Ultrasound-guided Musculoskeletal Procedures ,UCA -ARIA 3CONFIENZA s 'IOVANNI 3ERAFINI %NZO 3ILVESTRI Editors Ultrasound-guided Musculoskeletal Procedures The Upper Limb Editors Luca Maria Sconfienza Radiology Unit IRCCS Policlinico San Donato San Donato Milanese (MI), Italy Enzo Silvestri Radiology Unit Ospedale Evangelico Internazionale Genoa, Italy Giovanni Serafini Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy ISBN 978-88-470-2741-1 ISBN 978-88-470-2742-8 (eBook) DOI 10.1007/978-88-470-2742-8 Springer Milan Dordrecht Heidelberg London New York Library of Congress Control Number: 2012939782 © Springer-Verlag Italia 2012 This work is subject to copyright. 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The publisher makes no warranty, express or implied, with respect to the material contained herein. 7654321 2012 Cover design: Ikona S.r.l., Milan, Italy Typesetting: Grafiche Porpora S.r.l., Segrate (MI), Italy Printing and binding: Grafiche Porpora S.r.l., Segrate (MI), Italy Springer-Verlag Italia S.r.l. – Via Decembrio 28 – I-20137 Milan Springer is a part of Springer Science+Business Media (www.springer.com) 2013 2014 Preface Ultrasound is an emergent imaging modality that is widely used to assess disorders affecting the musculoskeletal system. Among its many features, it is the only imaging modality that is able to perform dynamic evaluations of the soft tissues related to the musculoskeletal system, and without patient exposure to ionizing radiation. Also, in expert hands, ultrasound enables the precise guidance of needles within soft tissues and joints, for use in a wide range of procedures. The idea of preparing a handbook was based on the frequent requests of our colleagues in other fields who were interested in learning ultrasoundguided procedures as applied to the musculoskeletal system. This text is extremely practical, offering point-by-point checklists for each procedure together with detailed anatomic schemes. Ultrasound images of the different applications are provided as well. We would also like to emphasize that this handbook is based both on our daily experience and on data obtained from the literature. It therefore describes different approaches for the same procedure, allowing the reader to select the most suitable for the particular application. Even though not all procedures are specifically included in the contents, readers should be able to extrapolate the appropriate ultrasound-guided technique for use in other anatomic districts. Finally, we acknowledge the work of our young colleagues, Alice Arcidiacono, Angelo Corazza, and Francesca Nosenzo, whose inputs were an invaluable contribution to this book. May 2012 Luca Maria Sconfienza Giovanni Serafini Enzo Silvestri V Contents 1 General Aspects of US-guided Musculoskeletal Procedures Armando Conchiglia, Lorenzo Maria Gregori, Luigi Zugaro and Carlo Masciocchi 1 Part I The Shoulder 2 The Shoulder: Focused US Anatomy and Examination Technique . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Enzo Silvestri and Davide Orlandi 13 3 Subacromial-Subdeltoid Bursa Injections . . . . . . . . . . . . . . . . Enzo Silvestri 25 4 Treament of Calcific Tendinitis of the Rotator Cuff . . . . . . . . Giovanni Serafini and Luca Maria Sconfienza 29 5 Calcific Enthesopathy Dry-Needling . . . . . . . . . . . . . . . . . . . . Francesca Lacelli 37 6 Hyaluronic Supplementation of the Subacromial Space . . . . Giovanni Serafini 41 7 Intra-articular Injections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Francesca Lacelli 45 8 Long Head of the Biceps Brachii Tendon Injection . . . . . . . . Luca Maria Sconfienza 51 9 Acromioclavicular Joint Injection . . . . . . . . . . . . . . . . . . . . . . Enzo Silvestri 55 VII VIII Contents Part II The Elbow 10 The Elbow: Focused US Anatomy and Examination Technique . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Enzo Silvestri and Emanuele Fabbro 61 11 Treatment of Lateral Epicondylitis . . . . . . . . . . . . . . . . . . . . . Giovanni Serafini 67 12 Treatment of Medial Epicondylitis . . . . . . . . . . . . . . . . . . . . . Enzo Silvestri 73 13 Olecranon Bursa Drainage . . . . . . . . . . . . . . . . . . . . . . . . . . . Francesca Lacelli 79 14 Intra-articular Injections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Luca Maria Sconfienza 83 Part III The Wrist 15 16 The Wrist: Focused US Anatomy and Examination Technique . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Enzo Silvestri and Giulio Ferrero 89 Treament of De Quervain’s Disease and Other Forms of Tenosynovitis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Giovanni Serafini 93 17 Articular Ganglia Drainage . . . . . . . . . . . . . . . . . . . . . . . . . . . Leonardo Callegari 97 18 Trapeziometacarpal Joint Injection . . . . . . . . . . . . . . . . . . . . Francesca Lacelli 101 19 Radiocarpal Joint Injections . . . . . . . . . . . . . . . . . . . . . . . . . . Luca Maria Sconfienza 105 Contents ix Part IV The Hand 20 The Hand: Focused US Anatomy and Examination Technique . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Francesca Lacelli and Chiara Martini 111 21 Treatment of Trigger Finger . . . . . . . . . . . . . . . . . . . . . . . . . . Leonardo Callegari 113 22 Intra-articular Injections: Metacarpophalangeal and Interphalangeal Joints . . . . . . . . . . . . . . . . . . . . . . . . . . . Luca Maria Sconfienza 119 Suggested Reading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121 Contributors Alice Arcidiacono Post-graduate School in Radiodiagnostics, University of Genoa, School of Medicine, Genoa, Italy Leonardo Callegari Radiology Unit B, Ospedale di Circolo, Fondazione Macchi, Varese, Italy Armando Conchiglia Radiology Department, Ospedale San Salvatore, University of L’Aquila, L’Aquila, Italy Angelo Corazza Post-graduate School in Radiodiagnostics, University of Genoa, School of Medicine, Genoa, Italy Emanuele Fabbro Post-graduate School in Radiodiagnostics, University of Genoa, School of Medicine, Genoa, Italy Giulio Ferrero Post-graduate School in Radiodiagnostics, University of Genoa, School of Medicine, Genoa, Italy Lorenzo Maria Gregori Radiology Department, Ospedale San Salvatore, University of L’Aquila, L’Aquila, Italy Francesca Lacelli Diagnostic Imaging Department, Ospedale S. Corona, ASL 2 Savonese, Pietra Ligure (SV), Italy Chiara Martini Post-graduate School in Radiodiagnostics, University of Genoa, School of Medicine, Genoa, Italy Carlo Masciocchi Radiology Department, Ospedale San Salvatore, University of L’Aquila, L’Aquila, Italy Francesca Nosenzo Post-graduate School in Radiodiagnostics, University of Genoa, School of Medicine, Genoa, Italy Davide Orlandi Post-graduate School in Radiodiagnostics, University of Genoa, School of Medicine, Genoa, Italy xi xii Contributors Luca Maria Sconfienza Radiology Unit, IRCCS Policlinico San Donato, San Donato Milanese (MI), Italy Giovanni Serafini Diagnostic Imaging Department, Ospedale S. Corona, ASL 2 Savonese, Pietra Ligure (SV), Italy Enzo Silvestri Genoa, Italy Radiology Unit, Ospedale Evangelico Internazionale, Luigi Zugaro Radiology Department, Ospedale San Salvatore, University of L’Aquila, L’Aquila, Italy 1 General Aspects of US-guided Musculoskeletal Procedures Armando Conchiglia, Lorenzo Maria Gregori, Luigi Zugaro and Carlo Masciocchi Ultrasonography (US) is a quick and non-invasive imaging modality that allows for the precise visualization of almost all soft-tissue components of the musculoskeletal system. Moreover, this modality also enables accurate guidance during interventional procedures, thus reducing the risks of complications. As US is relatively operatordependent, an effective scanning technique is strictly correlated with the ability to delineate US appearances. If clinical knowledge is the basic requirement for any diagnostic or therapeutic process, then US-guided interventional procedures analogously require thorough knowledge of the equipment being used. Also good technical skills are needed in order to extract the maximum amount of information that can be obtained with the available equipment, while avoiding the numerous pitfalls and artifacts of this imaging modality. Setting Room A proper setting for the room used in the interventional procedures is a prerequisite in ensur- ing high safety standards together with a smooth workflow. The suggested structural requirements are the following: • The rooms and spaces are related to the nature and extent of the activities performed. The minimum clearance should be 4 m, with a 1.5-m clearance around the bed • Chamber of observation • Medical staff preparation area • Storage area for clean material • Disposal area for soiled material • Waiting area • Toilet and sink for patients • Toilet and sink for medical staff. The suggested technical requirements are the following: • Adjustable (height and angular adjustments) surgical bed • Ventilation system capable of maintaining a constant air exchange within the room • Adjustable lighting system illuminating the surgical field • Medical gas pipeline systems • Emergency trolley • Emergency call system. US System Luigi Zugaro ( ) Radiology Department Ospedale S. Salvatore, University of l’Aquila L’Aquila, Italy While choosing the right US system can be extremely challenging, an informed and useful choice is more likely if the purchaser has a clear L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_1 © Springer-Verlag Italia 2012 1 2 concept of the US-guided interventional procedures that will be performed. In general, the basic requirements for dedicated interventional US equipment are: Ergonomics • System dimensions and steering. The system should be portable, allowing for transportation to remote clinics or for operating-theater work. Machines used regularly for mobile work should be robust and easy to move. Hand-held portable machines are an option. • Moveable (swivel and tilt) monitor and control panel, including height adjustment for different operators and situations. • Keyboard design facilitating access to the required functions, without the need for stretching or twisting. Materials • Long-lasting materials with high resistance to common antiseptics • Smooth surfaces that can be easily and quickly cleaned. Technical Requirements • Quick probe selection and switching process, simultaneous connection of several probes • Dynamic frequency capability • Dynamic focusing control, number and pattern of focal zones • Functions such as beam steering, sector angle adjustment, zoom, frame rate adjustment. Probes • High-frequency linear-array probes, operating with frequencies of 10 MHz or more, are mandatory • Compatibility with US guidance devices • Ergonomic handle shape to preserve a neutral wrist position • Probe design allowing use with either hand. US-guided Procedures Prior to any interventional procedure, a preliminary US evaluation of the affected site should be A. Conchiglia et al. performed in order to identify the most reliable procedure setting and to confirm the expected findings. This is extremely important because the patient’s condition may have changed since the previous examination, necessitating different treatment. Clinical History It is important to have at least basic information on the patient’s medical history. A brief preliminary talk, covering the following items, should be held with the patient or his/her physician: • Present complaint(s) • History of the present complaint(s) • Past medical history • Drug/allergy history • Family medical history • Personal and social history • Systems review. In general, the three most urgent considerations that must be carefully assessed before any US-guided interventional procedure are: • The presence of blood-thinning pathologies or the use of blood-thinning drugs that could cause severe bleeding during and after the procedure • The presence of drugs allergies • The presence of diabetes, which is a contraindication for steroid use. Explanation of Contraindications to the Interventional Procedure and Informed Consent Despite the minimal invasiveness of the interventional procedures described in this book, the patient must be provided with an accurate explanation of the possible contraindications related to the planned procedure. Although the complication rate associated with these procedures is extremely low, patients should be aware that their occurrence cannot be ruled out entirely. The subjects that must be clearly explained to the patient are the following: • Pain/soreness during the procedure 1 General Aspects of US-guided Musculoskeletal Procedures • Pain/soreness after the procedure and the possibility of steroid flare • Potential risk of joint infection • Potential risk of tendon rupture. After receiving this information, the patient must formally agree to the procedure by providing both verbal and written informed consent. Antisepsis All US-guided interventional procedures must be performed with aseptic techniques in order to avoid any risk of contamination by infectious organisms (bacteria, fungi, viruses) or other disease-causing microorganisms. The cornerstones of a safe US-guided interventional procedure are: • Antisepsis: transient microorganisms are removed from the skin using chemical solutions for disinfection. • Aseptic non-touch technique: ANTT minimizes the risk of infection by ensuring that only uncontaminated objects/fluids make contact with sterile/susceptible sites. The only part of sterile equipment that may be handled is that which will not be exposed to the susceptible site. Re-useable equipment employed during an aseptic procedure should be cleaned with wipes and must be fit for purpose, e.g., a steel dressing trolley for dressing changes. All packs/single-use equipment, e.g., dressing packs, cannula packs, and syringe packs, must be intact, with a still-valid expiration date, and without visible signs of contamination. • Operator sterility: accurate and effective hand hygiene is the most important component of good infection prevention and control, given that the hands are a common route of infection transmission. Transient bacteria can be removed by effective hand hygiene techniques, e.g., by washing the hands with an antimicrobial liquid soap and water, or by using an alcohol-based hand rub. Sterile gloves, coats and hats are mandatory. • Probe antisepsis: the US probe and probe wire are swiped with dedicated antiseptic tis- 3 sues; if required for the procedure, a sterile probe cover is used. • Patient antisepsis: the skin cannot be “sterilized” but certain chemical preparations reduce microbial levels. Our antisepsis procedure is composed of a first step in which a brown water-based povidone-iodine solution is used to mark the treated area and after 3–5 min (sufficient to let the antiseptic act), in the second step, a transparent solution of 70% isopropyl alcohol and 2% chlorhexidine is applied that disinfects by denaturing proteins and disrupting the cell wall of microorganisms in addition to being bactericidal and long-acting. Both steps are recommended for adequate skin decontamination prior to the insertion of an invasive device. • Surgical field: delimitation of the area to be operated on is performed by the operator using sterile technique, including adhesive sterile towels. • US contact gel: conventional US contact gel should not be used for aseptic US-guided procedures. However, contact gel is not generally used in short procedures (e.g., simple injections). For longer procedures, sterile contact gel can be applied. Needles and Syringes The wide range of different interventional procedures implies the use of several different kinds of needles. Needles of different diameters (measured in gauges, G; the lower the number, the higher the diameter) and lengths (measured in millimeters) are used for all procedures: • Superficial procedures are generally performed using thin (26–32G) and short (2–5 cm) needles. • Procedures that require the aspiration of dense collections, such as ganglions or calcifications, are performed using larger (14– 16G) needles. Needle length is strictly related to the depth of the target. • Spinal needles are used for deep locations, such as hip joints or in obese patients. The 4 A. Conchiglia et al. most common spinal needles used in these procedures are 9–12 cm and 16–22G. Syringes come with a number of designs for the area where the blade locks to the syringe body. Our preference is to use slip tip syringes as they are easiest