Outcome of short-term emergency department observation care of children with sickle cell disease and vaso-occlusive crises: initial experience from south-western Nigeria

Author:

Adegoke Samuel A1,Oladimeji O I2,Ologun B G2,Aladekomo T A1,Oyelami O A1

Affiliation:

1. Department of Paediatrics and Child Health, Obafemi Awolowo University (OAU), Ile-Ife, Nigeria

2. Department of Paediatrics, Wesley Guild Hospital Ilesa Unit, OAU Teaching Hospitals Complex, Ile-Ife, Nigeria

Abstract

Abstract Background Short-term emergency department (ED) observation care may prevent prolonged and unnecessary hospital admission in patients with sickle pain. This study highlights the outcomes of short-term ED care of acute pain in children with sickle cell disease (SCD). Methods Children aged 6 mo to 19 y with SCD and painful crises who were managed by short-term ED care from July 2017 to June 2019 were studied retrospectively. Biodata, pain score, type of care, length of hospital stay, inpatient transfer rate (the proportion that required transfer for full admission) and return rate (the proportion that returned to the hospital for retreatment of unresolved pain) were documented. Results From July 2017 to June 2019, 122 children with SCD were admitted to the ED for painful crises, of whom 118 (96.7%) with 167 hospital visits were managed by short-term ED observation care. The median length of stay was 10.5 h. In 50.3% of encounters, patients were successfully managed without requiring further care. However, in 17.4% of encounters, they had their ED observation care terminated and converted to full admission. The overall return rate for acute care within 1 wk for either persistence of symptoms or any other complaint was 31.7%. Conclusions Dedicated short-term ED observation care has the potential to provide effective and timely management of acute pain in children with SCD.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Medicine,Parasitology

Reference21 articles.

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3. Morbidity and mortality pattern in hospitalized children with sickle cell disorders at university college hospital Ibadan, Nigeria;Brown;Niger J Paed.,2013

4. Sickle cell disease clinical phenotypes in children from South-Western Nigeria;Adegoke;Niger J Clin Pract.,2015

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