S'abonner

Midazolam-Droperidol, Droperidol, or Olanzapine for Acute Agitation: A Randomized Clinical Trial - 19/04/17

Doi : 10.1016/j.annemergmed.2016.07.033 
David McD. Taylor, MD, MPH a, , Celene Y.L. Yap, MSc c, Jonathan C. Knott, MBBS, PhD d, Simone E. Taylor, PharmD b, Georgina A. Phillips, MBBS e, Jonathan Karro, MBBS e, Esther W. Chan, BPharm, PhD f, David C.M. Kong, BPharm, PhD c, David J. Castle, MD g
a Emergency Department, Austin Health, Heidelberg, Victoria, Australia 
b Pharmacy Department, Austin Health, Heidelberg, Victoria, Australia 
c Centre for Medicine Use and Safety, Monash University, Parkville, Victoria, Australia 
d Emergency Department, Royal Melbourne Hospital, Parkville, Victoria, Australia 
e Emergency Department, St Vincent’s Hospital, Victoria Parade, Victoria, Australia 
f Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong 
g St Vincent’s Hospital and the University of Melbourne, Fitzroy, Victoria, Australia 

Corresponding Author.

Abstract

Study objective

We aim to determine the most efficacious of 3 common medication regimens for the sedation of acutely agitated emergency department (ED) patients.

Methods

We undertook a randomized, controlled, double-blind, triple-dummy, clinical trial in 2 metropolitan EDs between October 2014 and August 2015. Patients aged 18 to 65 years and requiring intravenous medication sedation for acute agitation were enrolled and randomized to an intravenous bolus of midazolam 5 mg–droperidol 5 mg, droperidol 10 mg, or olanzapine 10 mg. Two additional doses were administered, if required: midazolam 5 mg, droperidol 5 mg, or olanzapine 5 mg. The primary outcome was the proportion of patients adequately sedated at 10 minutes.

Results

Three hundred forty-nine patients were randomized to the 3 groups. Baseline characteristics were similar across the groups. Ten minutes after the first dose, significantly more patients in the midazolam-droperidol group were adequately sedated compared with the droperidol and olanzapine groups: differences in proportions 25.0% (95% confidence interval [CI] 12.0% to 38.1%) and 25.4% (95% CI 12.7% to 38.3%), respectively. For times to sedation, the differences in medians between the midazolam-droperidol group and the droperidol and olanzapine groups were 6 (95% CI 3 to 8) and 6 (95% CI 3 to 7) minutes, respectively. Patients in the midazolam-droperidol group required fewer additional doses or alternative drugs to achieve adequate sedation. The 3 groups’ adverse event rates and lengths of stay did not differ.

Conclusion

Midazolam-droperidol combination therapy is superior, in the doses studied, to either droperidol or olanzapine monotherapy for intravenous sedation of the acutely agitated ED patient.

Le texte complet de cet article est disponible en PDF.

Plan


 Please see page 319 for the Editor’s Capsule Summary of this article.
 Supervising editor: Steven M. Green, MD
 Author contributions: All authors conceived and designed the study, contributed to the ethics committee (institutional review board) application, contributed to interpretation of the results, drafted the article, and contributed to its revision. DMcDT obtained the research funding. CYLY, SET, and DCMK prepared the study packs. DMcDT and CYLY supervised the study overall. JCK, GAP, and JK supervised the study at their respective sites. CYLY, JCK, GAP, and JK were responsible for all staff education. CYLY managed collation of the data and entry into the study database. DMcDT, CYLY, and JCK undertook the data analysis. DMcDT takes responsibility for the paper as a whole.
 Funding and support: By Annals policy, all authors are required to disclose any and all commercial, financial, and other relationships in any way related to the subject of this article as per ICMJE conflict of interest guidelines (see www.icmje.org/). The authors have stated that no such relationships exist. The study was supported by the Morson Taylor Research Award 2013 of the Australasian College for Emergency Medicine Foundation and the Austin Health Medical Research Foundation, 2014.
 Trial registration number: ACTRN12607000591459
 Neither of the funding organizations had any role in the design or execution of the study, or the data analysis or interpretation.
 A 8TPZ5TT survey is available with each research article published on the Web at www.annemergmed.com.
 A podcast for this article is available at www.annemergmed.com.


© 2016  American College of Emergency Physicians. Publié par Elsevier Masson SAS. Tous droits réservés.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 69 - N° 3

P. 318 - mars 2017 Retour au numéro
Article précédent Article précédent
  • Design: A Neglected Modality for Improvement
  • Robert L. Wears
| Article suivant Article suivant
  • A Prospective Observational Study of Patients Receiving Intravenous and Intramuscular Olanzapine in the Emergency Department
  • Jon B. Cole, Johanna C. Moore, Benjamin J. Dolan, Alex O’Brien-Lambert, Brandon J. Fryza, James R. Miner, Marc L. Martel

Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.

Déjà abonné à cette revue ?

Mon compte


Plateformes Elsevier Masson

Déclaration CNIL

EM-CONSULTE.COM est déclaré à la CNIL, déclaration n° 1286925.

En application de la loi nº78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, vous disposez des droits d'opposition (art.26 de la loi), d'accès (art.34 à 38 de la loi), et de rectification (art.36 de la loi) des données vous concernant. Ainsi, vous pouvez exiger que soient rectifiées, complétées, clarifiées, mises à jour ou effacées les informations vous concernant qui sont inexactes, incomplètes, équivoques, périmées ou dont la collecte ou l'utilisation ou la conservation est interdite.
Les informations personnelles concernant les visiteurs de notre site, y compris leur identité, sont confidentielles.
Le responsable du site s'engage sur l'honneur à respecter les conditions légales de confidentialité applicables en France et à ne pas divulguer ces informations à des tiers.


Tout le contenu de ce site: Copyright © 2024 Elsevier, ses concédants de licence et ses contributeurs. Tout les droits sont réservés, y compris ceux relatifs à l'exploration de textes et de données, a la formation en IA et aux technologies similaires. Pour tout contenu en libre accès, les conditions de licence Creative Commons s'appliquent.