Cicalese Erin, Shah Aashish, Bashqoy Ferras, Pierce Kristyn, Howell Heather, Desai Purnahamsi
Neonatology, New York University (NYU) Grossman School of Medicine, New York, USA.
Pediatrics, New York University (NYU) Grossman School of Medicine, New York, USA.
Cureus. 2025 Jun 14;17(6):e86005. doi: 10.7759/cureus.86005. eCollection 2025 Jun.
Prolonged sedation in premature infants often involves opioids and benzodiazepines, which can cause adverse effects and worse neurodevelopmental outcomes. Dexmedetomidine has emerged as a safer alternative with fewer side effects, but its long-term neurodevelopmental impact on very preterm infants remains unclear. Further research is needed to understand its effects on this vulnerable population.
The primary objective is to compare the neurodevelopmental outcomes of premature infants who received and did not receive dexmedetomidine infusions while intubated. The secondary objective is to compare the rate of unplanned extubations in these groups.
This was a retrospective cohort study deemed Institutional Review Board (IRB)-exempted by the New York University (NYU) IRB. The study population (n = 15) with a matched control cohort (n = 15) includes infants born under 32 weeks gestation or weighing less than 1,500 g who were intubated during their hospitalization and followed up at our high-risk follow-up program. Patients excluded from the study include those who did not survive to discharge, those lost to follow-up, or those with major congenital anomalies. The patient chart was reviewed for data on maternal characteristics and details from the infant's neonatal intensive care unit (NICU) admission. Data from follow-up visits at six months to two years of life included the Bayley Scales of Infant and Toddler Development, Fourth Edition (BSID-IV) scores. Data were analyzed using Mann-Whitney U testing and Fisher's exact testing.
There was no statistically significant difference (p = 0.373) in BSID-IV scores between the two groups. The overall number of unplanned extubations was not different between the two groups. When assessing unplanned extubations per intubation day, there was a trend toward fewer unplanned extubations in the dexmedetomidine group.
This study suggests that dexmedetomidine may be a safe and effective alternative to traditional sedatives for extremely premature infants, with no observed adverse effects on long-term neurodevelopmental outcomes and potential benefits in reducing extubation-related complications. However, larger, multi-center prospective studies are needed to confirm these findings and inform clinical practice.
早产儿长时间镇静常使用阿片类药物和苯二氮䓬类药物,这些药物会引起不良反应并导致更差的神经发育结局。右美托咪定已成为一种更安全的替代药物,副作用更少,但其对极早产儿的长期神经发育影响仍不明确。需要进一步研究以了解其对这一脆弱人群的影响。
主要目的是比较插管时接受和未接受右美托咪定输注的早产儿的神经发育结局。次要目的是比较这些组中意外拔管的发生率。
这是一项回顾性队列研究,纽约大学机构审查委员会(IRB)认定该研究无需IRB批准。研究人群(n = 15)与匹配的对照队列(n = 15)包括孕周小于32周或出生体重小于1500 g、住院期间接受插管并在我们的高危随访项目中进行随访的婴儿。排除在研究之外的患者包括未存活至出院者、失访者或患有重大先天性异常者。查阅患者病历以获取产妇特征数据以及婴儿新生儿重症监护病房(NICU)入院的详细信息。6个月至2岁随访时的数据包括贝利婴幼儿发育量表第四版(BSID-IV)评分。使用曼-惠特尼U检验和费舍尔精确检验对数据进行分析。
两组间BSID-IV评分无统计学显著差异(p = 0.373)。两组间意外拔管的总数没有差异。在评估每日插管的意外拔管情况时,右美托咪定组意外拔管有减少的趋势。
本研究表明,对于极早产儿,右美托咪定可能是传统镇静剂的一种安全有效的替代药物,未观察到对长期神经发育结局有不良影响,且在减少与拔管相关并发症方面可能有益。然而,需要更大规模的多中心前瞻性研究来证实这些发现并为临床实践提供依据。