Other disorders of hemostasis Flashcards

1
Q

heparin induced thrombocytopenia pathophys

A

heparin forms a complex with platelet factor 4, leading to formation of igG antibodies and consumption of platelets

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2
Q

DIC pathophys

A
  • widespread microthrombi lead to ischemia and infarction

- consumption of platelets and factors leads to bleeding

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3
Q

What disease processes may DIC occur secondarily to…

A

Obstetrics complications -tissue thromboplastin activates coagulation
Sepsis – endotoxins/cytokines induce Tissue factor
Adenocarcinoma - mucin activates coagulation
Acute promyelocytic leukemia -primary granules activate coagulation
Rattlesnake bite -venom activates coagulation

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4
Q

Lab findings in DIC

A
Decreased platelet count
Decreased fibrinogen
Increased PT/PTT
Microangiopathic hemolytic anemia
Elevated fibrin split products -D Dimer
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5
Q

Treatment of DIC

A

Treat underlying cause

Blood transfusion and cryoprecipitate as needed

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6
Q

alpha-2 antiplasmin function

A

inactivates plasmin

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7
Q

tPA function

A

activates plasminogen to plasmin

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8
Q

What are the two disorders of fibrinolysis?

A

Radial prostateectomy – release of urokinase activates plasmin
Cirrhosis of liver – reduced production of alpha-2 antiplasmin

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9
Q

presentation and lab findings of disorders of fibrinolysis

A

plasmin overactivity –> increased bleeding time
Increased PT/PTT
Increased bleeding time with normal platelets
Increased fibrinogen split products with absent D-Dimers(no fibrin thrombi present)

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10
Q

treatment of disorders of fibronolysis

A

aminocaproic acid (blocks activation of plasminogen)

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11
Q

how to distinguish thrombus from post mortem clot?

A

lines of zahn (alternating platelets/fibrin and RBC layers) and attachment to blood vessel wall

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12
Q

virchows triad

A

blood flow disruption, endothelial damage, hypercoaguable state

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13
Q

Lack of B12 or folate results in build up of what?

A

homocysteine

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14
Q

Homocysteine causes waht

A

endothelial damage

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15
Q

What is cystathionine beta synthase deficiency

A

Cause of high homocysteine with homocystinuria

CBS usually converts homocysteine to cystathione

Characterized by vessel thrombosis, mental retardation, lens dislocation and long fingers

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16
Q

What is factor V leiden?

A

A mutated form of factor V that lacks the cleavage site for deactivation by protein C and S

17
Q

What is prothrombin 20210A?

A

An inherited point mutation in prothrombin that results in increased gene expression

18
Q

What is ATIII deficiency and what will happen with heparin dosages?

A

ATIII usually inactivates thrombin and coag factors, thus with a deficiency PTT does not rise with standard heparin dosing

Must give high dose of heparin then switch to Coumadin

19
Q

How does estrogen effect coagulation?

A

Increases production of coag factors

20
Q

Atherosclerotic embolus histology

A

Will have cholesterol clefts

21
Q

Fat embolus histology

A

fat with bone marrow elements

22
Q

What is the cause of a gas embolus?

A

Usually from rapid ascent of a diver, as nitrogen gas precipitates out of blood, leading to the bends

23
Q

Symptoms of the ‘bends’

A

Joint, muscle pain. Respiratory symptoms

24
Q

Amniotic fluid embolus presentation

A

DIC, SOB, neurological symptoms

25
Q

Amniotic fluid embolism histology

A

squamous cells and keratin debris in embolus from fetal skin

26
Q

Death from PE is caused by what?

A

electromechanical dissociation in heart