Comparison of Nebulized Ketamine to Intravenous Subdissociative Dose Ketamine for Treating Acute Painful Conditions in the Emergency Department: A Prospective, Randomized, Double-Blind, Double-Dummy Controlled Trial.


Journal

Annals of emergency medicine
ISSN: 1097-6760
Titre abrégé: Ann Emerg Med
Pays: United States
ID NLM: 8002646

Informations de publication

Date de publication:
01 May 2024
Historique:
received: 05 01 2024
revised: 18 03 2024
accepted: 22 03 2024
medline: 5 5 2024
pubmed: 5 5 2024
entrez: 4 5 2024
Statut: aheadofprint

Résumé

We aimed to assess and compare the analgesic efficacy and adverse effects of intravenous subdissociative-dose ketamine to nebulized ketamine in emergency department (ED) patients with acute painful conditions. We conducted a prospective, randomized, double-blind, double-dummy clinical trial in adult patients (ages 18 and older) with a numerical rating scale pain score of ≥5. We randomized subjects to receive either a single dose of 0.3 mg/kg of intravenous (IV) ketamine or 0.75 mg/kg of nebulized ketamine through a breath-actuated nebulizer. Primary outcome was the difference in pain scores on the numerical rating scale between groups at 30 minutes postmedication administration. The secondary outcomes included the need for rescue analgesia, occurrences of adverse events in each group, and the difference in pain scores at 15, 30, 60, 90, and 120 minutes. We calculated a 95% confidence interval (CI) for a mean difference at 30 minutes, with a minimum clinically important difference set at 1.3 points. We enrolled 150 subjects (75 per group). Mean pain scores through numerical rating scale were 8.2 for both groups at baseline, which decreased to 3.6 and 3.8 at 30 minutes, yielding a mean difference of 0.23 (95% CI -1.32 to 0.857). We observed no clinically concerning changes in vital signs. No serious adverse events occurred in any of the groups throughout the study period. We found no difference between the administration of IV and nebulized ketamine for the short-term treatment of moderate to severe acute pain in the ED, with both treatments providing a clinically meaningful reduction in pain scores at 30 minutes.

Identifiants

pubmed: 38703175
pii: S0196-0644(24)00171-9
doi: 10.1016/j.annemergmed.2024.03.024
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American College of Emergency Physicians. Published by Elsevier Inc. All rights reserved.

Auteurs

Tommy Nguyen (T)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Mo Mai (M)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Amulya Choudhary (A)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Slavic Gitelman (S)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Jefferson Drapkin (J)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY. Electronic address: jdrapkin@maimonidesmed.org.

Antonios Likourezos (A)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Sarah Kabariti (S)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Rukhsana Hossain (R)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Karina Kun (K)

Department of Pharmacy, Maimonides Medical Center, Brooklyn, NY.

Ankit Gohel (A)

Department of Pharmacy, Maimonides Medical Center, Brooklyn, NY.

Patrizia Niceforo (P)

Department of Pharmacy, Maimonides Medical Center, Brooklyn, NY.

Michael Silver (M)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Sergey Motov (S)

Department of Emergency Medicine Maimonides Medical Center, Brooklyn, NY.

Classifications MeSH