Evidence-based mini-review: Are systemic corticosteroids an effective treatment for acute pain in sickle cell disease?

L. Vandy Black, Wally R. Smith

Research output: Contribution to journalArticle

Abstract

An 18-year-old African-American male with sickle cell disease (SCD) is admitted to the hospital with a vaso-occlusive pain crisis affecting his chest and right upper extremity. He has a history of asthma but does not have a fever or respiratory symptoms, and a chest X-ray is negative for an infiltrate. He is treated with intravenous fluids and morphine. You are asked about the potential efficacy of systemic corticosteroids as an adjunctive treatment for pain control.

Original languageEnglish (US)
Pages (from-to)416-417
Number of pages2
JournalHematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program
Volume2010
StatePublished - 2010

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Acute Pain
Sickle Cell Anemia
Adrenal Cortex Hormones
Thorax
Pain
Upper Extremity
African Americans
Morphine
Fever
Asthma
X-Rays
Therapeutics

ASJC Scopus subject areas

  • Medicine(all)

Cite this

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