Exam 34: Disorders of Secondary Hemostasis
Exam 1: Introduction30 Questions
Exam 2: Cellular Homeostasis40 Questions
Exam 3: Structure and Function of Hematopoietic Organs35 Questions
Exam 4: Hematopoiesis35 Questions
Exam 5: The Erythrocyte37 Questions
Exam 6: Hemoglobin40 Questions
Exam 7: Granulocytes and Monocytes30 Questions
Exam 8: Lymphocytes25 Questions
Exam 9: The Platelet16 Questions
Exam 10: The Complete Blood Count and Peripheral Blood Smear Evaluation35 Questions
Exam 11: Introduction to Anemia35 Questions
Exam 12: Anemias of Disordered Iron Metabolism and Heme Synthesis36 Questions
Exam 13: Hemoglobinopathies: Qualitative Defects33 Questions
Exam 14: Thalassemia32 Questions
Exam 15: Megaloblastic and Nonmegaloblastic Macrocytic Anemias34 Questions
Exam 16: Hypoproliferative Anemias32 Questions
Exam 17: Hemolytic Anemia: Membrane Defects36 Questions
Exam 18: Hemolytic Anemia: Enzyme Deficiencies36 Questions
Exam 19: Hemolytic Anemia: Immune Anemias30 Questions
Exam 20: Hemolytic Anemia: Nonimmune Defects30 Questions
Exam 21: Nonmalignant Disorders of Leukocytes: Granulocytes and Monocytes35 Questions
Exam 22: Nonmalignant Lymphocyte Disorders32 Questions
Exam 23: Introduction to Hematopoietic Neoplasms34 Questions
Exam 24: Myeloproliferative Neoplasms44 Questions
Exam 25: Myelodysplastic Syndromes34 Questions
Exam 26: Acute Myeloid Leukemias35 Questions
Exam 27: Precursor Lymphoid Neoplasms34 Questions
Exam 28: Mature Lymphoid Neoplasms39 Questions
Exam 29: Hematopoietic Stem Cell Transplantation41 Questions
Exam 30: Morphologic Analysis of Body Fluids in the Hematology Laboratory39 Questions
Exam 31: Primary Hemostasis35 Questions
Exam 32: Secondary Hemostasis and Fibrinolysis33 Questions
Exam 33: Disorders of Primary Hemostasis35 Questions
Exam 34: Disorders of Secondary Hemostasis34 Questions
Exam 35: Thrombophilia34 Questions
Exam 36: Hemostasis: Laboratory Testing and Instrumentation41 Questions
Exam 37: Hematology Procedures46 Questions
Exam 38: Bone Marrow Examination34 Questions
Exam 39: Automation in Hematology38 Questions
Exam 40: Flow Cytometry34 Questions
Exam 41: Chromosome Analysis of Hematopoietic and Lymphoid Disorders35 Questions
Exam 42: Molecular Analysis of Hematologic Diseases18 Questions
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A 34-year-old woman has just given birth to a healthy baby boy.After the delivery of the baby,the physician proceeds to deliver the placenta.After it has been extracted from the mother's uterus,the resident examines it and notes that it appears incomplete.They try to deliver the remainder but are unsuccessful.A few moments later,the mother loses consciousness,and is bleeding profusely from her uterus.Blood is collected,and the results follow. PT: 17 sec (RR: 11.3-12.8 sec)
INR: 3.02
APTT: 67 sec (RR: 23-32 sec)
D-dimer: 540 ng/mL (RR: <400 ng/mL)
Fibrinogen: 82 mg/dL (RR: 200-400 mg/dL)
Factor V assay: 12%
Based on this information,from what is the patient most likely suffering?
(Multiple Choice)
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How does von Willebrand's disease (VWD)differ from Bernard-Soulier syndrome?
Correlate the pathophysiology of both disorders in your response.Name at least two laboratory tests that differentiate each.
(Essay)
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What laboratory tests typically are utilized to detect lupus anticoagulants?
(Essay)
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Explain how liver disease can be differentiated from DIC through laboratory test analysis.
(Essay)
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Screening tests for the evaluation of VWD include the platelet count,APTT,PT,bleeding time,and/or PFA-100.Which of the following results would be evident in most cases of VWD?
(Multiple Choice)
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Explain the inheritance pattern of the following disorder and how it contributes to the clinical manifestations of each of the following disorders:a.Hemophilia A
(Essay)
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A preterm infant (29 weeks old)has a platelet count of 85 × 10⁹/L.Is this a normal or abnormal finding?
(Multiple Choice)
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A patient might be suffering from a coagulopathy.Which of the following physical manifestations would suggest a primary hemostatic pathway problem?
(Multiple Choice)
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Which of the following laboratory assays would be useful in identifying the presence of primary fibrinolysis?
(Multiple Choice)
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Which congenital deficiency(ies)is(are)suspected with a normal platelet count,an abnormal PT and APTT,and normal PFA-100 and thrombin time?
(Multiple Choice)
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A physician has confirmed von Willebrand's disease in a patient.Further testing is needed to determine which subtype the patient has.Multimer analysis is performed and comes back normal.What is the most probable explanation for this?
(Multiple Choice)
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A patient with a protein C deficiency is at risk for developing which of the following?
(Multiple Choice)
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What type of VWD is the only type to have a decreased platelet count?
(Multiple Choice)
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