LOW-INTENSITY ORAL ANTICOAGULATION IN SICKLE-CELL DISEASE REVERSES THE PRETHROMBOTIC STATE - PROMISES FOR TREATMENT

Increased plasma levels of prothrombin fragment 1 + 2 (F1 + 2) found in patients with sickle-cell disease reflect enhanced endogenous thrombin generation, We postulate that hypercoagulability contributes to vaso-occlusion. The intensity of acenocoumarol treatment required to reduce the F1 + 2 level to 50% of pretreatment level was investigated in seven patients with symptomatic sickle-cell anaemia during steady-state disease for a period of 2 months, All patients had increased levels of F1 + 2 compared with an age-matched control group. Normalization of the F1 + 2 was achieved at a median INR of 1 . 64 (range 1 . 18-2 . 2). it is concluded that low-intensity oral anticoagulation normalizes the hypercoagulability in sickle-cell disease.