Sedation Practices in Mechanically Ventilated Neurocritical Care Patients from 19 Countries: An International Cohort Study

dc.contributor.authorFeng S.N.
dc.contributor.authorLaws L.H.
dc.contributor.authorDiaz-Cruz C.
dc.contributor.authorCinotti R.
dc.contributor.authorSchultz M.J.
dc.contributor.authorAsehnoune K.
dc.contributor.authorStevens R.D.
dc.contributor.authorRobba C.
dc.contributor.authorCho S.M.
dc.contributor.correspondenceFeng S.N.
dc.contributor.otherMahidol University
dc.date.accessioned2025-01-27T18:23:19Z
dc.date.available2025-01-27T18:23:19Z
dc.date.issued2025-01-01
dc.description.abstractBackground: Our objective was to characterize the impact of common initial sedation practices on invasive mechanical ventilation (IMV) duration and in-hospital outcomes in patients with acute brain injury (ABI) and to elucidate variations in practices between high-income and middle-income countries. Methods: This was a post hoc analysis of a prospective observational data registry of neurocritically ill patients requiring IMV. The setting included 73 intensive care units (ICUs) in 18 countries, with a total of 1,450 patients with ABI requiring IMV. There were no interventions. Results: Patients were categorized into day 1 propofol, midazolam, propofol and midazolam, dexmedetomidine, or sodium thiopental. The primary outcome was duration of IMV. Secondary outcomes were ICU and hospital mortality, ICU length of stay, days to first extubation, extubation failure, and withdrawal of life-sustaining therapy. Multivariable analyses were adjusted for clinically preselected covariates. Of 1,450 included patients (median age 54 years, 66% male), 41.2% (n = 597) were started on propofol, 26.1% (n = 379) were started on midazolam, 19.9% were started on propofol and midazolam, 0.3% (n = 5) were started on sodium thiopental, 0.7% (n = 10) were started on dexmedetomidine, and 11.8% (n = 171) were treated without sedation. After adjustment, there was no significant difference in IMV duration between patients who received midazolam (aβ = 0.64, p = 0.43, 95% confidence interval [CI] − 0.96 to 2.24) or propofol and midazolam (aβ = 0.32, p = 0.46, 95% CI − 1.44 to 2.12) compared with patients who received propofol. Patients who were started on midazolam had an average length of ICU stay that was 2.78 days longer than patients started on propofol (p = 0.003, 95% CI 0.94–4.63). There were no differences in mortality, days to first extubation, extubation failure, or withdrawal of life-sustaining therapy. Patients from high-income countries (n = 1,125) were more likely to receive propofol on day 1 (45.7 vs. 25.5%), whereas patients from middle-income countries (n = 325) were more likely to receive midazolam (32.6 vs. 24.3%) (p < 0.001). Conclusions: In an international registry of patients with ABI requiring IMV, IMV duration did not differ significantly relative to initial sedation strategy. However, patients started on midazolam had longer ICU stay.
dc.identifier.citationNeurocritical Care (2025)
dc.identifier.doi10.1007/s12028-024-02200-1
dc.identifier.eissn15560961
dc.identifier.issn15416933
dc.identifier.pmid39776348
dc.identifier.scopus2-s2.0-85215527722
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/103058
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleSedation Practices in Mechanically Ventilated Neurocritical Care Patients from 19 Countries: An International Cohort Study
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85215527722&origin=inward
oaire.citation.titleNeurocritical Care
oairecerif.author.affiliationMahidol Oxford Tropical Medicine Research Unit
oairecerif.author.affiliationIRCCS San Martino Polyclinic Hospital
oairecerif.author.affiliationThomas Jefferson University Hospital
oairecerif.author.affiliationNantes Université
oairecerif.author.affiliationUniversity of Oxford
oairecerif.author.affiliationHôtel Dieu CHU de Nantes
oairecerif.author.affiliationUniversità degli Studi di Genova
oairecerif.author.affiliationMedizinische Universität Wien
oairecerif.author.affiliationAmsterdam UMC - University of Amsterdam
oairecerif.author.affiliationJohns Hopkins University School of Medicine

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