Rotation from methadone to buprenorphine using a micro-dosing regime in patients with opioid use disorder and serious mental illness: A case series

IF 3 3区 医学 Q2 SUBSTANCE ABUSE
Vivian C. Praeger, Matthew Y. Frei, Dan Pham, Adrian J. Praeger, Dan I. Lubman, Shalini Arunogiri
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引用次数: 0

Abstract

Introduction

Inducting buprenorphine from methadone has traditionally involved initial opioid withdrawal, with risk of mental state deterioration in patients with serious mental illness (SMI). Micro-dosing of buprenorphine, with small incremental doses, is a novel off-label approach to transitioning from methadone and does not require a period of methadone abstinence. Given the limited literature about buprenorphine microdosing, we aimed to evaluate the feasibility and safety of inducting buprenorphine in a series of patients on methadone with SMI.

Methods

For this retrospective case series, we reviewed the records of 16 patients with SMI at a Melbourne addiction treatment centre, from January 2021 to July 2022, who transitioned via micro-dosing, from high-dose methadone (>30 mg) to buprenorphine and depot-buprenorphine. Psychiatric diagnoses, mental state, other substance withdrawal, transfer success, transition time, opioid withdrawal symptoms and overall patient experience were collected via objective and subjective reporting.

Results

Methadone to buprenorphine transfer was completed by 88% of patients. Mental health measures remained stable with the exception of mildly increased anxiety. Median transfer time was 6.5 days for inpatients, 9 days for mixed setting and 10 days for outpatients. Most patients (93%) rated their experience ‘manageable’ reporting mild withdrawal symptoms. One patient met study criteria for precipitated withdrawal.

Discussion and Conclusions

This retrospective case series provides evidence that the use of a micro-dosing buprenorphine induction for methadone to buprenorphine transitions, including to depot-buprenorphine, has negligible risk, is tolerated by patients with SMI and is unlikely to precipitate an exacerbation of their mental illness.

在阿片类药物使用障碍和严重精神疾病患者中使用微量给药机制,从美沙酮轮换到丁丙诺啡:病例系列。
导言:传统上,从美沙酮诱导丁丙诺啡需要初始阿片类药物戒断,严重精神疾病(SMI)患者有精神状态恶化的风险。丁丙诺啡的微量给药,以小剂量递增的方式,是从美沙酮过渡到丁丙诺啡的一种标签外的新方法,而且不需要一段时间的美沙酮戒断期。鉴于有关丁丙诺啡微量给药的文献有限,我们旨在评估一系列服用美沙酮的 SMI 患者服用丁丙诺啡的可行性和安全性:在这项回顾性病例系列研究中,我们回顾了墨尔本一家戒毒治疗中心从 2021 年 1 月至 2022 年 7 月期间 16 名 SMI 患者的病历,这些患者通过微量给药从大剂量美沙酮(>30 毫克)过渡到丁丙诺啡和去甲丁丙诺啡。通过客观和主观报告收集了患者的精神诊断、精神状态、其他药物戒断情况、转院成功率、转院时间、阿片类药物戒断症状和总体体验:结果:88%的患者完成了美沙酮向丁丙诺啡的转移。除焦虑轻度增加外,心理健康指标保持稳定。住院患者的中位转移时间为 6.5 天,混合环境为 9 天,门诊患者为 10 天。大多数患者(93%)将其经历评为 "可控",并报告了轻微的戒断症状。有一名患者符合研究中的析出性戒断标准:这一回顾性系列病例提供的证据表明,使用微量丁丙诺啡诱导美沙酮向丁丙诺啡过渡(包括向去甲丁丙诺啡过渡)的风险可以忽略不计,SMI 患者可以耐受,并且不太可能导致其精神疾病恶化。
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来源期刊
Drug and alcohol review
Drug and alcohol review SUBSTANCE ABUSE-
CiteScore
4.80
自引率
10.50%
发文量
151
期刊介绍: Drug and Alcohol Review is an international meeting ground for the views, expertise and experience of all those involved in studying alcohol, tobacco and drug problems. Contributors to the Journal examine and report on alcohol and drug use from a wide range of clinical, biomedical, epidemiological, psychological and sociological perspectives. Drug and Alcohol Review particularly encourages the submission of papers which have a harm reduction perspective. However, all philosophies will find a place in the Journal: the principal criterion for publication of papers is their quality.
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