Literature DB >> 32765165

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

Hugo Paquin1, Evelyne D Trottier1, Yves Pastore2, Nancy Robitaille2, Marie-Joelle Dore Bergeron3, Benoit Bailey1.   

Abstract

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: 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: 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: 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.
© 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.

Entities:  

Keywords:  Hemoglobinopathies; Paediatric hematology; Pain; Sickle cell disease

Year:  2019        PMID: 32765165      PMCID: PMC7395317          DOI: 10.1093/pch/pxz022

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN: 1205-7088            Impact factor:   2.253


  37 in total

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Authors:  Deborah Tomlinson; Carl L von Baeyer; Jennifer N Stinson; Lillian Sung
Journal:  Pediatrics       Date:  2010-10-04       Impact factor: 7.124

Review 2.  Intranasal fentanyl in the treatment of acute pain--a systematic review.

Authors:  M S Hansen; O Mathiesen; S Trautner; J B Dahl
Journal:  Acta Anaesthesiol Scand       Date:  2012-01-19       Impact factor: 2.105

3.  Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease.

Authors:  Julie A Panepinto; David C Brousseau; Cheryl A Hillery; J Paul Scott
Journal:  Pediatr Blood Cancer       Date:  2005-02       Impact factor: 3.167

Review 4.  Intranasal fentanyl for pain management in children: a systematic review of the literature.

Authors:  Shawna Mudd
Journal:  J Pediatr Health Care       Date:  2010-06-17       Impact factor: 1.812

Review 5.  The management of painful crisis in sickle cell disease.

Authors:  Josh Wright; Sam H Ahmedzai
Journal:  Curr Opin Support Palliat Care       Date:  2010-06       Impact factor: 2.302

6.  Intranasal fentanyl for the prehospital management of acute pain in children.

Authors:  Adrian P Murphy; Macartan Hughes; Siobhan Mccoy; Gloria Crispino; Abel Wakai; Ronan O'Sullivan
Journal:  Eur J Emerg Med       Date:  2017-12       Impact factor: 2.799

7.  Retrospective evaluation of pain assessment and treatment for acute vasoocclusive episodes in children with sickle cell disease.

Authors:  William T Zempsky; Kristin A Loiselle; Kathleen McKay; Gabriella L Blake; J Nathan Hagstrom; Neil L Schechter; Zeev N Kain
Journal:  Pediatr Blood Cancer       Date:  2008-08       Impact factor: 3.167

8.  The implementation of intranasal fentanyl for children in a mixed adult and pediatric emergency department reduces time to analgesic administration.

Authors:  Anna Holdgate; Anthony Cao; Ka Mei Lo
Journal:  Acad Emerg Med       Date:  2010-02       Impact factor: 3.451

Review 9.  Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.

Authors:  Barbara P Yawn; George R Buchanan; Araba N Afenyi-Annan; Samir K Ballas; Kathryn L Hassell; Andra H James; Lanetta Jordan; Sophie M Lanzkron; Richard Lottenberg; William J Savage; Paula J Tanabe; Russell E Ware; M Hassan Murad; Jonathan C Goldsmith; Eduardo Ortiz; Robinson Fulwood; Ann Horton; Joylene John-Sowah
Journal:  JAMA       Date:  2014-09-10       Impact factor: 56.272

10.  Sickle cell disease related mortality in the United States (1999-2009).

Authors:  Dima Hamideh; Ofelia Alvarez
Journal:  Pediatr Blood Cancer       Date:  2013-04-23       Impact factor: 3.167

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Review 2.  Acute complications in children with sickle cell disease: Prevention and management.

Authors:  Carolyn E Beck; Evelyne D Trottier; Melanie Kirby-Allen; Yves Pastore
Journal:  Paediatr Child Health       Date:  2022-03-07       Impact factor: 2.253

3.  La prévention et la prise en charge des complications aiguës de l'anémie falciforme.

Authors:  Carolyn E Beck; Evelyne D Trottier; Melanie Kirby-Allen; Yves Pastore
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Review 4.  Commonly used agent for acute pain management of sickle cell anemia in Saudi Emergency Department: A narrative review.

Authors:  Reem A Hejazi; Nameer A Mandourah; Aryaf S Alsulami; Hussain T Bakhsh; Reem M Diri; Ahmad O Noor
Journal:  Saudi Pharm J       Date:  2021-02-16       Impact factor: 4.330

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