Incident Management System for the Covid-19 Response. Pan American Health Organization, 525 23rd St, Northwest Washington, DC 20037-2895.
Incident Management System for the Covid-19 Response. Pan American Health Organization, 525 23rd St, Northwest Washington, DC 20037-2895.
J Clin Epidemiol. 2022 Apr;144:43-55. doi: 10.1016/j.jclinepi.2021.12.018. Epub 2021 Dec 18.
The objective of this systematic review is to summarize the effects of ivermectin for the prevention and treatment of patients with COVID-19 and to assess inconsistencies in results from individual studies with focus on risk of bias due to methodological limitations.
We searched the L.OVE platform through July 6, 2021 and included randomized trials (RCTs) comparing ivermectin to standard or other active treatments. We conducted random-effects pairwise meta-analysis, assessed the certainty of evidence using the GRADE approach and performed sensitivity analysis excluding trials with risk of bias.
We included 29 RCTs which enrolled 5592 cases. Overall, the certainty of the evidence was very low to low suggesting that ivermectin may result in important benefits. However, after excluding trials classified as "high risk" or "some concerns" in the risk of bias assessment, most estimates of effect changed substantially: Compared to standard of care, low certainty evidence suggests that ivermectin may not reduce mortality (RD 7 fewer per 1000) nor mechanical ventilation (RD 6 more per 1000), and moderate certainty evidence shows that it probably does not increase symptom resolution or improvement (RD 14 more per 1000) nor viral clearance (RD 12 fewer per 1000).
Ivermectin may not improve clinically important outcomes in patients with COVID-19 and its effects as a prophylactic intervention in exposed individuals are uncertain. Previous reports concluding important benefits associated with ivermectin are based on potentially biased results reported by studies with substantial methodological limitations. Further research is needed.
本系统评价的目的是总结伊维菌素预防和治疗 COVID-19 患者的效果,并评估由于方法学局限性导致的个体研究结果的不一致性。
我们通过 2021 年 7 月 6 日在 L.OVE 平台上进行了检索,并纳入了比较伊维菌素与标准或其他活性治疗的随机对照试验(RCT)。我们进行了随机效应成对荟萃分析,使用 GRADE 方法评估证据的确定性,并进行了敏感性分析,排除了有偏倚风险的试验。
我们纳入了 29 项 RCT,共纳入了 5592 例病例。总体而言,证据的确定性非常低至低,表明伊维菌素可能带来重要的获益。然而,在排除了偏倚评估中被归类为“高风险”或“存在一些关注”的试验后,大多数效应估计值发生了显著变化:与标准治疗相比,低确定性证据表明伊维菌素可能不会降低死亡率(每 1000 人减少 7 例)或机械通气(每 1000 人增加 6 例),而中等确定性证据表明伊维菌素可能不会增加症状缓解或改善(每 1000 人增加 14 例)或病毒清除(每 1000 人减少 12 例)。
伊维菌素可能不会改善 COVID-19 患者的临床重要结局,其作为暴露个体的预防干预措施的效果也不确定。先前报告的与伊维菌素相关的重要获益是基于存在严重方法学局限性的研究报告的潜在有偏倚结果。需要进一步的研究。