Literature DB >> 28334590

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

Paula Tanabe, Caroline E Freiermuth, David M Cline, Susan Silva.   

Abstract

BACKGROUND: Guidelines recommend rapid, aggressive management of vaso-occlusive crisis (VOC) for patients with sickle cell disease (SCD). A large prospective research and quality improvement (QI) project was conducted to measure changes in clinical outcomes in two EDs-academic medical centers with emergency medicine residency programs and Level 1 trauma centers-during a 2.5-year time period (October 2011-March 2014).
METHODS: A QI team used a Plan-Do-Study-Act approach to modify and implement changes to opioid analgesic protocols for the emergency department (ED) treatment of VOC. Data were collected quarterly; the team reviewed the results and made modifications to improve outcomes. A structured health record review was conducted to assess clinical outcomes (10 records/quarter/site). Patient interviews were conducted to measure satisfaction with pain management. Outcomes were compared before (T1) and after (T2) implementation of an electronic health record (EHR).
RESULTS: One hundred ninety-six ED health records (118 unique patients, mean age = 32 [standard deviation, 11], 51% male) were analyzed. Before implementation, trends in decreasing time to initial analgesic administration were noted. There was a statistically significant increase in arrival to administration of first analgesic time between T1 and T2 at Site 1 but not at Site 2. Neither site showed significant changes in time between the administration of the first and second opioid doses, total opioid dose administered, or patient satisfaction.
CONCLUSION: While QI efforts initially shortened door-to-analgesic times, these gains were not sustained. The lessons learned can help other EDs improve the timely delivery of analgesics to patients with SCD.
Copyright © 2016 The Joint Commission. Published by Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 28334590     DOI: 10.1016/j.jcjq.2016.12.005

Source DB:  PubMed          Journal:  Jt Comm J Qual Patient Saf        ISSN: 1553-7250


  5 in total

Review 1.  Improving Emergency Department-Based Care of Sickle Cell Pain.

Authors:  Jeffrey A Glassberg
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

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

Authors:  Cagla S Muslu; Matthew Kopetsky; Mark Nimmer; Alexis Visotcky; Raphael Fraser; David C Brousseau
Journal:  Pediatr Blood Cancer       Date:  2020-07-02       Impact factor: 3.167

Review 3.  Key Components of Pain Management for Children and Adults with Sickle Cell Disease.

Authors:  Amanda M Brandow; Michael R DeBaun
Journal:  Hematol Oncol Clin North Am       Date:  2018-06       Impact factor: 3.722

4.  Emergency Department (ED), ED Observation, Day Hospital, and Hospital Admissions for Adults with Sickle Cell Disease.

Authors:  David M Cline; Susan Silva; Caroline E Freiermuth; Victoria Thornton; Paula Tanabe
Journal:  West J Emerg Med       Date:  2018-02-12

5.  Patient Perspectives of Sickle Cell Management in the Emergency Department.

Authors:  Nancy Crego; Rita Masese; Emily Bonnabeau; Christian Douglas; Gary Rains; Nirmish Shah; Paula Tanabe
Journal:  Crit Care Nurs Q       Date:  2021 Apr-Jun 01
  5 in total

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