Centre for Interdisciplinary Addiction Research of Hamburg University (CIAR), University Medical Center Hamburg-Eppendorf, Department of Psychiatry and Psychotherapy, Martinistr. 52, 20246 Hamburg, Germany.
University of Florence, Department of Psychiatry, AOU Careggi, Largo Brambilla, 3, 50134 Florence, Italy.
J Subst Abuse Treat. 2021 Aug;127:108350. doi: 10.1016/j.jsat.2021.108350. Epub 2021 Mar 4.
Since April 2015, slow-release oral morphine (SROM) has been approved for opioid agonist treatment (OAT) in Germany. Experimental studies show that benefits of SROM over methadone include less heroin craving, better tolerability, and higher patient satisfaction and mental stability. The SROMOS study (Efficacy and Tolerability of Slow-Release Oral Morphine in Opioid Substitution Treatment) aims to investigate the long-term effects (effectiveness and safety) of morphine substitution under routine care in Germany.
This is a prospective, noninterventional, naturalistic, observational study. Between July 2016 and November 2017, this study recruited patients in OAT who decided to switch to SROM from 23 outpatient addiction treatment centers in Germany. The study collected data on mental health (Brief Symptom Inventory - BSI-18), substance use, somatic health (Opiate Treatment Index Health-Symptoms-Scale - OTI-HSS), opioid craving (visual analogue scale), and withdrawal symptoms (Short Opiate Withdrawal Scale) at baseline (t0) and after 3 (t3), 6 (t6) and 12 (t12) months. Physicians documented side effects as adverse events (AEs) and adverse drug reactions (ADRs).
Three-quarters of the enrolled study participants (N = 180) were male. The average age was 44.4 years. Patients were opioid-dependent for 23 years and had been in OAT for almost seven years on average. After 12 months, 60.6% were still being treated with SROM. Mental health improved significantly under SROM treatment between t0 and t12. The intention-to-treat (ITT), as well as the per-protocol (PP) analysis, shows a statistically significant improvement of the mean Global Severity Index (GSI) of the BSI-18 value of 20% (ITT) and 24% (PP). Physical health also improved significantly under SROM treatment. There were no statistically significant changes in the use of cannabis, cocaine, amphetamines, and tranquillizers in the past 30 days, but heroin use, intravenous consumption, and the number of drinking days significantly decreased.
This study provides some of the first long-term data on OAT with SROM under routine care conditions. SROM treatment is an effective alternative for a subgroup of opioid-dependent patients with an unsatisfactory course of OAT or in cases where undesirable side effects due to alternative substances have occurred.
The study protocol was approved by the Ethics Committee of the Chamber of Physicians in Hamburg in March 2016 (No. PV5222). The study was conducted by following the Declaration of Helsinki and is registered with the German Register of Clinical Trials (DRKS, ID: DRKS00010712).
自 2015 年 4 月以来,缓释口服吗啡(SROM)已在德国获准用于阿片类药物激动剂治疗(OAT)。实验研究表明,SROM 相对于美沙酮的益处包括减少海洛因渴望、更好的耐受性以及更高的患者满意度和心理稳定性。SROMOS 研究(缓释口服吗啡在阿片类药物替代治疗中的疗效和耐受性)旨在研究德国常规护理下吗啡替代治疗的长期效果(疗效和安全性)。
这是一项前瞻性、非干预性、自然观察性研究。2016 年 7 月至 2017 年 11 月,本研究从德国 23 家门诊成瘾治疗中心招募了决定从 OAT 转为 SROM 的患者。该研究在基线(t0)和 3 个月(t3)、6 个月(t6)和 12 个月(t12)时收集了心理健康(Brief Symptom Inventory - BSI-18)、物质使用、躯体健康(阿片类药物治疗指数健康症状量表 - OTI-HSS)、阿片类药物渴望(视觉模拟量表)和戒断症状(短期阿片戒断量表)的数据。医生将不良反应(AE)和药物不良反应(ADR)记录为不良事件(AE)。
纳入研究的参与者中,有四分之三(N=180)为男性。平均年龄为 44.4 岁。患者依赖阿片类药物 23 年,平均接受 OAT 治疗近 7 年。12 个月后,仍有 60.6%的患者接受 SROM 治疗。SROM 治疗下,心理健康在治疗后 12 个月内显著改善。意向治疗(ITT)和方案治疗(PP)分析显示,BSI-18 的平均总体严重程度指数(GSI)值改善了 20%(ITT)和 24%(PP)。SROM 治疗也显著改善了躯体健康。在过去 30 天内,大麻、可卡因、安非他命和镇静剂的使用没有统计学上的显著变化,但海洛因使用、静脉注射消费和饮酒天数明显减少。
这项研究提供了一些关于常规护理下 OAT 中使用 SROM 的首次长期数据。对于 OAT 过程不理想或因替代物质发生不良副作用的阿片类药物依赖患者亚群,SROM 治疗是一种有效的替代方法。
该研究方案于 2016 年 3 月获得汉堡医师协会伦理委员会的批准(编号:PV5222)。该研究遵循《赫尔辛基宣言》进行,并在德国临床试验注册处(DRKS)注册(DRKS,ID:DRKS00010712)。