Review Questions Flashcards
What is the most common acquired bleeding disorder?
a. Trauma-induced coagulopathy
b. Vitamin K deficiency
c. Liver disease
d. VWD
a. Trauma-induced coagulopathy
Which is a typical form of anatomic bleeding?
a. Epistaxis
b. Menorrhagia
c. Hematemesis
d. Central nervous system bleed
d. Central nervous system bleed
What factor becomes deficient early in liver disease, and what assay does its deficiency prolong?
a. Prothrombin deficiency, the PT
b. Factor VII deficiency, the PT
c. FVIII deficiency, the PTT
d. Factor IX deficiency, the PTT
b. Factor VII deficiency, the PT
Which of the following conditions causes a prolonged thrombin time?
a. Antithrombin deficiency
b. Prothrombin deficiency
c. Hypofibrinogenemia
d. Warfarin therapy
c. Hypofibrinogenemia
In what type or subtype of VWD is the RIPA test result positive when ristocetin is used at a concentration of less than 0.5 mg/mL?
a. Subtype 2A
b. Subtype 2B
c. Subtype 2N
d. Type 3
b. Subtype 2B
What is the typical treatment for vitamin K deficiency when the patient is bleeding?
a. Vitamin K and plasma
b. Vitamin K and four-factor PCC
c. Vitamin K and platelet concentrate d. Vitamin K and FVIII concentrate
b. Vitamin K and four-factor PCC
- If a patient has anatomic soft tissue bleeding and poor wound healing, but the PT, PTT, TT, platelet count, and platelet functional assay results are normal, what factor deficiency is possible?
a. Fibrinogen
b. Prothrombin
c. Factor XII
d. Factor XIII
d. Factor XIII
What therapy may be used for a hemophilic boy who is bleeding and who has a high FVIII inhibitor titer?
a. rFVIIa
b. Plasma
c. Cryoprecipitate
d. FVIII concentrate
a. rFVIIa
What is the most prevalent form of VWD?
a. Type1
b. Type 2A
c. Type 2B
d.Type3
a. Type1
Which of the following assays is used to distinguish vitamin
K deficiency from liver disease?
a. PT
b. Protein C assay
c. Factor V assay
d. Factor VII assay
c. Factor V assay
Mucocutaneous hemorrhage is typical of:
a. Acquired hemorrhagic disorders
b. Localized hemorrhagic disorders
c. Defects in primary hemostasis
d. Defects in fibrinolysis
c. Defects in primary hemostasis