CLINICAL STEPS IN FIXED PROSTHODONTICS Introduction Dental prosthetics is an extremely vast and complex specialty. Perhaps that's why it is studied over the course of four semesters during dental school. What every student should understand is that the concepts studied serve as the foundation for future clinical reasoning, which is essential in the practice of dentistry. Another particularly important aspect is the importance of interdisciplinarity and collaboration that must exist among all clinical specialties so that the therapeutic decision and the medical act itself are most appropriate for each patient. The last few decades have revolutionized all branches of dental prosthetics. The emergence of new technologies, new equipment, and new concepts has made it possible to carry out more predictable, precise, and efficient treatments. Fixed dental prosthetics are extensively covered by international experts in various books and treaties. This course is a concise and up-to-date version of the most important clinical aspects of fixed prosthodontics, structured into 9 distinct chapters. The ultimate goal is for the student to use these concepts to understand how to examine a patient, analyze all the data for the purpose of making a correct diagnosis, and then decide on an appropriate treatment plan for each patient. This includes performing fixed prosthetic treatment steps according to standardized protocols. The authors of this course dedicated to students have tried to contribute personally regarding iconography and those small but incredibly important tips and tricks that help novice practitioners perfect their clinical skills. Prof. Dr. Anca Jivănescu CHAPTER 1. EXAMINATION, DIAGNOSIS, AND TREATMENT PLAN FOR FIXED PROSTHETIC RESTORATIONS The clinical examination phase is extremely important in establishing a fixed prosthetic restorative treatment. It begins with taking the patient's history, which is recommended to be done in a different environment than the consultation room. The questionnaire primarily aims to determine whether the patient is a candidate for fixed prosthetic restorative treatment and whether they desire to change the design of their smile. The time allocated for the examination phase is usually directly proportional to the difficulty of the patient's aesthetic or functional issues. It is very useful for the patient to complete a questionnaire while waiting, which can help clarify these issues. Smile Self-Assessment Questionnaire? (according to RE Goldstein, Change your smile) | Question | 1. Are you confident in your smile? | 2. Do you prefer to be photographed only from a certain | side of your face? | 3. Do you believe someone in your circle has a nicer | smile than yours? | 4. Do you browse through magazines and wish you had a | smile like a model? | 5. When you look through magazines, does the smile | catch your attention first? | 6. When you look in the mirror, do you see any flaws in | your teeth or gums? | 7. Would you like your teeth to be whiter? | 8. Are you satisfied with the way your gums look? | 9. Do you feel that too many or too few teeth are | prominent when you smile? Yes No | 10. Do you feel that your gums are not prominent enough when you smile? | 11. Are your teeth too long or too short? | 12. Are your teeth too wide or too narrow? | 13. Are your teeth too straight or too round? | 14. Are you satisfied with the way your teeth are aligned? The patient's response should not be suggested by the doctor . If the patient answers "no" to every question except questions No. 1, 8, and 14, it means they are satisfied with their smile. Aesthetic evaluation begins with observing facial elements. Even if the teeth appear attractive individually, if they do not harmonize with other facial structures, the overall impression will not be aesthetic. To achieve aesthetic restoration, the dentist must understand the shape, texture, and color of natural teeth and how these teeth relate to other facial structures. This information must then be conveyed to the dental laboratory to create the desired restoration. The examination will be done from the frontal and sagittal views. Facial symmetry and the proportionality of facial planes will be examined, which are attributes of an attractive face. If perceptible abnormalities such as skeletal asymmetries are present, interdisciplinary consultation (orthodontist, maxillofacial surgeon) will be sought. In most cases, there is a reduction in the lower facial height due to dental wear or disturbances in the eruption of posterior teeth. Restoring the vertical dimension of occlusion will often lead to a substantial improvement in facial appearance. One of the simplest methods to evaluate facial aesthetics in relation to the vertical dimension of occlusion is to observe the patient from the front with the lips at rest and the mandible in a relaxed position. In the case of patients without skeletal asymmetries or dento-facial anomalies, this position generates optimal facial beauty. If closing into maximum intercuspation results in a decrease in aesthetic appearance, it indicates an incorrect occlusal vertical dimension, i.e., too small. Ideally, when the patient closes from the rest position to maximum intercuspation, there should be a minor change in facial appearance. In most cases, patients fall into one of these two situations: excessive vertical overclosure of teeth with a reduced occlusal vertical dimension, or a reduced occlusal vertical dimension due to excessive tooth wear. The next step is to evaluate the patient sagittal. In cases of Angle Class I relationship, the facial plane is slightly convex, the vertical line connects the glabella with the pogonion, and the subnasale point is in the middle of the distance between them. Facial profiles with excessively convex or concave appearances cannot be modified solely through dental restorations. If the patient insists on changing their facial appearance, cephalometric analysis will be required to confirm the skeletal diagnosis. In cases where patients have moderate to excessive dental wear, the facial profile conforms to Angle Class III occlusion, which is due to the forward and upward rotation of the mandible as the teeth wear down. Evaluating the sagittal position of the lips will provide information about skeletal and dental relationships. The nasolabial angle in Caucasians is 90-100 degrees for men and 95-105 degrees for women. Dental restorations, by positioning the teeth more vestibular or oral, may have a relatively small effect on lip position. The position of the upper lip is most influenced by the maxillary bone and the cervical third of the incisors. Major changes in lip position can only be achieved through orthodontic or orthognathic treatment. Plastic surgery is used to enhance lip contour and reduce the nasolabial angle. The lower edge of the nose can create an aesthetic problem, resulting in an abnormal nasolabial angle. If changing the nasolabial angle is necessary for aesthetic reasons, plastic surgery is required. The relationship between the nose, lips, and chin can be evaluated using one of the three reference lines (Ricketts, Steiner, Burstone), serving as a guide for the lower third of the profile. (Fig.1.1) Fig.1.1. Examining the profile highlights the nasolabial angle and the E-Rickets plane. If the maxilla is prominent, the nasolabial angle is below 90 degrees, and the profile is convex. In these situations, consideration will be given to creating smaller, less dominant restorations in the frontal area. If the maxilla is retruded, the nasolabial angle is above 90 degrees, the profile is concave, and restorations placed more vestibular and prominent can be crafted. The relationship of the lips with these lines can help formulate the diagnosis and treatment plan regarding the position of the anterior teeth and the alveolus. Using these lines will demonstrate whether the lip is anterior or posterior to the ideal position, providing indications for the positioning of the teeth and alveolus. Lips situated anterior to the reference lines necessitate a more posterior placement of the teeth and alveolus. Lips situated posterior to these lines require anterior traction of the maxilla or mandible. This should be done after cephalometric analysis and interpretation by a specialist. Aesthetic modifications of lip position and the lower facial height can be achieved through surgical, orthodontic, or prosthetic treatment. The next step in aesthetic analysis is assessing the relationship between the lips and teeth, i.e., the visibility of the teeth, both statically and dynamically. In a 30-year-old woman, the degree of tooth visibility at rest is approximately 3.5mm. Prosthodontists recommend that the visibility of the front teeth at rest should be approximately 2mm. Between 2 and 4 mm is the visibility range that achieves maximum aesthetic effect for a woman. The size and position of the teeth, the length and mobility of the lips affect the disposition of the teeth, both statically and dynamically. The average length of the maxillary central incisor measures between 10-11mm. The average length of the lip is 20-22mm measured from the base of the nose to the upper lip edge. The mobility of the lip in a normal smile is approximately 7-8mm. When a person smiles, the tip of the maxillary canine comes very close to or touches the lower lip, while the maxillary incisors are positioned approximately 2-4mm from the lower lip. This position is influenced by the curvature of the lower lip and the incisal plane. All anterior teeth are displayed in a smile, and often the first and second premolars, and sometimes even the molars. If the patient exhibits inadequate or excessive visibility of the teeth during a smile, then these three parameters, namely static and dynamic lip position and lip length, are critical factors during treatment. If the patient shows more than 4mm of the maxillary central incisors in repose and the teeth need to be lengthened, this will be achieved by elongating the incisal edge. If the degree of tooth visibility is 3-4mm and it is found that the teeth are too short, then surgical crown lengthening is necessary. If the degree of tooth visibility at rest is insufficient but the length of the incisors and the mobility of the lips are normal, and the teeth are not adequately displayed during a smile, this indicates insufficient vertical dimension of occlusion (VDO). In this situation, it is not desirable to elongate the crowns of the teeth, but rather, the occlusion must be evaluated and VDO needs to be corrected. If excessive display of the upper incisors is observed at rest, with normal lip mobility and lip length, and more than 3mm of the gingival margin is visible during a smile, orthognathic surgical treatment is indicated. In clinical situations where the degree of tooth visibility at rest is normal, tooth length is within normal limits, but there are discrepancies in terms of the smile line and the degree of tooth visibility, it is not recommended to perform restorative treatments that compromise their structural integrity. If there is a moderate or severe distortion of the smile line, orthodontic treatment is preferred. In an aesthetic smile, there is what is called negative space, which is a reduced space between the posterior maxillary teeth and the buccal mucosa. If the space appears excessive during a smile, it can be corrected by slightly increasing the vestibular contour of the posterior teeth, especially when prosthetic restorative treatment is necessary. If the negative space is too small due to an exaggerated convexity of the vestibular surface of the posterior teeth, the effect will be inaesthetic. Ideally, the dental midline (interincisal line) should overlap with the facial midline. This doesn't always happen, but it has been observed that deviations from normal in the dental midline do not have a significant effect on dentofacial aesthetics if the two lines are parallel. If the deviation of the interincisal line from the facial midline is less than 4mm and parallel to the facial midline, it may not be perceived as inaesthetic by others. Dental midlines can be corrected through orthodontic or restorative treatment. Regarding the proportions of the maxillary teeth, many authors recommend using the golden proportion to define their optimal width as they move away from the midline. The maxillary central incisors should be relatively symmetrical and generally dominate the smile but not excessively. Recent studies in the literature have shown that measurements of contemporary individuals' anterior teeth do not always adhere strictly to the golden proportion. The relationship between the central incisor and lateral incisor is closer to the golden proportion in an aesthetic smile. The optimal width of the lateral incisor is 62%-65% of that of the central incisor. The canine does not follow the golden proportion rule and is approximately 75% of the optimal width of the maxillary lateral incisor. The positions of the front teeth can vary, with one lateral incisor typically more rotated than the other, one may be more palatalized, etc., and canines are generally in different vertical positions and angled differently. Establishing the correct gingival relationship with the lips and teeth is essential in an aesthetic composition. The gingival line (free gingival margin), gingival color, and gingival papilla contour should be evaluated separately. To achieve an aesthetic effect, the gingival line of the anterior teeth should be relatively parallel to the horizon and relatively symmetrical on both sides of the midline. It is not critical for the gingival line of the lateral incisor to be lower than that of the central incisor if it is not noticeable when the person smiles. The gingival contour in the vestibular area should have a scalloped appearance. To systematize this data, it is useful to complete a facial aesthetics assessment form. Facial Aesthetics Assessment Form 1. Facial Analysis A. Broad Smile 1. Position of the interpupillary line relative to the occlusal plane: parallel / deviated to the right / deviated to the left 2. Relationship of the interincisal line to the facial midline: symmetrical / deviated to the right / deviated to the left 3. Lip relationship to the midline: symmetrical / deviated to the right / deviated to the left B. Lips at Rest 1. Upper lip thickness: thick / medium / thin 2. Lower lip thickness: thick / medium / thin 3. Lip position: prominent / retruded 4. Degree of tooth visibility at rest 5. Upper: _______ mm 6. Lower: _______ mm C. Profile 1. Nasolabial angle: normal approximately 90° / maxillary prognathism < 90° / maxillary retrognathism > 90° 2. Ricketts' E-plane (from nose to chin): upper lip 4 mm from the E-plane / lower lip 2 mm from the E-plane / within normal limits / convex / concave 4. Dental Analysis A. Proportion of central incisors (measured with a caliper) • Width-to-length ratio (W:L) > 80% (ideal: L=80% of W:L) / < 80% B. Proportion between central incisor, lateral incisor, and canine (golden rule: 1.6:1:0.6) • Central incisor width: _______ mm • Lateral incisor width: _______ mm • Canine width: _______ mm C. Axial inclination (draw on the diagram the degree of inclination) • Gingival characteristics and dental height (draw on the diagram) • Mucogingival problems / Gingival asymmetry 5. Diagnostic Information After examination and evaluation, you can proceed to complete an aesthetic assessment table to summarize the main aesthetic issues and requirements. Aesthetic evaluation table (circle the correct answer and fill in the columns). Aesthetic Issue | Yes | No ---------------------------------------|-------|------1. Gingival Height Asymmetry Location: | | | | ---------------------------------------|-------|------2. Black Triangles Location: | | | Yes | No ---------------------------------------|-------|------3. Gingival Color Changes Location: | | | Yes | No ---------------------------------------|-------|------4. Over contoured Crowns Location: | | | Yes | No ---------------------------------------|-------|------5. Poor Marginal Adaptation Location: | | | Yes | No ---------------------------------------|-------|------6. Acute Periodontal Conditions Location: | | Yes | No ---------------------------------------|-------|------- | 7. Tooth Mobility or Furcation Involvement | | | Yes | No Location: | | ---------------------------------------|-------|------8. Endodontic Lesions | Location: | | Yes | No ---------------------------------------|-------|------9. Occlusion: Incisal Wear, | Wear Facets Location: | | Yes | No | | ---------------------------------------|-------|------10. Continuous Canine-to-Distal | Progression (Curve Overlap) Location: | | | Yes | No | ---------------------------------------|-------|------11. Presence of Tremors Location: | | | Yes | No ---------------------------------------|-------|------12. Presence of Diastema Size: | | | Yes | No ---------------------------------------|-------|------13. Dental Crowding Location: | | | Yes | No ---------------------------------------|-------|------14. Cracked or Fractured Teeth Location: | | | Yes | No ---------------------------------------|-------|------15. Discolored Teeth Location: | | | Yes | No ---------------------------------------|-------|------16. Surface Texture | | Smooth | Yes | No Moderate | Rough | | | ---------------------------------------|-------|------- Detailed clinical examination should be supplemented with photographic examination, mainly focusing on detailing the three aspects: • Facial composition; • Dento-labial composition (lips, gums, and teeth); • Dental composition (teeth and gums). Fig. 1.2. Facial Composition Fig. 1.3. Dento-Labial Composition (Lips, Gums, Teeth) Fig. 1.4. Dental Composition (Teeth and Gums) Once the basic assessment has been completed, the dentist has the necessary information to establish a general diagnosis. Answering the five basic questions makes the diagnostic process straightforward. Diagnosis always begins with an analysis of the patient's face. If the gingival positioning is incorrect or the smile is asymmetric, then the treatment plan becomes interdisciplinary, and the five basic questions help determine the aetiology of the discrepancies. Question 1: What are the facial proportions and skeletal relationships? For a proportional (balanced) appearance of the face, the dimensions of the middle and lower thirds should be 1:1. If the lower third of the face is larger compared to the middle third, the general diagnosis will be excessive vertical maxillary (EMV). This patient exposes a significant portion of the gingiva both in the anterior and posterior areas. This condition is related to the growth and development of the maxilla and mandible. The mandibular ramus is usually short, resulting in an obtuse angle with the mandibular plane. The maxilla grows excessively so that the maxillary teeth occlude with the mandibular teeth. If EMV leads to significant functional and/or aesthetic problems, the primary treatment is orthognathic surgery. This involves a Le Fort I osteotomy followed by immobilization of the maxilla. In some cases, the mandible will naturally rotate into a favourable occlusal position with the maxilla. If the mandible does not find a correct occlusal position, bilateral sagittal mandibular osteotomy will be performed. Overly large maxillae and those with width discrepancies can be treated with multiple osteotomies. If the patient chooses not to undergo orthognathic surgery, Botox treatment (Allergan) can be used to mask excessive gingival exposure. If the lower third of the face is shorter than the middle third, this is usually due to insufficient vertical development of the maxilla. In cases where insufficient maxillary development leads to significant functional and/or aesthetic problems, the primary treatment is again orthognathic surgery. This procedure typically involves maxillary osteotomy and bilateral sagittal mandibular osteotomy. Finally, the anterior-posterior relationship between the maxilla and mandible should be evaluated. Ricketts' aesthetic line (E-line) is a useful tool for assessing this relationship. In a sagittal view, a line is drawn from the nose to the chin. In a 1:1 representation of a young face, the upper lip should be 2 to 4 mm behind the line, and the lower lip should be 0 to 2 mm behind the line. A normal facial profile is straight. If the lower lip is more than 2 mm behind the line, the facial profile is convex, indicating a Class II Angle malocclusion. If the lower lip surpasses the line, the facial profile is concave, indicating a Class III Angle malocclusion. Question 2: What are the length and mobility of the upper lip? Upper Lip Length The average length of the upper lip in young women (25-30 years) is 20 to 22 mm, and in young men, it's 22 to 24 mm. Age is important because as the patient ages, the upper lip tends to lengthen. Typically, the upper lip will lengthen by 1 mm per decade starting at the age of 40. If the upper lip is shorter than normal, a significant portion of the gingiva will be exposed during a wide smile. Surgical procedures can lower the upper lip, but these interventions are not routine. By modifying labial behaviour, the patient can reduce the mobility of the upper lip. They are instructed to look in a mirror and learn to smile in a way that exposes as little gingiva as possible. This is an effective procedure if the patient practices the exercise in front of a mirror and works only for the rehearsed smile, not for emotional smiles. The primary treatment for a short upper lip is Botox. It is injected into the elevator muscles of the upper lip, temporarily paralyzing these muscles. In some circumstances, dermal injection can be used for the treatment of a short upper lip. Lip mobility Normal mobility of the upper lip, measured from rest to a wide smile, is 6 to 8 mm. Ideal mobility moves the upper lip toward the gingival line (a line drawn from canine to canine at the gingival level) in a wide smile. A hypermobile upper lip can move well above the gingival line, exposing a significant portion of the gingiva. Although not specifically related to sex or age, women tend to have greater lip mobility. When a hypermobile upper lip is encountered, it is often related to a longer upper lip, and the treatment options are limited. The patient should be aware that the upper lip is longer than normal and will continue to lengthen with age due to collagen loss and decreased muscle tone. A rarely used treatment is shortening the lip with plastic surgery, indicated only if the issue is a major aesthetic disadvantage for the patient. On the other hand, lengthening the incisal margins of the maxillary anterior teeth can be performed to make them more visible both at rest and in a wide smile. However, this can lead to significant over-dimensioning of the incisal margins from the canine to the first premolar. To correct excessive upper lip length, extensive coronal reshaping dental procedures are needed. Once the basic evaluation has been conducted, the dentist has the necessary information to obtain a general diagnosis. Getting answers to the five basic questions makes the diagnostic process straightforward. Diagnosis always begins with analysing the patient's face. If the positioning of the gums is incorrect or the smile is asymmetric, then the treatment plan becomes interdisciplinary, and the five basic questions help determine the aetiology. Hyperactive Upper Lip: The normal mobility of the upper lip, measured from rest to a wide smile, is 6 to 8 mm. Ideal mobility moves the upper lip towards the gingival line (a line drawn from canine to canine at the gingival level) during a wide smile. A hypermobile upper lip can move well beyond the gingival line, exposing a significant portion of the gum. Although not specifically related to gender or age, women tend to have greater lip mobility. When increased lip mobility is combined with anatomically shorter lips, increased gum exposure is more common, particularly in women compared to men. Botox injections, lip behaviour education, and plastic surgery can be helpful in this case. The hypertrophied nasal septum depressor muscles are sectioned, resulting in reduced lip mobility at the midline. However, this procedure does not address other facial muscles that can continue to cause significant lip mobility. Hypomobile Upper Lip: Reducing lip mobility can negatively affect smile dynamics. There are two different types of hypoactive smiles. First, the patient does not want or know how to smile normally. The patient may adopt a hypoactive smile to cover up an aesthetic deficit. Treating this deficiency creates the possibility of developing a more dynamic smile. If the patient does not know how to smile normally, lip muscle tonicity exercises should be performed to increase lip mobility. In the second type of hypoactive smile, the patient cannot smile too much. Often, the upper lip elevator muscles are limited due to the strong activation of the upper lip depressor muscles. If the depressor muscles are treated with Botox, the elevator muscles can increase upper lip mobility. Question 3: What is the relationship between the gingival line and the horizontal plane? When positioned correctly, maxillary anterior teeth exhibit symmetry with the gingival line. This is a line drawn from the gingival margin of a canine to the gingival margin of the contralateral canine. The central incisors should be in line, and the lateral incisors can be in line or up to 1.5 mm below the line, and this line should be parallel to the horizontal plane. Posterior teeth should maintain the same horizontal symmetry. When teeth erupt excessively/continuously, with alveolar process, a gingival line that is no longer straight but becomes straight and concave appears. It occurs more frequently in the anterior teeth, but it can occur anywhere in the oral cavity, involving a variable number of teeth. Continuous eruption generally occurs in three cases: 1. Continuous tooth eruption due to improper occlusal contact (Class II Angle malocclusion) or lack of antagonists. 2. Continuous tooth eruption due to attrition. 3. Occlusal plane modification due to excessive eruption or attrition. As teeth erupt, the dentogingival complex moves with them, resulting in an inaesthetic gingival line. There are three primary treatment strategies for this situation. The first and generally most desirable treatment is orthodontic intrusion of the teeth to their initial position. If continuous eruption occurred due to a lack of occlusal contact, the teeth may not require coronal restoration after intrusion. However, long-term retention of intruded teeth needs attention. This can be achieved by either establishing a new occlusal relationship with the presence of antagonists or by using a fixed or removable retention appliance. If extrusion occurred due to attrition, teeth would require coronal restorations at the completion of orthodontic treatment. A more traditional but generally less desirable treatment in a patient with dental wear is surgical crown lengthening and reestablishment of the initial gingival line position before restoration. There are several disadvantages to this treatment. Firstly, the surgical intervention will expose root surfaces, resulting in a less favourable surface for adhesive restorations. Secondly, due to the narrower root diameter, definitive restorations will have a triangular shape, which is less aesthetic. Thirdly, surgical intervention results in gingival margins with a more bulging appearance rather than a knife-edge appearance. The gingival margin should terminate on enamel, but when moved onto root surfaces, it will not heal in a knife-edge fashion. Lastly, surgical crown lengthening requires the removal of interproximal alveolar bone, typically resulting in open gingival embrasures. Ultimately, osteotomy will lead to an increased crown-to-root ratio. The third treatment option is to increase the vertical dimension of occlusion through orthodontic treatment or coronal restorations. This procedure does not directly treat excessive dental eruption. However, it provides interocclusal space for coronal restorations in patients with secondary attrition-related excessive dental eruption. Question 4: What is the length of the maxillary central incisor? When the maxillary central incisor is shorter than average (10-11 mm), there are three compatible aetiologies: 1. Microdontia 2. Loss of incisal length due to attrition 3. Pathological passive eruption If the aetiology is microdontia, the teeth will be proportionally smaller, and the enamelcement junction may be located in the sulcus. If the aetiology is the loss of incisal length due to attrition, the normal anatomy will be altered. If the aetiology is pathological passive eruption, the diagnosis should be made based on the response to question #5. Question 5: Is the enamel-cement junction palpable in the gingival sulcus? If the measured tooth is short, and the enamel-cement junction cannot be determined with a probe within the sulcus, the aetiology is pathological passive eruption. The gingival tissue has not migrated to its correct position, 1 to 2 mm from the enamel-cement junction, leading to excessive enamel coverage. The normal process of passive eruption is completed by the age of 15-16. Pathological passive eruption is surgically treated through crown lengthening surgery. Classification of Partial Edentulism In the case of partial edentulism, the prosthodontic diagnosis should take into account a universally accepted classification system. The most important classifications are: 1. Kennedy Classification 2.ACP Classification (American College of Prosthodontics) The Kennedy Classification comprises 4 classes: 1. Class I: Bilateral edentulous areas. 2. Class II: Unilateral edentulous areas. 3. Class III: Edentulous areas with teeth remaining both anterior (mesial) and posterior (distal). 4. Class IV: Edentulous areas in the anterior region on both sides of the midline. Applegate established some rules for applying the Kennedy Classification: • Non-recoverable teeth with extraction indications are not considered for classification (they are considered missing teeth). • Absent teeth that will not be prosthetically replaced are not considered for classification. This situation usually pertains to third molars or second molars without antagonists. • The most posterior (distal) edentulous space determines the class of edentulism. • Any additional edentulous space is termed as modification. • The extent and/or location of modifications are not specified. • Class IV does not present modifications ACP Classification of Partial Edentulism (American College of Prosthodontists) Within this classification, there are 4 diagnostic criteria: 1. Extent and topography of edentulous spaces 2. Condition of abutment teeth 3. Occlusal relationships 4. Edentulous ridges Each diagnostic criterion can be categorized into four classes: • Class I: Ideal or Minimal Impairment • Class II:Moderate involvement • Class III: Substantial involvement • Class IV: Severe involvement Criterion 1 – Extent and Topography of Edentulous Spaces Class 1 - Ideal or Minimally Affected Arches by Edentulism Single edentulous space located in a single arch that meets one of the following conditions: • Any maxillary frontal edentulous space that does not exceed 2 incisors • Any mandibular frontal edentulous space that does not exceed 4 incisors • Any maxillary or mandibular lateral edentulous space that does not exceed 2 premolars or one premolar and one molar Class 2 - Moderately Affected Arches by Edentulism Edentulous spaces present in both arches and meet one of the following conditions: • Any maxillary frontal edentulous space that does not exceed 2 incisors • Any mandibular frontal edentulous space that does not exceed 4 incisors • Any maxillary or mandibular lateral edentulous space that does not exceed 2 premolars or one premolar and one molar • Absence of a maxillary or mandibular canine Class 3 - Substantially Affected Arches by Edentulism • Any maxillary or mandibular lateral edentulous space involving more than 3 teeth or including 2 molars • Any anterior or posterior edentulous space involving more than 3 teeth Class 4 - Severely Affected Arches by Edentulism • Any edentulous space or combination of edentulous spaces requiring increased therapeutic compliance from the patient. Criterion 2 – Condition of Abutment Teeth Class 1 - Ideal or Minimally Affected Abutment Teeth: • No preparatory treatment is required Class 2 - Moderately Affected Abutment Teeth: • Insufficient dental structures to support intracoronal restorations in 1-2 sextants • Abutment teeth require limited preparatory treatment (periodontal, endodontic, orthodontic, etc.) in 1-2 sextants Class 3 - Substantially Affected Abutment Teeth: • Insufficient dental structures to support intra-coronal restorations in 3 sextants • Abutment teeth require limited pre-prosthetic treatment (periodontal, endodontic, orthodontic, etc.) in 3 sextants. Class 4 - Severely Affected Abutment Teeth: • Insufficient dental structures to support intra-coronal restorations in 4-6 sextants • Abutment teeth require limited preparatory treatment (periodontal, endodontic, orthodontic, etc.) in 4-6 sextants • Abutment teeth with a reserved prognosis. Criterion 3 – Occlusal Relationships Class 1 - Ideal or Minimally Affected Occlusal Relationships: • No occlusal preparatory treatment is required • Inter-arch and intermaxillary relationships of Class I Class 2 - Moderately Affected Occlusal Relationships: • Limited occlusal preparatory treatment is required, such as selective occlusal interference removal through grinding • Inter-arch and intermaxillary relationships of Class I Class 3 - Substantially Affected Occlusal Relationships: • Reconstruction of the occlusal scheme without altering the vertical dimension of occlusion • Inter-arch and intermaxillary relationships of Class II Class 4 - Severely Affected Occlusal Relationships: • Reconstruction of the occlusal scheme, altering the vertical dimension of occlusion • Inter-arch and intermaxillary relationships of Class II division 2 or Class III. Criterion 4 – Edentulous Ridges For partially edentulous cases, the classification of edentulous ridges is made according to the criteria for complete edentulism. The table below systematically presents the classes and diagnostic criteria for partial edentulism according to the American College of Prosthodontists (ACP). Class I II III IV Alveolar process bone height At least 21 mm X 16-20 mm X 11-15mm X Up to 10 mm X Maxillary Edentulous Ridge Morphology Type A - Resists vertical and horizontal displacement, X pterygomaxillary groove without torus Type B - Reduced lateral vestibular height, erased X pterygomaxillary groove, no torus interfering with the distal border of the prosthesis Type C - Reduced frontal vestibular height, minimal support, X resilient frontal ridge Type D - Reduced frontal and lateral vestibular height, X posterior torus, frontal hyperplasia Mandibular Muscle Insertions Type A - Corresponding fixed mucosa X Type B - No fixed mucosa in the frontal area, mentalis X muscle Type C - No fixed mucosa in the frontal area, mentalis X muscle, genioglossus muscle Type D - Fixed mucosa only on the lingual side X Type E - No fixed mucosa X Mandibulo-Maxillary Relationships Class I X X X X Class II X X Class III X X Need for Pre-prosthetic Surgical Interventions Minor interventions on soft tissues X Minor interventions on hard tissues X Simple implants X Implants with augmentation X Correction of dentofacial malformations X Hard tissue augmentation X Extensive soft tissue remodelling X Reduced Inter-arch Space 18-20 mm X Surgical correction required X Tongue Anatomy Hypertrophy (occupies interdental space) X Hyperactivity - with posterior position X Aggravating Factors (Modifiers) Oral manifestations of systemic conditions Mild Moderate X X Severe X Psychosocial Factors Moderate X Major Cranio-Mandibular Disorders X X Paraesthesia / Dysesthesia X Maxillofacial Defects X Ataxia X Refractory Patients X Once the general diagnosis has been established, an interdisciplinary treatment strategy can be developed. Determining the regional diagnosis (pulp status, periodontal condition, TMJ status, etc.) contributes to the development of the definitive sequential treatment plan. Bibliografy: 1. Winston W.L. Chee, BDS Dent Clin N Am 48 (2004). 2. R.Goldstein. Change your smile. 2012. 3. Dorin Bratu, Robert Nussbaum. Bazele clinice si tehnice ale protezarii fixe. 4. McGarry TJ, Nimmo A, Skiba JF, Ahlstrom RH, Smith CR., Koumjian JH. Classification sistem for partial edentulism. J Prosthodont 2002. 5. Irfan Ahmad. Prosthodontics at a glance, Wyley 2015. 