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Haemostasis
haemostasis is a process to prevent and
stop bleeding, meaning to keep blood
within a damaged blood vessel.
Stages
1. Vasoconstriction
2.primary haemostasis
Haemostasis Pathway
Injury
Primary haemostasis sec: haemostasis
Collagen exposure
Platelet adhesion Coagulation Cascade
Release reaction
Platelet aggregation Fibrin
Primary haemo: plug Sec: Haemo: Plug
Integrity of Haemostasis
Depends on:
1. Vessel wall
2. Platelets (no. and function)
3. Coagulation factors
Primary haemostasis
Vessel Wall
• Release tissue factor that initiates
coagulation cascade.
• Exposed collagen results in platelet
adhesion (using vWF as a bridge).
• That leads to platelet plug formation and
stop the bleeding temporarily
Thrombocytopenia
Causes
Low production of platelets (aplastic)
increase consumption of Platelets(DIC)
Increase destruction of platelets(ITP,
TTP)
Low Platelet production
• N = 150 – 450k
• Excessive bleed / Spontaneous bleed(nose, mouth
andsmall cut bleeding)
• Mucosal surfaces / Skin (petechiae & ecchymosis)
• Immune Mediated Thrombocytopenia
• Drug induced(chloramphenicol)
• Haemolytic Uraemic Syndrome
Platelet Dysfunction
• Abnormal platelet aggregation
• Normal platelet count
• Excessive / spontaneous bleed
• Mucosa / Skin
• Inherited disorders
• Drug induced
Secondary
haemostasis
Coagulation cascade begins
Eccymoses
Coagulation Factors Deficiency
• Spontaneous bleeding into deep tissues
• Increased post-traumatic haemorrhage
• Factor 8 – Haemophilia A
• Factor 7 – 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.
Haemoarthroses
Other causes of
factors Def:
Liver Disease
• Mixed – both coag deficiency and platelet
problem
• Reduced coag factor synthesis
(1, 2, 5, 7, 9, 10)
• Cirrhosis  Hypersplenism 
Thrombocytopenia
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)
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
DIC
Consequence of Thrombosis:
1. Tissue infarction  Renal impairment
2. CVA
3. PE
4. DVT
5. Consequence of Bleeding:
6. Purpura
7. GI Bleed
Other Disorders
• Vitamin K deficiency
• Autoantibodies to coag factors
• Haemorrhagic disease of the newborn
• Massive transfusion
Question
Which one of them is due to
thrombocytopenia and which from
coagulation disorder?
PT/iNR. aPTT.
Extrinsic pathway. Intrinsic pathway
FACTOR vii. FACTOR VIII
Common pathway. Common pathway
Factor I,ii,v,x. Factor I,ki,v,x
Warfarin. Heparin
Normal range
PT =8.4 - 13.0 sec
APTT= 23-31.4 sec
INR =0.8 - 1.2 sec
Platelets =150 -450k
Fibrinogen= 130- 330 mg/dl
Bleeding time= 2- 6 mints
Clotting time=2- 8 mints
Investigations for Bleeding
Condition Test
Wall Defect All tests are normal.
Low Platelet Low platelet count + bleeding time
Platelet Dysf Normal platelet count + bleeding time
Haemophilia APPT
vWD APPT + bleeding time
Liver Disease INR + APPT + platelet count
Drug Induced INR + APPT + plasma level
DIC All tests are abnormal.
Thank you All

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Stop Bleeding Process

  • 1. Haemostasis haemostasis is a process to prevent and stop bleeding, meaning to keep blood within a damaged blood vessel. Stages 1. Vasoconstriction 2.primary haemostasis
  • 2. Haemostasis Pathway Injury Primary haemostasis sec: haemostasis Collagen exposure Platelet adhesion Coagulation Cascade Release reaction Platelet aggregation Fibrin Primary haemo: plug Sec: Haemo: Plug
  • 3. 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). • That leads to platelet plug formation and stop the bleeding temporarily
  • 6. Thrombocytopenia Causes Low production of platelets (aplastic) increase consumption of Platelets(DIC) Increase destruction of platelets(ITP, TTP)
  • 7. Low Platelet production • N = 150 – 450k • Excessive bleed / Spontaneous bleed(nose, mouth andsmall cut bleeding) • Mucosal surfaces / Skin (petechiae & ecchymosis) • Immune Mediated Thrombocytopenia • Drug induced(chloramphenicol) • Haemolytic Uraemic Syndrome
  • 8. Platelet Dysfunction • Abnormal platelet aggregation • Normal platelet count • Excessive / spontaneous bleed • Mucosa / Skin • Inherited disorders • Drug induced
  • 11.
  • 12. Coagulation Factors Deficiency • Spontaneous bleeding into deep tissues • Increased post-traumatic haemorrhage • Factor 8 – Haemophilia A • Factor 7 – 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.
  • 15. Liver Disease • Mixed – both coag deficiency and platelet problem • Reduced coag factor synthesis (1, 2, 5, 7, 9, 10) • Cirrhosis  Hypersplenism  Thrombocytopenia
  • 16.
  • 17. 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)
  • 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. DIC Consequence of Thrombosis: 1. Tissue infarction  Renal impairment 2. CVA 3. PE 4. DVT 5. Consequence of Bleeding: 6. Purpura 7. GI Bleed
  • 20. Other Disorders • Vitamin K deficiency • Autoantibodies to coag factors • Haemorrhagic disease of the newborn • Massive transfusion
  • 21.
  • 22.
  • 23.
  • 24.
  • 25.
  • 26. Question Which one of them is due to thrombocytopenia and which from coagulation disorder?
  • 27.
  • 28.
  • 29.
  • 30. PT/iNR. aPTT. Extrinsic pathway. Intrinsic pathway FACTOR vii. FACTOR VIII Common pathway. Common pathway Factor I,ii,v,x. Factor I,ki,v,x Warfarin. Heparin
  • 31. Normal range PT =8.4 - 13.0 sec APTT= 23-31.4 sec INR =0.8 - 1.2 sec Platelets =150 -450k Fibrinogen= 130- 330 mg/dl Bleeding time= 2- 6 mints Clotting time=2- 8 mints
  • 32.
  • 33. Investigations for Bleeding Condition Test Wall Defect All tests are normal. Low Platelet Low platelet count + bleeding time Platelet Dysf Normal platelet count + bleeding time Haemophilia APPT vWD APPT + bleeding time Liver Disease INR + APPT + platelet count Drug Induced INR + APPT + plasma level DIC All tests are abnormal.
  • 34.
  • 35.
  • 36.
  • 37.