4.3 Article

Brain Injury and Development in Preterm Infants Exposed to Fentanyl

期刊

ANNALS OF PHARMACOTHERAPY
卷 49, 期 12, 页码 1291-1297

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/1060028015606732

关键词

premature infant; magnetic resonance imaging; neonatal intensive care; analgesics; opioid analgesics

资金

  1. National Institute of Child Health and Development [R01 HD057098]
  2. Intellectual and Developmental Disabilities Research Center at Washington University [NIH/NICHD P30 HD062171]
  3. Doris Duke Charitable Foundation
  4. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [P30HD062171, R01HD057098, U54HD087011] Funding Source: NIH RePORTER
  5. NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES [UL1TR000448, KL2TR000450] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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 mu g/kg, interquartile range 1-441 mu g/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.

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