Holzapfel Lindsay, Arnold Cody, Tyson Jon, Shapiro Steven, Reynolds Eric, Pedroza Claudia, Stephens Emily, Kleinfeld Alan, Huber Andrew, Rysavy Matthew, Khan Amir, Del Mar Romero Lopez Maria
The University of Texas Health Science Center at Houston.
Stanford University.
Res Sq. 2023 Mar 7:rs.3.rs-2566352. doi: 10.21203/rs.3.rs-2566352/v1.
: Bilirubin neurotoxicity ( ) occurs in premature infants at lower total serum bilirubin levels than term infants and causes neurodevelopmental impairment. Usual dose lipid infusions in preterm infants may increase free fatty acids sufficiently to cause bilirubin displacement from albumin, increasing passage of unbound bilirubin ( ) into the brain leading to BN and neurodevelopmental impairment not reliably identifiable in infancy. These risks may be influenced by whether cycled or continuous phototherapy is used to control bilirubin levels. : To assess differences in wave V latency measured by brainstem auditory evoked responses ( ) at 34-36 weeks gestational age in infants born ≤750 g or <27 weeks' gestational age randomized to receive usual or reduced dose lipid emulsion (half of the usual dose) irrespective of whether cycled or continuous phototherapy is administered. : Pilot factorial randomized controlled trial ( ) of lipid dosing (usual and reduced) with treatment groups balanced between cycled or continuous phototherapy assignment. Eligible infants are born at ≤750 g or <27 weeks' gestational age enrolled in the NICHD Neonatal Research Network RCT of cycled or continuous phototherapy. Infants will randomize 1:1 to reduced or usual dose lipid assignment during the first 2 weeks after birth and stratified by phototherapy assignment. Free fatty acids and UB will be measured daily using a novel probe. BAER testing will be performed at 34-36 weeks postmenstrual age or prior to discharge. Blinded neurodevelopmental assessments will be performed at 22-26 months. Intention-to-treat analyses will be performed with generalized linear mixed models with lipid dose and phototherapy assignments as random effects covariates, and assessment for interactions. Bayesian analyses will be performed as a secondary analysis. Pragmatic trials are needed to evaluate whether lipid emulsion dosing modifies the effect of phototherapy on BN. This factorial design presents a unique opportunity to evaluate both therapies and their interaction. This study aims to address basic controversial questions about the relationships between lipid administration, free fatty acids, UB, and BN. Findings suggesting a reduced lipid dose can diminish the risk of BN would support the need for a large multicenter RCT of reduced versus usual lipid dosing. : Clinical Trials.gov, NCT04584983, Registered 14 October 2020, https://clinicaltrials.gov/ct2/show/NCT04584983 : Version 3.2 (10/5/2022).
胆红素神经毒性( )在早产婴儿中发生时的总血清胆红素水平低于足月儿,并会导致神经发育障碍。早产儿常用剂量的脂质输注可能会使游离脂肪酸充分增加,导致胆红素从白蛋白上解离,增加未结合胆红素( )进入大脑的量,从而导致胆红素神经毒性和婴儿期无法可靠识别的神经发育障碍。这些风险可能会受到采用循环光疗还是持续光疗来控制胆红素水平的影响。 :评估出生体重≤750克或孕周<27周的婴儿在34 - 36周胎龄时,通过脑干听觉诱发电位( )测量的V波潜伏期的差异,这些婴儿被随机分配接受常规剂量或减少剂量的脂质乳剂(常规剂量的一半),无论采用循环光疗还是持续光疗。 :脂质剂量(常规和减少剂量)的探索性析因随机对照试验( ),治疗组在循环光疗或持续光疗分配之间保持平衡。符合条件的婴儿为出生体重≤750克或孕周<27周,参加美国国立儿童健康与人类发展研究所(NICHD)关于循环光疗或持续光疗的新生儿研究网络随机对照试验。婴儿将在出生后的前2周内以1:1的比例随机分配到减少剂量或常规剂量的脂质组,并按光疗分配进行分层。每天使用新型探头测量游离脂肪酸和未结合胆红素。脑干听觉诱发电位测试将在孕龄34 - 36周或出院前进行。在22 - 26个月时进行盲法神经发育评估。将使用广义线性混合模型进行意向性分析,将脂质剂量和光疗分配作为随机效应协变量,并评估相互作用。将进行贝叶斯分析作为次要分析。 需要进行实用性试验来评估脂质乳剂剂量是否会改变光疗对胆红素神经毒性的影响。这种析因设计提供了一个独特的机会来评估两种疗法及其相互作用。本研究旨在解决关于脂质给药、游离脂肪酸、未结合胆红素和胆红素神经毒性之间关系的基本争议问题。表明减少脂质剂量可以降低胆红素神经毒性风险的研究结果将支持开展一项关于减少脂质剂量与常规脂质剂量对比的大型多中心随机对照试验的必要性。 :ClinicalTrials.gov,NCT04584983,2020年10月14日注册,https://clinicaltrials.gov/ct2/show/NCT04584983 :版本3.2(2022年10月5日)