The management of pain in sickle cell disease

Pediatr Clin North Am. 2000 Jun;47(3):699-710. doi: 10.1016/s0031-3955(05)70233-9.

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.

Publication types

  • Review

MeSH terms

  • Acute Disease
  • Analgesics, Opioid / therapeutic use
  • Anemia, Sickle Cell / complications*
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Child
  • Child, Preschool
  • Cognitive Behavioral Therapy
  • Combined Modality Therapy
  • Humans
  • Pain / etiology*
  • Pain Management*
  • Physical Therapy Modalities

Substances

  • Analgesics, Opioid
  • Anti-Inflammatory Agents, Non-Steroidal