Medically Compromised

Question 1

Clotting factor deficiencies

Answer 1

Hemophilia A and B

Von Willebrand’s

Question 2

Primary hemostasis

Answer 2

Platelet plug

Question 3

Secondary hemostasis

Answer 3

fibrin clot

Question 4

Decrease in Factor 8

Answer 4

Hemophilia A

Question 5

Decrease in Factor 9

Answer 5

Hemophilia B

Question 6

This binds to Factor 8, which then binds to platelets to activate the coagulation cascade.

Answer 6

vWF

Question 7

This activates Factor 10 in the INTRINSIC pathway.

Answer 7

Factor 8

Question 8

X-linked recessive disorder.

Answer 8

Hem A and B

Question 9

Only males are affected by this disease.

Answer 9

Hem A and B

Question 10

Known as Christmas Disease

Answer 10

Hemophilia B

Question 11

Needed for platelet adhesion.

Answer 11

vWF

Question 12

Can be autosomal dominant or acquired.

Answer 12

von Willebrand’s disease

Question 13

This is prolonged in Hemophilia A and B, and von Willebrand’s.

Answer 13

Partial Thromboplastin Time

Question 14

Test of the intrinsic pathway.

Answer 14

Partial Thromboplastin Time

Question 15

Normal Partial Thromboplastin Time

Answer 15

24-38 seconds

Question 16

Normal Prothrombin Time

Answer 16

11-17 seconds

Question 17

Assesses platelet function

Answer 17

Bleeding time.

Question 18

The time it takes to stop bleeding.

Answer 18

Bleeding Time

Question 19

This blood disease has increased bleeding time.

Answer 19

von Willebrand’s.

Question 20

Joint and muscle hemorrhages are common in this disease.

Answer 20

Hemophilia

Question 21

T/F: Non-invasive endo is preferred over extractions in people with bleeding disorders.

Answer 21

True

Question 22

Avoid prescribing these medications in someone with a bleeding disorder. Cause increased bleeding.

Answer 22

Aspirin or Ibuprofen