AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic Instructor Serial/Semester Location Start/Finish Time Date LESSON OBJECTIVE Performance: To gain an understanding of Critical Care Hematologic disorders. Conditions: The student will be presented a powerpoint presentation by the instructor and will have all necessary references made available to him/her. Standard: 1. Given the five elements of the nursing care process and a scenario of a critical care patient with a hematological disorder, determine approaches for patient care by correctly responding to written, oral, and experiential assessment measures TEACHING POINTS 1. Describe the functions of the hematologic system 6. 2. 3. 7. 8 4. 5. Describe the composition of blood Describe the physiologic effect of neutropenia on the critically ill patient Discuss splenomegaly Differentiate the etiology/pathophysiology, assessment, diagnosis, medical managment and nursing interventions for Idiopathic Thrombocytopenic Purpura and Trombotic Thrombocytopenic Purpura Identify the etiology/pathophysiology, assessment, diagnosis, medical management and nursing interventions for Disseminated Intravascular Coagulation 9. 10. INSTRUCTIONAL STRATEGY Interactive Lecture Method: Instructor Media: Classroom Environment: OTHER LESSON SPECIFICATIONS Knowledge Lesson Type of Lesson: 1/50 Ratio: Resources: . End of Lesson Test: None Instructional Time: 204 Reference(s): Click here to enter reference(s). Minutes LESSON PLAN APPROVAL Signature of Standards Officer Date AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic INTRODUCTION Allocated Time: Review: 5 Minutes You have had previous anatomy and physiology lectures in your combat medic training, this lecture will build upon prior instruction. Objective: To discuss/describe topics related to the nursing process. Importance: Nurses work in various health care settings so it is important to gain an understanding of this subject as it will apply to your clinical practice. Fit: Hematology, also spelled haematology (from the Greek αἷμα haima "blood" and -λoγία), is the branch of biology physiology, internal medicine, pathology, clinical laboratory work, and pediatrics that is concerned with the study of blood, the blood-forming organs, and blood diseases. Hematology includes the study of etiology, diagnosis, treatment, prognosis, and prevention of blood diseases. The laboratory work that goes into the study of blood is frequently performed by a medical technologist. Hematologists physicians also very frequently do further study in oncology - the medical treatment of cancer. Blood diseases affect the production of blood and its components, such as blood cells, hemoglobin, blood proteins, the mechanism of coagulation, etc. Approach: You will be presented the subject in lecture format and will be tested using a written exam at a later date. Control Statement: If you have any questions during the lesson please feel free to ask. BODY 1. Teaching Point: Describe the functions of the hematologic system Minutes Allocated Time: Introduction: Learner Participation: Knowledge Lesson Please follow along with your hand outs and take notes. Skill Lesson Powerpoint presentation with associated handouts. Learning Support: 1. Functions of the Hematological System a. Respiration i. RBCs transport oxygen to the tissue ii. RBCs transport carbon dioxide to the lungs b. Nutrition i. return proteins and fats from the GI tract ii. transport vitamins and minerals iii. conveyance of necessary electrolytes c. Excretion i. waste produces (such as BUN, creatinine) ii. carry cellular debris to necessary organs to be excreted (i.e., the kidney) 1 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic d. Defense i. blood is route for first line cellular defense against infection ii. conveys clotting mechanisms to inhibit bleeding iii. mode of arrival for healing processes Knowledge Lesson: Question: Answer: Check on Learning In a knowledge lesson, pose questions to the class. Click here to enter the question. Click here to enter the answer. Skill Lesson: In a skill lesson, provide practice and watch students perform a skill. 