Major candidate variables to guide personalised treatment with steroids in critically ill patients with COVID-19: CIBERESUCICOVID study
| dc.contributor.author | Torres, Antoni | |
| dc.contributor.author | Motos, Anna | |
| dc.contributor.author | Cillóniz, Catia | |
| dc.contributor.author | Ceccato, Adrián | |
| dc.contributor.author | Fernández Barat, Laia | |
| dc.contributor.author | Gabarrús, Albert | |
| dc.contributor.author | Bermejo Martín, Jesús | |
| dc.contributor.author | Lorente Balanza, José Ángel | |
| dc.contributor.author | Peñuelas, Óscar | |
| dc.contributor.author | Barbé, Ferran | |
| dc.contributor.author | Et al. | |
| dc.date.accessioned | 2022-09-12T08:33:07Z | |
| dc.date.available | 2022-09-12T08:33:07Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | Purpose: Although there is evidence supporting the benefits of corticosteroids in patients affected with severe coronavirus disease 2019 (COVID-19), there is little information related to their potential benefits or harm in some subgroups of patients admitted to the intensive care unit (ICU) with COVID-19. We aim to investigate to find candidate variables to guide personalized treatment with steroids in critically ill patients with COVID-19. Methods: Multicentre, observational cohort study including consecutive COVID-19 patients admitted to 55 Spanish ICUs. The primary outcome was 90-day mortality. Subsequent analyses in clinically relevant subgroups by age, ICU baseline illness severity, organ damage, laboratory findings and mechanical ventilation were performed. High doses of corticosteroids (≥ 12 mg/day equivalent dexamethasone dose), early administration of corticosteroid treatment (< 7 days since symptom onset) and long term of corticosteroids (≥ 10 days) were also investigated. Results: Between February 2020 and October 2021, 4226 patients were included. Of these, 3592 (85%) patients had received systemic corticosteroids during hospitalisation. In the propensity-adjusted multivariable analysis, the use of corticosteroids was protective for 90-day mortality in the overall population (HR 0.77 [0.65-0.92], p = 0.003) and in-hospital mortality (SHR 0.70 [0.58-0.84], p < 0.001). Significant effect modification was found after adjustment for covariates using propensity score for age (p = 0.001 interaction term), Sequential Organ Failure Assessment (SOFA) score (p = 0.014 interaction term), and mechanical ventilation (p = 0.001 interaction term). We observed a beneficial effect of corticosteroids on 90-day mortality in various patient subgroups, including those patients aged ≥ 60 years; those with higher baseline severity; and those receiving invasive mechanical ventilation at ICU admission. Early administration was associated with a higher risk of 90-day mortality in the overall population (HR 1.32 [1.14-1.53], p < 0.001). Long-term use was associated with a lower risk of 90-day mortality in the overall population (HR 0.71 [0.61-0.82], p < 0.001). No effect was found regarding the dosage of corticosteroids. Moreover, the use of corticosteroids was associated with an increased risk of nosocomial bacterial pneumonia and hyperglycaemia. Conclusion: Corticosteroid in ICU-admitted patients with COVID-19 may be administered based on age, severity, baseline inflammation, and invasive mechanical ventilation. Early administration since symptom onset may prove harmful. | spa |
| dc.description.filiation | UEM | spa |
| dc.description.impact | 38.9 Q1 JCR 2022 | spa |
| dc.description.impact | 6.229 Q1 SJR 2022 | spa |
| dc.description.impact | No data IDR 2022 | spa |
| dc.description.sponsorship | Instituto de Salud Carlos III de Madrid (ISCIII) (COV20/00110) | spa |
| dc.description.sponsorship | Centro de Investigacion Biomedica En Red-Enfermedades Respiratorias (CIBERES) | spa |
| dc.description.sponsorship | Instituto de Salud Carlos III European Commission Miguel Servet 2020: CP20/00041 | spa |
| dc.description.sponsorship | Instituto de Salud Carlos III (PI19/00207) | spa |
| dc.identifier.citation | Torres, A., Motos, A., Cillóniz, C., Ceccato, A., Fernández-Barat, L., Gabarrús, A., Bermejo-Martín, J., Ferrer, R., Riera, J., Pérez-Arnal, R., García-Gasulla, D., Peñuelas, O., Lorente, J. A., Gonzalo-Calvo, D., Almansa, R., Menéndez, R., Palomeque, A., Villar, R. A., Añón, J. M., … Santacoloma, B. (2022). Major candidate variables to guide personalised treatment with steroids in critically ill patients with COVID-19: CIBERESUCICOVID study. Intensive Care Medicine, 48(7), 850–864. https://doi.org/10.1007/s00134-022-06726-w | spa |
| dc.identifier.doi | 10.1007/s00134-022-06726-w | |
| dc.identifier.issn | 0342-4642 | |
| dc.identifier.issn | 1432-1238 | |
| dc.identifier.uri | http://hdl.handle.net/11268/11585 | |
| dc.language.iso | eng | spa |
| dc.peerreviewed | Si | spa |
| dc.relation.publisherversion | https://doi.org/10.1007/s00134-022-06726-w | spa |
| dc.rights.accessRights | open access | spa |
| dc.subject.other | Infecciones por coronavirus | spa |
| dc.subject.unesco | Tratamiento médico | spa |
| dc.subject.unesco | Enfermedad transmisible | spa |
| dc.title | Major candidate variables to guide personalised treatment with steroids in critically ill patients with COVID-19: CIBERESUCICOVID study | spa |
| dc.type | journal article | spa |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 91e712d1-cbf0-4eab-9536-461d26ddbddf | |
| relation.isAuthorOfPublication.latestForDiscovery | 91e712d1-cbf0-4eab-9536-461d26ddbddf |

