Patterns of publicly funded naltrexone use among patients diagnosed with alcohol use disorder in Ontario

Author:

Tourchian Nima1,McCormack Daniel2,Leece Pamela345,Tadrous Mina126,Gomes Tara127ORCID

Affiliation:

1. Leslie Dan Faculty of Pharmacy, University of Toronto , 144 College St, Toronto, Ontario, M5S 3M2 , Canada

2. ICES , 2075 Bayview Ave., Toronto, Ontario, M4N 3M5 , Canada

3. Public Health Ontario , 480 University Ave. #300, Toronto, Ontario, M5G 1V2 , Canada

4. Department of Family and Community Medicine, University of Toronto , 500 University Ave.,Toronto, Ontario, M5G 1V7 , Canada

5. Dalla Lana School of Public Health, University of Toronto , 155 College St., Toronto, Ontario, M5T 3M7 , Canada

6. Women’s College Hospital , 76 Grenville St., Toronto, Ontario, M5S 1B2 , Canada

7. Li Ka Shing Knowledge Institute of St. Michael’s Hospital , 30 Bond St., Toronto, Ontario, M5B 1W8 , Canada

Abstract

Abstract Aims Naltrexone is recommended first-line to manage alcohol use disorder (AUD). With previous studies indicating poor retention on naltrexone, we determined duration of naltrexone use and assessed the association between prescription setting and time to discontinuation in Ontario. Methods We conducted a retrospective population-based cohort study among Ontario public drug beneficiaries diagnosed with AUD who initiated publicly funded naltrexone from June 2018 to September 2019. The primary outcome was time to naltrexone discontinuation, with a secondary analysis assessing receipt of at least one prescription refill. We used Cox proportional hazards models and logistic regression to test the association between prescription setting and each medication persistence outcome. Results Among 2531 new naltrexone patients with AUD, the median duration of naltrexone use was 31 days and 394 (15.6%) continued naltrexone for 6 months or longer. There was no association between setting of initiation and duration of naltrexone use; however, those initiating naltrexone following an acute inpatient hospital stay were more likely to fill a second prescription (aOR 1.43, 95% CI 0.96–2.14), while those initiating after an ED visit were less likely to be dispensed a second prescription (aOR = 0.69, 95% CI 0.52–0.90) compared to those starting in a physician’s office. Conclusion Persistence on naltrexone to treat an AUD is low, regardless of the setting of initiation. Further research is needed to elucidate the barriers encountered by patients with AUD that lead to poor treatment persistence in order to develop interventions that facilitate patient-centered access to evidence-based treatment for AUD in the province.

Funder

Ontario Ministry of Health

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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