2. Teaching Point: Describe the composition of blood Minutes Allocated Time: Introduction: Learner Participation: Knowledge Lesson Please follow along with your hand outs and take notes. Skill Lesson Powerpoint presentation with associated handouts. Learning Support: 2. Composition of Blood a. Cellular Components i. Red Blood Cells (RBCs): 5 million cells/mm3 ii. White Blood Cells (WBCs): 5000-10,000 cells/m3 1. Granulocytes 2. Neutrophils: 50-70% 3. Eosinophils: 1-5% 4. Basophils: 0.05-1% 5. Monocytes (+ macrophages): 1-8% 6. Lymphocytes: 20-40% 7. B lymphocytes 8. T lymphocytes iii. Platelets (thrombocytes) 1. 150,000-400,000 cells/mm3 iv. Plasma 1. 55% of blood 2. Water (92%) 3. Protein (7%) 4. Albumin and other plasma proteins v. Immunoglobulins (alpha, beta and gamma) 1. Clotting Factors vi. Other 1. Respiratory gases 2 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic 2. Metabolites 3. Enzymes 4. Hormones Knowledge Lesson: Question: Answer: Check on Learning In a knowledge lesson, pose questions to the class. Click here to enter the question. Click here to enter the answer. Skill Lesson: In a skill lesson, provide practice and watch students perform a skill. 3. Teaching Point: Describe the physiologic effect of neutropenia on the critically ill patient Minutes Allocated Time: Introduction: Learner Participation: Knowledge Lesson Please follow along with your hand outs and take notes. Skill Lesson Powerpoint presentation with associated handouts. Learning Support: 3. Neutropenia a. Absolute Neutrophil Count (ANC) of <1000 cells/ml i. Significant Risk of Infection when ANC < 500 cells/ml occurs as a result of decreased production or excess destruction of neutrophils b. Etiologies i. extremes in age ii. malnutrition iii. irradiation/chemical (benzene) iv. drugs 1. ETOH, chemotherapy, antibiotics, etc. v. stress vi. surgery c. Immune Impairment & Increased Infections i. renal failure, AIDS, anemia, DM, leukemia d. Infections i. typhoid, hepatitis, measles, influenza, malaria, VRE, disseminated TB, etc. Knowledge Lesson: Question: Answer: Check on Learning In a knowledge lesson, pose questions to the class. Click here to enter the question. Click here to enter the answer. Skill Lesson: In a skill lesson, provide practice and watch students perform a skill. 3 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic 4. Teaching Point: Discuss splenomegaly Minutes Allocated Time: Introduction: Learner Participation: Knowledge Lesson Please follow along with your hand outs and take notes. Skill Lesson Powerpoint presentation with associated handouts. Learning Support: 4. Splenomegaly a. Fever; flushed, warm skin b. Tachycardia c. Chills d. Cough e. Change in sputum color f. Ulcerative mouth lesions g. Sore throat; dysphagia h. Difficulty/burning on urination i. Fatigue; malaise; joint pain j. Patient Management k. Identify Risk Factors l. Enhance Generation of Cells i. granulocytes, macrophages, or both m. Therapies to Stimulate Immune System i. bone marrow growth factors (Neupogen) ii. also known as colony-stimulating factors n. Decrease Risk for Infection i. decrease exposure to exogenous organisms ii. decrease number of normal endogenous organisms iii. avoid indwelling catheters iv. meticulous care of all lines v. frequent oral and skin care vi. consistent use of standard precautions o. Early Detection of Infections p. Appropriate Use of Antibiotics i. prophylactics may be ordered for prevention q. Adequate Nutrition i. high protein, high caloric diet essential ii. enteral feeding may be warranted r. Patient Participation in Care i. establish patient readiness/ability to learn s. Assist Patient with Verbalization of Fears i. anxiety-producing information at patient comfort level t. Encourage Patient to Participate in ADLs 4 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic u. Nursing Diagnosis i. risk for infection related to neutropenia ii. Signs/Symptoms 1. Fever; flushed, warm skin 2. Tachycardia 3. Chills 4. Cough 5. Change in sputum color 6. Ulcerative mouth lesions 7. Sore throat; dysphagia 8. Difficulty/burning on urination 9. Fatigue; malaise; joint pain Knowledge Lesson: Question: Answer: Check on Learning In a knowledge lesson, pose questions to the class. Click here to enter the question. Click here to enter the answer. Skill Lesson: In a skill lesson, provide practice and watch students perform a skill. 