PharmacoEpidemiology and Drug Safety Research Group, Department of Pharmacy, University of Oslo, Oslo, Norway.
PharmaTox Strategic Research Initiative, Faculty of Mathematics and Natural Sciences, University of Oslo, Oslo, Norway.
JAMA Netw Open. 2019 Apr 5;2(4):e191435. doi: 10.1001/jamanetworkopen.2019.1435.
The reproductive safety of benzodiazepine/z-hypnotic exposure on child longer-term developmental risks remains unresolved.
To quantify the association of motor, communication, and attention-deficit/hyperactivity disorder (ADHD) symptoms in preschoolers with gestational benzodiazepine/z-hypnotic exposure by timing and duration and coexposure to opioids or antidepressants.
DESIGN, SETTING, AND PARTICIPANTS: Nationwide, population-based Norwegian Mother and Child Cohort Study, recruiting pregnant women from 1999 to 2008, with child follow-up from ages 6, 18, and 36 months to ages 5, 7, and 8 years. Follow-up of teenagers is ongoing. The study included women with depressive/anxiety (n = 4195), sleeping (n = 5260), or pain-related (n = 26 631) disorders before and/or during pregnancy.
For the timing analyses, children exposed to benzodiazepines/z-hypnotics in midpregnancy (weeks 17-28) or late pregnancy (week 29 or later) vs those born to nonmedicated women. For the duration and coexposure analyses, benzodiazepine/z-hypnotic treatment for multiple 4-week intervals vs 1 and co-use of benzodiazepine/z-hypnotic with opioids or antidepressants vs sole benzodiazepine/z-hypnotic use.
Parent-reported motor and communication skills (Ages and Stages Questionnaires) and ADHD symptoms (Conners' Parent Rating Scale-Revised) at child median age of 5.1 years (interquartile range, 5.0-5.3 years) as standardized mean scores. General linear propensity score-adjusted and marginal structural models were fitted. Analyses were stratified by maternal disorder.
Of 41 146 eligible pregnancy-child dyads, 36 086 children (18 330 boys and 17 756 girls) were included, of whom 283 (0.8%) were prenatally exposed to benzodiazepines/z-hypnotics (134 in the depressive/anxiety, 60 in the sleeping, and 89 in the pain-related disorders). There was no increased risk for greater ADHD symptoms or fine motor deficits after intrauterine benzodiazepine/z-hypnotic exposure at different time points. Children born to women with depressive/anxiety disorders who took benzodiazepines/z-hypnotics in late pregnancy had greater gross motor (weighted β, 0.67; 95% CI, 0.21-1.13) and communication (weighted β, 0.35; 95% CI, 0.04-0.65) deficits than unexposed children. There was no evidence for substantial duration or coexposure associations.
These findings suggest no substantial detrimental risk on child fine motor and ADHD symptoms after prenatal benzodiazepine/z-hypnotic exposure alone or in combination with opioids or antidepressants. Residual confounding by indication and/or a higher drug dose regimen among women with anxiety/depression may explain the moderate association of gross motor and communication deficits with late-pregnancy benzodiazepine/z-hypnotic use.
苯二氮䓬/镇静催眠药暴露对儿童长期发育风险的生殖安全性仍未解决。
通过时间和持续时间以及同时暴露于阿片类药物或抗抑郁药,量化与妊娠期间苯二氮䓬/镇静催眠剂暴露相关的学龄前儿童运动、沟通和注意力缺陷/多动障碍(ADHD)症状的关联。
设计、地点和参与者:全国性的挪威母亲和儿童队列研究,招募了 1999 年至 2008 年期间的孕妇,对儿童从 6 个月、18 个月和 36 个月龄随访至 5 岁、7 岁和 8 岁。青少年的随访仍在进行中。该研究包括患有抑郁/焦虑症(n=4195)、睡眠障碍(n=5260)或疼痛相关疾病(n=26631)的妇女,这些疾病在妊娠前和/或妊娠期间存在。
对于时间分析,在妊娠中期(17-28 周)或妊娠晚期(第 29 周或以后)暴露于苯二氮䓬/镇静催眠药的儿童与未接受药物治疗的女性所生的儿童相比。对于持续时间和共同暴露分析,使用多个 4 周间隔的苯二氮䓬/镇静催眠药治疗与使用 1 个和共同使用苯二氮䓬/镇静催眠药与阿片类药物或抗抑郁药与单独使用苯二氮䓬/镇静催眠药相比。
儿童在 5.1 岁(中位数年龄,5.0-5.3 岁;四分位距)时的父母报告的运动和沟通技能(年龄和阶段问卷)和 ADHD 症状(康纳斯父母评定量表修订版)的标准化平均分数。使用一般线性倾向得分调整和边缘结构模型进行拟合。分析按产妇疾病进行分层。
在 41146 名合格的妊娠-儿童对子中,纳入了 36086 名儿童(18330 名男孩和 17756 名女孩),其中 283 名(0.8%)儿童在子宫内暴露于苯二氮䓬/镇静催眠药(抑郁/焦虑症 134 名,睡眠障碍 60 名,疼痛相关疾病 89 名)。宫内苯二氮䓬/镇静催眠药暴露在不同时间点与 ADHD 症状或精细运动缺陷的风险增加无关。患有抑郁/焦虑症的女性在妊娠晚期使用苯二氮䓬/镇静催眠药的儿童,与未暴露的儿童相比,粗大运动(加权β,0.67;95%置信区间,0.21-1.13)和沟通(加权β,0.35;95%置信区间,0.04-0.65)缺陷更为明显。没有证据表明存在实质性的持续时间或共同暴露关联。
这些发现表明,在妊娠期间单独或与阿片类药物或抗抑郁药联合使用苯二氮䓬/镇静催眠药后,儿童的精细运动和 ADHD 症状不会出现实质性的不良风险。焦虑/抑郁妇女中可能存在残余混杂因素和/或更高的药物剂量方案,这可能解释了妊娠晚期使用苯二氮䓬/镇静催眠药与粗大运动和沟通缺陷的中度关联。