Thromboembolic Disorders Flashcards

1
Q

leading cause of maternal mortality

A

deep venous thrombosis

pulmonary embolism

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2
Q

the most constant predisposing factor for venous thrombosis

A

stasis

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3
Q

coagulation factors increased in pregnancy

A

fibrinogen
factor VII
factor VIII
von willebrand

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4
Q

the most important risk factor in developing thromboembolism

A

genetically determined thrombophilia

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5
Q

thrombin (IIa) acts in what coagulation cascade pathway?

A

intrinsic pathway

common pathway

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6
Q

the most thrombogenic of the heritable thrombophilia

A

antithrombin deficiency

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7
Q

antithrombin deficiency type that results in reduced synthesis of biologically normal antithrombin

A

type I deficiency

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8
Q

antithrombin deficiency type that is characterized by normal levels of antithrombin with reduced functional activity

A

type II deficiency

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9
Q

lethal antithrombin deficiency

A

homozygous antithrombin deficiency

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10
Q

treatment function of antithrombin

A

target towards the COMMON PATHWAY

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11
Q

treatment for antithrombin

A

low molecular weight heparin (LMWH)

recombinant human antithrombin concentration infusion

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12
Q

helps inactivates procoagulant Va and VIIa

A

protein S

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13
Q

vitamin K dependent glycoprotein that increases throughout the fist half of pregnancy

A

protein C

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14
Q

anticoagulant and inflammatory regulatory pathways

A

protein C

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15
Q

inhibits the synthesis of of PAI

A

activated protein c

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16
Q

activated protein c

A

thrombin + thrombomodulin

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17
Q

extensive thromboses in the micronutrition soon after birth leading to skin necrosis

A

purpura fulminans

18
Q

activated protein c resistance aka

A

factor leiden mutation

19
Q

most common heritable thrombophilia

A

heterozygous inheritance for factor V leiden

20
Q

mutation in factor v gene; substitution of _________ for aginine at position 506

A

glutamine

21
Q

second most inherited thrombophilia

A

prothrombin G20210A mutation (PGM)

22
Q

mutation in prothrombin = excessive prothrombin accumulation

A

PGM

23
Q

mutation of enzyme 5,10-methylene-tetrahydrofolate reductase

A

hyperhomocysteinemia

24
Q

deficiencies of folic acid, vitamin b6, vitamin b12

A

hyperhomocysteinemia

25
Q

fasting threshold to define hyperhomocysteinemia

A

> 12umol/L

26
Q

most common acquired thrombophilia

A

antiphospholipid antibody syndrome

27
Q

antibodies against phospholipid-binding proteins such as B2-glycoprotein I

A

antiphospholipid antibody syndrome

28
Q

APAS clinical feature; vascular thromboses

A
  • one unexplained fetal death at or beyond 10 weeks
  • one preterm before 34 weeks because of eclampsia, severe preeclampsia, placental insufficiency
  • unexplained consecutive spontaneous abortion before 10 weeks
29
Q

most commonly involve in APAS

A

lower extremity

30
Q

when other veins are involved in APAS

A

catastrophic APAS

31
Q

thrombophilia screening is indicated for persons:

A

with history of venous thromboembolism
first degree relative before 50
experienced fetal loss

32
Q

most common venous thromboses that are confined to the deep veins of the lower extremity

A

DVT

33
Q

most commonly affected vein in DVT

A

iliofemoral vein

34
Q

homans sign

A

DVT

35
Q

initial diagnostic test of DVT

A

compression ultrasonography

36
Q

diagnosis for DVT is based on

A

based on:
the compressibility
typical echoarchitecture of a thrombosed vein

37
Q

useful diagnosis for DVT

A

MRI

38
Q

gold standard to exclude lower extremity DVT

A

venography

39
Q

initial treatment for thromboembolism

A

unfractionated heparin

40
Q

preferred test to assess heparin anticoagulation

A

anti-factor Xa levels

41
Q

greater activity against factor Xa than thrombin

A

LMWH