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Eur. J. Clin. Invest. · Feb 2021
High-Dose Methylprednisolone in Nonintubated Patients with Severe COVID-19 Pneumonia.
- Aikaterini Papamanoli, Jeanwoo Yoo, Prabhjot Grewal, William Predun, Jessica Hotelling, Robin Jacob, Azad Mojahedi, Hal A Skopicki, Mohamed Mansour, Luis A Marcos, and Andreas P Kalogeropoulos.
- Division of Infectious Diseases, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.
- Eur. J. Clin. Invest. 2021 Feb 1; 51 (2): e13458e13458.
BackgroundRecent trials with dexamethasone and hydrocortisone have demonstrated benefit in patients with coronavirus disease 2019 (COVID-19). Data on methylprednisolone are limited.MethodsRetrospective cohort of consecutive adults with severe COVID-19 pneumonia on high-flow oxygen (FiO2 ≥ 50%) admitted to an academic centre in New York, from 1 March to 15 April 2020. We used inverse probability of treatment weights to estimate the effect of methylprednisolone on clinical outcomes and intensive care resource utilization.ResultsOf 447 patients, 153 (34.2%) received methylprednisolone and 294 (65.8%) received no corticosteroids. At 28 days, 102 patients (22.8%) had died and 115 (25.7%) received mechanical ventilation. In weighted analyses, risk for death or mechanical ventilation was 37% lower with methylprednisolone (hazard ratio 0.63; 95% CI 0.47-0.86; P = .003), driven by less frequent mechanical ventilation (subhazard ratio 0.56; 95% CI 0.40-0.79; P = .001); mortality did not differ between groups. The methylprednisolone group had 2.8 more ventilator-free days (95% CI 0.5-5.1; P = .017) and 2.6 more intensive care-free days (95% CI 0.2-4.9; P = .033) during the first 28 days. Complication rates were not higher with methylprednisolone.ConclusionsIn nonintubated patients with severe COVID-19 pneumonia, methylprednisolone was associated with reduced need for mechanical ventilation and less-intensive care resource utilization without excess complications.© 2020 Stichting European Society for Clinical Investigation Journal Foundation. Published by John Wiley & Sons Ltd.
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