Background Dysregulated systemic inflammation is the primary driver of mortality in severe coronavirus disease 2019 (COVID-19) pneumonia. Current guidelines favour a 7-10-day course of any glucocorticoid equivalent to dexamethasone 6 mg daily. A comparative randomised controlled trial (RCT) with a higher dose and a longer duration of intervention was lacking.Methods We conducted a multicentre, open-label RCT to investigate methylprednisolone 80 mg as a continuous daily infusion for 8 days followed by slow tapering versus dexamethasone 6 mg once daily for up to 10 days in adult patients with COVID-19 pneumonia requiring oxygen or noninvasive respiratory support. The primary outcome was reduction in 28-day mortality. Secondary outcomes were mechanical ventilation-free days at 28 days, need for intensive care unit (ICU) referral, length of hospitalisation, need for tracheostomy, and changes in C-reactive protein (CRP) levels, arterial oxygen tension/inspiratory oxygen fraction (PaO2/FIO2) ratio and World Health Organization Clinical Progression Scale at days 3, 7 and 14.Results 677 randomised patients were included. Findings are reported as methylprednisolone (n=337) versus dexamethasone (n=340). By day 28, there were no significant differences in mortality (35 (10.4%) versus 41 (12.1%); p=0.49) nor in median mechanical ventilation-free days (median (interquartile range (IQR)) 23 (14) versus 24 (16) days; p=0.49). ICU referral was necessary in 41 (12.2%) versus 45 (13.2%) (p=0.68) and tracheostomy in 8 (2.4%) versus 9 (2.6%) (p=0.82). Survivors in the methylprednisolone group required a longer median (IQR) hospitalisation (15 (11) versus 14 (11) days; p=0.005) and experienced an improvement in CRP levels, but not in PaO2/FIO2 ratio, at days 7 and 14. There were no differences in disease progression at the prespecified time-points.Conclusion Prolonged, higher dose methylprednisolone did not reduce mortality at 28 days compared with conventional dexamethasone in COVID-19 pneumonia.

Prolonged higher dose methylprednisolone versus conventional dexamethasone in COVID-19 pneumonia: a randomised controlled trial (MEDEAS)

Carrozzi, Laura;Rafanelli, Annalisa;Casto, Elisabetta;
2023-01-01

Abstract

Background Dysregulated systemic inflammation is the primary driver of mortality in severe coronavirus disease 2019 (COVID-19) pneumonia. Current guidelines favour a 7-10-day course of any glucocorticoid equivalent to dexamethasone 6 mg daily. A comparative randomised controlled trial (RCT) with a higher dose and a longer duration of intervention was lacking.Methods We conducted a multicentre, open-label RCT to investigate methylprednisolone 80 mg as a continuous daily infusion for 8 days followed by slow tapering versus dexamethasone 6 mg once daily for up to 10 days in adult patients with COVID-19 pneumonia requiring oxygen or noninvasive respiratory support. The primary outcome was reduction in 28-day mortality. Secondary outcomes were mechanical ventilation-free days at 28 days, need for intensive care unit (ICU) referral, length of hospitalisation, need for tracheostomy, and changes in C-reactive protein (CRP) levels, arterial oxygen tension/inspiratory oxygen fraction (PaO2/FIO2) ratio and World Health Organization Clinical Progression Scale at days 3, 7 and 14.Results 677 randomised patients were included. Findings are reported as methylprednisolone (n=337) versus dexamethasone (n=340). By day 28, there were no significant differences in mortality (35 (10.4%) versus 41 (12.1%); p=0.49) nor in median mechanical ventilation-free days (median (interquartile range (IQR)) 23 (14) versus 24 (16) days; p=0.49). ICU referral was necessary in 41 (12.2%) versus 45 (13.2%) (p=0.68) and tracheostomy in 8 (2.4%) versus 9 (2.6%) (p=0.82). Survivors in the methylprednisolone group required a longer median (IQR) hospitalisation (15 (11) versus 14 (11) days; p=0.005) and experienced an improvement in CRP levels, but not in PaO2/FIO2 ratio, at days 7 and 14. There were no differences in disease progression at the prespecified time-points.Conclusion Prolonged, higher dose methylprednisolone did not reduce mortality at 28 days compared with conventional dexamethasone in COVID-19 pneumonia.
2023
Salton, Francesco; Confalonieri, Paola; Centanni, Stefano; Mondoni, Michele; Petrosillo, Nicola; Bonfanti, Paolo; Lapadula, Giuseppe; Lacedonia, Donato; Voza, Antonio; Carpenè, Nicoletta; Montico, Marcella; Reccardini, Nicolò; Meduri, Gianfranco Umberto; Ruaro, Barbara; Confalonieri, Marco; Citton, Gloria Maria; Lapadula, Giulia; Bozzi, Chiara; Tavano, Stefano; Pozzan, Riccardo; Andrisano, Alessia Giovanna; Jaber, Mohamad; Mari, Marco; Trotta, Liliana; Mondini, Lucrezia; Barbieri, Mariangela; Ruggero, Luca; Antonaglia, Caterina; Soave, Sara; Torregiani, Chiara; Bogatec, Tjaša; Baccelli, Andrea; Nalesso, Giulia; Re, Beatrice; Pavesi, Stefano; Barbaro, Maria Pia Foschino; Giuliani, Antonella; Ravaglia, Claudia; Poletti, Venerino; Scala, Raffaele; Guidelli, Luca; Golfi, Nicoletta; Vianello, Andrea; Achille, Alessia; Lucernoni, Paolo; Gaccione, Anna Talia; Romagnoli, Micaela; Fraccaro, Alessia; Malacchini, Nicola; Malerba, Mario; Ragnoli, Beatrice; Zamparelli, Alessandro Sanduzzi; Bocchino, Marialuisa; Blasi, Francesco; Spotti, Maura; Miele, Carmen; Piedepalumbo, Federica; Barone, Ivan; Baglioni, Stefano; Dodaj, Meridiana; Franco, Cosimo; Andrani, Francesco; Mangia, Angelo; Mancini, Annalisa; Carrozzi, Laura; Rafanelli, Annalisa; Casto, Elisabetta; Rogliani, Paola; Ora, Josuel; Carpagnano, Giovanna Elisiana; Di Lecce, Valentina; Tamburrini, Mario; Papi, Alberto; Contoli, Marco; Luzzati, Roberto; Zatta, Marta; Di Bella, Stefano; Caraffa, Emanuela; Francisci, Daniela; Tosti, Andrea; Pallotto, Carlo; De Rosa, Francesco Giuseppe; Pecori, Alessio; Franceschini, Marta; Carlin, Massimiliano; Orsini, Valentina; Spolti, Anna; Inannace, Marta; Santantonio, Teresa; Meli, Rossella; Sauro, Sara; Fedeli, Carlo; Mangini, Elisabetta; Biolo, Gianni; Nunnari, Alessio; Pietrangelo, Antonello; Corradini, Elena; Bocchi, Davide; Boarini, Chiara; Zucchetto, Antonella; Lanini, Simone
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1184128
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