6. Robbins, Rousse. Global Diagnosis. Quintessence 2016. CHAPTER 2. COMMUNICATION METHODS DOCTOR-PATIENT-DENTAL TECHNICIAN The success of a prosthetic restorative treatment that fulfils optimal aesthetic and functional desires is based on a thorough examination and effective communication between the doctor and the patient, as well as between the doctor and the dental technician. Most dentists diagnose aesthetic problems using traditional means of radiography and clinical examination. The therapeutic decision is based on each doctor's own vision and experience. Clinicians' concepts of facial aesthetics may or may not coincide with patients' perceptions and desires. This is where most communication problems often begin. First and foremost, a therapeutic strategy, a systematic approach to aesthetic problems, must be mentally developed. This means identifying the problem and visualizing the therapeutic solution, together with the patient and the dental technician. Identifying problems requires a systematic analysis in three stages of the patient's aesthetic needs: • Aesthetic evaluation form; • Computerized simulation; • Diagnostic models and wax-up. Through visual explanations, images, photographs, and models, the risk of misunderstanding within the team of specialists (doctor-technician) or between the doctor and the patient is minimized. The most common classical means of visualization and communication are: • Study models; • Diagnostic wax or composite resin modelling; • Use of markers (outlining on the model or in the oral cavity); • Direct testing modelling in the oral cavity (with wax or composite resins); • Photographs of other patients with similar problems and their resolution methods. Unfortunately, these methods are often inadequate for helping the patient understand how a treatment or restoration will change their appearance or facial features. Most patients know very little about the potential of dental aesthetics, especially the limitations of aesthetic restorative treatments. Therefore, they sometimes have unrealistic expectations, which, if not clarified from the beginning, can lead to disillusionment, failures, and dissatisfied patients. The more efficient the communication with the patient, the greater the chances of successfully completing the treatment and satisfying the patient. Traditional doctor-patient communication methods have several advantages but also some disadvantages. Therefore, the most appropriate method should be selected based on the clinical situation. 2.1. STUDY MODELS Study models are the most common and frequently used means of communication with the patient, as well as with the dental technician. These allow the doctor to develop the treatment plan and analyse possible therapeutic alternatives. Unfortunately, these models have limited possibilities for demonstrating to the patient what is intended to be achieved with specialized treatment. In the absence of the color of natural teeth and surrounding tissues (lips, gingival tissues), the teeth in study models can hardly fit into a final image of dentofacial aesthetics. Often, patients cannot imagine what can be achieved in the end by just observing these monochromatic models. (Fig. 2.1.) Fig. 2.1. Rarely can patients visualize treatment results on study models. 2.2. DIAGNOSTIC MODELING ON STUDY MODELS (WAX-UP TECHNIQUE) Modifications performed on study models involve the sectioning or repositioning of crowded or spaced teeth, with or without the addition of wax, to simulate the expected treatment results. Wax-up diagnostic model represents a precise method for measuring and assessing tooth proportions. Although it efficiently facilitates communication between the dentist and the dental laboratory, diagnostic model entails additional costs, especially in terms of time. Moreover, it often cannot convincingly visualize for the patient the goals of aesthetic treatment. On the study model, wax or resin will be added to conform to certain facets (Fig. 2.2). These can subsequently be tested in the patient's oral cavity and serve as a useful guide when elongating clinical crowns or altering the shape and position of teeth. If mutually agreed upon by the dentist and the patient, they can be used as a model for the final restorations. Fig. 2.2. Because wax or resin diagnostic models come in different colors (green, yellow, blue), patients may have difficulty visualizing treatment results. 2.3. SIMULATION OF CORONAL CONTOURS USING IN-MOUTH MARKERS Alcohol-soluble markers provide a simple and cost-effective way to highlight minor changes in tooth shape. By using a black marker on the dry tooth surface, the areas that need to be removed can be outlined. When the patient looks into a mirror from a distance of 30cm, can visualize the effects of cosmetic contouring, as the black color of the marker matches the background of the oral cavity behind the teeth. This technique can easily simulate the removal of dental tissues and cosmetic reshaping but cannot highlight other treatments such as whitening or veneers. Fig. 2.3.a. Initial situation. b. Using a black marker to simulate necessary coronal reshaping. In this case, simple subtractive reshaping is insufficient, so diagnostic model(diagnostic cast) is required. 2.4. PHOTOS OF PATIENTS WITH SIMILAR ISSUES A common and effective way to present therapeutic solutions is by creating albums with photos of other patients who have had various dental aesthetic issues and how they were resolved. These albums can be made available to the patient in the waiting room, serving as an educational and informative tool. Through the photos in the albums, we can showcase the therapeutic options available and actively involve the patient in the treatment plan. These photos of other patients are impersonal and can only be considered a starting point that can enhance the patient's understanding of aesthetic treatments. However, for the patient, it may be challenging to imagine how their aesthetic appearance will change with the planned treatment just by looking at pictures of other patients with similar issues. Fig. 2.4. Photos of other patients with similar situations can be suggestive for visualizing therapeutic possibilities: a. Initial situation; b. Final smile. 2.5. DIRECT IN-MOUTH TESTING MODELS (MOCK-UP TECHNIQUE) If contour changes to the teeth are required through addition, they can be done directly in the patient's oral cavity using tooth-colored wax or composite resin. These are molded directly onto the tooth surface, and this technique is called mock-up. The technique is quite time consuming and cannot be used when orthodontic or periodontal surgery is required. Fig. 2.5. By modelling with white wax or composite resin directly on the tooth surface, certain coronal reshaping can be simulated. There are several basic rules for diagnostic cast based on specific aesthetic principles: • Start with the central incisors, which are considered dominant teeth (the width/height ratio is 80%). Provide the technician with information about the tooth's length as determined during the aesthetic analysis. • Aim for symmetry with respect to the midline. • Apply the golden proportion principle for correct tooth modelling. • Apply the principle of distal axial inclination direction. • Incisal embrasures should progressively increase in size from incisors to premolars. • Model angular lines parallel to the long axis of the teeth. • Model incisal contour and texture according to age and gender. • Ensure the correct positioning of gingival height and gingival zenith. 2.6. TESTING PROVISIONAL RESTORATIONS For patients seeking a highly customized outcome in aesthetic restorative treatment, more detailed visualization methods are required. One such method involves creating a conformer using the thermo-vacuum forming technique, made from transparent foil over a study model. Resins matching the tooth or gingival tissue color are applied to this conformer to simulate the desired changes. This so-called diagnostic prosthesis can produce a realistic effect of the intended modifications, both in terms of color, shape, and tooth position. In cases of patients with protruding front teeth, this method is contraindicated, as it will exacerbate the malposition and have the opposite effect to the desired one. This technique is even more time consuming than diagnostic wax modelling. It is recommended only for very demanding and difficult patients who want to know the exact aesthetic final result. Naturally, these patients will incur additional charges. In more challenging situations involving radical changes to smile design, it is advisable to create a provisional test restoration. This allows for effective communication with both the patient and the dental laboratory. With this method, the patient can directly visualize changes in tooth shape and size and participate in potential adjustments through suggestions. Through these provisional restorations, the patient does not need to rely on imagination ("how will the restoration look?") but can see the modification of the smile design directly in the oral cavity. In addition to aesthetics, phonetics (fricative and sibilant sounds) can be checked, and, in the end, comfort and the impact on the patient's psyche are evaluated. It is recommended that until the patient accepts the provisional restoration, the definitive restoration should not be initiated. Once the provisional restorations are accepted, they will be duplicated in the laboratory and serve as a guide for creating the final restorations. Below is a case of a patient who requested replacement of an unsatisfactory fixed prosthesis in the frontal zone (Fig.2.6). After diagnostic wax modelling and the creation of a putty silicon key (Fig.2.7), the provisional restoration was fabricated (Fig.2.8). Only after the patient expressed satisfaction with the shape and arrangement of the teeth did we proceed with the definitive restoration (Fig.2.9). Fig.2.6. Patient requiring a change in smile design. Fig.2.7. Provisional test restoration. Fig. 2.8. Temporary Test Restoration in the Oral Cavity Fig. 2.9. Definitive Restoration a. on the Model and b. in the Oral Cavity 2.8. OTHER MEANS OF COMMUNICATION WITH THE LABORATORY Most often, to facilitate communication and visualize the effects of aesthetic treatments, two or three of the mentioned methods are combined. In the case of patients with multiple aesthetic issues, such as diastema in the maxillary teeth, crowding of the mandibular front teeth, and the need for coronal contouring, multiple visualization and communication methods are necessary. In these situations, both diagnostic wax modelling or resin modelling for closing diastemas and modelling for coronal contouring of the lower front teeth are needed, and finally, marking new demarcation lines (e.g., shortening some teeth, shifting proximal lines). Certainly, all these methods require a lot of time and skill on the part of the dentist. Often, the dental laboratory is not immediately adjacent to the dental office, and the dental technician is not always available. Therefore, it is necessary to transmit explicit data related to the patient and what is desired as the outcome of aesthetic restorative treatment. The most common means of communication with the dental laboratory are: • Digital photography • Modified shade guides • Lip impression 2.8.1. DIGITAL PHOTOGRAPHY The popularity of digital photography in the field of dentistry has increased in recent years. This method offers several advantages and benefits in our profession. It is relatively easy to use, with the dentist requiring basic knowledge of photographic techniques and computer use to maximize its potential. Currently, it cannot be said that the digital photography method is standardized. Digital cameras interpret color differently, making standardization difficult. Factors such as lighting, the angle at which the photo is taken, and environmental factors will alter color perception. It is essential to use digital photography as an adjunct to other techniques and take several serial photos using proper lighting to provide as much necessary color analysis information as possible. To use the information provided by digital photography effectively, several factors should be considered. Firstly, it is advisable to use different backgrounds (usually a neutral gray background) and take photos from different angles. Vectorization involves taking photos from different angles to visualize interproximal areas of enamel unsupported by dentin without the yellowish-red reflection of proximal teeth. It has been found that an angle of 67-70 degrees with the buccal surface of the tooth is best for highlighting hue and saturation. For brightness, a 90-degree angle should be used. Through digital photography, various facial parameters can be communicated, such as facial shape, profile, lip tone, relationships with the gingival margin, incisal length, translucency degree, or other characteristics. To capture tooth shape and color more accurately, it is recommended to use higher zoom levels, holding the teeth from the shade guide close to the respective tooth. Fig.2.10. With the help of digital photography, the dentist can convey certain color, translucency, and texture characteristics. For surface shape and gloss, the teeth should be cleaned and dried; then, images should be captured perpendicular to the tooth surface. A dark-colored background should be used to increase contrast. It is quite challenging to distinguish whether a tooth has low gloss, is dehydrated, or has undergone a bleaching process, but this issue can be clarified through anamnesis. When lenses are positioned perpendicular to the tooth surface, light can reflect to the camera like a mirror. Using a polarized light filter will cancel out the reflected light, making color determination easier. Brightness can be more easily appreciated in blackand-white photos. Images should be captured at a 1:1 ratio to capture surface characteristics. For accurate color recording, it is desirable to use a dual (bilateral) flash with color correction. The optimal settings for DSLR digital cameras are as follows: F-Stop = 28-32; manual settings; shutter speed = 1/25-1/250; ISO = 100-200, manual focus. Fig. 2.11. Digital camera with dual bilateral flash. To highlight the degree of translucency, photos should be overexposed, a black background should be used, and photos should be taken at a 60-degree angle. To observe the degree of opalescence through photos, certain conditions must be met; this will allow for precise measurement of enamel thickness for future ceramic restorations. A dark background will reduce reflection, which is accentuated by the flash. Red color reflections come from soft tissues, pass through the enamel, mix with the blue ones, greatly reducing the opalescence effect. If a black background is used, the contrast between the blue opalescence of the enamel and the red-yellow underlying dentin is increased. Exposure variations are called bracketing and can be done in several ways, most commonly by adjusting the aperture. Closing the aperture allows less light to pass to the digital sensors. For a photograph to be as useful as possible in transmitting color, it is recommended to use different backgrounds, angles, and apertures. Surface texture and gloss can have a significant effect on the final restoration's appearance. If these characteristics are not accurately replicated, many restorations will not have a natural appearance, even if the color is suitable. The smoother the tooth surface (and more reflective), the brighter it appears. To counteract this issue, some cameras use filters to eliminate surface gloss. Systems that do not use such filters record overly high brightness values, which can have undesirable effects on the aesthetics of the future restoration. 2.8.2. MODIFIED SHADE GUIDES Natural teeth do not have a uniform color, making it challenging to find a perfectly matching shade in existing shade guides. In cases where an appropriate color cannot be found in the shade guides, modified shade guides are used. A tooth with higher brightness (V) and lower saturation (C) values is selected from the shade guide. On this sample, prepared with a bur to create a rough surface, surface colors are applied to modify the color, making it as similar as possible to the natural tooth. This sample is sent to the laboratory and serves as a perfect guide for selecting the color of the future restoration. This method is useful, especially when a highly individualized restoration is desired with various special effects, such as mimicking fissures, proximal discolorations, decalcification white spots, etc., or in the case of covering a single incisor that must harmonize perfectly with its counterpart. (Fig.2.12.a,b). F Fig. 2.12. a. Pigments are applied to the tooth's surface on the shade guide to transfer all surface characteristics to the laboratory. b. Selecting the color with the modified tooth from the shade guide. No matter how accurate an impression is, it is not possible to reproduce the surface texture precisely on plaster models. Even high-quality photographic images do not provide conclusive information about the texture and gloss of natural teeth. To provide the technician with the most precise information regarding these characteristics, teeth from denture sets with gloss and texture as similar as possible to natural teeth can be selected and sent to the laboratory. These will serve as a guide for the future restoration. 2.1.9.3. LIP IMPRESSION AND FACIAL MASK In an aesthetic treatment plan, obtaining a lip model can be very useful. Lip impression is usually done with standard materials, typically irreversible hydrocolloids. The lip model, or the so-called facial mask, represents a three-dimensional model that is applied directly to the models mounted in the articulator. These models will serve as a guide for the technician to evaluate and modify the smile line, occlusal plane, oral corridor, tooth and gingival display mode. One of the most well-known systems for lip impression and facial mask creation is the Kalco system from Zhermack, which includes special impression spoons, impression material (alginate), and silicon used to create the facial mask. After lip impression with the impression spoon and irreversible hydrocolloid, the facial mask is created, which is applied to the models mounted in the articulator. This will be an important guide for the technician in creating the fixed prosthesis. Fig.2.13. Impression spoons (Kalco system). Fig.2.14. Lip impression with alginate. Fig. 2.15. Lip impression after removal from the oral cavity. Fig. 2.16. Facial Mask on the Articulator Fig. 2.17. Achieving prosthetic restoration and testing in the articulator with a facial mask. Lip impression is essential when aiming for a change in the position of the upper front teeth. With its help, a diagnostic cast can be achieved in a more realistic position. In cases of immediate complete denture placement, the model obtained through lip impression can be used to achieve a more natural arrangement of teeth in the prosthesis, as it provides valuable information regarding the smile line, position of the lower lip, buccal corridor, and midline. The conventional means and methods described in this chapter are accessible to any practitioner, but they often require a significant amount of time and may not always yield conclusive results. Virtual simulation (Digital Smile Design) Computerized imaging represents a modern, more sophisticated, yet much faster and efficient alternative for patient evaluation and communication. Dentists can currently take advantage of the benefits offered by the integration of digital technologies into the routine of dental laboratories, such as the so-called virtual or digital wax-up and digital surgical guides. To encourage patient involvement and active participation in the treatment plan development, it's advisable to perform computerized simulations right in front of the patient. Certain modifications, such as teeth whitening, cosmetic contouring, or tooth replacement, can be done quickly, in a matter of minutes, right in front of the patient. However, there are certain situations that require a more careful study of captured images, and in many cases, it's beneficial for the dentist to perform the simulation in the absence of the patient (14). There are indeed several virtual smile design systems available, ranging from the classic Digital Smile Design (DSD) introduced by Christian Coachman to those associated with CAD/CAM systems (e.g., Cerec Smile Design, Romexis Smile Design, Medit Smile Design). CHAPTER 3. PREPROSTHETIC TREATMENT Edentulism refers to the absence of one or more dental units, which can vary in terms of location, frequency, or extent. Depending on the location, size, and duration of the edentulous space, disturbances can occur in all functions of the stomatognathic system, including mastication, phonation, and aesthetic function. Following the loss of a tooth over time, a series of changes occur. These changes lead to the atrophy of the alveolar ridge in the affected area, migration of adjacent teeth towards the edentulous space, the development of parafunctional muscle activity resulting in the formation of wear facets. Depending on the body's ability to adapt to the new situation, temporomandibular joint dysfunction may develop consequently (1). The migration of adjacent teeth towards the edentulous space can occur horizontally due to the available space and lack of support, thus disrupting the position of teeth within the arch. This tilting of adjacent teeth creates additional areas for food retention, which are difficult to clean. The change in the axis of the teeth results in a non-physiological distribution of occlusal forces, which were originally aligned with the long axis of the tooth until the edentulous space and tooth tilting occurred (Fig. 1, 2). The action of the force arm, which shifts eccentrically from the long axis of the tooth during tilting, combined with food retention and the negative impact of food impaction, can lead to the development of periodontal lesions such as periodontal pockets. Over time, these pockets can lead to the loss of adjacent teeth to the edentulous space. Additionally, there is a disturbance in the balance of the opposing dental arch, where the tooth opposing the edentulous space begins to migrate vertically. This vertical movement can be of two types: - Egression, where the tooth moves vertically, bringing the alveolar bone along with it. - Extrusion, where the tooth migrates vertically while the alveolar bone remains in its original position. When dental extrusion begins, if timely intervention is not carried out, it can lead to the exposure of the root portion of the tooth. This results in dental sensitivity because the cementum layer covering the tooth's root is porous and lacks the ability to isolate the enamel from the aggressive factors in the oral cavity. The porous structure of root cementum significantly increases susceptibility to dental caries. Fig. 3.1. Migration of teeth in the horizontal and vertical planes. Fig. 3.2. The loss of the canine resulted in the tilting, mesialization, and vertical migration of the upper premolar. In these two types of vertical migration of antagonistic teeth in the edentulous gap, if timely intervention is not carried out, they can continue until they encounter the edentulous ridge and may cause ulcerative lesions that accentuate vertical bone loss in the edentulous ridge. Furthermore, the vertical migration of antagonistic teeth in the edentulous gap can disrupt mandibular propulsion movements, blocking this type of movement. Any treatment plan and any pre-prosthetic therapy should be guided, according to Körber (4), by the following 12 questions: 1. What is the extent and topography of the edentulous gaps? 2. Is the occlusal relief intact or not? 3. What is the periodontal status of the abutment teeth? 4. Is it necessary to immobilize the remaining teeth? 5. Are occlusal relationships normal or pathological? 6. Are occlusal ratios physiological or not? 7. Is mandibular dynamics disturbed or not? 8. Are occlusal stops multiple, symmetrical, and uniform? 9. Is neuro-muscular function normal or disturbed? 10. What is the quality of oral hygiene? 11. Is preventive action needed for dental caries of the remaining teeth? 12. Does individual aesthetics need improvement or not? Prosthetic treatment is dictated by: - The number of remaining teeth. - Their topographical arrangement. - The existing occlusal stops. - The periodontal status of each abutment tooth. The analysis of occlusal relief integrity is performed both in the oral cavity and, more accurately, on study models that must faithfully represent the situation in the oral cavity. Prosthetic restoration should precisely replicate the occlusal relief of the opposing teeth (5). In cases where both arches are being treated, fixed prosthetic restorations for each arch will be designed in an articulator, considering the principles of functional occlusion and the individual characteristics of mandibular position and movements. 1. Preprosthetic Periodontal Treatment The periodontal status of the future abutment teeth is crucial for the long-term success of the upcoming restoration. Before commencing any prosthetic treatment, it is essential to provide appropriate periodontal therapy for each abutment tooth. In cases where teeth exhibit pronounced mobility, this can be reduced through guided tissue regeneration techniques and endodontic treatment for teeth with this issue. For teeth with periodontal conditions, it is crucial to reduce the force arm and direct occlusal forces along the long axis of the abutment teeth by establishing functional occlusion. Malocclusions result in the mobilization of abutment teeth. Abutment teeth that are mispositioned (tilted, egressed, extruded) can be orthodontically corrected if the patient is willing to accept the treatment plan. Teeth with significant mobility should be temporarily stabilized during preprosthetic treatments to prevent dental migration and promote tooth stability until the periodontal therapy is completed. Normally, patients have two types of occlusion: - Point centric, where the MIP (Maximum Intercuspation Position) coincides with the CR (centric relation). - Long centric, where MIP does not coincide with CR. Some patients may have interferences that lead to lateral, protrusive, or retrusive jaw movements. These interferences should be identified and eliminated during preprosthetic treatment so that the patient can adapt comfortably. When assessing mandibular dynamics, the patient should perform mouthopening movements. In cases where there is asymmetry in the movement, it may be due to myalgia or arthralgia or prolonged functional disorders that need to be identified and addressed. Patients who do not maintain proper dental hygiene should be motivated to achieve proper hygiene. Otherwise, prosthetic restoration will have a limited lifespan. Before commencing prosthetic treatment, the entire oral cavity should be cleaned, and all carious lesions must be removed. In the stage of selecting abutment teeth, the following factors should be considered (1): a) Status of the dental crowns: - Intact - With lesions - With restorations - Absent b) Root morphology c) Crown-to-root ratio d) Endodontic status: - Vital teeth - Non-vital teeth - Teeth with complete or incomplete root canal fillings - Teeth with apical resection e) Tooth implantation: - Normal - Tilted - Twisted When selecting an abutment tooth, its crown may not always have an ideal morphology and may present carious lesions, dystrophies, traumatic injuries, which need to be corrected through reconstruction. Thanks to new materials and modern techniques, most of these crown lesions can be restored. Crowns with extensive and deep lesions can also be salvaged. These may require: - Endodontic treatment, followed by the reconstruction of the coronal portion using corono-radicular devices that can be custom-made in the dental laboratory or prefabricated metal or non-metal devices like posts. - In cases of short clinical crowns due to dental abrasion or when crown lesions extend subgingival, surgical lengthening is necessary to increase the retention surface for the future crown. - Guided by the principle that the edge of the future prosthetic restoration should be supported by healthy dental tissues, in cases where crown lesions extend subgingival, the same approach is adopted, and crown lengthening is extended beyond the restored area to achieve the effect of encirclement or ferrule effect. There are two ways to achieve crown lengthening: either through gingivectomy or through gingivo-alveoloplasty. Gingivectomy is typically performed in cases of gingival hyperplasia and can be done using: - A scalpel - Electrocautery - Laser - Zirconia oxide burs for mucosal procedures. Gingivo-alveoloplasty is performed when a greater crown lengthening is required, and intervention on the alveolar bone is necessary for remodelling. Both crown lengthening procedures are also used in situations where, for aesthetic reasons, it is necessary to modify uneven gingival margins to achieve a special aesthetic effect in patients with a gummy smile. To ensure predictable results, surgical guides and provisional restorations should be used to guide the healing process. The root configuration of the abutment tooth influences its value because all occlusal forces acting on it are transmitted to the alveolar bone through the root. Oval or flattened roots with a greater buccal-oral diameter than mesio-distal ones are more valuable than round roots in cross-section. Molars with divergent roots provide better periodontal support than molars with converging roots and a conical shape. Fig. 3.3. The molar with divergent roots (a) is a more valuable abutment than one with fused roots (b). The buccal-oral diameter of the root of the maxillary premolar (a) is larger than that of the maxillary central incisor, which has a spherical root in cross-section (b). This makes the premolar a more valuable abutment tooth, even though both have the same root surface area. In the case of single-rooted teeth, those with long roots and potential curves in the apical third are preferred. In the situation of multi-rooted teeth with periodontal issues, there are significant challenges in achieving prosthetic restoration. The biggest problems arise when the periodontal lesion leads to exposure of the furcation because it is very difficult for the clinician to access the area for scaling and root planning, and on the other hand, the patient cannot properly clean this area. If these two problems can be satisfactorily resolved, these teeth have a better prognosis than a single-rooted tooth with the same degree of implantation. The root morphology of the abutment tooth is crucial in the periodontal therapy preceding prosthetic treatment. SRP (scaling and root planning) is the treatment of choice for achieving therapeutic success. Ideally, attempts should be made to achieve guided tissue regeneration through bone augmentations and connective tissue grafts to cover these defects and increase the degree of implantation of these teeth. The crown-to-root ratio is represented by the length of the crown measured from the incisal or occlusal edge of the tooth to the level of the alveolar crest, relative to the length of the intraosseous root. Ideally, the crown-to-root ratio is 1/1.5-2. The minimum acceptable ratio for abutment teeth is 1/1. In the presence of an equal periodontal ligament space, the displacement of the crown of a tooth with reduced bone support is greater than that of a tooth that has not experienced bone loss (Nyman and Lindhe). Root exposure is considered a pathological retraction of the supporting periodontal tissue that occurs because of minor or major periodontal conditions. This periodontal retraction alters the clinical crown-to-root ratio. During repeated marginal gingivitis and periodontitis, gingival retraction and alveolar bone loss occur, leading to a decrease in the degree of implantation of the tooth in the alveolar bone. As a result, the extracoronal force arm of the tooth increases, amplifying the harmful forces acting on the tooth. A crown-to-root ratio less than 1/1 is only accepted in cases where the antagonists of fixed restoration are represented by artificial teeth (complete dentures). In the case of teeth with periapical pathology that can be resolved through conservative endodontic treatment, the crown-to-root ratio will not be affected. However, when periapical pathology can only be resolved surgically, efforts should be made to minimize the amount of root resection so that the crown-to-root ratio is minimally influenced. The endodontic status of these abutment teeth is a crucial element in their selection. The preference is for using vital abutment teeth. However, in many situations due to past carious conditions, direct pulp capping, migrations, torsions, or lack of parallelism, pulpectomy may be necessary for prosthetic purposes to prevent complications resulting from pulp necrosis. This is because addressing endodontic problems later requires perforating the prosthetic restoration to gain access to the root canals. The loss of hard dental tissues by creating an access cavity for subsequent endodontic treatment results in undermining the resistance of the abutment tooth, and crown perforation reduces its retention. Future prosthetic abutments may have an correct endodontic treatment, but in most cases, root canal treatments are incorrect, often being incompletely obturated. In fortunate cases, incomplete treatments do not result in periapical pathology, but most of the time, incomplete obturations lead to periapical pathology. Depending on the quality and the length of the root canal obturation, the approach to this problem is either the correct redoing of the root canal treatment or the surgical resolution of periapical pathology by root apex resection. The second option has a significant drawback, namely a decrease in root implantation. The decision not to perform pulpectomy for prosthetic purposes can lead to false conclusions and incorrect clinical decisions that will be regretted later, causing discomfort to both the patient and the dentist, and ultimately increasing costs. Evaluating the periodontal status of future abutment teeth is essential for the long-term success of the future prosthetic restoration. The degree of periodontal involvement in abutment teeth can range from mild, as seen in gingivitis, where only the gingiva is affected due to irritation from dental plaque. This type of gingivitis can be relatively easily resolved by changing the patient's oral hygiene habits, adopting proper toothbrushing techniques, and using additional oral hygiene tools such as dental floss, interdental brushes, and oral irrigators. In the case of periodontitis, the problems become more complicated because other components of the periodontium are involved, including the periodontal ligament, alveolar bone, and root cementum. Gingivitis and periodontitis should be treated during the pre-prosthetic treatment phase because dental mobility and pain worsen during chewing, causing discomfort to the patient. Inflammation of the periodontium reduces the ability of abutment teeth to respond to functional demands. Therefore, prosthetic restorations designed to stimulate healthy periodontal tissues can have an irritating effect on periodontal tissues affected by periodontal disease. Periodontal diseases often lead to changes in tooth positions. If prosthetic restorations are applied to teeth without prior periodontal therapy, they will further irritate the periodontium and reduce the lifespan of the abutment tooth. Fixed prostheses made on models based on impressions of gingiva affected by periodontal disease will not fit correctly when the gingiva heals after subsequent periodontal treatment. Any periodontal healing is accompanied by gingival recession, which exposes the edge of the prosthetic restoration and creates inappropriate retentive spaces between teeth, leading to plaque accumulation and resulting in inflammation of the residual alveolar crest mucosa and gingiva of the abutment teeth, perpetuating this vicious cycle. To establish the future margins of the preparation on the future abutment tooth, the position of the healthy gingival sulcus must be determined before starting the preparation. For patients with advanced periodontal disease, the treatment sequence should be as follows: - Irrecoverable teeth should be extracted, and temporary prostheses with provisional cervical margins should be made, which will be contoured after periodontal healing. - Completion of periodontal treatment. Teeth with divergent roots are more valuable abutments than those with fused roots. - Approximately two months after completing periodontal treatment, when the gingival tissue and gingival sulcus have stabilized, the cervical contour of the preparation is contoured. Periodontal therapy begins with a clinical examination, where the patient's oral hygiene level is assessed. A periodontal evaluation at the gingival level assesses the color, texture, tendency to bleed, and contour of the gingiva. Then, the height of keratinized gingiva and attached gingiva is evaluated. The examination of the gingival sulcus is done by periodontal probing after complete cleaning and the removal of all gingival irritation factors. The examination of periodontal pockets is mandatory by periodontal probing and radiological examination. These examinations can determine whether the periodontal pockets are false or true. False periodontal pockets appear because of the increase in volume of the gum in response to an irritating factor without affecting the periodontal ligament. This type of lesion falls under the category of gingivitis. True periodontal pockets occur with the destruction of supporting periodontal tissue. These can be classified into supraalveolar pockets, where the bottom of the periodontal pocket