Suppr超能文献

降低新冠病毒疾病住院率的门诊治疗方案:一项随机对照试验的系统评价和荟萃分析

Outpatient regimens to reduce COVID-19 hospitalisations: a systematic review and meta-analysis of randomized controlled trials.

作者信息

Sullivan David J, Focosi Daniele, Hanley Daniel F, Cruciani Mario, Franchini Massimo, Ou Jiangda, Casadevall Arturo, Paneth Nigel

出版信息

medRxiv. 2023 Jun 26:2022.05.24.22275478. doi: 10.1101/2022.05.24.22275478.

Abstract

BACKGROUND

During pandemics, early outpatient treatments reduce the health system burden. Randomized controlled trials (RCTs) in COVID-19 outpatients have tested therapeutic agents, but no RCT or systematic review has been conducted comparing the efficacy of the main outpatient treatment classes to each other. We aimed in this systematic review of outpatient RCTs in COVID-19 to compare hospitalisation rate reductions with four classes of treatment: convalescent plasma, monoclonal antibodies, small molecule antivirals and repurposed drugs.

METHODS

We conducted a systematic review and meta-analysis of all COVID-19 outpatient RCTs that included the endpoint of progression to hospitalisation. We assembled, from multiple published and preprint databases, participant characteristics, hospitalisations, resolution of symptoms and mortality from January 2020 to May 21, 2023. The risk of bias from COVID-NMA was incorporated into the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system. We measured heterogeneity with I . Meta-analysis by a random or fixed effect model dependent on significant heterogeneity (I >50%) was performed. The protocol was registered in PROSPERO, CRD42022369181.

FINDINGS

The search identified 281 studies of which 54 RCTs for 30 diverse interventions were included in the final analysis. These trials, performed largely in unvaccinated cohorts during pre-Omicron waves, focused on populations with at least one COVID-19 hospitalisation risk factor. Grouping by class, monoclonal antibodies (OR=0.31 [95% CI=0.24-0.40]) had highest efficacy, followed by COVID-19 convalescent plasma (CCP) (OR=0.69 [95% CI=0.53 to 0.90]) and small molecule antivirals (OR=0.78 [95% CI=0.48-1.33]) for hospital reduction. Repurposed drugs (OR=0.82 [95% CI-0.72-0.93]) had lower efficacy.

INTERPRETATION

Inasmuch as omicron sublineages (XBB and BQ.1.1) are now resistant to monoclonal antibodies, oral antivirals are the preferred treatment in outpatients where available, but intravenous interventions from convalescent plasma to remdesivir are also effective and necessary in constrained medical resource settings or for acute and chronic COVID-19 in the immunocompromised.

FUNDING

US Department of Defense and National Institute of Health.

RESEARCH IN CONTEXT

We systematically searched the published and preprint data bases for outpatient randomized clinical trials of treatment of COVID-19 disease with hospitalisation as an endpoint. Previous systematic reviews and meta-analyses have confined the reviews to specific classes such as convalescent plasma, monoclonal antibodies, small molecule antivirals or repurposed drugs. Few comparisons have been made between these therapeutic classes. The trials took place both in the pre-vaccination and the vaccination era, spanning periods with dominance of different COVID variants. We sought to compare efficacy between the four classes of treatments listed above when used in outpatient COVID-19 patients as shown in randomized, placebo-controlled trials.

ADDED VALUE OF THIS STUDY

This systematic review and meta-analysis brings together trials that assessed hospitalisation rates in diverse COVID-19 outpatient populations varying in age and comorbidities, permitting us to assess the efficacy of interventions both within and across therapeutic classes. While heterogeneity exists within and between these intervention classes, the meta-analysis can be placed in context of trial diverse populations over variant time periods of the pandemic. At present most of the world population has either had COVID-19 or been vaccinated with a high seropositivity rate, indicating that future placebo-controlled trials will be limited because of the sample sizes required to document hospitalisation outcomes.

IMPLICATIONS OF ALL THE AVAILABLE EVIDENCE

Numerous diverse therapeutic tools need to be ready for a resilient response to changing SARS-CoV-2 variants in both immunocompetent and immunocompromised COVID-19 outpatient populations. To date few head-to-head randomized controlled trials (RCTs) has compared treatment options for COVID-19 outpatients, making comparisons and treatment choices difficult. This systematic review compares outcomes among RCTs of outpatient therapy for COVID-19, taking into account time between onset of symptoms and treatment administration. We found that small-chemical antivirals, convalescent plasma and monoclonal antibodies had comparable efficacy between classes and amongst interventions within the four classes. Monoclonals have lost efficacy with viral mutation, and chemical antivirals have contraindications and adverse events, while intravenous interventions like convalescent plasma or remdesivir remain resilient options for the immunocompromised, and, in the case of CCP, in resource constrained settings with limited availability of oral drugs.

