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González, Jessica; Benítez, Iván D; de Gonzalo-Calvo, David; Torres, Gerard; de Batlle, Jordi; Gómez, Silvia; Moncusí-Moix, Anna; Carmona, Paola; Santisteve, Sally; Monge, Aida; Gort-Paniello, Clara; Zuil, María; Cabo-Gambín, Ramón; Manzano Senra, Carlos; Vengoechea Aragoncillo, José Javier; Vaca, Rafaela; Minguez, Olga; Aguilar, María; Ferrer, Ricard; Ceccato, Adrián; Fernández, Laia; Motos, Ana; Riera, Jordi; Menéndez, Rosario; Garcia-Gasulla, Darío; Peñuelas, Oscar; Labarca, Gonzalo; Caballero, Jesús; Barberà, Carme; Torres, Antoni; Barbé, Ferran
Critical care (London, England), 01/2022, Letnik: 26, Številka: 1Journal Article
We evaluated whether the time between first respiratory support and intubation of patients receiving invasive mechanical ventilation (IMV) due to COVID-19 was associated with mortality or pulmonary sequelae. Prospective cohort of critical COVID-19 patients on IMV. Patients were classified as early intubation if they were intubated within the first 48 h from the first respiratory support or delayed intubation if they were intubated later. Surviving patients were evaluated after hospital discharge. We included 205 patients (140 with early IMV and 65 with delayed IMV). The median p ;p age was 63 56.0; 70.0 years, and 74.1% were male. The survival analysis showed a significant increase in the risk of mortality in the delayed group with an adjusted hazard ratio (HR) of 2.45 (95% CI 1.29-4.65). The continuous predictor time to IMV showed a nonlinear association with the risk of in-hospital mortality. A multivariate mortality model showed that delay of IMV was a factor associated with mortality (HR of 2.40; 95% CI 1.42-4.1). During follow-up, patients in the delayed group showed a worse DLCO (mean difference of - 10.77 (95% CI - 18.40 to - 3.15), with a greater number of affected lobes (+ 1.51 95% CI 0.89-2.13) and a greater TSS (+ 4.35 95% CI 2.41-6.27) in the chest CT scan. Among critically ill patients with COVID-19 who required IMV, the delay in intubation from the first respiratory support was associated with an increase in hospital mortality and worse pulmonary sequelae during follow-up.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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in: SICRIS
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