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暴露于芬太尼的早产儿的脑损伤与发育

Brain Injury and Development in Preterm Infants Exposed to Fentanyl.

作者信息

McPherson Christopher, Haslam Matthew, Pineda Roberta, Rogers Cynthia, Neil Jeffrey J, Inder Terrie E

机构信息

Brigham and Women's Hospital, Boston, MA, USA

Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Ann Pharmacother. 2015 Dec;49(12):1291-7. doi: 10.1177/1060028015606732. Epub 2015 Sep 14.

Abstract

BACKGROUND

Fentanyl is commonly used in preterm infants. Relatively little is known regarding the neurodevelopmental outcomes of preterm infants exposed to fentanyl.

OBJECTIVE

To investigate the association between cumulative fentanyl dose and brain injury and diameters in a cohort of preterm infants.

METHODS

Data on demographics, perinatal course, and neonatal course, including total fentanyl exposure prior to term equivalent age, were retrospectively evaluated for 103 infants born at ≤30 weeks gestational age (mean gestational age 26.9 ± 1.8 weeks) who underwent magnetic resonance imaging at term equivalent age. Magnetic resonance images were evaluated for brain injury and regional brain diameters. Developmental testing was conducted at term equivalent and 2 years of age.

RESULTS

Seventy-eight infants (76%) received fentanyl (median cumulative dose 3 µg/kg, interquartile range 1-441 µg/kg). Cumulative fentanyl dose in the first week of life correlated with the incidence of cerebellar hemorrhage after correction for covariates (odds ratio 2.1, 95% confidence interval 1.1-4.1). Cumulative fentanyl dose before term equivalent age correlated with reductions in transverse cerebellar diameter after correction for covariates, including the presence of cerebellar hemorrhage (r = 0.461, P = 0.002). No correlation was detected between cumulative fentanyl dose and development at 2 years of age.

CONCLUSIONS

Higher cumulative fentanyl dose in preterm infants correlated with a higher incidence of cerebellar injury and lower cerebellar diameter at term equivalent age. Our findings must be taken with caution, but emphasize the need for future prospective trials examining the risks and benefits of commonly used analgesic agents in preterm infants.

摘要

背景

芬太尼常用于早产儿。对于接触芬太尼的早产儿的神经发育结局,人们了解相对较少。

目的

研究一组早产儿中芬太尼累积剂量与脑损伤及脑径之间的关联。

方法

对103例孕龄≤30周(平均孕龄26.9±1.8周)且在足月矫正年龄时接受磁共振成像检查的婴儿,回顾性评估其人口统计学、围产期及新生儿期情况,包括足月矫正年龄前的芬太尼总暴露量。对磁共振图像进行脑损伤及脑区直径评估。在足月矫正年龄及2岁时进行发育测试。

结果

78例婴儿(76%)接受了芬太尼治疗(累积剂量中位数为3μg/kg,四分位间距为1 - 441μg/kg)。校正协变量后,出生后第一周的芬太尼累积剂量与小脑出血发生率相关(比值比2.1,95%置信区间1.1 - 4.1)。校正包括小脑出血在内的协变量后,足月矫正年龄前的芬太尼累积剂量与小脑横径减小相关(r = 0.461,P = 0.002)。未检测到芬太尼累积剂量与2岁时的发育之间存在相关性。

结论

早产儿中较高的芬太尼累积剂量与足月矫正年龄时较高的小脑损伤发生率及较小的小脑直径相关。我们的研究结果必须谨慎看待,但强调未来需要进行前瞻性试验来研究常用镇痛剂在早产儿中的风险和益处。

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