Höck Michaela, Posod Anna, Waltner-Romen Maria, Kiechl-Kohlendorfer Ursula, Griesmaier Elke
Department of Paediatrics II (Neonatology) Medical University of Innsbruck Innsbruck Austria.
Paediatr Neonatal Pain. 2020 Nov 27;3(1):29-35. doi: 10.1002/pne2.12042. eCollection 2021 Mar.
LISA is a promising method in improving preterm outcome. The aim of this study was to assess whether the INSURE (intubation-surfactant extubation) technique or LISA (less invasive surfactant administration) procedure for surfactant administration is associated with more pain-relieving interventions after the intervention in preterm infants.
Preterm infants born at <32 weeks gestational age admitted to the Neonatal Intensive Care Unit of Innsbruck University hospital between Jan 2012 and June 2017 subjected to INSURE or LISA were included in the study, which was performed as a retrospective analysis of routinely collected data. Pain assessments were made bedside using the Bernese Pain Scale for Neonates.
During the study period 15 preterm infants (median gestational age 30.7 weeks; range: 25.9-32.0 weeks) were subjected to INSURE technique and 59 (median gestational age 29.4 weeks; range: 25.1-31.4 weeks) to LISA. Infants subjected to LISA showed a higher need for nonpharmacological pain-relieving interventions in the first three days of life.
LISA procedure compared to INSURE technique was associated with a higher need for pain-relieving interventions in the first three days of life. Prospective randomized controlled trials are needed to optimize this less invasive method for surfactant application with special focus on pain in neonates.
肺表面活性物质注入系统(LISA)是一种有望改善早产结局的方法。本研究旨在评估在早产婴儿中,用于给予肺表面活性物质的INSURE(气管插管-肺表面活性物质-拔管)技术或LISA(微创肺表面活性物质给药)操作在干预后是否与更多的疼痛缓解干预措施相关。
纳入2012年1月至2017年6月间入住因斯布鲁克大学医院新生儿重症监护病房、胎龄<32周且接受了INSURE或LISA操作的早产婴儿,该研究是对常规收集数据进行的回顾性分析。使用伯尔尼新生儿疼痛量表在床边进行疼痛评估。
在研究期间,15例早产婴儿(中位胎龄30.7周;范围:25.9 - 32.0周)接受了INSURE技术,59例(中位胎龄29.4周;范围:25.1 - 31.4周)接受了LISA操作。接受LISA操作的婴儿在出生后的前三天对非药物性疼痛缓解干预措施的需求更高。
与INSURE技术相比,LISA操作在出生后的前三天与更高的疼痛缓解干预措施需求相关。需要进行前瞻性随机对照试验,以优化这种微创的肺表面活性物质应用方法,特别关注新生儿的疼痛问题。