Mordal Jon, Juya Farid, Holtan Line, Vederhus John-Kåre, Opheim Arild, Brenna Ida H, Enger Asle E, Weimand Bente, Solli Kristin Klemmetsby, Tanum Lars
Division of Mental Health and Addiction, Vestfold Hospital Trust, Tønsberg, 3103, Norway.
Mental Health Services, Akershus University Hospital, Lørenskog, 1478, Norway.
Addict Sci Clin Pract. 2025 Jun 16;20(1):50. doi: 10.1186/s13722-025-00576-9.
For people with opioid use disorder (OUD), extended-release naltrexone (XR-NTX) is an effective antagonist treatment option. However, successful opioid tapering and abstinence is a prerequisite for XR-NTX induction and has repeatedly been reported as a major barrier to effective treatment. The aims of this study were to describe XR-NTX induction rates, reasons for incomplete induction, and extraordinary complications reported during the induction phase. We also compared sociodemographic and clinical variables among those who did and did not complete induction onto XR-NTX.
This naturalistic, multicenter, and open-label Norwegian study of XR-NTX included men and women aged 18-65 who had severe OUD. Most participants were referred to inpatient medically managed opioid withdrawal and received individualized pharmacological and psychosocial treatment according to clinical assessment and national guidelines. After opioid withdrawal, the participants underwent a minimum of three opioid-free days prior to XR-NTX induction. Variables were collected through baseline assessments and a retrospective patient chart review. XR-NTX induction completers and non-completers were compared via bivariate and logistic regression analyses.
Of 129 participants with recent opioid use at inclusion, 106 (82%) completed XR-NTX induction. Induction was initiated in an inpatient setting for 116 participants (90%) and extraordinary complications were noted for 19 (15%) patients. Withdrawal symptoms and ambivalence were the most common reasons for non-completion, each noted in 75% of the cases. As compared with those who successfully completed induction, non-completers more often reported lifetime hepatitis (78% vs. 52%, p = 0.017), had a longer period of current substance use (mean 119 vs. 54 months, p = 0.001), and more frequently used methadone prior to study inclusion (43% vs. 8%, p < 001). In logistic regression analyses, methadone use was the only significant factor and was negatively associated with completion (odds ratio 0.20, 95% confidence interval = 0.05-0.72, p = 0.014).
The results demonstrate the safety, efficacy and tolerability of a Norwegian opioid withdrawal and XR-NTX induction procedure. Although the present induction rate was high, our findings indicate that methadone users need special attention and tailored interventions regarding opioid withdrawal management and XR-NTX induction.
The study is registered at clinicaltrials.gov (NCT03647774).
对于患有阿片类药物使用障碍(OUD)的人来说,长效纳曲酮(XR-NTX)是一种有效的拮抗剂治疗选择。然而,成功的阿片类药物减量和戒断是启动XR-NTX治疗的先决条件,并且多次被报道为有效治疗的主要障碍。本研究的目的是描述XR-NTX的启动率、启动不完全的原因以及启动阶段报告的特殊并发症。我们还比较了完成和未完成XR-NTX启动的患者的社会人口统计学和临床变量。
这项关于XR-NTX的自然主义、多中心、开放标签的挪威研究纳入了年龄在18-65岁之间患有严重OUD的男性和女性。大多数参与者被转介到住院接受药物管理的阿片类药物戒断治疗,并根据临床评估和国家指南接受个体化的药物和心理社会治疗。在阿片类药物戒断后,参与者在启动XR-NTX之前至少经历了三天无阿片类药物的时间。通过基线评估和回顾性患者病历审查收集变量。通过双变量和逻辑回归分析比较XR-NTX启动完成者和未完成者。
在纳入研究时近期使用过阿片类药物的129名参与者中,106名(82%)完成了XR-NTX启动。116名参与者(90%)在住院环境中启动了治疗,19名(15%)患者出现了特殊并发症。戒断症状和矛盾心理是未完成启动的最常见原因,各有75%的病例出现。与成功完成启动的参与者相比,未完成者更常报告有终身性肝炎(78%对52%,p = 0.017),当前物质使用时间更长(平均119个月对54个月,p = 0.001),并且在纳入研究之前更频繁地使用美沙酮(43%对8%,p < 0.001)。在逻辑回归分析中,美沙酮的使用是唯一的显著因素,并且与完成启动呈负相关(优势比0.20,95%置信区间 = 0.05-0.72,p = 0.014)。
结果证明了挪威阿片类药物戒断和XR-NTX启动程序的安全性、有效性和耐受性。尽管目前的启动率很高,但我们的研究结果表明,美沙酮使用者在阿片类药物戒断管理和XR-NTX启动方面需要特别关注和量身定制的干预措施。
该研究已在clinicaltrials.gov注册(NCT03647774)。