Division of Neonatology, Pediatric Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
Department of Neonatology and Pediatric Intensive Care Medicine, University Children's Hospital, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Pediatr Res. 2021 Feb;89(3):540-548. doi: 10.1038/s41390-020-0979-2. Epub 2020 May 26.
Providing optimal pain relief is a challenging task when caring for premature infants. The aim of this study was to compare the long-term cognitive, motor, and behavioral outcomes of preterm infants before and after the implementation of a pain and sedation protocol. In addition, we investigated whether the increased opiate administration resulting after the implementation process had an impact on these outcomes.
Cognitive outcomes were evaluated using the Kaufman Assessment Battery for Children (KABC), neuromotor examinations were based on Amiel-Tison, and behavioral outcomes were assessed using the parent-reported Child Behavior Checklist (CBCL).
One hundred extremely preterm infants were included in the study (control group, n = 53; intervention group, n = 47). No significant differences were found in cognitive and motor outcomes at preschool age. However, every increase in the cumulative opiate exposure for each 100 mg/kg was weakly significantly associated with a higher risk for autism spectrum features (adjusted odds ratio (aOR) = 1.822, 95% confidence interval (CI) [1.231-2.697]; P = 0.03) and withdrawn behavior (aOR = 1.822, 95% CI [1.231-2.697]; P = 0.03) at preschool age.
Increased neonatal cumulative opiate exposure did not alter cognitive and motor outcomes but may represent a risk factor for autism spectrum and withdrawn behavior at preschool age.
The implementation of a protocol for the management of pain and sedation in preterm infants resulted in increased cumulative opiate exposure. Our study adds further evidence that increased neonatal opiate exposure did not alter cognitive and motor outcomes but may yield a potential risk factor for autism spectrum disorders and withdrawn behavior at preschool age. A vigilant use of opiates is recommended. Further studies are needed looking for novel pain management strategies and drugs providing optimal pain relief with minimal neurotoxicity.
在早产儿护理中,提供最佳的疼痛缓解是一项具有挑战性的任务。本研究旨在比较实施疼痛和镇静方案前后早产儿的长期认知、运动和行为结果。此外,我们还研究了实施过程后阿片类药物用量增加是否会对这些结果产生影响。
使用 Kaufman 儿童评估量表(KABC)评估认知结果,基于 Amiel-Tison 进行神经运动检查,使用父母报告的儿童行为检查表(CBCL)评估行为结果。
本研究共纳入 100 例极早产儿(对照组,n=53;干预组,n=47)。在学龄前,认知和运动结果无显著差异。然而,每增加 100mg/kg 的累积阿片类药物暴露量,自闭症谱系特征的风险就会略有显著增加(调整后的优势比(aOR)=1.822,95%置信区间(CI)[1.231-2.697];P=0.03),以及退缩行为(aOR=1.822,95% CI [1.231-2.697];P=0.03)。
新生儿累积阿片类药物暴露量的增加并未改变认知和运动结果,但可能是学龄前自闭症谱系和退缩行为的危险因素。
在早产儿中实施疼痛和镇静管理方案导致累积阿片类药物暴露量增加。我们的研究进一步证明,新生儿阿片类药物暴露量的增加并未改变认知和运动结果,但可能成为学龄前自闭症谱系障碍和退缩行为的潜在危险因素。建议谨慎使用阿片类药物。需要进一步研究寻找新的疼痛管理策略和药物,以提供最佳的疼痛缓解,同时最小化神经毒性。