Exam 33: Coagulation Procedures
Exam 1: Morphology of Human Blood and Marrow Cells: Hematopoiesis28 Questions
Exam 2: Bone Marrow29 Questions
Exam 3: The Red Blood Cell: Structure and Function64 Questions
Exam 4: Anemia: Diagnosis and Clinical Considerations33 Questions
Exam 5: Evaluation of Red Blood Cell Morphology and Introduction to Platelet and White Blood Cell Morphology29 Questions
Exam 6: Iron Metabolism and Hypochromic Anemias31 Questions
Exam 7: Megaloblastic Anemias29 Questions
Exam 8: Aplastic Anemia Including Pure Red Cell Aplasia and Congenital Dyserythropoietic Anemia and Paroxysmal Nocturnal Hemoglobinuria48 Questions
Exam 9: Introduction to Hemolytic Anemias: Intracorpuscular Defects: I Hereditary Defects of the Red Cell Membrane36 Questions
Exam 10: Hemolytic Anemias: Intracorpuscular Defects: II Hereditary Enzyme Deficiencies20 Questions
Exam 11: Hemolytic Anemias: Intracorpuscular Defects: III the Hemoglobinopathies75 Questions
Exam 12: Hemolytic Anemias: Intracorpuscular Defects: Iv Thalassemia30 Questions
Exam 13: Hemolytic Anemias: Extracorpuscular Defects51 Questions
Exam 14: Hypoproliferative Anemia: Anemia Associated With Systemic Diseases32 Questions
Exam 15: Cell Biology, Disorders of Neutrophils, Infectious Mononucleosis, and Reactive Lymphocytosis44 Questions
Exam 16: Introduction to Leukemia and the Acute Leukemias74 Questions
Exam 17: Chronic Myeloproliferative Disorders I: Chronic Myelogenous Leukemia24 Questions
Exam 18: Chronic Myeloproliferative Disorders Ii: Polycythemia Vera, Essential Thrombocythemia, and Idiopathic Myelofibrosis56 Questions
Exam 19: Myelodysplastic Syndromes28 Questions
Exam 20: Chronic Lymphocytic Leukemia and Related Lymphoproliferative Disorders29 Questions
Exam 21: The Lymphomas41 Questions
Exam 22: Multiple Myeloma and Related Plasma Cell Disorders45 Questions
Exam 23: Lipid Lysosomal Storage Diseases and Histiocytosis37 Questions
Exam 24: Introduction to Hemostasis113 Questions
Exam 25: Disorders of Primary Hemostasis: Quantitative and Qualitative Platelet Disorders and Vascular Disorders62 Questions
Exam 26: Disorders of Plasma Clotting Factors48 Questions
Exam 27: Interaction of the Fibrinolytic, Coagulation, and Kinin Systems; Disseminated Intravascular Coagulation; and Related Pathology44 Questions
Exam 28: Introduction to Thrombosis and Anticoagulant Therapy66 Questions
Exam 29: Quality Control in the Hematology Laboratory22 Questions
Exam 30: Body Fluid Examination: the Qualitative, Quantitative, and Morphologic Analysis of Serous, Cerebrospinal, and Synovial Fluids36 Questions
Exam 31: Hematology Methods114 Questions
Exam 32: Principles of Automated Differential Analysis25 Questions
Exam 33: Coagulation Procedures61 Questions
Exam 34: Applications of Flow Cytometry to Hematology and Hemostasis20 Questions
Exam 35: Molecular Diagnostic Techniques in Hematopathology34 Questions
Exam 36: Special Stainscytochemistry38 Questions
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The reptilase test will be abnormally prolonged:
Free
(Multiple Choice)
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Correct Answer:
A
Enzyme-specific synthetic substrates used in coagulation studies are based on the principle of amino acids of the substrate on the protein molecule fitting into the active sites and the binding sites of the __________.
Free
(Multiple Choice)
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Correct Answer:
B
Synthetic chromogenic and fluorogenic assays are available for coagulation studies in the evaluation of:
Free
(Multiple Choice)
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Correct Answer:
E
In the presence of a factor VIII inhibitor, the Bethesda titer should be determined in the management of a patient with __________ when therapy involves Factor VIII concentrates.
(Multiple Choice)
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The __________ is the assay used for the one-stage quantitative method for factors VIII, IX, XI, and XII?
(Multiple Choice)
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In the one-stage quantitative assay for factors II, V, VII, and X the __________ is the test system used, with specific-factor-deficient plasmas added to normalize all other factors but the one being measured.
(Multiple Choice)
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In the fibrinogen activity assay, a prolonged clotting time obtained when testing patient plasma indicates:
(Multiple Choice)
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In the absence of factor XIII, the hydrogen-bonded fibrin polymers are soluble in __________ or 1% monochloroacetic acid.
(Multiple Choice)
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When a factor deficiency is present, there will be a correction of the abnormal APTT by __________ of normal plasma.
(Multiple Choice)
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In the factor XIII screening test, the presence of a formal clot after 24 hours indicates a plasma factor XIII concentration of __________ of normal.
(Multiple Choice)
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What is the anticoagulant used in a sample to be tested for APTT?
(Multiple Choice)
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If fibrin is discovered in a citrated plasma sample, the following test(s) will not be affected and can still be run:
(Multiple Choice)
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In performing a one-stage quantitative assay method for factor II, results are obtained from an activity curve made from dilutions of normal reference plasma and factor __________ plasma.
(Multiple Choice)
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Reptilase hydrolyzes the fibrinopeptide __________ from the intact fibrinogen molecule in contrast to thrombin, which hydrolyzes fibrinopeptide __________ from fibrinogen.
(Multiple Choice)
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Stabilization of the fibrin clot depends on plasma factor __________, which converts hydrogen bonds to covalent bonds by transamination.
(Multiple Choice)
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The PT test is sensitive to the vitamin __________ factors and therefore useful as a means of monitoring oral anticoagulant therapy.
(Multiple Choice)
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A thrombin time test was performed and the resulting clotting time exceeded the reference range. A 1:1 mixing study with normal pooled plasma was done that corrected the result to the normal range. Which abnormality is suspected?
(Multiple Choice)
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