Seliga-Siwecka Joanna, Chmielewska Anna, Jasińska Katarzyna
Neonatal and Intensive Care Department, The Medical University of Warsaw, 2 Karowa Street, 00-315, Warsaw, Poland.
Department of Clinical Sciences, Umeå University, Umeå, Sweden.
Trials. 2020 Nov 23;21(1):946. doi: 10.1186/s13063-020-04841-x.
Human milk is recommended for all very low birth weight infants. Breastmilk is highly variable in nutrient content, failing to meet the nutritional demands of this group. Fortification of human milk is recommended to prevent extrauterine growth retardation and associated poor neurodevelopmental outcome. However, standard fortification with fixed dose multicomponent fortifier does not account for the variability in milk composition. Targeted fortification is a promising alternative and needs further investigation.
This randomized controlled trial will recruit preterm infants (≤ 32 weeks of gestation) within the first 7 days of life. After reaching 80 ml/kg/day of enteral feeding, patients will be randomized to receive standard fortification (HMF, Nutricia) or targeted fortification (modular components: Bebilon Bialka, Nutricia-protein; Polycal, Nutricia-carbohydrates; Calogen, Nutricia-lipids). The intervention will continue until 37 weeks of post-conception age or hospital discharge. Parents and outcome assessors will be blinded to the intervention. The primary outcome measure is velocity of weight, length, and head growth until 36 weeks post-conceptional age or discharge. Secondary outcomes include neurodevelopment at 12 months assessed with Bayley Scale of Development III, repeated at 36 months; body composition at discharge and at 4 months; and incidence of necrotizing enterocolitis, sepsis, retinopathy of prematurity, and bronchopulmonary dysplasia.
Targeted fortification has previously been shown as doable in the neonatal intensive care unit context. If it shows to improve growth and neonatal outcome, choosing the targeted fortification as a first line nutritional approach in very low birth weight infants may become a recommendation.
ClinicalTrials.gov NCT03775785 , Registered on July 2019.
推荐所有极低出生体重儿食用母乳。母乳的营养成分差异很大,无法满足这一群体的营养需求。建议强化母乳以预防宫外生长迟缓及相关的不良神经发育结局。然而,使用固定剂量多成分强化剂进行标准强化并未考虑到母乳成分的变异性。针对性强化是一种有前景的替代方法,需要进一步研究。
这项随机对照试验将纳入出生后7天内的早产儿(胎龄≤32周)。在达到每日肠内喂养80毫升/千克后,患者将被随机分组,分别接受标准强化(纽迪希亚的人乳强化剂)或针对性强化(模块化成分:贝比龙比亚尔卡、纽迪希亚蛋白质;聚卡,纽迪希亚碳水化合物;卡洛金,纽迪希亚脂质)。干预将持续至孕龄37周或出院。家长和结局评估者将对干预措施不知情。主要结局指标是至孕龄36周或出院时的体重、身长和头围生长速度。次要结局包括12个月时使用贝利婴幼儿发展量表第三版评估的神经发育情况,并在36个月时重复评估;出院时及4个月时的身体成分;以及坏死性小肠结肠炎、败血症、早产儿视网膜病变和支气管肺发育不良的发生率。
此前已证明在新生儿重症监护病房环境下针对性强化是可行的。如果它显示能改善生长和新生儿结局,那么在极低出生体重儿中选择针对性强化作为一线营养方法可能会成为一项推荐。
ClinicalTrials.gov NCT03775785,于2019年7月注册。