is located coronally to the level of the adjacent alveolar bone and infra-alveolar pockets, where the bottom of the pocket is positioned apically to the level of the adjacent bone. The presence of true periodontal pockets requires preprosthetic periodontal treatment until the moment when we obtain healthy periodontal tissue. Assessment of abutment tooth mobility is a vital stage in the lifetime of the future prosthetic restoration(2). Physiologic mobility in single-rooted teeth is up to 0.15 mm and in multiple-root teeth it is 0.10 mm. Increased tooth mobility (greater than physiological) can be transient, reversible or irreversible. Transitory tooth mobility usually occurs after laborious tooth extractions, in teeth that have undergone periodontal surgical procedures, or in patients who have received orthodontic treatment. Usually, this type of tooth mobility is reversible after the natural reorganization of the periodontium and tissue healing. There are three degrees of tooth mobility: Grade I tooth mobility is slightly more pronounced than physiological mobility, but the incisal edge or occlusal surface during tooth movement does not exceed 1mm in the buccolingual direction. Grade II tooth mobility involves movement both in the vestibulooral and mesio-distal directions, exceeding a value of 1 mm; Grade III tooth mobility is highly pronounced and occurs in the vestibulo-oral, mesio-distal and axial directions. Increased physiological tooth mobility can occur during pregnancy, tooth eruption, in acute inflammations of the apical periodontium or in teeth with hooks that have functionally overstressed the tooth. This type of mobility is reduced when the causative factor is removed. Pathological tooth mobility appears in: - periodontal disease with the reduction of the periodontal ligament and the reduction of the alveolar bone level; - gingival inflammation extends to the supporting ligament and bone; - physicochemical changes due to hormonal treatments. - due to osteomyelitis, tumors, traumas, traumatic occlusion and bruxism; - due to metabolic diseases such as diabetes. Transient tooth mobility can be of a prosthetic nature, for example a hook or a means of stabilizing a removable prosthesis or an incorrectly distributed extension can lead to the appearance of tooth mobility, but when the determining factor is removed the mobility will be reduced. Superficial or deep periodontal inflammations, tartar accumulations, septic pulpal inflammations that spread into the periodontal space can increase tooth mobility. Dental migrations of the tilting type led to a modification of the axis in which the tooth receives forces, lead to the appearance of premature contacts and interferences leading to overloading of the tooth and the widening of the periodontal space. In all these situations, if the causative factor is detected and removed, dental mobility will disappear. If the periodontal insufficiency and the destruction of the alveolar bone is massive, the inversion of the crown-root ratio occurs in favour of the root and the force arm increases, which leads to the development of irreversible dental mobility. In this situation, the only treatment that can help is guided tissue regeneration. Many times, the abutment teeth are in malposition. The malposition can be primary or secondary to extractions, periodontal diseases, interferences, traumatic occlusion. Usually, in patients who had extractions and did not follow prosthetic treatment, a series of dental movements of the teeth adjacent to the edentulous gap and of the antagonistic teeth to the gap begin. These dental movements occur due to the loss of contact areas with neighbouring teeth. Usually, the adjacent teeth to the edentulous gap begin to migrate towards each other through a translational movement, which later, under the influence of occlusal forces and the interferences caused by the displacements, turns into tilting and sometimes rotations of the teeth occur. The tooth opposing the gap, no longer having an antagonist, begins to egress or extrude. These tooth movements alter the occlusal plane and reduce the available prosthetic space thus making it difficult to develop an optimal prosthetic plan. In the situation where the movements of the teeth are not very pronounced, corrections can be solved by selective grinding, but the significant disadvantage will be that the abutment teeth will no longer receive the occlusal forces in the long axis, these forces will act para-axially, and over time a periodontal overload of the abutment tooth will occur. If the abutment tooth has a tipping degree greater than 25º, it can no longer be used as a post tooth because the occlusal forces will act completely outside the long axis of the tooth and will accelerate the destruction of the supporting periodontal tissue and the resorption of the alveolar bone. Orthodontic treatment aims to correct tilted, rotated or egressed/extruded teeth so that the occlusal plane is corrected, and by repositioning the abutment teeth, the contact points with neighbouring teeth are restored, the gap is recalibrated and the axis of the remaining teeth can be corrected so that the abutment teeth or the teeth adjacent to an implant prosthetic restoration to be able to correctly receive the occlusal forces. Through the changes obtained with the help of orthodontic treatment, the aesthetic aspect of the final restoration is improved, and optimal conditions can be created for the realization of a prosthetic restoration that will function in optimal conditions for as long as possible. Fig.3.4. Fixed orthodontic device for correcting the position of the second molar tilted towards the mesial: A) occlusal aspect; B) vestibular aspect (1) By correcting the axes of the remaining teeth from a prophylactic perspective, the retentive and food impact areas are solved, thus preventing the appearance of periodontal pockets. Interdisciplinary orthodontic-prosthetic treatment has the result of offering the possibility of increasing the quality of prosthetic treatment by eliminating compromise solutions, but unfortunately, many patients and doctors refuse this type of treatment due to the time factor, preferring faster solutions but which unfortunately are more radical and invas Chapter 4. DENTAL PREPARATIONS IN FIXED PROSTHODONTICS Because dental hard tissues do not have the regenerative potential that most tissues of the human body have, when they are lost due to carious or traumatic processes, they must be replaced in order to restore form and function. Most of the time, this replacement involves a preparation/preparation of the remaining tissues in order to optimize the consecutive clinical-technical stages. Therefore, it is necessary to consider biological, mechanical and aesthetic factors, which are interrelated. The preparation of the teeth to achieve correct and durable prosthetic restorations must take into account all these factors at the same time, and their simultaneous maximum satisfaction is often impossible. Thus, the prosthetist is often put in a position to find the best compromise. Biological considerations: - Protecting adjacent teeth during preparation; - Protection of soft tissues (marginal periodontium, lips, cheeks); - Protecting the pulp from thermal, chemical, bacterial trauma; - Conserving dental hard tissues (axial preparation, marginal preparation, placement of prosthetic restoration edges, marginal adaptation, marginal geometry); - Occlusal considerations; - Preventing fractures. Mechanical considerations: - Retention form (amplitude and direction of dislocating forces, geometry of the preparation – height, diameter, taper, size and texture of the prepared surface, cementation interface, cement type, thickness of the cement film); - Stability; - Resistance. Aesthetic considerations: - all-ceramic full crown; - Total physiognomic metal-ceramic crowns; - New generation polymers; - Edges placed subgingival. These principles are further elaborated in specialized textbooks (such as Rosenstiel, Schillingburg, Bratu) and are not the focus of this work. However, we will emphasize essential points that help students and young dentists in their day-to-day practice. 1. Preparation must ensure maximum preservation of dental hard tissues. In the case of vital teeth, conservative preparation minimizes the possibility of adverse pulpal effects following the preparation trauma itself, as well as during other clinical stages (gingival sulcus displacement, impression, temporary fixed prosthesis fabrication, framework try-in/other checks, temporary/final cementation, etc.). In the case of non-vital teeth, conservative preparation enhances the structural resistance of the tooth, minimizing the risk of fracture under masticatory forces. A minimally invasive and maximally conservative approach can be achieved by: - Choosing inlays and partial crowns instead of full crowns. - Ensuring minimal taper of the preparation. - Anatomical preparation of the occlusal surface. - Opting for a minimally invasive marginal/terminal design. - Keeping apical preparation minimal/minimal invasion at the gingival sulcus. - Orthodontic repositioning when a convenient preparation for parallelism among multiple abutments would compromise pulp vitality. 2. Any preparation, for any type of fixed prosthetic restoration, involves a certain degree of tissue sacrifice, no matter how minimally invasive the restoration may be. Exceptions are certain no-prep restorations. This applies both to single-tooth restorations and when preparing for an abutment of a fixed prosthetic restoration. Thus, the student and young dentist must make a correct and informed decision when choosing a specific prosthetic restoration over another. Ideally, when the clinical situation allows, the restoration of choice should be a conservative one. In case of failure, the practitioner can then consider a more invasive restoration. 3. An optimal preparation is essential for the adaptation of the prosthetic restoration, ultimately influencing the long-term success of the treatment. 4. There is no clinical consensus regarding the best preparation technique or the best marginal preparation, which can indeed make therapeutic decisions challenging for students and young dentists. However, there are certain recommendations aimed at improving marginal adaptation, enhancing aesthetics, and minimizing marginal stress levels. 5. There is no clinical consensus even in recommending the ideal instrumentation for a specific preparation (Beuer). 6. In current prosthodontics, the concept of overcontouring is relative (BOP technique - Ignacio Loi). Overcontouring is allowed under the condition that the emergence profile is correct, the marginal area of the prosthetic piece is properly shaped, finished, and polished, and its marginal adaptation is precise. We will not dwell on traditional preparations that, in the absence of current adhesive systems and techniques, were designed with additional retention features such as grooves, pits, boxes, assuming a greater tissue sacrifice to provide retention for fixed prostheses. Considering that classical preparations are extensively detailed in dedicated specialty textbooks and are mostly focused on mixed metal-ceramic and metal-polymeric fixed prosthetic restorations, we will emphasize innovative, modern preparations, and concepts oriented towards maximum tissue conservation in the following. It's important to note that preparations should be kept within enamel, and unnecessary dentin exposure should be avoided. Modern preparations can be successfully used for mixed metal-ceramic fixed prostheses, provided that a correct design is implemented, and modern adhesive protocols characteristic of allceramic systems are used. Any fixed prosthesis requires a certain minimum thickness to ensure the mechanical strength of the material/materials from which it is made. Thus, a less resistant material (e.g., feldspathic ceramic) requires a greater thickness than a material with higher resistance (e.g., zirconium oxide). A layered mixed fixed prosthesis requires a larger prosthetic space than a monolithic fixed prosthesis. The required thickness of a fixed prosthesis must always be correlated with the prosthetic space, both axially and incisal/occlusal. Therefore, when it is necessary to achieve an increase in volume through prosthetic treatment, tissue reduction during preparation will be less (or non-existent in no-prep treatments) compared to situations where this is not desired. Examples include cases with pronounced dental wear, abrasion, attrition, erosions, certain traumas, where volume augmentation is done purely additively, sometimes entirely non-invasive, through vestibular and palatal veneers, as well as adhesive-fixed table-top restorations to hard dental tissues. In some cases, minimal tissue invasion is required by rounding and finishing certain edges to facilitate subsequent clinical and technical steps. A thorough case documentation and planning is essential before commencing the treatment stages. Preparation for dental crowns In relation to the free gingival crest, the terminations can be placed supragingival, epigingival, or subgingival. It is universally accepted that supragingival placement offers the most advantages. The termination should follow the free gingival crest, parallel to the clinical crown, concave towards incisal/occlusal on the vestibular and oral aspects, and convex towards incisal/occlusal on the proximal surfaces (mesial+distal). This is essential in preparing teeth with periodontal involvement. The following preparation steps are aimed at teeth in an ideal position, whose longitudinal axis coincides with the prosthetic axis of the future restoration. In cases of migrated, tilted, translated, rotated, extruded, or intruded abutment teeth, the ideal treatment of choice is interdisciplinary, involving orthodontics followed by prosthetics. While there is currently a consensus regarding the preparation of axial and occlusal surfaces, as well as the incisal edge, there are no specific guidelines for the universal use of a particular marginal preparation/ideal termination. Setting aside older classifications of prosthetic terminations associated with crown preparations, in modern prosthodontics, we can systematize as follows: 1. Preparations without a precise margin, also known as vertical preparations (similar to tangential, knife-edge, or feather edge preparations), brought to the forefront and strongly supported by Ignacio Loi through the BOPT technique. 2. Preparations with a precise margin, also known as horizontal preparations, including preparations with a shoulder and chamfer, as well as their variations (straight shoulder, straight shoulder with rounded internal angle, inclined shoulder, bevelled shoulder, deep chamfer, long chamfer, etc.). In this category, we will exemplify and describe in detail the preparation with a straight shoulder with a rounded internal angle and the chamfer preparation. These preparations share with traditional shoulder preparations only the advantage of a precise margin, without the tissue invasion typically associated with traditional shoulder preparations. It's about rounded internal angle shoulders and conservative chamfers, measuring 0.3-0.8mm, rather than extensive straight shoulders at a 90º angle with widths of 1mm, 1.2mm, or even 1.5mm, as described in traditional techniques and recommended for metalceramic and metal-polymer fixed prostheses, as well as traditional all-ceramic/polymer jacket crowns. Advocates of vertical preparation argue for its universal indications based on: 1. Minimally invasive nature: Vertical preparation is characterized by its minimally invasive approach, preserving more of the natural tooth structure, which is beneficial for long-term dental health. 2. Creation of a terminal zone instead of a line: This approach allows dental technicians greater flexibility in achieving marginal adaptation and optimal aesthetics by creating a terminal zone rather than a sharp line. 3. Biological considerations: Vertical preparation can have biological advantages by modifying and maturing periprosthetic gingival epithelium. This leads to the subsequent development of healthy epithelium through directed over contouring, often facilitated with provisional restorations. Practically, this results in a new emergence profile, eliminating the amelocemental junction and creating a new cemento-prosthetic junction. This allows for superior aesthetics through the harmonization of adjacent preparation margins and the achievement of optimal symmetry. The adoption of minimally invasive concepts in modern prosthodontics has been made possible due to the evolution of dental materials. Currently, optimal aesthetic results can be achieved using polycrystalline ceramic materials with increased strength, even though a decade ago, these materials did not excel in terms of aesthetics. Research in the field of materials for fixed prostheses has led to: - Improvement in the aesthetics of polycrystalline ceramic materials through increased translucency. - The ability to create monolithic fixed prostheses from lithium disilicate and zirconium oxide ceramic materials. - The possibility of creating thinner restorations by enhancing the intrinsic mechanical strength properties of materials, allowing for more conservative preparations. - Enhanced quality and properties of adhesive agents and the development of clear adhesive fixation protocols, leading to improved durability of fixed prostheses (e.g., primer 10-MDP for adhesive bonding of ZrO2 fixed prosthetic restorations). In a didactic manner, we will divide the preparation stages into common stages and specific stages (preparation of the terminal zone). In cases where an increase in coronary volume is desired in the end, preparation will be performed through a previously obtained mock-up. Preparation for veneer crowns In the anterior region: 1. Preparation of the incisal edge In the posterior region: 1. Preparation of the occlusal surface For the upper incisors For didactic purposes, this can be divided into: Typically, it is performed perpendicular to the 1.1. Reduction of the internal occlusal surface; direction of action/axis of the mandibular frontals in 1.2. Bevelling of the supporting cusps. maximum intercuspation. Thus, in the case of a psalidodont occlusion, the Reduction should be carried out while respecting the section direction will be oriented buccal-palatal, anatomy of the occlusal surface, conservatively, ensuring respectively inciso-cervical. maximum thickness of TDD (tooth tissue remaining) near In the case of a labiodont ( head to head)occlusion, the pulp horns. This ensures correct adaptation and the preparation of the incisal edge will be done optimal resistance for future fixed prosthetic restorations straight. and facilitates subsequent clinical and technical steps. For the lower incisors, the incisal reduction will be performed perpendicular to their axis. It is considered optimal to obtain a prosthetic incisal/occlusal clearance of 1.5-2mm. Anatomic reduction can be achieved through the prior preparation of depth-marking grooves made with specific instruments and by using silicone condensation keys/conformers. Methods for preparing orientation grooves 1. Classic Method: According to Schillingburg, Rosenstiel, Bratu, using cylindrical-conical diamond instruments with rounded tips. 2. Modern Method: Using specialized instruments designed for this purpose, which enable controlled and uniform penetration into the TDD (remaining tooth tissue) at a desired depth while following the anatomy of the occlusal surface. (ex. DM05, DM10, DM15, DM20 – Komet, MADC – NTI, 828 – Meisinger) These instruments also allow for the creation of a more favourable pattern or layout of the grooves, making it possible for subsequent preparation perpendicular to their direction. This ensures increased tissue preservation by avoiding the engagement of rotary instruments in the grooves and further deepening. In case these special instruments are unavailable, a similar pattern of orientation grooves can be created using spherical diamond instruments with a diameter identical to the desired reduction. 1.1. Reduction of the internal occlusal surface is achieved by removing the islands of remaining TDD (tooth tissue) between the orientation grooves, using cylindrical or cylindrical-conical diamond instruments with rounded tips, oriented buccal or palatal and kept parallel to the cuspal inclintion being prepared, performing mesio-distal brushing movements. 1.2. Bevelling the supporting cusps is an extremely important stage, common to all extra-coronal preparations on teeth in the lateral areas of the arches. It ensures the attainment of optimal prosthetic space at this level, depending on the material strength of the future fixed prosthesis. In this case as well, the creation of depth orientation grooves is recommended, either using the classic or modern approach with specialized instruments. Bevelling the supporting cusps is done by maintaining cylindrical or cylindrical-conical diamond instruments with rounded tips, in a buccal-oral direction, parallel to the external cusp incline, at a 45-degree angle to the long axis of the tooth. Precise, fine mesio-distal movements are performed during this process. As the preparation progresses toward the proximal areas, rotational movements can be associated, following the tooth's anatomy closely. Preparation of the axial surfaces 2. Preparation of the vestibular surface It will always be performed anatomically. Thus, both in the anterior and lateral areas of the arches, the preparation will be carried out in two planes, delimited by the anatomical equator. 2.1. Preparation in the incisal/occlusal plane, parallel to the vestibular surface at a supra-equatorial level. 2.2. Preparation in the cervical plane, along the tooth's axis, respecting the axis of insertion of the future fixed prosthesis. In the first stage, orientation grooves will be prepared. For objective reasons, we recommend creating horizontal grooves, which allow for a more conservative subsequent preparation technique. Their depth should be approximately 1.5mm in the equatorial area and 1.5 to a maximum of 2mm towards the incisal/occlusal area. The preparation in the incisal/occlusal plane (supra-equatorial) will be performed using cylindrical or cylindrical-conical diamond instruments with rounded tips. These instruments should be maintained inciso/occluso-cervically parallel to the vestibular surface at this level, with brushing movements in the mesiodistal direction across the tooth surface. Experienced practitioners may also use specialized instruments such as flame-shaped or tapered ones for this purpose. Preparation in the cervical plane (sub-equatorial) is carried out using specific instruments, depending on the desired margin termination/preparation: 2.2.1. Cylindrical or cylindrical-conical diamond instruments with rounded tips, for preparations with chamfers. 2.2.2. Cylindrical or cylindrical-conical diamond instruments with flat tips and rounded angles, for preparations with a straight shoulder and rounded internal angle. 2.2.3. Flame-shaped diamond instruments, for vertical preparations without a precise limit. The advantages of cylindrical instruments lie in the fact that they occupy a smaller volume compared to cylindrical-conical ones for the same tip shape. This allows for better access to proximal areas, minimizing the risk of touching the proximal surfaces of adjacent teeth to the preparation. On the other hand, to achieve optimal convergence of opposing axial surfaces, these instruments need to be tilted, requiring more experienced practitioners and greater attention; otherwise, it may result in retentive areas. 2.2.1. Preparation with a chamfer of the cervical area of the vestibular surface It can be achieved with: - Cylindrical-conical instruments with rounded tips maintained along the tooth's axis. Cylindrical instruments with rounded tips inclined with the base toward the tooth's axis and the tip outward, so that in the end, an ideal convergence of 6º is achieved with the cervical area of the opposing axial surface (oral). It is crucial that for a flawless chamfer-type preparation configuration, the diamond instruments with rounded tips are inserted into the marginal TDD (tooth tissue remaining) for half of their diameter, preventing the creation of a preparation into the canal and an unsupported enamel ledge in the marginal area. We recommend using cylindrical/cylindrical-conical instruments with a tip radius of 0.3-0.8mm, and in the case of cylindrical-conical instruments, an angle of 2-3º with the axis of the bur, ideally ensuring a convergence of 4-6º between opposing axial walls. Using these instruments, tissue reduction at the marginal level ranges between 0.3-0.8mm. 2.2.2. Preparation with a rounded internal angle shoulder of the cervical area of the vestibular surface The preparation technique is similar to the one described earlier. Cylindrical-conical instruments with straight tips and rounded angles, maintained along the axis, or cylindrical instruments with straight tips and rounded angles, inclined at 2-3º relative to the tooth's axis, will be used. We recommend creating shoulder configurations of 0.3 to a maximum of 1mm, considering that all current classes of materials designed for fixed prostheses meet the mechanical strength requirements, especially when a well-established adhesive fixation protocol is used. 2.2.3. Vertical preparation of the cervical area of the vestibular surface (vertical preparation, tangential) The preparation is carried out using flame-shaped diamond instruments, maintained along the tooth's axis and moved in the mesio-distal direction, with the tip following the contour of the free gingival crest. The objective of this preparation is to achieve at this level a terminal transition zone between the prepared area and the unprepared remaining tooth tissue (TDD) that is smooth and without any visually detectable or palpable demarcation. Vertical preparation can be performed both supragingival and subgingival, but within the BOP (Biologically Oriented Preparation Technique) described by Ignacio Loi, it is done subgingival. Vertical preparation offers conservative advantages, ensuring minimal reduction of hard dental tissues around the neck of the tooth. Fixed prostheses obtained on teeth prepared vertically will invariably have overcontour, with a different emergence profile compared to the original tooth. However, this is a controlled, non-retentive over contouring, designed correctly to protect the marginal periodontium, provided there is optimal marginal adaptation of the prosthetic piece and minimal invasion of the sulcus. 3. Preparation of the oral surface In the anterior region In the posterior region For the mandible - the technique described for the We will uniformly address the preparation of the preparation of the cervical area of the vestibular surface oral surface of both maxillary and mandibular will be used. Please refer to sections 2.2.1, 2.2.2, 2.2.3. anterior teeth, emphasizing the similarities rather Objectives: than the differences, as clinical variety is a distinct - Maintain the correct axis. consideration. - Achieve the ideal convergence of 6º. For any maxillary or mandibular anterior tooth, - Follow the contour of the free gingival crest. there is generally a concave area toward the For the maxilla - the technique described for the incisal edge and a convex area toward the preparation of the cervical area of the vestibular surface cervical region. will also be employed. Please refer to sections 2.2.1, 2.2.2, In general, for a guided, minimally invasive 2.2.3. preparation, we recommend the use of horizontal orientation grooves and silicone keys. Objectives: To prepare the concave area of the oral surface, - Maintain the correct axis. instruments like rugby/football American-shaped - Achieve the ideal convergence of 6º. diamond burs, egg-shaped burs, etc., will be - Follow the contour of the free gingival crest. used. The choice of diamond instruments will be based on the For the convex area, corresponding to the cervical desired marginal preparation, with cylindrical-conical region (also referred to as subcingular - Bratu), diamond instruments maintained along the tooth's axis and the preparation technique described for the cylindrical instruments inclined with the tip outward to cervical/sub-equatorial area of the vestibular achieve occlusal convergence (6º) of opposing axial areas. surface will be employed, depending on the desired marginal preparation/termination. This involves maintaining cylindrical-conical diamond instruments along the tooth's axis and cylindrical instruments inclined with the tip outward to achieve occlusal convergence (6º) of opposing axial areas. The tip of the rotary instrument will follow the free gingival crest at this level, and the preparation can be placed supra, epi, or subgingival. Please refer to sections 2.2.1, 2.2.2, 2.2.3. 4. Preparation of the proximal surfaces The objectives of the preparation are as follows: - Protecting the proximal surfaces of adjacent teeth during preparation. - Minimizing tissue reduction according to the desired preparation. - - Achieving minimal/optimal occlusal convergence of opposing proximal surfaces. - - Maintaining the preparation axis. Following the free gingival crest. Ensuring the marginal preparation is parallel to the free gingival crest, regardless of whether it is placed supragingival, epigingival, or subgingival. The proximal surfaces will be prepared using the technique described for the cervical/sub-equatorial area of the vestibular surface, depending on the desired marginal preparation. Protection of adjacent teeth can be accomplished using matrices such as Safeguard, Fenderwedge, metal bands, wedges, or other suitable methods. These are recommended, especially for students and less experienced prosthodontists. However, considering that the cervical area of the proximal surfaces is invariably located approximately 11.5mm further inside the tooth compared to the proximal contact point, preparation at this level can be performed by separating a thin layer of tooth tissue, which can be subsequently removed using hand instruments. Small-diameter rotary instruments (e.g., flame-shaped, tapered) have an advantage in this regard. Among cylindrical and cylindrical-conical instruments with identical tip diameters, cylindrical ones offer a clear advantage due to their smaller profile for the same tip diameter/curvature radius. CAD/CAM CROWN PREPARATION GUIDE Ideal Posterior Crown Preparation • Rounded Internal Angles • Reduction by 1.5-2 mm at the occlusal level and 1 mm at the margin. • Chamfer preparation at the margin with an occlusal convergence ranging from 6-10o Ideal Anterior Crown Preparation • Reduction of 1-1.5 mm of the vestibular and lingual surfaces • Reduction at the incisal level by 1-2 mm • Chamfer preparation at the margin • The preparation should follow a three-dimensional reduction based on the anatomical shape of the tooth. CONSIDERATIONS TO AVOID IN PREPARATION: Knife-edge" or "feather-edge" margins • Due to possible complications in milling and the material's limitations, knife-edge or feather-edge margins should be avoided. Reduction at the margin (marginal level) by 1 mm with an occlusal convergence of 6-10 0 Avoiding Retentive Features • The presence of these can lead to insufficient material thickness in the areas trapped between these retentive features. Avoidance of Preparations with High Convergence • Preparations with a high degree of convergence can also create challenges during scanning. • To eliminate this drawback, it should be ensured that the entire margin of the preparation is visible from the occlusal aspect. Avoidance of Sharp Angles If the diameter of the bur is larger than the apex of the preparation, overcontouring may occur during milling. This can happen in cases of lower incisor preparation or when the angles of the preparations are not rounded. Avoidance of Thin Walls After Endodontic Treatments One should avoid thin walls after endodontic treatments, as they may potentially lead to fractures over time. Additionally, it should be ensured that the access area is not less than 1.5 mm to prevent failure. Supragingival margins are ideal, as there is no need to hide the metal collar. PREPARATION GUIDE FOR INLAYS AND ONLAYS • The preparation termination should have well-defined margins for easier identification. • • Occlusal reduction >1.5 mm • • Internal axial walls with 6-10 degrees of convergence 0 • • The lines forming the internal angles should be rounded • • Interproximal bevel of 100-120o • • At the margin, the preparation edges will be capped. • • Isthmus depth of 1.5-2.0 mm • • Isthmus width of 1.5-2.0 mm • The termination of the preparation should have well-defined angles for easier identification. • • Occlusal reduction of 1.5-2.0 mm • Internal axial walls 6-10 0 • • The lines forming the internal angles should be rounded • Interproximal bevel 100-120o ASPECTS TO AVOID IN PREPARATIONS • To avoid over contouring, the oclusal margin design that follows the existing occlusal anatomy cannot have a diameter smaller than 1 mm. • Knife-edge or feather-edge margins will result in thin margins of the milled ceramic, potentially causing fractures later on. • Parallel walls and sharp internal angles can lead to misfit of the restoration. • Interproximal concavities will result in over contouring and uncovered margins. • Insufficient isthmus width will result in a fragile restoration. GUIDE FOR VENEER PREPARATION MARGINAL INCISAL PREPARATION • To uniformly prepare the thickness of the enamel on the labial surface, a diamond bur with a rounded tip and medium grit should be used. • • The depth of the preparation will be located between 0.5-0.8 mm. • • Incisal reduction of 1-1.5 mm. • • The total height from margin to incisal edge cannot exceed 9.5 mm. EXTENDED INCISAL MARGINAL PREPARATION • Additional reductions may be necessary for masking certain deficits or for layering techniques. FENESTRATED PREPARATION • Proper chamfer preparation of interproximal and cervical margins provides the necessary space for ceramics ASPECTS TO AVOID IN PREPARATIONS ROUNDED INCISAL EDGE • This type of preparation can cause tilting or fracturing of the restoration margin. • Rounded margins • Retentivities • Insertion axis • A retention-based preparation can lead to issues for digital design software due to an inappropriate insertion axis. CAD/CAM CROWN PREPAARATION GUIDE IDEAL POSTERIOR CROWN PREPARATION • Rounded internal angles • Reduction by 1.5-2 mm at the occlusal level and 1 mm at the margin level • Chamfer preparation at the margin level with a convergence angle between 6-10 degrees IDEAL ANTERIOR CROWN PREPARATION • Reduction of 1-1.5 mm on the vestibular and lingual surfaces • Reduction of 1-2 mm at the incisal level • Chamfer preparation at the margin level • The preparation should follow a three-plane reduction based on the tooth's anatomical shape. ASPECTS TO AVOID IN PREPARATION: "KNIFE-EDGE" OR "FEATHER" EDGES • Due to possible complications during milling and material limitations, "knife-edge" or "feather" edges should be avoided. • Reduction at the margin level by 1 mm and an occlusal convergence of 6-10 degrees. AVOIDING RETENTIONS • Their presence can lead to insufficient material thickness in areas blocked by these retentions. AVOIDING HIGH CONVERGENCE PREPARATIONS • Preparations with a high degree of convergence can also lead to scanning difficulties. • To eliminate this issue, it should be ensured that the entire margin of the preparation is visible from the occlusal view. AVOIDING SHARP ANGLES If the diameter of the bur is larger than the apex of the preparation, overcontouring may occur during milling. This can happen in cases of preparing lower incisors or when the angles of the preparations are not rounded. AVOIDING THIN WALLS AFTER ENDODONTIC TREATMENTS Thin walls after endodontic treatments should be avoided, as they can potentially lead to fractures over time. Additionally, it should be ensured that the access area is not less than 1.5 mm to prevent failure. Supragingival margins are ideal as there's no need to hide the metal collar. PREPARATION GUIDE FOR INLAYS AND ONLAYS • The preparation termination should have well-defined margins for easier identification. • Occlusal reduction >1.5 mm • Internal axial walls with 6-10 degrees of convergence • Lines forming internal angles should be rounded • Interproximal bevelling of 100-120 degrees • At the margin level, the preparation edges will be capped. • Depth of isthmus: 1.5-2.0 mm • Width of isthmus: 1.5-2.0 mm • The termination of the preparation should have well-defined angles for easier identification. • Occlusal reduction: 1.5-2.0 mm • Internal axial walls: 6-10 degrees of convergence • Lines forming internal angles should be rounded • Interproximal bevelling: 100-120 degrees ASPECTS TO AVOID IN PREPARATIONS • To avoid over contouring, the design of the occlusal margin following the existing occlusal anatomy cannot have a diameter smaller than 1 mm. • "Knife-edge" or "feather" edges will result in thin edges of the milled ceramic, potentially causing fractures later on. • Parallel walls and sharp internal angles can lead to restoration misfit. • Interproximal concavities will cause over contouring and uncovered margins. • Insufficient width of the isthmus will result in a fragile restoration. PREPARATION GUIDE FOR VENEERS IDEAL VENEER PREPARATION FLAT INCISAL MARGINAL PREPARATION • To uniformly prepare the thickness of the enamel on the labial surface, a diamond bur with a rounded tip of medium grit will be used. • Preparation depth will be between 0.5-0.8 mm • Incisal reduction of 1-1.5 mm • The total height from margin to incisal edge should not exceed 9.5 mm. EXTENDED INCISAL MARGINAL PREPARATION • Additional reductions may be necessary for masking certain deficiencies or for layering techniques. FENESTRATED PREPARATION • Proper chamfer preparation of interproximal and cervical margins provides the necessary space for ceramic. ASPECTS TO AVOID IN INCISAL MARGIN PREPARATIONS • This type of preparation can cause tilting or fracturing of the restoration margin. • Rounded margins • Retentions • Insertion axis • Preparations with retentions can lead to issues for digital design software due to an inadequate insertion axis. CHAPTER 5. IMPRESSION IN FIXED PROSTHODONTICS The faithful reproduction of all elements within the prosthetic field, i.e., transferring data from the oral cavity to the dental laboratory, has always been a challenge for clinicians. Impression-taking is a crucial clinical step in the fabrication of fixed prosthetic restorations (FPR). The efficiency of prosthetic treatment through any type of FPR largely depends on the precision of dental impressions. Over the years, both impression techniques and materials have evolved, rendering several previously successful methods obsolete. GENERAL INFORMATION: An impression represents a negative replica of the anatomical structures within the oral cavity. Based on the impression, a working model is fabricated in the dental laboratory, where the future fixed prosthetic restoration will be crafted. The choice of impression materials and techniques in conventional practice is based on several criteria: • The fidelity of the impression material or the availability of modern equipment for material homogenization and dosing. • The time available to the practitioner for impression-taking. • The dimensional stability of the impression material. • The specific characteristics of the prosthetic field closely related to the desired fixed prosthesis. • The ability to store and repeatedly fabricate the model. • The specifics of the methods and materials available for creating the model. Other clinical aspects to consider when deciding on the selection of impression material and technique include: • The presence of cavities and undercuts that may pose challenges to accurately recording details with the impression material. • Recording cervical margins becomes problematic when they are located juxtagingival or even subgingival. If the finish line is not well-defined in the working model, even a slight deviation, such as a few tenths of a millimetre, can result in a conjunctival fixed prosthesis. Furthermore, a portion of the unprepared dental surface must also be replicated. Its presence in the working model allows the dental technician to create prosthetic surfaces that best match the emergence profile most tolerated by the marginal periodontium. To achieve this, temporary gingival enlargement is performed to ensure access for the impression material. • The need to control oral fluids, such as blood, sulcular fluid, and saliva. Minor bleeding may occur due to marginal periodontal inflammation (preliminary periodontal treatment is essential) or operative aggressions during abutment preparation using rotary instruments and gingival sulcus widening manoeuvres. Mild bleeding is rapidly controlled if the gingiva is healthy. Haemostatic agents like 15-20% ferric sulfate (e.g., Astringedent by Bisco) or aluminium sulfate are used for this purpose. Sulcular fluid secretion increases in the presence of even minor inflammation, often becoming unavoidable during temporary gingival sulcus widening, regardless of the technique used. When recording an area that requires precision in a wet environment, it emphasizes the need to use impression materials capable of wetting the surfaces effectively. Stages of Prosthetic Field Impression • Fluid Control • Gingival Displacement • Impression Materials • Impression Trays • Impression Techniques 1. Fluid Control: Fluid control represents achieving the best possible isolation of the prosthetic field to be impressed. This is accomplished using cotton rolls, standard saliva ejectors, and surgical aspirators. Both cotton rolls and aspirators are disposable and need to be replaced due to moisture. Saliva ejectors, when placed sublingually, help in suctioning saliva secreted by the salivary glands to maintain a well-isolated prosthetic field. In cases of excessive salivary flow, whether it's physiological or pathological, additional measures are taken to ensure a faithful impression. This includes the use of anti-sialagogue medication such as Atropine, Dicyclomine, or Clonidine. Modern tools for aspiration, removal of soft tissues, and illumination, like Isolite or Re-Leaf (Kulzer), are very helpful in preparing the operating field for impressions. 