Literature DB >> 32928464

A Multiyear Cross-sectional Study of Guideline Adherence for the Timeliness of Opioid Administration in Children With Sickle Cell Pain Crisis.

David C Brousseau1, Elizabeth R Alpern2, James M Chamberlain3, Angela M Ellison4, Lalit Bajaj5, Daniel M Cohen6, Selena Hariharan7, Lawrence J Cook8, Monica Harding8, Julie Panepinto9.   

Abstract

STUDY
OBJECTIVE: The National Heart, Lung, and Blood Institute evidence-based guidelines for timeliness of opioid administration for sickle cell disease (SCD) pain crises recommend an initial opioid within 1 hour of arrival, with subsequent dosing every 30 minutes until pain is controlled. No multisite studies have evaluated guideline adherence, to our knowledge. Our objective was to determine guideline adherence across a multicenter network.
METHODS: We conducted a multiyear cross-sectional analysis of children with SCD who presented between January 1, 2016, and December 31, 2018, to 7 emergency departments (EDs) within the Pediatric Emergency Care Applied Research Network. Visits for uncomplicated pain crisis were included, defined with an International Classification of Diseases, Ninth Revision (ICD-9) and ICD-10 code for SCD crisis and receipt of an opioid, excluding visits with other SCD complications or temperature exceeding 38.5°C (101.3°F). Times were extracted from the electronic record. Guideline adherence was assessed across sites and calendar years.
RESULTS: A total of 4,578 visits were included. The median time to first opioid receipt was 62 minutes (interquartile range 42 to 93 minutes); between the first and second opioid receipt, 60 minutes (interquartile range 39 to 93 minutes). Overall, 48% of visits (95% confidence interval 47% to 50%) were guideline adherent for first opioid. Of 3,538 visits with a second opioid, 15% (95% confidence interval 14% to 16%) were guideline adherent. Site variation in adherence existed for time to first opioid (range 22% to 70%) and time between first and second opioid (range 2% to 36%; both P<.001). There was no change in timeliness to first dose or time between doses across years (P>.05 for both).
CONCLUSION: Guideline adherence for timeliness of SCD treatment is poor, with half of visits adherent for time to first opioid and one seventh adherent for second dose. Dissemination and implementation research/quality improvement efforts are critical to improve care across EDs.
Copyright © 2020 American College of Emergency Physicians. Published by Elsevier Inc. All rights reserved.

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Year:  2020        PMID: 32928464      PMCID: PMC8689682          DOI: 10.1016/j.annemergmed.2020.08.006

Source DB:  PubMed          Journal:  Ann Emerg Med        ISSN: 0196-0644            Impact factor:   5.721


  20 in total

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Authors:  M D Cabana; C S Rand; N R Powe; A W Wu; M H Wilson; P A Abboud; H R Rubin
Journal:  JAMA       Date:  1999-10-20       Impact factor: 56.272

2.  Translating Clinical Guidelines Into Practice: Challenges and Opportunities in a Dynamic Health Care Environment.

Authors:  Emily B Vander Schaaf; Carl J Seashore; Greg D Randolph
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3.  The Pediatric Emergency Care Applied Research Network Registry: A Multicenter Electronic Health Record Registry of Pediatric Emergency Care.

Authors:  Sara J Deakyne Davies; Robert W Grundmeier; Diego A Campos; Katie L Hayes; Jamie Bell; Evaline A Alessandrini; Lalit Bajaj; James M Chamberlain; Marc H Gorelick; Rene Enriquez; T Charles Casper; Beth Scheid; Marlena Kittick; J Michael Dean; Elizabeth R Alpern
Journal:  Appl Clin Inform       Date:  2018-05-23       Impact factor: 2.342

4.  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

5.  Race matters: perceptions of race and racism in a sickle cell center.

Authors:  Stephen C Nelson; Heather W Hackman
Journal:  Pediatr Blood Cancer       Date:  2012-09-28       Impact factor: 3.167

6.  Sickle cell-related pain: perceptions of medical practitioners.

Authors:  B S Shapiro; L J Benjamin; R Payne; G Heidrich
Journal:  J Pain Symptom Manage       Date:  1997-09       Impact factor: 3.612

7.  Acute care utilization and rehospitalizations for sickle cell disease.

Authors:  David C Brousseau; Pamela L Owens; Andrew L Mosso; Julie A Panepinto; Claudia A Steiner
Journal:  JAMA       Date:  2010-04-07       Impact factor: 56.272

8.  Management of sickle cell pain crisis in the emergency department at teaching hospitals.

Authors:  R Silbergleit; M O Jancis; R M McNamara
Journal:  J Emerg Med       Date:  1999 Jul-Aug       Impact factor: 1.484

9.  The cost of health care for children and adults with sickle cell disease.

Authors:  Teresa L Kauf; Thomas D Coates; Liu Huazhi; Nikita Mody-Patel; Abraham G Hartzema
Journal:  Am J Hematol       Date:  2009-06       Impact factor: 10.047

10.  Management of Chronic Pain in Adults Living With Sickle Cell Disease in the Era of the Opioid Epidemic: A Qualitative Study.

Authors:  Cynthia B Sinha; Nitya Bakshi; Diana Ross; Lakshmanan Krishnamurti
Journal:  JAMA Netw Open       Date:  2019-05-03
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Authors:  Chris A Rees; David C Brousseau; Fahd A Ahmad; Jonathan Bennett; Seema Bhatt; Amanda Bogie; Kathleen M Brown; T Charles Casper; Laura L Chapman; Corrie E Chumpitazi; Daniel M Cohen; Carlton Dampier; Angela M Ellison; Hartmut Grasemann; Robert W Hickey; Lewis L Hsu; Peter A Lane; Nitya Bakshi; Sara Leibovich; Prabhumallikarjun Patil; Elizabeth C Powell; Rachel Richards; Syana Sarnaik; Debra L Weiner; Claudia R Morris
Journal:  Am J Hematol       Date:  2022-09-05       Impact factor: 13.265

  1 in total

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