Hemorrhagic Disorders and Laboratory Assessment Flashcards
1
Q
- What is the most common acquired bleeding disorder?
a. Vitamin K deficiency
b. Liver disease
c. ACOTS
d. VWD
A
c. ACOTS
2
Q
- Which is a typical form of anatomic bleeding?
a. Epistaxis
b. Menorrhagia
c. Hematemesis
d. Soft tissue bleed
A
d. Soft tissue bleed
3
Q
- What factor deficiency has the speediest effect on the prothrombin time?
a. Prothrombin deficiency
b. Factor VII deficiency
c. Factor VIII deficiency
d. Factor IX deficiency
A
b. Factor VII deficiency
4
Q
- Which of the following conditions causes a prolonged
thrombin time?
a. Antithrombin deficiency
b. Prothrombin deficiency
c. Hypofibrinogenemia
d. Warfarin therapy
A
c. Hypofibrinogenemia
5
Q
- In what 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
A
b. Subtype 2B
6
Q
- What is the typical treatment for vitamin K deficiency when
the patient is bleeding?
a. Vitamin K and PCC
b. Vitamin K and plasma
c. Vitamin K and platelet concentrate
d. Vitamin K and factor VIII concentrate
A
b. Vitamin K and plasma
7
Q
- If a patient has anatomic soft tissue bleeding and poor
wound healing, but the PT, PTT, thrombin time, platelet
count, and platelet functional assay results are normal,
what factor deficiency is indicated?
a. Fibrinogen
b. Prothrombin
c. Factor XII
d. Factor XIII
A
d. Factor XIII
8
Q
- What therapy may be used for a hemophilic boy who is
bleeding and who has a high titer of factor VIII inhibitor?
a. rFVIIa
b. Plasma
c. Cryoprecipitate
d. Factor VIII concentrate
A
a. rFVIIa
9
Q
- What is the most prevalent form of VWD?
a. Type 1
b. Type 2A
c. Type 2B
d. Type 3
A
a. Type 1
10
Q
- 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
A
c. Factor V assay
11
Q
- Mucocutaneous hemorrhage is typical of:
a. Acquired hemorrhagic disorders
b. Localized hemorrhagic disorders
c. Defects in primary hemostasis
d. Defects in fibrinolysis
A
c. Defects in primary hemostasi