Reducing Time to Analgesia for Sickle Cell Pain Episode Treatment in the Pediatric Emergency Department

Standardizing care with an order set increased the number of pain assessments. Incorporation of the SCD home pain action plan into the ED treatment pathway decreased the time to analgesia.

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Publication Details

Journal
Pediatric Quality and Safety
Published
2025-05-01
DOI
https://doi.org/10.1097/pq9.0000000000000821
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Reducing Time to Analgesia for Sickle Cell Pain Episode Treatment in the Pediatric Emergency Department

Jaime Kaye Otillio, Emmanuel J. Volanakis, S. Barron Frazier, Michael R. DeBaun et al.
Pediatric Quality and Safety
Hemoglobinopathies and Related Disorders
article

Reducing Time to Analgesia for Sickle Cell Pain Episode Treatment in the Pediatric Emergency Department

Jaime Kaye Otillio, Emmanuel J. Volanakis, S. Barron Frazier, Michael R. DeBaun, Amelia Wong, Christine M. Smith, Lacey Noffsinger, Jeannie Byrd, Abby K. Fahnestock
article en

Abstract

Standardizing care with an order set increased the number of pain assessments. Incorporation of the SCD home pain action plan into the ED treatment pathway decreased the time to analgesia.

Pediatric Quality and SafetyVol. 10(3)
Vanderbilt University Medical Center (US)
Openalex Percentile: Top 82%
Hemoglobinopathies and Related Disorders
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