2. Gingival Displacement (Temporary Gingival Enlargement): Gingival displacement involves introducing elastic impression materials into the oral cavity in a semi-fluid state. Since these materials are slightly compressible, they may not effectively displace the free gingiva and interdental papilla. The inherent elasticity of soft tissues contributes to creating a virtual space in the gingival sulcus. If, however, the impression material manages to penetrate the sulcus, the margins will inevitably become thin, fragile, and prone to deformation under the pressure of gypsum or the materials used to create the working model. To achieve a faithful reproduction of the terminal area of the abutment, gingival sulcus preparation is required, with the following objectives: temporary displacement of gingival tissues from the tooth surfaces to expose the cervical area and a portion of the underlying surface. This ensures vertical access for the fluid elastomer. Creating a space horizontally to ensure sufficient margin thickness in the impression and to avoid distortion, a prerequisite for accuracy. Gingival retraction must be maintained throughout the intraoral hardening of the impression material to avoid negatively affecting its mechanical properties. Various techniques and materials for effective widening of the gingival sulcus around tooth preparations or abutments are used, which can be divided into: a) Mechanical methods involving unimpregnated retraction cords of various dimensions, provisional crowns that, when removed, reveal the gingival sulcus, and copper bands prepared to suitable abutment diameters. Mechanical-chemical methods involving retraction cords impregnated with substances like epinephrine, aluminium chloride, ferric sulphate, all used in normal concentrations that do not adversely affect the periodontal status through gingival retraction with tissue loss. In the case of epinephrine, caution should be exercised in individuals with heart conditions due to an increase in blood pressure and heart rate. b) Mechanical-chemical methods - EXPASYL is a mixture of Aluminium chloride and kaolin that, once injected, increases in volume. After rinsing, the gingival sulcus remains dilated for a few minutes, allowing for a precise impression. The same effect is achieved with products like Magic Foam cord, Retraction Paste (3M ESPE), or Traxodent (Premier). -Reversible hydrocolloids (agar-agar) injected at the gingival sulcus level. Gingival retraction with retraction cords Gingival retraction cords can be twisted, braided, which in turn can be with a solid or hollow center. There are also woven retraction cords that have a hollow center, being much more compressive and more difficult to remove from the sulcus. These can absorb up to 2.5 times more solution than the twisted ones, but they are more often cut and caught by burs than the others. The practical procedure for inserting retraction cords involves checking the status of the soft tissue. It is checked for bleeding; if bleeding is present, haemostasis is performed. If bleeding persists even after the removal of provisional restorations, the marginal adaptation of provisional restorations is checked, and they are finished and polished before proceeding with the impression. The impression field is isolated using cotton rolls, and saliva aspiration is performed simultaneously. The depth of the gingivo-dental sulcus is measured with a periodontal probe to choose the correct thickness of the retraction cord. The cord is impregnated with an astringent substance, wrapped around the tooth, and inserted into the gingivo-dental sulcus. The insertion starts from the mesial or distal proximal area and continues incrementally until it encircles the entire cervical circumference of the abutment, and then the insertion point is revisited. During cord insertion, excessive pressure should be avoided as it can cause injuries at the epithelial attachment and gingival tissue, leading to bleeding, especially in non-keratinized and slightly inflamed gingiva. Various techniques or procedures for cord insertion are described in the literature, involving the use of a single cord or two cords. A) The single-cord technique is the choice in most cases due to its simplicity and speed. The depth of the sulcus, measured with a periodontal probe, dictates the diameter of the cord to be used. For example, 1mm corresponds to #0, and 0.5mm corresponds to #00. This single-cord technique is especially suitable for anterior and posterior teeth, for epigingival or supragingival preparations. In the case of subgingival preparations, the gingiva may collapse over the inserted cord, and the impression material may not penetrate deep enough into the gingival sulcus to create an adequately voluminous impression, resulting in clear indications of the preparations. Therefore, after inserting the cord, it should be visible in the sulcus, and if it's not visible, it means the cord has been chosen too thin. Once inserted, it is left in the gingival sulcus for about 5 minutes before careful removal, just before injecting the impression material. B) The double-cord technique, using two cords for gingival retraction, is a technique that requires more time to perform and is particularly suitable for subgingival preparations. The steps for this technique involve starting with the insertion of a thinner cord, size #00 or #000, deep into the gingival sulcus, right at the base of the sulcus under the margin of the preparation. This is done to have better control over moisture and potential local bleeding. Then, a thicker cord is placed above the first cord and left in place for about 5 minutes. This last cord is removed just before inserting the impression material, ensuring temporary widening of the gingival sulcus. Electrosurgical Method: This method is performed using an electric scalpel under local anesthesia. Contact with metallic objects inside the oral cavity should be avoided as much as possible, and it is contraindicated for individuals with pacemakers or when the gingiva is thin and adherent. The effect achieved by gingival retraction should persist throughout the impression process and should not disappear immediately after removing the cord or widening the gingival sulcus. In this case, the effort put into achieving retraction would become pointless. The factors that influence the choice of a gingival retraction method include: • General factors: diabetes, heart disease, pacemaker, hypertension, hyperthyroidism, allergic conditions. • Local factors: the placement of the cervical margin of the preparation. • Periodontal conditions: thin and adherent gingiva, thickness of the vestibular alveolar bone, nature and extent of gingival recession inherent in any method. Gingival retraction using a laser beam is easier and often does not require anesthesia. It is performed with a diode laser and provides superior healing compared to the electrosurgical method. In conclusion, whichever method of gingival retraction we choose, it should be easy to apply, not painful during insertion, have a rapid action with a sufficiently longlasting effect to allow the necessary clinical maneuvers for impression taking, should not cause bleeding, and should not have general side effects such as increased heart rate, elevated blood pressure, allergies, gingival recessions, or necrosis. Impression in Fixed Prosthodontics Impression Materials To achieve superior impressions from a technical and clinical perspective, impression materials must meet certain characteristics: - Plasticity: This represents the material's ability to be deformed and shaped under minimal pressure and functional movements, thereby recording all morphological and functional details of the prosthetic field without distortion. - Setting Time: It should be short but sufficient to meet the clinical requirements of the impression phase. - Fidelity: Fidelity is the material's capacity to record the finest details of the prosthetic field. - Elasticity: Elasticity refers to the material's property to allow the impression to be removed from the prosthetic field (with varying degrees of retention) and then return to its initial shape. - Mechanical Strength: This is the material's ability to resist breakage during removal from the field, transport, and model casting. - Dimensional Stability: Dimensional stability represents the material's ability not to undergo plastic deformation during removal, storage, transport, and casting under the temperature and humidity conditions of the clinic and laboratory. Ideally, materials with the lowest possible shrinkage coefficient are sought. - Compatibility with Model Materials: Both the properties of the impression materials and those used for model casting need to be known to determine the appropriate combinations to use. Clinical Properties of Impression Materials - Hydrophilicity: The impression material should be capable of replacing moisture and forming intimate contact with the tooth and soft tissues. It should not contain any bubbles or voids. - Flexibility: The impression should be easy to remove after being fixed in the oral cavity. - Elastic Recovery: An impression should return to its original size after removal from irregular surfaces in the oral cavity. - Resistance to Tear: It should resist tearing after removal from the oral cavity and when separated from the model. - Detail Reproduction: The impression material should reproduce even the finest details of oral tissues and accurately transfer those details onto gypsum models. The image below represents the main impression materials. Reversible Elastic Impression Materials In dentistry, reversible elastic impression materials are represented by reversible hydrocolloids. Reversible hydrocolloids were the first elastic impression materials to appear. The main substance is a gel based on agar-agar, which becomes plastic when exposed to heat. The term "hydrocolloid" comes from the fact that these materials form colloidal solutions in the form of a gel with water during the final setting phase. The term "reversible" indicates the ability to return to a sol (fluid) state after having been turned into a gel. Some commercial names for these materials include Hydrocolloid (KENT DENTAL) and Hydrocolloid (KERR). The primary component of a reversible hydrocolloid is agar-agar (gelatin). Agaragar liquefies, transitioning from a gel to a sol state between 71°C and 100°C and gels again, transitioning from a sol to a gel state between 30°C and 50°C. The gel structure is formed from microscopic fibers and chains of colloidal particles, creating a network that retains water in its interstices. In dry conditions, the gel loses water through "sweating" and retracts, while in a moist environment, the gel can absorb water through imbibition. The table below presents the main advantages and disadvantages of common impression materials. Advantages Disadvantages Indications Irreversible Rapidity, Cost-effective, Low precision Study and diagnostic Hydrocolloids Immediate pouring models, Preliminary impression, Impression of antagonists Condensation Easy to use, Short Hydrophobic, Silicon Weak stability setting time, Different Fixed prosthodontics viscosities Addition Stability, Easy to use, Hydrophobic Silicon Variable working/setting (problematic time, Odorless, subgingival Tasteless, High crown precision, Multiple impressions), model pouring, Some materials Different viscosities, release H2 Fixed prosthodontics/implants High tear strength, Single or dual-phase impression Polyether Dimensional stability, Short working Fixed Most used in fixed time, Material prosthodontics/implants prosthodontics, becomes very Excellent precision, rigid after Easy to use (automix), setting, Cannot Short setting time, High pour multiple tear strength, models Hydrophilic, Different viscosities, Single or dual-phase impression The indications for reversible impression materials include fidelity, which is higher than that of alginates but inferior to synthetic elastomers. They were neglected for a while and used mostly in dental technology laboratories for duplicating models. Corrections to the impression are not possible, but the material can be re-liquefied, and the impression can be retaken on the same patient. Currently, these materials are being reintroduced and successfully used in dental offices for impression-taking of preparations (inlays/onlays, crowns, etc.) or for duplicating models in dental technology laboratories. Contraindications for reversible impression materials are when it is not possible to achieve quality conditioning of the gingival sulcus, in the case of knife-edge preparations that result in very thin impression margins, in simultaneous bilateral preparations at the premolar and molar levels, and in patients with macroglossia and/or excessive lingual mobility. The disadvantages of using reversible impression materials include a more challenging and time-consuming technique, relatively brittle material, very limited dimensional stability after gelation (the model must be poured immediately), models can only be made from gypsum, high initial investment for accessories, and lower patient comfort. Irreversible Elastic Materials Irreversible hydrocolloids: - Alginates - Synthetic elastomers: • Polysulfides • Silicones • Polyethers Alginate From a chemical standpoint, these consist of a long chain of cyclic molecules, similar in composition to sugar. They are presented in powder form, which, upon adding water and stirring, transforms into a paste or gel that becomes irreversible. The commercial presentation of alginates is as a powder in a tightly sealable container when not in use. It also includes a container for the proper dosage of the powder into the mixing bowl to achieve the desired quality for impressions. After adding water to the powder and mixing, it reaches a sol state, which is then loaded onto the impression spoon, smoothed gently with moistened fingers to reduce air inclusions, and then applied to the prosthetic field. After a few minutes (2-4 minutes, depending on the manufacturer), the material hardens, changing from a sol to a gel-like consistency, at which point it can be removed from the prosthetic field. The material is soft, rubbery, moist, and fragile, and its resistance is low during removal. Due to its composition and structure, it is susceptible to dehydration, and structural changes may occur within it. Therefore, it is recommended to pour the gypsum model as quickly as possible (within 30 minutes) or keep the alginate impression in a moist environment for a short period, such as covering it with a moist towel and sealing it tightly. Some commercial names for alginates include Alginoplast (Bayer), Xantalgin (Bayer), Ypeen (Spofa), Orthoprint (Zhermack). They are typically presented as powder in boxes or bags of different colors, with variations based on the type of gelation: • Type I (rapid gelation) • Type II (normal gelation) • And by purpose: • Class A (for single-tooth prostheses) • Class B (for arches) • Class C (for study models and individual impressions). As for its composition, alginic acid is derived from marine plants. The sodium and potassium salts of this acid have properties that make them suitable as impression materials, and the transition from sol to gel occurs upon contact with water. Synthetic Elastomers Based on their composition, elastomers are divided into polysulfides, silicones (condensation and addition types), and polyethers. Depending on their consistency, they are classified into four categories: • Type I: Putties (Putty) • Type II: High viscosity for coarse impressions (Heavy-bodied) • Type III: Medium viscosity for a wide range of impressions (Regular) • Type IV: Low viscosity (fluid) for syringe injection techniques Polysulfides These materials, called polysulfides, mercaptans, thiocauchuks, or thiokols, derive their name from the first product introduced to the market, "Thiokol," in 1953. Commercial names include Permlastic and Unilastic (Kerr), and they are presented as two-paste systems (base and accelerator) in three consistency variants. Composition: The base primarily contains a polysulfide polymer, while the accelerator contains lead dioxide. Due to the lead dioxide, these materials are dark brown or gray and have an unpleasant odour due to sulphur. Properties: • Hydrophobic • High, medium, or low consistency • Excellent dimensional stability with a contraction of 0.40-0.45% over 24 hours • Very good fidelity for fluid forms, decreasing with increased viscosity • Good mechanical strength • Shelf life of 18 months • Radiopacity Disadvantages: Unpleasant odour and long setting time. Indications: • Chitinous variants are used in double-mix techniques as support materials for fluid ones. • Variants with normal consistency are used in total and partial edentulism for the final impression. • Fluid variants are used to capture fine details during the fabrication of single-tooth prostheses and bridges. Regarding contraindications, these materials have virtually no contraindications regarding the type of impressed field but target individuals who exhibit intolerance (allergic reactions) to the chemical constituents of polysulfides. Silicones Silicones represent a new class of impression materials designed to overcome the drawbacks of polysulfides. They can be further categorized into condensation and addition silicones. Condensation Silicones Properties: • Excellent fidelity for fluid forms, decreasing with increased consistency • Dimensional stability: undergo significant shrinkage after setting, 0.60% for putty and 0.38% for fluid (greater than polysulfides) • Model pouring should be done rapidly, within 60 minutes • Pleasant taste and odour • Shelf life of 12 months • Hydrophobic materials Addition Silicones Presentation: They are presented as two-paste systems (base and accelerator) in five consistency variants: putty, high, medium, fluid, and very fluid. Properties: • Hydrophobic (though hydrophilic variants are also available) • Excellent fidelity for fluid forms, decreasing with increased consistency • Excellent dimensional stability (0.05% in 24 hours, the lowest among all elastic materials) • Good tear resistance • Models can be poured up to 7 days, thanks to their outstanding stability and ease of pouring • Perfect models without air bubbles in hydrophilic ones • Pleasant color, odour, and taste • Shelf life of 24 months • Higher cost. Indications: These materials are indicated for all types of impression of prosthetic fields for fixed prostheses, functional impression of partially or totally edentulous prosthetic fields. Contraindications: • Individuals with intolerance or allergic reactions to some chemical components of the bases or accelerators of polysulfides. Polyethers Polyethers are presented as two-paste systems (base and accelerator), with the base tube having a much larger orifice than the accelerator tube (an 8:1 ratio) and in two consistency variants: low and high. Properties: • Hydrophilic materials • High and low consistency • Very good dimensional stability with 0.12% contraction at 24 hours • Good fidelity • Removal from the field is more challenging as they become harder and less flexible after setting • Models can be poured up to 7 days • Shelf life of 24 months • These materials cannot be exposed to water as they have high absorption capacity and deform easily. Impression Techniques in Fixed Prosthodontics The classification of impression procedures for the prosthetic field in fixed prosthodontics is based on the working steps and is divided into two categories: 1. Single-step (monophase) 2. Two-step (biphasic) They are further categorized based on the number of components used into: - monocomponent impressions. - bicomponent impressions. In the specialized literature, the following nomenclature for the classification of impression techniques (Witz 1977) has been established: Unimaxillar Impression: 1. Conventional or single-step impression 2. Two-step impression 3. Wash impression (two-phase) 4. Double-mix impression 5. Compound impression (sandwich) 6. Impression for FPD (Fixed Partial Denture) Bimaxillar Impression: • Single-unit impression with thermoplastic or synthetic elastomers in a copper ring. • Bimaxillary impression with thermoplastic material and synthetic elastomers or with synthetic elastomers paste and fluid in a special spoon. For all elastomeric impressions, gingival sulcus preparation is required. The technique of using addition silicones for a single-step impression with two different material consistencies is illustrated in the images below. Single-Step Impression (Monophase): Indications: • Impressions of antagonistic arches • Preliminary impressions for making models on which individual trays are fabricated. Final Impressions with Synthetic Elastomers. Monophase impressions can be made using: • Standard trays - irreversible hydrocolloids • Individual trays - synthetic elastomers • Special trays - reversible hydrocolloids In a monophase impression, the chosen impression material is placed in a universal tray and positioned in the prosthetic field. This impression is used to record the antagonistic teeth and is typically made using irreversible hydrocolloids. For all impressions using synthetic elastomers, gingival retraction is necessary. Two-Step Impression: After gingival retraction, elastomeric fluid is injected onto the prepared tooth and into the gingival sulcus. In the second step, the prepared solid silicone, along with the catalyst, is placed in a universal tray and positioned in the prosthetic field to encase the fluid silicone. This category can also include injection impression techniques. The impression is obtained in two phases. In the first phase, the solid elastomer (putty) is prepared and placed in a universal tray equipped with efficient retention systems (2mm holes), and it is placed in the prosthetic field. After the material sets, the impression is removed from the prosthetic field. Gingival sulcus retraction is performed between the two phases of impression making. The impression created by the putty elastomer is prepared as follows: the surface is washed under a stream of water, dried with an air jet from the dental unit, and any excess material is removed from the retentive regions. Triangular grooves (bounded by 2 walls) are cut at the level of the vestibular and oral (tooth) faces, which continue the vestibular and palatal or lingual side (inferior). The purpose of these grooves is to allow the excess fluid silicone to flow out and ensure proper reseating of the impression on the prosthetic field. The presence of grooves prevents deformation of the initial impression due to overpressure. An alternative to this technique involves reducing the size of the tray during impression making when the material is still pliable. In the second phase, fluid silicone(light body) is prepared and introduced into a syringe for injection into the gingival sulcus, onto the prepared tooth, neighbouring teeth, and into the impressions made in the first phase using the putty silicon. The tray containing the impression and fluid elastomer is repositioned in the oral cavity on the prosthetic field in the same position. After setting (2-4 minutes), the impression is removed, washed, and dried. Examination of the impression shows that the fluid material, which has a different color than the putty consistency material, delineates the boundaries of the abutment preparation and the depths of the sulci. Each edentulous space or gap is well-defined by a ring-like prominence that extends 0.5-1 mm beyond the impression surface into the gingival sulcus. Between the abutment impression and the adjacent teeth, mesial and distal, a wall with thickness indicates the space created for the future prosthetic restoration, and the inclined parts of the impressions show the negative relief of the occlusal surfaces. The material used for recording details can detach from the putty material, if the surface of the initial impression has not been thoroughly dried - this is a possible defect that necessitates repeating the impression from phase II. Advantages of Conventional Impressions: • The technique is well-known and widely accepted. • Most dentists are reluctant to adopt new concepts once they are accustomed to the traditional technique. • The equipment is simple, and the technique is relatively easy to learn. • Cost varies from low to moderate. • The accuracy of impressions using addition silicones and poly-ethers is recognized. Disadvantages of Conventional Impressions: • Conventional impressions can be messy, leaving material residues on patients' skin, mucous membranes, and between their teeth, which must be removed. Material residues can scatter throughout the dental office, on gloves, floors, instruments, etc. • Discomfort for patients, with some experiencing a heightened sense of nausea. • Errors due to the incorporation of air bubbles and debris can lead to inaccuracies in the model. • Inventory management for impression trays and materials. • Additional costs for courier services, sending models to the lab, etc. Digital Impressions The digital era necessitates a transition from conventional to digital impressions. Will digital impressions improve and simplify the impression-taking process? Will they benefit patients? Will the cost of digital impressions be comparable to conventional ones? An estimated 334 million impressions are taken worldwide annually, with 55 million in the USA alone. Among these, 59% are considered inadequate. For both conventional and digital techniques, precise tooth preparation is essential. Digital impressions do not tolerate approximations. Gingival groove preparation is just as crucial as in conventional impressions. Advantages and Disadvantages of Digital Impressions: 1. The technique is not familiar to all dentists and convincing some that it is a better method can be challenging. 2. Complexity - the equipment is sophisticated, although it has simplified considerably in recent times. Training and instruction are required to master the technique. 3. Equipment costs are high, but after amortization, it becomes more cost-effective than conventional impressions. 4. Comparative studies on precision show some similarity between digital and conventional impressions. However, long-term clinical studies are needed to determine if these systems are superior in terms of restoration accuracy. 5. Simplicity becomes like conventional impressions after mastering and deepening the technique. 6. Eliminates office "mess" (additional waste). 7. Eliminates patient discomfort. 8. No risk of inaccuracies due to the incorporation of air bubbles. However, attention must be paid when recording data to avoid artifacts caused by saliva, debris in the oral cavity, or gingival margins. 9. No need to store or acquire trays and impression materials. 10. Eliminates the risk of contamination and the need for impression disinfection. 11. Eliminates the need for long-term model storage. Introduction to CAD/CAM Technology in Dentistry: The first attempts to apply CAD/CAM technology in dentistry began in the 1970s. Young and Altschuler introduced the idea of using optical instrumentation to develop a layered intraoral surface map in 1977. Francois Duret conceptualized how digital technology used in industry could be adapted to dentistry to obtain digital impressions. Duret's innovative idea dates to 1970, which he further developed in his doctoral thesis completed in 1972. The principle involves using a laser beam to obtain a digital impression based on the biphasic profilometry principle, which can then be transferred to a computerized design and manufacturing system. This is essentially the concept of CAD/CAM applied to the fabrication of various dental restorations. At the time, his enthusiasm was not widely shared. The first functional 3D intraoral camera for capturing intraoral images was called RedCam (using infrared laser radiation as a light source, later replaced by BlueCam – blue laser radiation) (Mormann et al., 1987). Today, an optical interference-free intraoral camera that provides a real-time, high-definition, color image, called Primescan, is the latest addition to the CEREC family and is among the top intraoral scanners. Conventional vs. Digital Impressions: Why use digital impressions? The answer is the same as for why we use cell phones, GPS, computers, etc. These technologies increase our efficiency and the quality of medical care. Digital impressions make the lives of dentists easier, better, more efficient, and increase patient satisfaction (Seelbach et al., 2013; Lee & Galucci, 2013). What can we evaluate with a conventional impression? Margin quality, whether it captured the entire area of interest, but the quality of the preparation can only be assessed after the model is poured. Statistically, over 50% of conventional impressions do not record the entire margin of the preparations (Christensen, 2005). With digital impressions, it is possible to evaluate the magnified image of the preparation in real-time on the monitor screen. Deficiencies that can be addressed on the spot, while the patient is still in the chair, such as the degree of preparation inclination, margin quality, retentive features, and interocclusal space, are highlighted using various color codes, with micron precision. Digital impressions eliminate the risk of material distortion, porosity, and tensile forces that can lead to distortion in conventional impressions. Research shows that the accuracy and precision of digital impressions are like conventional ones (Leu, 2008; Holmes, 1898; Endel & Mehl, 2011, 2013, 2015; Patzelt, 2014). Additionally, because digital impressions do not require the pouring of a model, there is no risk of gypsum expansion. Models produced from digital impressions are either 3D printed or milled from a block of material. CAD/CAM-produced models have acceptable clinical accuracy (50 microns) (Endel & Mehl, 2011; Patzelt, 2014). Digital impressions increase the efficiency and profitability of dental practices, being faster than conventional ones (Patzelt, 2014). Retaking a digital impression takes seconds and costs nothing. It eliminates the need for disinfection and impression storage. Only the tip (wand) of the scanner is autoclaved for each patient. Despite these advantages, there is still room for improvement, and manufacturers introduce new enhancements to digital impression systems each year. In the last 20 years, intraoral scanning devices have evolved significantly, to the point where conventional impression-taking techniques are predicted to become obsolete in the near future. CHAPTER 6. PROVISIONAL FIXED PARTIAL DENTAL PROSTHESES Provisional Fixed Prosthetic Restorations (PFPR) represent an important intermediate stage in the process of obtaining the definitive prosthetic restoration, designed to improve the aesthetics and enhance the function of the temporary dental prosthesis over a limited period of time (Glossary of Prosthodontic Terms). The term "provisional" emphasizes the temporary nature of the restoration, which is also referred to in the literature as a transitional, interim, or temporary restoration. In the construction of PFPR, the clinician must focus on both protecting and stabilizing dental structures and achieving the most accurate restoration of aesthetic, masticatory, and phonetic functions. The ultimate success of fixed prosthetic restorations and collaboration with the patient depend on the quality standards of this treatment phase. In the treatment of partial edentulism with fixed prostheses, PFPR must fulfil several objectives, including: • Diagnosis clarification. • Refinement of the treatment plan. • Patient's motivation for the treatment plan. • Communication of information to the laboratory. • Healing of remaining tissues. • Establishing occlusal and VDO (vertical dimension of occlusion) • Restoration and evaluation of phonetics, mastication, and facial plans. aesthetics. • Prevention of dental migrations. • Assessment of the parallelism of prepared teeth. Depending on the intended and actual duration, two categories can be distinguished: • Short-term PFPR. • Long-term PFPR, which can be maintained in the prosthetic field for up to 2 years. The concept of long-term provisional prosthetic restoration is relatively recent and refers to those temporary fixed prostheses that need to be maintained in the arch for several months, even 1-2 years, to allow for the consolidation of orthodontic, surgical, or implant prosthodontic outcomes. 