Cameron Colin, Watson Diane, Robinson Jeffrey
From the Integrated Forensic Program, Royal Ottawa Health Care Group, Department of Psychiatry, University of Ottawa, Ottawa, Ontario, Canada.
J Clin Psychopharmacol. 2014 Oct;34(5):559-64. doi: 10.1097/JCP.0000000000000180.
Nabilone is a synthetic cannabinoid that has shown promise for the treatment of posttraumatic stress disorder (PTSD)-related insomnia and nightmares as well as efficacy in the management of chronic pain. It has also been proposed for harm reduction in cannabis dependence. Its effectiveness for management of concurrent disorders in seriously mentally ill correctional populations has not been evaluated. This retrospective study of 104 male inmates with serious mental illness prescribed nabilone analyzes the indications, efficacy, and safety of its use. Medications discontinued with the initiation of nabilone were also reviewed. The results showed nabilone targeting a mean of 3.5 indications per patient, thus likely reducing polypharmacy risk. The mean final dosage was 4.0 mg. Results indicated significant improvement in PTSD-associated insomnia, nightmares, PTSD symptoms, and Global Assessment of Functioning and subjective improvement in chronic pain. Medications associated with greater risk for adverse effects or abuse than nabilone were often able to be discontinued with the initiation of nabilone, most often antipsychotics and sedative/hypnotics. There was no evidence of abuse within this high-risk population or reduction of efficacy when nabilone was given in powder form with water rather than as a capsule. This study supports the promise of nabilone as a safe, effective treatment for concurrent disorders in seriously mentally ill correctional populations. Prospective, randomized controlled trials are required to confirm our preliminary results. Follow-up in the community will be required to confirm effectiveness in harm reduction.
纳必隆是一种合成大麻素,已显示出在治疗创伤后应激障碍(PTSD)相关失眠和噩梦方面具有前景,以及在慢性疼痛管理方面具有疗效。它还被提议用于减少大麻依赖的危害。其对严重精神疾病惩教人群中并发疾病管理的有效性尚未得到评估。这项对104名开具纳必隆处方的患有严重精神疾病的男性囚犯的回顾性研究分析了其使用的适应症、疗效和安全性。还审查了开始使用纳必隆时停用的药物。结果显示,纳必隆针对每位患者平均3.5种适应症,因此可能降低多药联用风险。平均最终剂量为4.0毫克。结果表明,PTSD相关失眠、噩梦、PTSD症状以及功能总体评估有显著改善,慢性疼痛有主观改善。与纳必隆相比具有更高不良反应或滥用风险的药物,在开始使用纳必隆时通常能够停用,最常见的是抗精神病药物和镇静/催眠药物。在这个高风险人群中没有滥用的证据,并且当纳必隆以粉末形式与水混合而非制成胶囊给药时,也没有疗效降低的情况。这项研究支持了纳必隆作为一种安全、有效的治疗方法用于严重精神疾病惩教人群并发疾病的前景。需要进行前瞻性、随机对照试验来证实我们的初步结果。还需要在社区进行随访以确认其在减少危害方面的有效性。