to connect to the needle for all procedures that do not involve high pressure; in that case, we use Luer-lock ones which assure a screw lock mechanism by simply twisting syringe and needle together. The choice of syringe size strictly depends on the amount of fluid to inject/drain. For the most common upper limb procedures, we recommend the following: • 1–2 ml: used around the hand/wrist for very small joint injections (MCP, PIP, DIP) and for the treatment of trigger finger and tenosynovitis. • 5–10 ml: used to inject sub-acromial bursa, the drainage of small collections, and to drain tennis/golfer’s elbow. • 20 ml: used for calcification lavage and aspiration, or the evacuation of fluid collections. How Is the Needle Inserted? Guidance of the needle under US can be performed with either the lateral or co-axial approach. In the former, the needle is kept perpendicular to the US beam and is inserted on the short side of the probe. In the latter, the needle is inserted on the long side of the probe, parallel to the US beam. The lateral approach has the advantage of excellent visibility of the needle, which, however, crosses a larger amount of tissue before reaching the target than is the case with the co-axial approach. On the other hand, the coaxial approach is burdened by a reduced needle visibility, but it can be used when the space around the target is greatly restricted. However, adequate experience is needed to achieve satisfactory results (Fig. 1.1a-b). a b Fig. 1.1 a In US-guided lateral approach the needle is inserted on the short side of the probe allowing for an excellent visibility. b In USguided coaxial approach the needle is inserted on the long side of the probe, allowing for a reduced path in soft tissues but a poor visibility 1 General Aspects of US-guided Musculoskeletal Procedures Drugs Local Anesthetics The important role played by local anesthetics is due to their ability to interrupt neural conduction, by inhibiting the influx of sodium ions. In most cases, this inhibitory activity follows their diffusion through the neural membrane into the axoplasm, where they enter sodium channels. The local anesthetic molecule consists of three components, a lipophilic aromatic ring, an intermediate ester or amide chain, and a terminal amine, each of which confers distinct properties to the molecule. The aromatic ring improves the lipid solubility of the compound, which in turn enhances diffusion through both nerve sheaths and the neural membranes of the individual axons comprising a nerve trunk. This property correlates with drug power, as a greater portion of an administered dose thereby enters neurons. US-guided interventional procedures usually require local anesthesia to minimize pain and discomfort. The type and amount of anesthetic used depends largely on the procedure itself and the involved anatomical location. Fast-acting local anesthetics, such as a 100 mg/5 ml lidocaine solution (2%), are injected with a small needle around and within the area to be treated. Patients will initially experience a brief stinging sensation related to the needle and the anesthetic being introduced; bicarbonates buffering significantly reduces this type of sensation. Within seconds, typically, the area becomes numb. Lidocaine solutions are also an option for US-guided diagnostic nerve blocks, with the anesthetic injected around the nerve over the level of the suspected pathology. Long-acting local anesthetics, such as a 25 mg/10 ml bupivacaine hydrochloride solution (0.25%), are injected in association with corticosteroids for local relief at sites of musculoskeletal discomfort (articular and extra-articular) and for therapeutic nerve blocks. 5 Adverse Effects The patient may experience temporary side effects after local anesthetic administration, but persistent problems are rare. Side effects can include: • Numbness of the tongue • Dizziness • Blurred vision • Muscle twitching Local anesthetics depress the central nervous system in a dose-dependent manner. Convulsive seizures are the principal life-threatening consequence of an overdose. Evidence of lidocaine toxicity may occur at concentrations of 5 g/ml, but convulsive seizures not until 8 g/ml. In addition to neural blockade, the peripheral actions of most local anesthetics include varying degrees of vasodilation, which in turn contributes to the hypotension observed after the administration of larger doses. It must be borne in mind that, as central nervous system depressants, local anesthetics potentiate any respiratory depression associated with the use of sedatives and opioids. Contrary to conventional thought, doses calculated as mg/years of age or mg/kg body weight do not predict the systemic serum concentration of the local anesthetic. Furthermore, considerations of the toxicity of any drug class must include the activity of not only the drug but also its metabolites. Local anesthetics are no exception. It is not unusual for patients to claim that they are allergic to local anesthetics. Upon careful questioning, however, it becomes apparent that what they experienced was either a syncopal episode associated with the injection or cardiac palpitations attributed to epinephrine either contained in the solution or released endogenously. Although rare, allergic reactions to local anesthetics have been reported in the scientific literature, but in none of these cases was there a confirmed IgE-mediated hypersensitivity reaction. Nevertheless, patients have occasionally experienced symptoms consistent with an allergic reaction to amide local anesthetics. These episodes generally have been attributed to the preservatives (methylparaben) or antioxidants (bisulfites) contained in the solution. 6 Corticosteroids Inflammation is one of the body’s first reactions to injury. The increase in local blood flow transports polymorphonuclear leukocytes, macrophages, and plasma proteins to the injured area, where a redistribution of arteriolar flow produces stasis and hypoxia at the injury site. The resulting infiltration of the affected tissues by leukocytes, plasma proteins, and fluid causes the redness, swelling, and pain that are characteristic of inflammation. The causes of inflammatory muscle and joint injuries including: • Degenerative joint disease • Tendinopathy • Bursitis • Arthritis • Trauma. Initially, the inflammatory reaction serves several important purposes. For example, the influx of leukocytes facilitates phagocytosis, allowing the removal of damaged cells and other particulate matter. The mechanism of corticosteroid action includes a reduction of the inflammatory reaction by limiting capillary dilatation and the permeability of the vascular structures. These drugs restrict the accumulation of polymorphonuclear leukocytes and macrophages, reduce the release of vasoactive kinins, and inhibit the release of destructive enzymes that attack the injury debris and destroy normal tissue indiscriminately. Steroids have variable structures, functions, and sites of action. In addition to the steroids found in nature, there are many that have been synthetically produced. These molecules differ mostly with respect to the functional groups attached to their carbon rings. The synthetic corticosteroids most commonly used in radiology procedures are derivatives of prednisolone (an analogue of cortisol). All have anti-inflammatory potencies per dose unit that are somewhat greater than that of cortisol. Corticosteroid preparations can be either soluble or insoluble. Most corticosteroid preparations contain corticosteroid esters, which are highly insoluble in water and thus form microcrystalline suspensions. A. Conchiglia et al. Dexamethasone-type preparations, however, are not esters and are freely soluble in water; hence, the preparation is clear (i.e., non-particulate). The potential advantage of corticosteroid ester preparations is that they require hydrolysis by cellular esterases to release the active moiety; consequently, their actions in the joint are longer-lasting than those of non-ester preparations. By contrast, freely water-soluble preparations, such as dexamethasone sodium phosphate and betamethasone sodium phosphate, are taken up rapidly by cells and thus have a quicker onset of effect but with a concomitant reduced duration of action. Soluble preparations must be used in all cases in which there is the risk of inadvertent intra-arterial injection, as it could result in embolic infarction from particulate corticosteroid esters. The duration of action of corticosteroids can be estimated based on their biologic half-life, pharmaceutical half-life, or duration of clinical benefit. While the duration of clinical benefit is the most practical assessment, it is unfortunately the most subjective and differs widely in literature reports, without statistically significant differences. As previously explained, ester preparations of a corticosteroid would be expected to have a longer half-life, since release of the active moiety relies on the activities of the patient’s own hydrolytic enzymes (esterases). Corticosteroids are sometimes administered after admixture with other agents in the same syringe. The potential advantages over a dualsyringe technique is the reduced chance of inadvertent needle movement during syringe exchange and a marginally reduced procedure time. Adverse Effects The established adverse effects associated with corticosteroid injections include the following: • Infection • Post-injection flares • Local tissue atrophy • Tendon rupture • Cartilage damage • Flushing • Increased blood glucose levels. 1 General Aspects of US-guided Musculoskeletal Procedures The most feared complication after steroid injection is infection. With the use of good sterile technique, however, the incidence of this complication is as low as 0.01–0.03%. The most common adverse effect is the post-injection flare, which is a local increase in inflammation that develops within hours and can last 2–3 days. The prevalence of post-injection flare is 2–25% and does not predict a poor response to therapy. The cause of the flare may be the previously described microcrystalline steroid esters, which may incite a crystal-induced arthritis, or possibly a chemical within the drug formulation. Local tissue necrosis, calcification, and tendon rupture have been associated with extra-articular injections of the corticosteroid formulation triamcinolone hexacetonide. Accordingly, it is recommended that this particular drug be administered only under US guidance, even though it is a very effective medication, with a clinical benefit of up to several months. There are a number of soft-tissue adverse effects associated with the local injection of corticosteroids, namely, skin atrophy and depigmentation, as well as fat necrosis. These are most noticeable after the injection of superficial structures (e.g., ganglia and tendon sheaths) but can also be seen after an intra-articular injection, presumably due to the reflux of corticosteroid along the needle track. Corticosteroids increase protein catabolism, and the possibility of tendon rupture associated with intratendinous corticosteroid injection is well recognized, implying that peritendinous injections should be performed with caution. US guidance will increase injection accuracy. Systemic effects do occur following softtissue or intra-articular injections but are generally believed to have minimal clinical importance. Nevertheless, it is important for the treating radiologist to be aware that intra-articular corticosteroids do exert variable systemic effects. Patients with diabetes who are administered such injections should thus be warned to expect a slight increase in their blood glucose level. 7 Hyaluronic Acid The administration of hyaluronic acid with USguided intra-articular injection, referred to as viscosupplementation, has been demonstrated to be effective in the treatment of moderate and severe osteoarthritis. The aim of the procedure is to reduce disability and pain by restoring the physiological properties of the synovial fluid and thereby improving articular function and the recovery of working and social activity. The intra-articular administration of hyaluronic acid has a role not only in restoring the viscoelastic properties of synovial fluid (pure mechanical effect), but also in stimulating the endogenous production of hyaluronic acid by articular chondrocytes and synoviocytes through the release of products based on hyaluronic acid. Hyaluronic acid is a polysaccharide member of the group of glycosaminoglycans. It is a polymer with a very high molecular mass and consists of repeating units of N-acetylglucosamine and glucuronic acid linked together by glycosidic bonds. It is present in the superficial layers of cartilage, the intercellular matrix of the joint capsule, synovial tissue, and synovial fluid. Hyaluronic acid is highly absorbent with visco-elastic properties: viscosity (lubrication) in case of static compressive strength and elasticity (shock-absorbing) in response to dynamic shear and compressive forces. Hyaluronic acid can be classified according to its molecular mass: • Low (up to 1000 kDa) • Average (1000–4000 kDa) • High (> 4000 kDa). These differences in molecular mass translate into different effects; low molecular mass forms have greater tissue penetration, producing a higher concentration of the product around the cell surface and a more powerful pharmacological response by chondrocytes. The stabilization of aggregates at high density and high molecular mass (> 2000 kDa) results in the reduced motility of single hyaluronic acid molecules, preventing their rapid degradation by synovial cells, which take up only free molecules. The prolonged half-life of these preparations within the joint 8 (approximately 4 weeks) allows the long-term treatment of osteoarthritis with only a single hyaluronic acid injection. Platelet-Rich Plasma Autologous platelet-rich plasma (PRP) is derived from three components (platelet concentrate, cryoprecipitate of fibrinogen, and thrombin) of whole blood withdrawn from the patient and combined at the moment of administration. The growth factors contained in the platelets, including transforming growth factor-β (TGF-β), platelet-derived growth factor (PDGF), fibroblastic growth factor (FGF), and insulin-like growth factor (IGF), are physiologically involved in tissue repair mechanisms and are concentrated in PRP, thus promoting healing of the injured tissue. Preparations of PRP are obtained from the transfusion medicine service of the hospital or prepared using disposable kits. Following activation with 1–2 ml of 10% calcium gluconate solution, autologous PRP must be injected immediately to prevent gelification. A. Conchiglia et al. The role of PRP in oral, plastic, maxillofacial and orthopedic surgery has been studied; for example, in the treatment of tendinosis, a fast and durable recovery of tendon structure was demonstrated. However other studies, also conducted on large series, concluded that PRP is no more effective than placebo. These issues need to be addressed before PRP can be used routinely. Post-procedural Care After the interventional procedure the treated skin is covered with a plaster and a compressive dressing and the patient is instructed to apply an instant ice bag over the treated area. Patients should be monitored for the after-effects of anesthesia for at least half an hour after the procedure. After they have been instructed regarding the management of possible complications, such as pain and skin reddening, in the following hours/ days, they can be discharged from the hospital/ clinic. Fig. 1.2 A well-organized tray containing all the required materials is strongly recommended and includes syringes, anesthetic, antiseptic solutions, saline solution, containers, sterile tissues, gloves, and drugs 1 General Aspects of US-guided Musculoskeletal Procedures General Workflow for US-Guided Interventional Procedures • Verbal and written informed consent is obtained after the patient has received a comprehensive explanation of the risks and possible complications associated with the procedure. Local regulations may vary among different countries and hospitals. A representative of the pertinent institution should be involved in formulating an appropriate informed consent form. • Pre-interventional planning should include a deep knowledge of the procedure and of the materials, as well as a preliminary US