Evidence map›Paper›PMID 42685097›Full record

ArticlePloS one2026

Comparative associations of Anakinra and Tocilizumab initiation with in-hospital mortality in severe COVID-19: A single-center sequential cohort study.

Fevzi Necati Avsar, Nihat Kılıcaslan, Tuncay Sahutoglu

Abstract readComparative Study
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Fevzi Necati AvsarDepartment of Internal Medicine, Sanliurfa Mehmet Akif Inan Training and Research Hospital, University of Health Sciences, Türkiye.ORCID https://orcid.org/0000-0002-5131-6983
Nihat KılıcaslanDepartment of Radiology, Sanliurfa Mehmet Akif Inan Training and Research Hospital, University of Health Sciences, Türkiye.
Tuncay SahutogluDivision of Nephrology, Department of Internal Medicine, Sanliurfa Mehmet Akif Inan Training and Research Hospital, University of Health Sciences, Türkiye.ORCID https://orcid.org/0000-0003-2015-4421

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterleukin-1 and interleukin-6 blockade have been widely used in severe COVID-19, but comparative real-world evidence regarding anakinra and tocilizumab in critically ill patients remains limited. We evaluated the associations of first initiation of anakinra or tocilizumab with 28-day and overall in-hospital mortality.

methodsThis single-center retrospective ICU cohort included adults with severe COVID-19. During hospital days 2-10, daily actions were classified as anakinra initiation, tocilizumab initiation, or control/defer. Calibrated overlap-weighted modified-Poisson models estimated associations with 28-day and overall in-hospital mortality; ferritin-adjusted sensitivity analyses were performed.

resultsOf 306 patients, 241 patients contributed 1,297 eligible person-days. Calibration met the prespecified balance criterion for the included covariates, although effective support for tocilizumab initiation remained limited. For 28-day in-hospital mortality, adjusted RRs versus control/defer were 0.99 (95% CI, 0.80-1.22) for anakinra and 0.99 (95% CI, 0.71-1.37) for tocilizumab. No clear associations were identified in the head-to-head comparison or for overall in-hospital mortality; ferritin-adjusted estimates were similar.

conclusionsIn this retrospective ICU cohort, neither anakinra nor tocilizumab initiation showed a clear association with 28-day or overall in-hospital mortality. Estimates were imprecise, particularly for tocilizumab, and remain susceptible to residual confounding.

Indexed as

Antibodies, Monoclonal, HumanizedCOVID-19 Drug TreatmentHospital MortalityInterleukin 1 Receptor Antagonist ProteinAgedCOVID-19FemaleHumansIntensive Care UnitsMaleMiddle AgedRetrospective StudiesSARS-CoV-2Antibodies, Monoclonal, HumanizedInterleukin 1 Receptor Antagonist Proteintocilizumab

Identifiers

PMID42685097
PMCPMC13537557

What Socratic holds

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Registered trials

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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 Socratic graph.