The role of corticosteroids in severe viral pneumonia: lessons from COVID-19 and influenza

Gordon et al., Pneumonia, doi:10.1186/s41479-025-00192-w, Feb 2026
Review of corticosteroid use in influenza and COVID-19 severe pneumonia. In influenza, the weight of evidence associates corticosteroid therapy with increased mortality, delayed viral clearance, and higher rates of secondary infection. In COVID-19, the RECOVERY trial established low-dose dexamethasone as standard of care in severe and critical disease, with the greatest mortality benefit seen in mechanically ventilated patients.
However, authors present evidence that this benefit does not extend to all hospitalized patients. In the RECOVERY trial itself, patients not receiving respiratory support at randomization showed no mortality reduction. Several studies found that corticosteroids given to non-ventilated patients or those with low inflammatory profiles were associated with increased mortality, severe ARDS, or septic shock. Data on patients receiving high-flow or simple oxygen remain inconclusive. The authors also note that timing matters: benefit was greater when treatment began after seven or more days of symptoms rather than early in the disease course, and that higher doses and longer durations did not improve survival. Authors conclude that corticosteroid therapy is context-dependent, and that a personalized approach guided by real-time inflammatory and virological monitoring is needed to optimize outcomes.
Gordon et al., 5 Feb 2026, China, peer-reviewed, 2 authors, study period 11 March, 2020 - 13 April, 2020. Contact: ramirez_pau@gva.es.
Abstract: ## REVIEW The role of corticosteroids in severe viral pneumonia: lessons from COVID-19 and influenza Monica Gordon 1 and Paula Ramirez 1* Abstract Background Corticosteroids have long been used as immunomodulatory agents in viral respiratory infections, but their role in influenza and COVID-19 remains controversial. While both diseases share overlapping pathogenic mechanisms involving hyperinflammation and immune dysregulation, clinical evidence suggests divergent outcomes in response to corticosteroid therapy. Objective This review critically examines the evidence regarding corticosteroid use in influenza and COVID-19, focusing on their impact on mortality, disease progression, and secondary infections. Methods A narrative review was conducted including randomized controlled trials, meta-analyses, and major observational studies published between 2000 and 2025. Data were analyzed comparatively for influenza (seasonal and pandemic strains) and SARS-CoV-2 infection. Results In influenza, most studies associate corticosteroid administration-particularly at high doses or prolonged courses-with increased mortality, delayed viral clearance, and higher rates of secondary bacterial pneumonia. Conversely, in COVID-19, randomized trials such as RECOVERY demonstrated that low-to-moderate doses of dexamethasone significantly reduce mortality in patients requiring oxygen or mechanical ventilation, without clear benefit in mild disease. These opposing outcomes highlight the importance of timing, dosing, and patient selection, reflecting distinct immunopathological trajectories between the two infections. Conclusions Corticosteroid therapy exerts context-dependent effects in viral pneumonia. While detrimental in most cases of influenza, it is beneficial in severe COVID-19 when guided by systemic inflammation. Future strategies should focus on personalized and real-time immune monitoring to tailor immunomodulatory interventions to each patient's inflammatory and virological status. *Correspondence: Paula Ramirez ramirez\_pau@gva.es 1 Critical Care Department, Hospital Universitario y Politécnico la Fe, Valencia, Spain Open Access © The Author(s) 2026. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit h t t p : / / c r e a t i v e c o m m o n s . o r g / l i c e n s e s / b y n c n d / 4 . 0 /.
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Please send us corrections, updates, or comments. c19early involves the extraction of 200,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. IMA and WCH provide treatment protocols.
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