Caulfield Mackenzie Duncan Gregory, Brar Rupinder, Sutherland Christy, Nolan Seonaid
Department of Family Medicine, University of Calgary, Calgary, Alberta, Canada.
Department of Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.
BMJ Case Rep. 2020 Mar 25;13(3):e233715. doi: 10.1136/bcr-2019-233715.
In the wake of North America's opioid crisis, access to evidence-based treatment for opioid use disorder (OUD) is of critical importance. While buprenorphine/naloxone and methadone are currently indicated as first-line medications for the treatment of OUD, there are a proportion of individuals who do not benefit from these therapies. Recent Canadian guidelines suggest the use of alternate therapies, including slow-release oral morphine or injectable opioid agonist therapy (iOAT) for individuals unsuccessful with either methadone or buprenorphine/naloxone. While the guidelines highlight the need to intensify OUD treatment as disease severity increases, equally important is the consideration for deintensification of treatment (eg, from iOAT to an oral opioid agonist treatment (OAT) option) following successful stabilisation. Literature addressing how best to accomplish this, however, is currently lacking. Accordingly, the case presented here describes a patient that successfully transitions from iOAT to oral buprenorphine/naloxone using a novel induction approach termed microdosing.
在北美阿片类药物危机之后,获得基于证据的阿片类药物使用障碍(OUD)治疗至关重要。虽然丁丙诺啡/纳洛酮和美沙酮目前被指定为治疗OUD的一线药物,但仍有一部分人无法从这些疗法中获益。加拿大最近的指南建议使用替代疗法,包括缓释口服吗啡或注射用阿片类激动剂疗法(iOAT),用于对美沙酮或丁丙诺啡/纳洛酮治疗无效的个体。虽然指南强调随着疾病严重程度的增加需要加强OUD治疗,但同样重要的是在成功稳定后考虑减少治疗强度(例如,从iOAT转换为口服阿片类激动剂治疗(OAT)方案)。然而,目前缺乏关于如何最好地实现这一点的文献。因此,这里介绍的病例描述了一名患者,他使用一种称为微剂量给药的新型诱导方法成功地从iOAT过渡到口服丁丙诺啡/纳洛酮。