6.1. Objectives of PFPR PFPR must fulfil a series of objectives, including: • Pulp protection. • Enamel surface protection. • Marginal periodontal protection. • Ensuring dimensional stability of the lower face. • Maintaining occlusal function. • Accessibility for proper hygiene. • Ensuring resistance and retention. • Ensuring appropriate aesthetics. • Prefiguring or supporting subsequent treatment stages. 6.1.1. Protection of pulp vitality from mechanical, thermal, chemical, and bacterial factors is achieved through: - Proper adaptation of PFPR to the abutment. - Covering the terminal area of the preparation with PFPR. - Preventing marginal saliva infiltration. - Choosing a thermally insulating material for PFPR construction. 6.1.2. Protection of enamel surfaces: PFPR prevents the fracture of the prepared abutment, or the edges of the preparation exposed to masticatory forces. 6.1.3. Marginal periodontal protection is achieved through proper PFPR conformation. To prevent gingival hypertrophy/inflammation, PFPR over contouring should be avoided. PFPR over contouring can cause gingival retractions. If it is a fixed provisional prosthesis with multiple elements (a provisional bridge), correct embrasures and hygiene spaces must be ensured. A properly designed and executed provisional restoration at the cervical level provides optimal conditions for impression of the terminal area and gingival sulcus. 6.1.4. Positional stability: PFPR prevents dental migrations of the abutments and antagonistic teeth. By preparing the abutments, the contact area with neighbouring and antagonistic teeth is lost, and the role of PFPR is to maintain positional stability by restoring occlusion and interproximal contact morphology, thus preventing vertical and horizontal migrations of abutments (mesialization, distalization), as well as vertical migrations of antagonistic teeth. These position changes result in mal-adaptations of definitive restorations, the need for subsequent adjustments, and sometimes the need to remake the definitive restoration. 6.1.5. Maintenance of occlusal function is achieved by: - Restoring contacts and relationships with the opposing arch. - Preserving occlusal stops. - The ability to test a new VDO (vertical dimension of occlusion). 6.1.6. Maintaining proper hygiene involves creating PFPR with open embrasures, a suitable design that allows the patient to establish a correct hygiene program, which will later be continued for the hygiene of future definitive fixed prosthetic restorations. 6.1.7. Ensuring resistance and retention. To prevent PFPR from fracturing under the action of masticatory forces, the clinician must pay special attention to the choice of material for construction and ensure optimal thickness and adequate retention at the abutment level. 6.1.8. Physiognomic function is of paramount importance in fixed prosthodontic treatment, especially in the frontal and premolar regions. The provisional prosthesis can prefigure the shape, color, and alignment of the future prosthetic restoration, playing a crucial role when effective communication with the patient is needed to modify the smile design. 6.1.9. By prefiguring or supporting subsequent treatment stages, PFPR allows for control of the preparations. Thus, it can be checked whether the preparation is sufficient both axially and occlusally, whether the abutments present retentive features, and whether they are parallel. The advantages of provisional prostheses include: • Providing physical and psychological comfort to the patient. • Educating the patient to maintain proper oral hygiene, necessary for future definitive fixed prosthetic restorations. • Refining the treatment plan. • Facilitating communication with the dental laboratory. • Correctly shaping the gingival tissue in the terminal area of the preparation, allowing for precise impression. The disadvantages of provisional prostheses include: • additional working time. • associated costs. • decementation or fracture of PFPR. • if the aesthetics of PFPR differ significantly from those of the definitive restoration, patients may have difficulty accepting the final prosthetic treatment. • allergic reactions to PFPR materials. • reversible or irreversible pulp inflammation following certain fabrication techniques (Bratu). 6.2. Classification of Provisional Restorations Provisional restorations can be classified based on their method of fabrication. Industrially obtained ones are only suitable for single-tooth provisional restorations and include aluminium crowns, anatomically contoured metal crowns, celluloid formers, and prefabricated polycarbonate crowns. Individually customized provisional restorations, made in the dental office or dental laboratory, can be crafted from a wide range of polymers and composite resins using various technical methods. Another classification of provisional restorations pertains to the fabrication technique, which can be either direct, performed in the dental office by the dentist directly on the patient's prosthodontic field, or indirect, where provisional restorations are created on a gypsum model in the dental laboratory. Depending on the number of teeth replaced, provisional restorations can be classified into: 1. 2. Single-tooth provisional restorations: • Temporary crowns - full or partial coverage. • Temporary inlays. • Temporary core-build-ups. • Temporary veneers. Partial fixed provisional prostheses: • Emergency prostheses - mainly used in the anterior region, post-extraction, or post-traumatic. • Protective prostheses - for vital abutment teeth. • Testing prostheses - serving as a guide to check occlusal, physiognomic, and phonetic functions of the future definitive restoration. • Waiting prostheses - belonging to the long-term type: • Space maintainers. 3. • Periodontal immobilization systems. • Post-surgical fixed partial prostheses. • Post-implant fixed partial prostheses. • Post-orthodontic fixed partial prostheses. • Socio-economic compromise fixed partial prostheses. Temporary removable partial prostheses (TRPP): - Emergency TRPP - after multiple tooth extractions or damage to existing TRPP. - Testing TRPP - physiognomic, occlusal, phonatory. - Waiting TRPP - for delaying definitive treatment. - TRPP with occlusal splint - if occlusal splint application is necessary for protection against parafunctional habits. - Space maintainers TRPP. - Post-surgical TRPP - after oral and maxillofacial surgery. - Socio-economic compromise TRPP. a. b. Fig. 6.1. Testing provisional restoration for veneers (a. initial situation, b. provisional after wax-up). 6.3. Materials for Fabricating PFPR Currently, there are numerous materials designed for provisional restorations, and they must meet the following criteria: • Biocompatibility (non-toxic and non-allergenic). • Compatibility with other materials (such as provisional cements). • Dimensional stability. • Low thermal conductivity. • Ease of preparation and manipulation. • Acceptance by the patient (non-irritating). • Easy adjustability and optimization. • Cost-effectiveness. Polymers intended for PFPR can be classified as follows: a. Self-polymerizing methyl or ethyl methacrylate-based resins. b. Thermally polymerizing resins for PFPR (longer duration). c. Photopolymerizing composite diacrylic resins. d. Dual-cured composite diacrylic resins e. Polymethyl methacrylate (PMMA), available in pre-polymerized blocks for CAD/CAM technology. Polymers and composite materials can be grouped as follows: auto- or thermal polymerizing acrylic resins, polycarbonate resins, self-polymerizing epiminic resins, composite diacrylic resins, acetal resins, auto-ligth-polymerizing/dual-cured resins, and glass fiber-reinforced resins. MATERIAL Advantages Disadvantages Metal prefabricated, no need for index Requires significant adjusments, poor aesthetics Polycarbonate prefabricated prefabricated, no need for index crowns Methyl methacrylate Ethyl-methacrylate Bis -acryl Major adjustments needed for marginal fit, contact points and occlusion Good strength and aesthetics, easy to Strong exothermic reaction, contraction, repair, multiple units, last long require shaping, laboratory involved Less exothermic reaction than PMMA, easy Less wear-resistant than PMMA, contraction, to repair shorter lifespan The most popular material (available in High costs, requires index, difficult to line, not syringes), significantly reduces exothermic suitable for long-span bridges reaction, no unpleasant odor, can be used for long term ususe, easy to handle UDMA Photopolymerizable, good mechanical High costs, requires index, exothermic properties, good aesthetics, easier to line reaction due to photopolymerization than bis-acryl Diacrylic resins Excellent aesthetics, ideal for temporary High costs, time-consuming veneers, can be used with or without shaping, no need for temporary cement Modified composites Low viscosity, ideal for provisional inlays, no The material is less resistant, poor need for index, temporary cement interproximal and occlusal contacts, difficult to remove from retentive areas TYPE Commercial name Manufacturer Advantages Disadvantages Methylmetaacrylate Alike Jet GC America Lang Dental - Good marginal adaptation - Good tranversal strength - Good polishablility -Durability Ethylmetaacrylate Snap Parkell -good polishability -minimal exothermic reaction -low volumetric contraction -chromatic stability - strong exothermic reaction -low abrasion resistance -pulpal toxicity due to residual monomer -high volumetric contraction -self-polymerizing -low hardness -low transversal strength -low durability -low fracture resistance -self-polymerizing Vinyl-ethylmethacrylate Trim II Bosworth -good polishability -minimal exotgermic reaction -good abrasion resistance -flexibility -chromatic stability Methyl-ethylmetaacrylate Unifast-LC GC America -good marginal adaptation -good transversal strength -good polishability -durability -dual polymerization BIS-acryl composite Luxatemp Turbotemp 2 Protemp II Temphase Goregeous Temp Zenith-DMG Oanvi lle Engineering 3M- ESPE Kerr DenMat -good marginal adaptation -minimal exothermic reaction -good abrasion resistance -good transverse strength -low volumetric contraction -dual polymerization -excellent polishability Compozit BISGMA TempSpan Pentron Clinical Tech -good marginal adaptation -good polishability -very low exothermic reaction -good abrasion resistance -good transverse strength -very low volumetric contraction -thin layer of unpolymerized oxygen -good chromatic stability -can be repaired with flow or hybrid composite -low hardness -low transversal strength -self-polymerizing -low fracture resistance -low surface hardness -low chromatic stability -fragility -thick layer of unpolymerized oxygen -higher cost compared to methacrylates -difficulty in repair -limited color selection The choice of the appropriate material for provisional fixed prosthetic restorations depends on several factors, including the fabrication technique, the extent of edentulism, the duration of PFPR usage, and the equipment available in the clinic or laboratory. 1. Acrylic Resins: • Self-curing and heat-curing types - Used in both direct and indirect techniques - Bicomponent system (powder and liquid) - Exothermic polymerization reaction, which can be harmful to dental pulp - Suitable for extensive PFPRs using the indirect technique - Heat-cured acrylic resins: § High aesthetic and mechanical qualities, chromatic stability, suitable for long-term PFPRs. 2. Polycarbonate Resins: - Granules of thermoplastic, reversible, injectable polymers - Used in the direct technique - Suitable for anterior teeth PFPRs - Superior properties compared to acrylic resins, autoclavable - Requires special injection equipment if fabricated in the clinic or available as prefabricated polycarbonate crowns. 3. Epimine Resins: - Available in a self-polymerizing, two-component system (base and catalyst) - Suitable for PFPRs made using the direct technique due to reduced toxicity and minimal exothermic reaction - Disadvantages include reduced chromatic stability, marginal adaptation, and mediocre wear resistance. 4. Composite Diacrylic Resins: - Photopolymerizable - Exhibit high values of chromatic, mechanical, and chemical resistance, with minimal contraction during polymerization - Suitable for both direct and indirect techniques for anterior and support zone PFPRs 5. High cost is a disadvantage. Acetal Resins: - Processed through thermos-injection - Outstanding characteristics: aesthetics, strength, resilience, biocompatibility, dimensional stability, easy processing. 6. Dual Resins: - self-photopolymerizable - Initial polymerization begins during mixing of the two components, transforming the material into an elastic phase that remains until final photopolymerization - Highest modulus of elasticity and remarkable fracture resistance. 7. Glass Fiber-Reinforced Resins: - New materials promoted by the Tragis-Vectris system - Suitable for long-term PFPRs (2-5 years) - Advantages include optimal aesthetics, minimal technical errors, excellent marginal adaptation, and resistance to masticatory forces. 8. Composite Bis-Acryl Resins: - Presented in an auto-mixable system - Suitable for long-term PFPRs, both single- and multi-toothed, in anterior and posterior regions, inlays, onlays, and prefabricated composite crowns - Advantages include excellent aesthetics, faithful marginal adaptation, easy cleaning, easy handling, superior mechanical properties, minimal contraction, and low setting temperature. Fig. 6.2. Bis-acryl resin, a two-component paste-paste system in a cartridge. The development in the field of nanotechnology has led to changes in the field of RPP, which has expanded by introducing prefabricated composite crowns for single-unit RPP, creating a hybrid between the advantageous results of auto mixable materials (aesthetics, adaptation, fidelity) and prefabricated crowns (material, time, and experience savings). Prefabricated RPP made of composite initially comes in a malleable state, like wax, and can be easily adapted and shaped to the dental preparation. Photopolymerization defines a resilient, finishable, polishable temporary crown. Advantages: optimal aesthetics, reduced working time, reduced costs (no need for impressions). 4. Techniques for obtaining prefabricated crowns 4.1 Prefabricated crowns • Materials used for prefabricated crowns: - polycarbonate. - aluminium. - tin-silver. - nickel-chrome; - composite resins. 4.1.1 Polycarbonate prefabricated crowns: - Suitable for both anterior and posterior regions; - Objectives: gingival protection, maintenance of occlusal relationships, restoration of contact area with adjacent teeth; - Working stages include: - color selection; - adaptation of the crown to the prepared abutment; - lining with self-polymerizing acrylic resin; - verification, adjustment, and polishing of the margins - verification of occlusal plane and occlusal stops; - checking the adaptation of the crown to the abutment; provisional fixation of the crown. - Working technique - for crown selection, the clinician determines the mesio-distal diameter of the tooth to be prepared, either intraorally or on a model - after preparing the abutment, the provisional crown will be adapted in relation to the adjacent teeth. If the crown is too long, it will be shortened at the cervical level using a handpiecemounted bur, following the gingival contour of the abutment. In case difficulties arise during the insertion of the provisional crown, it will be narrowed mesio-distally without compromising the proximal contacts with adjacent teeth. - Lining the temporary crown with self-curing acrylic resin will provide optimal retention and adaptation. - Prior to lining, the abutment and adjacent tissues are coated with Vaseline. - The acrylic resin is prepared in a dappen dish and the resulting resin paste is loaded into the polycarbonate crown and applied onto the abutment under pressure, to ensure registration of the gingival area. -pressure is maintained on the temporary crown until the resin regains its shape memory, visible in the cervical area, after which the clinician begins mobilizing the crown and repositioning it on the abutment - before final setting, the crown should be left in lukewarm water for 5 minutes for complete polymerization - if the new temporary crown fits perfectly, it will be processed, finished, and temporarily fixed 4.1.2. Prefabricated metal crowns: - indicated for posterior regions; - similar objectives to polycarbonate temporary crowns; - advantages: easy adaptability, well tolerated at the gingival level 4.2. Direct fabrication technique for temporary crowns: - eliminates laboratory procedures; - advantages: time and cost savings; - disadvantages: risk of tissue trauma during polymerization (due to temperature increase), inadequate marginal adaptation; - indications: single or multiple unit temporary crowns with a reduced number of teeth 4.2.1. Direct fabrication technique using custom trays Custom trays are auxiliary means for fabricating temporary crowns that reproduce the negative shape of the teeth before they are prepared or the modified tooth shapes with wax on a gypsum model (wax-up) Types of trays: prefabricated industrial trays and trays made in the dental office 4.2.1.1. - High-consistency silicone impression material (to be easily trimmed into the desired shape) is the most suitable direct tray: - advantages: flexibility, low cost, easy trimming; - disadvantages: sometimes difficult to reproduce surface details of the teeth. Fig. 6. Silicon index for creating provisional restoration. 4.2.1.2 - Thermoplastic films - made of propylene acetate or cellulose, with a thickness of 0.5mm - are heated and adapted to the gypsum model under vacuum - advantages: the transparency of the film provides constant visual control during the working time, ensures correct positioning of the conformer on the prosthetic field, and reduces working time. Fig. 7. Conformer obtained through thermo-vacuum forming. - the conformers will be perforated with a probe, towards the outside, in order to allow the RPP material to vent without creating any depletion in the thickness of the crown. 4.2.2. The steps for direct technique in the fabrication of RPD are as follows: 1. obtaining a conforming structure, in the form of an impression; 2. relieving the conforming structure to ensure optimal adaptation; 3. creating grooves on the vestibular and oral surfaces of the impression to guide excess material flow out of the conforming structure; 4. removing excess material after polymerization reaction; 5. when using thermoplastic foil conforming structures, photopolymerizable/dual resins can be chosen for RPD; 6. conforming the gingival margins; 7. verifying adaptation on the prosthetic field and occlusal plane; 8. finishing and polishing the RPD; 9. temporary fixation. 4.2.2.1. Fabrication of RPD through direct technique in the conforming impression - a high-consistency silicone-based impression material will be used to create the conforming impression - the prosthetic field will be impressed using a standard tray in a single-step impression technique (with two consistency types) - after removing the impression from the oral cavity, it will be trimmed to remove excess material for easy reinsertion. -the clinician prepares the abutment and after its completion, checks the adaptation of the conformer - Both the preparation and the adjacent area are lubricated with Vaseline - The chosen material for making the RPP is applied with the help of a dispenser and a nozzle, ready homogenized, inside the conformer at the level of the area to be restored - The conformer is applied to the prosthetic field and polymerization is awaited - If the RPP is over-contoured, the margins will be reduced by finishing - If the RPP has defects and gaps, they will be corrected with flowable composite - If the adaptation of the RPP is adequate, it will be finished with burs, brushes, and finishing paste. Fig. 8. Inserting the provisional restoration material into the silicone key. 4.3. The combined technique for the fabrication of RPD - consists of creating a RPD in the laboratory, based on the diagnostic model. This restoration is thin and not adapted to abutments, therefore it requires lining in the oral cavity. The advantages are: - reduced working time for the clinician; - increased biocompatibility due to the reduced amount of heat released intraoral; 3.1. The steps in the combined technique are: 1. taking an impression of the initial situation in a previous appointment; 2. removing the material corresponding to the gingival groove from the impression, thus widening the area of the cervical margin; 3. applying the material for the RPD inside the impression, on the teeth to be restored; 4. positioning the impression on the prosthesis field, on the prepared teeth; 5. polymerizing the impression; 6. removing the excess material; 7. polishing and finishing the RPD; 8. temporarily fixing the RPD. Fig. 9. Proper adaptation and contouring of RPP (Removable Partial Denture) margins. 4.4. Indirect technique for making RPD - obtained exclusively outside the oral cavity, without risks for the patient - after preparing the abutments, the prosthetic field is imprinted - a working model is poured - RPD is fabricated on the model. - Advantages: - abutments and marginal tissues are not exposed to polymerization - increased biocompatibility - optimal marginal adaptation (Bratu) - clinical steps: 1. Determining the color; 2. Tooth preparation; 3. Choosing the impression tray; 4. Highlighting the terminal area of the preparation; 5. Impressing the prosthetic field; 6. Pouring the model and performing laboratory steps; 7. RPD is checked in the oral cavity - proximal contact areas; - contour and possible surface defects; - occlusal and marginal adaptation. 8. Defects will be corrected by resin augmentation; 9. Provisional fixation. In order to visualize the aesthetic aspect of the future final prosthetic restoration and to improve clinician-patient communication, modern prosthodontics introduces new techniques: • Computer simulations • Wax modelling on a wax-up model • Intraoral mock-up modelling a. Computer simulations: - consist of the need for digital software -hardware tools through which the user can create the future virtual aesthetic aspect - necessary tools: - cameras and photo and video scanners - monitors and tablets - specialized programs that can communicate with CAD-CAM technologies have raised the standards of classical prosthodontics. Advantages are: - speed, efficiency - Disadvantages: - high costs for equipment, - sometimes the inability to accurately reproduce the virtual design in the oral cavity (Ionas) b. Wax modelling on a wax-up model: - the future RPD will be modelled in wax on the study model - indications: - choosing the treatment plan; - possibility of effective communication with the patient and presentation of the treatment plan. - making the silicone key. - advantages: - reduced time due to technical steps performed in the dental laboratory - the patient can visualize and suggest modifications regarding the aspect of the final restoration - perfect cervical adaptation - high aesthetics - disadvantages: - requires two treatment sessions - dental laboratory costs - Steps of fabrication of RPD modelled in wax on the wax-up model - the prosthetic field of the initial situation is impressed, with one session before starting the prosthetic treatment - based on this impression, a diagnostic model (wax-up) -the technician shapes the wax model based on the diagnostic model, and then duplicates the diagnostic model. -The technician creates a conformer based on the duplicated model. - Using the duplicated model, the technician prepares the future abutments. -The indirect classic technique is used to create the RPD on the abutments of the duplicated model. -Once the prosthodontist completes the abutment preparation, they will check the fit of the RPD received from the laboratory (which may not have an optimal fit with the prepared teeth). If adjustments are necessary, the RPD will be optimized. -The preparations and adjacent tissues are lubricated with petroleum jelly, and the clinician will line the RPD using a direct technique. - The RPD is then finished and temporarily fixed. c. Intraoral Mock-up: - It involves modifying the physiognomy directly in the oral cavity by applying composite material to the dental structures without using an adhesive system. - Indications: - Single-tooth structures in the frontal or lateral area (Ardu). - Advantages:- Rapid presentation of the result. - Requires only one session. - Disadvantages:- Requires an experienced clinician for the shaping. - Time-consuming treatment session (Ionas). Conclusion: With numerous technological options available for RPD fabrication, it is the clinician's duty to select the appropriate type of restoration for each individual case. 5. Fixation of RPD During the provisional fixation period, the following are monitored: • Proximal, occlusal, and alveolar ridge relationships • Esthetics • Soft tissue behaviour • Oral hygiene Qualities of materials used for cementing RPD: • Biocompatibility • Optimal marginal closure • Easy preparation, adequate working and setting time • Chemical compatibility with the polymer • Mechanical strength • Easy removal of excess material Removal of RPD should be easy, without affecting soft and hard tissues and without compromising the restoration. Stages of cementation: • Isolation of the prosthetic field • Preparation of the provisional fixation material • Loading of the RPD with the fixation material • Insertion of the RPD into the oral cavity, verification of correct positioning •Removal of excess cement CHAPTER 7. MODERN METHODS OF CHOOSING, COMMUNICATING AND REPRODUCING COLOR IN DENTAL PROSTHETICS The major advantages of the computerized methods of choosing and communicating the color are primarily objectivity and precision and can be concretized as follows: - they are not influenced by the surrounding environment. - they are not influenced by light; - the results are reproducible. The three large classes of devices for measuring color are: - RGB devices, - spectrophotometers - colorimeters. Devices that capture image information (for red, blue, and green) to create a color image are called RGB devices. Most digital cameras and video cameras belong to this category. Most RGB devices are based on the most basic electronic color determination system, but they show a certain degree of subjectivity because they cannot monitor certain variables. Color is determined using data captured by the digital camera. The accuracy of the information obtained with the help of these RGB devices is questionable since it is not based on an objective measurement. These systems are useful as a starting point for the information that will be transmitted to the dental laboratory. One such RGB system is Shade Scan by Cynovad (Fig.) With the help of this device, the appearance and color of the teeth can be perceived in a similar way to the human eye, but with the accuracy and consistency of a computer. During a few minutes, the image of the tooth is captured by scanning and will be sent to the laboratory. The software of this system records the data related to the three color parameters and elaborates the chromatic map of the tooth. The Cynovad Shade Scan system is an RGB device that records the chromatic characteristics of the teeth The times of using this device are: inserting the Shade Disk in the upper part of the part (Fig.4.6), applying the protective device and self-calibration. Then the screen of this scanner will be applied in contact and parallel to the surface of the tooth, after which the image will be captured, which will be transmitted through the Shade - Port system to the computer, where the image will be analyzed through the Shade Scan software (Fig. 4.7 ). Fig.4.6. Inserarea discului Shade Fig.4.7. Utilizarea soft-ului pentru alegerea Disk culorii şi întocmirea hărţii cromatice Digi Color is a system developed by O'Brien Dental Lab, which presents a complex program with multiple facets, which combines digital photography, color selection with color keys and photo analysis with the help of software that will be able to prepare a color map useful for the dental laboratory dental technique (Fig.4.16). With the help of a high-resolution digital camera, a photo is taken that will be printed on a special paper and sent to the dental laboratory. After the color analysis, the software will develop the chromatic map, through which the photographic image is obtained by color sections, giving the technician clear information regarding the choice of the optimal ceramic color set for each individual section. Fig. 4.16. The Digi Color system software analyzes the photographic image and creates the color map (in the image there is a tooth from the color key) The "Clear Match" system is a color communication software between the doctor and the laboratory, which uses mathematical analysis to determine the color of the teeth in a few seconds. The system requires a computer with the specific software installed and a digital camera, no other investments are required (Fig. 4.17). The stages of choosing the color using the Clear Match system are: 1. capturing the image with the digital camera, storing the image in the patient's file or integrating it into other software (Vipersoft® or Dentrix®); 2. choosing the color by recording the three color parameters H, V, C (hue, brightness and saturation) through a mathematical analysis system and obtaining a color map. 3. sending the information to the laboratory via e-mail; 4. comparing the results; the system presenting the possibility of evaluation by percentage differences of the initial image of the tooth with the one at the end of the treatment. Fig. 4.17. The Clear Match system allows the analysis of the color of the entire surface of the tooth, the creation of the color map and the transmission of information via electronic mail to the dental laboratory. Spectrophotometers The spectrophotometer is a device that consists of 3 main elements: a light source, the system for transmitting light to the object and receiving the light reflected from the object, and a spectrophotometer that determines the intensity of the received light as a function of wavelength. The Vita Easyshade system has a CPU for spectral data analysis and color determination to match the classic Vita system Vitapan 3D Master (Fig.4.18.). It is a portable intraoral spectrophotometer, easy to use. It consists of a base unit and a handle that connects to the base unit via a fiber optic cable. The handpiece contains a fiber optic assembly for illuminating and receiving light from the tooth, as well as a multiple spectrophotometer and a microprocessor for communication with the base unit. The communication between the handpiece and the base is done via USB. The basic unit contains a set of lamps, CPU, a fluorescent vacuum display with touch screen system and a removable calibration system. There are both RS232 and USB interfaces for connection with external computers. The system uses a 20Watt stabilized tungsten halogen bulb, with a color temperature of 3350 °K and a continuous light source for the entire spectrum. The lamp requires 15 seconds to warm up and stabilize, and the average life of the lamp is 100 hours. The Easyshade handpiece contains 3 separate spectrophotometers. One spectrophotometer continuously monitors the output signal from the lamp during the calibration and measurement process, and the other two are used to analyse the light that is reflected by the tooth. Spectrophotometers have separate receiving elements, located at different distances from the light source, and measure the color of a material (tooth or ceramic) for different depths. Fig. 4.18. Vita Easyshade system For infection control, a disposable polyurethane sleeve is applied over the handpiece. The process of determining color is based on comparison. A ceramic block of known color will be used for calibration. Several determinations are made for calibration: the first ones are with the lamp in the off position, and the following ones with the lamp in the on position, to illuminate the calibration block. The data obtained from the spectrophotometers will be transformed into a spectral curve (Fig.4.19), which is very useful especially in the research activity. Fig. 4.19. The data obtained with the help of spectrophotometers are more difficult to transpose in the daily activity in the offices, but they are extremely useful in the research activity. Widespread use of spectrophotometers in dentistry, both in research and in the clinical field, has been less extensive since the equipment required is expensive and sophisticated. Until recently, it was difficult to measure tooth color in vivo with the help of spectrophotometers. The best research spectrophotometer used is called spherical optics, where the object is placed inside the apparatus and exposed to light from different directions and angles. This results in the most accurate spectral analysis of the object. (Fig.4.20). Spectrophotometers for dental use cannot obtain the same degree of illumination all around (360 degrees), since the tooth cannot be placed inside the device. The light is directed onto the surface of the tooth. Fig. 4.20. A light exposure all around (360 degrees) cannot be obtained Fig.4.21. For clinical use of in clinical conditions (in offices) only in spectrophotometers, the best research conditions (15) setting is 45/0 (illumination at 45 degrees and observation at 0 degrees) (15) There are two settings used in reflectance spectrophotometers: illumination at 0 degrees and observation at 45 degrees (0/45), respectively illumination at 45 degrees and observation at 0 degrees (45/0). For clinical observation, only the second variant (45/0) can be used (Fig. 4.21). A spectrophotometer designed for clinical observation is the SpectroShade from MHT. (Fig.4.22.) This system uses two digital cameras, connected by optical fiber with a spectrophotometer that measures the teeth color parameters. The system is based on a multimodal mechanism, with a dual light source, which illuminates the teeth and allows translucency and reflectivity to be read. SpectroShade has the ability to display color results in an advanced graphic (Fig.4.23). Fig. 4.22. The Spectro Shade spectrophotometer of the MHT company 4.23. The Spectro Shade system offers the possibility to draw up the color map of the entire tooth quickly and precisely 4.2.3. Colorimeters Much of the research in the field of dental medicine regarding the color of natural teeth and ceramic restorations, both in vivo and in vitro, has been done with the help of colorimeters. They are designed to measure color as perceived by the human eye. A colorimeter filters light into three or four areas of the visible spectrum to determine the color of an object, but they are less accurate than spectrophotometers. A high-performance colorimeter is the X-Rite ShadeVision (Fig. 4.24), which shows remarkable efficiency, because it stores the data related to the three-color parameters (hue, saturation and brightness), unlike spectrophotometers that record at least 16 points of reflectance. A colorimeter can give information about color, similar to that provided by a spectrophotometer, but simplifying the process, eliminating a lot of data related to the spectral analysis that is obtained with the help of spectrophotometers, data that is not necessarily necessary. The stages of color determination through technological methods as in the case of traditional methods, the stages of color determination with the help of technological systems are the following: • -color analysis; • - color communication; • - color interpretation; • - making the restoration; • -checking the color of the restoration Color analysis Most technological color determination systems use the ΔE of the CIEL*a*b* system to determine the color difference between the tooth to be restored and a chosen color. This difference is the smallest distance in the CIEL*a*b* color space, between the colors that are compared and is determined by the following equation: ΔE=(ΔL*2+Δ a*2+ Δ b*2)1/2 L* - represents brightness (from white to black); a*- corresponds to the red-green axis (positive values indicate red, negative values indicate green); b*- corresponds to the yellow-blue axis (a positive value indicates yellow, a negative value indicates blue). ΔL, Δ a, Δ b, as well as ΔE are graphically represented in a numerical form in the Shade Vision and ShadeEye system, with the help of the Shade Match digital system. The SpectroShade system allows changing the chosen color depending on the different ΔE values, which will increase the accuracy of the initial choice. With the help of digital analysis, the goal is to obtain the lowest value of ΔE, which indicates the most accurate determination of the color, in the three areas of the tooth (gingival, middle, and incisal). This value is not directional, i.e. it does not indicate whether one color is darker or lighter than another. The ΔL value is the most important parameter, because the human eye can detect