5. Teaching Point: Differentiate the etiology/pathophysiology, assessment, diagnosis, medical managment and nursing interventions for Idiopathic Thrombocytopenic Purpura and Trombotic Thrombocytopenic Purpura Minutes Allocated Time: Introduction: Learner Participation: Knowledge Lesson Please follow along with your hand outs and take notes. Skill Lesson Powerpoint presentation with associated handouts. Learning Support: 5. Thrombocytopenia a. Causes i. Bone Marrow Suppression Decreased Platelet Production ii. Aplastic anemia iii. Burns iv. Chemotherapy v. Radiation b. Interference with Platelet Production i. Alcohol ii. Histamine-2 blockers iii. Hormones iv. Thiazide diuretics c. Platelet Destruction artificial heart valves cardiopulmonary bypass machine i. heparin 5 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic ii. infection iii. sulfonamides iv. Septra/Bactrim v. transfusions d. Immune Response Against Platelets i. Idiopathic Thrombocytopenic Purpura ii. Thrombotic Thrombocytopenic Purpura iii. Mononucleosis iv. Vaccinations e. Interference with Platelet Function i. catecholamines 1. DM 2. SLE (systemic lupus erythematosus) 3. Thyrotoxicosis (Grave’s disease) 4. uremia 5. medications a. Aminoglycosides, NSAIDS, Dextran, Diazepam, Digitoxin, Loop diuretics, Phenytoin, Salicylates, Tricyclic antidepressants, Vitamin E 6. ITP a. Thrombocytopenia without evidence of toxic exposure i. absence of disease associated with decreased platelets b. Immunological Mechanism Involving IgG Antiplatelet Antibodies i. platelets removed by spleen from circulation ii. acute and chronic from have been identified iii. exhibit normal production with decreased platelet survival without splenomegaly c. Acute i. most common cause of thrombocytopenia without anemia or neutropenia ii. 95% of Patients are Children between 2 and 6 years of age iii. history of recent viral illness iv. 85% Complete Recovery Rate with Rare Recurrence d. Chronic i. adults 20-40 years of age (usually) e. Gradual Onset i. many remissions and exacerbations f. Exacerbations i. often correlate with cyclic metabolic changes g. Forerunner of Other Autoimmune Dis. i. SLE, lymphoma, autoimmune hemolytic anemia ii. 25-30% of Chronic ITP Patients have SLE h. Other as a complication of many systemic disorders i. Signs and Symptoms are Indistinguishable j. Diseases Include 6 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic i. Lymphoma ii. SLE iii. Infectious mononucleosis iv. Thyrotoxicosis v. Severe infection k. Clinical Manifestations i. petechiae, purpura and ecchymosis ii. oozing from mucous membranes iii. Platelet Count <150,000/ul iv. Spontaneous Hemorrhage <20,000/ul v. Fatal Hemorrhage Risk if <10,000/ul l. Medical Management i. Platelet Transfusions ii. Attempt to Maintain Single Donor 1. decrease exposure to multiple antigens 2. fever/allergic reactions- multiple transfusions iii. Corticosteroids iv. IV IgG v. Plasmapheresis vi. Splenectomy vii. Monitor CBC- report values <50,000/ul viii. Monitor for Bleeding 1. esp. mucous membranes ix. Recognize/Limit Interventions 1. that can deplete or shorten life of platelets 2. medications, fever, high metabolic activity 7. Thrombotic Thrombocytopenic Purpura a. More Common in Females b. Middle to Late Adulthood i. peak incidence in the 40s c. Rarely Seen in Infants and the Elderly d. Clinical Manifestations i. Thrombocytopenia ii. Low Red Blood Cell Count iii. Neurological Abnormalities iv. Petechiae, Purpura and Ecchymosis v. Oozing from Mucous Membranes vi. Fever, Weakness, Fatigue vii. Pallor, Shortness of Breath viii. LOC, Headache, Confusion, Speech Changes e. Medical Management i. Medical Management ii. Plasmapheresis with Plasma Exchange 7 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic iii. Nursing Interventions 1. same as with ITP 2. monitor end organ function closely 3. i.e. uop, ABG, neuro status iv. Report changes in end organ function Knowledge Lesson: Question: Answer: Check on Learning In a knowledge lesson, pose questions to the class. Click here to enter the question. Click here to enter the answer. Skill Lesson: In a skill lesson, provide practice and watch students perform a skill. 