Ling Walter, Hillhouse Maureen P, Saxon Andrew J, Mooney Larissa J, Thomas Christie M, Ang Alfonso, Matthews Abigail G, Hasson Albert, Annon Jeffrey, Sparenborg Steve, Liu David S, McCormack Jennifer, Church Sarah, Swafford William, Drexler Karen, Schuman Carolyn, Ross Stephen, Wiest Katharina, Korthuis P Todd, Lawson William, Brigham Gregory S, Knox Patricia C, Dawes Michael, Rotrosen John
University of California, Los Angeles, CA, USA.
Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA.
Addiction. 2016 Aug;111(8):1416-27. doi: 10.1111/add.13375. Epub 2016 Apr 21.
To examine the safety and effectiveness of buprenorphine + naloxone sublingual tablets (BUP, as Suboxone(®) ) provided after administration of extended-release injectable naltrexone (XR-NTX, as Vivitrol(®) ) to reduce cocaine use in participants who met DSM-IV criteria for cocaine dependence and past or current opioid dependence or abuse.
This multi-centered, double-blind, placebo-controlled study, conducted under the auspices of the National Drug Abuse Treatment Clinical Trials Network, randomly assigned 302 participants at sites in California, Oregon, Washington, Colorado, Texas, Georgia, Ohio, New York and Washington DC, USA to one of three conditions provided with XR-NTX: 4 mg/day BUP (BUP4, n = 100), 16 mg/day BUP (BUP16, n = 100, or no buprenorphine (placebo; PLB, n = 102). Participants received pharmacotherapy for 8 weeks, with three clinic visits per week. Cognitive behavioral therapy was provided weekly. Follow-up assessments occurred at 1 and 3 months post-intervention. The planned primary outcome was urine drug screen (UDS)-corrected, self-reported cocaine use during the last 4 weeks of treatment. Planned secondary analyses assessed cocaine use by UDS, medication adherence, retention and adverse events.
No group differences were found between groups for the primary outcome (BUP4 versus PLB, P = 0.262; BUP16 versus PLB, P = 0.185). Longitudinal analysis of UDS data during the evaluation period using generalized linear mixed equations found a statistically significant difference between BUP16 and PLB [P = 0.022, odds ratio (OR) = 1.71] but not for BUP4 (P = 0.105, OR = 1.05). No secondary outcome differences across groups were found for adherence, retention or adverse events.
Buprenorphine + naloxone, used in combination with naltrexone, may be associated with reductions in cocaine use among people who meet DSM-IV criteria for cocaine dependence and past or current opioid dependence or abuse.
研究在给符合《精神疾病诊断与统计手册》第四版(DSM-IV)可卡因依赖标准且有过或目前存在阿片类药物依赖或滥用的参与者注射长效纳曲酮(XR-NTX,商品名Vivitrol)后,给予丁丙诺啡 + 纳洛酮舌下片(BUP,商品名Suboxone)以减少可卡因使用的安全性和有效性。
本多中心、双盲、安慰剂对照研究在美国国家药物滥用治疗临床试验网络的支持下进行,将美国加利福尼亚州、俄勒冈州、华盛顿州、科罗拉多州、得克萨斯州、佐治亚州、俄亥俄州、纽约州和华盛顿特区各研究点的302名参与者随机分配至接受XR-NTX的三种情况之一:4毫克/天丁丙诺啡(BUP4,n = 100)、16毫克/天丁丙诺啡(BUP16,n = 100)或不使用丁丙诺啡(安慰剂;PLB,n = 102)。参与者接受8周的药物治疗,每周进行三次门诊就诊。每周提供认知行为疗法。干预后1个月和3个月进行随访评估。计划的主要结局是治疗最后4周经尿液药物筛查(UDS)校正的自我报告可卡因使用情况。计划的次要分析评估通过UDS检测的可卡因使用情况、药物依从性、留存率和不良事件。
主要结局在各治疗组间未发现差异(BUP4与PLB相比,P = 0.262;BUP16与PLB相比,P = 0.185)。在评估期内使用广义线性混合方程对UDS数据进行纵向分析发现,BUP16与PLB之间存在统计学显著差异[P = 0.022,比值比(OR)= 1.71],但BUP4组未发现差异(P = 0.105,OR = 1.05)。在依从性、留存率或不良事件方面,各治疗组间未发现次要结局差异。
丁丙诺啡 + 纳洛酮与纳曲酮联合使用,可能会使符合DSM-IV可卡因依赖标准且有过或目前存在阿片类药物依赖或滥用的人群的可卡因使用量减少。