evaluation of the lesion. • Patient positioning on the bed or operating table is particularly important, with the comfort of both the patient and the operator confirmed in order to avoid any sudden movements by either one. • Operator sterility should be performed as described above. • Both the US equipment and the probe are swiped with dedicated antiseptic tissues and, if required for the procedure, a sterile probe cover is used. • All devices and drugs should be prepared in full sterility before the procedure commences. The availability of an organized tray with all materials is recommended (Fig. 1.2). • Operating field delimitation with adhesive sterile towels should be performed by the sterile operator. • Skin antisepsis should be as accurate as possible. While the skin cannot be “sterilized,” certain chemical preparations reduce microbial levels. We recommend a 2-step antisepsis procedure: (1) the area to be treated is wiped with a brown water-based 5% povidone-iodine solution; (2) after 3–5 min (time required to let this antiseptic to act), the same area is wiped with a transparent 2% chlorhexidine-based solution, which denatures the proteins and disrupts the cell walls of contaminating organisms, is bactericidal, and is long-acting. This second step improves skin sterility and avoids staining of the US probe. • Antiseptic solutions usually create a good coupling between the skin and the US probe. When longer procedures are performed (e.g., the treatment of calcific tendinitis), a small amount of sterile contact gel can be used. 9 Part I The Shoulder 2 The Shoulder: Focused US Anatomy and Examination Technique Enzo Silvestri and Davide Orlandi The shoulder can be subdivided into three compartments: anterior, lateral, and posterior. Anterior Compartment Long Head of the Biceps Brachii Tendon Anatomy This tendon originates from the bicipital anchor, on the apex of the glenoid labrum. It courses laterally and anteriorly, turning distally inside the bicipital groove. It ends at its myotendinous junction, located under the insertion of the pectoralis major tendon on the anterior humeral diaphysis. Scanning Technique The patient is seated opposite the examiner, with his or her forearm 90° flexed and the arm resting on the thigh, slightly internally rotated, palm facing up. The transducer is placed in a horizontal position on the anterior aspect of the shoulder, to localize the bicipital groove (between the lesser and greater humeral tuberosities). Between the two bony structures, the long head of the biceps brachii tendon can be visualized on an axial scan as an oval-shaped, hyperechoic structure with a fibrillar echotexture. The probe is then glided caudally, to evaluate the vertical part of the tendon up to the myotendinous junction, followed by a 90° clockwise rotation to evaluate the tendon along its long axis. Enzo Silvestri ( ) Radiology Unit Ospedale Evangelico Internazionale Genoa, Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_2 © Springer-Verlag Italia 2012 13 14 E. Silvestri and D. Orlandi a b c Fig. 2.1 Evaluation of the long head of the biceps brachii tendon. a The probe and patient are positioned for an evaluation of the long head of the biceps tendon on a short-axis scan. b Anatomical scheme of the long head of the biceps brachii tendon as seen along its short-axis (arrowheads). GT greater tuberosity, LT lesser tuberosity. c US short-axis scan of the long head of the biceps brachii tendon (arrowheads). D deltoid muscle 2 The Shoulder: Focused US Anatomy and Examination Technique 15 a b c Fig. 2.2 Evaluation of the long head of the biceps brachii tendon. a The probe and patient are positioned for an evaluation of the long head of the biceps tendon on a long-axis scan. b Anatomical scheme of the long head of the biceps brachii tendon as seen along its long axis (arrowheads). H humerus. c US long-axis scan of the long head of the biceps brachii tendon (arrowheads). D deltoid muscle 16 E. Silvestri and D. Orlandi Subscapularis Tendon Anatomy The subscapularis muscle originates from the subscapularis fossa, on the anterior aspect of the scapula. It runs laterally and anteriorly and its distal tendon inserts on the anterior aspect of the humeral head. Most fibers insert on the lesser tuberosity, while others contribute to the stability of the biceps tendon, inserting on the greater tuberosity and on the bicipital pulley. Scanning Technique With the operator holding the probe on the bicipital groove, the patient performs an extrarotation of the forearm to extract the subscapularis tendon, allowing its visualization on a longitudinal scan, while the elbow is kept as close as possible to the thoracic wall. With the probe turned 90° clockwise, the subscapularis tendon can be assessed on its short axis, thus demonstrating the alternation of tendinous and muscular fibers. a b c Fig. 2.3 Evaluation of the subscapularis tendon. a The probe and patient are positioned for an evaluation of the subscapularis tendon on a long-axis scan. b Anatomical scheme of the subscapularis tendon (SSC) as seen along its long axis. H humerus. c US long-axis scan of the SSC. D deltoid muscle 2 The Shoulder: Focused US Anatomy and Examination Technique 17 a b c Fig. 2.4 Evaluation of the subscapularis tendon. a The probe and patient are positioned for an evaluation of the subscapularis tendon on a short-axis scan. b Anatomical scheme of the subscapularis tendon as seen along its short axis (arrowheads). H humerus. c US short-axis scan of the subscapularis tendon (arrowheads). D deltoid muscle 18 E. Silvestri and D. Orlandi Glenohumeral Anterior Recess The probe is placed in the same position used to evaluate the subscapularis tendon along its long axis and is then moved medially, which allows visualization of the articular cortex of the humeral head. This structure appears as a spherically curved echogenic line, while the cortical surface of the anterior glenoid rim is seen as a triangular echogenic structure just medial to this line. The coracoid process partially hinders the articular space. The anterior glenoid labrum may occasionally be seen as a well-defined, triangular, echogenic structure. a b c Fig. 2.5 Evaluation of the glenohumeral anterior recess. a The probe and patient are positioned for an evaluation of the glenohumeral anterior recess. b Anatomical scheme of the glenohumeral anterior recess (arrow). H humerus, SSC subscapularis, C coracoid process, G glenoid. c US scan of the glenohumeral anterior recess (arrow) 2 The Shoulder: Focused US Anatomy and Examination Technique Lateral Compartment Supraspinatus Tendon Subacromial-Subdeltoid Bursa The subacromial subdeltoid (SASD) bursa is a wide mucous bursa covering the rotator cuff as a cap. It acts as a local attrition attenuator and facilitates gliding of the supraspinatus tendon underneath the acromion during arm abduction. This structure consists of a subacromial portion (located between the superior face of the joint capsule and the inferior surface of the acromion) and a subdeltoid portion (located deep to the deltoid muscle), which may extend laterally and inferiorly as far as 3 cm below the greater tuberosity. In a minority of patients, a subcoracoid extension is present. When the rotator cuff is intact, this bursa does not communicate with the articular joint space. In normal conditions, the SASD bursa appears as a 2-mm-thick structure made up of a thin inner layer of hypoechoic fluid between two layers of hyperechoic peribursal fat. The synovial membrane of the bursa cannot be depicted with US. Anatomy 19 The supraspinatus muscle is located in the fossa supraspinata of the scapula. Its tendon courses laterally and slightly anteriorly, inserting on the upper portion of the greater tuberosity. A few fibers are sent also to the bicipital pulley. Scanning Technique The patient places his or her hand on the homolateral iliac wing, with the elbow as medial as possible. Starting from the bicipital groove, the probe is shifted cranially and laterally in an axial-oblique fashion along the major axis of the supraspinatus tendon, posterior to the biceps tendon. A correct scan is obtained when the humeral head cartilage, the anatomical neck of the humerus, and the greater humeral tuberosity are seen together. Anisotropy artifacts may particularly disturb the insertional area of the tendon on the humeral neck. These artifacts can be avoided by slightly tilting the probe laterally such that the US beam is as perpendicular as possible to the tendon fibers. The probe should then be rotated 90° clockwise to assess the tendon’s short axis. 20 E. Silvestri and D. Orlandi a b c Fig. 2.6 Evaluation of the supraspinatus tendon. a The probe and patient are positioned for an evaluation of both the supraspinatus tendon on a long-axis scan and the SASD bursa. b Anatomical scheme of the supraspinatus tendon (SSP) as seen along its long axis. GT greater humeral tuberosity, arrow SASD bursa. c US long-axis scan of the SSP. Arrow SASD bursa, D deltoid muscle, asterisks articular cartilage. The arrowhead indicates the critical zone of the SSP where anisotropy artifacts may occur 2 The Shoulder: Focused US Anatomy and Examination Technique Posterior Compartment Infraspinatus and Teres Minor Tendons Anatomy The infraspinatus and teres minor muscles arise from the fossa infraspinata of the scapula, the former cranial to the latter. Both tendons course laterally and cranially, inserting on the posterior aspect of the greater tuberosity. a 21 Scanning Technique The patient sits opposite the examiner, elbow flexed and palm on the opposite shoulder. The probe should be oriented vertically to localize the scapular spine, which separates the fossa supraspinata from the fossa infraspinata. Within the latter, the infraspinatus and teres minor muscles can be seen along their short axis with a sagittal US scan. The probe should then be shifted laterally to assess both tendons on a short-axis view. The longitudinal axis of each tendon can be studied by rotating the probe 90°. b c d Fig. 2.7 Evaluation of the extra-rotator tendons. The patient (a) and probe (b) are positioned for an evaluation of the extra-rotator tendons on a long-axis scan. c Anatomical scheme of the infraspinatus tendon (ISP) as seen along its long axis. GT greater humeral tuberosity, MJ myotendinous junction. d US long-axis scan of the ISP. Asterisk indicates the enthesis of the ISP, where anisotropy artifacts may occur 22 E. Silvestri and D. Orlandi Glenohumeral Posterior Joint Recess The probe is placed in the same position used to evaluate the insertional portion of the infraspinatus tendon along its long axis. It is then moved medially to visualize the articular cortex of the humeral head, which appears as a spherically curved echogenic line, while the cortical surface of the posterior glenoid rim is seen as a triangular echogenic structure just medial to this line, and the fibrocartilaginous posterior glenoid labrum as a well-defined, triangular, echogenic structure. a b c Fig. 2.8 Evaluation of the glenohumeral posterior recess. a The probe and patient are positioned for an evaluation of the glenohumeral posterior recess. b Anatomical scheme of the glenohumeral posterior recess (arrow). H humerus, ISP infraspinatus, asterisks humeral cartilage, G glenoid, arrowheads glenoid labrum. c US scan of the glenohumeral posterior recess (arrow). D deltoid muscle 2 The Shoulder: Focused US Anatomy and Examination Technique Acromioclavicular Joint The patient is seated opposite the examiner and the probe is placed on a coronal-oblique plane on the top of his or her shoulder. The two bony struc- 23 tures of the acromion and the clavicle are demonstrated as two linear hyperechoic lines, while the articular joint space appears as an anechoic triangular structure between them. a b c Fig. 2.9 Evaluation of the acromioclavicular joint. a The probe and patient are positioned for an evaluation of the acromioclavicular joint. b Anatomical scheme of the acromioclavicular joint. Arrow joint space, arrowheads joint capsule, A acromion, C clavicle. c US scan of the acromioclavicular joint 3 Subacromial-Subdeltoid Bursa Injections Enzo Silvestri Essentials Etiology The general term “bursitis” indicates a nonspecific inflammatory condition of the synovial walls of the bursa, an anatomical entity with the mechanical function of reducing friction between sliding structures (e.g., tendon and cortical bone, tendon and muscle). Primary bursitis commonly originates from rheumatoid arthritis, gout, tuberculosis, polymyalgia rheumatica, and other pathological conditions. The bursa may become secondarily inflamed in rotator cuff tendinopathy/ tears, with or without joint effusion. Bursitis also occurs in the setting of anterosuperior impingement due to overhead activities. Isolated septic bursitis is more likely in very young infants or in elderly patients with chronic debilitating disorders, or it may derive from the accidental introduction of bacteria during nonsterile percutaneous procedures. Epidemiology Subacromial-subdeltoid (SASD) bursitis is the most common finding on US evaluation for painEnzo Silvestri ( ) Radiology Unit Ospedale Evangelico Internazionale Genoa, Italy ful shoulder. Minor asymptomatic abnormalities of this structure can be observed in up to 78% of patients. Clinical Presentation Patients with acute SASD bursitis usually report a restriction of abduction movements without previous trauma. Pain usually worsens during the night but also when performing overhead activities, and is typically reported on the lateral and anterior aspects of the shoulder. Patients with chronic SASD bursitis often complain of a dull shoulder ache, with tenderness over the greater trochanter and beneath the deltoid muscle. Ultrasound Diagnosis Under normal conditions, the SASD bursa appears as a 2-mm-thick structure made up of an inner layer of hypoechoic fluid between two layers of hyperechoic peribursal fat. The synovial membrane of the bursa is not normally depicted on US. Since intrabursal fluid can migrate depending on gravity and arm positioning, the various portions of the SASD bursa should be systematically assessed. In subacromial impingement, the bursa has thickened walls and may contain fluid as a result of chronic inflammation. Dynamic examination with the use of longitudinal scans L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_3 © Springer-Verlag Italia 2012 25 26 during abduction of the arm can underline even small intrabursal effusions, demonstrating the “notch sign” in the upper profile of the bursa at the level where it passes under the coracoacromial ligament. Care should be taken not to apply excessive pressure with the probe over the bursa. An effusion in both bursal and joint synovial spaces is considered indicative of a full-thickness tear of the rotator cuff. In the case of acute bursitis, the effusion may be consistent, with findings of a hypervascular flow in the synovial walls and peribursal tissues at Doppler examination. Occasionally (synovial osteochondromatosis, rheumatoid arthritis), round hyperechoic bodies (nodules) are found within the bursal space. Septic bursitis may include a complex effusion containing debris and septations. The bursal walls may be thickened, with peribursal hypoechoic strands reflecting edema in the surrounding soft tissues as associated findings. Treatment Options Oral anti-inflammatory drugs and intrabursal steroids are usually indicated in the acute phase E. Silvestri of the pathology. In chronic unresponsive cases, surgical removal is suggested. Interventional Procedure Indications Acute or chronic painful bursitis. Suspected or known septic bursitis can be drained but steroid injection should be avoided. Objective To deliver anti-inflammatory drugs into the bursal space. Equipment - 1 syringe (2 ml) 20G needle Lidocaine (2–5 ml) Long-acting steroid (1 ml, 40 mg/ml) Plaster Ice pack. 3 Subacromial-Subdeltoid Bursa Injections Our Procedure Fig. 3.1a STEP 1 After an accurate disinfection of both the skin and the probe, a longitudinal US scan is obtained to visualize the bursal effusion (Fig. 3.1a). The most distended bursal recess is selected as the target. Fig. 3.1b Fig. 3.1c STEP 2 As shown in Fig. 3.1b,c, the needle (arrowheads) is inserted with a lateral approach to the probe in order to reach the bursal space along a parallel path relative to the probe. A small amount of local anesthetic (asterisks) is injected into the bursal space to confirm correct positioning of the needle tip. Gently advancing the needle into the bursa while injecting can help to debride thickened and collapsed bursal walls. The anatomical scheme and the US image show the position of the needle with respect to the humeral head (H) and the supraspinatus tendon (SSP). 