Division of Neurotoxicology, National Center for Toxicological Research/Food and Drug Administration, Jefferson, AR, United States; Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR 72079, USA.
Neurotoxicol Teratol. 2012 Jan-Feb;34(1):47-55. doi: 10.1016/j.ntt.2011.10.008. Epub 2011 Nov 7.
Use of preemptive analgesia in Neonatal Intensive Care Units is recommended for severe and/or invasive procedures. However, the potential long-term consequences of such analgesia, which may be prolonged, are only beginning to be studied. In this pilot study, a subset of subjects previously enrolled in the Neurological Outcomes and Preemptive Analgesia in Neonates (NEOPAIN) trial was assessed at early childhood. These ex-preterm infants (born at 23-32 weeks of gestational age) required intubation within 72 h postpartum and were randomized to receive either preemptive morphine analgesia (maximum of 14 days) or placebo within 8h post-intubation. At 5-7 years of age, neuropsychological outcomes, morphometrics, adaptive behavior, parent-rated behavior, motivation, and short-term memory were measured. Although overall IQ and academic achievement did not differ between the morphine treated (n=14) and placebo (n=5) groups, preemptive morphine analgesia was associated with distinct differences in other outcome variables. Head circumference of morphine treated children was approximately 7% smaller (Cohen'sd: 2.83, effect size large) and body weight was approximately 4% less (Cohen'sd: 0.81, effect size large); however, height did not differ. In the short-term memory task (delayed matching to sample), morphine treated children exhibited significantly longer choice response latencies than placebo children (3.86±0.33 and 2.71±0.24 s, respectively) (p<0.03) and completed approximately 27% less of the task than placebo children (Cohen'sd: 0.96, effect size large). Parents described morphine treated children as having more social problems, an effect specific to creating and maintaining friendships (Cohen'sd: -0.83, effect size large). Despite the small sample size and the preliminary nature of this study, these results are strongly suggestive of long-lasting effects of preemptive morphine analgesia. A larger investigation with more comprehensive assessments of some of these key features will enable a more complete understanding of the relationship between preemptive morphine treatment and long-term neurocognitive, behavioral, and adaptive outcomes.
在新生儿重症监护病房中,建议对严重和/或有创性操作使用预防性镇痛。然而,这种可能持续时间较长的镇痛的潜在长期后果才刚刚开始研究。在这项初步研究中,对先前参加新生儿神经结局和预防性镇痛(NEOPAIN)试验的一部分受试者在幼儿期进行了评估。这些早产儿(胎龄 23-32 周)出生后 72 小时内需要插管,并在插管后 8 小时内随机接受预防性吗啡镇痛(最多 14 天)或安慰剂。在 5-7 岁时,测量了神经心理学结果、形态计量学、适应行为、父母评定行为、动机和短期记忆。尽管吗啡治疗组(n=14)和安慰剂组(n=5)的总体智商和学业成绩没有差异,但预防性吗啡镇痛与其他结局变量的明显差异有关。接受吗啡治疗的儿童的头围约小 7%(Cohen'sd:2.83,大效应量),体重约轻 4%(Cohen'sd:0.81,大效应量);然而,身高没有差异。在短期记忆任务(延迟匹配样本)中,接受吗啡治疗的儿童的选择反应时明显长于安慰剂儿童(分别为 3.86±0.33 和 2.71±0.24 秒)(p<0.03),并且完成任务的比例约低于安慰剂儿童(Cohen'sd:0.96,大效应量)。父母描述接受吗啡治疗的儿童有更多的社交问题,这种影响特定于建立和维持友谊(Cohen'sd:-0.83,大效应量)。尽管样本量小,且这项研究初步,但这些结果强烈提示预防性吗啡镇痛具有持久的影响。更大规模的研究,更全面地评估其中一些关键特征,将能够更全面地了解预防性吗啡治疗与长期神经认知、行为和适应结局之间的关系。