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Remdesivir in adults with severe COVID-19: a randomised, double-blind, placebo-controlled, multicentre trial.瑞德西韦治疗成人重症 COVID-19 的随机、双盲、安慰剂对照、多中心临床试验。
Lancet. 2020 May 16;395(10236):1569-1578. doi: 10.1016/S0140-6736(20)31022-9. Epub 2020 Apr 29.
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A Trial of Lopinavir-Ritonavir in Covid-19.洛匹那韦-利托那韦治疗新冠肺炎的试验
N Engl J Med. 2020 May 21;382(21):e68. doi: 10.1056/NEJMc2008043. Epub 2020 May 5.
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Diagnosis and Treatment Protocol for Novel Coronavirus Pneumonia (Trial Version 7).新型冠状病毒肺炎诊疗方案(试行第七版)
Chin Med J (Engl). 2020 May 5;133(9):1087-1095. doi: 10.1097/CM9.0000000000000819.
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A Trial of Lopinavir-Ritonavir in Adults Hospitalized with Severe Covid-19.洛匹那韦-利托那韦治疗成人重症 COVID-19 患者的临床试验。
N Engl J Med. 2020 May 7;382(19):1787-1799. doi: 10.1056/NEJMoa2001282. Epub 2020 Mar 18.
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First Case of 2019 Novel Coronavirus in the United States.美国首例 2019 新型冠状病毒病例。
N Engl J Med. 2020 Mar 5;382(10):929-936. doi: 10.1056/NEJMoa2001191. Epub 2020 Jan 31.
6
A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster.一个涉及 2019 年新型冠状病毒的家庭聚集性肺炎病例,提示存在人际传播:一项家庭聚集性研究。
Lancet. 2020 Feb 15;395(10223):514-523. doi: 10.1016/S0140-6736(20)30154-9. Epub 2020 Jan 24.
7
A Novel Coronavirus from Patients with Pneumonia in China, 2019.2019 年中国肺炎患者中的一种新型冠状病毒。
N Engl J Med. 2020 Feb 20;382(8):727-733. doi: 10.1056/NEJMoa2001017. Epub 2020 Jan 24.
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Network meta-analysis: an introduction for clinicians.网状Meta分析:临床医生指南
Intern Emerg Med. 2017 Feb;12(1):103-111. doi: 10.1007/s11739-016-1583-7. Epub 2016 Dec 2.
9
Comparative safety and effectiveness of cognitive enhancers for Alzheimer's dementia: protocol for a systematic review and individual patient data network meta-analysis.用于阿尔茨海默病痴呆症的认知增强剂的比较安全性和有效性:系统评价和个体患者数据网络荟萃分析方案
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Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation.系统评价和荟萃分析议定书的首选报告项目(PRISMA-P)2015:详细说明和解释。
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比较 COVID-19 患者抗病毒药物的有效性和安全性:系统评价和个体患者数据网络荟萃分析方案。

Comparative effectiveness and safety of antiviral agents for patients with COVID-19: Protocol for a systematic review and individual-patient data network meta-analysis.

机构信息

Department of Hospital-Acquired Infection Control, Peking University People's Hospital, Beijing, The People's Republic of China.

Department of Hospital-Acquired Infection Control, Beijing Jishuitan Hospital, Beijing, The People's Republic of China.

出版信息

PLoS One. 2020 Nov 9;15(11):e0241947. doi: 10.1371/journal.pone.0241947. eCollection 2020.

DOI:10.1371/journal.pone.0241947
PMID:33166346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7652299/
Abstract

BACKGROUND

A recent cluster of pneumonia cases in Wuhan, China, has been caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We propose the protocol described below to perform an individual-patient data (IPD) network meta-analysis (NMA) in order to evaluate the efficacies of different antiviral drugs to treat patients with coronavirus disease 2019 (COVID-19).

MATERIALS AND METHODS

We will search the Medline, EMBASE, Cochrane Library, SinoMed, CNKI and VIP databases from their inceptions through July 2020. There will be no restrictions on language, publication year, or publication type. Randomized clinical trials (RCTs) and prospective cohort studies with antiviral treatments for COVID-19 will be considered. Two reviewers will independently select studies and collect data. Risk-of-bias assessments will be completed using the Cochrane risk-of-bias scale. Primary outcome will be the COVID-19 recovery rate. We will combine aggregated data from IPD with the NMA in a single model, compare the effects of different antiviral drugs on patient-relevant efficacy, and rank the results to decide which is the most effective.

TRIAL REGISTRATION

PROSPERO registration number: CRD42020167038.

摘要

背景

近期在中国武汉发生了一组肺炎病例,其病因是严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)。我们提出了如下方案,以便开展个体化患者数据(IPD)网络荟萃分析(NMA),从而评估不同抗病毒药物治疗 2019 冠状病毒病(COVID-19)患者的疗效。

材料与方法

我们将从各数据库建库起至 2020 年 7 月检索 Medline、EMBASE、Cochrane 图书馆、中国生物医学文献数据库(SinoMed)、中国知网(CNKI)和维普中文期刊服务平台(VIP)。检索语种、发表年份和文献类型均不受限制。我们将纳入使用抗病毒药物治疗 COVID-19 的随机对照试验(RCT)和前瞻性队列研究。两名评审员将独立筛选研究并提取数据。使用 Cochrane 偏倚风险评估工具评估偏倚风险。主要结局指标为 COVID-19 康复率。我们将在单一模型中合并 IPD 的汇总数据和 NMA,比较不同抗病毒药物对患者相关疗效的影响,并对结果进行排名,以确定哪种药物最有效。

注册

PROSPERO 注册号:CRD42020167038。