Module 9: Part 4 (68-88) Flashcards

1
Q

______ is the most common cause of thrombocytopenia
in pregnancy

A

Gestational thrombocytopenia (GT)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Gestational thrombocytopenia (GT) is usually a PLT count below ____

A

150

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is Gestational Thrombocytopenia?

A

Mild thrombocytopenia occurring during the third trimester with spontaneous
resolution in postpartum period

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

A small subset of women with GT may develop more significant declines in platelet
count and ________

A

reduction in antithrombin III associated with preeclampsia, HELLP
syndrome or acute fatty liver of pregnancy, ITP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

With Autoimmune Thrombocytopenic Purpura (ATP) _______ are responsible for the increased platelet destruction

A

IgG antibodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Antibodies directed against platelet antigens are produced primarily in the _____, where phagocytosis by macrophages occur. Also can occur in ____ and _____

A

spleen
the liver and bone marrow.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

For autoimmune thrombocytopenic purpura (ATP) when would you administer corticosteroids? If there is no response to steroids what would you give?

A

Corticosteroids are administered if the platelet count is < 20-30k before
the onset of labor or <50k at the time of delivery

High dose IV immune globin if no response to steroids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the 5 things included in the classic pentad that defines Thrombotic thrombocytopenia purpura (TTP) ?

A
  1. Thrombocytopenia (as low as 20K)
  2. Microangiopathic hemolytic anemia
  3. Fever
  4. Neurologic signs such as photophobia, headache, and seizures
  5. Renal failure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

_____ is the hallmark of TTP

A

DIC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Associated with congenital or acquired deficiency of
the enzyme ADAMTS13

A

Thrombotic
thrombocytopenia
purpura (TTP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

ADAMTS13 is responsible for _____

A

cleaving vWF multimers.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Decreased levels of ____ in the acute phase of TTP/normal in remission

A

vWF

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What helps differentiate TTP from DIC?

A

The presence of vWF (but not fibrinogen) in
platelet aggregates helps differentiate TTP from
DIC. (In patients with DIC, fibrinogen but not vWF is found in platelet aggregates.)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

______ appears to be a precipitating event in both initial and recurrent episodes of TTP

A

Pregnancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Diagnosis may be confounded by a misdiagnosis of HELLP syndrome although concurrent diagnosis have been reported

A

Thrombotic
Thrombocytopenic
Purpura (TTP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Is neuraxial anesthesia recommended for pts with Thrombotic Thrombocytopenic Purpura (TTP) ? Why or why not?

A

Because of the coagulopathy present, neuraxial
anesthesia is not recommended

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

vWF has two primary roles in coagulation. What are they?

A

it forms a complex with factor VIII
it mediates platelet adhesion by binding to platelets and collagen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Which type of Von Willebrand’s Disease is the most common congenital bleeding disorder?

A

Type 1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Von Willebrand’s Disease Type 1

A

vWF functions normally but the level is decreased
Both vWF and factor VIII increase in normal pregnancy so antenatal bleeding is rare

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is Von Willebrand Disease type 2?

A

includes a family of disorders characterized by
qualitative dysfunction of vWF, with normal plasma concentrations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What are Von Willebrand Disease type 2A and 2M? What occurs?

A

Type 2A and 2M lead to platelet aggregation, in type 2B vWF increases binding between platelets leading to accelerated platelet turnover and thrombocytopenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Von Willebrand disease type 2 is (less/more) common

A

less

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Which type of Von Willebrand disease is a severe quantitative deficiency in vWF?

A

type 3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Levels of what factors should be determined during pregnancy especially in the 3rd trimester w/ Von Willebrand disease?

A

factor VIII and vWF ristocetin cofactor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What can be administered for acute bleeding for pts with Von Willebrand disease?

A

FFP or cryoprecipitate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What is administered IV as labor begins for pts with von willebrand diseae types 1 or 2A? When should it be repeated?

A

0.3 mcg/kg of desmopressin (DDAVP) is administered IV as labor begins and the dose is repeated every 12 to 24 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

What are the classifications of Von Willebrand’s disease?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

What kind of coagulopathy is DIC?

A

acquired

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

DIC results from an abnormal activation of the
coagulation system which leads to:

A
  • Formation of large amounts of thrombin
  • Activation of the fibrinolytic system
  • Depletion of coagulation factors
  • Hemorrhage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

What are the most frequent causes of DIC?

A

Preeclampsia, placental abruption, sepsis, retained dead fetus syndrome, PPH, acute fatty liver of pregnancy, AFE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Pathogenesis of DIC

A
32
Q

Range of Normal Results for Coagulation Tests in Pregnancy

A
33
Q

What 2 lab findings with DIC are decreased?

A

PLT count
fibrinogen

34
Q

In DIC there are variable increases in ___ and ___

A

PT
aPTT

35
Q

There are higher concentrations of what lab values in DIC?

A

D-dimer, fibrin monomer and fibrin
degradation products

36
Q

Viscoelastic monitoring confirms what 3 things associated with DIC?

A

delayed clot activation, decreased clot strength, and evidence of fibrinolysis

37
Q

What are the therapeutic goals for DIC?

A

 Treat or remove the precipitating cause (evacuation of the uterine contents)
 Replace depleted coagulation factors
 Stop on-going proteolytic activity; i.e., both the coagulation and fibrinolytic pathways
 Provide multi-system support as required

38
Q

What all is included in the treatment of DIC pt in active bleeding or for invasive procedures?

