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Sedation - Effects of disorders of abuse on therapeutic efficacy (SEDATE): A retrospective cohort study.
Albala, Lorenzo; Loesche, Michael A; Hayes, Bryan D; McEvoy, Dustin S; Filbin, Michael; Dutta, Sayon; Eyre, Andrew J.
Afiliação
  • Albala L; Department of Emergency Medicine, Massachusetts General Hospital, Boston, MA, United States of America. Electronic address: lalbala@partners.org.
  • Loesche MA; Department of Emergency Medicine, Massachusetts General Hospital, Boston, MA, United States of America.
  • Hayes BD; Department of Emergency Medicine, Massachusetts General Hospital, Boston, MA, United States of America; Department of Pharmacy, Massachusetts General Hospital, Boston, MA, United States of America.
  • McEvoy DS; Digital Health eCare, Mass General Brigham, Boston, MA, United States of America.
  • Filbin M; Department of Emergency Medicine, Massachusetts General Hospital, Boston, MA, United States of America.
  • Dutta S; Department of Emergency Medicine, Massachusetts General Hospital, Boston, MA, United States of America; Digital Health eCare, Mass General Brigham, Boston, MA, United States of America.
  • Eyre AJ; Department of Emergency Medicine, Brigham and Women's Hospital, Boston, MA, United States of America.
Am J Emerg Med ; 49: 294-299, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34182272
ABSTRACT

BACKGROUND:

The impact of alcohol or opioid use disorders on medication dosing for procedural sedation in the emergency department (ED) is unclear, as most of the literature is from gastrointestinal endoscopy. Exploring how these patient factors affect sedative and analgesic medications may inform more nuanced sedation strategies in the emergency department.

METHODS:

This was a retrospective chart-review cohort study across five EDs from 2015 to 2020. Included were adult patients who underwent procedural sedation in the ED, categorized into three a priori groups alcohol use disorder (AUD), opioid use disorder (OUD), and individuals with neither (non-SUD). Wilcoxon test was used to compare the time-averaged dose of agents between groups. Logistic regression was used to model multi-agent sedations. The propofol time-averaged dose was the primary outcome. Secondary outcomes included other agents, sedation duration, and switching to other agents.

RESULTS:

2725 sedations were included in the analysis. 59 patients had a history of AUD, and 40 had a history of OUD. Time-averaged doses of medications did not differ significantly between AUD and non-SUD patients. Likewise, patients with OUD did not receive different doses of medications compared to non-SUD. The propofol doses for non-SUD, AUD, and OUD were 0.033 IQR 0.04; 0.042 IQR 0.05; and 0.058 IQR 0.04 mg/kg*min, respectively. Sedation duration was not different across groups. Having AUD or OUD is not associated with increased odds of requiring multiple sedative agents.

CONCLUSION:

Although sedation in patients with AUD or OUD may be associated with significant case bias, these patient factors did not significantly alter outcomes compared to the general population. This study suggests there is no evidence to proactively adjust medication strategy in ED patients with AUD or OUD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Relacionados ao Uso de Substâncias / Relação Dose-Resposta a Droga / Hipnóticos e Sedativos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Emerg Med Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Relacionados ao Uso de Substâncias / Relação Dose-Resposta a Droga / Hipnóticos e Sedativos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Emerg Med Ano de publicação: 2021 Tipo de documento: Article