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撒哈拉以南非洲抗逆转录病毒治疗时代的严重药物不良反应:系统评价。

Serious adverse drug reactions in sub-Saharan Africa in the era of antiretroviral treatment: A systematic review.

机构信息

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

出版信息

Pharmacol Res Perspect. 2021 Dec;9(6):e00875. doi: 10.1002/prp2.875.

Abstract

We aimed to summarize and describe the burden of serious adverse drug reactions (ADRs) in sub-Saharan Africa (SSA) in the era of antiretroviral therapy. We searched Medline, CINAHL, Africa-Wide Information, Scopus, and Web of Science, without language restriction up to March 2021. We hand-searched reference lists, conference abstracts, and dissertation databases. We included studies reporting proportions of admissions attributed to ADRs, admissions prolonged by ADRs, or in-hospital deaths attributed to ADRs. Two reviewers independently screened the studies, reviewed the study quality using a previously published tool, and extracted the data. We tested for heterogeneity using I -statistics and summarized the study results using medians and interquartile ranges. Subgroup analyses summarized the results by study quality, setting, methodology, and population. From 1005 unique references identified, we included 15 studies. Median study quality was 7/10; heterogeneity was very high. Median [IQR] proportion of admissions attributed to ADRs was 4.8% [1.5% to 7.0%] (14 studies) and 6.4% [4.0% to 8.4%] in nine active surveillance studies in adults. Two pediatric studies reported the proportion of admissions prolonged by ADRs (0.29% and 0.99%). Three studies reported the proportion of in-hospital deaths attributed to ADRs (2.5%, 13%, and 16%). Antiretroviral and antituberculosis drugs were often implicated in serious ADRs. Evidence of the burden of serious ADRs in SSA is patchy and heterogeneous. A few high-quality studies suggest that the burden is considerable, and that it reflects the regional impact of the HIV pandemic. Further characterization of this burden is required, ideally in studies of standardized methodology.

摘要

我们旨在总结和描述抗逆转录病毒治疗时代撒哈拉以南非洲(SSA)严重药物不良反应(ADR)的负担。我们检索了 Medline、CINAHL、Africa-Wide Information、Scopus 和 Web of Science,没有语言限制,检索截至 2021 年 3 月。我们手工检索了参考文献列表、会议摘要和论文数据库。我们纳入了报告归因于 ADR 的住院比例、因 ADR 而延长的住院时间或归因于 ADR 的院内死亡比例的研究。两名审查员独立筛选研究,使用先前发表的工具评估研究质量,并提取数据。我们使用 I 统计量检测异质性,并使用中位数和四分位距总结研究结果。亚组分析根据研究质量、研究地点、研究方法和研究人群总结了结果。从 1005 条独特的参考文献中,我们纳入了 15 项研究。中位数研究质量为 7/10;异质性非常高。归因于 ADR 的住院比例中位数 [四分位距] 为 4.8% [1.5%至 7.0%](14 项研究),9 项成人主动监测研究中为 6.4% [4.0%至 8.4%]。两项儿科研究报告了归因于 ADR 的住院时间延长的比例(0.29%和 0.99%)。三项研究报告了归因于 ADR 的院内死亡比例(2.5%、13%和 16%)。抗逆转录病毒和抗结核药物常与严重 ADR 相关。SSA 严重 ADR 负担的证据参差不齐且存在异质性。少数高质量研究表明,负担相当大,反映了 HIV 大流行对该地区的影响。需要进一步描述这种负担,理想情况下在标准化方法的研究中进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96bf/8569857/49a0ad50bfbc/PRP2-9-e00875-g002.jpg

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