Primary Coagulation Factors Flashcards

1
Q

Prekallikrein (PK)Name(s)PathwayCharacteristic

A

Name:Fletcher factorPathway:IntrinsicCharacteristic: Functions with HMWK and factor XII

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2
Q

HMWKName(s)PathwayCharacteristic

A

Name:High Molecular Weight KilinogenPathway: IntrinsicCharacteristic:co factor in kallikrein & factor XII activation, necessary in factor XIIa activation of XI, precursor for bradykinin (potent dilator & inducer of smooth muscle contraction)

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3
Q

IName(s)PathwayCharacteristic

A

Name:FibrinogenPathway: BOTHCharacteristic:synthesized in liver, also acute phase reactant

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4
Q

IIName(s)PathwayCharacteristic

A

Name: ProthrombinPathway:BOTHCharacteristic: Vitamin K dependent

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5
Q

IIIName(s)PathwayCharacteristic

A

Name: Tissue FactorPathway: ExtrinsicCharacteristic: Released after tissue injury

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6
Q

IV Name(s)PathwayCharacteristic

A

Name: CalciumPathway:BOTHCharacteristic: Necessary for activation of factor IX, X, for conversion of prothrombin to thrombin by Xa and for polymerization of fibrin monomers

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7
Q

VName(s)PathwayCharacteristic

A

Name: Proaccelerin, labile factor, accelerator globulinPathway: BOTHCharacteristic: Protein co-factor; also important co-factor in activated protein C’s ability to function as a physiologic anticoagulant

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8
Q

VI (same as Va)Name(s)PathwayCharacteristic

A

Name:AccelerinPathway: BOTHCharacteristic: NOT USED

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9
Q

VIIPathwayCharacteristic

A

Pathway: ExtrinsicCharacteristic: Vit K dependent

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10
Q

VIIIName(s)PathwayCharacteristic

A

Name: Antihemophilic factor APathway: IntrinsicCharacteristic: Protein co-factor on X chromosome; synthesized in the liver, but also in endothelial cells in all tissue; common deficiency - Hemophilia B

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11
Q

IXName(s)PathwayCharacteristic

A

Name: Christmas factor, antihemophilic factor BPathway: IntrinsicCharacteristic: Vit K dependent; deficiency - Hemophilia B

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12
Q

XName(s)PathwayCharacteristic

A

Name: Stuart Prower FactorPathway: BOTHCharacteristic: Vit K dependent; key entry protein in the common pathway; rare congenital deficiencies, acquired deficiency associated with amyloidosis

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13
Q

XIName(s)PathwayCharacteristic

A

Name: Plasma thromboplastin atecedent (PTA)Pathway: IntrinsicCharacteristic: synthesized in liver; third most common deficiency, but rare bleeding diathesis

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14
Q

XIIName(s)PathwayCharacteristic

A

Name: Hageman FactorPathway: IntrinsicCharacteristic: Activated in vivo by cell components such as fatty acids, endotoxin, cerebrosides; associated with activation of complement and fibinolysis

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15
Q

XIIIName(s)PathwayCharacteristic

A

Name: Protransglutaminase, fibrino ligasePathway: BOTHCharacteristic: stabilizes conversion of fibrin monomer to polymerized fibrin & a stable clot; synthesized in liver and is present in platelets; deficiencies associated with delayed wound healing & recurrent spontaneous abortion

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