dc.contributor.author | Aragon, Romina E. | |
dc.contributor.author | Proano, Alvaro | |
dc.contributor.author | Mongilardi, Nicole | |
dc.contributor.author | de Ferrari, Aldo | |
dc.contributor.author | Herrera, Phabiola | |
dc.contributor.author | Roldan, Rollin | |
dc.contributor.author | Paz, Enrique | |
dc.contributor.author | Jaymez, Amador A. | |
dc.contributor.author | Chirinos, Eduardo | |
dc.contributor.author | Portugal, Jose | |
dc.contributor.author | Quispe, Rocio | |
dc.contributor.author | Brower, Roy G. | |
dc.contributor.author | Checkley, William | |
dc.date.accessioned | 2019-07-04T17:00:23Z | |
dc.date.available | 2019-07-04T17:00:23Z | |
dc.date.issued | 2019 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/6900 | |
dc.description.abstract | OBJECTIVES: We sought to study the association between sedation status, medications (benzodiazepines, opioids, and antipsychotics), and clinical outcomes in a resource-limited setting. DESIGN: A longitudinal study of critically ill participants on mechanical ventilation. SETTING: Five intensive care units (ICUs) in four public hospitals in Lima, Peru. PATIENTS: One thousand six hundred fifty-seven critically ill participants were assessed daily for sedation status during 28 days and vital status by day 90. RESULTS: After excluding data of participants without a Richmond Agitation Sedation Scale score and without sedation, we followed 1338 (81%) participants longitudinally for 18,645 ICU days. Deep sedation was present in 98% of participants at some point of the study and in 12,942 ICU days. Deep sedation was associated with higher mortality (interquartile odds ratio (OR) = 5.42, 4.23-6.95; p < 0.001) and a significant decrease in ventilator (- 7.27; p < 0.001), ICU (- 4.38; p < 0.001), and hospital (- 7.00; p < 0.001) free days. Agitation was also associated with higher mortality (OR = 39.9, 6.53-243, p < 0.001). The most commonly used sedatives were opioids and benzodiazepines (9259 and 8453 patient days respectively), and the latter were associated with a 41% higher mortality in participants with a higher cumulative dose (75th vs 25th percentile, interquartile OR = 1.41, 1.12-1.77; p < 0.01). The overall cumulative dose of benzodiazepines and opioids was high, 774.5 mg and 16.8 g, respectively, by day 7 and by day 28; these doses approximately doubled. Haloperidol was only used in 3% of ICU days; however, the use of it was associated with a 70% lower mortality (interquartile OR = 0.3, 0.22-0.44, p < 0.001). CONCLUSIONS: Deep sedation, agitation, and cumulative dose of benzodiazepines were all independently associated with higher 90-day mortality. Additionally, deep sedation was associated with less ventilator-, ICU-, and hospital-free days. In contrast, haloperidol was associated with lower mortality in our study. | en_US |
dc.language.iso | eng | |
dc.publisher | BioMed Central | |
dc.relation.ispartofseries | Critical Care | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | acute respiratory failure | en_US |
dc.subject | adult | en_US |
dc.subject | agitation | en_US |
dc.subject | anesthesia level | en_US |
dc.subject | APACHE | en_US |
dc.subject | Article | en_US |
dc.subject | artificial ventilation | en_US |
dc.subject | benzodiazepine derivative | en_US |
dc.subject | clinical assessment | en_US |
dc.subject | clinical outcome | en_US |
dc.subject | Clinical outcomes | en_US |
dc.subject | cohort analysis | en_US |
dc.subject | controlled study | en_US |
dc.subject | Critical illness | en_US |
dc.subject | critically ill patient | en_US |
dc.subject | deep sedation | en_US |
dc.subject | dexmedetomidine | en_US |
dc.subject | drug use | en_US |
dc.subject | female | en_US |
dc.subject | Glasgow coma scale | en_US |
dc.subject | haloperidol | en_US |
dc.subject | human | en_US |
dc.subject | intensive care unit | en_US |
dc.subject | length of stay | en_US |
dc.subject | longitudinal study | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | middle aged | en_US |
dc.subject | mortality rate | en_US |
dc.subject | mortality risk | en_US |
dc.subject | multicenter study | en_US |
dc.subject | narcotic analgesic agent | en_US |
dc.subject | observational study | en_US |
dc.subject | Peru | en_US |
dc.subject | prevalence | en_US |
dc.subject | priority journal | en_US |
dc.subject | propofol | en_US |
dc.subject | prospective study | en_US |
dc.subject | public hospital | en_US |
dc.subject | Ramsay Sedation Scale | en_US |
dc.subject | Richmond Agitation Sedation Scale | en_US |
dc.subject | sedation | en_US |
dc.subject | Sedation | en_US |
dc.subject | Sequential Organ Failure Assessment Score | en_US |
dc.subject | ventilated patient | en_US |
dc.title | Sedation practices and clinical outcomes in mechanically ventilated patients in a prospective multicenter cohort | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1186/s13054-019-2394-9 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.02.09 | |
dc.relation.issn | 1466-609X |
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