Does Prolonged Suffering Have to Be a Part of the Process? Methadone Initiations in the Fentanyl Era: A Lived Experience Narrative, Evidence Review, and Call to Action.

Brooke Jackson, Patricia Liu, David Lawrence
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Abstract

In a drug landscape dominated by the highly potent synthetic opioid fentanyl, traditional methadone initiation protocols increasingly fail people with opioid use disorder (OUD). While "low" initial dose selection and "slow" dose adjustment rates reduce risk for methadone-associated toxicity, they also result in weeks to months of unrelieved withdrawal symptoms and cravings, especially for people with high opioid tolerance from routine fentanyl use. For this growing population, "low-and-slow" forces a choice between 3 poor options: suffer weeks to months of withdrawal, self-manage withdrawal through non-prescribed substance use, or give up on treatment. Our commentary combines a Peer Support Specialist's lived experiences with methadone initiation and evidence from the peer-reviewed literature to illustrate this problem and the role of one potential solution: rapid methadone initiation (RMI), defined here as reaching a methadone dose of 80 mg or more within the first 7 days of treatment. For appropriately selected patients, RMI is associated with positive outcomes, including improved patient satisfaction, reduced readmission rates, and increased retention in care. Though regulations permit and growing evidence supports RMI, adoption remains limited. Our commentary, therefore, concludes by sharing frameworks to support providers in implementing RMI as a potential treatment option for people with OUD across applicable care settings. Methadone's life-saving potential depends on dosing that matches the physiological reality of fentanyl use. Collectively, addiction clinicians define the community standard of care. In the face of a transformed drug landscape, it is time for that standard to evolve to ensure that the option for rapid and effective relief becomes the rule, rather than the exception.

长期的痛苦一定是这个过程的一部分吗?芬太尼时代的美沙酮启动:生活经验叙述,证据审查和行动呼吁。
在一个由强效合成阿片类药物芬太尼主导的药物领域,传统的美沙酮起始方案越来越多地使阿片类药物使用障碍(OUD)患者失败。虽然“低”初始剂量选择和“慢”剂量调整率降低了美沙酮相关毒性的风险,但它们也导致数周至数月的戒断症状和渴望得不到缓解,特别是对于常规使用芬太尼的阿片类药物耐受性高的人。对于这一不断增长的人口,“低而慢”迫使他们在三种糟糕的选择之间做出选择:忍受数周到数月的戒断,通过非处方药物使用自我管理戒断,或者放弃治疗。我们的评论结合了同行支持专家的美沙酮起始的生活经验和同行评议文献的证据来说明这个问题和一种潜在解决方案的作用:美沙酮快速起始(RMI),这里定义为在治疗的前7天内美沙酮剂量达到80毫克或更多。对于适当选择的患者,RMI与积极的结果相关,包括患者满意度的提高,再入院率的降低和护理留置率的增加。尽管法规允许并且越来越多的证据支持RMI,但采用仍然有限。因此,我们的评论通过分享框架来结束,以支持提供者在适用的护理环境中实施RMI作为OUD患者的潜在治疗选择。美沙酮拯救生命的潜力取决于与芬太尼使用的生理现实相匹配的剂量。总的来说,成瘾临床医生定义了社区护理标准。面对变化的药物环境,现在是时候发展这一标准,以确保快速有效缓解的选择成为规则,而不是例外。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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