HEMA PART 5: PRACTICE QUESTIONS

1. It measures the capillaries’ resistance to pressure; correlates with the degree of

THROMBOCYTOPENIA?

2. QUICK’S Mtd is not repeated on the same arm for 3 days. TRUE or FALSE?

3. Rumple-Leede grade for 20-50 petechiae.

4. Positive result of Hirschboeck Mtd; reference range?

5. Dependent on the concentration of vWF; reference range?

6. Volume of blood and incubation temperature in Stefanini mtd.

7. Volume of blood and incubation temperature in MacFarlane mtd; Normal Value.

8. Severe fibrinogen deficiency may cause?

9. Reference range for Duke mtd and Ivy mtd respectively.

10. Uses blood pressure cuff in measuring bleeding time.

11. Purplish-red pinpoint hemorrhagic spots; 3mm in diameter.

12. Purpla skin discoloration; 1cm in diameter

13. Usually in irregular shape; 3cm or larger

14. Localized collection of extravasated blood.

15. These are produced by LIVER; circulates in the blood as zymogens along with nonenzymatic
factors and calcium.

16. This is also produced by ENDOTHELIAL CELLS.

 HEMA PART 5: PRACTICE QUESTIONS

17. No vWF = _____________

No FVIII = vWF remains intact

18. It is circulated in the blood as inactive until converted by enzymes to active protease. Factors: II, VII,
IX, X, XII.

19. vWF prolongs ________ from few minutes to ___ to 12 hours.

20. Serine Proteases: __________________

21. Cofactors: ________________________

22. Transglutamase: ___________________

23. The only substrate in the cascade does not become an activated enzyme; MOST
CONCENTRATED FACTOR.

24. What coagulation factor is involved when patients do not bleed even if hypercalcemic? *NO. AND
PREFERRED NAME

25. Coagulation factors associated with the Owren’s dse.

26. Serum Prothrombin Conversion Accelerator (SPCA).

27. Associated with NO BLEEDING HISTORY.

28. Later found out that this is the ACTIVATED FACTOR V.

28-41. Fill the box.

FACTOR PREFFERED NAME SYNONYMS NOTES
I
---

II Prothrombin (1)

III Tissue Factor

---

IV Calcium
---
 HEMA PART 5: PRACTICE QUESTIONS

V Labile factor, Accelerator Deficiency: Parahemophilia

globulin (aCg) or Owren;s dse

VII Proconvertin
---

VIII:C Antihemophilic Factor (AHF) (3)

IX Plasma Thromboplastin (4)

Component (PTC)

X Stuart-Power Factor (3)

---

XI Antihemophlic factor C

XII Glass Factor, Contact factor Deficiency: NO BLEEDING

HISTORY

XIII (3)
----

HMWK High Molecular Weight (4)

Kininogen ---

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