用伊维菌素治疗控制盘尾丝虫病后的严重不良事件:对报告病例的回顾。

Nana AY Twum-Danso
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引用次数: 68

摘要

本文总结了1989年1月1日至2001年12月31日通过被动监测系统在盘尾丝虫病群体治疗方案中使用Mectizan(R)(伊维菌素,默克,夏普和多美)治疗后报告的严重不良事件(SAEs)病例。在本报告所述期间,报告的约1.65亿例治疗中,共报告了207例SAE病例,每80万例治疗中报告的SAE累计发生率为1例。平均年龄40岁,男性占70%。伊维菌素摄入和发病之间的平均时间为1天。对于57%的病例(n = 118),这是他们第一次接触伊维菌素。大多数病例报告来自喀麦隆(n = 176;85%),在1989-1991年和1994-1995年,当该计划扩大到ivermectin-naïve人口时,SAE的发病率达到高峰。喀麦隆55%的病例(即176例中有97例)为脑病,报告发生在该国中南部地区;这些病例中有三分之二是与伊维菌素治疗暂时相关的“可能”或“可能”罗阿罗阿脑病病例。报告偏倚可以解释34个盘尾丝虫病流行国家之间SAE报告的部分差异,但不是全部差异,这些国家有或曾经有过大规模治疗项目。需要进一步的研究来理解喀麦隆中南部脑病病例的明显聚集性,因为单独的L. loa感染可能不能解释该地区这种类型的SAE发病率增加的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Serious adverse events following treatment with ivermectin for onchocerciasis control: a review of reported cases.

Serious adverse events following treatment with ivermectin for onchocerciasis control: a review of reported cases.

Serious adverse events following treatment with ivermectin for onchocerciasis control: a review of reported cases.

Serious adverse events following treatment with ivermectin for onchocerciasis control: a review of reported cases.

This paper presents a summary of reported cases of Serious Adverse Events (SAEs) following treatment with Mectizan(R) (ivermectin, Merck, Sharpe & Dohme) in onchocerciasis mass treatment programs from January 1, 1989 to December 31, 2001 through a passive surveillance system. A total of 207 SAE cases were reported out of approximately 165 million reported treatments delivered during the period under review, giving rise to a cumulative incidence of 1 reported SAE per 800,000 reported treatments. The mean age was 40 years and 70% of the cases were males. The mean time between ivermectin intake and onset of illness was 1 day. For 57% of the cases (n = 118), that was their first exposure to ivermectin. The majority of cases were reported from Cameroon (n = 176; 85%) with peaks in the incidence of SAE reporting in 1989-1991 and 1994-1995 when the program expanded to ivermectin-naïve populations. Fifty-five percent of the cases from Cameroon (i.e. 97 out of 176 cases) were encephalopathic and were reported from the central-southern region of the country; two-thirds of these cases were 'probable' or 'possible' cases of Loa loa encephalopathy temporally related to ivermectin treatment. Reporting bias may explain some but not all of the differences in SAE reporting between the 34 onchocerciasis-endemic countries that have, or have had, mass treatment programs. Further research is needed to understand the apparent clustering of encephalopathy cases in central-southern Cameroon since L. loa infection alone probably does not explain the increased incidence of this type of SAE from this region.

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