Literature DB >> 32614150

The association between timely opioid administration and hospitalization in children with sickle cell disease presenting to the emergency department in acute pain.

Cagla S Muslu1, Matthew Kopetsky2, Mark Nimmer1,3, Alexis Visotcky4, Raphael Fraser4, David C Brousseau1,3.   

Abstract

INTRODUCTION: The National Heart, Lung, and Blood Institute guidelines for sickle cell disease (SCD) pain crisis management recommend opioids within 60 minutes of emergency department (ED) registration and every 30 minutes thereafter until acute pain is managed. These guidelines are based on expert opinion without published, supporting data.
OBJECTIVE: To evaluate the association between timely ED opioid administration and hospitalization rates in children with SCD.
METHODS: Retrospective cohort of children presenting to a children's hospital ED with SCD pain between January 1, 2014, and April 30, 2018. Visits were extracted using ICD codes, chief complaints, and receipt of at least one opioid, and then reviewed to confirm the visit was an uncomplicated pain crisis. The primary outcome was hospitalization, yes or no. Generalized estimating equations were used to determine adjusted odds of hospitalization for the timely administration of initial and second doses of opioids.
RESULTS: Of the 902 eligible visits, 368 (40.8%) resulted in hospitalization. The mean (SD) age was 11.9 (± 5.2) years. The first opioid was administered within 60 minutes of arrival in 601 (66.6%) visits. The second opioid was administered within 30 minutes of the first in 84 (12.3%) visits. Receipt of the first opioid within 60 minutes of arrival was not associated with decreased hospitalization (1.30 [0.96-1.76]). However, receipt of the second dose within 30 minutes of the first was associated with decreased hospitalization (0.56 [0.33-0.94]).
CONCLUSION: This study suggests an association between children with SCD receiving a second dose within 30 minutes of the first opioid dose and decreased hospitalizations.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  emergency department; opioids; pain crisis; pain management; pediatrics; sickle cell disease

Year:  2020        PMID: 32614150      PMCID: PMC7674235          DOI: 10.1002/pbc.28268

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  18 in total

1.  Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999-2007.

Authors:  Hussain R Yusuf; Hani K Atrash; Scott D Grosse; Christopher S Parker; Althea M Grant
Journal:  Am J Prev Med       Date:  2010-04       Impact factor: 5.043

2.  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

3.  The number of people with sickle-cell disease in the United States: national and state estimates.

Authors:  David C Brousseau; Julie A Panepinto; Mark Nimmer; Raymond G Hoffmann
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

Review 4.  Pathogenesis and treatment of sickle cell disease.

Authors:  H F Bunn
Journal:  N Engl J Med       Date:  1997-09-11       Impact factor: 91.245

5.  Parents' pain medication underdosing is associated with more emergency department visits in sickle cell disease.

Authors:  Andrea K Morrison; Matthew P Myrvik; David C Brousseau; Amy L Drendel; J Paul Scott; Alexis Visotcky; Julie A Panepinto
Journal:  Pediatr Blood Cancer       Date:  2017-12-12       Impact factor: 3.167

6.  The burden of emergency department use for sickle-cell disease: an analysis of the national emergency department sample database.

Authors:  Sophie Lanzkron; C Patrick Carroll; Carlton Haywood
Journal:  Am J Hematol       Date:  2010-10       Impact factor: 10.047

7.  A Prospective Emergency Department Quality Improvement Project to Improve the Treatment of Vaso-Occlusive Crisis in Sickle Cell Disease: Lessons Learned.

Authors:  Paula Tanabe; Caroline E Freiermuth; David M Cline; Susan Silva
Journal:  Jt Comm J Qual Patient Saf       Date:  2017-01-13

8.  Emergency department crowding and analgesic delay in pediatric sickle cell pain crises.

Authors:  Rohit Shenoi; Long Ma; Dorothy Syblik; Shabana Yusuf
Journal:  Pediatr Emerg Care       Date:  2011-10       Impact factor: 1.454

9.  Emergency department management of acute pain episodes in sickle cell disease.

Authors:  Paula Tanabe; Randall Myers; Amy Zosel; Jane Brice; Altaf H Ansari; Julia Evans; Zoran Martinovich; Knox H Todd; Judith A Paice
Journal:  Acad Emerg Med       Date:  2007-03-26       Impact factor: 3.451

10.  Impact of emergency department care on outcomes of acute pain events in children with sickle cell disease.

Authors:  Amanda M Brandow; Mark Nimmer; Timothy Simmons; T Charles Casper; Lawrence J Cook; Corrie E Chumpitazi; J Paul Scott; Julie A Panepinto; David C Brousseau
Journal:  Am J Hematol       Date:  2016-09-03       Impact factor: 10.047

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