Princess Royal Maternity, Glasgow, UK; College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK; Department of Clinical Physics and Bio-engineering, Royal Hospital for Children, NHS Greater Glasgow & Clyde, Glasgow, UK.
Early Hum Dev. 2020 Nov;150:105188. doi: 10.1016/j.earlhumdev.2020.105188. Epub 2020 Sep 10.
Prenatal opioid exposure adversely impacts upon fetal growth and places the newborn at risk of neonatal opioid withdrawal. The severity and duration of opioid withdrawal cannot be predicted in the individual baby and may be contributed to by other drugs including benzodiazepines and alcohol as well as cigarette smoking. Mitigating factors include breastfeeding, rooming in and absence of maternal polypharmacy. Less well recognised are a variety of other complications associated with prenatal opioid exposure including epigenetic changes, effects on neurophysiological function and structural alterations to the developing brain. The visual system is significantly affected, with changes to both clinical and electrophysiological function persisting at least to mid-childhood. Longer term neurodevelopmental and behavioural outcomes are confounded by multiple factors including poverty, parent-child interaction and small study numbers, but systematic reviews consistently demonstrate poorer outcomes for those children and young people prenatally exposed to opioids. Crucially, manifestation of neonatal withdrawal is not a prerequisite for important long term problems including behavioural, emotional or motor function disorder, sensory or speech disorder, strabismus and nystagmus. A body of evidence supports an independent adverse effect of prenatal opioid exposure upon fetal brain development, mediated via a systemic neuro-inflammatory process. Children prenatally exposed to opioids should remain under appropriate follow up, at least until school entry, as difficulties may only become apparent in mid-childhood. Future studies of the management of opioid use disorder in pregnancy, including maintenance methadone, must include longer term outcomes for the baby.
产前阿片类药物暴露会对胎儿生长产生不利影响,并使新生儿面临新生儿阿片类药物戒断的风险。个体婴儿的阿片类药物戒断的严重程度和持续时间无法预测,并且可能由包括苯二氮䓬类药物和酒精以及吸烟在内的其他药物引起。减轻因素包括母乳喂养、母婴同室和没有母亲的多种药物治疗。不太被认识的是与产前阿片类药物暴露相关的各种其他并发症,包括表观遗传变化、对神经生理功能的影响以及对发育中大脑的结构改变。视觉系统受到显著影响,临床和电生理功能的变化至少持续到儿童中期。长期神经发育和行为结果受到多种因素的影响,包括贫困、亲子互动和研究数量少,但系统评价一致表明,那些在产前接触过阿片类药物的儿童和年轻人的结果较差。至关重要的是,新生儿戒断的表现并不是包括行为、情绪或运动功能障碍、感觉或言语障碍、斜视和眼球震颤在内的重要长期问题的先决条件。大量证据表明,产前阿片类药物暴露对胎儿大脑发育有独立的不良影响,这是通过全身神经炎症过程介导的。产前接触过阿片类药物的儿童至少应在入学前进行适当的随访,因为问题可能只会在儿童中期才变得明显。未来对妊娠期间阿片类药物使用障碍的管理研究,包括维持美沙酮,必须包括婴儿的长期结局。