1. Haemostasis Tiffany Shaw MBChB II 2002

2. Haemostasis Pathway Injury Collagen exposure Tissue Factor Platelet adhesion Coagulation Cascade Release reaction Platelet aggregation Fibrin Primary haemostatic plug Secondary haemostatic plug

3. Coagulation Cascade

4. Integrity of Haemostasis Depends on: 1.Vessel wall 2.Platelets (no. and function) 3.Coagulation factors

5. Vessel Wall Release tissue factor that initiates coagulation cascade. Exposed collagen results in platelet adhesion (using vWF as a bridge). Hereditary haemorrhagic telangiectasia Scurvy Senile purpura

6. Hereditary Haemorrhagic Telangiectasia

7. Low Platelet Number N = 150 – 450 Excessive bleed / Spontaneous bleed Mucosal surfaces / Skin Immune Mediated Thrombocytopenia Drug induced Haemolytic Uraemic Syndrome DIC

8. Platelet Dysfunction Abnormal platelet aggregation Normal platelet count Excessive / spontaneous bleed Mucosa / Skin Inherited disorders Drug induced

9. Eccymoses

10. Coagulation Factors Deficiency Spontaneous bleeding into deep tissues Increased post-traumatic haemorrhage Factor 8 – Haemophilia A Factor 9 – Haemophilia B vWF – Von Willebrand’s disease Von Willebrand’s Factor: Protein produced by endothelial cells which mediates platelet adhesion to endothelium and carries factor 8 in plasma.

11. Haemaphilia A Factor 8 deficiency 50 / million people Sex-linked Most detected in childhood Mild symptoms ~ spontaneous bleed Chronic joint disease after repeated bleed

12. Haemophilia B Factor 9 deficiency = Christmas disease Also sex-linked Similar presentation as haemophilia A Much rare

13. Haemoarthroses

14. Von Willebrand’s Disease vWF deficiency Autosomal dominant (F = M) Most common inherited bleeding disorder Bleeding from mucosa Excessive blood loss in trauma Bleeding into deep tissue (rarer)

15. Liver Disease Mixed – both coag deficiency and platelet problem Reduced coag factor synthesis (1, 2, 5, 7, 9, 10) Cirrhosis  Hypersplenism  Thrombocytopenia

16. DIC Generalised activation of coag cascade Wide-spread fibrin formation Thrombosis Low coag factor Bleeding

17. DIC Consequence of Thrombosis: 1.Tissue infarction  Renal impairment 2.CVA 3.PE 4.DVT Consequence of Bleeding: 1.Purpura 2.GI Bleed

18. DIC Causes of coag cascade activation: 1.Sepsis 2.Disseminated cancer 3.Obstetric complications (e.g. retained product of conception) 4.Fulminant liver disease 5.Anaphylaxis 6.AML

19. Drug Induced Coag Factor Def Heparin: Inactivates certain coag factors (e.g. 9a, 10a, 11a, 2) Also impairs platelet function Warfarin: Block synthesis of Vit K dependent factors (2, 7, 9, 10)

20. Other Disorders Vitamin K deficiency Autoantibodies to coag factors Haemorrhagic disease of the newborn Massive transfusion

21. Investigations for Bleeding 1.Platelet Count 2.Bleeding time 3.Activated Partial Thromboplastin Time 4.Prothrombin Time (INR) 5.Plasma level assay

22. Investigations for Bleeding ConditionTest Wall DefectAll tests are normal. Low PlateletLow platelet count + bleeding time Platelet DysfNormal platelet count + bleeding time Haemophilia APPT + Plasma level vWD APPT + bleeding time + plasma level Liver Disease INR + APPT + platelet count Drug Induced INR + APPT + plasma level DICAll tests are abnormal.

23. Management 1.Replace deficiency 2.Treat underlying cause 3.Reversal of drug effects 4.Supportive therapy

24. Extra Notes on ITP Platelets become coated by autoantibodies Removed by RES  reduced lifespan Low platelet count Acute / Chronic Purpura / Spontaneous bleed / Asymptomatic May resolve spontaneously or require medical treatment

25. Extra Notes on ITP Isolated low platelet count < 20 Increased megakaryocytes in bone marrow Normal INR + APPT Increased bleeding time

26. Extra Notes on ITP Mx: 1.Do nothing 2.Prednisolone 3.Splenectomy 4.Other immunosuppresives

27. Extra Notes on IPT May be associated with: Haematological malignancies Viral infections (e.g. HIV) C.T. disorders (e.g. SLE)  Test for c.t. disorders.

28. 70-Year-Old with ITP Incidental finding in 1993 Platelet count = 60 Asymptomatic Referred to haematologist Test for c.t. disorders U/S for spleen size Bone marrow biopsy

29. 70-Year-Old with ITP Negative for c.t. disorders Spleen size normal Bone marrow: increased megakaryoccytes Continue monitoring (weekly FBC)

30. 70-Year-Old with ITP December 1993 Bruising with minimal trauma Platelet count = 43 Start Prednisolone After 6/52  platelet count 190 Slowly dropped again after withdrawal Asymptomatic

31. 70-Year-Old with ITP Continue monitoring Platelet transfusion if serious bleeding occurs Consider splenectomy if worsens Discharged to GP last week