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伊维菌素用于预防和治疗 COVID-19 感染:系统评价、荟萃分析和试验序贯分析,为临床指南提供信息。

Ivermectin for Prevention and Treatment of COVID-19 Infection: A Systematic Review, Meta-analysis, and Trial Sequential Analysis to Inform Clinical Guidelines.

机构信息

Population Health Sciences Institute, Newcastle University, Newcastle Upon Tyne, United Kingdom.

Evidence-based Medicine Consultancy, Bath, United Kingdom.

出版信息

Am J Ther. 2021 Jun 21;28(4):e434-e460. doi: 10.1097/MJT.0000000000001402.

Abstract

BACKGROUND

Repurposed medicines may have a role against the SARS-CoV-2 virus. The antiparasitic ivermectin, with antiviral and anti-inflammatory properties, has now been tested in numerous clinical trials.

AREAS OF UNCERTAINTY

We assessed the efficacy of ivermectin treatment in reducing mortality, in secondary outcomes, and in chemoprophylaxis, among people with, or at high risk of, COVID-19 infection.

DATA SOURCES

We searched bibliographic databases up to April 25, 2021. Two review authors sifted for studies, extracted data, and assessed risk of bias. Meta-analyses were conducted and certainty of the evidence was assessed using the GRADE approach and additionally in trial sequential analyses for mortality. Twenty-four randomized controlled trials involving 3406 participants met review inclusion.

THERAPEUTIC ADVANCES

Meta-analysis of 15 trials found that ivermectin reduced risk of death compared with no ivermectin (average risk ratio 0.38, 95% confidence interval 0.19-0.73; n = 2438; I2 = 49%; moderate-certainty evidence). This result was confirmed in a trial sequential analysis using the same DerSimonian-Laird method that underpinned the unadjusted analysis. This was also robust against a trial sequential analysis using the Biggerstaff-Tweedie method. Low-certainty evidence found that ivermectin prophylaxis reduced COVID-19 infection by an average 86% (95% confidence interval 79%-91%). Secondary outcomes provided less certain evidence. Low-certainty evidence suggested that there may be no benefit with ivermectin for "need for mechanical ventilation," whereas effect estimates for "improvement" and "deterioration" clearly favored ivermectin use. Severe adverse events were rare among treatment trials and evidence of no difference was assessed as low certainty. Evidence on other secondary outcomes was very low certainty.

CONCLUSIONS

Moderate-certainty evidence finds that large reductions in COVID-19 deaths are possible using ivermectin. Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant impact on the SARS-CoV-2 pandemic globally.

摘要

背景

重新利用的药物可能在对抗 SARS-CoV-2 病毒方面发挥作用。具有抗病毒和抗炎特性的驱虫药伊维菌素已在众多临床试验中进行了测试。

不确定性领域

我们评估了伊维菌素治疗在降低死亡率、次要结局和 COVID-19 感染者或高危人群的化学预防方面的疗效。

数据来源

我们检索了截至 2021 年 4 月 25 日的文献数据库。两位综述作者筛选了研究,提取了数据,并评估了偏倚风险。进行了荟萃分析,并使用 GRADE 方法评估了证据的确定性,并在针对死亡率的试验序贯分析中进行了补充评估。24 项涉及 3406 名参与者的随机对照试验符合综述纳入标准。

治疗进展

对 15 项试验的荟萃分析发现,与未用伊维菌素相比,伊维菌素降低了死亡风险(平均风险比 0.38,95%置信区间 0.19-0.73;n = 2438;I2 = 49%;中等确定性证据)。使用相同的 DerSimonian-Laird 方法进行的试验序贯分析证实了这一结果,该方法是对未调整分析的补充。使用 Biggerstaff-Tweedie 方法进行的试验序贯分析也具有稳健性。低确定性证据表明,伊维菌素预防可使 COVID-19 感染平均减少 86%(95%置信区间 79%-91%)。次要结局提供的证据不太确定。低确定性证据表明,伊维菌素对“需要机械通气”可能没有益处,而“改善”和“恶化”的效果估计明显倾向于使用伊维菌素。治疗试验中严重不良事件罕见,评估为低确定性的无差异证据。其他次要结局的证据非常低确定性。

结论

中等确定性证据表明,使用伊维菌素可能会大大降低 COVID-19 死亡率。在临床病程早期使用伊维菌素可能会减少进展为严重疾病的人数。伊维菌素的明显安全性和低成本表明,它很可能对全球的 SARS-CoV-2 大流行产生重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46f9/8248252/a1e6ee081326/ajt-28-e434-g001.jpg

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