Evaluation of a clinical protocol using intranasal fentanyl for treatment of vaso-occlusive crisis in sickle cell patients in the emergency department.

Hemoglobinopathies Paediatric hematology Pain Sickle cell disease

Journal

Paediatrics & child health
ISSN: 1205-7088
Titre abrégé: Paediatr Child Health
Pays: England
ID NLM: 9815960

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 17 08 2018
accepted: 26 01 2019
entrez: 9 8 2020
pubmed: 9 8 2020
medline: 9 8 2020
Statut: ppublish

Résumé

Vaso-occlusive crisis (VOC) is one of the most frequent causes of emergency visits and admission in children with sickle cell disease (SCD). This study aims to evaluate whether the use of a new pain management pathway using intranasal (IN) fentanyl from triage leads to improved care, translated by a decrease in time to first opiate dose. We performed a retrospective chart review of patients with SCD who presented to the emergency department (ED) with VOC, in the period pre- (52 patients) and post- (44 patients) implementation period of the protocol. Time to first opiate was the primary outcome and was evaluated pre- and postimplementation. Patients received a first opiate dose within 52.3 minutes of registration (interquantile range [IQR] 30.6, 74.6), corresponding to a 41.4-minute reduction in the opiate administration time (95% confidence interval [CI] -56.1, -27.9). There was also a 43% increase in the number of patients treated with a nonintravenous (IV) opiate as first opiate dose (95% CI 26, 57). In patients who were discharged from the ED, there was a 49% decrease in the number of IV line insertions (95% CI -67, -22). There was no difference in the hospitalization rates (difference of 6 [95% CI -13, 25]). This study validates the use of our protocol using IN fentanyl as first treatment of VOC in the ED by significantly reducing the time to first opiate dose and the number of IVs.

Sections du résumé

BACKGROUND BACKGROUND
Vaso-occlusive crisis (VOC) is one of the most frequent causes of emergency visits and admission in children with sickle cell disease (SCD).
OBJECTIVES OBJECTIVE
This study aims to evaluate whether the use of a new pain management pathway using intranasal (IN) fentanyl from triage leads to improved care, translated by a decrease in time to first opiate dose.
METHODS METHODS
We performed a retrospective chart review of patients with SCD who presented to the emergency department (ED) with VOC, in the period pre- (52 patients) and post- (44 patients) implementation period of the protocol. Time to first opiate was the primary outcome and was evaluated pre- and postimplementation. Patients received a first opiate dose within 52.3 minutes of registration (interquantile range [IQR] 30.6, 74.6), corresponding to a 41.4-minute reduction in the opiate administration time (95% confidence interval [CI] -56.1, -27.9). There was also a 43% increase in the number of patients treated with a nonintravenous (IV) opiate as first opiate dose (95% CI 26, 57). In patients who were discharged from the ED, there was a 49% decrease in the number of IV line insertions (95% CI -67, -22). There was no difference in the hospitalization rates (difference of 6 [95% CI -13, 25]).
CONCLUSIONS CONCLUSIONS
This study validates the use of our protocol using IN fentanyl as first treatment of VOC in the ED by significantly reducing the time to first opiate dose and the number of IVs.

Identifiants

pubmed: 32765165
doi: 10.1093/pch/pxz022
pii: pxz022
pmc: PMC7395317
doi:

Types de publication

Journal Article

Langues

eng

Pagination

293-299

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the Canadian Paediatric Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Hugo Paquin (H)

Department of Pediatrics, Division of Pediatric Emergency Medicine, CHU Ste-Justine, Montréal, Quebec.

Evelyne D Trottier (ED)

Department of Pediatrics, Division of Pediatric Emergency Medicine, CHU Ste-Justine, Montréal, Quebec.

Yves Pastore (Y)

Department of Pediatrics, Division of Hematology and Oncology, CHU Ste-Justine, Montréal, Quebec.

Nancy Robitaille (N)

Department of Pediatrics, Division of Hematology and Oncology, CHU Ste-Justine, Montréal, Quebec.

Marie-Joelle Dore Bergeron (MJ)

Department of Pediatrics, CHU Ste-Justine, Montréal, Quebec.

Benoit Bailey (B)

Department of Pediatrics, Division of Pediatric Emergency Medicine, CHU Ste-Justine, Montréal, Quebec.

Classifications MeSH