coagulation disorders Flashcards
(34 cards)
haemostasis
arrest of bleeding
thrombosis
inappropriate formation of clots within vascular system
bleeding
failure of blood to clot in response to appropriate stimulus
stages of haemostasis
- vessel spasm
- formation of platelet plug
- blood coagulation or development of insoluble fibrin clot
- clot restriction
- clot dissolution
requirements of blood clotting process
platelets (produced in bone marrow)
Von Willebrand factor (generated in vessel endothelium)
clotting factors (synthesised in liver using Vit K)
clotting factor I
fibrinogen
clotting factor II
prothrombin
clotting factor III
thromboplastin
clotting factor IV
calcium
clotting factor VIII
anti-hemophilic factor
if don’t have = haemophilia A
intrinsic blood clotting pathway
disease within body triggers clot formation, vitamin K dependent
extrinsic blood clotting pathway
external stimulus triggers blood clot
terminal steps of blood clotting process
- calcium, factors V and X, platelet phospholipids combine to form prothrombin activator
- prothrombin activator converts prothrombin to thrombin
- this causes the conversion of fibrinogen to fibrin strands which create the insoluble clot
hypercoagulability states
increase risk of clot or thrombus formation in the arterial or venous circulations
caused by accelerated activity of coagulation system or increased platelet function
conditions that create increased platelet function
atherosclerosis, diabetes, smoking, elevated blood lipids and cholesterol, increased platelet levels
conditions that cause accelerated activity of coagulation system
pregnancy, peurperium (6 weeks after delivery), oral contraceptives, post-surgical state, immobility, congestive heart failure, malignant diseases
arterial thrombi
associated with conditions that produce turbulent blood flow and platelet adherence
venous thrombi
associated with conditions that cause stasis of blood flow with increased concentrations of coagulation factors
coagulation defects
impaired synthesis of coagulation factors
hereditary disorders - hemophilia A and Von Willebrand disease
conditions associated with disseminated intravascular coagulation
obstetric conditions, cancer, infections, shock, trauma and surgery, hematologic conditions
disseminated intravascular coagulation
plenty of blood clots and blockages = tissue and organ death, but some bleeding occurring too
hemophilia
inherited bleeding disorder in which there is a deficiency or lack of factor VIII (A) or IX (B)
detection of hemophilia
family history, symptoms (bruising, bleeding after minor surgery, muscle/joint/soft tissue bleeding), lab testing, hemostatic challenges (surgery, dental work, trauma)
types of bleeds
joint bleeding, muscle hemorrhage, soft tissue, life threatening and other