Exam 31: Disorders of Secondary Hemostasis
Exam 1: Introduction34 Questions
Exam 2: Cellular Homeostasis40 Questions
Exam 3: Hematopoiesis35 Questions
Exam 4: Structure and Function of Hematopoietic Organs34 Questions
Exam 5: The Erythrocyte33 Questions
Exam 6: Hemoglobin35 Questions
Exam 7: The Leukocyte37 Questions
Exam 8: Introduction to Anemia35 Questions
Exam 9: Anemias of Disordered Iron Metabolism and Heme Synthesis36 Questions
Exam 10: Hemoglobinopaties: Qualitative Defects33 Questions
Exam 11: Thalassemia32 Questions
Exam 12: Megaloblastic and Nonmegaloblastic Macrocytic Anemias67 Questions
Exam 13: Introduction to Hemolytic Anemia32 Questions
Exam 14: Hemolytic Anemia: Membrane Defects36 Questions
Exam 15: Hemolytic Anemia: Enzyme Deficiencies35 Questions
Exam 16: Hemolytic Anemia: Immune Anemias30 Questions
Exam 17: Hemolytic Anemia: Nonimmune Defects32 Questions
Exam 18: Nonmalignant Granulocyte and Monocyte Disorders23 Questions
Exam 19: Nonmalignant Lymphocyte Disorders32 Questions
Exam 20: Introduction to Hematopoietic Neoplasms34 Questions
Exam 21: Myeloproliferative Disorders41 Questions
Exam 22: Myelodysplastic Syndromes33 Questions
Exam 23: Acute Myeloid Leukemias35 Questions
Exam 24: Acute Lymphoblastic Leukemias35 Questions
Exam 25: Lymphoid Malignancies: Chronic Lymphoid Leukemias, Lymphomas, and Plasma Cell Neoplasms34 Questions
Exam 26: Hematopoietic Stem Cell Transplantation43 Questions
Exam 27: Morphologic Analysis of Body Fluids in the Hematology Laboratory39 Questions
Exam 28: Primary Hemostasis34 Questions
Exam 29: Secondary Hemostasis and Fibrinolysis33 Questions
Exam 30: Disorders of Primary Hemostasis33 Questions
Exam 31: Disorders of Secondary Hemostasis35 Questions
Exam 32: Thrombophilia35 Questions
Exam 33: Hematology Procedures and Hemostasis46 Questions
Exam 34: Bone Marrow Examination34 Questions
Exam 35: Automation in Hematology and Hemostasis39 Questions
Exam 36: Flow Cytometry35 Questions
Exam 37: Chromosome Analysis of Hematopoietic and Lymphoid Disorders35 Questions
Exam 38: Molecular Analysis of Hematologic Diseases15 Questions
Exam 39: Laboratory Testing in Coagulation39 Questions
Exam 40: Quality Assessment in the Hematology Laboratory41 Questions
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Deficiencies of the fibrin-forming proteins often have a delayed bleeding symptom that is due to which of the following?
Free
(Multiple Choice)
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Correct Answer:
D
Use this case to answer the following questions:
A 5-year-old boy visits his primary care physician after an accident on his bike.It was his first accident, and he fell on his knees.His mother noticed severe swelling in his knees and elbows, but thought that it was from the accident.She placed an ice pack on the affected areas and put him to rest.After a few days, the swelling had not improved, so she made an appointment to see his pediatrician.The physician asks him a few questions about the accident and then proceeds to perform a physical examination.The physician notes small hematomas on his elbows and knees and also on his upper torso.He draws blood, and the results are shown below. PT: 12.2 sec (RR: 11.3-12.8 sec)
INR: 1.12
APTT: 72 sec (RR: 23-32 sec)
Platelet aggregation studies: normal aggregation with all agonists
The physician admits him to the area hospital.
-What disorder is the patient most likely suffering from?
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(Multiple Choice)
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Correct Answer:
C
Which of the following laboratory assays would be useful in identifying presence of primary fibrinolysis?
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(Multiple Choice)
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Correct Answer:
B
George Jones is admitted to the hospital with abdominal pain.Upon physical examination, the attending physician notices a yellow ring around George's green eyes.George has a significant swelling in his abdomen, and has been suffering from swollen joints for the last month.The physician runs a battery of labs.The results are below: TEST George Jones Reference Range PT 16.8 11-13 INR 3.85 NA APTT 71 23-32 BT 5 2-6 Fibrinogen 275/ 200-400/ Factor X 22\% >50\% activity Factor II 21\% >50\% activity Factor VII 23\% >50\% activity Factor V 28\% >50\% activity Factor XII 95\% >50\% activity Factor XI 99\% >50\% activity Factor IX 30\% >50\% activity RIPA 95\% >50\% activity AST Elevated Normal ALT Elevated Nomal GGT Elevated Normal TBL Elevated Normal DBI Elevated Nomal Based on this information, from what is George most likely suffering?
(Multiple Choice)
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Explain how liver disease can be differentiated from DIC through laboratory test analysis.
(Essay)
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Which assay would assess for the presence of a circulating nonspecific inhibitor?
(Multiple Choice)
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What plasma factor levels can be expected in a female carrier of F-VIII or F-IX deficiency?
(Multiple Choice)
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What tests typically are utilized in the detection of lupus anticoagulants in the laboratory?
(Essay)
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Use this case to answer the following questions:
A 5-year-old boy visits his primary care physician after an accident on his bike.It was his first accident, and he fell on his knees.His mother noticed severe swelling in his knees and elbows, but thought that it was from the accident.She placed an ice pack on the affected areas and put him to rest.After a few days, the swelling had not improved, so she made an appointment to see his pediatrician.The physician asks him a few questions about the accident and then proceeds to perform a physical examination.The physician notes small hematomas on his elbows and knees and also on his upper torso.He draws blood, and the results are shown below. PT: 12.2 sec (RR: 11.3-12.8 sec)
INR: 1.12
APTT: 72 sec (RR: 23-32 sec)
Platelet aggregation studies: normal aggregation with all agonists
The physician admits him to the area hospital.
-Predict results that will confirm the patient's diagnosis.
(Multiple Choice)
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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 are shown below. 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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Interpret the following results: PT: 11.8 sec (RR: 11.2-13.8 sec)
INR: 1.07
APTT: 57 sec (RR: 23-32 sec)
BT: 12 min
Ristocetin aggregation: decreased aggregation
Based on this information, from what is the patient most likely suffering?
(Multiple Choice)
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A physician has confirmed von Willebrand's disease in his 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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Which of the following is used in the identification of a secondary hemostatic pathway anomaly?
(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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Explain how disseminated intravascular coagulation is not a primary disease state.Correlate etiology, pathophysiology, and laboratory analysis in your response.
(Essay)
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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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A patient has a prolonged PT.What can you infer from this result?
(Multiple Choice)
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Hemophilia A is caused by a deficiency in which of the following proteins?
(Multiple Choice)
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An advantage of prenatal diagnosis by genotypic analysis for hemophilia over phenotypic analysis is:
(Multiple Choice)
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