治疗合并感染的班氏丝虫病和盘尾丝虫病:阿苯达唑与伊维菌素治疗单独感染班氏丝虫病的安全性和有效性研究

William H Makunde, Leo M Kamugisha, Julius J Massaga, Rachel W Makunde, Zakana X Savael, Juma Akida, Fred M Salum, Mark J Taylor
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引用次数: 35

摘要

背景:为了联合使用伊维菌素和阿苯达唑消除淋巴丝虫病,评估同时感染淋巴丝虫病和盘尾丝虫病的个体不良事件增加的潜在风险是很重要的。比较阿苯达唑(400 mg)联合伊维菌素(150微克/kg)治疗班氏乌氏菌和盘尾丝虫病合并感染与单例班氏乌氏菌感染的安全性和有效性。方法:合并感染的安全性研究采用交叉、双盲设计,单独感染班氏丝虫病的安全性研究采用两种治疗方法比较的开放设计。对于合并感染,一组给予单剂量伊维菌素(150微克/千克)加阿苯达唑(400毫克)(a组),另一组给予安慰剂(B组)。5天后,治疗方案逆转,a组接受安慰剂,B组接受治疗。对于单次班氏丝虫病感染,一组给予单剂量阿苯达唑(400 mg)加伊维菌素(150 μ g/kg) (C组),另一组给予单剂量阿苯达唑(400 mg) (D组)。在入院第1天、第0天、第2、3、7天采集血液和皮肤标本,评估药物的安全性和有效性。随访12个月,采集血液和皮肤标本,评估药物疗效。在治疗后的前48小时内,每6小时对研究个体进行临床监测,并在住院期间和随访期间进行常规临床检查。结果:在同时感染班氏丝虫病和盘尾丝虫病的患者中,伊维菌素和阿苯达唑治疗是安全且耐受的。两组间生理指标差异无统计学意义(p < 0.05)。合并感染个体的不良事件发生率为63% (5/8,A组,阿苯达唑+伊维菌素)和57% (4/7,B组,安慰剂),为轻或中度强度。单次bancrofti感染的不良事件发生率为50% (6/12,C组,阿苯达唑+伊维菌素)和38% (5/13,D组,阿苯达唑),其发生率与合并感染的发生率相似。治疗组间不良事件发生率无差异。阿苯达唑和伊维菌素治疗后微丝虫病的减少在单一感染组和合并感染组之间没有显著差异。结论:伊维菌素联合阿苯达唑治疗盘尾丝虫病合并感染是一种安全、耐受的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Treatment of co-infection with bancroftian filariasis and onchocerciasis: a safety and efficacy study of albendazole with ivermectin compared to treatment of single infection with bancroftian filariasis.

Treatment of co-infection with bancroftian filariasis and onchocerciasis: a safety and efficacy study of albendazole with ivermectin compared to treatment of single infection with bancroftian filariasis.

Treatment of co-infection with bancroftian filariasis and onchocerciasis: a safety and efficacy study of albendazole with ivermectin compared to treatment of single infection with bancroftian filariasis.

Treatment of co-infection with bancroftian filariasis and onchocerciasis: a safety and efficacy study of albendazole with ivermectin compared to treatment of single infection with bancroftian filariasis.

BACKGROUND: In order to use a combination of ivermectin and albendazole for the elimination of lymphatic filariasis, it is important to assess the potential risk of increased adverse events in individuals infected with both lymphatic filariasis and onchocerciasis. We compared the safety and efficacy of albendazole (400 mg) in combination with ivermectin (150 micrograms/kg), for the treatment of co-infections of Wuchereria bancrofti and Onchocerca volvulus with single infection of W. bancrofti. METHODS: The safety study on co-infections was a crossover, double blind design, while for the single infection of bancroftian filariasis an open design comparing two treatments was used. For co-infection, one group was allocated a single dose of ivermectin (150 micrograms/kg) plus albendazole (400 mg) (Group A). The other group received placebo (Group B). Five days later the treatment regime was reversed, with the Group A receiving placebo and Group B receiving treatment. For the single bancroftian filariasis infection, one group received a single dose of albendazole (400 mg) plus ivermectin (150 microg/kg) (Group C) while the other group received a single dose of albendazole (400 mg) alone (Group D). Blood and skin specimens were collected on admission day, day 0, and on days 2, 3, and 7 to assess drug safety and efficacy. Thereafter, blood and skin specimens were collected during the 12 months follow up for the assessment of drug efficacy. Study individuals were clinically monitored every six hours during the first 48 hours following treatment, and routine clinical examinations were performed during the hospitalisation period and follow-up. RESULTS: In individuals co-infected with bancroftian filariasis and onchocerciasis, treatment with ivermectin and albendazole was safe and tolerable. Physiological indices showed no differences between groups with co-infection (W. bancrofti and O. volvulus) or single infection (W. bancrofti). The frequency of adverse events in co-infected individuals was 63% (5/8, Group A, albendazole + ivermectin) and 57% (4/7, Group B, placebo) and of mild or moderate intensity. In single W. bancrofti infection the frequency of adverse events was 50% (6/12, Group C, albendazole + ivermectin) and 38% (5/13, Group D, albendazole) and of a similar intensity to those experienced with co-infection. There were no differences in adverse events between treatment groups. There was no significant difference in the reduction of microfilaraemia following treatment with albendazole and ivermectin in groups with single or co-infection. CONCLUSION: Our findings suggest that ivermectin plus albendazole is a safe and tolerable treatment for co-infection of bancroftian filariasis and onchocerciasis.

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