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Dr Ambika Jawalkar
I. Platelet disorders
II. Coagulation disorders/defective
coagulation mechanism
III. Vascular disorders (Non-
thrombocytopenic purpura)
 Thrombocytopenic purpura – deficiency of
platelets
*essential / idiopathic(ITP)
*secondary
 Thrombasthenia – functional disorder of
platelets (defect in adhesion / aggregation)
eg: aspirin, large doses of penicillin, von
Willibrand’s disease
 Deficiency of clotting factors
* Hemophilia
 Vitamin K deficiency
 Anticoagulant overdose
 Disseminated intravascular clotting (DIC)
 Drug induced damage to capillary wall
 Deficiency of vitamin C – Scurvy
 Allergic purpura
 Infections
 Senile purpura
 Connective tissue diseases
 Group of bleeding disorders
 Characteristic features are,
*purple-colored petechial haemorrhages
*bruises in the skin
CAUSES:
1. Platelet disorders
Thrombocytopenic purpura – primary,
secondary
Thrombosthenic purpura – vWD
1. Vascular disorders – non-
thrombocytopenic purpura
“group of disorders occouring due to
heriditary deficiency of coagulation”
 Characterized by bleeding tendency &
increased clotting time.
 Hemoplilia A – 83% cases
* FactorVIII (Classic Hemophilia)
 Hemophilia B – 15% cases
* Factor IX (Christmas disease)
 Hemophilia C – 2% cases
* Factor XI (PTA deficiency)
TESTSTHAT DETECT
DEFECTS INTHP
 Bleeding time
 Capillary fragility test
 Platelet aggregation test
 Platelet adhesiveness test
TESTSTHAT DETECT
DEFECTS IN DHP
 Clotting time
 Prothrombin time
 Prothrombin
consumption time
 Partial thromboplastin
time (PTT)
 Activated partial
thromboplastin time
(aPTT)
 Thrombin time
 Clot retraction time
 Time lapse between the skin prick and
arrest of bleeding
 Estimated by Duke’s method & Ivy’s
method
 Normal values
by Duke’s method – 1-6 min.
by Ivy’s method – 3-6 min.
 BT is prolonged in Purpura & normal in
Hemophilia
 Time between skin prick & formation of
first fibrin thread
 Estimated by Capillary tube method & Lee-
White method
 Normal values
by capillary tube method is 3-6 min.
by lee-white method is 8-12 min.
 Prolonged in hemophila
 Quick’s one stage method
 Commercially available tissue
thromboplastin & CaCl2 is added to
oxalated or citrated plasma – incubated at
37oC
 Normal value is 11-16 sec.
 Extrinsic system is tested here.(no platelets
involved)
 Used to monitor anti-coagulant therapy
 Increased in liver failure, vit K deficiency
 Also known as KCCT – Kaolin cephalin
clotting time.
 Detects minute coagulation defects
 Normal is 40 sec.
 Measures intrinsic pathway
 Used to monitor Heparin therapy
 Is prolonged in Hemophilia, vWD
 Measures final step in coagulation i.e,
availability of functional fibrinogen
 Normal is 10 sec.
 Is prolonged in hypofibrinogenemia,
dysfibrinogenemia, DIC & hepain therapy.
 Measures time needed for contraction of an
undisturbed clot.
 Indicates function & number of platelets
 Normally begins within 2 hours and
completed within 24 hours
 Is retarded in thrombocytopenia
 Clot is small & soft in thromboasthenia

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Bleeding disorders

  • 2. I. Platelet disorders II. Coagulation disorders/defective coagulation mechanism III. Vascular disorders (Non- thrombocytopenic purpura)
  • 3.  Thrombocytopenic purpura – deficiency of platelets *essential / idiopathic(ITP) *secondary  Thrombasthenia – functional disorder of platelets (defect in adhesion / aggregation) eg: aspirin, large doses of penicillin, von Willibrand’s disease
  • 4.  Deficiency of clotting factors * Hemophilia  Vitamin K deficiency  Anticoagulant overdose  Disseminated intravascular clotting (DIC)
  • 5.  Drug induced damage to capillary wall  Deficiency of vitamin C – Scurvy  Allergic purpura  Infections  Senile purpura  Connective tissue diseases
  • 6.
  • 7.  Group of bleeding disorders  Characteristic features are, *purple-colored petechial haemorrhages *bruises in the skin
  • 8. CAUSES: 1. Platelet disorders Thrombocytopenic purpura – primary, secondary Thrombosthenic purpura – vWD 1. Vascular disorders – non- thrombocytopenic purpura
  • 9. “group of disorders occouring due to heriditary deficiency of coagulation”  Characterized by bleeding tendency & increased clotting time.  Hemoplilia A – 83% cases * FactorVIII (Classic Hemophilia)  Hemophilia B – 15% cases * Factor IX (Christmas disease)  Hemophilia C – 2% cases * Factor XI (PTA deficiency)
  • 10.
  • 11.
  • 12.
  • 13.
  • 14. TESTSTHAT DETECT DEFECTS INTHP  Bleeding time  Capillary fragility test  Platelet aggregation test  Platelet adhesiveness test TESTSTHAT DETECT DEFECTS IN DHP  Clotting time  Prothrombin time  Prothrombin consumption time  Partial thromboplastin time (PTT)  Activated partial thromboplastin time (aPTT)  Thrombin time  Clot retraction time
  • 15.  Time lapse between the skin prick and arrest of bleeding  Estimated by Duke’s method & Ivy’s method  Normal values by Duke’s method – 1-6 min. by Ivy’s method – 3-6 min.  BT is prolonged in Purpura & normal in Hemophilia
  • 16.  Time between skin prick & formation of first fibrin thread  Estimated by Capillary tube method & Lee- White method  Normal values by capillary tube method is 3-6 min. by lee-white method is 8-12 min.  Prolonged in hemophila
  • 17.  Quick’s one stage method  Commercially available tissue thromboplastin & CaCl2 is added to oxalated or citrated plasma – incubated at 37oC  Normal value is 11-16 sec.  Extrinsic system is tested here.(no platelets involved)  Used to monitor anti-coagulant therapy  Increased in liver failure, vit K deficiency
  • 18.  Also known as KCCT – Kaolin cephalin clotting time.  Detects minute coagulation defects  Normal is 40 sec.  Measures intrinsic pathway  Used to monitor Heparin therapy  Is prolonged in Hemophilia, vWD
  • 19.  Measures final step in coagulation i.e, availability of functional fibrinogen  Normal is 10 sec.  Is prolonged in hypofibrinogenemia, dysfibrinogenemia, DIC & hepain therapy.
  • 20.  Measures time needed for contraction of an undisturbed clot.  Indicates function & number of platelets  Normally begins within 2 hours and completed within 24 hours  Is retarded in thrombocytopenia  Clot is small & soft in thromboasthenia