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瑞德西韦、羟氯喹和洛匹那韦/利托那韦治疗 COVID-19 的不良反应:随机试验的系统评价和荟萃分析。

Adverse effects of remdesivir, hydroxychloroquine and lopinavir/ritonavir when used for COVID-19: systematic review and meta-analysis of randomised trials.

机构信息

Department of Internal Medicine, Hospital Alemán de Buenos Aires, Buenos Aires, Argentina

Department of Health Research Methods, Evidence, and Impact (HEI), McMaster University, Hamilton, Ontario, Canada.

出版信息

BMJ Open. 2022 Mar 2;12(3):e048502. doi: 10.1136/bmjopen-2020-048502.

Abstract

BACKGROUND

To summarise specific adverse effects of remdesivir, hydroxychloroquine and lopinavir/ritonavir in patients with COVID-19.

METHODS

We searched 32 databases through 27 October 2020. We included randomised trials comparing any of the drugs of interest to placebo or standard care, or against each other. We conducted fixed-effects pairwise meta-analysis and assessed the certainty of evidence using the grading of recommendations assessment, development and evaluation approach.

RESULTS

We included 16 randomised trials which enrolled 8152 patients. For most interventions and outcomes the certainty of the evidence was very low to low except for gastrointestinal adverse effects from hydroxychloroquine, which was moderate certainty. Compared with standard care or placebo, low certainty evidence suggests that remdesivir may not have an important effect on acute kidney injury (risk difference (RD) 8 fewer per 1000, 95% CI 27 fewer to 21 more) or cognitive dysfunction/delirium (RD 3 more per 1000, 95% CI 12 fewer to 19 more). Low certainty evidence suggests that hydroxychloroquine may increase the risk of cardiac toxicity (RD 10 more per 1000, 95% CI 0 more to 30 more) and cognitive dysfunction/delirium (RD 33 more per 1000, 95% CI 18 fewer to 84 more), whereas moderate certainty evidence suggests hydroxychloroquine probably increases the risk of diarrhoea (RD 106 more per 1000, 95% CI 48 more to 175 more) and nausea and/or vomiting (RD 62 more per 1000, 95% CI 23 more to 110 more) compared with standard care or placebo. Low certainty evidence suggests lopinavir/ritonavir may increase the risk of diarrhoea (RD 168 more per 1000, 95% CI 58 more to 330 more) and nausea and/or vomiting (RD 160 more per 1000, 95% CI 100 more to 210 more) compared with standard care or placebo.

DISCUSSION

Hydroxychloroquine probably increases the risk of diarrhoea and nausea and/or vomiting and may increase the risk of cardiac toxicity and cognitive dysfunction/delirium. Lopinavir/ritonavir may increase the risk of diarrhoea and nausea and/or vomiting. Remdesivir may have no important effect on risk of acute kidney injury or cognitive dysfunction/delirium. These findings provide important information to support the development of evidence-based management strategies for patients with COVID-19.

摘要

背景

总结瑞德西韦、羟氯喹和洛匹那韦/利托那韦在 COVID-19 患者中的特定不良反应。

方法

我们通过 27 个数据库检索了 32 个数据库,截止日期为 2020 年 10 月 27 日。我们纳入了比较任何感兴趣药物与安慰剂或标准治疗,或相互之间比较的随机试验。我们进行了固定效应的两两荟萃分析,并使用推荐评估、制定和评估方法对证据的确定性进行了评估。

结果

我们纳入了 16 项随机试验,共纳入了 8152 名患者。对于大多数干预措施和结局,除了羟氯喹引起的胃肠道不良反应的证据确定性为中高度外,其他的证据确定性都很低或很低。与标准治疗或安慰剂相比,低确定性证据表明,瑞德西韦可能对急性肾损伤没有重要影响(每 1000 人减少 8 例,95%CI 为 27 例减少至 21 例增加)或认知功能障碍/谵妄(每 1000 人增加 3 例,95%CI 为 12 例减少至 19 例增加)。低确定性证据表明,羟氯喹可能增加心脏毒性的风险(每 1000 人增加 10 例,95%CI 为 0 例至 30 例增加)和认知功能障碍/谵妄(每 1000 人增加 33 例,95%CI 为 18 例减少至 84 例增加),而中度确定性证据表明,羟氯喹可能增加腹泻的风险(每 1000 人增加 106 例,95%CI 为 48 例增加至 175 例增加)和恶心和/或呕吐(每 1000 人增加 62 例,95%CI 为 23 例增加至 110 例增加)与标准治疗或安慰剂相比。低确定性证据表明,洛匹那韦/利托那韦可能会增加腹泻的风险(每 1000 人增加 168 例,95%CI 为 58 例增加至 330 例增加)和恶心和/或呕吐(每 1000 人增加 160 例,95%CI 为 100 例增加至 210 例增加)与标准治疗或安慰剂相比。

讨论

羟氯喹可能增加腹泻和恶心和/或呕吐的风险,并且可能增加心脏毒性和认知功能障碍/谵妄的风险。洛匹那韦/利托那韦可能会增加腹泻和恶心和/或呕吐的风险。瑞德西韦可能对急性肾损伤或认知功能障碍/谵妄的风险没有重要影响。这些发现为支持 COVID-19 患者的循证管理策略的制定提供了重要信息。

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