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苯硝唑治疗慢性恰加斯病的安全性概况:一家转诊中心的经验和系统文献综述与荟萃分析。

Safety Profile of Benznidazole in the Treatment of Chronic Chagas Disease: Experience of a Referral Centre and Systematic Literature Review with Meta-Analysis.

机构信息

National Referral Unit for Tropical and Travel Medicine, Department of Internal Medicine, Hospital Universitario La Paz-Carlos III, IdiPAZ, Madrid, Spain.

Division of Infectious Diseases, University of Messina, Polyclinic "G. Martino", Messina, Italy.

出版信息

Drug Saf. 2018 Nov;41(11):1035-1048. doi: 10.1007/s40264-018-0696-5.

Abstract

INTRODUCTION

Benznidazole is the preferred drug for treatment of Chagas disease. However, it is toxic and of limited value in chronic infection.

OBJECTIVE

We aimed to estimate the rates of and factors related to adverse reactions (ARs) to benznidazole and treatment discontinuations (TDs).

METHODS

A meta-analysis was performed using an electronic search of the published literature with no language restrictions until June 2017. Prospective studies were included of chronically infected patients in which at least one treatment arm included benznidazole. Data were added from a prospective cohort of patients with Chagas disease at our centre (January 2007-June 2017). Weighted rates of ARs and TDs were estimated, and potentially related factors were analysed.

RESULTS

Some 413 studies were found, from which we chose 42 (nine clinical trials and 33 observational studies, including ours), comprising data for 7822 patients. The weighted rate of ARs to benznidazole was 44.1% (95% confidence interval [CI] 37.2-51.2). ARs were more frequent in adults than in children (51.6 vs. 24.5%), with the most common being skin reactions (34%), gastrointestinal complaints (12.6%) and neurological symptoms (11.5%). Grade 4 ARs were recorded in 3% of cases. The weighted rate of TDs was 11.4% (95% CI 8.5-14.5); TDs were more frequent in adults than in children (14.2 vs. 3.8%). In our cohort, only female sex was related to an increased rate of ARs but not to TDs.

CONCLUSION

Benznidazole had a poor tolerability profile, with a high incidence of TDs, especially in adult patients and women. Optimised dosing schedules and/or new drugs are urgently needed.

摘要

简介

苯唑硝唑是治疗恰加斯病的首选药物。然而,它在慢性感染中具有毒性且价值有限。

目的

我们旨在评估苯唑硝唑不良反应(ARs)的发生率和相关因素以及治疗中断(TDs)。

方法

使用电子搜索方法对已发表的文献进行了无语言限制的荟萃分析,检索时间截至 2017 年 6 月。纳入慢性感染患者的前瞻性研究,其中至少有一个治疗组包括苯唑硝唑。还从我们中心的恰加斯病前瞻性队列(2007 年 1 月至 2017 年 6 月)中添加了数据。估计 ARs 和 TDs 的加权发生率,并分析潜在相关因素。

结果

共发现 413 项研究,从中选择了 42 项(9 项临床试验和 33 项观察性研究,包括我们自己的研究),这些研究包含了 7822 名患者的数据。苯唑硝唑的 ARs 加权发生率为 44.1%(95%置信区间[CI]37.2-51.2)。成人的 ARs 发生率高于儿童(51.6%比 24.5%),最常见的是皮肤反应(34%)、胃肠道不适(12.6%)和神经系统症状(11.5%)。有 3%的病例记录到 4 级 ARs。TDs 的加权发生率为 11.4%(95%CI8.5-14.5);成人的 TDs 发生率高于儿童(14.2%比 3.8%)。在我们的队列中,只有女性与 ARs 发生率增加有关,而与 TDs 无关。

结论

苯唑硝唑的耐受性较差,TDs 的发生率较高,特别是在成年患者和女性中。迫切需要优化的剂量方案和/或新药。

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