Shenoy R K, Kumaraswami V, Rajan K, Thankom S
T.D. Medical College Hospital, Alleppey, Kerala, India.
Ann Trop Med Parasitol. 1993 Oct;87(5):459-67. doi: 10.1080/00034983.1993.11812796.
The use of ivermectin in lymphatic filariasis (both bancroftian and brugian) has been recently explored in several studies. We report in this paper, for the first time, a direct comparison of the efficacy and tolerability of single doses of ivermectin and diethylcarbamazine (DEC) in brugian filariasis. We also present our findings on the use of split doses of ivermectin and DEC on microfilaraemia levels and the occurrence of adverse reactions. Fifty male, asymptomatic microfilaremics drawn from the Alleppey District, Kerala, India, were allocated one of the following five treatment regimens in a double blind randomized study: (1) single oral 6 mg/kg dose of DEC; (2) single oral 6 mg/kg dose of DEC preceded by 1 mg/kg DEC primer; (3) single oral 220 micrograms/kg dose of ivermectin; (4) single oral 200 micrograms/kg dose of ivermectin preceded by a 20 micrograms/kg ivermectin primer; or (5) a single oral 400 micrograms/kg dose of ivermectin preceded by a 20 micrograms/kg ivermectin primer. The kinetics of microfilaria clearance differed in the two (DEC/ivermectin) groups in the first month post-treatment. At the end of 1 year there were no differences in the microfilaria levels in the two DEC-tested groups and the 420 micrograms/kg ivermectin group. The safety of the 400 micrograms/kg dose of ivermectin was established in this study which has also shown that, currently, this dose would be the best choice for brugian filariasis. Patients in the ivermectin groups had significantly lower adverse reaction scores than patients who had received DEC. There was no advantage in splitting the dose of either DEC or ivermectin, either in terms of efficacy or tolerability.(ABSTRACT TRUNCATED AT 250 WORDS)
近期多项研究探讨了伊维菌素在淋巴丝虫病(班氏丝虫病和布鲁氏丝虫病)中的应用。本文首次报告了单剂量伊维菌素与乙胺嗪(DEC)治疗布鲁氏丝虫病的疗效和耐受性的直接比较。我们还展示了关于分剂量使用伊维菌素和DEC对微丝蚴血症水平及不良反应发生情况的研究结果。在印度喀拉拉邦阿勒皮地区选取了50名无症状男性微丝蚴血症患者,在一项双盲随机研究中分配至以下五种治疗方案之一:(1)口服单剂量6mg/kg的DEC;(2)口服单剂量6mg/kg的DEC,之前先服用1mg/kg的DEC引物;(3)口服单剂量220μg/kg的伊维菌素;(4)口服单剂量200μg/kg的伊维菌素,之前先服用20μg/kg的伊维菌素引物;或(5)口服单剂量400μg/kg的伊维菌素,之前先服用20μg/kg的伊维菌素引物。治疗后第一个月,两组(DEC/伊维菌素)微丝蚴清除动力学有所不同。1年末,两个DEC测试组和420μg/kg伊维菌素组的微丝蚴水平无差异。本研究证实了400μg/kg剂量伊维菌素的安全性,还表明目前该剂量是治疗布鲁氏丝虫病的最佳选择。伊维菌素组患者的不良反应评分显著低于接受DEC治疗的患者。无论是DEC还是伊维菌素,分剂量在疗效或耐受性方面均无优势。(摘要截选至250词)