单剂量伊维菌素、乙基卡马嗪和阿苯达唑治疗Côte科特迪瓦淋巴丝虫病的疗效和安全性:一项开放标签随机对照试验

Catherine M Bjerum, Allassane F Ouattara, Méité Aboulaye, Olivier Kouadio, Vanga K Marius, Britt J Andersen, Gary J Weil, Benjamin G Koudou, Christopher L King
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引用次数: 0

摘要

背景:需要改进药物方案来加速非洲淋巴丝虫病的消除。本研究确定了伊维菌素+乙基卡马嗪+阿苯达唑(IDA)单次联合给药是否不劣于非洲许多lf流行地区使用的伊维菌素+阿苯达唑(IA)标准3年剂量。方法:在一项开放标签、单盲试验中,在Côte科特迪瓦接受治疗的未接受治疗的成人班氏乌chereria微丝虫病患者随机接受单剂量IDA (n = 43)或3年剂量IA (n = 52)。主要终点是36个月时微丝蚴(Mf)阴性的参与者比例。次要终点是6个月、12个月和24个月的Mf清除率;灭活成虫巢;和安全。结果IDA治疗后36个月,18/33 (55%;95% CI, 38-72%)与33/42 (79%;67-91%)合并IA (P = 0.045)。在6个月和12个月时,IDA在清除Mf方面分别优于IA(89%[77-99%]和71%[56-85%]),而IA分别为34%(20-48%)和26% (14-42%)(P < .001)。24个月时IDA与IA相当(61% [45-77%]vs 54% [38-72%];P = .53)。在各时间点,IDA对成虫的灭活效果均优于IA。两种治疗均耐受良好,无严重不良事件发生。结论单剂量IDA在减少24个月的总体Mf负担方面优于2剂量IA。再感染可能是IDA对Mf缺乏持续清除的原因。临床试验注册NCT02974049。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and Safety of a Single Dose of Ivermectin, Diethylcarbamazine, and Albendazole for Treatment of Lymphatic Filariasis in Côte d'Ivoire: An Open-label Randomized Controlled Trial.

Background: Improved drug regimens are needed to accelerate elimination of lymphatic filariasis in Africa. This study determined whether a single co-administered dose of ivermectin plus diethylcarbamazine plus albendazole [IDA] is noninferior to standard 3 annual doses of ivermectin plus albendazole (IA) used in many LF-endemic areas of Africa.

Methods: Treatment-naive adults with Wuchereria bancrofti microfilaremia in Côte d'Ivoire were randomized to receive a single dose of IDA (n = 43) or 3 annual doses of IA (n = 52) in an open-label, single-blinded trial. The primary endpoint was the proportion of participants who were microfilaria (Mf) negative at 36 months. Secondary endpoints were Mf clearance at 6, 12, and 24 months; inactivation of adult worm nests; and safety.

Results: At 36 months posttreatment with IDA, 18/33 (55%; 95% CI, 38-72%) cleared Mf versus 33/42 (79%; 67-91%) with IA (P = .045). At 6 and 12 months IDA was superior to IA in clearing Mf (89% [77-99%] and 71% [56-85%]), respectively, versus 34% (20-48%) and 26% (14-42%) (P < .001). IDA was equivalent to IA at 24 months (61% [45-77%] vs 54% [38-72%]; P = .53). IDA was superior to IA for inactivating adult worms at all time points. Both treatments were well tolerated, and there were no serious adverse events.

Conclusions: A single dose of IDA was superior to 2 doses of IA in reducing the overall Mf burden by 24 months. Reinfection may have contributed to the lack of sustained clearance of Mf with IDA.

Clinical trials registration: NCT02974049.

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