Impacts of an opioid overdose prevention intervention delivered subsequent to acute care.

Journal Article (Journal Article)

BACKGROUND: Opioid overdose is a major and increasing cause of injury and death. There is an urgent need for interventions to reduce overdose events among high-risk persons. METHODS: Adults at elevated risk for opioid overdose involving heroin or pharmaceutical opioids who had been cared for in an emergency department (ED) were randomised to overdose education combined with a brief behavioural intervention and take-home naloxone or usual care. Outcomes included: (1) time to first opioid overdose-related event resulting in medical attention or death using competing risks survival analysis; and (2) ED visit and hospitalisation rates, using negative binomial regression and adjusting for time at risk. RESULTS: During the follow-up period, 24% of the 241 participants had at least one overdose event, 85% had one or more ED visits and 55% had at least one hospitalisation, with no significant differences between intervention and comparison groups. The instantaneous risk of an overdose event was not significantly lower for the intervention group (sub-HR: 0.83; 95% CI 0.49 to 1.40). DISCUSSION: These null findings may be due in part to the severity of the population in terms of housing insecurity (70% impermanently housed), drug use, unemployment and acute healthcare issues. Given the high overdose and healthcare utilisation rates, more intensive interventions, such as direct referral and provision of housing and opioid agonist treatment medications, may be necessary to have a substantial impact on opioid overdoses for this high-acuity population in acute care settings. TRIAL REGISTRATION NUMBER: NCT0178830; Results.

Full Text

Duke Authors

Cited Authors

  • Banta-Green, CJ; Coffin, PO; Merrill, JO; Sears, JM; Dunn, C; Floyd, AS; Whiteside, LK; Yanez, ND; Donovan, DM

Published Date

  • June 2019

Published In

Volume / Issue

  • 25 / 3

Start / End Page

  • 191 - 198

PubMed ID

  • 29436397

Pubmed Central ID

  • PMC6800078

Electronic International Standard Serial Number (EISSN)

  • 1475-5785

Digital Object Identifier (DOI)

  • 10.1136/injuryprev-2017-042676

Language

  • eng

Conference Location

  • England