changes in brightness more easily than it can detect changes in hue. It has been shown that a value of ΔL less than 2 and a total difference ΔE less than 4 represents a clinically acceptable color. Digital analysis is faster and less subjective than conventional methods of color determination. The color is measured electronically, either with a colorimeter or with a spectrophotometer, and a color map is drawn up, visually checked, and sent to the technical laboratory dental. Color analysis also involves choosing the optimal material for each type of restoration, because the intrinsic properties of different materials can greatly affect the perception of the shade of the future restoration. Color communication A precise and efficient communication with the dental laboratory is the foundation of predictable and successful results in the case of aesthetic restorative treatment. With the help of technological systems, communication becomes much simpler and more precise, being carried out in electronic format. The images are captured and analysed by the existing processor in the office, and the information is then sent via electronic mail directly to the dental laboratory. It is good that, in addition to the information processed and transmitted in electronic format, digital color photos can also be sent, which can provide additional data regarding the appearance of the future restoration. Interpretation of the color In the dental laboratory, the technician will analyse the color map and interpret the photographs before proceeding to fabricate the restoration. The interpretation of data received via e-mail is subjective and depends on the knowledge and skills of the technician. It must take into account several factors that can change the perception of the color of a restoration, such as surface texture, anatomical shape, surface gloss and fluorescence. Fabrication of the restoration When fabricating a restoration, the technician must consider the intrinsic properties of the materials to obtain both the desired color and the appropriate translucency and opalescence. The devices that measure the color of the teeth on restricted areas (SM), help the technician to choose the color for the ceramic layers. Another parameter that must be considered is the age of the patient. The color of young patients shows a whitish tint with an increased brightness, which with age will turn into an orange color with a decreased brightness. As the patient gets older, the color may even have a brown tint, with a low degree of brightness. Increased calcification causes an increase in opacity, and with age the dentin becomes more opaque, darker in color and more visible through the thinned enamel layer. Restoration color verification Restoration color verification is significantly improved by the use of computerized techniques. For example, the Shade Vision system has a feature to virtually test the color of the restoration, and the SpectroShade system has a way for the technician to check the restoration electronically before sending it to the office. This check certifies the correctness and accuracy of the chosen color and reduces the number of failures, additional sessions needed to redo the restoration. Being introduced on the market of dental products for a relatively short time, and with predilection for equipping dental technical laboratories, a series of clinical studies are still needed, which highlight the superiority of these digital color selection systems and certify their profitability. The table below compares the advantages and disadvantages of traditional and digital color selection systems Table 6.2. Advantages and disadvantages of traditional and modern color selection systems System Benefits Disadvantage Conventional low cost subjectivity inconsistency ease of use in manufacturing visual manipulation can be the choice of color is transported affected by the environment, by the lighting conditions Digital more objectively, increased costs; the color can be checked in the interpretation of the the laboratory, report depends on the uninfluenced by the technician; environment, the lighting is not easy to transport conditions increases (e.g. Cynovad and Spectro productivity (reduce Shade) working time, fewer failures) CHAPTER 8. ALL-CERAMIC SYSTEMS Contemporary prosthodontics is overwhelmed by the multitude of ceramic materials available on the market, making the material selection process difficult for the clinician. Achieving successful clinical results involves two important factors: (1) knowledge and proper selection of the material and (2) the skill of the practitioner which includes proper handling of the material and proper communication with the dental laboratory. WHAT ARE DENTAL CERAMICS? A ceramic is a product made from a non-metallic inorganic material processed by firing at high temperature to achieve desired mechanical and optical properties. The advent of all-ceramic materials has radically changed the therapeutic workflow from preparation to cementation (da Silva LH, 2017; Bajraktarova-Valjakova E, 2018). All-ceramic systems are biocompatible, have acceptable long-term clinical strength and are aesthetically superior. The use of ceramics in dentistry started to become popular in the sec. The aesthetic characteristics of this material compared to other materials used are largely responsible for its popularity in the 18th century. Alexis Duchateu, a pharmacist in Paris integrated dental ceramics, and later in 1903, Charles Land created the first all-ceramic inlays, onlays and crowns using fired ceramics (Mörmann WH, 2002). Technical performance led to the development of new biocompatible ceramic materials with excellent aesthetics and greatly improved optical properties, but also with superior mechanical properties and reduced plaque retention (Zarone F, 2011; Bajraktarova-Valijakova, 2018). For their everyday use in dentistry, ceramics must meet specific criteria: (1) hardness similar to dental tissues and prevent crack propagation, (2) adequate mechanical strength to withstand occlusal forces, (3) superior optical and aesthetic properties, and (4) predictable in vivo performance that provides long-lasting restorations. An ideal ceramic material should be translucent at the incisal margins, opaque in the cervical area, provide adequate strength and allow preservation of tooth structures. They can be successfully used for all types of prosthetic restorations(unidental crowns, inlays ,onlays and veneers (Nikolopoulou F, 2014; Edelhoff, 2011). Dental ceramics can be classified into two broad categories: -1. silica-based - feldspathic ceramics, leucite-reinforced ceramics, lithium disilicate-based ceramics, -2. oxide-based - zirconium oxide, Y-TZP and aluminium oxide (Allied Market Research, 2017). Glass ceramics The anorganic phase of ceramics is composed of a residual glass phase to which finely dispersed crystalline phases are added (Gracis S, 2016; Shenoy A, 2010). The crystalline phase can contain between 0.5% to 99.0% of the composition, but typically contains 30% to 70% of the final composition (Montazerian M, 2017). The type, size and volume fraction of the crystalline phase together with the distribution in the glass matrix are among the important factors in controlling mechanical and aesthetic properties such as hardness and translucency of the final material. In addition, the presence of crystalline phase improves the mechanical strength of the final material by inhibiting crack propagation (Fu L, 2020). The glassy phase also contributes to the improvement of mechanical properties through marginal grain deposition. Advantages of glassy ceramic matrix over traditional ceramics include ease of synthesis process, low shrinkage and improved translucency due to decreased internal light scattering (Ho GW, 2011; Fu L, 2020). Glazed ceramic matrix is divided into two subcategories: natural materials such as feldspathic ceramics and synthetic materials such as lithium disilicate. Feldspar ceramics Feldspar ceramics are known as traditional dental ceramics which are based on a ternary system composed of natural feldspars (potassium/sodium aluminosilicate), kaolin (Al2O3.SiO2.2H2O), quartz (SiO2), and a few metal oxides as additives (Saint-Jean SJ, 2014). During the fabrication process, fused feldspar provides a glassy matrix for the distribution of a disordered silicon tetrahedron lattice. Feldspar ceramics are silicon-based ceramics available in sintered or milled form, which have a low to medium flexural strength (65-120 Mpa)(Li R,2014). This class of materials can be produced in different shades with different degree of opacity and translucency by adding metal oxide pigments. In dentistry, opaque feldspathic ceramics are used as a first layer that protects the underlying metal, followed by a layer of ceramic enamel to reproduce the natural color of the tooth. Despite their advantageous properties, feldspathic ceramics are limited to low-stress anterior applications due to lower flexural strength and increased brittleness. The perceived color of natural teeth is the result of dentin reflection modified by absorption, dispersion, and enamel thickness (da Silva LH, 2017). Translucent porcelain may have a greater effect on the colour of the facets than opaque substrate. There is a significant correlation between core thickness ratio, ceramic veneer and restoration colour. Even when there is adequate thickness, clinically appropriate shades are difficult to achieve because there is a wide range of translucency between the core materials of all ceramic systems at clinically relevant thicknesses. Clinicians claim that porcelain with high opacity could be used to reduce the colour difference of porcelain veneers when cementing on a dark or substantially discoloured tooth. Various manufacturers have introduced the high opacity porcelain system and claim superior colour stability on any substrate. These ceramics are considered to be the most conservative and generally the most translucent ceramic materials, but they are also the least durable. The high transparency of the material and its aesthetics create the illusion of natural teeth. Stratified feldspathic veneers are indicated in the restoration of dyschromic teeth because the layered porcelain powders offer more flexibility in terms of alternating between opacity and translucent areas. Because it can be layered in very thin layers that are applied directly to enamel, this ceramic is considered to be the material that allows the greatest preservation of remaining tooth structures. If we refer to ceramic veneers, they require a thickness of 0.2-0.3 mm for each shade changed. Many dentists choose feldspathic veneers because they can be made thinner than pressed ceramics. Vitablocs (Vita Zahnfabrik, Bad Säckingen, Germany) are among the most widely used digitally milled feldspathic ceramics (CAM) with an average flexural strength of 154 MPa. Feldspar ceramic restorations that are bonded directly to the glaze have proven to be successful in the long term. Leucit-reinforced ceramics Leucite-reinforced ceramics are silicon-based ceramics available in sintered, pressed or milled form. It contains up to 45% leucite by volume, which has a medium bending strength (120-140 MPa) and compressive strength. Leucite crystals can stop the propagation of cracks and contribute to an increased strength of the ceramic mass (Fasbinder DJ, 2002). Lithium disilicate Synthetic glass ceramics emerged as an alternative to natural glass ceramics, with a higher volume fraction of the crystalline phase distributed in the glass matrix. Currently, lithium disilicate glass ceramics are among the most popular dental restorative materials (Montazerian M, 2017). Lithium disilicate is a silicon-based ceramic available in sintered, pressed or milled form (Zarone F, 2016). Lithium disilicate glass ceramics are based on the SiO2Li2O system composed of randomly oriented lithium disilicate crystals, resembling fine platelets, or rods at concentrations higher than 70% and a lower concentration of lithium orthophosphate (Li3PO4) crystals dispersed heterogeneously in the glass matrix (SaintJean SJ, 2014; Ho GW, 2011). The higher concentration of crystalline phase and tighter interconnection of the synthetic glass ceramic matrix exhibit significantly higher strength of about 350 MPa and fracture toughness of 2.5 MPa m1/2 compared to natural feldspathic porcelain (Ho GW, 2011; Ritzberger, 2010). Secondary to the improved mechanical properties, this restorative material can have a wide range of applications, including resin-cemented veneers, crowns, and 3-unit bridges up to the second premolar. IPS e.max (Ivoclar Vivadent, Schaan, Liechtenstein), a lithium disilicate ceramic, was developed in part by Prof. Wolfram Holland at Ivoclar Vivadent. After the development of clinical applications, the material was released to the dental community about 12 years ago. This ceramic material is much researched, and many authors have described its physical properties. The effects of lithium disilicate on fracture potential and tensile strength have been tested, as well as the effects of physiological ageing in aqueous media, abrasivity, wear, and surface roughness. The results of the studies revealed that almost all clinical requirements considered ideal for dental ceramics used in clinical practice have been met or exceeded. Celtra Duo (Densply Sirona,York, PA) is one of the newest lithium silicatebased ceramics available on the market. It is a zirconia-reinforced lithium silicate, containing around 10% zirconium oxide. The manufacturer claims that the smaller crystal size and ultrafine microstructure material lead to increased mechanical strength. Celtra Duo lithium silicate-based ceramics are available in pressable or milled form and can be used for crowns, partially cemented crowns (inlays, onlays, veneers) (Lawson NC, 2016). Another lithium disilicate-based ceramic material is GC Initial LiSi Press (GC America, Alsio, IL) which have high strength and density. This new lithium disilicate ceramic provides an even distribution of microcrystals, leading to excellent mechanical and optical properties. Recommended indications for pressed ceramics are crowns, inlays, onlays, veneers, and 3-unit fixed partial dentures up to the second premolar (Hallmann L, 2019). Monolithic full-contour restorations adhesively fixed with resin cement are fabricated from lithium disilicate even for higher stress situations at the molar level. Lithium disilicate attests to the safety of its use for any kind of single restorations or small fixed partial dental prostheses in the frontal area. Due to the glassy properties of this material, adhesive cementation is recommended. However, bonding to dentin gives less predictable results for these restorations because of the flexibility of dentin. Enamel bonded restorations are much more predictable, as enamel is known to have a significantly higher rigidity than dentin. Aluminium oxide (alumina) Alumina (Al2O3) is a naturally occurring oxide with a wide range of industrial applications, such as abrasive materials secondary to its high hardness. In addition to high hardness, superior wear and corrosion resistance along with biocompatibility have made this material a popular candidate in dental medicine (Ben-Nissan B, 2008). The very fine grain size of medical-grade alumina ceramics prevents static fatigue and deflects cracks while under load. All these properties have made alumina a desirable substrate for a wide range of medical applications, including dental restorations and orthopaedic applications. However, alumina ceramics are prone to mass fracture due to their high elasticity (Scherrer SS, 2008). Nobel Biocare's Procera AllCeram (Zürich, Switzerland) (the first dense polycrystalline ceramic) and In-Ceram AL, a product of VITA Zahnfabrik, are the best known representatives of this type of ceramic. Zirconium oxide (Zirconia) Zirconium oxide ceramics use CAD-CAM techniques to fabricate a wide range of prosthetic restorations, crowns, bridges, implant abutments, mobile and removable dentures. Y-TZP zirconium oxide is milled in the presintered phase, then sintered to reduce its volume by about 20% (Shenoy A, 2010). Zirconia (zirconium dioxide) is a polycrystalline ceramic with excellent hardness, strength and fatigue resistance. Depending on the temperature, this polymorphic ceramic can be formed of 3 different crystallographic phases, such as the cubic phase formed at temperatures above 2300°C, the tetragonal phase at temperatures between 1100°C and 2300°C, and the monocyclic phase occurring at room temperature up to 1100°C (Bona AD, 2015; Manziuc M-M, 2019). By adding stabilizing oxides, such as magnesium, yttrium, cerium is developing the characteristic of transformation toughning - the so-called martensitic transformation. Partially stabilised in the tetragonal phase under the action of mechanical stimuli, it transforms into the monocyclic phase, which is much more stable and achieves a volume increase of 4%. This growth stops cracks propagating in the material through compression, giving zirconium oxide its reputation as a smart material. The stable crystalline phase for zirconia at room temperature and atmospheric pressure is monocyclic. The monocyclic phase transitions into the tetragonal phase at around 1170 °C with a shrinkage of about 5% and a slight expansion during cooling. With increasing temperature up to 2370 °C, zirconia passes from tetragonal to cubic phase with a subsequent change in volume of 2.3% (Bona AD, 2015). Zirconia has similar elasticity to stainless steel but superior biocompatibility. In addition, low plaque retention results in the maintenance of good periodontal health after the application of restorations made of this material (Gautam C, 2016). There are probably over 50 different zirconia-based ceramics and often the technician or clinician has no idea what the manufacturing standards were for a particular zirconia block or disc used to fabricate restorations from different sources. The fatigue strength depends on the manufacturing standard applied by the manufacturer. Yttria-stabilised zirconia (flexural strength >900 MPa) is indicated for clinical situations including anterior and posterior crowns, inlays, implant bridges/crowns, 3-unit fixed dentures, fixed arch restorations (up to 14 units)(DC-Zircon). Zirconium dioxide can also be used when a large amount of dental tissue is missing or when there is a risk of bending and stress, for posterior unidentate restorations and for posterior multi-unit fixed restorations, or when adhesive cementation is problematic due to subgingival margins. The flexural strength of widely used zirconia-based dental ceramics ranges from 1.0 to 1.4 GPa (Glidewell [Newport Beach, CA] BruxZir Solid Zirconia, 1-1.4 GPa; Ivoclar Vivadent Zenostar T, 1.2 GPa; Katana Zirconia [Kuraray Noritake Dental Inc., Okayama, Japan]). Due to their high opacity, several studies have attempted to increase the translucency of zirconia materials by modifying their microstructure, including decreasing their aluminium content, increasing their density, decreasing their grain size, adding zirconia in the cubic phase, and decreasing the amount of impurities and structural defects (Bajraktarova-Valjakova E, 2017). Crystalline grain size is the microstructural feature that is closely related to the translucency adjustment of polycrystalline ceramics. The creation of ceramic materials with high translucency has been achieved in the past by increasing grain size during sintering. Larger grains lead to a smaller number of neighbouring grains, thus reducing light scattering. For Y-TZP, larger grains have been shown to be detrimental to both mechanical properties and tetragonal phase stability. Therefore, zirconia translucency cannot be achieved by increasing the grain size. Low translucency has made ceramic materials from zirconia to be a little more aesthetic and it was a challenge for the technician to achieve aesthetic results. An alternative method of fabricating Y-TZP with high translucency is achieved by significantly decreasing the grain size. However, the grain size should be decreased until a critical value is reached which results in the attenuation of the socalled birefringence phenomenon . Birefringence occurs in Y-TZP due to the large amount of tetragonal crystalline phase (>90%), which is a crystal that has different refractive indices depending on the crystallographic orientation in the microstructure. Such anisotropic behaviour related to refractive index variation causes light scattering. Another way to overcome the effects of light scattering, is the use of cubic zirconia, which provides optical isotropic behaviour, increasing translucency (Bajraktarova-Valjakova E, 2017). However, the increase in translucency (due to the increase in the content of the cubic structure) leads to a decrease in bending strength. The flexural strength of translucent(super and ultratranslucent) zirconia ranges from 500 to 800 MPa (Glidewell BrixZir Anterior and Ivoclar Weiland Zenostar MT, and Katana [Noritake] STML, 750 MPa and UTML 560 MPa). It has been reported that zirconia translucency is variably dependent on processing method, manufacturer formulation, and laboratory sintering times and temperatures. Updated classification of ceramic materials(Mc Laren) Another more updated classification of all-ceramic materials was developed by Edward Mc Laren in 2015. According to this classification there are 4 main classes of ceramic materials: CLASS I (Powder/Liquid or Feldspar Ceramic) Powder and liquid ceramics are created from materials containing silicon dioxide, a glass matrix and varying amounts of crystalline phase within that glass matrix (example: Creation Porcelain, Jensen Dental, www.jensendental.com; Ceramco3, DENTSPLYInternational, www.dentsply.com; EX-3, Kuraray Noritake Dental, Inc., www.kuraraynoritake.com). Class I ceramics include feldspathic ceramics. Feldspathic materials currently available include : Vita VM 13, Vita Zahnfabrik, www.vita-zahnfabrik.com; Vintage Halo, Shofu, www.shofu.com. Class I ceramic materials are handmade. They are the most conservative and generally the most translucent ceramic materials, but they are also the least durable. Powder and liquid ceramics are ideal for cases where we have significant amounts of glaze remaining. Because it can be layered in very thin layers that are applied directly to the enamel, this ceramic is the material that allows the greatest preservation of remaining tooth structure. If we refer to ceramic veneers, Class I ceramics require a thickness of 0.2 mm to 0.3 mm for each shade changed. This class of material is most suitable for anterior restorations, but can occasionally be used for premolars and rarely for molars, providing all parameters at a very low risk level. CLASS -II (Glass ceramics) The composition of Class II ceramics is similar to that of Class I, as both ceramics possess a glassy matrix, but the two classes differ in their crystal phase ratios and crystal types. In Class II ceramics, crystal types can be added to the glass or grown in the glassy matrix. - CLASS-II a Materials in this subdivision have a low-moderate leucite content (less than 50%). Such materials (e.g. IPS Empress® CAD, Ivoclar Vivadent, www.ivoclarvivadent.com; Authentic®, Jenson Dental; VITABLOCS® Mark II, VITA Zahnfabrik) contain less than 50% crystals and behave more like glass, requiring bonding. Like all Class II materials, which have come to be known as glass ceramics, CL-IIa materials have the same clinical indications as Class I, i.e. anterior teeth, premolars and in rare situations molars. In addition, their clinical success in situations of increased occlusal stress or when we have more exposed dentin has been documented over time. They are very translucent, but require slightly larger sizes for processing and aesthetics/shade matching (e.g. a minimum thickness of 0.8 mm to layer this ceramic). Materials in this sub-category have demonstrated increased strength. These dense materials containing glass and leucite are suitable for thicker veneers, crowns in the front, inlays and posterior onlays, but only when long-term adhesion can be ensured. CLASS-II b This is a new sub-category that has a moderate to high content (more than 50%) of crystals containing glass or glassy ceramics. It presents itself as a homogeneous glass, which after secondary treatment creates and grows crystals. This process provides improved physical and mechanical properties by increasing the number of crystals and generating compressive stress around the crystals. An example of a material in this subcategory is lithium disilicate (e.g. IPS e.max®, Ivoclar Vivadent). CLASS III (High strength crystalline ceramics) Class III materials are high strength crystalline ceramics that have little or no crystalline phase and are also produced by industrial processes. - CLASS III a CL-IIIa materials are manufactured by creating a porous matrix that is formed into a block and then processed into its final form using CAD/CAM technology, after which a second phase follows when a material melts and fills the pores of the first material. This material is disappearing from the market, being replaced entirely by 100% polycrystalline ceramics. - CLASS III b High strength, 100% crystalline ceramic CL-IIIb was originally represented by alumina-based materials (e.g. Procera®, Nobel Biocare, www.nobelbiocare.com). More recently, zirconium oxide based ones have been introduced (eg LAVA™, 3M ESPE, www.3MESPE.com; Prettau®, Zirkonzahn, www.zirkonzahn.com). Alumina systems have proven successful for single tooth restorations but have gradually been replaced by zirconia and lithium disilicate. Whether alumina or zirconia, both materials have demonstrated greater strength than CL-I and CL-II materials and can be used in the fabrication of a framework to replace the metal framework. These materials can be veneered with ceramic layers, resulting in superior strength and significantly improved aesthetics. Materials in Class III typically require a thickness of 1.2 mm to 1.5 mm, depending on the color of the substrate. Currently, more translucent versions are being used for monolithic restorations in zirconia. The first material commercially available in this category was BruxZir® by Glidewell Laboratories. Zirconia used in dental laboratories is typically supplied in the form of presintered discs. There is currently a wide range of zirconium oxide-based materials used for prosthetic restorations. This class of materials has evolved significantly in recent years, with the emergence of translucent, super, and ultra-translucent materials designed for esthetic monolithic restorations. Manufacturers recommend adhering to minimum dimensions for connectors when fabricating fixed prostheses to avoid failures. The maximum mesiodistal distance between abutment teeth for zirconia should ideally not exceed 25 mm. As indicated by fractographic studies (Rekow, 2011), most fractures in all-ceramic fixed prostheses occur due to stress concentration at the connector area. Zirconia-based materials, especially the newer ones with increased translucency, allow the creation of monolithic fixed prostheses that can have sufficient thickness, eliminating the need for veneering with ceramic. In the last five years, zirconium oxide-based ceramics have emerged that are super-translucent or ultra-translucent but have lower strength, approximately 600 MPa, which affects the range of indications and cementation procedures. Class IV (Metal-Ceramic) Materials in class IV are essentially materials from class I fused with a metal substrate, allowing their use in clinical situations with increased stress where conventional crowns are necessary. Like class III materials, class IV materials, namely metal-ceramics, demonstrate higher strength, but their aesthetic characteristics are limited. Metal-ceramic materials require a thickness of at least 1 mm to achieve a natural-looking esthetic. Metal-ceramics exhibit similar qualities to class III materials based on zirconia, but they are not as sensitive to ceramic firing, unlike zirconia. The materials in CL-I can be aesthetically enhanced by using a metal framework with a higher gold content (e.g., Captek™, Argen USA Inc., www.captek.com). The chemical composition and characteristics of today's dental ceramic materials provide a framework for determining the class of ceramics that can be used for a specific clinical case. However, there are other factors that influence material selection, including the preservation of tooth structure, the possibility of adhesive cementation, aesthetic requirements, smile design, and tooth shade. Class I and Class II materials offer improved aesthetics but have lower strength. It's important to note that all types of ceramics are less resistant to shear and fracture forces compared to compressive forces. However, by controlling the stress to which these materials are subjected, they can be successfully used in fixed prosthetic restorations. The use of integral ceramic systems for fixed prosthetic work has its limitations and specific requirements. Correct diagnosis and patient selection are critical factors for success. Other factors that may restrict the use of integral ceramic systems include limited interocclusal space, deep occlusion, severe bruxism, and parafunctional activity. The selection of integral ceramic systems depends on specific indications for each clinical case, and the clinician must pay attention to preparation details, adaptations, and the cementation protocol, considering the potential risks associated with each individual case. MATERIAL SELECTION FOR CERAMIC RESTORATIONS To choose the appropriate dental material, important parameters should be considered: 1. Position: The clinician should consider whether the restoration will be used for the anterior or posterior region. For anterior restorations, a more translucent ceramic material with lower mechanical strength leads to favourable aesthetic results. However, for posterior restorations where translucency is not important, a stronger ceramic material such as alumina, zirconia, or lithium disilicate is recommended. 2. Design: The clinician should consider the design of the ceramic restoration, whether it's a single unit or a multi-unit FDP (fixed dental prosthesis). Certainly, for multi-unit restorations, a stronger ceramic material is recommended. 3. Strength: It's necessary to assess the biomechanical risk and analyse occlusal forces. For medium to low biomechanical stresses, feldspathic ceramic or lithium disilicate is recommended. However, for medium to high occlusal demands, stronger ceramics such as alumina or zirconia are more suitable. 4. Substrate: The tooth or material substrate is one of the most important criteria for selecting ceramic restoration materials. There are three factors to consider: the percentage of remaining enamel, the percentage of remaining dentin, and the presence or absence of discoloration. In the anterior sextant, when there is more than 50% remaining enamel substrate, the use of feldspathic ceramic is favoured due to its increased translucency and optical properties. However, when the amount of remaining enamel is less than 50% in the presence of discoloration, lithium disilicate is the material that should be chosen. In the posterior sextants, feldspathic ceramic is contraindicated due to its low mechanical properties. For ceramic restorations made from lithium disilicate, the clinician should always consider adhesive bonding to the underlying tooth structure. For restorations made of alumina or zirconia, adhesive cementation is necessary only if retention is compromised (height <3mm and a convergence angle >20°). 5. Translucency: To achieve successful aesthetic results, it is important to consider the translucency versus opacity of the ceramic restoration material. Generally, in the aesthetic zone, a material with high translucency is desired, while for the posterior region, high opacity is favorable. FACTORS INFLUENCING THE CHOICE OF CERAMIC MATERIAL AND RESTORATION TYPE Mechano-chemical properties, biological factors, as well as aesthetic requirements are the foundation for selecting an "allceramic" material from which a fixed prosthetic restoration will be made. From the range of aesthetic materials available in the dental products market, the decision for a specific material should be based on the individual clinical situation, analysing the advantages and disadvantages of each material to choose the optimal one. Restorations in the frontal zone pose an aesthetic risk when modifying the smile design is desired. This risk involves either altering the proportions and ratios of the teeth, making minor positional and alignment changes, or modifying the color in the context of the facial features and the lines that characterize it. When it is necessary to mask the discoloration of an abutment or when a higher degree of translucency is required to achieve the most natural tooth appearance, the choice of the appropriate material should be based on the optical properties of each material. To prevent occlusal risks, restorations should be carried out after a proper occlusal analysis of the models mounted in the articulator, in order to anticipate signs or symptoms of TMJ pathology or occlusal disorders of muscular origin. If dealing with a patient at high occlusal risk, special attention is required when selecting the ceramic material for the restoration, especially for patients with bruxism. When restoring the entire arch, extra attention to detail is necessary to ensure occlusal harmony that provides a healthy stomatognathic system while minimizing stress on the restoration. When opting for all-ceramic adhesive cemented restorations, the amount of remaining enamel is essential for the success of the restoration. The minimally invasive and conservative principle is a crucial requirement in tooth preparation for all-ceramic restorations. The quality and quantity of dentin at the cementation interface can compromise the longevity of the restoration, especially if it is sclerotic or carious. If there is increased sensitivity to cold, it indicates that the collagen network in the dentin has been significantly altered, which will also compromise the adhesion of the final restoration. Additionally, if proper isolation cannot be achieved during an adhesive cementation procedure, failure is imminent. In the case of subgingival preparations, patients with limited mouth opening, or any other situation where proper isolation is impossible, choosing an allceramic system that can be conventionally cemented (CIS, CIMR) is preferred. Strength of Ceramic Materials Based on compressive and fracture strength, ceramic materials can be ranked in the following decreasing order: zirconium oxide-based ceramics (800-1200 MPa), alumina-infiltrated ceramics (236-600 MPa), lithium disilicate ceramics (300-500 MPa), leucite ceramics, and feldspathic ceramics (between 100-120 MPa) (Lawson NC, 2016). Translucency of Ceramic Materials Ceramics with moderate translucency and opacity are indicated for discolorations, metal-ceramic crowns, and implant abutments. Although these materials can mask discolorations, there are situations where a more opaque material is necessary. Among these moderately translucent materials, nano-ceramic resin materials (Lava Ultimate [3M ESPE]) and lithium disilicate (e.max Ivoclar Vivadent, LT, or MT) can be mentioned. Ceramic materials with minimal translucency and high opacity (capable of covering discolorations) include CAD/CAM blocks made of zirconium oxide and yttrium-stabilized zirconium oxide, aluminium oxide and zirconium oxide coping, CAD/CAM blocks made of lithium disilicate (e.max HT), and monolithic zirconium oxide. Fully opaque materials include: • Monolithic zirconium oxide • Pressed-to-metal (PTM) systems (Authentic, Jensen Industries) • Ceramic veneering for metal frameworks made of noble alloys, semi-noble alloys, titanium (Titanium, Platinumpalladium/high gold hybrid: Captek). Based on these classifications, we can make an informed choice of the appropriate material depending on the prosthetic restoration we are planning to create. The probability of survival for all-ceramic prostheses increases with the increase in the modulus of elasticity. Periodically, ceramic surfaces need to be polished (using polishing stones and rubber wheels designed for ceramics) to reduce the potential for wear by the enamel surfaces of opposing teeth. The thickness of connectors should be adjusted depending on the material from which they are constructed. For lithium disilicate, the occlusal-gingival thickness should be around 4-5mm, and the buccal-lingual thickness should be 3-4mm. For YTPZ polycrystalline D, the dimensions are OG (occlusal-gingival) = 2.8mm and D (V-L) (buccal-lingual) = 2.7mm. Especially in the anterior zone, where aesthetic requirements are the most demanding, knowledge of each material's characteristics allows us to thin the connector to the maximum extent possible, helping us achieve the final aesthetic result without compromising the structural strength and creating adequate space for interdental papillae, which should be between 45mm in the cervico-incisal direction from the free gingival margin. Longevity and Prognosis of All-Ceramic Restorations It is widely accepted that fracture is the most common cause of failures in all-ceramic