TY - JOUR KW - Adolescent KW - Adult KW - Aged KW - Child KW - Clinical Trials as Topic KW - Dapsone KW - Drug Therapy, Combination KW - Female KW - Humans KW - leprosy KW - Male KW - Methods KW - Middle Aged KW - Random Allocation KW - Rifampin AU - Yawalkar S J AU - McDougall A C AU - Languillon J AU - Ghosh S AU - Hajra S K AU - Opromolla D V AU - Tonello C J AB -

In an international multicentre controlled single-blind trial of 93 previously untreated lepromatous leprosy patients the therapeutic effects of adding rifampicin, 450 mg/day orally or 1,200 mg once monthly in a single oral dose, to dapsone (50 mg/day orally) for the first 6 months of treatment were compared. Clinical and histopathological improvements and bacteriological regression, indicated by the decreases in the bacterial and morphological indices of the skin and nose-blow smears, were satisfactory and practically identical after 6 months' treatment. The once-monthly rifampicin schedule was better tolerated than the daily one. In view of the good therapeutic efficacy and tolerability, the much lower cost of treatment (about one-tenth of that of the daily rifampicin regimen) and the possibility of administration under supervision, once-monthly rifampicin given in a single oral 1,200 mg dose should be recommended, along with a standard dapsone regimen, for large-scale, initial, and intensive combination treatment of patients with lepromatous and borderline-lepromatous leprosy, to help prevent an increase in dapsone resistance. A third antileprosy drug (e.g., clofazimine) may be added to this initial dual-treatment regimen.

BT - Lancet (London, England) C1 - http://www.ncbi.nlm.nih.gov/pubmed/6122970?dopt=Abstract DA - 1982 May 29 DO - 10.1016/s0140-6736(82)92334-0 IS - 8283 J2 - Lancet LA - eng N2 -

In an international multicentre controlled single-blind trial of 93 previously untreated lepromatous leprosy patients the therapeutic effects of adding rifampicin, 450 mg/day orally or 1,200 mg once monthly in a single oral dose, to dapsone (50 mg/day orally) for the first 6 months of treatment were compared. Clinical and histopathological improvements and bacteriological regression, indicated by the decreases in the bacterial and morphological indices of the skin and nose-blow smears, were satisfactory and practically identical after 6 months' treatment. The once-monthly rifampicin schedule was better tolerated than the daily one. In view of the good therapeutic efficacy and tolerability, the much lower cost of treatment (about one-tenth of that of the daily rifampicin regimen) and the possibility of administration under supervision, once-monthly rifampicin given in a single oral 1,200 mg dose should be recommended, along with a standard dapsone regimen, for large-scale, initial, and intensive combination treatment of patients with lepromatous and borderline-lepromatous leprosy, to help prevent an increase in dapsone resistance. A third antileprosy drug (e.g., clofazimine) may be added to this initial dual-treatment regimen.

PY - 1982 SP - 1199 EP - 202 T2 - Lancet (London, England) TI - Once-monthly rifampicin plus daily dapsone in initial treatment of lepromatous leprosy. VL - 1 SN - 0140-6736 ER -