Resumen
Background: The shift from prescription to illicit drugs involved in drug poisoning deaths raises questions about the current utility of prescription drug monitoring program (PDMP) data to inform drug poisoning (overdose) prevention efforts. In this study, we describe relations between specific drugs involved in Kentucky drug poisoning deaths and antecedent controlled substance (CS) dispensing. Methods: The study used linked death certificates and PDMP data for 2,248 Kentucky resident drug poisoning deaths in 2021. Death certificate literal text analysis identified drugs mentioned with involvement (DMI) in drug poisoning deaths. We characterized the concordance between each DMI and the CS dispensing history for this drug at varying timepoints since 2008. Results: Overall, 25.5% of all decedents had dispensed CS in the month before fatal drug poisoning. Over 80% of decedents were dispensed opioid(s) since 2008; the percentage was similar regardless of opioid involvement in the poisoning death. One-third of decedents had dispensed buprenorphine for treatment of opioid use disorder since 2008, but only 6.1% had dispensed buprenorphine in the month preceding death. Fentanyl/fentanyl analogs were DMI in 1,568 (69.8%) deaths, yet only 3% had received a fentanyl prescription since 2008. The highest concordance in the month preceding death was observed for clonazepam (43.6%). Conclusion: Overall, concordance between CS dispensing history and the drugs involved in poisoning deaths was low, suggesting a need to reevaluate the complex relationships between prescription medication exposure and overdose death and to expand harm reduction interventions both within and outside the healthcare system to reduce drug poisoning mortality.
| Idioma original | English |
|---|---|
| Número de artículo | 53 |
| Publicación | Substance Abuse: Treatment, Prevention, and Policy |
| Volumen | 18 |
| N.º | 1 |
| DOI | |
| Estado | Published - dic 2023 |
Nota bibliográfica
Publisher Copyright:© 2023, BioMed Central Ltd., part of Springer Nature.
Financiación
The authors would like to thank the Kentucky All Schedule Prescription Electronic Program and the Kentucky Office of Vital Statistics for their support of this study, and Dr. Holly Hedegaard and Dr. Bruce Goldberger for review of the manuscript. This study was funded by the US Food and Drug Administration (FDA) HHSF223201810183C. The contents of this article are solely the responsibility of the authors and do not necessarily represent the official views of the US Food and Drug Administration.
| Financiadores | Número del financiador |
|---|---|
| Kentucky All Schedule Prescription Electronic Program | |
| Kentucky Office of Vital Statistics | |
| U.S. Food and Drug Administration | HHSF223201810183C |
| U.S. Food and Drug Administration |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- Health Policy
- Psychiatry and Mental health
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