Comparison of the efficacy and safety of 12-month low-dose factor VIII tertiary prophylaxis vs on-demand treatment in severe haemophilia A children.

Abstract

Prophylaxis has commonly become standard treatment for severe haemophilia patients. The World Federation of Hemophilia (WFH) recommends low-dose prophylaxis in countries with resource constraints. To determine efficacy and safety of low-dose factor VIII (FVIII) tertiary prophylaxis compared to on-demand treatment in severe haemophilia A children in Indonesia. Eligible patients were randomly assigned to prophylaxis and on-demand groups. Patients in the prophylaxis group received infusion of FVIII 10IU/kg body weight, two times per week. Primary outcomes were the numbers of joint bleeding and total bleeding episodes; secondary outcomes were evidence of FVIII inhibitor, Hemophilia Joint Health Score (HJHS) and Hemophilia Early Arthropathy Detection Ultrasound (HEAD-US) score. Patients were monitored for 12months. Fifty patients, all with tertiary prophylaxis, 4-18years of age, were randomized into prophylaxis (n=25) and on-demand (n=25) groups. The mean follow-up time was 12.8±0.86 vs 12.3±0.54months, respectively. Numbers of total and joint bleeding episodes were significantly lower in the prophylaxis group (P<0.001, 95% CI -24.6;-10.7 and P<0.001, 95% CI -14;-3, respectively). The prophylaxis group showed improvement of joint function (P=0.004; CI 95% -3;-0.5); on the contrary, we found deterioration in the on-demand group (P=0.001; CI 95% 1;3). HEAD-US scores showed improvement at month 6 in the prophylaxis group, but there was no significant difference between groups at month 12. Low-dose FVIII tertiary prophylaxis was effective in reducing joint bleeding episodes and improvement of HJHS compared to on-demand FVIII treatment in severe haemophilia A children.