27 28 E. Silvestri STEP 3 Once correct positioning of the needle tip has been confirmed, the steroid can be injected into the bursa, leaving the needle in place and replacing the syringe used to administer the anesthetic with one containing steroid. The needle is then removed and a plaster is applied at the puncture site together with an ice pack. Post-procedural Care After treatment, patients should avoid exertion and overhead movements for 5–10 days. Pain may occur after treatment and is managed with oral NSAIDs. 4 Treament of Calcific Tendinitis of the Rotator Cuff Giovanni Serafini and Luca Maria Sconfienza Essentials Etiology The term “calcific tendinitis” refers to the intratendinous deposition of calcium, predominantly hydroxyapatite, that can affect every tendon in the body and especially the rotator cuff. This pathological condition is a dynamic process that evolves through four stages: pre-calcific, calcific, resorptive, and post-calcific. In the precalcific stage, microtraumatic factors associated with a local decrease in blood supply can lead to intratendinous fibrocartilaginous metaplasia, with resulting calcification. The subsequent calcific phase is considered as a resting period. Eventually, triggered by unknown factors, there is resorption of the deposit, accompanied by vascular invasion, the migration of phagocytic cells with dissolution of the calcific focus (resulting in a “toothpaste” appearance of the calcific deposit), and edema from intratendinous pressure, such that the condition becomes symptomatic. After resorption, in the post-calcific or reparative phase, fibroblasts restore the normal tendinous collagen pattern. Giovanni Serafini ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy Epidemiology Rotator cuff calcific tendinitis is a commonly seen condition, occurring in up to 20% of painful shoulders and up to 7.5% of asymptomatic shoulders. It is more frequent in women in their 40s and 50s and seems not to be related to physical activity. The supraspinatus tendon (80% of cases), followed by the infraspinatus (15% of cases) and subscapularis (5% of cases) tendons, is the most commonly affected cuff tendon. The lower third of the infraspinatus tendon, the critical zone of the supraspinatus tendon, and the pre-insertional fibers of the subscapularis tendon are the most frequently affected locations. This condition is typically associated with an intact rotator cuff. Clinical Presentation The pre-calcific phase is usually asymptomatic. The typical clinical manifestation is low-grade subacute pain that usually increases at night and corresponds to the calcific stage, variably associated with mechanical symptoms according to the size of the deposit. In many cases, however, rotator cuff calcific tendinitis can be a highly disabling disorder, with sharp acute pain that limits shoulder movement and is resistant to high doses of oral anti-inflammatory drugs. This clinical presentation usually coincides with the resorptive stage; fever, reflecting rupture of the calcifi- L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_4 © Springer-Verlag Italia 2012 29 30 cation into the adjacent structures, is occasionally reported. However, the acute phase of calcific tendinitis of the rotator cuff is regarded as a selfhealing condition, with spontaneous resolution in 7–10 days. Ultrasound Diagnosis Three types of calcifications have been described: type I consists of a hyper-reflexive lesion with a well-circumscribed dorsal acoustic shadow; type II deposits are well-circumscribed, homogeneous hyperechoic foci with a faint posterior shadow; type III are amorphous, inhomogeneous hyperechoic foci without posterior acoustic shadow. The consistency is solid for deposits of types I and II and semi-liquid for type III calcifications. G. Serafini and L.M. Sconfienza Interventional Procedure Indications The US-guided percutaneous treatment of calcific tendinitis of the rotator cuff is always and immediately indicated in the acute phase of the pathology, with US findings of type II or III calcifications. In case of mildly symptomatic type I calcifications, elective treatment should be considered. Percutaneous treatment is not indicated if the calcification has migrated into the bursal space or is eroding the humeral cortical bone, or if it is very small (< 5 mm). Objective To dissolve and aspirate the calcific material using an US-guided, double-needle procedure. Treatment Options Asymptomatic cases usually do not require treatment, as the process is self-healing. In patients with mild symptoms, the disease can be managed conservatively with physical therapy and a short course of oral NSAIDs. Lithotripsy is only partially effective. An alternative therapeutic approach is to extract the calcific material in an arthroscopy or imaging-guided procedure. Equipment - Two 16G needles One 10-cm 18/20G needle (optional) Inox bowl (to collect the washing fluid) Sterile saline solution (100–200 ml) warmed to about 38–40°C Two syringes (20 ml and 3 ml) Lidocaine (10 ml) Steroid (1 ml, 40 mg/ml) Plaster Ice pack. 4 Treament of Calcific Tendinitis of the Rotator Cuff Our Procedure Fig. 4.1a Fig. 4.1b Fig. 4.1c STEP 1 The patient is either placed in the supine position (subscapularis and supraspinatus calcifications) or is prone (infraspinatus or teres minor calcifications), as seen in Fig. 4.1a. A correct US scan should demonstrate the target calcification (C) according to its major axis (Figs. 4.1b, c). After sterile preparation of the skin and probe, a small amount of local anesthesia is injected under US guidance and using an in-plane approach along the path of the needle (arrowheads), in the SASD bursa (asterisks), and around the calcification (C) (Fig. 4.1a). H humeral head. 31 32 G. Serafini and L.M. Sconfienza Fig. 4.2a Fig. 4.2b Fig. 4.2c STEP 2 As shown in Fig. 4.2a–c, the first needle (arrowheads) is inserted into the lowest portion of the calcification (C), maintaining the bevel (arrow) open towards the probe. H humerus. 4 Treament of Calcific Tendinitis of the Rotator Cuff 33 Fig. 4.3a Fig. 4.3b c d Fig. 4.3c-d STEP 3 A second needle (curved arrows) is inserted into the calcification (C) parallel and superficial to the first (Fig.4.3a–c, arrowheads), and its tip is rotated 180° in order to create a correct washing circuit. As shown in Fig. 4.3c, the deeper needle needs to be inserted first, to avoid artifacts (circles) caused by the second, more superficial needle. Needle bavel (arrow) is opened upwards. Figure 4.3d shows both needles (arrowheads and curved arrows) within the calcification. H humerus. 34 G. Serafini and L.M. Sconfienza Fig. 4.4a Fig. 4.4b Fig. 4.4c STEP 4 A 20-ml syringe filled with warm sterile water is connected to one of the needles (arrowheads and curved arrows) and a gentle, intermittent pressure is applied. If the positioning is correct, a slight expansion of the calcification can be visualized. If no washing fluid exits and the needles are correctly positioned, an 18G spinal needle could be inserted into one or both 16G needles to slightly penetrate the target calcification, creating enough space for circulation of the fluid. The washing fluid exiting from the second needle is collected in the inox bowl, positioned as shown in Fig. 4.4a. Washing of the target continues until complete emptying of the calcification (C) is demonstrated, as shown in Fig. 4.4b,c. Arrowheads first needle, curved arrow second needle, H humerus. 4 Treament of Calcific Tendinitis of the Rotator Cuff Fig. 4.5a Fig. 4.5b Fig. 4.5c STEP 5 At the end of the procedure, one needle is removed and the 1-ml syringe is connected to the remaining needle (Fig.4.5a). This needle (arrowheads) is then displaced into the SASD bursa (Fig. 4.5b) and 1 ml of steroid is injected (asterisks). A plaster is then applied to the skin at the puncture site and an ice pack is placed over the shoulder. H humerus, C treated calcification. Post-procedural Care The patient is kept under observation for at least 30 min. The ice pack over the treated shoulder should be maintained for at least 2 h. Patients should avoid overhead movements and the carrying of heavy weights for up to 15 days. Pain may occur after treatment and is managed with oral NSAIDs. Post-procedural bursitis is seen in about 15% of patients within approximately 2 months after treatment. In these cases, an intrabursal steroid injection may be useful. 35 5 Calcific Enthesopathy Dry-Needling Francesca Lacelli Essentials Etiology Calcific enthesopathy of the rotator cuff represents a common and mostly asymptomatic US finding. Unlike calcific tendinopathy, in which a calcification develops from fibrocartilaginous metaplasia 1–2 cm away from the insertional tendinous area, in this condition tiny calcifications are found in the insertional area of the rotator cuff tendons and are usually coupled to degenerative alterations of the pre-insertional tendinous portion. Epidemiology The exact incidence of this condition cannot be estimated because of the broad range of degenerative or inflammatory conditions that may result in calcific enthesopathy. Males and females are equally affected. Clinical Presentation Patients with symptomatic calcific enthesopathy report well-circumscribed pain at the level of the greater trochanter (supraspinatus, infraspinatus, or teres minor insertional areas) or of the lesser trochanter (subscapularis insertion). The pain is worsened by applied pressure, either by the examiner’s finger or by the probe during the examination. Ultrasound Diagnosis Tiny, irregular hyperechoic insertional calcifications in a setting of degenerative tendinopathy. The calcifications are close to the humeral cortical bone and may present as an irregularity in the hyperechoic profile of the latter. Treatment Options Physiotherapy should always be considered. In symptomatic cases, a percutaneous procedure or surgical tendinous debridement is needed. Francesca Lacelli ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_5 © Springer-Verlag Italia 2012 37 38 F. Lacelli Interventional Procedure material; to produce slight intratendinous bleeding that will in turn promote healing of the tendon. Indications Symptomatic insertional calcific enthesopathy in one or more tendons of the rotator cuff. Objective To fragment the tiny insertional calcifications in order to accelerate the resorption of calcific Equipment - 1 syringe (5–10 ml) 18G needle Lidocaine (5–10 ml) Long-acting steroid (1 ml, 40 mg/ml) Plaster Ice pack. Our Procedure Fig. 5.1a STEP 1 After sterile preparation of both the skin and the US probe, the affected area is visualized with a longitudinal scan according to the respective tendon. A small amount of local anesthetic is injected under US guidance and with an in-plane approach along the path of the needle, into the SASD bursa, and around the insertional calcifications (see Fig. 3.1a–c). 5 Calcific Enthesopathy Dry-Needling 39 Fig. 5.1b c d e f Fig. 5.1c-f STEP 2 As shown in Fig. 5.1a–f, consecutive dry-needling punctures (arrowheads) are performed on the calcifications (arrow) to fragment the small calcific deposits and to produce slight bleeding into the insertional tendinous portion. The probe should also be shifted anteriorly and posteriorly to target the treatment towards all the calcifications. H humerus. 40 F. Lacelli Fig. 5.2 STEP 3 At the end of the procedure, 1 ml of steroid (asterisks) is injected (arrowheads) into the SASD bursa (Fig. 5.2) and the cutaneous point of insertion is covered with a plaster. An ice pack is applied over the shoulder. Post-procedural Care The patient is kept under observation for at least 30 min. The ice pack over the treated shoulder should be maintained for at least 2 h. Patients should avoid overhead movements and the carrying of heavy weights for up to 15 days. Pain may occur after treatment and is managed using oral NSAIDs. Post-procedural bursitis is seen in about 15% of patients within approximately 2 months after treatment. In these cases, an intrabursal steroid injection may be useful. 6 Hyaluronic Supplementation of the Subacromial Space Giovanni Serafini Essentials Etiology Cuff tear arthropathy is the association of a massive rotator cuff tear and shoulder osteoarthritis, with progressive superior migration of the humeral head, acetabulization of the shoulder, and collapse of the humeral head. Poor vascularity, the inferior mechanical properties of an aging rotator cuff, type III acromions, and subacromial impingement are the most outstanding factors leading to this condition. Epidemiology Most commonly, an elderly patient will present with massive rotator cuff tears altering the biomechanics of the shoulder and leading to progressive superior migration of the humeral head. The end-stage of cuff tear arthropathy is the acetabulization of the shoulder, with collapse of the humeral head. Giovanni Serafini ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy Clinical Presentation The main symptoms of cuff tear athropathy are functional limitation, weakness, and pain in the shoulder. There is an inability to perform either abduction or extra-rotation movements. Patients often complain of difficulty carrying out daily activities, such as combing their hair, clasping a bra behind their back, reaching behind their back, or sleeping on the affected shoulder. Weakness can appear during lifting or in rotating the arm. Pain while performing overhead activities and at night is common; it is usually located over the outside of the shoulder and upper arm. Crepitus or a crackling sensation may also be noted when the shoulder is moved in certain positions. Ultrasound Diagnosis A massive rotator cuff tear is diagnosed when a complete rupture of at least two tendons of the rotator cuff is identified. Treatment Options Several different surgical treatment options for cuff tear arthropathy have been proposed. However, in elderly patients, surgery may be more frequently associated with complications or may be precluded due to concurrent medical conditions. Viscosupplementation can help in the conservative management of this condition. L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_6 © Springer-Verlag Italia 2012 41 42 G. Serafini Interventional Procedure Indications Cuff tear arthropathy. Percutaneous treatment is not indicated in case of a recent history of shoulder trauma. Objective To inject a viscosupplement into the subacromial space so as to facilitate gliding of the acromial and humeral cortical bones in the acromial-humeral articulation. Equipment - Two syringes (5 ml and 10 ml) Lidocaine (2–5 ml) High-molecular-weight hyaluronic acid (6 ml) 18G needle Plaster. Our Procedure Fig. 6.1a Fig. 6.1b STEP 1 The subacromial space is visualized on a coronal US scan that includes the acromial superolateral cortical bone and the superior aspect of the humeral head (Fig. 6.1a, b); A acromion, H humeral head. Local anesthetic is injected along the path of the 18G needle under US guidance with an in-plane approach and an oblique direction (lateral to medial and superior to inferior) to reach the subacromial space. 6 Hyaluronic Supplementation of the Subacromial Space Fig. 6.1c STEP 2 As shown in Fig. 6.1c, once the subacromial space is reached by the needle (arrowheads), a syringe pre-filled with 6 ml of high-molecular-weight hyaluronic acid is attached to the needle, and the operator slowly and gently injects the drug into the subacromial space (asterisk). There should be no resistance against the injection; if this is not the case, a slight retraction of the needle may be necessary. A plaster is then applied to the skin at the puncture site. Post-procedural Care The injection should be repeated after one week. Treatment can be repeated in case of pain recurrence. 