Literature DB >> 17389246

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

Paula Tanabe1, Randall Myers, Amy Zosel, Jane Brice, Altaf H Ansari, Julia Evans, Zoran Martinovich, Knox H Todd, Judith A Paice.   

Abstract

OBJECTIVES: To characterize the initial management of patients with sickle cell disease and an acute pain episode, to compare these practices with the American Pain Society Guideline for the Management of Acute and Chronic Pain in Sickle-Cell Disease in the emergency department, and to identify factors associated with a delay in receiving an initial analgesic.
METHODS: This was a multicenter retrospective design. Consecutive patients with an emergency department visit in 2004 for an acute pain episode related to sickle cell disease were included. Exclusion criteria included age younger than 18 years. A structured medical record review was used to abstract data, including the following outcome variables: analgesic agent and dose, route, and time to administration of initial analgesic. Additional variables included demographics, triage level, intravenous access, and study site. Mann-Whitney U test or Kruskal-Wallis test and multivariate regression were used to identify differences in time to receiving an initial analgesic between groups.
RESULTS: There were 612 patient visits, with 159 unique patients. Median time to administration of an initial analgesic was 90 minutes (25th to 75th interquartile range, 54-159 minutes). During 87% of visits, patients received the recommended agent (morphine or hydromorphone); 92% received the recommended dose, and 55% received the drug by the recommended route (intravenously or subcutaneously). Longer times to administration occurred in female patients (mean difference, 21 minutes; 95% confidence interval = 7 to 36 minutes; p = 0.003) and patients assigned triage level 3, 4, or 5 versus 1 or 2 (mean difference, 45 minutes; 95% confidence interval = 29 to 61 minutes; p = 0.00). Patients from study sites 1 and 2 also experienced longer delays.
CONCLUSIONS: Patients with an acute painful episode related to sickle cell disease experienced significant delays to administration of an initial analgesic.

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Year:  2007        PMID: 17389246     DOI: 10.1197/j.aem.2006.11.033

Source DB:  PubMed          Journal:  Acad Emerg Med        ISSN: 1069-6563            Impact factor:   3.451


  31 in total

1.  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

2.  The National Heart, Lung, and Blood Institute Strategic Vision Implementation for Health Equity Research.

Authors:  George A Mensah; Catherine M Stoney; Michelle M Freemer; Sharon Smith; Michael M Engelgau; W Keith Hoots; James P Kiley; David C Goff
Journal:  Ethn Dis       Date:  2019-02-21       Impact factor: 1.847

3.  A Survey of the Pain Management of Acute Painful Crisis among Patients with Sickle Cell Disease at Two Centres in Jamaica.

Authors:  R Augier; S Jenkins; S Bortolusso Ali; I Tennant; J Williams-Johnson; M Reid
Journal:  West Indian Med J       Date:  2014-06-12       Impact factor: 0.171

Review 4.  Reducing Health Care Disparities in Sickle Cell Disease: A Review.

Authors:  LaTasha Lee; Kim Smith-Whitley; Sonja Banks; Gary Puckrein
Journal:  Public Health Rep       Date:  2019-10-10       Impact factor: 2.792

Review 5.  Optimizing the care model for an uncomplicated acute pain episode in sickle cell disease.

Authors:  Paul Telfer; Banu Kaya
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

6.  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

7.  Impact of early analgesia on hospitalization outcomes for sickle cell pain crisis.

Authors:  Jason Payne; Inmaculada Aban; Lee M Hilliard; Jennifer Madison; Christina Bemrich-Stolz; Thomas H Howard; Amanda Brandow; Emily Waite; Jeffrey D Lebensburger
Journal:  Pediatr Blood Cancer       Date:  2018-08-27       Impact factor: 3.167

8.  Experiences of Pediatric Patients With Sickle Cell Disease in Rural Emergency Departments.

Authors:  Kristen J Alston; Cecelia R Valrie; Christy Walcott; Tamara D Warner; Beng Fuh
Journal:  J Pediatr Hematol Oncol       Date:  2015-04       Impact factor: 1.289

9.  The impact of race and disease on sickle cell patient wait times in the emergency department.

Authors:  Carlton Haywood; Paula Tanabe; Rakhi Naik; Mary Catherine Beach; Sophie Lanzkron
Journal:  Am J Emerg Med       Date:  2013-02-04       Impact factor: 2.469

Review 10.  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

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