Bloomfield Frank H, Harding Jane E, Meyer Michael P, Alsweiler Jane M, Jiang Yannan, Wall Clare R, Alexander Tanith
Liggins Institute, University of Auckland, Private Bag, Auckland, 92019, New Zealand.
Newborn Services, Auckland City Hospital, Auckland, New Zealand.
BMC Pediatr. 2018 Jul 7;18(1):220. doi: 10.1186/s12887-018-1195-7.
Babies born at moderate-late preterm gestations account for > 80% of all preterm births. Although survival is excellent, these babies are at increased risk of adverse neurodevelopmental outcomes. They also are at increased risk of adverse long-term health outcomes, such as cardiovascular disease, obesity and diabetes. There is little evidence guiding optimal nutritional practices in these babies; practice, therefore, varies widely. This factorial design clinical trial will address the role of parenteral nutrition, milk supplementation and exposure of the preterm infant to taste and smell with each feed on time to tolerance of full feeds, adiposity, and neurodevelopment at 2 years.
METHODS/DESIGN: The DIAMOND trial is a multi-centre, factorial, randomised, controlled clinical trial. A total of 528 babies born between 32 and 35 weeks' gestation receiving intravenous fluids and whose mothers intend to breastfeed will be randomised to one of eight treatment conditions that include a combination of each of the three interventions: (i) intravenous amino acid solution vs. intravenous dextrose solution until full milk feeds established; (ii) milk supplement vs. exclusive breastmilk, and (iii) taste/smell given or not given before gastric tube feeds. Babies will be excluded if a particular mode of nutrition is clinically indicated or there is a congenital abnormality. Primary study outcome: For parenteral nutrition and milk supplement interventions, body composition at 4 months' corrected age. For taste/smell intervention, time to full enteral feeds defined as 150 ml.kg.day or exclusive breastfeeding.
Days to full sucking feeds; days in hospital; body composition at discharge; growth to 2 years' corrected age; development at 2 years' corrected age; breastfeeding rates.
This trial will provide the first direct evidence to inform feeding practices in moderate- to late-preterm infants that will optimise their growth, metabolic and developmental outcomes.
Australian New Zealand Clinical Trials Registry - ACTRN12616001199404 . This trial is endorsed by the IMPACT clinical trials network ( https://impact.psanz.com.au ).
中度晚期早产儿占所有早产婴儿的80%以上。尽管存活率很高,但这些婴儿出现不良神经发育结局的风险增加。他们出现心血管疾病、肥胖和糖尿病等不良长期健康结局的风险也增加。几乎没有证据指导这些婴儿的最佳营养实践;因此,实践差异很大。这项析因设计临床试验将探讨肠外营养、补充奶类以及每次喂养时让早产儿接触味觉和嗅觉对其完全耐受全量喂养的时间、肥胖程度和2岁时神经发育的作用。
方法/设计:钻石试验是一项多中心、析因、随机对照临床试验。共有528名孕32至35周出生、接受静脉输液且母亲打算母乳喂养的婴儿将被随机分配到八种治疗方案之一,这些方案包括三种干预措施的每种组合:(i)在完全建立奶类喂养前,静脉输注氨基酸溶液与静脉输注葡萄糖溶液;(ii)补充奶类与纯母乳喂养;(iii)在鼻饲前给予或不给予味觉/嗅觉刺激。如果临床上有特定的营养方式指征或存在先天性异常,则将婴儿排除。主要研究结局:对于肠外营养和补充奶类干预措施,矫正年龄4个月时的身体成分。对于味觉/嗅觉干预措施,达到全肠道喂养的时间定义为150毫升·千克·天或纯母乳喂养。
完全吸吮喂养的天数;住院天数;出院时的身体成分;矫正年龄2岁时的生长情况;矫正年龄2岁时的发育情况;母乳喂养率。
这项试验将提供首个直接证据,为中度至晚期早产儿的喂养实践提供参考,以优化其生长、代谢和发育结局。
澳大利亚新西兰临床试验注册中心 - ACTRN12616001199404 。本试验得到IMPACT临床试验网络(https://impact.psanz.com.au )的认可。