Worley Matthew J, Heinzerling Keith G, Shoptaw Steven, Ling Walter
Department of Psychiatry, University of California, San Diego, CA, USA.
Veterans Affairs San Diego Healthcare System, San Diego, CA, USA.
Addiction. 2017 Jul;112(7):1202-1209. doi: 10.1111/add.13782. Epub 2017 Feb 28.
Buprenorphine-naloxone (BUP-NLX) can be used to manage prescription opioid addiction among persons with chronic pain, but post-treatment relapse is common and difficult to predict. This study estimated whether changes in pain over time and pain volatility during BUP-NLX maintenance would predict opioid use during the taper BUP-NLX taper.
Secondary analysis of a multi-site clinical trial for prescription opioid addiction, using data obtained during a 12-week BUP-NLX stabilization and 4-week BUP-NLX taper.
Community clinics affiliated with a national clinical trials network in 10 US cities.
Subjects with chronic pain who entered the BUP-NLX taper phase (n = 125) with enrollment occurring from June 2006 to July 2009 (52% male, 88% Caucasian, 31% married).
Outcomes were weekly biologically verified and self-reported opioid use from the 4-week taper phase. Predictors were estimates of baseline severity, rate of change and volatility in pain from weekly self-reports during the 12-week maintenance phase.
Controlling for baseline pain and treatment condition, increased pain [odds ratio (OR) = 2.38, P = 0.02] and greater pain volatility (OR = 2.43, P = 0.04) predicted greater odds of positive opioid urine screen during BUP-NLX taper. Increased pain (IRR = 1.40, P = 0.04) and greater pain volatility [incidence-rate ratio (IRR) = 1.66, P = 0.009] also predicted greater frequency of self-reported opioid use.
Adults with chronic pain receiving out-patient treatment with buprenorphine-naloxone (BUP-NLX) for prescription opioid addiction have an elevated risk for opioid use when tapering off maintenance treatment. Those with relative persistence in pain over time and greater volatility in pain during treatment are less likely to sustain abstinence during BUP-NLX taper.
丁丙诺啡 - 纳洛酮(BUP-NLX)可用于治疗慢性疼痛患者的处方阿片类药物成瘾,但治疗后复发很常见且难以预测。本研究评估了在BUP-NLX维持治疗期间疼痛随时间的变化以及疼痛波动性是否能预测BUP-NLX减量期的阿片类药物使用情况。
对一项关于处方阿片类药物成瘾的多中心临床试验进行二次分析,使用在12周BUP-NLX稳定期和4周BUP-NLX减量期获得的数据。
美国10个城市中隶属于一个国家临床试验网络的社区诊所。
患有慢性疼痛且进入BUP-NLX减量期的受试者(n = 125),入组时间为2006年6月至2009年7月(52%为男性,88%为白种人,31%已婚)。
结局为4周减量期内每周经生物学验证和自我报告的阿片类药物使用情况。预测因素为12周维持期内每周自我报告的疼痛基线严重程度、变化率和波动性估计值。
在控制基线疼痛和治疗条件后,疼痛增加[比值比(OR)= 2.38,P = 0.02]以及疼痛波动性更大(OR = 2.43,P = 0.04)预测在BUP-NLX减量期阿片类药物尿液筛查呈阳性的几率更高。疼痛增加(发病率比(IRR)= 1.40,P = 0.04)以及疼痛波动性更大[发病率比(IRR)= 1.66,P = 0.009]也预测自我报告的阿片类药物使用频率更高。
接受丁丙诺啡 - 纳洛酮(BUP-NLX)门诊治疗处方阿片类药物成瘾的慢性疼痛成年人在维持治疗减量时阿片类药物使用风险升高。那些疼痛随时间相对持续且治疗期间疼痛波动性更大的人在BUP-NLX减量期维持戒断的可能性较小。