Evidence map›Paper›PMID 34882805›Full record

ArticleJournal of medical virology2022

Efficacy and safety of current treatment interventions for patients with severe COVID-19 infection: A network meta-analysis of randomized controlled trials.

Qinglin Cheng, Gang Zhao, Junfang Chen, Qingjun Jia, Zijian Fang

Open access · greenAbstract readNetwork Meta-Analysis
In one paragraph

Article in Journal of medical virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  5. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Qinglin ChengDivision of Infectious Diseases, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.ORCID 0000-0003-2899-7626
Gang ZhaoDivision of Infectious Diseases, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.ORCID 0000-0002-5564-911X
Junfang ChenDivision of Infectious Diseases, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
Qingjun JiaDivision of Infectious Diseases, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
Zijian FangDivision of Infectious Diseases, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
Hangzhou Center for Disease Control and Prevention · CNHangzhou Normal University · CN

Funding

Basic Public Welfare Research Project of Zhejiang Province LGF21H260007Medical Science and Technology Project of Zhejiang Province 2021PY065
6 · The paper itself

Abstract

This study aimed to assess the efficacy and safety of different medications available at present for severe coronavirus disease 2019 (COVID-19) infection. We searched databases for randomized controlled trials (RCTs) published up to April 30, 2021, with Chinese or English language restriction, of medications recommended for patients (aged 18 years or older) with severe COVID-19 infection. We extracted data on trials and patient characteristics, and the following primary outcomes: all-cause mortality (ACM), and treatment-emergent adverse events (TEAEs). We identified 1855 abstracts and of these included 15 RCTs comprising 3073 participants through database searches and other sources. In terms of efficacy, compared with the standard of care (SOC) group, no significant decrease in ACM was found in α-lipoic acid, convalescent plasma (CP), azithromycin, tocilizumab, methylprednisolone, interferon beta, CP/SOC, high dosage sarilumab, low dosage sarilumab, remdesivir, lopinavir-ritonavir, auxora, and placebo group. Compared with placebo, we found that a significant decrease in ACM was only found in methylprednisolone (odds ratio [OR]: 0.16, 95% confidence interval [CI]: 0.03-0.75]. With respect to TEAEs, the CP group showed lower TEAEs than placebo (OR: 0.07, 95% CI: 0.01-0.58) or SOC (OR: 0.05, 95% CI: 0.01-0.42) group for the therapy of severe COVID-19 patients. This study only demonstrated that methylprednisolone was superior to placebo in treating patients with severe COVID-19 infection. Meanwhile, this further confirmed that the safety of other treatment interventions might be inferior to CP for the therapy of severe COVID-19 patients.

Indexed as

COVID-19HumansSARS-CoV-2Severity of Illness IndexTreatment Outcomeefficacynetwork meta-analysisrandomized controlled trialssafetysevere COVID-19

Identifiers

PMID34882805
PMCPMC9015508
OpenAlexW4200585865

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.