6. Teaching Point: Identify the etiology/pathophysiology, assessment, diagnosis, medical management and nursing interventions for Disseminated Intravascular Coagulation Minutes Allocated Time: Introduction: Learner Participation: Knowledge Lesson Please follow along with your hand outs and take notes. Skill Lesson Powerpoint presentation with associated handouts. Learning Support: 8. DIC a. Etiology/Pathophysiology i. Serious Disorder of Hemostasis 1. microsvascular coagulation 2. depletion of clotting factors and hemorrhage ii. Mortality Rate of 80 - 90% iii. Acute, Chronic and Subacute Forms iv. Acute DIC 1. develops rapidly 2. most serious form of acquired coagulopathy v. Chronic DIC 1. most often caused by malignancy 2. also from renal, liver or metabolic disease vi. Subacute DIC 1. no clinical signs or symptoms 2. laboratory abnormalities b. Normal Hemostasis i. Vessel Spasm 1. contraction of blood vessel immediately after damage to control the loss of blood 2. effect lasts for about 30 minutes ii. Platelet Plug 8 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic 1. platelets activated (become sticky), clump together, adhere to damaged blood vessel 2. controls blood loss if vessel break is small c. Clotting cascade i. Damaged Blood Vessels/Tissues 1. elease substances that activate clotting cascade ii. Intrinsic and Extrinsic Pathways 1. both end in final common pathway iii. Prothrombin is Converted to Thrombin iv. Thrombin Degrades Fibrinogen into Fibrin v. Fibrin Threads are Relatively Insoluble 1. maintain the stability of a clot vi. Fibrin Enmeshes with the Platelet Plug vii. Serum is Released, Clot is Stable viii. Fibrinolysis 1. breakdown of clot ix. Tissue Plasminogen Activator (t-PA) 1. present in lining of all blood vessels 2. released after clot formation 3. converts plasminogen into plasmin x. Plasmin Dissolves Fibrin/Clot 1. perfusion through blood vessel reestablished xi. Normal Clotting Cascade Overstimulated 1. massive tissue destruction 2. damage to endothelial cells xii. Thrombin Produced xiii. Fibrin Produced xiv. Clotting Factors Consumed xv. Fibrin Strands in Microvasculature xvi. Clotting in Microvasculature 1. causes organ ischemia and necrosis 2. skin, lungs, kidneys especially damaged 3. thrombophlebitis, PE, CVA, GI bleeding, renal failure thrombosis xvii. RBCs Damaged 1. schistocytes a. lost ability to carry oxygen xviii. Clotting Cascade Stimulated Fibrinolysis Stimulated 1. degrade clot once stable-reestablish perfusion xix. Fibrinolysis 1. breakdown of fibrin 2. release of fibrin degradation products xx. Fibrin Degradation Products 1. potent anticoagulants that interfere with thrombin, fibrin and platelet activity 9 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic xxi. Consumption of Clotting Factors 1. at sites where a clot is not needed 2. leads to body depletion 3. results in an inability to form clots as needed xxii. Assessment/Clinical Manifestations xxiii. Recognition of Risk Factors xxiv. Microvascular Thrombosis Develops 1. organ ischemia and necrosis 2. mental status changes xxv. Angina xxvi. Hypoxemia xxvii. Decreased Urine Output xxviii. Nonspecific Hepatitis xxix. Depletion of Clotting Factors & Clot Lysis 1. excessive bleeding 2. occult blood 3. gingival bleeding, petechiae, ecchymoses xxx. Overt Bleeding from Three Unrelated Sites 1. must consider bleeding in unseen spaces a. i.e. peritoneum and retroperitoneal space xxxi. May Exhibit Signs/Symptoms of Shock xxxii. Increased d-dimer xxxiii. byproducts of fibrin breakdown xxxiv. FSPs/FDPs 1. byproducts of fibrin breakdown 2. non-specific to identify clot lysis xxxv. Increased Coagulation Times xxxvi. Decreased Antithrombin III 1. substance that binds with heparin 2. decreased ATIII increases likelihood of clots d. Medical Management i. Goals ii. Identify/Treat Underlying Cause iii. DIC is a secondary process 1. stop the abnormal coagulation 2. control the bleeding iv. Correct