Citation

Sullivan MD, Howe CQ. Pain 2013; 154(Suppl 1): S94-S100.

Affiliation

Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA. Electronic address: sullimar@uw.edu.

Copyright

(Copyright © 2013, Lippincott, Williams and Wilkins)

DOI

10.1016/j.pain.2013.09.009

PMID

24036286

Abstract

Opioid therapy offers the promise of reducing the burden of chronic pain in not just individual patients, but among the broad population of patients with chronic pain. Randomized trials have demonstrated that opioid therapy for up to 12-16weeks is superior to placebo, but have not addressed longer-term use. In the United States, opioid sales have quadrupled during 2000-2010, with parallel increases in opioid accidental overdose deaths and substance abuse admissions. Clinical use of long-term opioid therapy is characterized by a pattern of adverse selection, where high-risk patients are prescribed high-risk opioid regimens. This adverse selection may link these trends in use, abuse, and overdose. Long-term opioid therapy appears to be associated with iatrogenic harm to the patients who receive the prescriptions and to the general population. The United States has, in effect, conducted an experiment of population-wide treatment of chronic pain with long-term opioid therapy. The population-wide benefits have been hard to demonstrate, but the harms are now well demonstrated.

Language: en