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Int. J. Clin. Pract. · Sep 2021
Impact of intermediate to high-doses of methylprednisolone on mortality rate in patients with COVID-19 pneumonia-induced severe systemic inflammation.
- Mónica Climente-Martí, Oreto Ruiz-Millo, Ian López-Cruz, Ángel Atienza-García, Eva Martínez-Moragón, Emilio Garijo-Gómez, María Luisa López-Grima, Rafael Zaragoza-Crespo, Juan Vicente Llau-Pitarch, Daniel Bautista-Rentero, José Miguel Nogueira-Coito, Tomás Ripollés-González, María Antonia Marco-Artal, Ramón Romero-Serrano, Francisco Dolz-Sinisterra, Rosario López-Estudillo, and Doctor Peset COVID-19 Working Group.
- Pharmacy Department, Doctor Peset University Hospital, Valencia, Spain.
- Int. J. Clin. Pract. 2021 Sep 1; 75 (9): e14479e14479.
IntroductionIn addition to respiratory support needs, patients' characteristics to guide indication or timing of corticosteroid treatment in COVID-19 patients are not completely established. This study aimed to evaluate the impact of methylprednisolone on mortality rate in patients with COVID-19 pneumonia-induced severe systemic inflammation (PI-SSI).MethodsBetween 9 March and 5 May 2020 (final follow-up on 2 July 2020), a retrospective cohort study was conducted in hospitalised patients with COVID-19 PI-SSI (≥2 inflammatory biomarkers [IBs]: temperature ≥38℃, lymphocyte ≤800 cell/µL, C-reactive protein ≥100 mg/L, lactate dehydrogenase ≥300 units/L, ferritin ≥1000 mcg/L, D-dimer ≥500 ng/mL). Patients received 0.5-1.0 mg/kg of methylprednisolone for 5-10 days or standard of care. The primary outcome was 28-day all-cause mortality. Secondary outcomes included ≥2 points improvement on a 7-item WHO-scale (Day 14), transfer to intensive care unit (ICU) (Day 28) and adverse effects. Kaplan-Meier method and Cox proportional hazard regression were implemented to analyse the time to event outcomes.ResultsA total of 142 patients (corticosteroid group n = 72, control group n = 70) were included. A significant reduction in 28-day all-cause mortality was shown with methylprednisolone in patients with respiratory support (HR: 0.15; 95% CI 0.03-0.71), with ≥3 (HR: 0.17; 95% CI 0.05-0.61) or ≥4 altered IB (HR: 0.15; 95% CI 0.04-0.54) and in patients with both respiratory support and ≥3 (HR: 0.11; 95% CI 0.02-0.53] or ≥4 altered IB (HR: 0.14; 95% CI 0.04-0.51). No significant differences were found in secondary outcomes.ConclusionIntermediate to high doses of methylprednisolone, initiated between 5 and 12 days after symptom onset, was associated with a significant reduction in 28-day all-cause mortality in patients with COVID-19 pneumonia and ≥3 o ≥ 4 altered IB, independently of the need of respiratory support.© 2021 John Wiley & Sons Ltd.
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