Department of Pediatrics, The Warren Alpert Medical School of Brown University, Providence, RI, USA.
Addiction. 2012 Nov;107 Suppl 1(0 1):63-73. doi: 10.1111/j.1360-0443.2012.04040.x.
To determine the effects of in utero exposure to methadone or buprenorphine on infant neurobehavior.
Three sites from the Maternal Opioid Treatment: Human Experimental Research (MOTHER) study, a double-blind, double-dummy, randomized clinical trial participated in this substudy.
Medical Centers that provided comprehensive maternal care to opioid-dependent pregnant women in Baltimore, MD, Providence, RI and Vienna, Austria.
Thirty-nine full-term infants.
The Neonatal Intensive Care Unit (NICU) Network Neurobehavioral Scale (NNNS) was administered to a subgroup of infants on postpartum days 3, 5, 7, 10, 14-15 and 28-30.
While neurobehavior improved for both medication conditions over time, infants exposed in utero to buprenorphine exhibited fewer stress-abstinence signs (P < 0.001), were less excitable (P < 0.001) and less over-aroused (P < 0.01), exhibited less hypertonia (P < 0.007), had better self-regulation (P < 0.04) and required less handling (P < 0.001) to maintain a quiet alert state relative to in utero methadone-exposed infants. Infants who were older when they began morphine treatment for withdrawal had higher self-regulation scores (P < 0.01), and demonstrated the least amount of excitability (P < 0.02) and hypertonia (P < 0.02) on average. Quality of movement was correlated negatively with peak NAS score (P < 0.01), number of days treated with morphine for NAS (P < 0.01) and total amount of morphine received (P < 0.03). Excitability scores were related positively to total morphine dose (P < 0.03).
While neurobehavior improves during the first month of postnatal life for in utero agonist medication-exposed neonates, buprenorphine exposure results in superior neurobehavioral scores and less severe withdrawal than does methadone exposure.
确定胎儿暴露于美沙酮或丁丙诺啡对婴儿神经行为的影响。
来自母体阿片类药物治疗:人类实验研究(MOTHER)研究的三个地点,这是一项双盲、双模拟、随机临床试验,参与了这项子研究。
在巴尔的摩、MD、普罗维登斯、RI 和维也纳、奥地利为阿片类药物依赖孕妇提供全面母婴护理的医疗中心。
39 名足月婴儿。
新生儿重症监护病房(NICU)网络神经行为量表(NNNS)在产后第 3、5、7、10、14-15 和 28-30 天对婴儿进行了亚组评估。
尽管两种药物治疗的神经行为都随着时间的推移而改善,但胎儿暴露于丁丙诺啡的婴儿表现出更少的戒断应激迹象(P < 0.001),兴奋性较低(P < 0.001),过度兴奋程度较低(P < 0.01),张力较高(P < 0.007),自我调节能力较好(P < 0.04),需要较少的处理(P < 0.001)以维持安静警觉状态,与胎儿暴露于美沙酮的婴儿相比。开始用吗啡治疗戒断时年龄较大的婴儿自我调节评分较高(P < 0.01),平均表现出最低的兴奋性(P < 0.02)和张力过高(P < 0.02)。运动质量与 NAS 评分峰值呈负相关(P < 0.01),与用吗啡治疗 NAS 的天数(P < 0.01)和接受的吗啡总量(P < 0.03)呈负相关。兴奋评分与总吗啡剂量呈正相关(P < 0.03)。
虽然胎儿暴露于阿片类激动剂药物的新生儿在出生后第一个月的神经行为会改善,但与美沙酮暴露相比,丁丙诺啡暴露导致更好的神经行为评分和更轻的戒断症状。