TY - JOUR
T1 - Prolonged higher dose methylprednisolone versus conventional dexamethasone in COVID-19 pneumonia
T2 - a randomised controlled trial (MEDEAS)
AU - MEDEAS Collaborative Group
AU - Salton, Francesco
AU - Confalonieri, Paola
AU - Centanni, Stefano
AU - Mondoni, Michele
AU - Petrosillo, Nicola
AU - Bonfanti, Paolo
AU - Lapadula, Giuseppe
AU - Lacedonia, Donato
AU - Voza, Antonio
AU - Carpenè, Nicoletta
AU - Montico, Marcella
AU - Reccardini, Nicolò
AU - Meduri, Gianfranco Umberto
AU - Ruaro, Barbara
AU - Confalonieri, Marco
AU - Citton, Gloria Maria
AU - Bozzi, Chiara
AU - Tavano, Stefano
AU - Pozzan, Riccardo
AU - Andrisano, Alessia Giovanna
AU - Jaber, Mohamad
AU - Mari, Marco
AU - Trotta, Liliana
AU - Mondini, Lucrezia
AU - Barbieri, Mariangela
AU - Ruggero, Luca
AU - Antonaglia, Caterina
AU - Soave, Sara
AU - Torregiani, Chiara
AU - Bogatec, Tjaša
AU - Baccelli, Andrea
AU - Nalesso, Giulia
AU - Re, Beatrice
AU - Pavesi, Stefano
AU - Barbaro, Maria Pia Foschino
AU - Giuliani, Antonella
AU - Ravaglia, Claudia
AU - Poletti, Venerino
AU - Scala, Raffaele
AU - Guidelli, Luca
AU - Golfi, Nicoletta
AU - Vianello, Andrea
AU - Achille, Alessia
AU - Lucernoni, Paolo
AU - Gaccione, Anna Talia
AU - Romagnoli, Micaela
AU - Fraccaro, Alessia
AU - Malacchini, Nicola
AU - Malerba, Mario
AU - Ragnoli, Beatrice
N1 - Publisher Copyright:
Copyright © The authors 2023.
PY - 2023/4
Y1 - 2023/4
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85148936444
U2 - 10.1183/13993003.01514-2022
DO - 10.1183/13993003.01514-2022
M3 - Article
SN - 0903-1936
VL - 61
JO - European Respiratory Journal
JF - European Respiratory Journal
IS - 4
M1 - 2201514
ER -