Hypotension, Hypoxemia, acidosis v. Intubate & Mechanically Ventilate prn vi. Volume Replacement - NS or LR vii. Blood Volume Expanders, as ordered viii. Blood Products 1. replace platelet deficiency & clotting factors 2. treat hemorrhage 10 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic ix. Platelets for Consumptive Thrombocytopenia x. FFP 1. clotting factor replacement xi. Cryoprecipitate 1. fibrinogen and Factor VIII replacement xii. RBCs 1. hemorrhage replacement a. to maintain oxygen carrying capacity xiii. Medications 1. Heparin a. potent thrombin inhibitor b. prevents thrombus formation c. blocks process that initiates DIC d. may increase the risk of bleeding i. use in controversial e. administered in low-dose, i.e. 500u/hr 2. Vitamin K i. critical to the production of clotting factors ii. may be administered SQ or IV 3. Antithrombin III a. inhibits thrombin b. enhances action of heparin c. ATIII Deficit No Response to Heparin d. due to above relationship e. may shorten course of DIC,increase survival f. must infuse slowly due to risk for hypotension 4. Aminocaproic Acid a. inhibits fibrinolysis b. interferes with plasmin activity c. given with heparin to prevent lysis of existing clots e. Nursing Interventions i. Goals 1. Recognize/Prevent Thrombotic and Hemorrhagic Events 2. Identify Patients at Risk 3. Continuous Assessment 4. Pain Management 5. Administer Medications as Ordered 6. Monitor Lab Values 7. Control Bleeding a. avoid invasive procedures, as able b. Avoid Dressing Changes c. reinforce- avoid disrupting an unstable clot f. Diagnosis 11 AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic i. History and Physical 1. include identification of risk factors ii. Clinical Presentation 1. abs iii. Thrombocytopenia 1. decreased fibrinogen 2. increased FDP/FSP 3. fibrin degradation products/fibrin split products Knowledge Lesson: Question: Answer: Check on Learning In a knowledge lesson, pose questions to the class. Click here to enter the question. Click here to enter the answer. Skill Lesson: In a skill lesson, provide practice and watch students perform a skill. END OF LESSON TEST Allocated Time: Instructions: Test Questions or Performance Expected: Test Key: 0 Minutes You will be tested on this subject at a later date. You will be expected to review and study the material taught in this session in order to pass the associated written test. If you have difficulty with the material please see me so we can review together. None. CONCLUSION Allocated Time: Summary: 5 Minutes Review and re-emphasize the difficult Teaching Points below. 1. 2. 3. 4. 5. 6. 7. 8 9. 10. 12 Describe the functions of the hematologic system Describe the composition of blood Describe the physiologic effect of neutropenia on the critically ill patient Discuss splenomegaly Differentiate the etiology/pathophysiology, assessment, diagnosis, medical managment and nursing interventions for Idiopathic Thrombocytopenic Purpura and Trombotic Thrombocytopenic Purpura Identify the etiology/pathophysiology, assessment, diagnosis, medical management and nursing interventions for Disseminated Intravascular Coagulation AFAMS Master Lesson Plan (MLP) Nursing Program Critical Care-Hematologic Closing Statement: Nurses work in various health care settings so it is important to gain an understanding of this subject as it will apply to your clinical practice. Re-motivating Statement: Hematology, also spelled haematology (from the Greek αἷμα haima "blood" and -λoγία), is the branch of biology physiology, internal medicine, pathology, clinical laboratory work, and pediatrics that is concerned with the study of blood, the blood-forming organs, and blood diseases. Hematology includes the study of etiology, diagnosis, treatment, prognosis, and prevention of blood diseases. The laboratory work that goes into the study of blood is frequently performed by a medical technologist. Hematologists physicians also very frequently do further study in oncology - the medical treatment of cancer. Blood diseases affect the production of blood and its components, such as blood cells, hemoglobin, blood proteins, the mechanism of coagulation, etc. 13