CTBT
CTBT
CTBT
Hemostasis or
haemostasis
Is
constrict.
Platelet plug formation - Platelets
adhere to damaged endothelium to form
platelet plug (primary hemostasis) and
then degranulate.
Blood coagulation - Clots form upon the
conversion of fibrinogen to fibrin, and its
addition to the platelet plug (secondary
hemostasis).
EXTRINSC
Tisue Thromboplastin
XII
XI
IX
VIII
VII
X
FIBRINOGEN
(I)
V
PROTHROMBIN
(II)
THROMBIN
(III)
FIBRIN
FIBRINOLYTIC PHASE
ANTICLOTTING
MECHANISMS ARE
ACTIVATED TO ALLOW CLOT
DISINTEGRATION AND REPAIR OF THE
DAMAGED VESSEL.
HEMOSTASIS
DEPENDENT
UPON:
VESSEL DEFECTS
PLATELET DISORDERS
FACTOR DEFICIENCIES
VESSEL DEFECTS
VITAMIN C DEFICIENCY
BACTERIAL & VIRAL INFECTIONS
ACQUIRED
PLATELET DISORDERS
THROMBOCYTOPENIA
(INADEQUATE NUMBER OF PLATELETS)
Causes
DRUG INDUCED
BONE MARROW FAILURE
HYPERSPLENISM
OTHER CAUSES
THROMBOCYTOPATHY
)ADEQUATE NUMBER BUT ABNORMAL
FUNCTION .(
causes
UREMIA
INHERITED DISORDERS
MYELOPROLIFERATIVE DISORDERS
DRUG INDUCED(ASPIRIN,
NSAIDS)
FACTOR DEFICIENCIES
Inherited:
1.
HEMOPHILIA A
2.
HEMOPHILIA B
3.
VON WILLEBRANDS
DISEASE
Acquired:
1.
Anticoagulant
therapy
2.
Liver diseases
3.
DIC
LABORATORY EVALUATION
PLATELET
COUNT
BLEEDING TIME (BT)
Clotting time (CT)
PROTHROMBIN TIME (PT)
Activated PARTIAL THROMBOPLASTIN
TIME (APTT)
100,000 - 400,000
CELLS/MM3
Thrombocytopenia
100,000>
BLEEDING TIME
PROVIDES ASSESSMENT OF
NORMAL VALUE
2-8 MINUTES
Material
1.
2.
3.
4.
5.
6.
PROTHROMBIN TIME
Measures Effectiveness of the Extrinsic
Pathway
NORMAL VALUE
10-15 SECS
PT
The prothrombin time: is therefore the time required for the plasma
to clot after an excess of thromboplastin and an optimal
concentration of calcium have been added.
EXTRINSC
Tisue Thromboplastin
XII
XI
IX
VIII
VII
X
FIBRINOGEN
(I)
V
PROTHROMBIN
(II)
THROMBIN
(III)
FIBRIN
?When is it ordered
Vitamin K deficiency
DIC
liver disease
a deficiency in one or more of the following factors:
I, II, V, VII, X.
Anticoagulant (warfarin)
INR
NORMAL VALUE
25-40 SECS
PTT
EXTRINSC
Tisue Thromboplastin
XII
XI
IX
VIII
VII
X
FIBRINOGEN
(I)
V
PROTHROMBIN
(II)
THROMBIN
(III)
FIBRIN
Normal
?When is it ordered
use of heparin.
e.g hemophilia
DIC
Liver disease
EXTRINSC
Tisue Thromboplastin
XII
XI
IX
VIII
VII
X
FIBRINOGEN
(I)
V
PROTHROMBIN
(II)
THROMBIN
(III)
FIBRIN
FACTOR DEFICIENCIES
Inherited:
1.
Acquired:
1.
Anticoagulant
therapy
2.
Liver diseases
3.
DIC
HEMOPHILIA A
2.
HEMOPHILIA B
3.
VON
WILLEBRANDS
DISEASE
HEMOPHILIA
10-15%
B (Christmas Disease)
of all Hemophiliacs
Deficiency of Factor IX
Lab Test - Prolonged PTT
VON
WILLEBRANDS DISEASE
Deficiency
ANTICOAGULANTS
1.
2.
ANTICOAGULANTS
Coumadins
Heparin
Liver Disease
DIC
Condition
Prothrombi
n
time
Partial
thromboplastin
time
Bleeding
time
Platelet
count
unaffected
prolonged
prolonged
unaffected
Vitamin K deficiency or
Warfarin
prolonged
prolonged
unaffected unaffected
Uremia
unaffected
unaffected
prolonged
Haemophilia
unaffected
prolonged
unaffected unaffected
Factor V deficiency
prolonged
prolonged
unaffected unaffected
Aspirin
unaffected
unaffected
prolonged
unaffected
Thrombocytopenia
unaffected
unaffected
prolonged
decreased
prolonged
prolonged
prolonged
decreased
Disseminated intravascular
coagulation
prolonged
prolonged
prolonged
decreased
Bernard-Soulier syndrome
unaffected
unaffected
prolonged
decreased
unaffected
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