Buprenorphine in the workers' compensation setting

J Opioid Manag. 2014 Jul-Aug;10(4):277-83. doi: 10.5055/jom.2014.0215.

Abstract

Buprenorphine is approved by the Food and Drug Administration for the treatment of chronic pain in low-dose transdermal patch formulations and for the treatment of addiction in high-dose sublingual tablets and films. Clinicians often prescribe these high-dose preparations "off label" for pain management. In the workers' compensation setting, it is particularly important to consider factors such as a) if the injured person has, and is being treated for co-occurring addiction as well as pain; b) if alternative therapies, including opioid withdrawal, were considered prior to initiating buprenorphine treatment; and c) the anticipated duration of treatment. This article reviews buprenorphine's approved indications, formulations, pharmacology, clinical efficacy, and special considerations in the workers' compensation setting.

Publication types

  • Review

MeSH terms

  • Administration, Sublingual
  • Analgesics, Opioid / administration & dosage
  • Analgesics, Opioid / adverse effects
  • Analgesics, Opioid / chemistry
  • Analgesics, Opioid / therapeutic use*
  • Buprenorphine / administration & dosage
  • Buprenorphine / adverse effects
  • Buprenorphine / chemistry
  • Buprenorphine / therapeutic use*
  • Drug Administration Schedule
  • Drug Approval
  • Humans
  • Occupational Diseases / diagnosis
  • Occupational Diseases / drug therapy*
  • Occupational Diseases / etiology
  • Occupational Health*
  • Off-Label Use
  • Opioid-Related Disorders / etiology
  • Opioid-Related Disorders / prevention & control
  • Patient Selection
  • Risk Assessment
  • Risk Factors
  • Tablets
  • Workers' Compensation*

Substances

  • Analgesics, Opioid
  • Tablets
  • Buprenorphine