Physiology Flashcards

(22 cards)

1
Q

Blood typing refers to what?

A

Antigen found on the RBC

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2
Q

Who gets RhoGAM?

A

Pregnant mothers who are Rh-, to prevent development of materal anti-Rh IgG

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3
Q

What factors activate X–>Xa

A

VIIa, VIIIa (cofactor), and IXa

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4
Q

What factors activate II (thrombin)–>IIa

A

Xa and Va (cofactor)

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5
Q

Hemophilia A

A

Deficiency of factor VIII (XR)

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6
Q

Hemophilia B

A

Deficiency of factor IX (XR)

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7
Q

Hemophilia C

A

Deficiency of factor XI (AR)

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8
Q

What is the enzyme that reduced vitamin K?

A

Epoxide reductase (Oxidized Vit K->reduced Vit K)

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9
Q

Activated protein C has what function?

A

Inactivates cofactors Va and VIIIa

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10
Q

What factor does vWF carry and protect?

A

VIII

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11
Q

Antithrombin inhibits activated forms of which factors?

A

II, VII, IX, X, XI, XII.

Mainly II and Xa

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12
Q

Factor V leiden mutation

A

Produces a factor V that is resistant to inhibition by activated protein C

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13
Q

What Rx indirectly decrease GpIIb/IIIa?

A

Clopidogrel, prasugrel, ticlopidine

Inhibit the ADP receptor that produces GpIIb/IIIa

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14
Q

What Rx directly decrease GpIIb/IIIa?

A

Eptifibatide, abciximab, and tirofiban
(Inhibit GpIIb/IIIa directly)
EAT GPIIb/IIIa

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15
Q

What Rx activates vWF to bind GpIb?

A

Ristocetin

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16
Q

Failure of agglutination with ristocetin occurs in?

A

vonWillebrand diease and Bernard-Soulier syndrome

17
Q

Bernard-Soulier syndrome is a deficiency in what?

A

GPIa receptor

18
Q

What’s in the endothelial cells that gets released during clotting?

A

vWF+VIII
Thromboplastin
tPA, PGI2

19
Q

Whats inside the platelet that gets released during clotting?

A

vWF

Fibrinogen

20
Q

Glanzmann thrombasthenia

A

Deficiency in GpbII/aIII (platelets can’t aggregate

21
Q

von Willebrand disease

A

Platelets can’t adhere to the wound area

22
Q

von Willebrand disease test results

A

Normal PTT, increased bleeding time