Evidence map›Paper›PMID 36326309›Full record

SynthesisTurkish journal of medical sciences2022

The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis.

Hamna Malık, Hira Bınt Abdul Jabbar, Farah Latıf, Azza Sarfraz, Zouina Sarfraz, Muzna Sarfraz

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Turkish journal of medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Trial
  2. Article
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

6 authors at 4 institutions in 2 countries.

Hamna MalıkResearch, Services Institute of Medical Sciences, Lahore, Pakistan.
Hira Bınt Abdul JabbarResearch, King Edward Medical University, Lahore, Pakistan.
Farah LatıfResearch and Publications, Fatima Jinnah Medical University, Lahore, Pakistan.
Azza SarfrazPediatrics and Child Health, The Aga Khan University, Karachi, Pakistan.
Zouina SarfrazResearch and Publications, Fatima Jinnah Medical University, Lahore, Pakistan.
Muzna SarfrazResearch, King Edward Medical University, Lahore, Pakistan.
King Edward Medical University · PKAga Khan University · PKAT Sciences (United States) · USFatima Jinnah Medical University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs SARS-CoV-2 continues to spread worldwide, this study brings to light the link that anakinra, a recombinant IL-1 receptor antagonist, has in averting grave clinical outcomes. The objectives of this meta-analysis are to investigate the effects of anakinra in interventional groups compared to control/standard of care groups on mortality along with the provision of a prevalence estimate of the variables associated with death (C-reactive protein-CRP, ferritin, acute respiratory distress syndrome-ARDS).

methodsAccording to the PRISMA 2020 statement guidelines, a systematic search was conducted from December 19, 2020, until December 10, 2021, with keywords including COVID-19, coronavirus, SARS-CoV-2, anakinra, mortality, across the following databases: PubMed/MEDLINE, Scopus, Web of Science, CINAHL Plus, and Cochrane. A random-effects model was applied using RevMan 5.4 for all statistical analyses.

resultsThe meta-analysis pooled in 1297 participants with 565 (43.6%) patients in the anakinra group. When comparing to the control/standard of care group, the anakinra group had a much lower risk of death (RR = 0.47. 95% CI = 0.37-0.59, Z = 6.44; P < 0.001). In addition to the risk of death being reduced by around 50% in the interventional group, prognostic indicators such as CRP and ferritin were improved with fewer occurrences of severe ARDS. DISCUSSION: Patients with COVID-19 pneumonia may be treated with anakinra as a safe and viable treatment modality to defer adverse outcomes such as a death in the 28-day period. Despite an auspicious premise, our findings must be used with caution as adequately powered randomized, placebo-controlled trials are required to corroborate these findings.

Indexed as

COVID-19 Drug TreatmentRespiratory Distress SyndromeFerritinsHumansInterleukin 1 Receptor Antagonist ProteinSARS-CoV-2FerritinsInterleukin 1 Receptor Antagonist ProteinAnakinraCOVID-19cytokine stormmeta-analysismortality

Identifiers

PMID36326309
PMCPMC10390186
OpenAlexW4285225585

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.