Deck 17: Defects of Plasma Clotting Factors
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Deck 17: Defects of Plasma Clotting Factors
1
Clotting factors must be present at a minimum of which percentage for hemostasis to be achieved?
A) 20%
B) 30%
C) 50%
D) 75%
A) 20%
B) 30%
C) 50%
D) 75%
B
2
Which result will be within reference range in a patient with dysfibrinogenemia?
A) Thrombin time
B) Activated partial thromboplastin time
C) Immunologic fibrinogen level
D) Protein electrophoresis
A) Thrombin time
B) Activated partial thromboplastin time
C) Immunologic fibrinogen level
D) Protein electrophoresis
C
3
The following laboratory results have been obtained for a 40-year-old woman: PT = 20 seconds (reference range is 11 to 15 seconds), aPTT = 50 seconds (reference range is 22 to 40 seconds), and thrombin time = 18 seconds (reference range is 11 to 15 seconds).What factor deficiency is most likely?
A) Factor VII deficiency
B) Factor VIII deficiency
C) Factor X deficiency
D) Factor XIII deficiency
A) Factor VII deficiency
B) Factor VIII deficiency
C) Factor X deficiency
D) Factor XIII deficiency
C
4
Which of the following is the most useful in differentiating hemophilia A from hemophilia B?
A) A familial pattern of inheritance
B) Patient's history
C) Activated partial thromboplastin time
D) Factor assays
A) A familial pattern of inheritance
B) Patient's history
C) Activated partial thromboplastin time
D) Factor assays
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5
Which of the following assays will be abnormal with hemophilia A?
A) Platelet count
B) Bleeding time
C) PT
D) aPTT
A) Platelet count
B) Bleeding time
C) PT
D) aPTT
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6
A prolonged aPTT is corrected with factor VIIIdeficient plasma but not with factor IXdeficient plasma.What factor is deficient?
A) IX
B) XIII
C) V
D) X
A) IX
B) XIII
C) V
D) X
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7
A man with hemophilia A and an unaffected female can produce a:
A) Female carrier
B) Male carrier
C) Male with hemophilia A
D) Normal female
A) Female carrier
B) Male carrier
C) Male with hemophilia A
D) Normal female
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8
Factor XI deficiency is also known as:
A) Christmas disease
B) Hemophilia A
C) Hemophilia C
D) Fitzgerald factor deficiency
A) Christmas disease
B) Hemophilia A
C) Hemophilia C
D) Fitzgerald factor deficiency
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9
Long-term antibiotic therapy is a cause of bleeding because it disrupts:
A) Vitamin K synthesis
B) Contact activation
C) Platelet aggregation
D) Fibrinolytic activity
A) Vitamin K synthesis
B) Contact activation
C) Platelet aggregation
D) Fibrinolytic activity
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10
Christmas disease is another name for:
A) Hemophilia A
B) Hemophilia B
C) von Willebrand's disease
D) Factor VII deficiency
A) Hemophilia A
B) Hemophilia B
C) von Willebrand's disease
D) Factor VII deficiency
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11
Which platelet response(s) is usually associated with hemophilia A?
A) Defective ADP release; normal response to ADP
B) Decreased amount of ADP in platelets
C) Absent aggregation to epinephrine, ADP, and collagen
D) Normal platelet aggregation
A) Defective ADP release; normal response to ADP
B) Decreased amount of ADP in platelets
C) Absent aggregation to epinephrine, ADP, and collagen
D) Normal platelet aggregation
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12
Treatment of patients with factor II, VII, or X deficiency consists of:
A) Administration of prothrombin complex concentrate
B) Administration of cryoprecipitate
C) Administration of FFP
D) Administration of whole blood
A) Administration of prothrombin complex concentrate
B) Administration of cryoprecipitate
C) Administration of FFP
D) Administration of whole blood
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13
Keloid scar formation is most commonly associated with:
A) Factor VIII deficiency
B) Factor IX deficiency
C) Factor XII deficiency
D) Factor XIII deficiency
A) Factor VIII deficiency
B) Factor IX deficiency
C) Factor XII deficiency
D) Factor XIII deficiency
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14
The only clotting factor not synthesized exclusively by the liver is:
A) Factor V
B) Factor VII
C) Factor VIII
D) Factor IX
A) Factor V
B) Factor VII
C) Factor VIII
D) Factor IX
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15
The treatment of choice for hemophilia A individuals is:
A) Cryoprecipitate
B) Factor VIII concentrate
C) Prothrombin complex
D) DDAVP
A) Cryoprecipitate
B) Factor VIII concentrate
C) Prothrombin complex
D) DDAVP
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16
Hemophilia B is best treated with:
A) A mixture of factors II, VII, IX, and X
B) Factor X concentrate
C) Factor VIII concentrate
D) Vitamin K
A) A mixture of factors II, VII, IX, and X
B) Factor X concentrate
C) Factor VIII concentrate
D) Vitamin K
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17
Factor assays measure the percentage of activity of a given factor by mixing the patient's plasma with:
A) Normal plasma
B) Adsorbed plasma
C) Factor-deficient plasma
D) Factor-specific plasma
A) Normal plasma
B) Adsorbed plasma
C) Factor-deficient plasma
D) Factor-specific plasma
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18
Which of the following is the most prevalent inherited bleeding disorder?
A) von Willebrand disease
B) Hemophilia A
C) Factor VII deficiency
D) Factor XII deficiency
A) von Willebrand disease
B) Hemophilia A
C) Factor VII deficiency
D) Factor XII deficiency
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19
Factor V Leiden is a genetic mutation of:
A) Factor IV
B) Factor V
C) The prothrombin molecule
D) Hemophilia A
A) Factor IV
B) Factor V
C) The prothrombin molecule
D) Hemophilia A
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20
All of the following may lead to deficiencies of clotting factors except:
A) Renal disease
B) Liver disease
C) Autoimmune disease
D) Cardiovascular disease
A) Renal disease
B) Liver disease
C) Autoimmune disease
D) Cardiovascular disease
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