A

 Transfuse FFP (15 – 30 mL/kg) to maintain the PT and aPTT within 1.5 x normal values
 Cryoprecipitate or fibrinogen concentrate to
maintain the fibrinogen concentration above 200 mg/dL
 Platelets to maintain platelet count >50,000/uL

39
Q

How should you transfuse FFP for a DIC pt with active bleeding or for invasive procedures? What do you want to maintain the PT and aPTT within?

A

Transfuse FFP (15 – 30 mL/kg) to maintain the PT and aPTT within 1.5 x normal values

40
Q

Why would you give Cryoprecipitate or fibrinogen concentrate to a pt in DIC with active bleeding or an invasive procedure?

A

to maintain the fibrinogen concentration above 200 mg/dL

41
Q

You would give PLTs to a DIC pt with active bleeding or an invasive procedure to maintain a PLT count > _____

A

50,000/uL

42
Q

Diagnosis + Management of DIC in Pregnancy

A
43
Q

A congenital deficiency in anticoagulant activity
occurs in >____% of women with pregnancy-related venous thrombosis

A

50

44
Q

What are the most common
thrombophilia diagnosed in pregnancy?

A

Factor V Leiden mutation, prothrombin mutation, protein C deficiency, protein S deficiency, and antithrombin III deficiency

45
Q

Venous thromboses are more common than arterial T/F

A

TRUE

46
Q

Incidence of hypercoaguable states increases with:

A

surgery, pregnancy, oral
contraceptive use, immobilization

47
Q

ACOG and ACCP recommend _____ for pregnancies complicated by inherited thrombophilia

A

thromboprophylaxis

48
Q

What is the most common hereditary thrombophilia?

A

Factor V Leiden

49
Q

Individuals with Factor V Leiden have what?

A

have a point mutation in the factor V gene that produces a single amino acid switch (arginine to glutamine) that makes the protein resistant to inactivation by activated protein C.

50
Q

This mutant protein persists longer in circulation owing to its slower degradation by activated protein C, leading to a hypercoagulable state

A

Factor V Leiden

51
Q

Factor V Leiden makes up ___% of all obstetric thromboembolic events

A

40

52
Q

Conflicting data regarding association with placental abruption, severe preeclampsia, IUGR

A

Factor V Leiden

53
Q

Risk for thrombosis in pregnancy is increased up to 5-fold with which deficiencies?

A

antithrombin 3
protein C

54
Q

What all does Antithrombin III inactivate?

A

thrombin and factors IXa, Xa, XIa, and XIIa

55
Q

Where is antithrombin III synthesized?

A

in liver and endothelial cells

56
Q

Antithrombin III activity is potentiated by ____

A

heparin

57
Q

What is the incidence of antithrombin III in the general population?

A

0.02 to 0.4%

58
Q

How much does the risk for thrombosis increase for pregnant pts when they have antithrombin III deficiency?

A

Risk increases from 3% to 7% among those with
Antithrombin III def. and no prior thromboembolism
to 40% in those with prior venous thromboembolism

59
Q

For Antithrombin III deficiency which types is quantitative and which is qualitative?

A

Type 1 = quantitative
Type 2 = qualitative

60
Q

Why might heparin not ensure effective thromboprophlaxis in pts with antithrombin III deficiency?

A

Heparin acts by potentiating activity of antithrombin
III…. If antithrombin III levels are decreased, then
heparin may not ensure effective
thromboprophylaxis

61
Q

What is proposed for perioperative or peripartum therapy for pts with ATIII deficiency and venous thromboembolism history?

A

Antithrombin III replacement, with or without heparin

62
Q

Protein C is a ______-dependent protein

A

vitamin K

63
Q

Where is Protein C synthesized? What does it do?

A

synthesized in the liver and inhibits blood
coagulation by proteolytic activation of factors V and VIII

64
Q

When does Protein C deficiency occur?

A

when the gene for protein C on both chromosomes #2 is affected

65
Q

Deficiency is defined by an activity level of <____%

A

50

66
Q

Incidence in general population of protein C deficiency is approx. ____%

A

0.3

67
Q

Protein C levels increase ____% in pregnancy but
attenuated in Protein C deficiency

A

35

68
Q

How much does the risk for thrombosis increase for pregnant pts when they have protein C deficiency?

A

Risk is less than 1% among those without previous thrombosis to as high as 17 % with a previous history of thrombosis

69
Q

When should a pt with protein C deficiency be treated with LMWH?

A

During delivery and up to 6 weeks after

70
Q

______ acts as a cofactor for protein C

A

Protein S

71
Q

The plasma levels of protein S normally (increase/decrease) during pregnancy

A

decrease

72
Q

The plasma levels of protein C normally (increase/decrease) during pregnancy

A

increase

73
Q

What is the incidence of Protein S deficiency?

A

less than 0.2%

74
Q

2-4 increased risk of VTE with what condition?

A

Protein S Deficiency

75
Q

The risk for antepartum and postpartum venous
thromboembolism is low in patients with protein C or protein S deficiency T/F

A

TRUE

76
Q

Thromboprophylaxis for pts w/ protein C or protein S deficiency is not indicated unless the patient has a history of venous thromboembolism or additional risk factors
are present T/F

A

TRUE