The management of pain in sickle cell disease

M. Yaster, S. Kost-Byerly, L. G. Maxwell

Research output: Contribution to journalArticlepeer-review

Abstract

The pain of vaso-occlusive crisis in patients with sickle cell disease is excruciating, incapacitating, and sometimes refractory to even the most advanced analgesic treatments. A comprehensive, multimodal approach to therapy that includes education, cognitive therapies, anti-inflammatory drugs, opioids, and psychostimulant adjuvant drugs has been presented. Until a cure for the underlying disease is found, these are the best approaches available. The authors hope that future research will find even better modalities of analgesic care.

Original languageEnglish (US)
Pages (from-to)699-710
Number of pages12
JournalPediatric clinics of North America
Volume47
Issue number3
DOIs
StatePublished - 2000

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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