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一种利用透皮芬太尼桥接和药代动力学诱导剂的高效且平稳的美沙酮转换为丁丙诺啡的方案:斯坦丘方法。

An Efficient and Smooth Methadone-to-Buprenorphine Transition Protocol Utilizing a Transdermal Fentanyl Bridge and a Pharmacokinetic Inducer: The Stanciu Method.

作者信息

Stanciu Cornel N, Gibson Stephen, Teja Nikhil, Healey Christopher J

机构信息

Psychiatry, Geisel School of Medicine, Concord, USA.

Pharmacy, New Hampshire Hospital, Concord, USA.

出版信息

Cureus. 2020 May 27;12(5):e8310. doi: 10.7759/cureus.8310.

Abstract

The traditional method of transitioning from methadone to buprenorphine requires a gradual dose reduction to a low dose of 30 mg daily, followed by cessation, and addressing withdrawal symptoms prior to the initiation of buprenorphine. This process can be time-consuming and is also associated with tremendous patient suffering and adverse outcomes. In recent years, several protocols have emerged based on the notion of blunting the shift from full receptor activation to partial receptor activation via an intermediate "bridge". This typically is required for the time period needed for the acting full agonist, methadone, to undergo biotransformation and clearance. In this report, we present an inadvertent case where transdermal fentanyl as a transitional bridge was utilized along with an inducer of methadone's metabolism to speed up the course, and urine acidification to enhance clearance. Our patient was transitioned from moderate-dose methadone, without encountering any withdrawal symptoms in the process, in three days. This method presents yet another option for select candidates, and it allows physicians to individualize methadone-to-buprenorphine transitions.

摘要

从美沙酮转换为丁丙诺啡的传统方法需要逐步减少剂量至每日30毫克的低剂量,然后停药,并在开始使用丁丙诺啡之前处理戒断症状。这个过程可能很耗时,并且还会给患者带来巨大痛苦和不良后果。近年来,基于通过中间“桥梁”来减弱从完全受体激活到部分受体激活转变的概念,出现了几种方案。这通常是作用性完全激动剂美沙酮进行生物转化和清除所需的时间段所必需的。在本报告中,我们介绍了一个意外案例,其中使用透皮芬太尼作为过渡桥梁,并联合使用美沙酮代谢诱导剂来加快进程,以及通过尿液酸化来增强清除。我们的患者从中等剂量美沙酮转换过来,在此过程中未出现任何戒断症状,用时三天。这种方法为特定候选人提供了另一种选择,并且使医生能够个性化美沙酮到丁丙诺啡的转换过程。

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