bleeding and thrmobosis Flashcards

(32 cards)

1
Q

balance between pro-coagulant and anti coagulant forces

A

human hemostatic system

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2
Q

regulated to promote blood flow and will have blood clot rapidly to stop and prevent excanguination

A

hemostasis

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3
Q

platelet adhesion is mediated by a multimeric protein called?

A

VWF (Von Willebrand Factor)

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4
Q

the major plasma inhibitor of thrombin and the other cloting factors in coagulation

A

antithrombin

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5
Q

is a plasma glycoprotein became an anticoagulant when it is activated by thrombin with the presence of thrombomodulin which is a trans membrane proteoglycan binding site for thrombin on endothelial cells surface

A

protein C

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6
Q

once protein C is activated it acts as an anticoagulant by cleaving and inactivating activated factor V and VIII, which accelerated by co-factor ___

A

protein S

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7
Q

deficiency of protein C will lead to?

A

hypercoagulable state

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8
Q

is a plasma protease inhibitor that regulates the TF induced extrinsic pathway of coagulation

A

tissue factor pathway inhibitor

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9
Q

where does tissue factor pathway inhibitor bounds to ?

A

lipoprotein and can also be released by heparin from endothelial cells which is bound to glycosaminoglycan and from platelets

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10
Q

major protease enzyme of fibrinolytic system

A

PLASMIN

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11
Q

markers use to exclude the diagnosis of DVT and pulmonary embolism

A

D-Dimer assays

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12
Q

defects in platelet adhesion

A

von willebrand diseaes
bernard-soulier syndrome

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13
Q

defects of platelet agg

A

glanzmann thrombasthenia
afibrinogenemia

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14
Q

defects of platelet secretion

A

disease COX activity
granule storage pool defects
nonspecific inherited secretory defects
nonspecific drug disease
uremia
platelet coating

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15
Q

defect of platelet coag

A

scott’s syndrome

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16
Q

some risk factors of thrombosis (venous inherited)

A

factor V leiden
prothrombin G20210A
antithrombin deficiency
Protein C deficiency
Protein S deficiency

17
Q

some risk factors for thrombosis (venous acquired)

A

age
previous thrombosis
immobilization
major surgery
pregnancy and puerperium
hospitalization
obesity
infection
smoking

18
Q

prolonged prothombin time lab eval

A

factor vii deficiency
factor k deficient
warfarin anticoagulation
direct Xa inhibitors

19
Q

prolonged pTT and PT disorders

A

factor 2, 5 ,10 or fibrinogen deficiency
vitamin K defiiency - late
direct thrombin inhibitors

20
Q

deals with the preservation of blood fluidity and to limit blood clotting under normal condition in focal sites of vascular injury

A

antithrombic mechanism

21
Q

what does tissue factor pathway inhibitor INHIBITS?

A

TF/Factor VIIa/Factor Xa complex

22
Q

physiologic regulation of fibrnolysis in 3 levels

A
  1. plasminogens activates inhibitors
  2. thrombin-activatable fibrinolysis inhibitor
  3. A2 - asntplasmin inhibits plasmin
23
Q

herbs with potential antiplatelet activity

A

gingko
garlic
bilberry
ginger
dong quai
feverfew
asian ginseng
american ginseng

24
Q

coumarin containing herbs

A

motherwort
chamomile
horse chestnut
red clover
fenugreek

25
abnormalities of prolonged activated partial thromboplastin time aPTT
no bleeding - decrease factor XII, high molecular weight kininogen variable, mild bleeding - decrease factor X1, mild decrease factor VIII and factor IX frequent, severe bleeding - severe deficiency of factors VIII and IX heparin and direct thrombin inhibitors
26
abrnomalities of prolonged prothrombin time (PT)
factor VII deficiency vitamin K deficiency - early warfarin anticoagulation direct Xa inhibitors
27
abnormalities of prolonged aPTT and PT
factor II, V, X or fibrinogen deficiency Viramin K deficiency - late direct thrombin inhibitors
28
abnormalities of prolonged thrombin time
heparin or heparin like inhibitors direct thrombin inhibitors mild or no bleeding - dysfibrinogenemia frequent, severe bleeding - afibrinogenemia
29
abnormalities of prolonged PT and.or aPTT not corrected with mixing with normal plasma
bleeding lupus anticoagulant disseminated intravascular coagulation heparin or direct thrombin inhibitors
30
abnormalities of abnormal clot solubility
factor XIII deficiency inhibitors or defective cross linking
31
abnormalities of rapid clot lysis
deficiency of a2- antiplasmin or plasminogen activator inhibitor 1 treatment with fibrinolytic therapy
32