43 7 Intra-articular Injections Francesca Lacelli Essentials Intra-articular injections of the shoulder can be performed in the treatment of a variety of pathological conditions. The drugs administered in these cases may be anti-inflammatory agents, such as the use of steroids for the various forms of capsulitis, or viscosupplements such as hyaluronic acid, which are injected to decelerate the physiological process of osteoarthritis. Adhesive Capsulitis Etiology Adhesive capsulitis of the shoulder (frozen shoulder) is a common disease with unclear pathogenesis, resulting in chronic inflammation of the capsular tissues and abnormal tissue repair with fibrosis. Epidemiology Approximately 2% of the general population is affected, with a peak incidence between 40 and 60 years and a slight female predominance. Francesca Lacelli ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy Clinical Presentation This condition is classified as primary idiopathic when there is no detectable underlying causes for the symptoms, or as secondary to shoulder affections, either traumatic or non-traumatic, that determine secondary pain and stiffness. A recognized different form of secondary frozen shoulder is seen in diabetic patients and tends to be more severe and protracted. The diagnosis is essentially clinical. Patients report increasing pain, especially at night, and a progressively reduced range of motion. In most cases, adhesive capsulitis is considered as a self-limiting disorder but it lasts for years in up to 40% of patients. Treatment Options Conservative treatment includes physical therapy, anti-inflammatory and analgesic medications, and oral administration or intra-articular injections of steroids. Interventional Procedure Indications Intra-articular injection of steroids. Primary idiopathic or secondary adhesive capsulitis, degenerative osteoarthritis associated with articular effusion. Contraindicated in diabetes-related secondary adhesive capsulitis. L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_7 © Springer-Verlag Italia 2012 45 46 F. Lacelli Intra-articular injection of hyaluronic acid. Degenerative osteoarthritis without articular effusion. Equipment - Objective - 1 syringe (2–5 ml) 20G spinal needle Long-acting steroid (1 ml, 40 mg/ml) or lowmolecular-weight hyaluronic acid (2 ml) Plaster. To deliver anti-inflammatory or viscosupplement drugs within the joint space. Our Procedure Intra-articular joint injections of the shoulder can be performed with either an anterior or a posterior approach. The anterior approach suffers from the deep location of the joint with respect to the skin surface, as well as the presence of the coracoid process, which makes it extremely difficult to accurately visualize the needle tip. Thus, the posterior approach is generally more convenient. This procedure can also be used for the injection of contrast agents within the joint for purposes of arthrography. Anterior Approach Fig. 7.1a STEP 1 The patient is placed in the supine position, with the forearm flexed 90° and the hand lying on the abdomen. An anterior axial US scan is performed at the level of the coracoid process. The correct scanning plane should reveal the coracoid at the middle third of its height, the subscapularis tendon on its long axis, and the humeral lesser tuberosity (Fig. 7.1a). 7 Intra-articular Injections Fig. 7.1b STEP 2 The space between the coracoid and the humeral head is centered at the middle of the scanning plane and a 20G needle (arrow) is inserted perpendicular to the skin, at the middle of the probe (Fig. 7.1b) between the humeral head (H) and the glenoid (G) and the coracoid (C). Passage of the needle tip into the glenohumeral joint is generally associated with a distinct feeling of capsular resistance followed by the sensation of a resistance-free space. Fig. 7.1c STEP 3 Once correct intra-articular positioning of the needle tip has been confirmed (asterisk), the drug can be injected (Fig. 7.1c). There should be no resistance to the injection; if this is not the case, a short retraction (1–2 mm) of the needle should be considered because the needle tip could be pointed against the humeral cartilage or into the anterior glenoid labrum. At the end of the injection, the needle can be removed and a plaster applied at the cutaneous site of approach. C coracoid, SSC subscapularis tendon, G glenoid. 47 48 F. Lacelli Posterior Approach Fig. 7.2a Fig. 7.2b Fig. 7.2c Lateral Approach STEP 1 The patient is in a prone position with the upper arm not completely abducted and the forearm flexed, in order to avoid tension on the posterior joint capsule (Fig. 7.2a). A longitudinal US scan of the posterior articular recess is performed. The transducer is aligned with the long axis of the musculotendinous junction of the infraspinatus muscle, just inferior to the scapular spine, with the posterior glenoid rim and posterior glenohumeral joint line centered in the field of view (Fig. 7.2b,c). Transducer angulation is adjusted to clearly show the contours of the posterior glenoid rim, the posterior glenoid labrum, and the humeral head. The articular cortex of the humeral head appears as a spherically curved echogenic line, and the cortical surface of the posterior glenoid rim as a triangular echogenic structure just medial to this line. The fibrocartilaginous posterior glenoid labrum is seen as a well-defined, triangular, and uniformly echogenic structure. 7 Intra-articular Injections Fig. 7.3a Fig. 7.3b Co-axial Approach STEP 1 A co-axial out-of-plane approach is also possible (Fig. 7.3a-b), although the needle will be less visible. The passage of the needle tip (arrow) into the glenohumeral joint is generally associated with a distinct feeling of capsular resistance followed by the sensation of a resistance-free space. The asterisk indicates the distended posterior glenohumeral joint recess. G glenoid, H humerus, D deltoid. STEP 2 Once correct intra-articular positioning of the needle tip has been confirmed, the drug can be injected. There should be no resistance to injection; if this is not the case, a short retraction (1–2 mm) of the needle should be considered because the needle tip could be pointed against the humeral cartilage or into the posterior glenoid labrum. Distension of the articular capsule is usually not visible because of the small amount of fluid injected. At the end of the injection, the needle can be removed and a plaster applied at the cutaneous site of the approach. Post-procedural Care The patient should be kept under observation for at least 30 min after the procedure. Pain may occur after treatment and is managed with oral NSAIDs. 49 8 Long Head of the Biceps Brachii Tendon Injection Luca Maria Sconfienza Essentials Etiology Pathologies of the LHBB include synovial effusion, synovial hypertrophy and, rarely, calcifications. Tenosynovitis can be found alone or, more often, associated with glenohumeral effusion since the joint space is usually in communication with the sheath of this tendon. Ultrasound Diagnosis An anechoic fluid collection around the fibrillar tendinous structure of the LHBB can be demonstrated on axial and longitudinal scans. If thickening of the synovial component of the sheath and power-Doppler signs of hypervascularity are present, a rheumatic condition should be suspected. Treatment Options Epidemiology A small amount of fluid within the sheath of the LHBB is a common and asymptomatic finding and is typically associated with glenohumeral joint effusion. Conspicuous effusions are usually symptomatic. Physiotherapy is the treatment of choice. In the acute phase, the percutaneous injection of steroids can have a prompt effect on pain, while aspiration is usually required when a large amount of fluid is present. Clinical Presentation Pain is usually described as originating from the anterior aspect of the shoulder and irradiating anteriorly down the humerus. The onset is typically subacute or chronic. Luca Maria Sconfienza ( ) Radiology Unit IRCCS Policlinico San Donato San Donato Milanese (MI), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_8 © Springer-Verlag Italia 2012 51 52 L.M. Sconfienza Interventional Procedure Equipment Indications - Symptomatic effusion in the sheath of the LHBB tendon. 1 syringe (2 ml) 22G needle Lidocaine (2 ml) Long-acting steroid (1 ml, 40 mg/ml) Plaster. Objective To inject a small amount of steroid in the distended sheath of the LHBB. Our Procedure Fig. 8.1a STEP 1 The patient is placed in the supine position with his or her hand in a neutral position (Fig. 8.1a). The LHBB tendon is seen on an axial scan, starting from the bicipital groove and moving the probe caudally to identify the level of larger effusion. 8 Long Head of the Biceps Brachii Tendon Injection Fig. 8.1b Fig. 8.1c Fig. 8.1d STEP 2 The needle is inserted with an in-plane approach lateral to the probe (Fig. 8.1b,c) and advanced towards the tendon (arrows) while a small amount of local anesthetic is injected along the path. Once the needle (arrowheads) has reached the distended synovial sheath (Fig. 8.1c, asterisk), the fluid content is drained (Fig. 8.1d, asterisk). H humerus. 53 54 L.M. Sconfienza Fig. 8.1e STEP 3 The syringe with the steroid is then connected to the needle and the drug is injected (Fig. 8.1e, asterisks), avoiding penetration of the tendon (arrows) by the needle tip (arrowheads). The needle is removed and a plaster applied on the skin. Post-procedural Care The patient is kept under observation for at least 10 min. Pain may occur after treatment and is managed with oral NSAIDs. After treatment, patients should avoid heavy activities and refrain from overhead movements for 5–10 days. 9 Acromioclavicular Joint Injection Enzo Silvestri Essentials Etiology The most common AC joint pathologies that can be treated using a percutaneous approach include osteoarthritis and osteolysis of the distal clavicle. Osteoarthritis usually develops secondary to previous trauma, while osteolysis of the distal clavicle may be associated with repetitive weight training involving the shoulder. The history and physical examination are extremely important in diagnosing these conditions. Clinical Presentation Patients usually have insidious onset of pain. On physical examination, there is tenderness to palpation of the AC joint. A lump over the joint space indicates the presence of a cyst arising from the articular capsule and is usually associated with a degenerative shoulder arthropathy. Pain occurs with active or passive adduction of the shoulder and may be exacerbated by asking the patient to hold the opposite shoulder while pushing the elbow cranially against resistance. Ultrasound Diagnosis Epidemiology Degeneration of the AC joint typically affects middle-aged patients and is often associated with rotator cuff disorders. However, it is also found in young athletes (20s to 30s) with repetitive falls on the shoulder. Degenerative changes of the AC joint include an irregular profile of the cortical bone surfaces of the distal clavicle and acromion, associated with an articular joint effusion and a thickened capsule. Treatment Options Physiotherapy is the preferred treatment. Steroids or hyaluronic acid can help in reducing pain and thus in facilitating rehabilitation. Enzo Silvestri ( ) Radiology Unit Ospedale Evangelico Internazionale Genoa, Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_9 © Springer-Verlag Italia 2012 55 56 E. Silvestri et al. Interventional Procedure Equipment Indications - Osteoarthritis and osteolysis of the distal clavicle. Contraindicated in the acute or subacute phase of traumatic injury. - 1 syringe (2 ml) 23G needle Long-acting steroid (1 ml, 40 mg/ml) and/or low-molecular-weight hyaluronic acid (1 ml) Plaster. Objective To deliver steroid or hyaluronic acid in the AC joint space. Local anesthetic can be used as a diagnostic tool to assess the origin of shoulder pain. Our Procedure Fig. 9.1 STEP 1 The patient is seated opposite the examiner in a neutral position, with the hand lying on the thigh (Fig. 9.1). An out-of-plane co-axial approach is suggested, but an in-plane lateral approach is also possible. 9 Acromioclavicular Joint Injection Fig. 9.2a Fig. 9.2b Fig. 9.2c STEP 2 With an out-of-plane co-axial approach (Fig. 9.2a–c), the AC joint is visualized at the middle of a coronal scan (A and C) and the needle is inserted perpendicularly to the skin at the exact half of the probe. A clear sensation of resistance should be appreciated as the joint capsule is passed (arrowheads). The probe is gradually tilted towards the needle such that the needle tip (arrow) can be seen as a hyperechoic dot in the distended articular space (asterisk). There should be no resistance during the injection. With an in-plane approach, the AC joint space is visualized on a sagittal US scan. The needle is inserted lateral to the probe and advanced with a 30–45° inclination. 57 58 E. Silvestri et al. Post-procedural Care The patient is kept under observation for at least 10 min. An ice pack over the treated shoulder should be maintained for at least 1 h. Pain may occur after treatment and is managed using oral NSAIDs. Patients should avoid overhead movements and carrying heavy weights for up to 3 days. Part II The Elbow The Elbow: Focused US Anatomy and Examination Technique 10 Enzo Silvestri and Emanuele Fabbro The elbow is divided into four compartments: anterior, lateral, medial, and posterior. Anterior Compartment Distal Tendon of the Biceps Brachii Anatomy The tendon originates from the distal portion of the biceps brachii muscle. It courses obliquely from anterior to posterior, inserting on the bicipital tuberosity of the radius and surrounded by the bicipitoradial bursa. Scanning Technique The patient’s forearm is positioned as supinated as possible on the table to improve tendon visibility. The probe must be placed longitudinally to evaluate the tendon along its long axis up to the insertion on the radial tuberosity. Due to the tendon’s oblique course, which becomes deeper as it courses distally, it is important to press the distal edge of the probe on the patient’s skin to avoid anisotropy artifacts. Enzo Silvestri ( ) Radiology Unit Ospedale Evangelico Internazionale Genoa, Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_10 © Springer-Verlag Italia 2012 61 62 E. Silvestri and E. Fabbro a b c Fig. 10.1 Evaluation of the biceps brachii distal tendon. a The probe and patient are positioned for an evaluation of the biceps brachii distal tendon on a long-axis scan. b Anatomical scheme of the biceps brachii distal tendon (arrowheads). RT radial tuberosity, RH radial head. c US long-axis scan of the biceps brachii distal tendon (arrowheads) 10 The Elbow: Focused US Anatomy and Examination Technique Lateral Compartment Common Extensor Tendon Anatomy The extensor tendon complex is composed of several tendons: extensor carpi radialis brevis, extensor carpi ulnaris, extensor digitorum communis, and extensor digiti quinti. Normally, all of them have a fibrillar echogenic structure. 63 Scanning Technique With the patient’s forearm slightly flexed, the probe is placed on the lateral epicondyle to evaluate the tendon complex on a longitudinal scan. Occasionally, it is possible to differentiate the lateral collateral ligament from the tendon, based on their echotexture. a b c Fig. 10.2 Evaluation of the common extensor tendon. a The probe and patient are positioned for an evaluation of the common extensor tendon on a long-axis scan. b Anatomical scheme of the common extensor tendon (arrowheads). LE lateral epicondyle, RH radial head. c US long-axis scan of the common extensor tendon (arrowheads) 64 E. Silvestri and E. Fabbro Radial-Humeral Joint Anatomy The radial-humeral joint comprises the capitulum humeri and the radial proximal epiphysis, each covered by hyaline cartilage. The annular ligament accrues from the anterior edge of the radial notch of the ulna and inserts on the posterior edge of the radial notch. It is involved in passive stabilization of the elbow joint. Scanning Technique The probe is placed in the same position used to evaluate the common extensor tendon. A longitudinal scan allows visualization of the underlying radial-humeral synovial meniscus filling in the gap of the lateral surface of the radial-humeral joint. The radial head and the annular ligament can be correctly assessed by having the patient pronate and supinate the forearm. a b c Fig. 10.3 Evaluation of the radial-humeral joint. a The probe and the patient are positioned for an evaluation of the radial-humeral joint on a long-axis scan. b Anatomical scheme of the radial-humeral joint. c US long-axis scan of the radial-humeral joint. The articular space (arrow) can be seen between the capitulum humeri (CH) and the radial head (RH). The synovial meniscus (asterisk) is also visible 10 The Elbow: Focused US Anatomy and Examination Technique Medial Compartment Common Flexor Tendon Anatomy The common flexor tendon is composed of the pronator teres, flexor carpi radialis, flexor digitorum superficialis, palmaris longus, and flexor carpi ulnaris. The tendon is shorter and flatter than the common extensor tendon. 