Mills Kimberly P, Lean Rachel E, Smyser Christopher D, Inder Terrie, Rogers Cynthia, McPherson Christopher C
Department of Pharmacy, St. Louis Children's Hospital, St. Louis, MO, United States.
Department of Psychiatry, Washington University in St. Louis, St. Louis, MO, United States.
Front Pain Res (Lausanne). 2022 Mar 1;3:836705. doi: 10.3389/fpain.2022.836705. eCollection 2022.
To evaluate the association between cumulative fentanyl dose during neonatal intensive care and 5-year neurodevelopmental and socioemotional outcomes in very preterm infants.
Patient demographics and clinical factors during the perinatal and neonatal course were collected in 84 patients born between 23- and 30-weeks gestational age (GA). Cumulative fentanyl dose during neonatal intensive care was calculated. Developmental testing at age 5 years included the Wechsler Preschool and Primary Scale of Intelligence Full-Scale Intelligence Quotient, Third Edition, Clinical Evaluation of Language Fundamentals-Preschool, Second Edition, Movement Assessment Battery for Children, Second Edition (MABC-2), and Shape School Assessment. Socioemotional outcomes were assessed via caregiver's responses on the Child Behavior Checklist/1.5-5 (CBCL/1.5-5.5) and Social Responsiveness Scale, Second Edition (SRS-2). Covariates were identified on bivariate analysis ( < 0.1). Linear regression models related outcome measures to the log of cumulative fentanyl dose adjusted for covariates.
Higher cumulative fentanyl dose was associated with lower composite motor scores on bivariate analysis ( < 0.01). Cumulative fentanyl dose did not correlate with composite intelligence quotient, language, or executive function. The Clinical Risk Index for Babies score, log of mechanical ventilation, inotrope, and anesthesia duration, and log of cumulative midazolam and hydrocortisone dose were also associated with MABC-2 scores ( < 0.1). Cumulative fentanyl dose was not associated with composite MABC-2 scores on multiple linear regression. Higher cumulative fentanyl dose was associated with decreased socioemotional problems based on caregiver's response on CBCL/1.5-5.5 t-scores driven by fewer symptoms of depression. The McMaster Family Assessment Device general functioning scale score, maternal age, GA, log of total parenteral nutrition days, patent ductus arteriosus requiring treatment, and log of inotrope hours were also associated with CBCL/1.5-5.5 t-scores ( < 0.1). Cumulative fentanyl dose ( = 0.039) and family dysfunction score ( = 0.002) remained significant after controlling for covariates on multiple linear regression.
Cumulative fentanyl dose during neonatal intensive care did not correlate with 5-year motor, cognitive, or language outcomes after controlling for other variables. Fentanyl dose was associated with caregiver reported total socioemotional problems on the CBCL/1.5-5.5 on multivariate modeling. Additional long-term studies are needed to fully elucidate the safety of fentanyl in very preterm neonates.
评估新生儿重症监护期间芬太尼累积剂量与极早产儿5岁时神经发育及社会情感结局之间的关联。
收集了84例孕龄在23至30周之间出生的患者围产期和新生儿期的人口统计学及临床因素。计算新生儿重症监护期间的芬太尼累积剂量。5岁时的发育测试包括韦氏学前及初小儿童智力量表第三版全量表智商、语言基本能力临床评估学前版第二版、儿童运动评估量表第二版(MABC - 2)以及形状学校评估。社会情感结局通过照顾者对儿童行为检查表/1.5 - 5岁版(CBCL/1.5 - 5.5)和社会反应量表第二版(SRS - 2)的回答进行评估。在双变量分析(P < 0.1)中确定协变量。线性回归模型将结局指标与经协变量调整后的芬太尼累积剂量的对数相关联。
在双变量分析中,较高的芬太尼累积剂量与较低的综合运动评分相关(P < 0.01)。芬太尼累积剂量与综合智商、语言或执行功能无关。婴儿临床风险指数评分、机械通气时间的对数、血管活性药物使用情况、麻醉持续时间以及咪达唑仑和氢化可的松累积剂量的对数也与MABC - 2评分相关(P < 0.1)。在多元线性回归中,芬太尼累积剂量与综合MABC - 2评分无关。基于照顾者对CBCL/1.5 - 5.5 t评分的回答,较高的芬太尼累积剂量与社会情感问题减少相关,这是由较少的抑郁症状驱动的。麦克马斯特家庭评估设备总体功能量表评分、母亲年龄、孕龄、全胃肠外营养天数的对数、需要治疗的动脉导管未闭以及血管活性药物使用小时数的对数也与CBCL/1.5 - 5.5 t评分相关(P < 0.1)。在多元线性回归中控制协变量后,芬太尼累积剂量(P = 0.039)和家庭功能障碍评分(P = 0.002)仍然显著。
在控制其他变量后,新生儿重症监护期间的芬太尼累积剂量与5岁时的运动、认知或语言结局无关。在多变量建模中,芬太尼剂量与照顾者报告的CBCL/1.5 - 5.5上的总体社会情感问题相关。需要更多长期研究来充分阐明芬太尼在极早产儿中的安全性。