Author:
Varisco Tyler J.,Fish Hannah,Bolin Joshua,Dadiomov David,Hill Lucas G.,Essien Ekere J.,Wanat Matthew A.,Ginsburg Diane,Waggener Jeanne,Yazdanfard Sahar,Song Juhyeon,Chi Whanhui,Thornton Douglas
Abstract
Abstract
Background
Less than half of community pharmacies in the United States stock buprenorphine products indicated for the treatment of opioid use disorder. This lack of access to buprenorphine in community pharmacies is a significant barrier to care. To address this issue, this protocol outlines a comprehensive approach to develop a practice guideline aimed at improving access to safe and effective opioid use disorder treatment in community pharmacies.
Methods
The guideline development process will proceed in three phases, following a technique closely aligned with the Institute of Medicine’s guidance on guideline development. The first phase will involve conducting qualitative interviews with pharmacists in three states to identify their beliefs toward buprenorphine dispensing. As limitations on buprenorphine supply are related to constraints at all levels of the drug supply and regulatory system, the second phase, we will recruit representatives from regulatory agencies, pharmacy organizations, the Drug Enforcement Administration, pharmaceutical wholesalers as well as addiction medicine physicians and psychiatric pharmacists to develop consensus recommendations through a modified Delphi design. This will be followed by a public comment period and external expert review of the recommendations led by the National Association of Boards of Pharmacy. Finally, in the third phase, a national, mixed media dissemination campaign will be led by the National Community Pharmacists Association (NCPA) to convey recommendations to practicing pharmacists.
Discussion
The guideline development process aims to incorporate the perspectives of multiple stakeholders and emphasize the importance of addressing the regulatory and pharmacy-specific aspects of care in addition to clinical evidence and guidance. The development of this guideline will provide targeted, multidisciplinary guidance for pharmacists, improving access to safe and effective opioid use disorder treatment in the community setting.
Preregistration
This protocol was registered with the Open Science Framework in March of 2023. Registration may be found at: https://doi.org/10.17605/OSF.IO/6S9DY.
Funder
Foundation for Opioid Response Efforts
Publisher
Springer Science and Business Media LLC
Reference37 articles.
1. Substance Abuse and Mental Health Services Administration. Treatment Improvement Protocol #63: Medications for opioid use disorder: for healthcare and addiction professionals, policymakers, patients, and families. 2021.
2. Congress US. H.R.2634 - Drug Addiction Treatment Act of 2000. 2000.
3. Beetham T, Saloner B, Wakeman SE, Gaye M, Barnett ML. Access to Office-based Buprenorphine Treatment in Areas with High Rates of opioid-related mortality: an audit study. Ann Intern Med. 2019;171(1):1–9.
4. Suarez E Jr., Bartholomew TS, Plesons M, Ciraldo K, Ostrer L, Serota DP, et al. Adaptation of the Tele-Harm reduction intervention to promote initiation and retention in buprenorphine treatment among people who inject drugs: a retrospective cohort study. Ann Med. 2023;55(1):733–43.
5. Molfenter T, Jacobson N, Kim JS, Horst J, Kim H, Madden L, et al. Building medication for opioid use disorder prescriber capacity during the opioid epidemic: prescriber recruitment trends and methods. J Subst Use Addict Treat. 2023;147:208975.