65 Scanning Technique With the patient’s forearm slightly flexed and externally rotated, the proximal edge of the probe is placed over the medial epicondyle (epitrochlea) to scan the common flexor tendon along its long axis. a b c Fig. 10.4 Evaluation of the common flexor tendon. a The probe and patient are positioned for an evaluation pf the common flexor tendon on a long-axis scan. b Anatomical scheme of the common flexor tendon (arrowheads). ME medial epicondyle, U ulna. c US long-axis scan of the common flexor tendon (arrowheads) 66 E. Silvestri and E. Fabbro Posterior Compartment Triceps Brachii Muscle and Tendon Anatomy The distal triceps tendon consists of the myotendinous junction of the three bellies forming the triceps muscle (long, medial, and lateral heads); the tendon inserts approximately 1 cm distal to the apex of the olecranon. Scanning Technique The triceps brachii muscle and tendon must be evaluated on long- and short-axis scans, positioning the elbow flexed 90°, the arm intrarotated, and the palm placed on the table. The US beam should be maintained as perpendicular as possible to the tendon fibers to avoid anisotropy artifacts. Olecranon Fossa and Posterior Olecranon Recess The posterior olecranon recess and the olecranic fossa can be assessed on longitudinal scans. The olecranon fossa appears as a wide concavity filled with a fat pad, localized deep to the triceps muscle and cranially to the distal humeral epicondyle. The olecranon process is visualized as a hyperechoic curvilinear bony structure covered by the synovial olecranon bursa. It is not visible under normal conditions. With the patients elbow flexed 90°, dynamic flexion and extension scans are used to assess the presence of intra-articular effusion. a b c Fig. 10.5 Evaluation of the posterior compartment of the elbow. a The probe and patient are positioned for an evaluation of the posterior compartment of the elbow on a long-axis scan. b Anatomical scheme of the posterior compartment of the elbow. c US long-axis scan of the posterior compartment of the elbow. The triceps tendon (arrowheads) inserts on the olecranon process (O). The posterior joint recess (arrow) and the olecranic fossa (OF) are also seen Treatment of Lateral Epicondylitis 11 Giovanni Serafini Essentials Etiology Epicondylitis is one of the most commonly diagnosed musculoskeletal disorders of the upperextremity. Lateral epicondylitis, also known as “tennis elbow,” is a painful condition of the tendinous origin of the wrist extensor muscles. Anatomically, the three major components of the common extensor tendon are the extensor carpi radialis brevis, the extensor digitorum, and the extensor carpi ulnaris tendon. Injury is due to repetitive stress on the common extensor tendon around its attachment to the lateral humeral epicondyle in response to manual tasks, forceful activities, or sports that require high force combined with high repetition or awkward posture (tennis, water polo, baseball, fencing). Epidemiology Lateral epicondylitis is more common than medial epicondylitis and generally affects individuals 40–60 years old, with equal prevalence among males and females. Clinical Presentation The main symptom is pain, which is localized in the lateral elbow region, corresponding to the lateral epicondyle of the humerus. It is typically related to activity and exacerbated by wrist and hand movements. Pain may radiate into the forearm and impair handgrip. Clinical tests, consisting of active and resisted movements of the extensor muscles of the forearm, provoke epicondylar pain (Cozen’s sign: pain with resisted wrist extension). During clinical examination, a typical tenderness at the lateral side of the elbow will often become apparent. Symptom duration usually ranges from a few weeks to a few months. Diagnosis In most cases, imaging is not necessary since the diagnosis of lateral epicondylitis is usually clinical, based on symptoms and findings during the physical examination. Imaging can be used to evaluate the extent of tissue damage, to exclude other causes of elbow pain, when the clinical presentation is atypical, or to confirm the diagnosis in patients not responding to treatment. Giovanni Serafini ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_11 © Springer-Verlag Italia 2012 67 68 In epicondylitis, the tendon can be thicker or thinner than normal, of poor definition, of decreased echogenicity, and accompanied by peritendinous effusion. In addition, the extensor tendon complex may show alterations in intratendinous vascularity. In severe cases, partial- or full-thickness tendon tears are seen as focal anechogenic areas with loss of the normal fibrillar pattern. G. Serafini Interventional Procedure Indications Insertional overload tendinopathy of the common extensor tendon. Contraindicated in case of traumatic lesions of the common extensor tendon. Objective Treatment Options First-line therapy usually consists of ice application, immobility of the upper limb, and NSAIDs. Shockwave therapy can reduce symptoms in the middle term. Surgical debridement is reserved for refractory cases. US-guided scarification (dry needling) can be considered as a minimally invasive option. To cause local hyperemia and bleeding into the tendon, thus promoting post-procedural plateletsinduced recovery phenomena. Equipment - 1 syringe (5–10 ml) 1 syringe (1–2 ml) 20G needle Lidocaine (5–10 ml) Long-acting steroid (1 ml, 40 mg/ml) Plaster. 11 Treatment of Lateral Epicondylitis Our Procedure Fig. 11.1a Fig. 11.1b Fig. 11.1c STEP 1 The patient is seated opposite the operator. The elbow is flexed 90° and the thumb points upward (Fig. 11.1a). The common extensor tendon is visualized by means of a longitudinal scan. The proximal portion of the probe is placed on the hyperechoic bony line of the lateral epicondyle (LE), while the distal part of the probe is aligned according to the common extensor tendon. The 20G needle (arrowheads) is inserted with an in-plane approach (Fig. 11.1b), in either a distal-proximal or a proximal-distal direction. Anesthetic (asterisks) is injected along the path of the needle, in the peritendinous soft tissues (Fig. 11.1c), and in the degenerated portions of the common extensor tendon (CET). RH radial head. 69 70 G. Serafini Fig. 11.2a Fig. 11.2b STEP 2 Figure 11.2a,b shows the needle (arrowheads) during a series of 15–20 repeated punctures (dry-needling) on the insertional portion of the tendon (CET), hitting also the periostum that covers the lateral epicondyle (LE). The radial head (RH) is also visible. 11 Treatment of Lateral Epicondylitis Fig. 11.3a Fig. 11.3b STEP 3 The end of the procedure is shown in Fig. 11.3a,b. One ml of steroid (asterisks) is injected into the peritendinous soft tissues, superficially to the tendon enthesis (CET). The needle (arrowheads) is then removed and a plaster applied. LE lateral epicondyle, RH radial head. Post-procedural Care The patient is kept under observation for at least 10 min. Pain may occur after treatment and is managed with oral NSAIDs. Patients are advised to use an orthotic support and to reduce their manual activity, although no systematic rest period is suggested. 71 Treatment of Medial Epicondylitis 12 Enzo Silvestri Essentials Etiology Epitrochleitis, or medial epicondylitis, is the most commonly diagnosed musculoskeletal disorder of the medial elbow. Medial epicondylitis, also known as “golfers elbow,” is a painful condition of the tendinous origin of the wrist flexor muscles. Anatomically, the major components of the common flexor tendon include the pronator teres, flexor carpi radialis, palmaris longus, flexor carpi ulnaris, and flexor digitorum superficialis. This condition is caused by repetitive stress on the common flexor tendon around its attachment to the medial humeral epicondyle due to manual tasks, forceful activities, and sports that require high force combined with repetitive valgus stress on the elbow joint (golf, baseball, goalkeeper). Epidemiology Medial epicondylitis is less common than lateral epicondylitis, with males slightly more often affected than females. The typical age range is from 30 to 50 years. Enzo Silvestri ( ) Radiology Unit Ospedale Evangelico Internazionale Genoa, Italy Clinical Presentation The main symptom is pain, which is localized in the medial elbow region, corresponding to the medial epicondyle of the humerus. Pain is typically related to activity and is exacerbated by wrist and hand movements. Moreover, it may radiate into the forearm and impair handgrip. Clinical tests, consisting of active and resisted movements of the flexor muscles of the forearm, provoke epitrochlear pain with resisted wrist flexion. During clinical examination, a typical tenderness at the medial side of the elbow will become apparent. The duration of epitrochleitis symptoms usually ranges from a few weeks to a few months. Diagnosis In most cases, imaging is not needed since the diagnose of medial epicondylitis is usually clinical, based on symptoms and findings during the physical examination. Diagnostic imaging can be used to evaluate the extent of tissue damage, to exclude other causes of elbow pain, when the clinical presentation is atypical, or to confirm the diagnosis in patients not responding to treatment. Ultrasound can demonstrate thinning or thickening of the tendon, sometimes associated with a peritendinous effusion. Also, tendon vascularity, evaluated using power Doppler, may be increased. More rarely, partial tears are seen. L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_12 © Springer-Verlag Italia 2012 73 74 E. Silvestri Treatment Options Objective First-line therapy usually consists of ice application, immobility of the upper limb, the use of orthotic devices, and NSAIDs. Shockwave therapy can reduce symptoms in the middle term. Surgical debridement is reserved for refractory cases. US-guided scarification (dry needling) can be considered as a minimally invasive option. To cause local hyperemia and bleeding into the tendon, thus promoting relevant post-procedural platelets-induced recovery phenomena. Interventional Procedure Indications Equipment - 1 syringe (5–10 ml) 1 syringe (1–2 ml) 20G needle Lidocaine (5–10 ml) Long-acting steroid (1 ml, 40 mg/ml) Plaster. Insertional overload tendinopathy of the common flexor tendon. Contraindicated in case of traumatic lesions of the common flexor tendon. Our Procedure Fig. 12.1a STEP 1 The patient is seated opposite the operator. The elbow is flexed 90° and the thumb points laterally (see Fig. 10.4a). The common flexor tendon (CFT) is visualized by means of a longitudinal scan. The proximal portion of the probe is placed on the hyperechoic bony line of the medial epicondyle (ME), while the distal part of the probe is aligned according to the common flexor tendon (see Fig. 10.4b,c). 12 Treatment of Medial Epicondylitis Fig. 12.1b Fig. 12.1c STEP 2 A 20G needle (arrowheads) is inserted with an in-plane approach, in either a distal-proximal or a proximal-distal direction (Fig. 12.1a–c), while a small amount of anesthetic (asterisks) is injected along the path of the needle, in the peritendinous soft tissues, and in the degenerated portions of the common flexor tendon (CFT). ME medial epicondyle. 75 76 E. Silvestri Fig. 12.2a Fig. 12.2b STEP 3 A series of 15–20 repeated punctures (dry needling, arrowheads) are performed in the insertional degenerated portions of the tendon (CFT), hitting also the periostium covering the medial epicondyle (Fig. 12.2a,b). ME medial epicondyle, arrow needle tip. 12 Treatment of Medial Epicondylitis Fig. 12.3a Fig. 12.3b STEP 4 At the end of the procedure, 1 ml of steroid (asterisks) is injected in the peritendinous soft tissues superficially to the tendinous insertion (CFT) (Fig. 12.3a,b). The needle (arrowheads) is then removed and a plaster applied. ME medial epicondyle, U ulna. Post-procedural Care The patient is kept under observation for at least 10 min. Pain may occur after treatment and is managed with oral NSAIDs. Patients are advised to use an orthotic support and to reduce their manual activity, although no systematic rest period is suggested. 77 Olecranon Bursa Drainage 13 Francesca Lacelli Essentials Epidemiology Olecranon bursitis is a relatively common condition that typically affects men between the ages of 30 and 60 years. It is characterized by an inflammatory process with fluid distension or hypertrophy of the synovial membrane. Clinical Presentation Patients usually complain of swelling in the olecranon region. Pain can vary from a subtle discomfort to an intense symptomatology. Pressure or active and passive movements may result in a worsening of symptoms. If fever is present, the diagnosis of septic bursitis must be considered. Ultrasound Diagnosis Etiology The most common cause of olecranon bursitis is local contusion: 66% of cases are aseptic and usually occur when trauma or repeated small injuries lead to bleeding into the bursa or the release of inflammatory mediators (student’s elbow, miner’s elbow). Bursitis can also develop secondary to calcific enthesopathy of the distal triceps tendon, systemic disorders such as rheumatoid arthritis, gout, hydroxyapatite and calcium pyrophosphate deposition diseases, septic conditions, or chronic hemodialysis. Francesca Lacelli ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy Olecranon bursitis is seen as a localized fluid collection and synovial wall hypertrophy. Color- and power-Doppler imaging demonstrate soft-tissue hyperemia. Both edema of the surrounding soft tissues and cellulitis are frequently associated with hemorrhagic and septic bursitis. In patients with chronic renal failure, it is common to identify a calcified bursitis. The presence of synovial proliferation and fibrosis suggests a differential diagnosis that includes solid tumor and chronic bursitis. In patients with rheumatoid arthritis, subcutaneous nodules can be seen in the olecranon region and along the proximal ulna. Fluid collection can lead to bursal rupture dissecting the superficial soft tissues. Treatment Options Most patients respond to conservative management, including ice, activity modification, and L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_13 © Springer-Verlag Italia 2012 79 80 F. Lacelli NSAIDs. In cases of septic bursitis, oral antibiotics may be administered. Drainage in the acute phases usually relieves swelling and discomfort, while steroid injection is performed in chronic or recurrent bursitis. Objective To drain distended olecranic bursa. To deliver anti-inflammatory drugs into the bursal space. Equipment Interventional Procedure Indications - Chronic or recurrent bursitis non-responsive to conservative treatment. Septic bursitis can be drained but steroid should not be injected. - 1 syringe (1 ml) 1 syringe to drain the bursal effusion (up to 20 ml) 14G–20G simple needle or shielded cannula Long-acting steroid (1 ml, 40 mg/ml) Plaster. Our Procedure Fig. 13.1a Fig. 13.1b STEP 1 The patient is positioned prone, with the forearm flexed and the hand lying on the examination table (Fig. 13.1a). This position can help to squeeze the bursa in case of a drainage procedure to address a consistent effusion. A longitudinal US scan is performed on the olecranic region (O) to assess the anatomical extension of the bursa and to identify the enlarged bursa (asterisks) (Fig. 13.1b). 13 Olecranon Bursa Drainage Fig. 13.2a Fig. 13.2b Fig. 13.2c STEP 2 A needle connected to a syringe is inserted with an in-plane approach until the tip enters the bursa (Fig. 13.2a). In some patients the bursal content is very dense, such that drainage is extremely challenging. In these cases, a larger shielded cannula (Fig. 13.2b,c, arrowheads) and the application of manual compression over the bursa (asterisks) may be helpful. A biopsy handle may also be used to obtain a more effective vacuum. T triceps tendon, O olecranon. 