Dale Terasaki1, Christopher Smith2, Susan L Calcaterra2. 1. Addition Medicine Fellowship, University of Colorado Hospital, CeDAR, Aurora, Colorado. 2. Department of Medicine, Hospital Medicine, University of Colorado Hospital, Aurora, Colorado.
Abstract
STUDY OBJECTIVE: Buprenorphine, a partial μ-opioid agonist, is an effective treatment for opioid use disorder that conventionally requires symptoms of withdrawal before initiation to avoid precipitating withdrawal. Our institution implemented a microdosing approach to transition patients from full μ-opioid agonists to buprenorphine without requiring patients to undergo a period of opioid abstinence. Little has been published about this strategy in the inpatient setting in the United States, and even less has been published dealing with the transition from methadone to buprenorphine. Our objective was to demonstrate that a microdosing protocol to transition patients from methadone to buprenorphine can be feasibly implemented in a U.S. hospital setting. DESIGN: Case series. PATIENTS: Three hospitalized adults with opioid use disorder who received a 1-week buprenorphine microdosing protocol. MEASUREMENTS AND MAIN RESULTS: In January 2019, we implemented a 1-week buprenorphine microdosing protocol for hospitalized adult patients with opioid use disorder who were initially stabilized on methadone and wished to start buprenorphine. We gave low-dose buprenorphine concurrently with each patient's full dose of methadone, and the buprenorphine dose was gradually titrated up over 7 days. On day 8, methadone was abruptly discontinued. The buprenorphine dose was further increased based on clinical judgment. All three patients were successfully transitioned from methadone 40-100 mg/day to buprenorphine 12-16 mg/day with minimal symptoms of opioid withdrawal. One patient relapsed and was lost to follow-up; two remained in treatment. CONCLUSION: A protocol using microdosing of buprenorphine can successfully transition patients receiving full μ-opioid agonist therapy, including methadone, to buprenorphine without the need for a period of opioid abstinence.
STUDY OBJECTIVE:Buprenorphine, a partial μ-opioid agonist, is an effective treatment for opioid use disorder that conventionally requires symptoms of withdrawal before initiation to avoid precipitating withdrawal. Our institution implemented a microdosing approach to transition patients from full μ-opioid agonists to buprenorphine without requiring patients to undergo a period of opioid abstinence. Little has been published about this strategy in the inpatient setting in the United States, and even less has been published dealing with the transition from methadone to buprenorphine. Our objective was to demonstrate that a microdosing protocol to transition patients from methadone to buprenorphine can be feasibly implemented in a U.S. hospital setting. DESIGN: Case series. PATIENTS: Three hospitalized adults with opioid use disorder who received a 1-week buprenorphine microdosing protocol. MEASUREMENTS AND MAIN RESULTS: In January 2019, we implemented a 1-week buprenorphine microdosing protocol for hospitalized adult patients with opioid use disorder who were initially stabilized on methadone and wished to start buprenorphine. We gave low-dose buprenorphine concurrently with each patient's full dose of methadone, and the buprenorphine dose was gradually titrated up over 7 days. On day 8, methadone was abruptly discontinued. The buprenorphine dose was further increased based on clinical judgment. All three patients were successfully transitioned from methadone 40-100 mg/day to buprenorphine 12-16 mg/day with minimal symptoms of opioid withdrawal. One patient relapsed and was lost to follow-up; two remained in treatment. CONCLUSION: A protocol using microdosing of buprenorphine can successfully transition patients receiving full μ-opioid agonist therapy, including methadone, to buprenorphine without the need for a period of opioid abstinence.
Authors: Elenore P Bhatraju; Natasha Ludwig-Barron; Julian Takagi-Stewart; Harveen K Sandhu; Jared W Klein; Judith I Tsui Journal: Drug Alcohol Depend Date: 2020-08-27 Impact factor: 4.492