Literature DB >> 24517964

The proportion of potentially preventable emergency department visits by patients with sickle cell disease.

Mark Nimmer1, Raymond G Hoffmann, Mahua Dasgupta, Julie Panepinto, David C Brousseau.   

Abstract

BACKGROUND: Emergency department (ED) visits by children with sickle cell disease (SCD) are often classified as urgent based on resource utilization. This classification may not accurately reflect the potentially preventable nature of SCD visits. We sought to determine the proportion of SCD crisis-related pediatric ED visits that are possibly preventable. PROCEDURE: We reviewed 2 years of ED visits with a diagnosis of SCD with crisis at a hospital with an established sickle cell program. Criteria for preventable visits were predefined by pediatric hematologists. Non-pain-related chief complaints requiring emergent evaluation or painful episodes preceded by 2 opioid doses were considered not preventable; others were potentially preventable.
RESULTS: The study included 603 visits by 187 patients; 33% were potentially preventable. Overall, 29% of visits were emergent based on non-pain-related emergent complaints. Of the remaining pain-related visits, 26% were preceded by 2 or more doses of opioids at home. Visits by children with asthma were 0.58 times as likely to be preventable, due to more non-pain-related emergent chief complaints (32%) and more children (36%) taking 2 or more opioid doses.
CONCLUSIONS: Approximately two thirds of SCD crisis-related pediatric ED visits are not immediately preventable; that percentage is higher in children with asthma.

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Year:  2015        PMID: 24517964     DOI: 10.1097/MPH.0000000000000124

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  6 in total

1.  Community Health Workers as Support for Sickle Cell Care.

Authors:  Lewis L Hsu; Nancy S Green; E Donnell Ivy; Cindy E Neunert; Arlene Smaldone; Shirley Johnson; Sheila Castillo; Amparo Castillo; Trevor Thompson; Kisha Hampton; John J Strouse; Rosalyn Stewart; TaLana Hughes; Sonja Banks; Kim Smith-Whitley; Allison King; Mary Brown; Kwaku Ohene-Frempong; Wally R Smith; Molly Martin
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

2.  Care Coordination for Children With Sickle Cell Disease: A Longitudinal Study of Parent Perspectives and Acute Care Utilization.

Authors:  Tiffany L Rattler; Annette M Walder; Hua Feng; Jean L Raphael
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

3.  Emergency department utilization by Californians with sickle cell disease, 2005-2014.

Authors:  Susan T Paulukonis; Lisa B Feuchtbaum; Thomas D Coates; Lynne D Neumayr; Marsha J Treadwell; Elliott P Vichinsky; Mary M Hulihan
Journal:  Pediatr Blood Cancer       Date:  2016-12-21       Impact factor: 3.167

4.  Biopsychosocial Factors Associated with Parenting Stress in Pediatric Sickle Cell Disease.

Authors:  Yelena L Johnson; Kerri Woodward; Carlton Dampier; Lindsey Cohen; Soumitri Sil
Journal:  J Clin Psychol Med Settings       Date:  2022-01-07

5.  Management of Sickle Cell Disease Super Utilizers.

Authors:  Gary A Johnson
Journal:  West J Emerg Med       Date:  2017-01-30

6.  Emergency department utilization for sickle cell disease in St. Vincent and the Grenadines.

Authors:  Shelly-Ann Williams; Shakel Henson; Shenese Trimmingham; Jill Newman; Julie Kanter
Journal:  Pan Afr Med J       Date:  2021-01-29
  6 in total

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