Grunau Ruth E, Weinberg Joanne, Whitfield Michael F
Centre for Community Child Health Research, British Columbia Research Institute for Children's & Women's Health, Vancouver, British Columbia, Canada.
Pediatrics. 2004 Jul;114(1):e77-84. doi: 10.1542/peds.114.1.e77.
Stress systems may be altered in the long term in preterm infants for multiple reasons, including early exposure to procedural pain in neonatal intensive care. This question has received little attention beyond hospital discharge. Stress responses (cortisol) to visual novelty in preterm infants who were born at extremely low gestational age (ELGA; < or =28 weeks), very low gestational age (VLGA; 29-32 weeks), and term were compared at 8 months of age corrected for prematurity (corrected chronological age [CCA]). In addition, among the preterm infants, we evaluated whether cortisol levels at 8 months were related to neonatal exposure to procedural pain and morphine in the neonatal intensive care unit.
Seventy-six infants, 54 preterm (< or =32 weeks' GA at birth) and 22 term-born infants who were seen at 8 months CCA composed the study sample, after excluding those with major sensory, motor, or cognitive impairment. Salivary cortisol was measured before (basal) and 20 minutes after introduction of novel toys (post 1) and after developmental assessment (post 2).
Salivary cortisol was significantly higher in ELGA infants at 8 months, compared with the VLGA and term groups before and after introduction of visual novelty. Term-born and VLGA infants showed a slight decrease in cortisol when playing with novel toys, whereas the ELGA group showed higher basal and sustained levels of cortisol. After controlling for early illness severity and duration of supplemental oxygen, higher basal cortisol levels in preterm infants at 8 months' CCA were associated with higher number of neonatal skin-breaking procedures. In contrast, cortisol responses to novelty were predicted equally well by neonatal pain or GA at birth. No relationship between morphine dosing and cortisol response was demonstrated in these infants.
ELGA preterm infants show a different pattern of cortisol levels before and after positive stimulation of visual novelty than more maturely born, VLGA preterm and term-born infants. Exposure to high numbers of skin-breaking procedures may contribute to "resetting" basal arousal systems in preterm infants.
由于多种原因,包括在新生儿重症监护室早期暴露于程序性疼痛,早产儿的应激系统可能会长期改变。这个问题在出院后很少受到关注。比较了极早早产儿(ELGA;胎龄≤28周)、极低出生体重早产儿(VLGA;胎龄29 - 32周)和足月儿在矫正胎龄8个月(矫正月龄[CCA])时对视觉新奇刺激的应激反应(皮质醇)。此外,在早产儿中,我们评估了8个月时的皮质醇水平是否与新生儿重症监护室中程序性疼痛和吗啡暴露有关。
76名婴儿组成研究样本,其中54名早产儿(出生时胎龄≤32周)和22名足月儿,在矫正月龄8个月时接受检查,排除了有严重感觉、运动或认知障碍的婴儿。在引入新玩具前(基础值)、引入后20分钟(刺激后1)和发育评估后(刺激后2)测量唾液皮质醇。
与VLGA组和足月儿组相比,ELGA组婴儿在8个月时,引入视觉新奇刺激前后唾液皮质醇水平显著更高。足月儿和VLGA组婴儿在玩新玩具时皮质醇略有下降,而ELGA组婴儿基础皮质醇水平较高且持续升高。在控制早期疾病严重程度和吸氧持续时间后,矫正月龄8个月时早产儿较高的基础皮质醇水平与更多的新生儿皮肤穿刺操作次数相关。相比之下,新生儿疼痛或出生时的胎龄对皮质醇对新奇刺激的反应预测效果相同。在这些婴儿中未发现吗啡剂量与皮质醇反应之间的关系。
与出生时胎龄较大的VLGA早产儿和足月儿相比,ELGA早产儿在视觉新奇刺激阳性激发前后的皮质醇水平模式不同。暴露于大量皮肤穿刺操作可能有助于“重置”早产儿的基础觉醒系统。