Department of Pharmacy Practice, College of Pharmacy, University of Rhode Island, 7 Greenhouse Road, Suite 265F, Kingston, RI, 02881, USA.
College of Health Sciences, University of Rhode Island, Kingston, RI, USA.
Drug Saf. 2021 Aug;44(8):863-875. doi: 10.1007/s40264-021-01080-0. Epub 2021 Jun 7.
Several studies have reported increasing prevalence of prescription opioid use among pregnant women. However, little is known regarding the effects of maternal opioid use on neurodevelopmental disorders in early childhood in pregnant women with no evidence of opioid use disorders or drug dependence.
The aim of this study was to quantify the association between prenatal opioid exposure from maternal prescription use and neurodevelopmental outcomes in early childhood.
This retrospective study included pregnant women aged 12-55 years and their live-birth infants born from 2010 to 2012 present in Optum's deidentified Clinformatics® Data Mart database. Eligible infants born to mothers without opioid use disorders or drug dependence were followed till occurrence of neurodevelopmental disorders, loss to follow-up, or study end (December 31, 2017), whichever came first. Propensity score by fine stratification was applied to adjust for confounding by demographic characteristics, obstetric characteristics, maternal comorbid mental and pain conditions, and measures of burden of illnesses and to obtain adjusted hazard ratios (HR) and 95% confidence intervals (CI). Exposed and unexposed infants were compared on the incidence of neurodevelopmental disorders.
Of 24,910 newborns, 7.6% (1899) were prenatally exposed to prescription opioids. Overall, 1562 children were diagnosed with neurodevelopmental disorders, with crude incidence rates of 2.9 per 100 person-years in exposed children versus 2.5 per 100 person-years in unexposed children. After adjustment, we observed no association between fetal opioid exposure and the risk of neurodevelopmental disorders (HR 1.10; 95% CI 0.92-1.32). However, increased risk of neurodevelopmental disorders were observed in children with longer cumulative exposure duration (HR 1.70; 95% CI 1.05-2.96) or high cumulative opioid doses (HR 1.22; 95% CI 1.01-1.54).
In pregnant women without opioid use disorders or drug dependence, maternal opioid use was not associated with increased risk of neurodevelopmental disorders in early childhood. However, increased risks of early neurodevelopmental disorders were observed in children born to women receiving prescription opioids for longer duration and at higher doses during pregnancy.
多项研究报告称,孕妇中处方类阿片类药物的使用呈上升趋势。然而,对于没有阿片类药物使用障碍或药物依赖证据的孕妇,母体阿片类药物使用对其子女早期神经发育障碍的影响知之甚少。
本研究旨在定量评估来自母体处方类阿片类药物使用的产前暴露与儿童早期神经发育结局之间的关联。
本回顾性研究纳入了 2010 年至 2012 年期间 Optum 公司匿名的 Clinformatics® Data Mart 数据库中的年龄在 12-55 岁之间的孕妇及其活产婴儿。对没有阿片类药物使用障碍或药物依赖的母亲所生的婴儿进行随访,直至发生神经发育障碍、失访或研究结束(2017 年 12 月 31 日),以先发生者为准。采用精细分层倾向评分来调整混杂因素,包括人口统计学特征、产科特征、母体合并的精神和疼痛状况,以及疾病负担的衡量标准,以获得调整后的危险比(HR)和 95%置信区间(CI)。比较暴露组和未暴露组神经发育障碍的发生率。
在 24910 名新生儿中,7.6%(1899 名)在产前暴露于处方类阿片类药物。总体而言,有 1562 名儿童被诊断为神经发育障碍,暴露组的粗发病率为每 100 人年 2.9 例,未暴露组为每 100 人年 2.5 例。调整后,我们未观察到胎儿阿片类药物暴露与神经发育障碍风险之间存在关联(HR 1.10;95%CI 0.92-1.32)。然而,在累积暴露时间较长(HR 1.70;95%CI 1.05-2.96)或累积阿片类药物剂量较高(HR 1.22;95%CI 1.01-1.54)的儿童中,神经发育障碍的风险增加。
在没有阿片类药物使用障碍或药物依赖的孕妇中,母体阿片类药物使用与儿童早期神经发育障碍的风险增加无关。然而,在接受处方类阿片类药物治疗时间较长且剂量较高的孕妇所生的儿童中,早期神经发育障碍的风险增加。