Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-14T05:04:42.889Z Has data issue: false hasContentIssue false

P030: The FAN study: intranasal fentanyl and inhaled nitrous oxide for fracture reduction

Published online by Cambridge University Press:  02 June 2016

J. Hoeffe
Affiliation:
CHU Sainte Justine, Bern
E. D. Trottier
Affiliation:
CHU Sainte Justine, Bern
B. Bailey
Affiliation:
CHU Sainte Justine, Bern
D. Shellshear
Affiliation:
CHU Sainte Justine, Bern
M. Lagacé
Affiliation:
CHU Sainte Justine, Bern
C. Sutter
Affiliation:
CHU Sainte Justine, Bern
G. Grimard
Affiliation:
CHU Sainte Justine, Bern
R. Cook
Affiliation:
CHU Sainte Justine, Bern
F. Babl
Affiliation:
CHU Sainte Justine, Bern

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Introduction: Recently, intranasal (IN) fentanyl and inhaled nitrous oxide/oxygen (N2O) mixture have been increasingly used for procedural sedation and analgesia (PSA) alone or in combination. There is a lack of data on the efficacy of these combined agents. Methods: The objective was to evaluate the efficacy of IN fentanyl and N2O as PSA for the reduction of mildly-to-moderately displaced fractures and dislocations. We performed a prospective, observational cohort study between September 2014 and October 2015. Patients were recruited at CHU Sainte Justine (Montréal) and Royal Children Hospital (Melbourne, Australia). Patients aged 4 to 18 years were eligible if PSA consisted of IN fentanyl and N2O for the reduction of mildly-to-moderately displaced fractures or dislocations. Patients received at least IN fentanyl 1.5 mcg/kg (100 mcg max) and at least a 50/50% mixture of N2O with oxygen. Primary outcome was the efficacy of PSA measured by the patient assigned Facial Pain Scale-Revised (FPS-R). The Face, Legs, Activity, Cry, Consolability (FLACC) scale was also recorded. Depth of sedation was evaluated using University of Michigan Sedation Scale (UMSS). Adverse events were recorded following criteria of the Consensus Panel on Sedation Research of PERC/PECARN. Additional data concerning satisfaction or discomfort were evaluated via questionnaires, and follow-up telephone calls were made to elicit information on adverse events after discharge. Results: A total of 91 patients aged 9.7 ± 3.0 years were enrolled. There was no difference between the median FPS-R score during the procedure compared to before: Median 2 and 2 (median difference 0 [95% CI 0, 0]), respectively. The FLACC score was higher during the procedure than before: Median 4 and 0 (median difference 2 [95% CI 1, 3]). UMSS was 1 (95% CI 1, 2) during the procedure. 42 (46%) patients had adverse events, all mild: vertigo (20%), nausea (16%)]or vomiting (12%). A total of 85/88 (97%) parents and 82/85 (96%) ED physicians would want the same sedation in another procedure. Conclusion: PSA with IN fentanyl and N2O seems effective in our study, as evaluated by patient assigned FPS-R. Patients were minimally sedated. Adverse events were frequent but mild. Overall, parents and medical staff would want the same agents used in another procedure. Thus, PSA with IN fentanyl and N2O appears to be an attractive option for reduction of mildly displaced fractures or dislocations.

Type
Posters Presentations
Copyright
Copyright © Canadian Association of Emergency Physicians 2016