Hemostasis and heavy bleeding M Hellgren Sahlgrenska University Hospital Gothenburg.

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Presentation transcript:

Hemostasis and heavy bleeding M Hellgren Sahlgrenska University Hospital Gothenburg

SU

Damage Repair

Platelets leucocyte Von Willebrand factor erytrocyte Vasoconstriction What happens at the vessel wall? Baghaei & Stigendal 2009

VWF GPIb Fibrin GPIIb/IIIa (Fibrinogen receptor) GPIIb/IIIa (Fibrinogen receptor) Collagen GPIa/IIa Plateletplug ( 10min ) Baghaei & Stigendal 2009 Blood Coagulation starts

Platelet aggregation Platelet aggregation

Blood Coagulation TF FVIIa FXa Thrombin Fibrinogen Fibrin FXIa FIXa FVIIIa FVa FXIIIa PK- INR APTT Initiation Amplification Baghaei & Stigendal 2009 Platelet

Fibrinogen

Collet, J.-P. et al. J. Biol. Chem. 2003;278:

Fibrinogen Fibrin Fibrinogen-,fibrin degradation products D-dimers Plasminogen urokinase PAI-1 tPA PAI-2 TAFI Faktor V Plasmin Faktor VIII alfa 2 antiplasmin

Fibrinolysis at different fibrin net Collet JP et al. Aretrioscler Thromb Vasc Biol.2000;20:

Platelet plug Initiation thrombin-fibrin Amplification thrombin-fibrin Fibrinolysis D-dimer Fibrin

Hemostasis during pregnancy Bleeding Thrombosis

Hemostasis during pregnancy

Kjellberg et al 1999 F 1+2 Soluble fibrin D-dimer

Hellgren-81

Laboratory Analyses Global tests Laboratory Analyses Thromboelastogram APTT Sonoclot PK (INR) Platelets Fibrinogen D-dimer Antithrombin Blood sampling each (2) - 4-6:e hours

Routine laboratory analyses Third trimester Hemostasis APTT, s normal/short normal PK, INR < 0.9 < 1.6 Platelets, x 10 9 /L > 100 > 50 Fibrinogen, g/L > 3.0 g/l > D-dimer, mg/L < 2.0 mg/L ?? Antithrombin, kIE/L > 0.80 >0.80

Thromboelastograph

Thromboelastography (TEG)

TEG Normal values r = reaction time 6-9 min MA = maximal amplitude mm α° = speed of fibrin formation > 50° α°α° r MA Kang et al: Anesth Analg 1985:64: CoagulationFibrinolys

Thromboelastography

Platelet function Bleeding time ; prolonged = increased bleeding Multiplate: aggregation (ASA and platelet inhibitors ) Platelet adhesion (hereditary defect)

Acquired coagulation disorders Lokal consumption Dilution DIC Decreased synthesis Primary fibrinolys Sekundary fibrinolys Thrombocytopathy

Hemostasis disorders

Fibrinogen and heavy obstetric bleeding Charbit-et al 2007

Coagulation analyses 0-24h Charbit et al 2006

Abruptio placentae h, post partum HB, g/L TPK, x10 9 /L APTT,s Fib, g/L PK(INR) < AT,IE/L D-dimer, mg/L >8 >

Bleeding 25 L E-conc plasma platelets Cristalloids and colloids

Blood and plasmaproducts Bleeding Transfusion Less than 2-2,5 L Erythrocytes More than 2-2,5L Ery:plasma 1:1 Platelets each 4

Treatment Erythrocyte concentrat HB > 100 g/L Fresh frosen plasma factor V, VIII, other factors, inhibitors Stored plasma stabile factorerand inhibitors Platelet concentrate at bleeding > x10 9 /L Fibrinogen >2-2,5 g /L Cyklokapron mg /kg body weight iv Concomittant administration! 4:4:1 4 g fibrinogen

Fibrinolysis and uterine contractions t-PA Uterine contractions D-dimer

R-FVIIa (Novoseven®) NovoNordisk

Register study from Northern Europe n=113 improvement ( % ) 97 treatment80 16 prophylaxis 75 4 thromboembolism 5 death One myocardial infarction Bleeding from arterial aneurysm and liver Hypovolemic shock Sepsis Brain damage Alfirevic et al Obstet Gynecol 2007;110:1270-8

Novoseven aktivated factor VII 0,1 mg / kg b.w. Antithrombin < 0.5 IU/ L Temperature <35° C, pH<7.2 and normal Ca + + Other factor koncentrate in collaboration with expert in blood coagulations Additional treatment

Desmopressin (Octostim) Desmopressin v Willebrands factor FVIII, t-PA ASA dextran thrombocytopaties von Willebrands disease uremia liver cirrhosis