Rudolf Gregory, Walsh Jim, Plawman Abigail, Gianutsos Paul, Alto William, Mancl Lloyd, Rudolf Vania
a Department of Pain Services , Swedish Medical Center , Seattle , WA , USA.
b Addiction Recovery Service, Swedish Medical Center , Seattle , WA , USA.
Am J Drug Alcohol Abuse. 2018;44(3):302-309. doi: 10.1080/00952990.2017.1334209. Epub 2017 Aug 10.
The clinical feasibility of a novel non-opioid and benzodiazepine-free protocol was assessed for the treatment of medically supervised opioid withdrawal and transition to subsequent relapse prevention strategies.
A retrospective chart review of DSM-IV diagnosed opioid-dependent patients admitted for inpatient medically supervised withdrawal examined 84 subjects (52 males, 32 females) treated with a 4-day protocol of scheduled tizanidine, hydroxyzine, and gabapentin. Subjects also received ancillary medications as needed, and routine counseling. Primary outcomes were completion of medically supervised withdrawal, and initiation of injectable extended release (ER) naltrexone treatment. Secondary outcomes included the length of hospital stay, Clinical Opiate Withdrawal Scale (COWS) scores, and facilitation to substance use disorder treatment intervention. Ancillary medication use and adverse effects were also assessed.
A total of 79 (94%) of subjects completed medically supervised withdrawal. A total of 27 (32%) subjects chose to pursue transition to ER naltrexone, and 24 of the 27 (89%) successfully received the injection prior to hospital discharge. The protocol subjects had a mean length of hospital stay of 3.6 days, and the mean COWS scores was 3.3, 3.4, 2.8, and 2.4 on Day 1, 2, 3, and 4, respectively. Furthermore, 71 (85%) engaged in an inpatient or outpatient substance use disorder (SUD) treatment program following protocol completion.
This retrospective chart review suggests the feasibility of a novel protocol for medically supervised opioid withdrawal and transition to relapse prevention strategies, including injectable ER naltrexone. This withdrawal protocol does not utilize opioid agonists or other controlled substances..
评估了一种新型的无阿片类药物和苯二氮䓬类药物方案在医学监督下治疗阿片类药物戒断及过渡到后续预防复发策略的临床可行性。
对因住院接受医学监督下戒断而入院的DSM-IV诊断为阿片类药物依赖患者进行回顾性病历审查,研究了84名受试者(52名男性,32名女性),他们接受了为期4天的替扎尼定、羟嗪和加巴喷丁定时给药方案治疗。受试者还根据需要接受辅助药物治疗和常规咨询。主要结局是完成医学监督下的戒断,以及开始注射用缓释纳曲酮治疗。次要结局包括住院时间、临床阿片类药物戒断量表(COWS)评分,以及对物质使用障碍治疗干预的促进作用。还评估了辅助药物的使用和不良反应。
共有79名(94%)受试者完成了医学监督下的戒断。共有27名(32%)受试者选择过渡到缓释纳曲酮治疗,其中27名中的24名(89%)在出院前成功接受了注射。该方案受试者的平均住院时间为3.6天,第1、2、3和4天的平均COWS评分分别为3.3、3.4、2.8和2.4。此外,71名(85%)受试者在完成方案后参加了住院或门诊物质使用障碍(SUD)治疗项目。
这项回顾性病历审查表明,一种新型方案用于医学监督下的阿片类药物戒断及过渡到预防复发策略(包括注射用缓释纳曲酮)是可行的。这种戒断方案不使用阿片类激动剂或其他管制物质。