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Hand <strong>book</strong> <strong>for</strong> <strong>dental</strong> <strong>surgeons</strong> on <strong>dental</strong> management of persons with hemophilia and other haemostatic disorders<br />

HAEMATOLOGY AND HAEMOSTATIC DISORDERS<br />

Normal platelet count is 150000-450000 platelets per microlitre of blood. Symptoms do not arise and<br />

bleeding time remains normal until it is greater than 100000/micro litre. Mild prolongation bleeding time<br />

occurs when it is between 50000-100000/micro litre. Easy bruising manifested by skin purpura occurs after<br />

minor trauma and bleeding after mucous membrane surgery occurs when it is less than 50000/micro litre<br />

Spontaneous bleeding occurs when its value is less than 20000/micro litre. When qualitative platelet<br />

abnormality is present then there is normal platelet count and prolonged bleeding time. Bleeding time over 10<br />

minutes has increased risk of bleeding. Extensive bleeding occurs when bleeding time is greater than 15-20min.<br />

Due to cyclical variation level of V Wb factor occasionally bleeding time may be normal so repeated testing<br />

may be necessary to establish diagnosis.<br />

Plasma coagulation function is readily assessed by partial thromboplastin time (PTT). Prothrombin time<br />

(PT), thrombin time, clot solubility test and clot lyses test.<br />

When there is prolonged partial thromboplastin time ( normal is 25-35 seconds) and no clinical bleeding,<br />

then one could suspect deficiency of factor 12, HMWK, PK. When it is associated, with mild or rare bleeding<br />

then factor 11 deficiency might be present and when there is frequent severe bleeding then deficiency of factor<br />

8 & 9 should be suspected. Prolonged prothrombin time (normal is 10-15 sec) indicates deficiency of factor 7,<br />

vitamin k (early) or warfarin ingestion. When PT & PTT both are prolonged, it indicates deficiency of factor 2,<br />

5 & 10, vitamin k (late) or warfarin ingestion.<br />

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Hand <strong>book</strong> <strong>for</strong> <strong>dental</strong> <strong>surgeons</strong> on <strong>dental</strong> management of persons with hemophilia and other haemostatic disorders

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