Friends Research Institute, Baltimore, MD, USA.
Friends Research Institute, Baltimore, MD, USA.
Drug Alcohol Depend. 2021 Feb 1;219:108422. doi: 10.1016/j.drugalcdep.2020.108422. Epub 2020 Dec 9.
The distinct pharmacological properties and clinical uses of extended-release naltrexone (XR-NTX) and sublingual buprenorphine-naloxone (BUP-NX) present challenges in analyzing patient outcomes.
We conducted a secondary analysis of a multi-site randomized trial comparing XR-NTX with sublingual BUP-NX treatment for opioid use disorder initiated during inpatient detoxification and continued in outpatient treatment. Urine testing data for non-study opioids from the last 22 weeks of the 24-week trial were analyzed in both a per-protocol sample (n = 474 participants who received at least one dose of medication) and a completers sample (n = 211 participants who received all XR-NTX doses or all BUP-NX prescriptions). The present analyses sought to identify differences in the weekly percentages of opioid-positive urine tests between participants treated with the two medications.
The proportion of opioid-positive tests in both conditions was less than 20 % for 21 of the 22 weeks in the per-protocol sample and all 22 weeks in the completers sample. Generalized linear mixed model analyses revealed a significant treatment (XR-NTX vs. BUP-NX) X week (weeks 3-24) interaction in the per-protocol sample but not the completers sample. In the per-protocol analysis, the BUP-NX, compared to XR-NTX, had significantly greater proportions of opioid-positive tests in 14 out of the 22 weeks.
Longitudinal modeling approaches that utilize flexible procedures for handling missing data can offer a different perspective on study findings. Results from the present analyses suggest that XR-NTX appeared to be somewhat more effective than BUP-NX in reducing illicit opioid use in the per-protocol sample.
延长释放型纳曲酮(XR-NTX)和舌下丁丙诺啡-纳洛酮(BUP-NX)具有独特的药理学特性和临床用途,这给分析患者结局带来了挑战。
我们对一项多中心随机试验进行了二次分析,该试验比较了 XR-NTX 与舌下 BUP-NX 治疗在住院戒毒期间开始并在门诊治疗中继续的阿片类药物使用障碍。对 24 周试验的最后 22 周的非研究性阿片类药物的尿检测数据进行了分析,分析样本包括接受至少一剂药物的按方案样本(n=474 名参与者)和完成者样本(n=211 名接受所有 XR-NTX 剂量或所有 BUP-NX 处方的参与者)。本分析旨在确定两种药物治疗的参与者每周阿片类药物阳性尿液检测的百分比差异。
在按方案样本中,有 21 周(22 周中的 21 周)和所有 22 周(22 周中的 22 周)的条件下,阿片类药物阳性检测的比例均低于 20%。广义线性混合模型分析显示,在按方案样本中存在显著的治疗(XR-NTX 与 BUP-NX)X 周(第 3-24 周)交互作用,但在完成者样本中则不存在。在按方案分析中,与 XR-NTX 相比,BUP-NX 在 22 周中的 14 周中阿片类药物阳性检测的比例显著更高。
利用灵活的缺失数据处理程序的纵向建模方法可以为研究结果提供不同的视角。本分析结果表明,在按方案样本中,XR-NTX 似乎比 BUP-NX 更能有效减少非法阿片类药物的使用。