Pharmacy Department, Perth Children's Hospital, 15 Hospital Ave, Nedlands, WA, 6009, Australia.
Medical School, The University of Western Australia, Perth, WA, Australia.
BMC Pediatr. 2022 Aug 30;22(1):514. doi: 10.1186/s12887-022-03569-8.
Despite the wide use of parenteral nutrition (PN) in neonatal intensive care units (NICU), there is limited evidence regarding the optimal time to commence PN in term and late preterm infants. The recommendations from the recently published ESPGHAN/ESPEN/ESPR/CPEN and NICE guidelines are substantially different in this area, and surveys have reported variations in clinical practice. The aim of this randomised controlled trial (RCT) is to evaluate the benefits and risks of early versus late PN in term and late preterm infants.
METHODS/DESIGN: This study is a single-centre, non-blinded RCT in the NICU of Perth Children's Hospital, Western Australia.A total of 60 infants born ≥34 weeks of gestation who have a high likelihood of intolerance to enteral nutrition (EN) for at least 3-5 days will be randomised to early (day 1 or day 2 of admission) or late commencement (day 6 of admission) of PN after informed parental consent. In both groups, EN will be commenced as early as clinically feasible. Primary outcomes are plasma phenylalanine and plasma F-isoprostane levels on Day 4 and Day 8 of admission. Secondary outcomes are total and individual plasma amino acid profiles, plasma and red blood cell fatty acid profiles, in-hospital all-cause mortality, hospital-acquired infections, length of hospital/NICU stay, z scores and changes in z scores at discharge for weight, height and head circumference, time to full EN, duration of respiratory (mechanical, non-invasive) support, duration of inotropic support, the incidence of hyper and hypoglycaemia, incidence of metabolic acidosis, liver function, blood urea nitrogen, and C-reactive protein (CRP).
This RCT will examine the effects of early versus late PN in term and late preterm infants by comparing key biochemical and clinical outcomes and has the potential to identify underlying pathways for beneficial or harmful effects related to the timing of commencement of PN in such infants.
ANZCTR; ACTRN12620000324910 (3rd March 2020).
尽管肠外营养(PN)在新生儿重症监护病房(NICU)中广泛使用,但关于足月和晚期早产儿何时开始 PN 的最佳时间,证据有限。最近发表的 ESPGHAN/ESPEN/ESPR/CPEN 和 NICE 指南在这方面的建议有很大的不同,调查也报告了临床实践的差异。本随机对照试验(RCT)的目的是评估足月和晚期早产儿早期与晚期 PN 的益处和风险。
方法/设计:这是一项在西澳大利亚珀斯儿童医院 NICU 进行的单中心、非盲 RCT。共有 60 名胎龄≥34 周且极有可能不耐受肠内营养(EN)至少 3-5 天的婴儿将在知情父母同意后随机分为早期(入院第 1 天或第 2 天)或晚期(入院第 6 天)开始 PN。在两组中,只要临床可行,将尽早开始 EN。主要结局是入院第 4 天和第 8 天的血浆苯丙氨酸和血浆 F-异前列烷水平。次要结局是总血浆和单个氨基酸谱、血浆和红细胞脂肪酸谱、院内全因死亡率、医院获得性感染、住院/NICU 时间、出院时体重、身高和头围的 z 评分和变化、完全 EN 的时间、呼吸(机械、非侵入性)支持的持续时间、正性肌力支持的持续时间、高血糖和低血糖的发生率、代谢性酸中毒的发生率、肝功能、血尿素氮和 C 反应蛋白(CRP)。
本 RCT 将通过比较关键的生化和临床结局,研究早期与晚期 PN 在足月和晚期早产儿中的作用,并有可能确定与此类婴儿 PN 开始时间相关的有益或有害影响的潜在途径。
ANZCTR;ACTRN12620000324910(2020 年 3 月 3 日)。