Shaw Isaac Neeraj, Christian M, Jesudasan K, Kurian Nisha, Rao Geetha S
Schieffelin Leprosy Research & Training Centre, Karigiri, India.
Lepr Rev. 2003 Jun;74(2):141-7.
The World Health Organization (WHO) Field Trials of multidrug therapy (MDT) started at Schieffelin Leprosy Research and Training Centre (SLR & IC), Karigiri, India in December 1981. The patients were treated with two MDT regimens. The first (regimen A) consisted of 600mg rifampicin and 300mg of clofazimine given under supervision on 2 consecutive days monthly, 225mg injection of acedapsone bimonthly and dapsone 100mg daily. The second regimen (regimen B) was the conventional MDT (WHO/MDT), rifampicin 600mg and clofazimine 300mg supervised once a month, dapsone 100mg and clofazimine 50mg daily, unsupervised. Both the regimens were administered for a minimum period of 2 years or until skin smear negativity, whichever occurred later. Thirty-four newly detected previously untreated MB patients, 16 of whom received regimen A and 18 regimen B, were reassessed. Both regimens were well accepted and well tolerated by the patients. Clofazimine discolouration was the only adverse effect of MDT seen in these patients. After completion of treatment with MDT, the patients were followed up for a total duration of 466 person-years with a mean of 13.7 +/- 1.4 years per patient. No relapse was seen.
1981年12月,世界卫生组织(WHO)在印度卡里吉里的谢弗林麻风病研究与培训中心(SLR & IC)启动了多药联合疗法(MDT)的现场试验。患者接受了两种MDT方案治疗。第一种(方案A)包括每月连续2天在监督下给予600毫克利福平、300毫克氯法齐明,每两个月注射225毫克氨苯砜,以及每日100毫克氨苯砜。第二种方案(方案B)是传统的MDT(WHO/MDT),每月监督一次给予600毫克利福平、300毫克氯法齐明,每日100毫克氨苯砜和50毫克氯法齐明,无需监督。两种方案均至少给药2年或直至皮肤涂片转阴,以较晚发生者为准。对34例新发现的既往未治疗的多菌型患者进行了重新评估,其中16例接受方案A,18例接受方案B。两种方案患者均能很好地接受且耐受性良好。氯法齐明变色是这些患者中观察到的MDT唯一不良反应。MDT治疗完成后,对患者进行了总计466人年的随访,平均每位患者随访13.7±1.4年。未观察到复发情况。