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评价羟氯喹、洛匹那韦-利托那韦或地塞米松治疗 COVID-19 的观察性研究和随机对照试验的治疗效果的一致性:meta 流行病学研究。

Agreement of treatment effects from observational studies and randomized controlled trials evaluating hydroxychloroquine, lopinavir-ritonavir, or dexamethasone for covid-19: meta-epidemiological study.

机构信息

Yale School of Medicine, Yale University, New Haven, CT, USA.

Center for Science in the Public Interest, Washington, DC, USA.

出版信息

BMJ. 2022 May 10;377:e069400. doi: 10.1136/bmj-2021-069400.

Abstract

OBJECTIVE

To systematically identify, match, and compare treatment effects and study demographics from individual or meta-analysed observational studies and randomized controlled trials (RCTs) evaluating the same covid-19 treatments, comparators, and outcomes.

DESIGN

Meta-epidemiological study.

DATA SOURCES

National Institutes of Health Covid-19 Treatment Guidelines, a living review and network meta-analysis published in , a living systematic review with meta-analysis and trial sequential analysis in (The LIVING Project), and the Epistemonikos "Living OVerview of Evidence" (L·OVE) evidence database.

ELIGIBILITY CRITERIA FOR SELECTION OF STUDIES

RCTs in 's living review that directly compared any of the three most frequently studied therapeutic interventions for covid-19 across all data sources (that is, hydroxychloroquine, lopinavir-ritonavir, or dexamethasone) for any safety and efficacy outcomes. Observational studies that evaluated the same interventions, comparisons, and outcomes that were reported in 's living review.

DATA EXTRACTION AND SYNTHESIS

Safety and efficacy outcomes from observational studies were identified and treatment effects for dichotomous (odds ratios) or continuous (mean differences or ratios of means) outcomes were calculated and, when possible, meta-analyzed to match the treatment effects from individual RCTs or meta-analyses of RCTs reported in 's living review with the same interventions, comparisons, and outcomes (that is, matched pairs). The analysis compared the distribution of study demographics and the agreement between treatment effects from matched pairs. Matched pairs were in agreement if both observational and RCT treatment effects were significantly increasing or decreasing (P<0.05) or if both treatment effects were not significant (P≥0.05).

RESULTS

17 new, independent meta-analyses of observational studies were conducted that compared hydroxychloroquine, lopinavir-ritonavir, or dexamethasone with an active or placebo comparator for any safety or efficacy outcomes in covid-19 treatment. These studies were matched and compared with 17 meta-analyses of RCTs reported in 's living review. 10 additional matched pairs with only one observational study and/or one RCT were identified. Across all 27 matched pairs, 22 had adequate reporting of demographical and clinical data for all individual studies. All 22 matched pairs had studies with overlapping distributions of sex, age, and disease severity. Overall, 21 (78%) of the 27 matched pairs had treatment effects that were in agreement. Among the 17 matched pairs consisting of meta-analyses of observational studies and meta-analyses of RCTs, 14 (82%) were in agreement; seven (70%) of the 10 matched pairs consisting of at least one observational study or one RCT were in agreement. The 18 matched pairs with treatment effects for dichotomous outcomes had a higher proportion of agreement (n=16, 89%) than did the nine matched pairs with treatment effects for continuous outcomes (n=5, 56%).

CONCLUSIONS

Meta-analyses of observational studies and RCTs evaluating treatments for covid-19 have summary treatment effects that are generally in agreement. Although our evaluation is limited to three covid-19 treatments, these findings suggest that meta-analyzed evidence from observational studies might complement, but should not replace, evidence collected from RCTs.

摘要

目的

系统地识别、匹配和比较来自个体或荟萃分析观察性研究和随机对照试验(RCT)的治疗效果和研究人群,这些研究评估了相同的 COVID-19 治疗方法、对照方法和结局。

设计

荟萃流行病学研究。

数据来源

美国国立卫生研究院 COVID-19 治疗指南、发表在《柳叶刀》上的实时综述和网络荟萃分析、发表在《柳叶刀》上的实时系统评价和荟萃分析及试验序贯分析(LIVING 项目)以及 Epistemonikos“证据实时概述”(L·OVE)证据数据库。

研究入选标准

LIVING 项目实时综述中的 RCT,直接比较了所有数据源中 COVID-19 三种最常研究的治疗干预措施(即羟氯喹、洛匹那韦-利托那韦或地塞米松)的任何安全性和疗效结局。在 LIVING 项目实时综述中报告的评估相同干预措施、比较和结局的观察性研究。

数据提取和综合

从观察性研究中确定安全性和疗效结局,并计算二分类(比值比)或连续(均数差或均数比)结局的治疗效果,并尽可能进行荟萃分析,以匹配来自个体 RCT 或报告在 LIVING 项目实时综述中的 RCT 荟萃分析的相同干预措施、比较和结局(即配对)的治疗效果。分析比较了研究人群特征的分布和配对的治疗效果之间的一致性。如果观察性和 RCT 治疗效果都显著增加或减少(P<0.05)或如果两种治疗效果都不显著(P≥0.05),则认为配对是一致的。

结果

开展了 17 项新的、独立的羟氯喹、洛匹那韦-利托那韦或地塞米松与活性或安慰剂对照治疗 COVID-19 的任何安全性或疗效结局的观察性研究荟萃分析,并对其进行了匹配和比较。在 LIVING 项目实时综述中报告了 17 项 RCT 荟萃分析。还确定了 10 项只有一项观察性研究和/或一项 RCT 的额外配对。在所有 27 对配对中,22 对配对均有足够的个体研究人口统计学和临床数据报告。所有 22 对配对均有性别、年龄和疾病严重程度重叠分布的研究。总体而言,27 对配对中有 22 对配对的治疗效果一致。在由观察性研究荟萃分析和 RCT 荟萃分析组成的 17 对配对中,14 对(82%)一致;在由至少一项观察性研究或一项 RCT 组成的 10 对配对中,有 7 对(70%)一致。对于二分类结局的 18 对配对,其一致比例(n=16,89%)高于连续结局的 9 对配对(n=5,56%)。

结论

评估 COVID-19 治疗方法的观察性研究和 RCT 的荟萃分析汇总治疗效果通常是一致的。尽管我们的评估仅限于三种 COVID-19 治疗方法,但这些发现表明,来自观察性研究的荟萃分析证据可能会补充但不能替代从 RCT 收集的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1df9/9086409/de1eab33da53/mono069400.f1.jpg

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