restorations, regardless of the fabrication method. More translucent ceramics are more brittle than the opaquer ones (Denry I, 2014), which means that the ideal ceramic material for all applications has not yet become a reality. Regarding the marginal adaptation of all-ceramic restorations, it is influenced by several sources of error related to scanning, design, limitations of the milling process, and the fractures that may occur during milling. Nakamura (2003) and Santos (2013) have highlighted marginal discrepancies ranging from 53-67 microns, and these discrepancies tend to increase with more angled preparations (Nakamura M, 1978; Santos, 2013). CAD/CAM materials with the most studies to date are the ones that appeared first, namely ceramic blocks. The 10-year survival rate of leucite ceramics has exceeded 90%, according to studies by Della Bona and Kelly (Della Bona, 2008). In addition, ceramics with a high glass content are sensitive to stress corrosion due to the wet oral environment, which can initiate and propagate cracks (Shenoy, 2010). The current formula of lithium disilicate in the CAD/CAM version has been available only since the late 2000s. There are already several studies, and their number is increasing over the years (Fasbinder, 2010). Monolithic restorations made of cubic zirconia have proven to have better light transmission than layered ones. Depending on the differences between them in terms of crystalline phase, processing method, the loads they are subjected to, clinical studies have shown survival rates of over 90% (Strub, 2013). Wear/fracture of ceramic restorations can occur during milling, other laboratory stages, cementation, or during function. Defects that can occur in ceramic masses during the milling process can act as stress concentration factors that can initiate a crack in the material, leading to subsequent fracture. Another cause of defects can be attributed to laboratory handling, particularly sandblasting treatment to prepare the restoration before veneering with ceramic. The damage resulting from this process may not be immediately visible but can compromise fatigue resistance in zirconia and alumina restorations (Denry I, 2013). The survival rate for CAD/CAM fixed zirconia prostheses varies around 70-80% (Raidgorski, 2012), with the major causes of failure being material chipping, delamination, intermediate framework fracture, and issues related to the abutment teeth. Clinical experience highlights that there are many factors that can affect the occlusion of crowns made through conventional techniques. Errors in achieving optimal occlusion can also occur with CAD/CAM techniques, as the design and milling steps can introduce occlusal errors. Differences in occlusal contacts can exist between the proposed design and the milled crown. Some materials, like leucite-based and disilicate ceramics, pose fewer problems for intraoral occlusal adjustments compared to strong materials like zirconia, which can create significant challenges for clinicians during occlusal adjustment and subsequent polishing. Normal occlusal forces range between 9 and 180N, with a duration of 0.2-0.33 seconds during chewing (Larson, 2009). The maximum bite force in young individuals falls between 516-532 N in the posterior region. Occlusal forces are greater towards the back, with the second molar bearing over 55% of the maximum bite force, while incisors handle about 20%. When these forces are directed onto a single tooth covered with a restoration, the resulting stress can be amplified. MOD cavities can weaken the remaining dental structure. For crown restorations, inclined planes and cusp inclinations receive higher forces, and maintaining occlusal contact points, not contact zones, is recommended to minimize apical stress. In the case of crowns, widening the contact area acts like a "snowshoe" that distributes chewing forces over a larger surface, reducing stress within the crown and the risk of fracture. Caution is advised when opting for all-ceramic restorations in high-stress molar areas. When multiple fixed prosthetic restorations are indicated, zirconia is the material of choice, but careful consideration is needed when deciding the size and shape of the connector, particularly regarding the gingival aspect (rounded, concave). Abrasive adjustments should be avoided after the fixed prosthesis has been milled and sintered. Concerning wear on opposing teeth, well-polished zirconia is less abrasive than glazed and pigmented zirconia or conventional ceramics. In terms of aesthetic limitations of CAD/CAM crowns, there are several aspects to consider to minimize aesthetic risk. After removal from the milling machine, restorations made from feldspathic and leucite ceramics can be finely polished and then cemented, especially in posterior and intracoronal restorations. For the anterior region, aesthetic limitations require staining/pigmentation before glazing. However, this is often insufficient to meet the aesthetic preferences of patients, especially those with complex intrinsic coloration of adjacent teeth to the future prosthetic restoration. In this situation, instead of full-contour milling, a coping is produced, allowing the technician to apply successive layers of ceramics with different colors to mimic the appearance of natural teeth. The choice of the most suitable ceramic material depends on the individual clinical case, which imposes specific aesthetic and strength requirements. More translucent materials are more aesthetic but less resistant, while opaque materials like zirconia offer strength suitable for a wide range of prosthetic restorations. FIXED PROSTHETIC RESTORATIONS WITH IN-OFFICE CAD/CAM SYSTEMS Materials for in-office CAD/CAM prosthetic restorations "The widespread use of CAD/CAM restorations in the dental office has expanded the variety of restorative materials. For practitioners, choosing the appropriate material is challenging due to the wide array of materials available in the market. The first in-office CAD/CAM inlay was produced in 1985 from a ceramic block containing fine filler feldspathic ceramic (Vita Mark 1, Vita Zahufabrik). Feldspathic ceramic was initially used for small occlusal inlays, but the desire to extend the indications for CAD/CAM restorations (onlays, crowns) led practitioners to work with mechanically stronger materials. This led to the development of leucitereinforced ceramics. To allow for rapid milling, some materials are marketed in a pre-crystallized form. Crystallization is necessary after milling to achieve the desired shade and final mechanical strength. In recent years, softer but less brittle materials have emerged, namely resin composite materials. They are much less mechanically robust but have the property of deforming before fracturing, unlike ceramic materials. The next step was to enhance the mechanical bonds of these resins by incorporating ceramic particles. Currently, manufacturers are attempting to combine the advantages of these two material families, offering a ceramic network infiltrated with resin polymers. Presently, manufacturers offer over 20 types of CAD/CAM blocks for in-office use. These are available in different sizes, shades, and translucencies and may require post-milling treatment, which varies depending on the material type. The blocks of materials used for CAD/CAM restorations are homogeneous, dense, and free from imperfections. These materials are available in various chromatic ranges and translucencies, allowing for improved aesthetics in restorations. Surface characterization and pigmentation, followed by firing, can be performed for aesthetic perfection. Ten years ago, there were only about 5 materials available for computerized milling, but today there are over 50 diverse materials to choose from based on each clinical case. This includes a wide range of materials, from ceramics to composites, hybrid materials, and metals (Van Noort, 2012; Fasbinder, 2010). It is known that restorations created with in-office CAD/CAM systems are monolithic, meaning the entire restoration is composed of a single material, unlike bilayer restorations that consist of a core (substrate) onto which a veneer layer is applied. Monolithic restorations have some unique characteristics. Being industrially produced, they have a dense, homogeneous structure without porosities, maximizing the physical properties of the material. They are delivered in the form of blocks specific to each milling machine. Milling machines use a subtractive (wet milling) system to shape the desired contour of the restoration created by digital design. After milling, depending on the characteristics of each material, a specific time and technique are allocated to complete the restoration. These materials are suitable for either hard milling (hard state) or soft milling (soft state). Hard milling refers to the milled block being in its final microstructural form. After milling, it only needs polishing or glazing before cementation. Soft milling refers to blocks that are milled in the so-called green form, which subsequently needs to undergo heat processes to reach the final microstructural form. Hard milling refers to composites, hybrid composite/ceramic materials, and certain ceramics, which are typically used for single-unit restorations (Miyazaky, 2009; Levine, 2009)." Classification of CAD/CAM Dental Materials for In-Office Use CAD/CAM dental materials for in-office use can be classified from a clinical perspective into four generations. 1. First Generation - Feldspathic Ceramics Materials of the first generation belong to the category of feldspathic ceramics (e.g., Vita Mark II, Vita) and leucite-reinforced glass ceramics with low to medium leucite content (e.g., Empress CAD, Ivoclar). They were introduced for commercial use before the 1990s and occupied over 90% of the market until the 2000s. They were also the most studied materials in terms of longevity. When indications and operator times are strictly adhered to, the success rate is sufficiently high. Some of the first CAD/CAM blocks were Vita Mark II (Vita, Germany), introduced in 1991. Feldspathic ceramics used for veneering metal frameworks are pressed at high pressure and temperature. It is currently one of the most widely used ceramic blocks with a broad range of indications, such as crowns, especially in the anterior region, inlays/onlays, and facades. Being a less resistant ceramic, if sufficient thickness is not ensured, fractures can occur. After adhesive cementation, the strength can increase to 350 MPa. Aesthetic characteristics are good, with the material exhibiting exceptional translucency but no fluorescence. Recently introduced Trilux blocks have three color gradation levels, while TriluxForte has four color gradation levels, and RealLife blocks (Vita) have two levels of translucency, dentin and enamel. As Vita Mark II blocks do not exhibit fluorescence, after polishing and cementation, the restoration will have a darker shade. This should be considered when selecting the acrylic cement. It is important to use an appropriate cementation protocol and not sandblast the restoration's inner surface, as microcracks may occur. Feldspathic ceramic blocks introduced more recently by Dentsply/Sirona CEREC Blocks have their own color key to facilitate block color selection. IPS Empress CAD (Ivoclar), a leucite ceramic, contains approximately 35-45% leucite load, similar to IPS Empress 1, but with smaller particle sizes between 1 and 5 microns. The presence of the glassy component in these materials allows them to be etched with hydrofluoric acid, treated with silane coupling agent, and then adhesively cemented (bonded) to the prepared tooth with resin cements. Shear bond strength is approximately 160 MPa, which increases through the adhesive cementation process. Currently, they are available in three translucency variants (HT, LT, and Multi), with the latter being the most aesthetic. Suitable blocks with different gripping chucks are available for each type of milling machine. 2. Second Generation - Reinforced Ceramics with Increased Leucite Content (E.g., e.max CAD) The second generation is represented by fortified ceramics with increased leucite content based on lithium disilicate, with e.max CAD by Ivoclar being the most representative. It consists of approximately 40% 0.2-1 micron-sized lithium disilicate crystals, offering much better flexural and fracture strength compared to feldspathic ceramic materials (which have low glassy content). They are sold in a partially crystallized (soft) state, allowing for easier milling, followed by a crystallization completion process through firing in a ceramic oven at around 850°C for 25 minutes. In its uncrystallized state, the blocks are ivory-colored and achieve the desired color after crystallization, with a contraction of approximately 0.2%. The final result is a ceramic glass with granules of about 1.5 microns and 70% volume within a glassy matrix. E.max CAD exhibits characteristics similar to Vita blocks but also has fluorescence, extending its indications to anterior restorations. They are available in over twenty different chromatic shades and three different translucencies (low, high, and medium), providing versatility in their applications. Another category of materials that emerged after 2013 is zirconia lithium silicate (ZLS) or zirconia-reinforced lithium silicate. It consists of spherical particles with dimensions of 400-500 nm infiltrated into a lithium silicate matrix. Vita Suprinity (Vita) and CeltraDuo (Dentsply) are part of this category, developed through the collaboration of Dentsply Degudent and Vita but marketed separately. Two types of blocks are available, tooth-colored and transparent. The transparent ones undergo a crystallization process at 840°C and transform into the desired tooth color. This material exhibits increased translucency but lower strength (200 MPa). If subjected to post-thermal treatment, the strength increases to 370 MPa, according to studies by Larson in 2013. 3. Third Generation - Hybrid Materials Recently, so-called nanoceramic resins and hybrid ceramic materials have been introduced. They combine the ease of manipulation similar to composites with the strength and final lustre of ceramics. These materials can be easily milled and have less abrasive effects on opposing teeth. Lava Ultimate (3MESPE) contains silicon particles of 20 nm, zirconia particles of 4-11 nm, which is approximately 80% ceramic load. It is the third generation of ceramic materials launched in the USA in 2011. This hybrid material offers improved strength (250 MPa), increased elasticity, and is less brittle. Currently, there are nine different colors and two different translucencies (LT and HT) available for this material. After milling, restorations are polished using suitable rubbers, brushes, and pastes and can be cemented. Initially, indications were extensive, but they have now been restricted to single-unit inlay/onlay restorations. The company 3M ESPE has withdrawn the indication for crowns. Lava Ultimate (3MESPE) Cerasmart by GC belongs to the same category of nanoceramic materials, with the advantage of fluorescence closer to dental structures and is considered to absorb forces due to its structural flexibility (force-absorbing nano-ceramic resin) (Sorrentino, 2018). Vita Enamic (Vita, Germany) is also part of the hybrid ceramic group and consists of a double network structure in which ceramic and polymer are interconnected. According to the manufacturer, the material combines the advantages of composites and ceramics in a single product, offering strength and elasticity, thus preventing fractures. On the other hand, the polymer network reduces the risk of being brittle. The flexural strength is 170 MPa, relatively low. Milling time is greatly reduced (approximately 30%), but the adhesive cementation protocol ensures an increase in strength. Approximately 100 restorations can be produced with a single bur. This Cerasmart GC material is suitable for detailed milling (inlay/onlay). Vita Enamic has multiple advantages, including stopping the propagation of fissures, a feature present in zirconia oxide. However, there are some controversies regarding the use of these materials in posterior areas with high stress concentration. 4. Fourth Generation - Monolithic Zirconia (FCZ)** The fourth generation of in-office CAD/CAM materials refers to full contour zirconia (FCZ) or monolithic zirconia. Zirconium oxide (zirconia) was introduced in dentistry over 15 years ago, but over time, it has continuously improved in terms of clinical and aesthetic performance. Zirconia-based ceramics have become among the most popular types of all-ceramic restorations today. They use CAD/CAM technology to manufacture a wide range of prosthetic restorations, including crowns, bridges, implant abutments, removable and retrievable prostheses, etc. Zirconium oxide (YTZP) is milled in a pre-sintered state, followed by a volume reduction of approximately 20% during sintering. Since 2013, pre-sintered zirconia blocks have been marketed for soft milling in the dental office. Zirconia ceramics can be manufactured by two methods: - Milling an enlarged refractory model, isostatic pressing of zirconia powder, sintering, and then veneering with ceramic (Procera Zirconia). - Milling a digitally enlarged restoration from a partially sintered block to compensate for sintering shrinkage. This compensation can be achieved through digital data manipulation, ensuring uniform and controlled volumetric shrinkage. After soft milling of colored blocks, they undergo sintering at a temperature below 1500°C (approximately 7 hours), followed by the final polishing process. During sintering, zirconia contracts and becomes denser. As the material does not have a glassy phase, it is rather opaque. By varying the composition or the sintering process temperature, zirconia's translucency can be manipulated. Currently, there are zirconium oxide-based materials that exhibit increasing levels of translucency, allowing for the creation of aesthetic monolithic restorations, especially in the anterior region. The current trend is to produce monolithic restorations as one of the most common sources of failure is the fracture/cracking of the veneering material. Additionally, the entire manufacturing process is simplified by creating monolithic restorations. A recently introduced material is e.max ZirCAD Prime, which combines 3YTPZ and 5YTPZ in its composition, providing incisal translucency (from 5YTPZ) and structural strength in the cervical half (from 3YTPZ). Zirconia-based ceramics can be manufactured through milling a block of dense sintered material in a soft, partially sintered, or green state. Hard (tough) milling of zirconia ceramics requires more robust milling machines, typically found in dental laboratories. Supporters of hard milling believe that the edges are much more accurate, but critics argue that this milling process can induce microcracks in the material. Tool wear is much faster, explaining the decline of this type of milling in favour of soft milling. Possibly in the future, with the introduction of ultrasonic milling technologies (specifically diamond instruments accelerated by ultrasonic piezoelectric vibration), hard milling may regain popularity. The clinical stages of making prosthetic restorations with in-office CAD/CAM systems are as follows: The concept of same-day dentistry (restorations in a single session) is possible with the help of in-office CAD/CAM systems. The digital steps, after preparing the abutment and preparing the gingival sulcus for impression, are as follows: 1. Entering patient data into the digital software. 2. Intraoral scanning (of the preparation, adjacent teeth, antagonists, and occlusion). 3. Creating the digital design. 4. Milling the ceramic block. 5. Adapting and cementing the restoration. Fig. 8.2. Entering data into the Romexis software. Fig. 8.3. Intraoral scanning with the Planscan Planmeca scanner. Fig. 8.4. The digital model. Fig. 8.5. The digital design of the crown. Fig. 8.6. Sending the digital design to the milling machine. a b Fig. 8.7. Ceramic crown a. after milling and b. after glazing and polishing. Chapter 9. CEMENTATION OF ALL-CERAMIC RESTORATIONS The main objective of cementing prosthetic restorations is to achieve a tight seal between the preparation surface and the restoration. This aims primarily to maintain pulp vitality and periodontal health and, secondarily, to ensure prosthesis retention. The bond between the preparation and the restoration involves creating an intimate adhesion between the preparation, cement, and prosthesis, making it crucial for the physical properties of the fixing material to align with the intended purpose. Fifty years ago, dentists had limited choices for restoration materials and cementation. Over the subsequent decades, there have been significant changes with the introduction of new materials. Responding to market demand, dental product manufacturers have developed non-metallic materials with greatly improved esthetic appearances, mimicking natural tooth aesthetics. Although zinc phosphate cements have been used in dentistry for over a century, their low strength, poor aesthetics, complex mixing protocols, potential for sensitivity, inadequate adhesion, and high solubility make them a poor choice for many contemporary applications. In response to the heightened expectations of modern restorations, new categories of cements have been created. Consequently, today's practitioners are faced with a multitude of restoration materials, bonding cements, and clinical scenarios, sometimes causing confusion. Dental cement should ideally possess the physical, biological, mechanical, and handling properties necessary to ensure restoration retention on the substrate. These properties include: • Biocompatibility with pulp and soft tissues surrounding teeth. • Favourable physical properties, such as low solubility, extended working time, quick setting time, radiopacity, and appropriate film thickness to facilitate proper seating of the restoration. • Mechanical properties, including good adhesion to both substrate and restoration material, as well as high shear, tensile, and compressive strength. • Ease of mixing and removal of excess material. Classification of cements All permanent cements can be classified into one of two major categories: conventional cements and adhesive cements. Conventional cements achieve retention through mechanical interlocking with restoration and substrate surfaces. Examples include zinc phosphate cements, carboxylate cements, glass ionomer cements, and resin-modified glass ionomer cements. Adhesive cements, on the other hand, provide stronger bonds with substantially higher adhesive properties, offering increased retention and support for low-strength restorations. Glass Ionomer Cements Glass ionomer cements were developed as a combination of silicate and polycarboxylate cements to provide fluoride release (from silicate cements) and adhesion to enamel and, to a lesser extent, dentin (from polycarboxylate cements). They consist of a powder containing fluoroaluminosilicates and a liquid containing polyacrylic acid and tartaric acid. When polyacrylic acid reacts with the external surface of particles in traditional glass ionomer cements, calcium, aluminium, and fluoride ions are released. Gelation occurs when a significant amount of metal ions is present. The material continues to harden for an additional 24 hours. Conventional glass ionomer cements have poor bond strength to tooth structures, moderate compressive strength (85 to 126 MPa), and low tensile strength (6 to 7 MPa). Because the physical qualities of traditional glass ionomer cement can vary widely depending on the powder-to-liquid ratio, proper manufacturer's mixing instructions must be followed. The constant, longterm fluoride release and fluoride recharge capabilities of conventional glass ionomer cement are considered favourable for caries prevention, but adhesion strength between traditional glass ionomer cement and dentin is reduced when dentin is too wet, contributing to post-cementation discomfort. Therefore, wet dentin surfaces must be dried with cotton before cementation. It has been noted that the solubility of conventional glass ionomer cement increases with early contamination by water and saliva, while the final hardness is found to decrease. When working with conventional glass ionomer cement, a coating agent (e.g., Ketac Glaze, 3M ESPE) or petroleum jelly should be used to protect the material at the restoration margins. Additionally, conventional glass ionomer cement exhibits high resistance to acid attack and bleaching, which may not make it the best choice for individuals with gastroesophageal reflux disease or those seeking whitening treatment. Resin-Modified Glass Ionomer Cements Resin-modified glass ionomer cements combine the chemistry and technology of both conventional cement and resin. This type of dental cement was created to address two major deficiencies of conventional glass ionomer cement: early sensitivity to moisture contamination and high solubility. Resin-modified glass ionomers were developed by replacing methacrylate monomers with some of the polyacrylic acid in traditional glass ionomer cements. Compared to conventional glass ionomer cement, resin-modified glass ionomer cement has demonstrated improved adhesion to tooth structure, higher compressive strength, and lower solubility, ensuring long-term margin stability and reduced post-cementation sensitivity while maintaining high fluoride release comparable to conventional glass ionomer cement. Resin-modified glass ionomer cements have a low bond strength to tooth substrate (approximately 8 MPa), high compressive strength (93-226 MPa), and high tensile strength (13-24 MPa). Patients with restorations cemented with resin-modified glass ionomer cement have shown the least post-cementation sensitivity compared to those cemented using conventional glass ionomer or zinc phosphate cements at all time intervals studied in various in vivo studies. The setting reaction of this cement is a two-stage process involving an acidbase reaction and polymerization. Once the powder and liquid are combined, an acidbase reaction occurs, resulting in the formation of polyacrylic salt. Polymerization can be initiated either by light or by enough free radicals. Resin Cements In the mid-1970s, resin cements were introduced as an alternative to acid-base reaction cements. Bisphenol-A-glycidyl methacrylate (Bis-GMA) resin, as well as other modified methacrylates from composite resin, is used to create resin cements. These cements have a polymerization-based setting reaction. Advantages of resin cements include excellent compressive and tensile strength, strong adhesion, low solubility, and adequate aesthetics. These characteristics allow them to be used in cases where retention is a concern, as well as for low-strength restorations or when aesthetics need to be considered (e.g., glass ceramic and composite resin restorations). Some resin cements incorporate filler materials like ytterbium trifluoride or aluminium and barium fluorosilicate, which can release fluoride after setting. This suggests that resin cement may have cariostatic properties. For all cementation applications, self-curing and dual-curing resin cements can be used. Resin cements that are light-cured should only be used for glass ceramic veneers or minimally invasive restorations with a thickness under 0.8 mm. According to some manufacturers, dual-curing resin cement improves long-term color stability. Without using light curing, dual-curing resin cement has been found to have lower bond strength and microhardness. Therefore, it is essential to light-cure all dual-curing resin cements for an adequate period at all accessible restoration margins. Resin cements can be classified based on their bonding mechanism, namely total etch, self-etch, and self-adhesive. Total etch systems generally involve three steps: acid etching, rinsing, and gentle drying. Then, bonding agents are applied and cured, followed by the application and bonding of the resin cement. In a self-etch system, the first two steps are replaced by a self-etch bonding agent that combines conditioner, primer, and adhesive. Self-adhesive resin cements were created and debuted in 2002 to improve ease of use. Despite the fact that this category of resin cements does not really have a long clinical history, it is already the most preferred. The first product, RelyX Unicem from 3M ESPE, has been thoroughly researched and is widely used worldwide. To maximize their effectiveness, such cements do not require surface pre-treatment or bonding agents. As a result, compared to traditional resin cements, the sensitivity of the technique in cementing with self-adhesive resin cement has been substantially reduced, but the adhesion is also lower than in the case of adhesive cements. The translucency of this type of cement is good, being available in chromatic shades for different clinical circumstances. Polymer degradation over time is still a problem with resin-containing dental cements (adhesive resin cement and resin-modified glass ionomer). Indications of different cements for indirect restorations The lifetime of a restoration is strongly influenced by the selection of the dental cement or the inappropriate handling of the chosen material. Clinicians must select dental cements based on physical, mechanical, aesthetic, and handling characteristics, as well as cost and method requirements. Due to the different composition and characteristics, cement selection and cementation technique is extremely important for the long-term clinical success of allceramic restorations. In the dental medicine of the last decades, a marked evolution has been highlighted at the level of bonding agents, adhesive systems and resin cements. The adhesion mechanism is quite different for dentine and enamel. Cements have been developed to achieve a bond with the organic phase of dentin through the dentinal adhesion system. Cements that adhere to the organic phase of dentin using the dentin adhesion system are called "resin cements" or "composite resin cements". These adhesion systems are based on the formation of a hybrid layer with the collagen fibers of the dentine structure. All glass ceramic restorations must be demineralized with hydrofluoric acid, then treated with a silane-based primer, bonding agent and resin cement. High-strength ceramic restorations with zirconium oxide or aluminium oxide infrastructure are not acid- etched and therefore cannot be bonded. To fix this type of restorations, it is necessary to use a surface treatment, which includes sandblasting, the application of silanes and special primers. There is no ideal dental cement that meets all biomechanical requirements. In the current conditions, when new materials and techniques appear, the cementation of new types of all-ceramic restorations is no longer a routine act. Knowing the qualities and drawbacks of each cement, the doctor will choose the type of product that best corresponds to each clinical situation. The cements used in dentistry are classified according to several criteria: the adhesion mechanism, the adhesion system, respectively the polymerization mechanism. 9.1 CLASSIFICATION OF CEMENTS ACCORDING TO THE ADHESION MECHANISM v Polycarboxylate cement, glass ionomer (hybrid ionomer) v Resin cement v Resin modified glass ionomer cement [RMGICs] v Dimethylacrylate cement - with/without microfilling 9.2. CLASSIFICATION OF CEMENTS ACCORDING TO THE ADHESION SYSTEM: v Adhesion to the tooth surface through the adhesion system of enamel and dentin v Adhesion using a metallic primer v Adhesion to the ceramic restoration by treating the ceramic surface with a silane coupling agent. 9.3 CLASSIFICATION OF DENTAL CEMENTS BASED ON THE POLYMERIZATION MECHANISM: v Light-cured cements v Chemically cured (self-cured) cements v Dual-cure cements (auto- and light-cured). Table 9.1. Classification of resin cements based on the polymerization mechanism Classification of resin cements based on polymerization mechanism Resin Cement Light-Cured Polymerization Method Photo-initiators activated by light Dual-Cured Chemical reaction and light Self-Cured Chemical reaction between two materials Characteristics Indications ❖ Extended working ❖ Esthetic restorations time ❖ Non-metallic ❖ Chromatic stability restorations ❖ Translucent ceramics, thin ceramic layer ❖ Strong adhesion ❖ Opaque ceramics ❖ Aesthetic ❖ Non-metallic ❖ Easy to use restorations Used in areas where ❖ Metallic restorations light curing is ❖ Endodontic posts challenging 9.3.1 Light-Cured Resin Cements These utilize photo initiators activated by light. The ability of light to penetrate all areas and activate photo initiators is crucial for this type of cement. An advantage of light-cured cements is the improved working time compared to other types of cements. Their chromatic stability is compared to that of dual-cured or self-cured resin cements. These cements are suitable for non-metallic restorations. Light-cured resins are recommended when cementing fully ceramic restorations with reduced thickness and translucency, allowing light transmission to reach the resin cement, or non-metallic orthodontic appliances and non-metallic immobilization devices. Some common light-cured cements include: v RelyX™ Veneer Cement (3M ESPE, www.3MESPE.com) v Variolink® Esthetic Dual LC (Ivoclar Vivadent Inc.) v Choice™ 2 Light-Cured Veneer Cement (BISCO, Inc.) v Calibra® (Dentsply Caulk, Milford, DE) v Nexus®2 (Kerr Corporation, Orange, CA), Illusion™ (Bisco, Inc) v Insure® (Cosmedent, Inc, Chicago, IL). 9.3.2 Dual-Cured Resin Cements (Auto-Light Polymerizable) These can be activated through chemical means and light. They are recommended when the ceramic is too thick or too opaque to allow light transmission through the restoration. Dual-cured cements are used for any non-metallic restoration where there is a question about the ability of light to fully penetrate and quickly seal the margins. Examples of dual-cured cements include: v NX3 Nexus® Third Generation (Kerr Corporation) v RelyX™ Ultimate Resin Cement v Variolink® Esthetic Dual (Ivoclar Vivadent Inc.) v Panavia V5 (Kuraray America, Inc) v Bistite II DC (J. Morita USA, Inc, Irvine, CA) v Duo-link™ (Bisco, Inc). 9.3.3 Self-Cured Resin Cements These polymerize through a chemical reaction and are called self-cured. To initiate this polymerization reaction, the two pastes that make up the cement must be mixed. They are especially useful in areas where light polymerization is difficult, where light cannot penetrate, such as metallic restorations or metal-ceramic restorations, metallic endodontic posts, and ceramic restorations with a thickness > 3mm, which can result in a lack of light penetration. Some of these types of resin cements include: v Panavia™ (Kuraray Dental, www.kuraraydental.com) v C&B™ Cement (BISCO, Inc, Schaumburg, IL) v MultiLink® (Ivoclar Vivadent, Inc, Amherst) v C&B Metabond® (Parkell, Inc, Farmingdale, NY). 9.4. CLASSIFICATION OF RESIN CEMENTS ACCORDING TO THE ADHESIVE SYSTEM The adhesive system can be: v total-etch (total-demineralizing) v self-etch (self-demineralizing) v self-adhesive Table. 9.2. Classification of Resin Cements According to the Adhesive System Classification of Adhesive Cements by Adhesive Scheme Resin Cement Adhesive Scheme Characteristics Total-Etch Demineralization with 30%-40% phosphoric acid, followed by adhesive application ❖ Excellent cement-to-tooth bond strength ❖ Reduced microleakage ❖ Good long-term predictability ❖ Technique requires multiple steps Classification of Adhesive Cements by Adhesive Scheme Resin Cement Adhesive Scheme Characteristics Self-Etch Self-demineralizing primer, followed by pre-mixed cement application ❖ Easy to use (AutoDemineralizing) Auto-Adhesive ❖ Good bond strength ❖ Less error-prone technique Single component, phosphoric acid is included in the resin ❖ Capable of bonding to the surface of an untreated tooth ❖ "Selective demineralization" can be incorporated to enhance bond strength 9.4.1 Total-Etch Resin Cements These cements use the technique of acid etching of enamel and dentin with 3040% phosphoric acid. This demineralization procedure removes the smear layer, and dentinal tubules are opened. After demineralization, the adhesive is applied to the preparation to bond the cement to the tooth. These cements and the adhesives used with them can be either light-cured or dual-cured. Total-etch resin cements have significantly increased the bond strength of resinbased cements and reduced microleakage significantly. This category ensures the best cement-to-tooth bond but involves the most steps for bonding ceramics, composite resins, or metals to the tooth. This multi-step technique is complex and can compromise bonding effectiveness because each stage represents a potential source of e rror. 9.4.2 Self-Etch Resin Cements Self-etch systems use a self-etching primer to prepare the tooth surface, and the pre-mixed cement is applied over the primer. The bonds with dental structures using these cement categories are almost as good as those of total-etch cements. Self-etch cements are popular among dentists because they are easy to use. However, these cements have shown weaker enamel bond strength compared to total-etch systems. Therefore, total demineralization, the three-step adhesive system established over 30 years ago, still represents the gold standard in terms of versatility and durability. Resin cements incorporating self-etching primers reduce clinical steps, increase ease of handling, reduce the risk of operating errors, and sensitivity to the technique. It is imperative to follow the manufacturer's instructions during cementation with adhesive cement because researchers have discovered incompatibilities between dualcure resin cements and simplified adhesive systems. 