Hemostasis/Coagulation Flashcards
Activated by trauma
Extrinsic clotting pathway
Activated by damage to the internal surface of a vessel
Intrinsic clotting pathway
immediate vasoconstriction and formation of platelet plug at damaged site
Primary hemostasis
Clotting cascade and the formation of fibrin clot
Secondary hemostasis
bright, red blood in the stool
hematochezia
digested, dark blood in the stool
melena
blood in the urine
hematuria
coughing up blood
hemoptysis
heavy menstrual bleeding
menorrhagia
nose bleed
epitaxis
PT/INR
Lab - Extrinsic Pathway
aPTT
Lab - Intrinsic Pathway
Chemotherapy/radiation, cancer in the bone marrow, B12/folate deficiency
Decreased production - platelet disorders
Idiopathic thrombocytopenic purpura, heparin-induced thrombocytopenia, DIC, medications (thiazides, digoxin, heparin)
Decreased survival - platelet disorders
Splenomegaly (enlarged spleen can cause spleen dysfunction), hypothermia
Splenic sequestration - platelet disorders
Large blood transfusions, too much RBC and plasma/too few platelets
Dilution - platelet disorders
Platelet count < 100,000
Easy bruising, mucosal hemorrhage, petechiae, purpura, internal bleeding
Thrombocytopenia
“immune-to-platelets” = immune mediated destruction
Triggered by viral infection
Associated with autoimmune diseases: AIDS, lupus
ITP
Factor VIII deficiency, most common (85%), x-linked
Hemophilia A
Factor IX deficiency, “Christmas Disease”, x-linked
Hemophilia B
Spontaneous bleeding: joints, mucosa, GI, intracranial
Prolonged bleeding after minor procedures
Hemophilia
Complex, acquired disorder in which clotting and hemorrhage simultaneously occur
DIC
malnutrition, malabsorption, antibiotic treatment, anticoagulation therapy
can lead to Vit. K deficiency
II, VII, IX, X
Vit. K dependent clotting factors
Inhibits the activity of thrombin, works intrinsically
Heparin
Vit. K dependent, works extrinsically
Coumadin