TY - JOUR
T1 - Immunosuppressed patients with COVID-19 pneumonia in ICU: clinical characteristics and factors influencing outcomes
AU - CIBERESUCICOVID Project investigators (COV20/00110, ISCIII)
AU - Galli, Flavia
AU - Forin, Edoardo
AU - Motos, Ana
AU - Molina Saldarriaga, Francisco José
AU - Gabarrus, Albert
AU - Canseco, Joan
AU - Fernandez-Barat, Laia
AU - Barbeta, Enric
AU - Calabretta, Davide
AU - Ceccato, Adrian
AU - Bermejo-Martin, Jesus F
AU - Ferrer, Ricard
AU - Riera, Jordi
AU - Penuelas, Oscar
AU - Lorente, Jose Angel
AU - de Gonzalo-Calvo, David
AU - Menendez, Rosario
AU - Gonzalez, Jessica
AU - Palomeque, Andrea
AU - Soler-Comas, Alba
AU - Amaya-Villar, Rosario
AU - Anon, Jose Manuel
AU - Marino, Ana Balan
AU - Barbera, Carme
AU - Barberan, Jose
AU - Ortiz, Aaron Blandino
AU - Bustamante-Munguira, Elena
AU - Caballero, Jesus
AU - Canton-Bulnes, Maria Luisa
AU - Perez, Cristina Carbajales
AU - Carbonell, Nieves
AU - Catalan-Gonzalez, Mercedes
AU - de Frutos, Raul
AU - Franco, Nieves
AU - Galban, Cristobal
AU - Lago, Ana Lopez
AU - Gumucio-Sanguino, Victor D
AU - Del Carmen de la Torre, Maria
AU - Diaz, Emilio
AU - Estella, Angel
AU - Gallego Curto, Elena
AU - Garcia-Garmendia, Jose Luis
AU - Gomez, Jose Manuel
AU - Huerta, Arturo
AU - Jorge Garcia, Ruth Noemi
AU - Loza-Vazquez, Ana
AU - Marin-Corral, Judith
AU - Martin Delgado, Maria Cruz
AU - Martinez de la Gandara, Amalia
AU - Martinez Varela, Ignacio
N1 - © 2025. The Author(s).
PY - 2025/11/25
Y1 - 2025/11/25
N2 - Abstract
Introduction COVID-19 severely impacted global health, especially older adults and those with comorbidities. Immunosuppressed patients are at high risk for severe outcomes, yet studies yield conflicting mortality rates for this group. This study examines the clinical characteristics and outcomes of immunosuppressed (IS) versus nonimmunosuppressed
(nIS) patients with COVID-19 in ICUs.
Methods A multicenter, observational case–control study included 5,824 ICU patients with COVID-19 from the CIBERESUCICOVID study. Patients were categorized as IS or nIS based on history of transplantation, HIV, active neoplasia, and use of immunosuppressive drugs or corticosteroids. The primary outcome was 90-day mortality; secondary outcomes included in-hospital, 15-day, 30-day and 1-year mortality, ICU-free days, ventilator-free days, and hospital length of stay. Subgroup analyses examined vaccination status and tocilizumab treatment. Propensity score (PS) matching was used to obtain balance among the baseline variables in the two groups.
Results IS patients (n = 689, 11.8%) were older, had more comorbidities, and higher APACHE-II scores. After PS matching, IS patients had higher 90-day mortality (39 vs. 33%; HR 1.30, 95% CI 1.04 to 1.62), as well as higher in-hospital (37 vs. 29%; sHR 1.35, 95% CI 1.08 to 1.69), 30-day (28 vs 23%; HR 1.31, 95% CI 1.01 to 1.69) and 1-year mortality (45 vs. 38%; HR 1.26, 95% CI 1.02 to 1.57). Among IS patients, transplant recipients had significantly higher 90-day mortality after matching (HR 4.45, 95% CI 1.46 to 13.58). Vaccinated IS patients showed higher mortality than vaccinated nIS patients, though differences were not significant after PS matching. Tocilizumab treatment in IS patients was associated with reduced mortality; multivariable analysis confirmed a significant decrease in in-hospital mortality (sHR 0.56, 95% CI 0.42 to 0.76).
Conclusion Critical immunosuppressed patients with COVID-19 have higher mortality, particularly transplant recipients. Tocilizumab shows potential benefits for IS patients. These findings highlight the need for tailored therapeutic strategies for immunosuppressed individuals with severe COVID-19. Further research is needed to confirm these results in the current clinical context.
AB - Abstract
Introduction COVID-19 severely impacted global health, especially older adults and those with comorbidities. Immunosuppressed patients are at high risk for severe outcomes, yet studies yield conflicting mortality rates for this group. This study examines the clinical characteristics and outcomes of immunosuppressed (IS) versus nonimmunosuppressed
(nIS) patients with COVID-19 in ICUs.
Methods A multicenter, observational case–control study included 5,824 ICU patients with COVID-19 from the CIBERESUCICOVID study. Patients were categorized as IS or nIS based on history of transplantation, HIV, active neoplasia, and use of immunosuppressive drugs or corticosteroids. The primary outcome was 90-day mortality; secondary outcomes included in-hospital, 15-day, 30-day and 1-year mortality, ICU-free days, ventilator-free days, and hospital length of stay. Subgroup analyses examined vaccination status and tocilizumab treatment. Propensity score (PS) matching was used to obtain balance among the baseline variables in the two groups.
Results IS patients (n = 689, 11.8%) were older, had more comorbidities, and higher APACHE-II scores. After PS matching, IS patients had higher 90-day mortality (39 vs. 33%; HR 1.30, 95% CI 1.04 to 1.62), as well as higher in-hospital (37 vs. 29%; sHR 1.35, 95% CI 1.08 to 1.69), 30-day (28 vs 23%; HR 1.31, 95% CI 1.01 to 1.69) and 1-year mortality (45 vs. 38%; HR 1.26, 95% CI 1.02 to 1.57). Among IS patients, transplant recipients had significantly higher 90-day mortality after matching (HR 4.45, 95% CI 1.46 to 13.58). Vaccinated IS patients showed higher mortality than vaccinated nIS patients, though differences were not significant after PS matching. Tocilizumab treatment in IS patients was associated with reduced mortality; multivariable analysis confirmed a significant decrease in in-hospital mortality (sHR 0.56, 95% CI 0.42 to 0.76).
Conclusion Critical immunosuppressed patients with COVID-19 have higher mortality, particularly transplant recipients. Tocilizumab shows potential benefits for IS patients. These findings highlight the need for tailored therapeutic strategies for immunosuppressed individuals with severe COVID-19. Further research is needed to confirm these results in the current clinical context.
U2 - 10.1186/s41479-025-00181-z
DO - 10.1186/s41479-025-00181-z
M3 - Artículo en revista científica indexada
C2 - 41287034
SN - 2200-6133
VL - 17
SP - 30
JO - Pneumonia (Nathan Qld.)
JF - Pneumonia (Nathan Qld.)
IS - 1
ER -