Flashcard Review
What coagulation factors bind membrane surface?
5, 10
8, 9
7
Protein C, protein S, protein Z
What can stimulate micro particle formation?
Cytokines (TNFa, IL 6)
Thrombin
Shear stress
Hypoxia
Under normal conditions where do MP come from and what other cells can produce them in disease states ?
endothelial cells, platelets, monocytes
can also be made from granulocytes and erythrocytes
When thrombin binds thrombomodulin and this complex activates protein C, what does APC (with co-factor protein S) then inactivate? Where is this process most efficient?
Inactivates 5 and 8
Inactivates PAI-1 (inhibits the inhibitor- up regulates lysis of any fibrin formed)
aPC inactivates factor 5 better on ENDOTHELIAL SURFACE rather than platelet surface- efficient at limiting thrombin generation on healthy resting EC but not on activated platelets.
When thrombin binds thrombomodulin, what function does this complex have?
Activate TAFI
Action of TF-F7 complex?
Activates additional 7 as well as 9, 10.
3 phases of coagulation in the cell-based model version
1- Initiation - on surface of TF bearing cell- produces small amount of thrombin. Thrombin and factor 9 then diffuse away towards the platelet.
2- Amplification - Thrombin activates platelets, releasing VWF from factor 8, leading to activated f5, 8, 11.
3- Propagation - on surface of the platelet - factor 8 and 9 form tenase complex, producing large amount of factor 10 on platelet surface.
Factor 10 and 5 form prothrombinase which generates large amounts of thrombin on platelet surface
What does antithrombin inactivate?
Mainly 10 and thrombin
Also 9, 11, 12 and TF-7 complex
Adverse effects of lasix
- acute kidney injury
- low thiamine levels
- insulin inhibition -> hyperglycemia
- altered mucociliary clearance
- ototoxicity
- delayed wound healing
- interference with thyroid binding
- RAS activation
- dehydration
Calcium dependent clotting factors
5, 7, 8, 9, 10, 11
Protein C,
Protein S
Formula MAP
CO x SVR (aka ohms law)
For TEG does the pin or cup move?
Cup moves.
Causes of elevated PTT with normal PT
Inherited deficiencies, DIC, liver disease, unfractionated heparin therapy, artifact of collection
Causes of elevated PT with normal PTT
Inherited factor VII deficiency, early vitamin K deficiency or antagonism, DIC, warfarin treatment, liver disease (cholestatic, liver failure)
What is normal BMBT?
<4 minutes