What is Hemostasis?

Hemostasis
(A) Hemostatic efficacy of thrombin nanocomplexes in rat hepatic hemorrhage model. (B) Hemostatic efficacy of native thrombin in rat hepatic hemorrhage model. (C) Hemostatic efficacy of thrombin nanocomplexes in rat iliac artery hemorrhage model. (D) Hemostatic efficacy of native thrombin in rat iliac artery hemorrhage model. Nanocomplexation of thrombin with cationic amylose derivative for improved stability and hemostatic efficacy. Zhuang B, Li Z, Pang J, Li W, Huang P, Wang J, Zhou Y, Lin Q, Zhou Q, Ye X, Ye H, Liu Y, Zhang LM, Chen R - International journal of nanomedicine (2015). Not Altered. CC.

Hemostasis is the normal response to vascular injury that leads to clot formation and stabilization.

Hemostasis involves: 

  • Arteriolar vasoconstriction
  • Primary hemostasis
  • Secondary hemostasis
  • Clot stabilization

Key components of hemostasis include the endothelium, platelets, and the coagulation cascade.

What is Arteriolar Vasoconstriction?

Arteriolar vasoconstriction is the narrowing of the blood vessels resulting from the contraction of the muscular wall of the vessels.

What is Primary hemostasis?

Primary hemostasis is a pro coagulation clot-forming process associated with the initiation and formation of the platelet plug.

What is Secondary hemostasis?

Secondary hemostasis is also a pro-coagulation clot-forming process and it’s associated with the propagation of the clotting process via the intrinsic and extrinsic coagulation cascades.

What is Clot Stabilization?

Clot stabilization is the enhancing activation of procoagulants only at the site where a clot is desired by the coated platelets.

What is the Coagulation Cascade?

The coagulation cascade is the series of steps that occur during the formation of a blood clot after injury by activating a cascade of proteins called clotting factors.

The factors involved in the coagulation cascade include: 

  • Factor XIII
  • Factor XII
  • Factor XI
  • Factor X
  • Factor IX
  • Factor VIII
  • Factor VII
  • Factor VI
  • Factor V
  • Factor IV
  • Factor III
  • Factor II
  • Factor I
 NAMEFUNCTION
Factor XIIIFibrin-stabilizing factorCrosslinks Fibrin
Factor XIIHageman factorActivates Factor XI, VII and Prekallikrein
Factor XIPlasma thromboplastin antecedentActivates Factor IX
Factor XStuart-Prower factorActivates Factor II, forms prothrombinase complex with Factor V
Factor IXPlasma thromboplastin component, Christmas factorActivates Factor X, forms tenase complex with Factor VIII
Factor VIIIAntihemophilic factorCofactor of IX with which it forms tenase complex
Factor VIIStable factor or proconvertinActivates Factor IX, X
Factor VIUnassignedUnassigned
Factor VLabile factor or proaccelerinCofactor of X with which it forms prothrombinase complex
Factor IVIonized calcium (Ca++)Required for coagulation factors to bind to phospholipid (formerly known as factor IV)
Factor IIITissue thromboplastin (tissue factor)Cofactor of VIIa (formerly known as Factor III)
Factor IIProthrombinFactor IIa activates I, X, VII, VIII, XI, XIII, protein C, platelets
Factor IFibrinogenBlood clot formation (Fibrin)

What are Vitamin K Dependent Factors?

Vitamin K dependent factors include: 

Factors, 2, 7, 9, 10, protein C and protein S.