Bleeding Disorders Flashcards

1
Q

What are the characteristic hallmarks of platelet bleeding?

A

Superficial (skin)
Petichiae
Spontaneous
Mucousal

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2
Q

What are the characteristic hallmarks of factor bleeding?

A

Deep (joints)
Big bleeds
Trauma

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3
Q

What is the most common hereditary bleeding disorder?

A

Von Willebrand Disorder

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4
Q

What is the inheritance pattern of von Willebrand Disorder?

A

Autosomal dominant

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5
Q

What are the types of vWF disease and prevalence of each?

A

Type 1: Decreased vWF (70%)
Type 2: Abnormal vWF (25%)
Type 3: Absent vWF (5%)

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6
Q

What are the symptoms of vWF?

A
Mucosal bleeding (after dental surgery)
Deep joint bleeding when severe
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7
Q
What are the following tests like in vW Disease?
Bleeding time:
PTT:
INR:
vWF level:
Platelet aggregation:
A
Bleeding time: Prolonged
PTT: prolonged
INR: Normal
vWF level: Decreased (normal in type 2)
Platelet aggregation studies: abnormal
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8
Q

How do you treat VWD?

A

DDAVP, Cryoprecipitate, factor VIII

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9
Q

What does DDAVP do for vW disease?

A

Releases vWF from stores

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10
Q

What is the downside to long term factor VIII use for vWD?

A

Works less and less well over time because antibodies will be made against it

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11
Q

What is the inheritance pattern of Hemophilia?

A

X linked recessive (in most cases)

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12
Q

What is the most common factor deficiency?

A

Hemophilia A

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13
Q

What is the factor deficient in Hemophilia A?

A

Factor VIII

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14
Q

What does hemophilia A symptoms look like?

A

Deep joint bleeding, prolonged dental work bleeding

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15
Q
What do the following tests look like in Hemophilia A?
INR:
TT:
Platelet count:
Bleeding time:
PTT:
Factor VIII assays:
DNA studies:
A
INR: normal
TT:normal
Platelet count: normal
Bleeding time: normal
PTT: prolonged
Factor VIII assays: abnormal
DNA studies: abnormal
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16
Q

What is the treatment for Hemophilia A?

A

DDAVP

Factor VIII

17
Q

What factor is decreased in hemophilia B?

A

Factor IX

18
Q

What is abnormal in Bernard Soulier syndrome?

A

Glycoprotein 1b

19
Q

What do platelets look like in Bernard Soulier?

A

BIG. Like RBC big

20
Q

What is deficient in Glanzmann Thrombasthenia?

A

No IIb-IIIa

21
Q

What is deficient in Gray Platelet syndrome?

A

alpha granules

22
Q

Why is too much bleeding common in DIC?

A

Platelets and factors are used up

23
Q

What do you oftentimes on a blood smear see with DIC?

A

Microangiopathic hemolytic anemia