Evidence map›Paper›PMID 40619454›Full record

ArticleScientific reports2025

Tocilizumab as a targeted immunomodulatory therapy in the management of severe respiratory illnesses: a multicenter cohort study of COVID-19 patients.

Abbas Al Mutair, Saad Alhumaid, Gasmelseed Y Ahmad, Ali A Rabaan, Sameer A Alkubati, Hamdan Albaqawi, Awatif M Alrasheeday, Bushra Alshammari, Kawther Alsaleh, Richard Mottershead and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2025. 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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0citing papers 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

The trial behind it

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Abbas Al MutairResearch Center, Almoosa Health Group, Al-Ahsa, Saudi Arabia.
Saad AlhumaidSchool of Pharmacy and Pharmacology, University of Tasmania, Hobart, TAS, 7001, Australia.
Gasmelseed Y AhmadResearch Centre, Almoosa Specialist Hospital, Al-Ahsa, Saudi Arabia.
Ali A RabaanMolecular Diagnostic Laboratory, Johns Hopkins Aramco Healthcare, Dhahran, Saudi Arabia.
Sameer A AlkubatiMedical Surgical Nursing Department, College of Nursing, University of Hail, Hail, Saudi Arabia.
Hamdan AlbaqawiMedical Surgical Nursing Department, College of Nursing, University of Hail, Hail, Saudi Arabia.
Awatif M AlrasheedayNursing Administration Department, College of Nursing, University of Hail, Hail, Saudi Arabia.
Bushra AlshammariMedical Surgical Nursing Department, College of Nursing, University of Hail, Hail, Saudi Arabia.
Kawther AlsalehResearch Center, Almoosa Health Group, Al-Ahsa, Saudi Arabia.
Richard MottersheadCollege of Health Sciences, University of Sharjah, Sharjah, United Arab Emirates.
Muhammad DaniyalResearch Center, Almoosa Health Group, Al-Ahsa, Saudi Arabia. muhammad.daniyal@almoosahealth.com.sa.
Awad Al-OmariAlmana Health Group, Al Khobar, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory pandemics like COVID-19 continued to strain healthcare systems worldwide. Numerous antiviral, antimalarial, and anti-inflammatory treatments were administered to many patients to pursue effective therapeutics. This study aims to assess the efficacy of the anti-inflammatory agent tocilizumab for critically ill patients, specifically in managing respiratory illnesses. This multi-center cohort study included laboratory-confirmed SARS-CoV-2 patients as special cases admitted to the intensive care units (ICUs) of 15 hospitals across Saudi Arabia between March 1, 2020, and October 30, 2020. A total of 1470 critically ill patients with SARS-CoV-2 were included. The study included 1470 patients with a mean age of 55.9 ± 15.1 years; 1088 (74.0%) were male and 382 (26.0%) female. Among them, 29% received Tocilizumab, while 71% received other treatments such as remdesivir, hydroxychloroquine, corticosteroids, convalescent plasma, intravenous immunoglobulin, and plasmapheresis. The median Sequential Organ Failure Assessment (SOFA) score for the cohort was 5 [IQR 3-8], with lower scores observed in the Tocilizumab administered group (p = 0.143). ICU mortality was significantly lower in the tocilizumab group: 150/426 (35.2%) versus 457/1044 (43.8%), p = 0.004. The median length of ICU stay was longer in the Tocilizumab group (12 days; IQR 7-21) than in the non-Tocilizumab group (8 days; IQR 4-15). However, Tocilizumab use was associated with a reduced likelihood of prolonged ICU stay (adjusted OR 0.68; 95% CI 0.57-0.83; p < 0.001). Similarly, the median hospital stay was longer among Tocilizumab recipients (18 days; IQR 12-30) compared to non-recipients (14 days; IQR 8-23). Despite the longer duration, Tocilizumab was associated with a decreased likelihood of extended hospital stay (adjusted OR 0.72; 95% CI 0.57-0.91; p = 0.003). These findings support the beneficial role of Tocilizumab in managing acute respiratory illness due to COVID-19. This study suggests that tocilizumab, particularly when administered early, is associated with reduced mortality and improved outcomes in critically ill patients. These findings not only support the use of tocilizumab as a therapeutic option for severe cases of COVID-19 but also highlight its potential for future respiratory pandemics. Early intervention with tocilizumab may lead to significant benefits, offering a valuable treatment strategy with manageable adverse effects for critically ill patients in future global health crises.

Indexed as

Antibodies, Monoclonal, HumanizedCOVID-19COVID-19 Drug TreatmentAdultAgedCohort StudiesCritical IllnessFemaleHumansIntensive Care UnitsLength of StayMaleMiddle AgedSARS-CoV-2Saudi ArabiaTreatment OutcomeAntibodies, Monoclonal, HumanizedtocilizumabCOVID-19EfficacyMortalityRespiratory illnessSaudi ArabiaTocilizumab

Identifiers

PMID40619454
PMCPMC12230132

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.