9.4.3 Auto-Adhesive Resin Cements Auto-adhesive cements are single-component systems that have good bond strength to dentin, enamel, and ceramics without the need for separate bonding agents. These cements can adhere to an untreated tooth surface that has not been prepared or pre-treated with a demineralizing agent, primer, or bonding agent, allowing cementation in a single step. These cements contain phosphoric acid, which is introduced into the resin. Once mixing is initiated, phosphoric acid reacts with filler particles and dentin in the presence of water, forming a chemical bond. The resin is polymerized into a polymer, as is the case with composite resin adhesion. In the case of some cements in this category, enamel adhesion is improved when a demineralizing agent and adhesive agent are applied. This "selective demineralization" approach uses a demineralizing or self-demineralizing primer before applying the auto-adhesive resin cement. "Selective demineralization" of enamel and/or dentin surfaces and indirect restorations can improve the adhesion of auto-adhesive resin cements. Unlike the results obtained on enamel, when dentin is demineralized with phosphoric acid and a bonding agent is applied before cement application, the bond strength decreases. This negative effect of pre-demineralizing dentin for self-etch adhesives has been repeatedly documented in the literature. When tested without predemineralization, self-adhesive resin cements have proven to produce fairly strong bonds to dentin. Examples of auto-adhesive cements include: v RelyX™ Unicem (3M ESPE) v TheraCem® (BISCO, Inc.) v Maxcem Elite™ (Kerr Corporation) v SpeedCEM™ (Ivoclar Vivadent Inc.). Resin-based cements: composition, properties, manipulation Resin-based cements are composed of diacrylic resins and glass filler. They usually have a dual-polymerization mechanism. There are two types of "traditional" resin cements: those commonly used - dual-cure cements, and photopolymerizable cements. The most recent addition to the "family of resin cements" is the self-etching cements, which require tooth surface pre-treatment and can have many clinical advantages. Resin-based aesthetic cements require a binder for adhesion to the tooth and a primer for adhesion to the ceramic surface. Adhesive cements usually only require a binder for adhesion to the tooth. These cements should be selected when stronger adhesion and high mechanical strength values of ceramics are desired. Auto-adhesive cements are composed of diacrylic resins (with acidic and adhesive groups) and glass filler. They contain adhesive components that eliminate the need for a separate acid etching agent, primer, or bonding agent for adhesion to dental structures or zirconium oxide-based ceramics. Some products recommend the use of a silane primer for silica-based ceramics and a ceramic primer for zirconium oxide. Auto-adhesive cements have a dual polymerization mechanism. During polymerization, auto-adhesive cements change their pH from acidic (pH 2-3) to neutral (pH 5-6). The initial acidity allows them to etch dentin and adhere to dental structure. The physical properties of resin cements are under the standardization of the International Organization (ISO) standard No. 4049, which sets strict requirements for these cements. When selecting a cement, the requirement that the cement must comply with the standard is a good step in the final decision. This standard requires a minimum strength of 50 MPa and radiopacity equivalent to aluminum. At this moment, no other cement can meet the requirements imposed on resin cements. Systems range from the simplest to relatively complex kits designed for aesthetic restorations (ceramic veneers). For adhesion to dentin, alloys, and silicon substrates, specific bonding agents are available. Without these specific bonding agents, cements exhibit moderate adhesion strength to dentin. The use of bonding agents and primers is essential to achieve optimal results. Photopolymerizable cements have the highest adhesion capacity, are the most stable, and achieve the highest degree of conversion. In cases where we do not have the ability to penetrate the light source, self-adhesive resin is a better choice than dual-cure resin. For many of the cements used for veneer cementation, manufacturers provide the material primarily as a photopolymerizable material, with the option to add a dual-cure catalyst only if needed. Because all resin cements use dimethacrylates, the materials polymerize into densely cross-linked polymers that are highly resistant to moisture absorption, insoluble in oral fluids, and have high durability. Resin cements are similar to composite restorative materials but with low filler particle concentrations (50% to 70%). For proper use, pure resin cements require surface pretreatment of the tooth with 37% phosphoric acid and the application of a dentin bonding agent before applying the resin cement. These cements form a micromechanical bond both with the tooth structure on one side and with the restorative material on the other. Primers improve the adhesion between resin-based cements and various restorative materials and can be classified based on the substrate (glass ceramics, alumina, zirconia, alloys) they are designed for. Silanizing agents are used for glass ceramics (feldspathic ceramics, leucite-reinforced ceramics, lithium disilicate). Modern silanizing agents are available in single-bottle systems and have a longer shelf life. Ceramic primers based on acidic adhesive monomers are used with alumina and zirconia-based ceramics. The acidic adhesive monomer used in CLEARFIL CERAMIC PRIMER (Kuraray America, Inc) is a phosphoric acid ester known as 10 MDP. This primer also contains silane. It works on any type of ceramic. To extend the shelf life, an ethanol-based solvent is used. Metallic primers based on sulfuric methacrylates are used for cementing metal restorations. Some primers contain multiple active agents and can be used on multiple surfaces. Self-adhesive cements are available in capsule or automix syringe form. The capsule system works better for cementing a single unit, such as a crown or inlay. Cementing multiple units or a bridge can pose problems because it requires multiple capsules. Some manufacturers have tried to produce larger single doses available for cases with multiple units. The best solution for larger cementations is the automix syringe. It allows control over the amount of cement dispensed while the tip distributes it mixed and ready for use. Material loss is minimal with this device. For the cementation of endodontic posts, manufacturers have two delivery options. One uses an elongation cannula for single-dose capsules, and the other uses a tip extension for automix syringes. Many types of prosthetic restorations can be successfully cemented using self-adhesive resin cements, including metal crowns, all-ceramic pressed crowns, inlays, and onlays (including leucite ceramics, reinforced leucite, lithium disilicate, alumina, or zirconia oxide restorations), and metal-ceramic crowns. No cement will provide the optimal level of longevity without proper preparation, which includes good resistance and shape retention. Self-adhesive resins and resin cements, due to increased adhesion, can help compensate for minor issues such as excessive axial inclination or inadequate preparation height. However, no cement will secure the restoration in the long term when the preparation is inadequate. Mechanisms of Adhesion of Cements to Ceramic Adhesion to Glass Ceramic Generally, restorations made from feldspathic ceramic and leucitereinforced ceramic should be cemented with resin-based cements, either adhesive or aesthetic. These are recommended due to their superior mechanical properties and strong adhesion to dental structures compared to other cements. Resin-based adhesive cement significantly improves fracture resistance and marginal sealing of restorations compared to selfadhesive cement and zinc phosphate. Glass Ceramic Pretreatment Technique Normally, glass ceramic is pre-treated with hydrofluoric acid gel before silanization. Hydrofluoric acid etches the ceramic surface, and the etching time is crucial for each category of ceramic material (20 seconds, 60 seconds, and 90 seconds). Adhesion to Zirconia Oxide Zirconia is a non-glass ceramic, so it doesn't etch using traditional methods. The retention of zirconia-based ceramics depends on the mechanical abrasion of the surface and chemical bonding with an adhesive monomer from special primers or cements. An adhesive monomer, such as 10 MDP, adheres to zirconia-based ceramics. The phosphate ester group in the acid monomer results in a chemical bond to metal oxides (the oxidized surface of alloys) of zirconiabased ceramics and other ceramics. Therefore, it is effective to use resin-based adhesive and self-adhesive cements that include adhesive monomers for cementation. In the case of aesthetic resinbased cements, pre-treatment with a ceramic primer containing adhesive acid monomers is necessary. Zirconia Oxide Pre-treatment Techniques Among the techniques for promoting adhesion to zirconia-based ceramics, we mention sandblasting and tribochemical silica coating. These pre-treatments are used before using a silane-based adhesive, ceramic primer, adhesive cement, or self-adhesive. If a ceramic primer, adhesive cement, or self-adhesive containing an acidic adhesive monomer is used, the easiest method of surface abrasion for ceramics is sandblasting. Tribochemical silica coating creates a bond between silica and the treated surface through a chemo-mechanical reaction. After completing this reaction, the surface is salinized to achieve a chemical bond with it. The adhesion strength of resin-based cements (PANAVIA F 2.0/Kuraray America, Inc., RelyX ARC/3M ESPE, RelyX Unicem/3M ESPE) to Lava/3M ESPE has been improved by sandblasting and applying primer to the surface compared to leaving it untreated. Some studies have also shown that tribochemical silica coating (Rocatec Soft/3M ESPE) was better than sandblasting with 60 µm aluminum oxide. Tribochemical coating resulted in superior bond stability. A good method for promoting a chemical bond to zirconia-based ceramics is the use of a 10 MDP primer. Silanes cannot form a chemical bond with zirconia without containing acidic adhesive monomers such as 10 MDP. When resin-based cements are used, the internal surface of the restoration needs to be treated differently depending on the type of material (metal, ceramic, zirconia oxide). The enamel/dentin surface will need treatment with phosphoric acid, while the restoration surface will be treated with hydrofluoric acid, sandblasting, or silanization, depending on the type of restoration. Surface treatment for different ceramic materials is presented in Table 9.3 Surface treatment of the crown Chemical treatment of the crown Glass-containing ceramics (feldspathic, reinforced with leucite, lithium disilicate) Zirconia ( 3 si 5 mol % yttria ) After the try-in stage, cleaning with special solutions (Ivoclean, Zirclean), and then etching with 5% HF for 90 seconds (feldspathic), 60 seconds (leucite-reinforced), 20-30 seconds (lithium disilicate) Application of silane primer (pure silane or ceramic primer) and drying After the try-in stage, sandblasting with aluminum oxide 50 µm, 10 seconds at 1 bar (5% mol yttria) or 2 bars (3 mol% yttria). Applying 10 MDP primer (pure MDP, ceramic primer, or universal adhesive), and then drying. Resin-based adhesive cements Advantages, disadvantages, and clinical considerations The physical properties of resin cements are standardized under International Organization for Standardization (ISO) standard No 4049, which establishes strict requirements for these cements. This standard calls for a minimum strength of 50 MPa and radio-opacity equivalent to aluminium. Resin cements offer various solutions in many clinical situations. Systems range from the simplest to relatively complex kits designed for aesthetic restorations (ceramic veneers). There are two types of "traditional" resin cements: those that are commonly used - dual-cure cements, and those that are light-cured. Photopolymerizable cements produce the highest bond strength, are the most stable, and achieve the highest degree of conversion. Due to their chemical complexity, dual-cure systems have a lower conversion rate and the shortest lifespan. In cases where it is not possible to access a light source, self-adhesive resin is a better choice than dual-cure resin. This is reflected in the fact that for many of the cements intended for aesthetic purposes, manufacturers make the material primarily available as a light-curing material, with the option to add a dual-cure catalyst only if necessary. Since all resin cements use dimethacrylates, the materials polymerize into dense cross-linked polymers that are highly resistant to moisture absorption, insoluble in oral fluids, and have high durability. For proper use, pure resin cements require surface pre-treatment of the tooth with 37% phosphoric acid and the application of a dentin bonding agent before applying the resin cement. These cements form a micromechanical bond both with the tooth structure on one side and with the restorative material on the other side. There are two types of "traditional" resin cements: those that are commonly used - dual-cure cements and light-curable cements. The most recent addition to the "resin cement family" is selfdemineralizing cements that require pre-treatment of the tooth surface and can offer many clinical advantages. The capsule system works better for cementing a single unit, such as a crown or an inlay. Cementing multiple units or a bridge can pose challenges because it requires more capsules. Some manufacturers have attempted to produce larger single doses available for cases involving multiple units. The best solution for larger cementation procedures is the automix syringe. This allows for precise control of the amount of cement dispensed, while the tip delivers it pre-mixed and ready for use. Material wastage is minimal with this device. Because self-adhesive cements undergo dual polymerization, they are suitable for the cementation of endodontic posts as well. Many types of prosthetic restorations can be successfully cemented using self-demineralizing resin cements, including metal crowns, all-ceramic pressed crowns, inlays and onlays (including leucite ceramic, leucite-reinforced, lithium disilicate, alumina, or zirconia restorations), and metal-ceramic mixed crowns. It's important to note that, in general, the bond strength of selfdemineralizing resin cements is not as high as that of resin cements using the total-etch technique. New primers for metal and ceramics have emerged that have improved the bonding strength of cements to non-demineralized substrates, such as zirconium oxide and metal. Self-demineralizing adhesives and resin cements, thanks to their increased adhesion, can help compensate for minor issues such as excessive axial convergence of abutments or the absence of adequate axial height in the preparation. However, no cement will provide long-term fixation when the preparation is inadequate. An ideal bonding material should meet numerous requirements, including good sealing properties, durable adhesion to both the tooth and the restoration, sufficient mechanical strength, low viscosity, resistance to disintegration, tissue compatibility, and ease of handling. It is important that the use of a new cement is based on scientific evidence and a good understanding of the chemical and physical mechanisms of the cement. This should be followed by a study of the manufacturer's recommendations for the indicated steps, as new products often require procedures that may not be familiar to the practitioner. These new cements are often technique-sensitive, and incorrect application of the cement can lead to the failure of restorations. The requirements of an ideal cement used for cementing prosthetic restorations in routine practice are: biocompatibility, interface sealing, anticariogenic properties, adhesion and strength, radiopacity, viscosity and film thickness, solubility, and aesthetics. Glass ceramics (feldspathic, leucite-reinforced, lithium disilicate) should be cemented with adhesive resin cement or esthetic resinbased cement, using appropriate primers and bonding agents. Due to their increased strength, zirconia-based ceramics can be cemented with adhesive cements or traditional cements. Selfadhesive cements are easier to use than traditional ones. When better retention is required, zirconia restorations can be cemented with dual adhesive or aesthetic cements, using appropriate primers for both the tooth and ceramic. Table 9.4 presents the indications for different cements based on the prosthetic restoration material. Material restoratio n Zirconia Lithium disilicate Ceramics reinforced with leucite Treatment RPF Cement type Cementing conventional : only at restorations with Retention mechanics good Glue: cement resin self- adhesive Tooth preparation Cleaning preparation ( paste and brushing) Cleaning preparation ( paste and brushing ) Good insolation Cleaning preparation ( paste and brushing ) Diga insolation Glue: cement adhesive Acid engraving on phosphoric and / or resin base bonding conforming instructions manufacturer Glue: cement selfCleaning preparation adhesive ( paste and brushing ) based on resin Rubberdam insolation Cleaning preparation Glue: cement adhesive ( paste and brushing ) on rubberdam insolation resin base Acid engraving and / or bonding Conforming instructions manufacturer Cleaning preparation ( paste and brushing ) Glue: cement adhesive Rubberdam insolation on Acid engraving resin base and / or bonding conforming instructions manufacturer Sandblasting (aluminum oxide 50-60 µm, <2 bars) application of RMGI or SARC cement. Sandblasting (aluminum oxide 50-60 µm, <2 bars), Applying primer 10 MDP and then dual self-adhesive cement Sandblasting (aluminum oxide 50-60 µm, <2 bars) ,Applying 10 MDP bonding primer and then dual resin cement 5% HF acid etching for 20 seconds, applying silane primer, and then SARC cement. 5% HF acid etching for 20 seconds, applying silane primer ,Applying bonding agent, applying ARC cement 9.6% HF acid etching for 1 minute (maximum 2.5 minutes), applying silane primer, applying bonding agent, and applying dual resin cement. Resin nanocera mics Cleaning preparation ( paste and brushing ) Glue: cement adhesive rubberdam insolation on Acid engraving and / or resin base bonding Conforming instructions manufacturer Sandblasting(aluminum oxide 2550 µm, 1.5-2 bars), applying bonding agent, and then dual resin cement. How to choose a dental cement based on the clinical situation? In everyday practice, we encounter various clinical situations that require different operative protocols. Ideal situations are those in which the preparation margins are located supragingival. Other factors such as the restorative material and clinician preferences affect the choice of cement in many cases. The ability to clinically isolate the working area from contamination due to the presence of blood and other oral fluids is absolutely essential for the successful use of total-etch resin cements. Some dental materials cannot be cemented without the use of adhesive techniques due to the nature of the ceramic material, for example, pressed ceramic and lithium disilicate. Resin cements and total-etch techniques represent the technique and material for definitive cementation, providing optimal results in terms of sealing and retention of the restoration. Clinical timelines must be strictly adhered to for therapeutic success. Cementing ceramic veneers with light-curable resin cement like RelyX Veneer by 3M ESPE Procedure: v The ceramic veneer must be etched with hydrofluoric acid. This step is sometimes performed in the dental laboratory before the restoration is sent to the dental office. If it hasn't been done in the laboratory, the etching should be done in the dental office, following the protocol specific to the ceramic material, after the veneer trial has been completed. v If a provisional restoration has been previously applied, it should be removed. Then, the tooth should be cleaned using a fluoride-free pumice paste, followed by rinsing thoroughly with water and gently drying it. v Applying the dental dam. v Matrices are placed between the teeth to prevent unwanted adhesion of adjacent teeth. v The bonding area between the teeth is isolated, and Teflon tape is used if necessary to prevent contamination. v The final restoration is checked for both aesthetic and positional aspects. For this purpose, the veneer is placed with the translucent shade of the try-in paste (RelyX Try-in Paste). v If the restoration meets all criteria, the veneer is removed, thoroughly washed, both the tooth and the veneer are dried, and the adhesive step is initiated. v Saliva decontamination can be achieved using 35% phosphoric acid for 15 seconds, or with ethanol in an ultrasonic bath, or with special pastes (Ivoclean, Zirclean). Afterward, rinse and dry the veneer. v The hydrofluoric acid etching should only be done if it has not been performed in the laboratory. v A single layer of silane primer is applied to the bonding surface of the veneer and allowed to dry. v Phosphoric acid is applied to the enamel and dentin for 15 seconds. v It is rinsed for 10 seconds. v Using a separate applicator for each layer, two coats of universal adhesive are applied to both the enamel and dentin. v It is gently dried for 2-5 seconds. v It is not photopolymerized! v A single layer of adhesive is applied to the silanized surface of the veneer. v It is gently dried for 2-5 seconds. v It is not photopolymerized! v The previously selected shade of cement is applied to the veneer. v The veneer is placed with slight pressure. v It is photopolymerized for 2 seconds, and excess cement is cleaned from the margins. v Each area and margin of the veneer is photopolymerized for 40 seconds. v The margins and adaptation are rechecked. Cementing zirconia crowns with self-adhesive cement like RelyX U200 Working procedure v Removal of temporary restoration and cleaning of the prepared tooth. v Applying the rubber dam. v The inner surface of the ceramic crown is sandblasted, cleaned, and dried. v The cementing material component is applied to the mixing pad. v Mix the cement. v Apply the cementing material to the prosthetic restoration or on the prepared tooth. v Apply the restoration, polymerize with light, and remove excess. Self-adhesive resin cement demonstrates good adhesion to both enamel and dentin, easy manoeuvrability, a low risk of postoperative hypersensitivity, and easy excess removal. Clinical stages of bonding ceramic restorations Treating the internal surface of the prosthetic restoration by sandblasting, only for zirconia. - Etching with hydrofluoric acid only for glass ceramics. - Silanization - 1 minute, gentle drying, storage in the dark, monocomponent silane (silane + alcohol / acetone) or bicomponent (+ aqueous solution, must be applied after a few hours) - Applying the adhesive agent, compatible with the cement used Surface dental treatment - Cleaning with non-fluoridated abrasive paste - Bicarbonate air-polishing jet (air-flow). - Applying orthophosphoric acid (gel, not solution) 30-40% (30 seconds on enamel, 15 seconds on dentin to prevent collagen fiber collapse and compromise adhesion - Rinsing off the acid agent, gentle drying for 10 seconds. - Applying the primer to the dentin substrate for 30 seconds, then drying - Applying the adhesive agent to the hard dental tissues - Applying resin cement inside the full ceramic FPD (Fixed Partial Denture) and positioning it at the level of the dental preparation. - Pre-polymerization (using a curing light) until the bonding agent reaches a gel-like consistency. - Removal of excess cement and complete photopolymerization on all surfaces for 60-90 seconds (ceramic absorbs 40-50% of the light emitted by the curing light; when ceramic thickness is > 0.7mm, a dual-cure cement is chosen). Conclusion Dental prosthetics undergoes radical transformations with the advent of the digital era. From digital impressions to digital data manipulation for diagnosis and treatment planning, and to the production of CAD/CAM restorations, the way dental services are provided to patients has undergone a significant shift. Every day, new materials with biomechanical and aesthetic characteristics emerge, allowing them to withstand demands even in the most challenging situations. More studies and time are needed to evaluate the true clinical performance of these restorations. Through the continuous development of materials and technologies, the prosthetic treatment of partial edentulism poses a challenge for clinicians, with the ultimate goal being to choose the most suitable options for each specific clinical situation. To ensure the longevity of fixed prosthetic restorations, it is essential to perform each procedure with professionalism and responsibility, always keeping the best interests of the patients, the primary beneficiaries of our treatments, in mind. Every clinical step is crucial. To successfully complete a prosthetic restorative treatment, the student must recognize the role of wellacquired theoretical knowledge in formulating an accurate diagnosis, leading to an appropriate treatment plan. Following the execution of clinical procedures according to standardized protocols, which have proven to be essential in therapeutic success, clinical experience will accumulate and make everything more manageable and predictable. Bibliografy 1. da Silva LH, de Lima E, Miranda RBP, et al. Dental ceramics: a review of new materials and processing methods. Braz Oral Res 2017;31:133-46. 2. Bajraktarova-Valjakova E, Korunoska-Stevkovska V, Kapusevska B, et al. Contemporary dental ceramic materials, a review: chemical composition, physical and mechanical properties, indications for use. Open Access Maced J Med Sci 2018;6:1742-55. 3. Zarone F, Russo S, Sorrentino R. From porcelain-fused-to-metal to zirconia: clinical and experimental considerations. Dent Mater 2011;27:83-96. 4. Bajraktarova-Valjakova, Korunoska-Stevkovska, Kapusevska, et al. Contemporary Dental Ceramic Materials: Chemical Composition, Physical and Mechanical Properties. Open Access Macedonian Journal of Medical Sciences 2018;6(9): 1742-55. 5. Nikolopoulou F, Loukidis M, Proffesor A. Critical Review and evaluation of composite/ceramic onlays versus crowns. 2014. https://doi.org/10.4172/21577633.1000261. 6. Edelhoff D, Brix O. All-ceramic restorations in different indications: a case series. J Am Dent Assoc 2011; 142: 14S-9S. 7. Kelly JR, Benetti P. Ceramic materials in dentistry: historical evolution and current practice. Aust Dent J 2011;56:84-96. 8. Gracis S, Thompson V, Ferencz J, et al. A new classification system for Allceramic and ceramic-like restorative materials. Int J Prosthodont 2016;28:22735. 9. Shenoy A, Shenoy N. Dental ceramics: an update. J Conserv Dent 2010; 13: 195. 10. Saint-Jean SJ. Dental Glasses and Glass-ceramics. Adv. Ceram. Dent., Elsevier Inc.; 2014, p. 255-277. https://doi.org/10.1-16/B978-0-12-394619-5.000121-2. 11. Montazerian M, Zanotto ED. Restorative dental glass-ceramics: current status and trends. Clin. Appl. Biomater. State-of-the-Art Progress, Trends, Nov. Approaches, Springer International Publishing; 2017, p. 313-336. https://doi.org/10.1007/978-3-319-56059-5_9. 12. Fu L, Engqvist H, Xia W. Glass-Ceramics in Dentistry: A Review. Materials 2020; 13(5): 1049. 13. Ho GW, Matinlinna JP. Insights on Ceramics as Dental Materials. Part I: Ceramic Material Types in Dentistry. Silicon 2011;3: 109-15. 14. Fu L, Xie L, Fu W, et al. Ultrastrong translucent glass ceramic with nanocrystalline, biomimetic structure. Nano Lett 2018; 18: 7146-54. 15. Montazerian M, Zanotto ED. Bioactive and inert dental glass-ceramics. J Biomed Mater Res A 2017;105:619-39. 16. Ritzberger C, Apel E, Hö land W, et al. Properties and clinical application of three types of dental glass-ceramics and ceramics for CAD-CAM technologies. Materials (Basel) 2010;3:3700-13. 17. Lawson NC, Bansal R, Burgess JO. Wear, strength, modulus and hardness of CAD-CAM restorative materials. Dent Mater 2016;32(11):e275-83. 18. Hallmann L, Ulmer P, Gerngross MD, et al. Properties of hot-pressed lithium silicate glass-ceramics. Dent Mater 2019;35(5):713-29. 19. Mirmohammadi H. Resin-based ceramic matrix composite materials in dentistry. Adv. Ceram. Matrix Compos. Second Ed., Elsevier Inc.; 2018, p. 741-762. https://doi.org/10.1016/B978-0-08-102166-8.00030-X. 20. Code on Dental Procedures and Nomenclature (CDT) n.d. Available at https://www.ada.org/en/publications/cdt. Accessed March 13, 2020. 21. Ben-Nissan B, Choi AH, Cordingley R. Alumina ceramics. Bioceram. Their Clin. Appl., Elsevier Inc.; 2008, p. 223-242. https://doi.org/10.1533/9781845694227.2.223. 22. Scherrer SS, Quinn GD, Quinn JB. Fractographic failure analysis of a ProceraÒ 2008;24:1107-13. 23. Bona AD, Pecho OE, Alessandretti R. Zirconia as a dental biometal. Materials (Basel) 2015;8:4978-91. 24. Manziuc M-M, Gasparik C, Negucioiu M, et. al. Optical properties of translucent zirconia: a review of the literature. EuroBiotech J 2019;3:45-51. 25. Gautam C, Joyner J, Gautam A, et al. Zirconia based dental ceramics: structure, mechanical properties, biocompatibility and applications. Dalton Trans 2016;45:19194-215. 26. 1.Mörmann WH, Bindl A. All-ceramic, chair-side computer aided design/computer-aided machining restorations. Dent Clin North Am. 2002;46(2):405-426. 27. Allied Market Research. Dental CAD/CAM Materials & Systems Market by Product - Global Opportunity Analysis and Industry Forecast, 2017-2023. Allied Market Research web site.Published June 2017. 28. Li R, Kim W. Ceramic dental biomaterials and CAD/CAM technology: state of the art. J Prosthodont Res. 2014;58(4):208-216. 29. Fasbinder DJ. Restorative material options for CAD/CAM restorations. Compend Contin Educ Dent. 2002;23(10):911-916, 918, 920 passim; quiz 924. 30. Zarone F, Ferrarri M, Mangano FG, et al. Digitally oriented materials: focus on lithium disilicate ceramics. Int J Dent. 2016;2016:9840594. doi: 10.1155/2016/9840594. 31. Shenoy A, Shenoy N. Dental ceramics: an update. J Conserv Dent. 2010;13(4):195-203. 32. Bona AD, Pecho OE, Alessandretti R. Zirconia as a dental biomaterial. Materials (Basel). 2015;8(8):4978-4991. 33. Lawson NC, Bansal R, Burgess JO. Wear, strength, modulus and hardness of CAD/CAM restorative materials. Dent Mater. 2016 Nov;32(11):e275-e283. 34. Vagkopoulou T, Koutayas SO, Koidis P, et al. Zirconia in dentistry: part 1. Discovering the nature of an upcoming bioceramic. Eur J Esthet Dent. 2009;4(2):130-151. 35. Christensen GJ. Is the rush to all-ceramic crowns justified? J Am Dent Assoc 2014; 145 (2):192–4. 36. Makhija SK, Lawson NC, Gilbert GH, et al. Dentist material selection for single unitcrowns: findings from the National Dental Practice-Based Research Network. J Dent 2016; 55: 40–7. 37. Denry I, Kelly J. Emerging ceramic-based materials for dentistry. J Dent Res 2014; 93 (12):1235–42. 38. Zhang Y, Kelly JR. Dental ceramics for restoration and metal veneering. Dent Clin North Am 2017; 61 (4):797–819. 39. Christensen, G.J., (2005) The state of fixed prosthodontics impressions: room for improvement. Journal of the American Dental Association. 136, 343-346. 40. Miyazaky, T., Hotta, Y., Kunii, J., Kuriyama, S., & Tamaky, Y.(2009) A review of dental CAD/CAM: Current status and future perspectives from 20 years of experience. Dental Materials Journal, 28(1), 44-56. 41. Stookey S. Catalyzed crystallization of glass in theory and practice. Ind Eng Chem 1959; 51(7): 805–8. 42. Schweiger M, von Clausbruch SC, Ho¨land W, et al. Process for the preparation of shaped translucent lithium disilicate glass ceramic products. Google Patents; 2002. 43. Van Noort, R. (2012) The future of dental devices is digital. Dental Materials, 28(1), 3-12. 44. Fasbinder, D.J. (2010) Materials for chairside CAD/CAM restorations. Compend Contin Educ Dent, 31, 702-4,706, 708. 45. de Carvalho Ramos N, Campos TMB, de La Paz IS, et al. Microstructure characterization and SCG of newly engineered dental ceramics. Dent Mater 2016;. 46. Rauch A, Reich S, Dalchau L, et al. Clinical survival of chair-side generated monolithic lithium disilicate crowns: 10-year results. Clin Oral Investig 2018; 22(4):1763–9. 47. Levine, N. & (2009) To the sky and beyond. Dental Products Report, 116. 48. Plourde, J., Harsono, M., & Fox, L., et al. (2011) Marginal and internal fit of E4D CAD/CAM all-ceramic crowns, Journal of Dental Research, 90, 638. 49. Heintze, Siegward & Rousson, Valentin. (2010). Fracture rates of IPS Empress all-ceramic crowns-a systematic review. The International journal of prosthodontics. 23. 129-33. 50. Lien W, Roberts HW, Platt JA, et al. Microstructural evolution and physical behavior of a lithium disilicate glass–ceramic. Dent Mater 2015; 31(8): 928–40. 51. Holand W, Apel E, van‘t Hoen C, et al. Studies of crystal phase formations in high-strength lithium disilicate glass-ceramics. J Non Cryst Solids 2006; 352(38– 39):4041–50. 52. Gehrt M, Wolfart S, Rafai N, et al. Clinical results of lithium-disilicate crowns after up to 9 years of service. Clin Oral Investig 2013; 17(1):275–84. 53. Koller, M., Arnetzl, G.V., & Holly, L., et al. (2012) Lava ultimate resin nano ceramic for CAD/CAM: customization case study. International Journal of Computerized Dentistry, 15, 159-164. 54. Roberto Sorrentino*, Yuko Nagasawa, Arianna Infelise, Giovanni Bonadeo and Marco Ferrari. In Vitro Analysis of the Fracture Resistance of Cad-Cam Cerasmart Molar Crowns with Different Occlusal Thickness. Biomed J Sci & Tech Res. Volume 3- Issue 2: 2018 55. Simsek, H., & Derelioglu, S. (2016). In Vitro Comparative Analysis of Fracture Resistance in Inlay Restoration Prepared with CAD-CAM and Different Systems in the Primary Teeth. BioMed research international, 2016, 4292761.doi:10.1155/2016/4292761 56. Zimmermann M, Koller C, Mehl A, et al. Indirect zirconia-reinforced lithium silicate ceramic CAD/CAM restorations: preliminary clinical results after 12 months.Quintessence Int 2017;48(1):19–25. 57. Vichi A, Fonzar RF, Goracci C, et al. Effect of finishing and polishing on roughness and gloss of lithium disilicate and lithium silicate zirconia reinforced glass ceramic for CAD/CAM systems. Oper Dent 2018; 43(1):90–100. 58. Riquieri H, Monteiro JB, Viegas DC, et al. Impact of crystallization firing process on the microstructure and flexural strength of zirconia-reinforced lithium silicate glass-ceramics. Dent Mater 2018; 34(10):1483–91. 59. Sen N, Us YO. Mechanical and optical properties of monolithic CAD-CAM restorative materials. J Prosthet Dent 2018;119(4):593–9 60. Kelly JR, Denry I. Stabilized zirconia as a structural ceramic: an overview. Dent Mater 2008;24(3):289–98 61. Denry I, Kelly JR. State of the art of zirconia for dental applications. Dent Mater2008;24(3):299–307 62. Nakamura M. A newly developed bonding restoration material-Clearfil Bond System F. Kokubyo Gakkai Zasshi 1978; 45(1):234 [in Japanese]. 63. Santos, G.C.J., Santos, M.J., & Rizkalla, A.S., et al. (2013) Overview of CEREC CAD/CAM chairside system. General Dentistry, 61, 36-40.quiz 41 64. Della Bona, A. & Kelly, J.R. (2008) The clinical succes of all-ceramic restorations. Journal of the American Dental Association (1939), 139, (suppl), 8S-13S. 65. Shenoy, A. & Shenoy, N. (2010) Dental ceramics: An update. Journal of Conservative Dentistry, 13, 195-203. 66. Strub, J.R. & Malament, K.A (2013) Do zirconia ceramics have a future in restorative dentistry? The International Journal of Periodontics & Restorative Dentistry, 33, 259. 67. Denry, I. (2013) How and when does fabrication damage adversely affect the clinical performance of ceramic restorations? Dental Materials, 29, 85-96. 68. Raigrodski, A.J., Hillstead, M.B., & Meng, G.K., et al. (2012a) Survival and complications of zirconia-based fixed dental prostheses: a systematic review. The Journal of Prosthetic Dentistry, 107, 170-177. 69. Raigrodski, A.J., Yu, A., & Chiche, G.J., et al. (2012b) Clinical efficacy of veneered zirconium dioxide-based posterior partial fixed dental prostheses: fiveyear results. The Journal of Prosthetic Dentistry, 108, 214-222. 70. Larson, T.D. (2009a) Tooth wear: when to treat, why, and how. Part one. Northwest Dentistry, 88, 31-38 71. Larson, T.D. (2009b) Tooth wear: when to treat, why, and how. Part two. Northwest Dentistry, 88, 31-38 72. Janyavula, S., Lawson, N., & Cakir, D., et al. (2013) The wear of polished and glazed zirconia against enamel. The Journal of Prosthetic Dentistry, 109, 22-29.
0
You can add this document to your study collection(s)
Sign in Available only to authorized usersYou can add this document to your saved list
Sign in Available only to authorized users(For complaints, use another form )