摘要

背景

在大流行期间,早期门诊治疗可减轻卫生系统负担。针对新冠门诊患者的随机对照试验(RCT)已对治疗药物进行了测试,但尚未进行RCT或系统评价来比较主要门诊治疗类别之间的疗效。在这项针对新冠门诊RCT的系统评价中,我们旨在比较四类治疗方法(恢复期血浆、单克隆抗体、小分子抗病毒药物和重新利用的药物)降低住院率的效果。

方法

我们对所有以住院进展为终点的新冠门诊RCT进行了系统评价和荟萃分析。我们从多个已发表和预印本数据库中收集了2020年1月至2023年5月21日期间的参与者特征、住院情况、症状缓解情况和死亡率。将新冠网络荟萃分析的偏倚风险纳入推荐分级评估、制定和评价(GRADE)系统。我们用I²测量异质性。根据显著异质性(I²>50%),采用随机或固定效应模型进行荟萃分析。该方案已在国际前瞻性系统评价注册库(PROSPERO)注册,注册号为CRD42022369181。

结果

检索到281项研究,最终分析纳入了54项针对30种不同干预措施的RCT。这些试验主要在奥密克戎毒株出现之前的未接种疫苗人群中进行,重点关注至少有一个新冠住院风险因素的人群。按类别分组,单克隆抗体(OR=0.31 [95%CI=0.24 - 0.40])疗效最高,其次是新冠恢复期血浆(CCP)(OR=0.69 [95%CI=0.53至0.90])和小分子抗病毒药物(OR=0.78 [95%CI=0.48 - 1.33])用于降低住院率。重新利用的药物(OR=0.82 [95%CI - 0.72 - 0.93])疗效较低。

解读

鉴于奥密克戎亚谱系(XBB和BQ.1.1)现在对单克隆抗体耐药,在有口服抗病毒药物可用的门诊患者中,口服抗病毒药物是首选治疗方法,但在医疗资源有限的环境中,或对于免疫功能低下的急性和慢性新冠患者,从恢复期血浆到瑞德西韦的静脉干预也是有效且必要的。

资助

美国国防部和美国国立卫生研究院。

研究背景

我们系统检索了已发表和预印本数据库,以查找以住院为终点的新冠门诊随机临床试验。以往的系统评价和荟萃分析将评价局限于特定类别,如恢复期血浆、单克隆抗体、小分子抗病毒药物或重新利用的药物。这些治疗类别之间很少进行比较。试验在疫苗接种前和接种疫苗时代均有开展,涵盖了不同新冠病毒变种占主导的时期。我们试图比较上述四类治疗方法在新冠门诊患者中使用时的疗效,如随机、安慰剂对照试验所示。

本研究的新增价值

这项系统评价和荟萃分析汇集了评估不同年龄和合并症的新冠门诊患者住院率的试验,使我们能够评估治疗类别内部和之间干预措施的疗效。虽然这些干预类别内部和之间存在异质性,但荟萃分析可以放在大流行不同时期试验不同人群的背景下进行。目前世界上大多数人口要么感染过新冠病毒,要么接种了疫苗,血清阳性率很高,这表明由于记录住院结果所需的样本量,未来的安慰剂对照试验将受到限制。

现有所有证据的意义

需要准备多种不同的治疗工具,以便在免疫功能正常和免疫功能低下的新冠门诊患者中,对不断变化的新冠病毒变种做出有力反应。迄今为止,很少有直接比较新冠门诊患者治疗方案的随机对照试验(RCT),这使得比较和治疗选择变得困难。这项系统评价比较了新冠门诊治疗RCT的结果,同时考虑了症状出现到开始治疗的时间。我们发现,小分子抗病毒药物、恢复期血浆和单克隆抗体在类别之间以及四类干预措施中的疗效相当。单克隆抗体因病毒突变而失去疗效,化学抗病毒药物有禁忌症和不良事件,而像恢复期血浆或瑞德西韦这样的静脉干预措施对于免疫功能低下者以及在口服药物供应有限的资源受限环境中(如CCP的情况)仍然是可靠的选择。

相似文献

4
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.
7
Systemic treatments for metastatic cutaneous melanoma.转移性皮肤黑色素瘤的全身治疗
Cochrane Database Syst Rev. 2018 Feb 6;2(2):CD011123. doi: 10.1002/14651858.CD011123.pub2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验