Days spent on non-invasive ventilation support: can it determine when to initiate VV- ECMO? Observational study in a cohort of Covid-19 patients

dc.contributor.authorFuset, Maria Paz
dc.contributor.authorHernández Platero, Lluisa
dc.contributor.authorSabater Riera, Joan
dc.contributor.authorGordillo Benitez, Miguel
dc.contributor.authorPaolo, Fabio di
dc.contributor.authorCárdenas Campos, Paola
dc.contributor.authorMaisterra Santos, Krystel
dc.contributor.authorPons Serra, María
dc.contributor.authorSastre Pérez, Paola
dc.contributor.authorGarcía Zaloña, Alejandro
dc.contributor.authorPuentes Yañez, Javiera
dc.contributor.authorPérez Fernández, Xosé Luis
dc.date.accessioned2023-09-13T13:47:22Z
dc.date.available2023-09-13T13:47:22Z
dc.date.issued2023-08-26
dc.date.updated2023-09-12T13:23:47Z
dc.description.abstractBackground The study evaluates the impact of the time between commencing non-invasive ventilation (NIV) support and initiation of venovenous extracorporeal membrane oxygenation (VV-ECMO) in a cohort of critically ill patients with coronavirus disease 2019 (COVID-19) associated acute respiratory distress syndrome (ARDS).Methods Prospective observational study design in an intensive Care Unit (ICU) of a tertiary hospital in Barcelona (Spain). All patients requiring VV-ECMO support due to COVID-19 associated ARDS between March 2020 and January 2022 were analysed. Survival outcome was determined at 90 days after VV-ECMO initiation. Demographic data, comorbidities at ICU admission, RESP (respiratory ECMO survival prediction) score, antiviral and immunomodulatory treatments received, inflammatory biomarkers, the need for vasopressors, the thromboprophylaxis regimen received, and respiratory parameters including the length of intubation previous to ECMO and the length of each NIV support (high-flow nasal cannula, continuous positive airway pressure and bi-level positive airway pressure), were also collated in order to assess risk factors for day-90 mortality. The effect of the time lapse between NIV support and VV-ECMO on survival was evaluated using logistic regression and adjusting the association with all factors that were significant in the univariate analysis.Results Seventy-two patients finally received VV-ECMO support. At 90 days after commencing VV-ECMO 35 patients (48%) had died and 37 patients (52%) were alive. Multivariable analysis showed that at VV-ECMO initiation, age (p = 0.02), lactate (p = 0.001), and days from initiation of NIV support to starting VV-ECMO (p = 0.04) were all associated with day-90 mortality.Conclusions In our small cohort of VV-ECMO patients with COVID-19 associated ARDS, the time spent between initiation of NIV support and VV-ECMO (together with age and lactate) appeared to be a better predictor of mortality than the time between intubation and VV-ECMO.
dc.format.extent7 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn1471-2466
dc.identifier.pmid37626354
dc.identifier.urihttps://hdl.handle.net/2445/201908
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1186/s12890-023-02605-2
dc.relation.ispartofBMC Pulmonary Medicine, 2023, vol. 23, num. 1
dc.relation.urihttps://doi.org/10.1186/s12890-023-02605-2
dc.rightscc by (c) Fuset, María Paz et al., 2023
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationCOVID-19
dc.subject.classificationRespiració artificial
dc.subject.classificationComorbiditat
dc.subject.otherCOVID-19
dc.subject.otherArtificial respiration
dc.subject.otherComorbidity
dc.titleDays spent on non-invasive ventilation support: can it determine when to initiate VV- ECMO? Observational study in a cohort of Covid-19 patients
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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