81 82 F. Lacelli Fig. 13.3 STEP 3 When the bursa (asterisks) has been completely drained, a small amount of steroid (circles) is injected (Fig. 13.3). In case of infection, lavage using warm saline solution may help. In these cases, however, steroid injections are to be avoided. The needle is then removed and a plaster applied at the cutaneous puncture site. T triceps tendon, O olecranon. Post-procedural Care The patient is kept under observation for at least 10 min. Pain may occur after treatment and is managed with oral NSAIDs. The patient is advised to avoid stressing the olecranon region on hard surfaces for a few days. Intra-articular Injections 14 Luca Maria Sconfienza Essentials Interventional Procedure Treatment Options Indications Intra-articular injections of the elbow can be performed in the treatment of a variety of pathological conditions. The drugs administered in these cases may be an anti-inflammatory agent, such as the use of steroids for rheumatoid arthritis or crystal-induced arthropathies, or a viscosupplement, such as hyaluronic acid, which is injected in joints involved by osteoarthritis. Local anesthetic can be injected to assess the intra-articular relevance of referred pain or as short-term analgesia. In traumatic fractures of the radial head, aspiration and analgesic injection are an option. This procedure can also be used to inject contrast agent within the joint for arthrography. Intra-articular injection of steroids: rheumatoid arthritis, crystal arthropathies, degenerative osteoarthritis with articular effusion. Intra-articular injection of hyaluronic acid: degenerative osteoarthritis without articular effusion. Intra-articular injection of local anesthetic: assessment of intra-articular relevance of pain, traumatic fractures of the radial head. Objective To deliver anti-inflammatory or viscosupplement agents into the intra-articular joint space. Equipment - 1 syringe (2–5 ml) 21G needle Long-acting steroid (1 ml, 40 mg/ml) or lowmolecular-weight hyaluronic acid (2 ml) Plaster. Luca Maria Sconfienza ( ) Radiology Unit IRCCS Policlinico San Donato San Donato Milanese (MI), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_14 © Springer-Verlag Italia 2012 83 84 L. M. Sconfienza Our Procedure Fig. 14.1a STEP 1 The patient is seated facing the operator with the elbow flexed 90° and the hand in a neutral position. The transducer is aligned longitudinally to visualize the humeral-radial joint (Fig. 14.1a). A longitudinal US scan of the lateral articular recess is performed, examining the cortical bone of the capitulum humeri, the synovial meniscus, and the proximal radial epiphisis covered with hyaline cartilage. The humeral-radial joint line is then centered in the field of view (see Fig. 10.3). 14 Intra-articular Injections Fig. 14.1b Fig. 14.1c STEP 2 A 20G needle is inserted perpendicularly to the skin at the center of the probe, with an out-ofplane (coaxial) approach (Fig. 14.1b). Passage of the needle tip into the joint is generally associated with a distinct feeling of capsular resistance followed by the sensation of a resistance-free space. When the needle tip (arrow) reaches the US scanning plane (Fig. 14.1c), it is visualized as a hyperechoic dot appearing in the anechoic articular space between the capitulum humeri (CH) and the radial head (RH), underlying the common extensor tendon (CET). The injection should be made slowly but with consistent pressure. At the end of the injection, the needle can be removed and a plaster applied on the skin. Post-procedural Care The patient should be kept under observation for at least 30 min after the procedure. Pain may occur after treatment and is managed with oral NSAIDs. A short resting period of 1 or 2 days should be recommended. 85 Part III The Wrist The Wrist: Focused US Anatomy and Examination Technique 15 Enzo Silvestri and Giulio Ferrero Extensor Tendons Anatomy On the dorsal side of the wrist, the extensor tendons run within six compartments, numbered from 1 to 6, from the radial to the ulnar side. The first compartment consists of the abductor pollicis longus and extensor pollicis brevis tendons. The second comprises the extensor carpi radialis longus and brevis tendons. The third, separated from the second by the Lister tubercle, contains the extensor pollicis longus tendon. The fourth compartment is the widest, as it must accommodate the extensor indici and the four extensor digitorum tendons. The fifth consists of the extensor digiti quinti tendon, and the sixth the extensor carpi ulnaris tendon. Scanning Technique To evaluate the first compartment, the wrist must be kept in an intermediate position between pronation and supination and the probe must be placed on the lateral side of the radial styloid. The second to fifth compartments are evaluated with the palm facing down in a neutral position. The sixth compartment is assessed with the hand slightly bent on the radial side. Long- and shortaxis scans of each tendon up to its distal insertion must be obtained, also during finger flexion and extension. Enzo Silvestri ( ) Radiology Unit Ospedale Evangelico Internazionale Genoa, Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_14 © Springer-Verlag Italia 2012 89 90 E. Silvestri and G. Ferrero a b c d e f Fig. 15.1 a Overview of the extensor compartments of the wrist. b Abductor pollicis longus (APL) and extensor pollicis brevis (EPB) tendons. R radius. c Extensor carpi radialis longus (ECRL) and brevis (ECRB) tendons. d The extensor pollicis longus tendon (EPL) is separated from the second compartment by the Lister tubercle (L). The extensor digiti secundi (EDS) and the extensor digitorum communis (EDC) tendons are contained in the fourth compartment. e Extensor digitorum communis (EDC) and extensor digiti quinti (EDQ) within the fourth compartment. f Extensor carpi (ECU) tendon overlying the ulna (U). All tendons are stabilized by the extensor retinacula (arrowheads) 15 The Wrist: Focused US Anatomy and Examination Technique Carpal Joints 91 carpal joint. The trapezium also articulates with the first metacarpal bone. Anatomy The radiocarpal joint is formed by the radius, the radioulnar capsule recess, and three bones of the proximal carpal row: scaphoid, lunate, and triquetrum. Between the scaphoid and the lunate and between the lunate and the triquetrum there are two important ligaments that act as passive wrist stabilizers, the scapho-lunate and lunatetriquetrum. The integrity or interruption of these structures defines the distribution of drugs inside the compartments and their spread into the mid- Scanning Technique The radiocarpal joint can be assessed by placing the probe on the dorsal side of the wrist on a longitudinal scan. A small amount of effusion will stretch the proximal side of the capsule. The trapezium-metacarpal joint is scanned with the wrist kept in the same position used for the first dorsal compartment, with the probe aligned along a longitudinal axis. a b Fig. 15.2a,b Sagittal scan over the radio-midcarpal joints. The distal radius (R), lunate (L), and capitate (C) are seen. The radiocarpal (arrow) and the mid-carpal (arrowhead) joints are visible 92 E. Silvestri and G. Ferrero a b Fig. 15.3a,b Trapeziometacarpal joint. The articular space (arrow) can be seen between the trapezium (T) and the metacarpal base (M). The joint capsule (arrowheads) is visible as well Treament of De Quervain’s Disease and Other Forms of Tenosynovitis 16 Giovanni Serafini Essentials Epidemiology De Quervain’s disease occurs in 0.5% of males and 1.3% of females; in the latter, it is often associated with pregnancy and nursing. The prevalence and incidence of De Quervain’s tenosynovitis in primary care are not known. This disease has a considerable impact on daily activities. Etiology De Quervain’s disease is a chronic tenosynovitis of the first dorsal compartment of the wrist, caused by a thickening of the retinaculum. This impairs the normal sliding of the extensor pollicis brevis and abductor pollicis longus tendons. Retinaculum thickening reflects degenerative changes, such as myxoid degeneration, fibrocartilaginous metaplasia, and mucopolysaccharide deposition. This condition should be not confused with acute tenosynovitis, in which inflammation and synovial effusion within the tendon sheath are seen. Clinical Presentation Typical symptoms include pain or tenderness over the radial styloid, sometimes radiating to the thumb, forearm, or shoulder. On physical examination, swelling over the radial styloid with tenderness and crepitations on palpation may be noted. There may also be associated functional limitations. Finkelstein’s test (deviating the wrist to the ulnar side while grasping the thumb, resulting in pain) is typically positive. Ultrasound Diagnosis Retinaculum thickening in the extensor compartment can be seen on US. Power Doppler can be used to detect hypervascularity. A dynamic US evaluation may demonstrate the impaired mobility of the tendons within the compartment. In some cases, an accessory tendon or a fibrous hyperechoic septum separating the two tendons is seen. The detection of these findings is important as they imply an improvement or worsening of the disease. Treatment Options Giovanni Serafini ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy Therapy initially consists of resting the thumb and wrist with or without splinting and ice application. An intracompartmental injection can provide the complete relief of symptoms. In some L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_16 © Springer-Verlag Italia 2012 93 94 cases, however, surgery is needed to release the retinaculum or to remove the accessory tendon or the fibrous septum. Interventional Procedure Indications If the condition is symptomatic and limits daily life activities, then US-guided percutaneous treatment is indicated. There are no specific contraindications to this procedure. Objective Early or subacute De Quervain’s disease responds well to corticosteroid injection, with the G. Serafini anti-inflammatory effects possibly resulting in relief from both pain and swelling. Advanced disease stages, characterized by a severe stenosis of the compartment due to retinaculum thickening, may benefit from a first injection of steroid, followed by 1–2 weeks of delayed hyaluronic acid injection. This second step has the advantage of both improving tendon sliding and stretching the thickened retinaculum. Equipment - 25G or smaller needle 1 syringe (1–2 ml) Long-acting steroid (1 ml, 40 mg/ml) Low-molecular-weight hyaluronic acid (2 ml, optional) Plaster. 16 Treament of De Quervain’s Disease and Other Forms of Tenosynovitis Our Procedure Fig. 16.1a Fig. 16.1b Fig. 16.1c Lateral Approach The wrist must be placed in an intermediate position between pronation and supination (Fig. 16.1a). The probe is then positioned on the lateral side of the radial styloid to assess the first compartment along its short axis (Fig. 16.1b). APL abductor pollicis longus, EPB extensor pollicis brevis. We prefer to use a lateral approach to treat De Quervain’s disease (Fig. 16.1c). The needle (arrowheads) is inserted within the thickened retinaculum (arrows) and the drug (asterisks) is injected. The abductor pollicis longus (APL), extensor pollicis brevis (EPB), and extensor carpi radialis longus (ECRL, second compartment) can be seen. 95 96 G. Serafini Fig. 16.2a Fig. 16.2b Longitudinal Approach Note that a long-axis approach is also possible (Fig. 16.2a). In Fig. 16.2b, the needle (arrowheads) is inserted within the thickened retinaculum (arrows). The abductor pollicis longus (APL) is seen overlying the radius (R). Post-procedural Care The patient is kept under observation for at least 10 min. Pain may occur after treatment and is managed with oral NSAIDs. Patients are advised to reduce their manual activity, although no systematic rest period is suggested. Other Forms of Tenosynovitis of the Dorsal Compartments Not just the first compartment but also other extensor compartments can be affected by acute or chronic tenosynovitis, which can similarly cause pain and functional limitations. Acute tenosynovitis is characterized by a fluid effusion within the compartment or the tendon sheath, while in chronic tenosynovitis there is synovial thickening or proliferation. The sixth extensor compart- ment differs from the other five in that sheath effusion frequently occurs in conjunction with joint effusion, due to the physiological communication between the two structures. In this case, sheath effusion should not be treated. Also in these cases, steroid injection is a valid option, as it is able to reduce pain and effusion. Sometimes, hyaluronic acid is injected to improve tendon sliding and to stretch a retinaculum stenosis. The injection technique is similar to that described for De Quervain’s disease. Articular Ganglia Drainage 17 Leonardo Callegari Essentials Epidemiology Ganglion cysts are the most common benign soft-tissue lesions of the wrist. They occur three times more often in women than in men, are predominantly seen in young adults, and are rare in children. In 60–70% of affected individuals, the ganglion cyst is localized in the dorsal aspect of the wrist and communicates with the synovial joint via a pedicle that usually originates at the scapholunate ligament but also may arise from a number of other sites over the dorsal aspect of the wrist capsule. In 13–20% of the cases, ganglia are found on the volar side of the wrist. Etiology Ganglia are articular cysts that originate from the articular cavity. The exact mechanism of ganglion formation remains unknown. Clinical Presentation On examination, wrist ganglia are usually 1- to 2-cm lumps, but they are rarely accompanied by Leonardo Callegari ( ) Radiology Unit B Ospedale di Circolo, Fondazione Macchi Varese, Italy signs of inflammation. On palpation, they are a firm swelling well tethered in place by an attachment to the underlying joint capsule or tendon sheath. While ganglia are frequently asymptomatic, symptoms may include general wrist pain, especially during activities, functional limitation, or a decrease in grip strength. In some cases, ganglia may cause pain by compressing small branches of the peripheral nerves. Ultrasound Diagnosis Wrist ganglia have a typical cystic pattern on US, i.e., roundish or oval hypo/anechoic findings and well delimited by a thin and regular wall. When the cyst content is not exactly hypo/anechoic, the presence of a well-defined pedicle may help to differentiate a ganglia from other pathological conditions. Treatment Options Ganglion cyst can be treated conservatively, by percutaneous drainage, or surgically. Bandaging is the most common conservative treatment and is aimed at limiting wrist mobility. Percutaneous drainage is the second treatment option but about 50% of these treated ganglion cysts will relapse. However, as this procedure is relatively non-invasive, it can be repeated several times. In case of recurrent cysts, surgery, performed using an L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_17 © Springer-Verlag Italia 2012 97 98 L. Callegari arthroscopic or open-air approach, is the last option. It is associated with a 35% recurrence rate, especially in patients with a longer history and a larger ganglion cyst. Objective Interventional Procedure Equipment Indications - Articular ganglia can be treated to reduce pain or other symptoms. Asymptomatic ganglia can be drained also for aesthetic reasons. Ganglia drainage is aimed at reducing lesion volume. Steroid injection after drainage may help to keep the ganglia wall collapsed. 18G needle 1 syringe (10 ml) Lidocaine (2–4 ml) Long-acting steroid (1 ml, 40 mg/ml). Our Procedure Fig. 17.1a Fig. 17.1b STEP 1 The wrist should be positioned according to the ganglion’s location (Fig. 17.1a). Ganglia more commonly occur on the dorsal side of the wrist. The probe is usually positioned along the major axis of the ganglion. As seen in Fig. 17.1b, the ganglion (G) should be assessed also with respect to the other structures of the wrist. Particular attention should be paid to avoid injury of the radial artery (A) that frequently surrounds the ganglion. 17 Articular Ganglia Drainage Fig. 17.2a Fig. 17.2b STEP 2 Using an in-plane lateral approach (see Fig. 17.1a), a small amount of anesthesia is injected into the subcutaneous tissues around the ganglion (G). Then, a large-bore needle (arrowheads) is advanced within the ganglion (Fig. 17.2a,b), with care taken to avoid surrounding structures, such as the radial artery (A). R radius, S scaphoid. Fig. 17.3 STEP 3 The ganglion’s content is completely drained using a syringe (Fig. 17.3). Continuous US monitoring of the needle (arrowheads) is mandatory. This procedure is usually quite slow, as the material contained in the ganglion is often very dense. In these cases, a larger shielded cannula and the application of manual compression over the ganglion may be helpful. A biopsy handle may also be used to obtain a more effective vacuum. 