Associations between fentanyl use and initiation, persistence, and retention on medications for opioid use disorder among people living with uncontrolled HIV disease
Autor: | Laura C. Fanucchi, Pamela Vergara-Rodriguez, Ryan Cook, Randy Torralva, Caroline King, Paula J. Lum, Allan Rodriguez, P. Todd Korthuis, Hansel E. Tookes, Gregory M. Lucas, Canyon Foot, Elizabeth N. Waddell |
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Rok vydání: | 2021 |
Předmět: |
Male
Agonist medicine.medical_specialty medicine.drug_class Narcotic Antagonists HIV Infections Toxicology Article Naltrexone Fentanyl Internal medicine Humans Medicine Pharmacology (medical) Medical prescription Pharmacology business.industry Opioid use disorder Middle Aged Opioid-Related Disorders medicine.disease Buprenorphine Clinical trial Psychiatry and Mental health Delayed-Action Preparations business medicine.drug Methadone |
Zdroj: | Drug Alcohol Depend |
ISSN: | 0376-8716 |
Popis: | BACKGROUND. Associations between fentanyl use and initiation and retention on medications for opioid use disorder (MOUD) are poorly understood. METHODS. Data were from a multisite clinical trial comparing extended-release naltrexone (XRNTX) with treatment as usual (TAU; buprenorphine or methadone) to achieve HIV viral suppression among people with OUD and uncontrolled HIV disease. The exposure of interest was fentanyl use, as measured by urine drug screening. Outcomes were time to MOUD initiation, defined as date of first injection of XR-NTX, buprenorphine prescription, or methadone administration; MOUD persistence, the total number of injections, prescriptions, or administrations received over 24 weeks; and MOUD retention, having an injection, prescription, or administration during weeks 20 to 24. RESULTS. Participants (N = 111) averaged 47 years old and 62% were male. Just over half (57%) were Black and 13% were Hispanic. Sixty-four percent of participants tested positive for fentanyl at baseline. Participants with baseline fentanyl positivity were 11 times less likely to initiate XR-NTX than those negative for fentanyl (aHR = 0.09, 95% CI 0.03 to 0.24, p < .001), but there was no evidence that fentanyl use impacted the likelihood of TAU initiation (aHR = 1.50, 0.67 to 3.36, p = .323). Baseline fentanyl use was not associated with persistence or retention on any MOUD. CONCLUSIONS. Fentanyl use was a substantial barrier to XR-NTX initiation for the treatment of OUD in persons with uncontrolled HIV infection. There was no evidence that fentanyl use impacted partial/full agonist initiation and, once initiated, retention on any MOUD. |
Databáze: | OpenAIRE |
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