Wilder Christine M, Hosta Daniel, Winhusen Theresa
Addiction Sciences Division, Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, 3131 Harvey Avenue, Cincinnati, OH 45229, USA.
Department of Veterans Affairs Medical Center, 3200 Vine Street, Cincinnati, OH 45220, USA.
J Subst Abuse Treat. 2017 Sep;80:33-36. doi: 10.1016/j.jsat.2017.06.005. Epub 2017 Jun 23.
In non-pregnant individuals being treated for opioid use disorder (OUD) with methadone, doses ≥60mg per day are associated with improved treatment retention and decreased illicit opioid use. Although methadone remains the first line treatment for OUD in pregnant women, there are no studies replicating this finding in pregnancy.
We conducted a retrospective cohort study of 189 pregnant women treated with methadone for OUD from 2006 to 2013. Chart data collected included demographics, pregnancy dates, methadone doses, and urine drug screen (UDS) results.
Treatment retention at delivery was significantly higher for subjects taking ≥60mg of methadone (90.1% v. 74.1% p<0.005), as was treatment retention at 60days postpartum (71.6% v. 37.0%, p<0.0001). Percent of UDS results negative for illicit substances during pregnancy was also significantly higher for subjects taking ≥60mg (71.5% v. 58.0%, p<0.04). There was no significant difference in UDS results in the first 60days postpartum (63.9% v. 68.1%). Generalized linear models showed a significant positive relationship between methadone dose and treatment retention at delivery (p<0.02) and at 60days postpartum (p<0.004) as well as a significant positive relationship between length of time in treatment and treatment retention at delivery (p<0.04) and at 60days postpartum (p<0.007). Maternal age and percent of negative UDS results were not predictive of treatment retention in either model and there was no significant interaction effect between methadone dose and percent negative UDS results.
In this cohort, women taking ≥60mg of methadone during pregnancy were more likely to remain in treatment and to provide urine samples negative for illicit drugs. Multivariate modeling suggested a dose dependent response across the entire dose range, rather than a threshold effect at 60mg.
在使用美沙酮治疗阿片类物质使用障碍(OUD)的非孕妇中,每天剂量≥60毫克与治疗依从性提高及非法阿片类物质使用减少相关。尽管美沙酮仍是孕妇OUD的一线治疗药物,但尚无研究在孕期重复这一发现。
我们对2006年至2013年期间189例接受美沙酮治疗OUD的孕妇进行了一项回顾性队列研究。收集的病历数据包括人口统计学信息、妊娠日期、美沙酮剂量及尿液药物筛查(UDS)结果。
服用≥60毫克美沙酮的受试者分娩时的治疗依从性显著更高(90.1%对74.1%,p<0.005),产后60天时的治疗依从性也是如此(71.6%对37.0%,p<0.0001)。服用≥60毫克的受试者孕期UDS结果中非法物质呈阴性的百分比也显著更高(71.5%对58.0%,p<0.04)。产后前60天UDS结果无显著差异(63.9%对68.1%)。广义线性模型显示美沙酮剂量与分娩时(p<0.02)及产后60天时(p<0.004)的治疗依从性之间存在显著正相关,治疗时长与分娩时(p<0.04)及产后60天时(p<0.007)的治疗依从性之间也存在显著正相关。在两个模型中,产妇年龄及UDS结果呈阴性的百分比均不能预测治疗依从性,美沙酮剂量与UDS结果呈阴性的百分比之间无显著交互作用。
在该队列中,孕期服用≥60毫克美沙酮的女性更有可能持续接受治疗并提供非法药物呈阴性的尿液样本。多变量建模表明在整个剂量范围内存在剂量依赖性反应,而非60毫克时的阈值效应。