The management of pain in sickle cell disease

Pediatr Clin North Am. 1989 Aug;36(4):1029-45. doi: 10.1016/s0031-3955(16)36735-9.

Abstract

For people with sickle cell disease, vaso-occlusive crisis pain is a frequently encountered problem that poses unique and often perplexing challenges in management. This article reviews the natural history of vaso-occlusive crisis and discusses intervention appropriate for the care of patients with pain due to this chronic illness.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Analgesics / administration & dosage
  • Analgesics / adverse effects
  • Analgesics / therapeutic use
  • Anemia, Sickle Cell / complications*
  • Anemia, Sickle Cell / physiopathology
  • Anemia, Sickle Cell / psychology
  • Child
  • Child, Preschool
  • Chronic Disease
  • Emergency Service, Hospital
  • Humans
  • Male
  • Pain / etiology
  • Pain / psychology
  • Pain Management*
  • Pain Measurement / methods
  • Patient Admission
  • Patient Compliance
  • Sex Factors

Substances

  • Analgesics