Coffin Phillip Oliver, Santos Glenn-Milo, Matheson Tim, Behar Emily, Rowe Chris, Rubin Talia, Silvis Janelle, Vittinghoff Eric
San Francisco Department of Public Health, San Francisco, California, United States of America.
University of California San Francisco, San Francisco, California, United States of America.
PLoS One. 2017 Oct 19;12(10):e0183354. doi: 10.1371/journal.pone.0183354. eCollection 2017.
The United States is amidst an opioid epidemic, including synthetic opioids that may result in rapid death, leaving minimal opportunity for bystander rescue. We pilot tested a behavioral intervention to reduce the occurrence of opioid overdose among opioid dependent persons at high-risk for subsequent overdose.
We conducted a single-blinded randomized-controlled trial of a repeated dose motivational interviewing intervention (REBOOT) to reduce overdose versus treatment as usual, defined as information and referrals, over 16 months at the San Francisco Department of Public Health from 2014-2016. Participants were 18-65 years of age, had opioid use disorder by Structured Clinical Interview, active opioid use, opioid overdose within 5 years, and prior receipt of naloxone kits. The intervention was administered at months 0, 4, 8, and 12, preceded by the assessment which was also administered at month 16. Dual primary outcomes were any overdose event and number of events, collected by computer-assisted personal interview, as well as any fatal overdose events per vital records.
A total of 78 persons were screened and 63 enrolled. Mean age was 43 years, 67% were born male, 65% White, 17% African-American, and 14% Latino. Ninety-two percent of visits and 93% of counseling sessions were completed. At baseline, 33.3% of participants had experienced an overdose in the past four months, with a similar mean number of overdoses in both arms (p = 0.95); 29% overdosed during follow-up. By intention-to-treat, participants assigned to REBOOT were less likely to experience any overdose (incidence rate ratio [IRR] 0.62 [95%CI 0.41-0.92, p = 0.019) and experienced fewer overdose events (IRR 0.46, 95%CI 0.24-0.90, p = 0.023), findings that were robust to sensitivity analyses. There were no differences between arms in days of opioid use, substance use treatment, or naloxone carriage.
REBOOT reduced the occurrence of any opioid overdose and the number of overdoses.
clinicaltrials.gov NCT02093559.
美国正处于阿片类药物流行之中,包括可能导致迅速死亡的合成阿片类药物,这使得旁观者救援的机会微乎其微。我们进行了一项行为干预试验,以减少阿片类药物依赖且有后续过量用药高风险人群中阿片类药物过量的发生。
我们在2014年至2016年期间于旧金山公共卫生部开展了一项单盲随机对照试验,比较重复剂量动机性访谈干预(REBOOT)与常规治疗(定义为提供信息和转介服务)对减少过量用药的效果,为期16个月。参与者年龄在18至65岁之间,通过结构化临床访谈确诊患有阿片类药物使用障碍,有阿片类药物的使用行为,在5年内有过阿片类药物过量经历,且之前接受过纳洛酮试剂盒。干预在第0、4、8和12个月进行,干预前及第16个月进行评估。双重主要结局为任何过量用药事件及事件数量,通过计算机辅助个人访谈收集,以及根据生命记录获取的任何致命过量用药事件。
共筛查78人,63人入组。平均年龄43岁,67%为男性,65%为白人,17%为非裔美国人,14%为拉丁裔。92%的访视和93%的咨询课程完成。基线时,33.3%的参与者在过去四个月内有过过量用药经历,两组的过量用药平均次数相似(p = 0.95);随访期间29%的人出现过量用药。按意向性分析,分配到REBOOT组的参与者发生任何过量用药的可能性较小(发病率比[IRR] 0.62 [95%CI 0.41 - 0.92,p = 0.019]),且过量用药事件较少(IRR 0.46,95%CI 0.24 - 0.90,p = 0.023),这些结果在敏感性分析中很稳健。两组在阿片类药物使用天数、物质使用治疗或纳洛酮携带方面无差异。
REBOOT减少了任何阿片类药物过量的发生及过量用药事件的数量。
clinicaltrials.gov NCT02093559