99 100 L. Callegari Fig. 17.4 STEP 4 At the end of the procedure, a small amount of steroid (asterisks) is injected into the ganglion cavity (Fig. 17.4). Post-procedural Care A compressive bandage is applied to the involved site for 5-10 days in order to keep the ganglion wall collapsed and to minimize the probability of recurrence. Trapeziometacarpal Joint Injection 18 Francesca Lacelli Essentials Epidemiology Trapeziometacarpal osteoarthritis occurs most often in women over the age of 40. In approximately 80% of cases, it is associated with osteoarthritis between the trapezium and the base of the second metacarpal, and in 40% of cases with osteoarthritis between the trapezium and the scaphoid. Etiology The trapeziometacarpal joint may be involved by different kinds of arthritis. The most common is osteoarthritis, also known as rhizarthrosis, and it is a result of natural joint aging. As the degenerative process continues, the cartilage becomes increasingly thinner, and eventually disappears. At later stages, the articular space may be lost and osteophytes are frequently seen. There may also be progressive subluxation of the base of the first metacarpal bone. Clinical Presentation The typical symptom is pain that occurs either after prolonged activities or as a result of simple anteposition and opposition movements of the thumb. Pain is mostly reported over the volar side of the thumb base. Ultrasound Diagnosis The trapeziometacarpal joint is easily evaluated by placing the probe on the volar side of the carpus and detecting the joint along its long axis. US signs of rhizarthrosis are joint effusion, a reduction of the articular space, erosive phenomena, and osteophytes. Treatment Options Conservative treatment of trapeziometacarpal arthritis includes physiotherapy, orthopedic splinting, and drug injection. The aim is to control symptoms and to delay or avoid surgery. In case of severe arthritis or persisting symptoms despite conservative therapy, surgery is an option. Francesca Lacelli ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_18 © Springer-Verlag Italia 2012 101 102 Interventional Procedure Indications US-guided percutaneous treatment is indicated if the patient complains of pain and functional limitation. This form of therapy has been shown to delay surgery and in some cases to allow the patient to completely avoid it. Objective Steroid injection is useful in reducing both the inflammatory component of osteoarthritis and pain. Hyaluronic acid is injected 10–15 days later and improves joint mobility. The injection should be F. Lacelli repeated weekly, three times. This cycle can be repeated in case of pain recurrence. Early stages of the disease respond well to this form of treatment. In patients with later-stage disease, the outcome is worse and there is earlier symptom recurrence. Equipment - 25G or smaller needle 1 syringe (1–2 ml) Local anesthetic (0.5 ml) Long-lasting steroid (0.5 ml, 40 mg/ml) Low-molecular-weight hyaluronic acid (0.5– 1 ml) Plaster. Our Procedure Fig. 18.1a Co-axial Approach STEP 1 The wrist must be positioned in an intermediate position between pronation and supination. The probe is placed on the lateral side of the wrist along its long axis, visualizing the trapeziometacarpal joint along its long axis. The needle is inserted with a co-axial out-of-plane approach (Fig. 18.1a). 18 Trapeziometacarpal Joint Injection 103 Fig. 18.1b Fig. 18.1c STEP 2 The articular space (arrow) can be seen between the trapezium (T) and the metacarpal base (M). As shown in Fig. 18.1b,c, the needle is inserted in the joint space, where it is seen as a small hyperechoic dot (arrow). Steroid (asterisk) is then injected into the joint, distending the capsule (arrowheads). After 10–15 days, hyaluronic acid is injected according to the same technique. 104 F. Lacelli Fig. 18.2a Fig. 18.2b Fig. 18.2c Longitudinal Approach The procedure can also be performed using a lateral approach (Fig. 18.2a). The needle (arrowheads) is inserted in the joint space (Fig. 18.2b,c) and drug (asterisk) is then injected in the joint, distending the capsule (arrows). Delayed hyaluronic acid injection is performed as above. M metacarpal base, T trapezium. Post-procedural Care After treatment, patients should avoid heavy activities for 5–10 days. Pain may occur after treatment and is managed with oral NSAIDs. Radiocarpal Joint Injections 19 Luca Maria Sconfienza Similar to the other joints discussed thus far, intra-articular injections of the wrist can be performed to address a variety of pathological conditions. The drug of choice will depend on the condition and the treatment goals. The technique can also be used in the injection of intra-articular contrast agent for arthrography. Equipment - 21G–23G needle 1 syringe (3–5 ml) Local anesthetic (5 ml) and/or Long-lasting steroid (1 ml, 40 mg/ml) and/or Medium-molecular-weight hyaluronic acid (2 ml) Plaster. Indications Intra-articular injection of steroids: rheumatoid arthritis, crystal arthropathies, degenerative osteoarthritis with articular effusion. Intra-articular injection of hyaluronic acid: degenerative osteoarthritis without articular effusion. Intra-articular injection of local anesthetic: assessment of intra-articular relevance of pain, traumatic fractures of the radial head, short-term analgesia. Luca Maria Sconfienza ( ) Radiology Unit IRCCS Policlinico San Donato San Donato Milanese (MI), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_19 © Springer-Verlag Italia 2012 105 106 L.M. Sconfienza Our Procedure Fig. 19.1a STEP 1 The hand is positioned on the table with the palm facing down (Fig. 19.1a). The probe is placed over the relevant joint to be injected. To inject the radiocarpal joint, the probe is positioned on the dorsal side of the wrist along its long axis (see Fig. 15.2a); this also allows visualization of the distal radial epiphysis and the first carpal row (see Fig. 15.2b). 19 Radiocarpal Joint Injections 107 Fig. 19.1b Fig. 19.1c STEP 2 The needle is inserted into the joint using an out-of-plane co-axial approach (Fig. 19.1b). Fig. 19.1c shows the injection of steroid in a patient with rheumatoid arthritis accompanied by synovial proliferation. The needle (arrows) can be seen as a small hyperechoic dot within the synovial proliferation (asterisks). The latter arises between the carpal bones (CB). The extensor tendons (ET), radius (R), and metacarpal bone (M) are also seen. Post-procedural Care Patients should avoid heavy activities for 5–10 days. Pain may occur after treatment and is managed with oral NSAIDs. Part IV The Hand The Hand: Focused US Anatomy and Examination Technique 20 Francesca Lacelli and Chiara Martini Flexor Digitorum Tendons Anatomy There are nine flexor tendons for each hand, a flexor digitorum superficialis and a flexor digitorum profundus for each finger, from the second to the fifth. The thumb is provided with a single flexor tendon only. The flexor digitorum profundus tendon originates from the anterior and medial aspects of the ulna, while the flexor digitorum superficialis tendon has two heads: humero-ulnar and radial. Both muscles originate from long tendons that proximally enter the carpal tunnel and then insert on the fingers. Deep tendons run straight up to the bases of the distal phalanges, where they insert. Superficial tendons run up to the middle of the proximal phalanges, where they split into two branches that surround the deep tendons and insert on the head of the middle phalanges. The superficial and deep tendons have common tendon sheaths. Flexor tendons are kept in place by several fibrous bands referred to as pulleys. These structures are very thin and are occasionally seen US as thin hypoechoic bundles that overhang the tendons. Scanning Technique With the patient’s hand placed on the table with the palmar side facing up, the probe is placed at the carpal tunnel level and then is moved distally to follow the tendons until their insertions. Axial scans allow the changing relationship between superficial and deep flexor tendons to be assessed; longitudinal scans are useful for passive dynamic evaluation, e.g., in patients with tendon impingement under the pulleys. Metacarpophalangeal and Interphalangeal Joints Scanning Technique With the patient’s palm facing up, the probe is placed along the longitudinal axis over the pertinent joint. Each joint is renforced by a capsule and a palmar plate, which together form a capsuloligamentous complex that is located on the ventral side. A small amount of intra-articular fluid can be seen under normal conditions. Francesca Lacelli ( ) Diagnostic Imaging Department Ospedale S. Corona Pietra Ligure (SV), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_20 © Springer-Verlag Italia 2012 111 112 F. Lacelli and C. Martini a b Fig. 20.1 a The probe position and b a long-axis scan of the flexor tendons. The flexor digitorum superficialis (FDS) and flexor digitorum profundus (FDP) can be seen. The A1 reflection pulley is indicated (arrowheads). MH metacarpal head, PP proximal phalanx Fig. 20.2 Long-axis lateral scan of the second metacarpophalangeal joint. The joint space (arrow) is located between the metacarpal head (MH) and the proximal phalanx (PP) and surrounded by the joint capsule (arrowheads) Treatment of Trigger Finger 21 Leonardo Callegari Essentials Etiology Trigger finger is a stenosing tenosynovitis that originates from a thickening of the first annular (A1) pulley of the flexor tendons. In order of frequency, the thumb, annular, middle, little, and index fingers are affected. Most cases of trigger finger are idiopathic. In some patients, high pressures on the A1 pulley during maximum flexion may cause changes in the pulley itself, with hypertrophy and fibrocartilaginous metaplasia. It is thought that chronic, repetitive friction causes a nodule in the tendon as the fibers lose their normal arrangement. Clinical Presentation Symptoms include triggering or catching of the finger during movement, pain on passive extension, and locking. Clinically, finger clicking can be clearly perceived. Sometimes, a palpable nodule may be appreciated over the metacarpophalangeal joint. Ultrasound Diagnosis Hypoechoic thickening of the A1 pulley and nodular thickening of the flexor tendon can be demonstrated using US. Dynamic US scans can confirm the diagnosis of trigger finger when thickening of the pulley or the tendon cannot otherwise be detected. Epidemiology Trigger finger is one of the most common pathologies of the upper limb (28 cases per 100,000 per year). It is more frequent in women, with a peak of incidence between the age of 50 and 60. There may be an associated clinical condition (diabetes mellitus, rheumatoid arthritis, hypothyroidism, obesity). In other patients it is due to repetitive activities (work, sport). Alternative Treatments Alternative treatments of trigger finger include: splintage, if the symptoms are mild: simply resting the finger may be enough to relieve the problem; pharmacological therapy with NSAIDs; and surgical release of the A1 pulley by open or percutaneous techniques. Leonardo Callegari ( ) Radiology Unit B Ospedale di Circolo, Fondazione Macchi Varese, Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_21 © Springer-Verlag Italia 2012 113 114 Interventional Procedure Indications The US-guided percutaneous treatment of trigger finger is indicated when the patient complains of pain or functional limitation (presence of discomfort or blockage during movements of the finger, or an inability to actively achieve flexion). Objective The aim of steroid injection is to reduce pain and inflammation. A 10- to 15-day delayed injection L. Callegari of hyaluronic acid into the sheath is performed to improve tendon sliding under the pulley by stretching the A1 pulley fibrosis. Equipment - 25G needle Two syringes (2 ml) Lidocaine (0.5 ml) Long-acting steroid (1 ml, 40 mg/ml) Low-molecular-weight hyaluronic acid (1 ml) Plaster. 21 Treatment of Trigger Finger 115 Our Procedure Fig. 21.1a Fig. 21.1b Fig. 21.1c STEP 1 The patient is seated opposite the examiner with his or her hand placed on the table and the palm facing up (Fig. 21.1a). The probe is placed at the level of the metacarpophalangeal joint, along the major axis of the flexor tendons (Fig. 21.1b,c). Note the thickened pulley (arrows) and the chronic tenosynovitis (arrowheads). FDS flexor digitorum superficialis, FDP flexor digitorum profundus, MH metacarpophalangeal head, PP proximal phalanx. 116 L. Callegari Fig. 21.2a Fig. 21.2b Fig. 21.2c Fig. 21.3 Longitudinal Approach STEP 2 As seen in Fig. 21.2a–c, the needle (arrowheads) is inserted along a longitudinal axis with a distal-proximal approach and the anesthetic is injected within the tendon sheath (arrows indicate the A1 pulley), avoiding the tendons. FDS flexor digitorum superficialis, FDP flexor digitorum profundus. Then, with the needle (arrowhead) kept in place, steroid (asterisks) is injected within the sheath (Fig. 21.3), avoiding the tendons. 21 Treatment of Trigger Finger 117 Fig. 21.4a Fig. 21.4b Fig. 21.4c Lateral Approach STEP 2 A short-axis approach is also possible, as shown in Fig. 21.4a-c. In this case, the probe is oriented on the short axis of the tendons (FT) and the needle (arrowheads) is inserted laterally. Steroid (asterisk) is then injected. 118 L. Callegari Fig. 21.5 STEP 3 After 10–15 days, hyaluronic acid (asterisks) is injected using the same longitudinal or lateral injection technique (Fig. 21.5), avoiding the tendons. FDS flexor digitorum superficialis, FDP flexor digitorum profundus. Arrowheads indicate the needle. Post-procedural Care After hyaluronic acid has been injected into the sheath, passive flexion- extension movements of the treated finger should be performed in order to favor the homogeneous spreading of hyaluronic acid within the sheath. Intra-articular Injections: Metacarpophalangeal and Interphalangeal Joints 22 Luca Maria Sconfienza Essentials Intra-articular injections of drugs are an option also for the metacarpophalangeal and interphalangeal joints. They are administered as described for the others joints of the upper limb. Interventional Procedures Indications Intra-articular injection of steroids: rheumatoid arthritis, degenerative osteoarthritis with articular effusion. Intra-articular injection of hyaluronic acid: degenerative osteoarthritis without articular effusion. Intra-articular injection of local anesthetic: assessment of the intra-articular relevancy of pain, short-term analgesia. Objective The aim of injecting intra-articular steroids and anesthetic is to reduce inflammation and pain, improving joint functionality. The intra-articular injection of hyaluronic acid improves joint lubrication. Equipment - 23–35G or smaller needle 1 syringe (3–5 ml) Local anesthetic (1 ml) Steroid (0.5–1 ml, 40 mg/ml) Low-molecular-weight hyaluronic acid (1 ml) Plaster. Luca Maria Sconfienza ( ) Radiology Unit IRCCS Policlinico San Donato San Donato Milanese (MI), Italy L.M. Sconfienza, G. Serafini, E. Silvestri (eds.), Ultrasound-guided Musculoskeletal Procedures, DOI 10.1007/978-88-470-2741-1_22 © Springer-Verlag Italia 2012 119 120 L.M. Sconfienza Our Procedure Fig. 22.1a STEP 1 The patient is seated in front of the table, opposite the examiner, with his or her hand placed on the table, palm facing down (Fig. 22.1a). The probe is positioned on the dorsal side of the joint for treatment along the longitudinal axis. Fig. 22.1b Fig. 22.1c STEP 2 The needle is inserted out-of-plane in the ulnar or radial (Fig. 22.1b,c) side of the joint. Insertion of the needle is easier on the less degenerated side of the joint. A small amount of anesthetic is injected. In the next step, with the needle kept in place, steroid and then hyaluronic acid are injected within the joint capsule. MH metacarpophalangeal head, PP proximal phalanx. Arrowheads indicate the joint capsule, the arrow the needle tip, and asterisks the drugs. A similar approach can be used for the interphalangeal joints. although caution is needed to avoid injury to the interdigital neurovascular bundle. A palmar approach is also possible. 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