Literature DB >> 26412961

A Quality Improvement Initiative to Improve Emergency Department Care for Pediatric Patients with Sickle Cell Disease.

Marsha J Treadwell1, Michael Bell1, Sara A Leibovich1, Fernando Barreda1, Anne Marsh1, Ginny Gildengorin1, Claudia R Morris1.   

Abstract

OBJECTIVE: To determine whether a quality improvement (QI) initiative would result in more timely assessment and treatment of acute sickle cell-related pain for pediatric patients with sickle cell disease (SCD) treated in the emergency department (ED).
METHODS: We created and implemented a protocol for SCD pain management in the ED with the goals of improving (1) mean time from triage to first analgesic dose; (2) percentage of patients that received their first analgesic dose within 30 minutes of triage, and (3) percentage of patients who had pain assessment performed within 30 minutes of triage and who were re-assessed within 30 minutes after the first analgesic dose.
RESULTS: Significant improvements were achieved between baseline (55 patient visits) and post order set implementation (165 visits) in time from triage to administration of first analgesic (decreased from 89.9 ± 50.5 to 35.2 ± 22.8 minutes, P < 0.001); percentage of patient visits receiving pain medications within 30 minutes of triage (from 7% to 53%, P < 0.001); percentage of patient visits assessed within 30 minutes of triage (from 64% to 99.4%, P < 0.001); and percentage of patient visits re-assessed within 30 minutes of initial analgesic (from 54% to 86%, P < 0.001).
CONCLUSIONS: Implementation of a QI initiative in the ED led to expeditious care for pediatric patients with SCD presenting with pain. A QI framework provided us with unique challenges but also invaluable lessons as we address our objective of decreasing the quality gap in SCD medical care.

Entities:  

Year:  2014        PMID: 26412961      PMCID: PMC4580258     

Source DB:  PubMed          Journal:  J Clin Outcomes Manag        ISSN: 1079-6533


  25 in total

1.  Guidelines for the management of the acute painful crisis in sickle cell disease.

Authors:  David C Rees; Ade D Olujohungbe; Norman E Parker; Adrian D Stephens; Paul Telfer; Josh Wright
Journal:  Br J Haematol       Date:  2003-03       Impact factor: 6.998

2.  A comparison of analgesic management for emergency department patients with sickle cell disease and renal colic.

Authors:  Matthew P Lazio; Heather H Costello; D Mark Courtney; Zoran Martinovich; Randall Myers; Amy Zosel; Paula Tanabe
Journal:  Clin J Pain       Date:  2010 Mar-Apr       Impact factor: 3.442

3.  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

4.  Evaluation and Treatment of Sickle Cell Pain in the Emergency Department: Paths to a Better Future.

Authors:  William T Zempsky
Journal:  Clin Pediatr Emerg Med       Date:  2010-12-01

5.  Treatment of sickle cell pain: fostering trust and justice.

Authors:  William T Zempsky
Journal:  JAMA       Date:  2009-12-09       Impact factor: 56.272

6.  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

7.  Adult emergency department patients with sickle cell pain crisis: results from a quality improvement learning collaborative model to improve analgesic management.

Authors:  Paula Tanabe; John W Hafner; Zoran Martinovich; Nicole Artz
Journal:  Acad Emerg Med       Date:  2012-04       Impact factor: 3.451

8.  Pain management and symptoms of substance dependence among patients with sickle cell disease.

Authors:  James Elander; Joanne Lusher; David Bevan; Paul Telfer
Journal:  Soc Sci Med       Date:  2003-11       Impact factor: 4.634

9.  Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: an educational void.

Authors:  Lawrence R Solomon
Journal:  Blood       Date:  2007-10-16       Impact factor: 22.113

10.  Daily assessment of pain in adults with sickle cell disease.

Authors:  Wally R Smith; Lynne T Penberthy; Viktor E Bovbjerg; Donna K McClish; John D Roberts; Bassam Dahman; Imoigele P Aisiku; James L Levenson; Susan D Roseff
Journal:  Ann Intern Med       Date:  2008-01-15       Impact factor: 25.391

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