Division of Neonatology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
JAMA Pediatr. 2021 Aug 1;175(8):790-796. doi: 10.1001/jamapediatrics.2021.0678.
Fortification of expressed breast milk (EBM) using commercially available human milk fortifiers (HMF) increases short-term weight and length in preterm very low-birth-weight (VLBW) neonates. However, the high cost and increased risk of feed intolerance limit their widespread use. Preterm formula powder fortification (PTF) might be a better alternative in resource-limited settings.
To demonstrate that fortification of EBM by preterm formula powder is noninferior to fortification by HMF, in terms of short-term weight gain, in VLBW neonates.
DESIGN, SETTING, AND PARTICIPANTS: Open-label, noninferiority, randomized trial conducted from December 2017 to June 2019 at a level 3 neonatal unit in India. The trial enrolled preterm (born at or before 34 weeks of gestation) VLBW neonates receiving at least 100 mL/kg/d of feeds and consuming 75% of milk or more as EBM.
Neonates were randomly assigned to receive fortification by either PTF or HMF. Calcium, phosphorus, iron, vitamin D, and multivitamins were supplemented in PTF and only vitamin D in the HMF group to meet the recommended dietary allowances.
The primary outcome was the weight gain until discharge from the hospital or 40 weeks' postmenstrual age, whichever was earlier; the prespecified noninferiority margin was 2 g/kg/d. Secondary outcomes included morbidities such as necrotizing enterocolitis, feed intolerance, and extrauterine growth restriction (<10th percentile on the Fenton chart at 40 weeks' postmenstrual age).
Of the 123 neonates enrolled, 60 and 63 were randomized to the PTF and HMF groups, respectively. The mean gestation (30.5 vs 29.9 weeks) and birth weight (1161 vs 1119 g) were comparable between the groups. There was no difference in the mean (SD) weight gain between the PTF and HMF groups (15.7 [3.9] vs 16.3 [4.0] g/kg/d; mean difference, -0.5 g/kg/d; 95% CI, -1.9 to 0.7). The lower bound of 95% CI did not cross the noninferiority margin. The incidence of feed intolerance was lower in the PTF group (1.4 vs 6.8 per 1000 patient-days; incidence rate ratio 0.19; 95% CI, 0.04 to 0.95), and fewer neonates required withholding of fortification for 24 hours or more (5% vs 22%; risk ratio, 0.22; 95% CI, 0.07 to 0.75). The incidence of necrotizing enterocolitis stage II or more (0 vs 5%) and extrauterine growth restriction (73% vs 81%) was comparable between the groups.
Fortification with preterm formula powder is not inferior to fortification with human milk fortifiers in preterm neonates. Given the possible reduction in feed intolerance and lower costs, preterm formula might be a better option for fortification, especially in resource-restricted settings.
Clinical Trial Registry, India Identifier: CTRI/2017/11/010593.
使用市售人乳强化剂(HMF)强化母乳可增加早产儿极低出生体重儿(VLBW)的短期体重和身长。然而,其高成本和增加的不耐受风险限制了其广泛应用。早产儿配方粉强化(PTF)可能是资源有限环境下更好的选择。
证明在早产儿中,PTF 强化 EBM 在短期体重增加方面不劣于 HMF 强化,以达到 VLBW 新生儿的效果。
设计、地点和参与者:这是一项在印度三级新生儿单位于 2017 年 12 月至 2019 年 6 月期间进行的开放性、非劣效性、随机试验。试验纳入了接受至少 100 mL/kg/d 的喂养且至少 75%的奶量为 EBM 的早产儿(出生时胎龄为 34 周或更早)。
新生儿被随机分配接受 PTF 或 HMF 强化。PTF 中补充钙、磷、铁、维生素 D 和多种维生素,而 HMF 组仅补充维生素 D,以满足推荐的膳食摄入量。
主要结局是出院或 40 周校正后至出院的体重增加,以先到者为准;预设的非劣效性边界为 2 g/kg/d。次要结局包括坏死性小肠结肠炎、不耐受和宫外生长受限等并发症(40 周校正后在 Fenton 图表上的第 10 个百分位数以下)。
在纳入的 123 名新生儿中,60 名和 63 名分别随机分配到 PTF 和 HMF 组。两组的平均胎龄(30.5 周比 29.9 周)和出生体重(1161 克比 1119 克)相当。PTF 组和 HMF 组的平均(SD)体重增加量无差异(15.7 [3.9] g/kg/d 比 16.3 [4.0] g/kg/d;平均差值,-0.5 g/kg/d;95%CI,-1.9 至 0.7)。95%CI 的下限未越过非劣效性边界。PTF 组不耐受的发生率较低(1000 患者天 1.4 例比 6.8 例;发生率比,0.19;95%CI,0.04 至 0.95),需要停止强化治疗 24 小时或更长时间的新生儿较少(5%比 22%;风险比,0.22;95%CI,0.07 至 0.75)。坏死性小肠结肠炎 II 期或更高级别(0 比 5%)和宫外生长受限(73%比 81%)的发生率在两组间相似。
早产儿配方粉强化在早产儿中不劣于 HMF 强化。鉴于不耐受的可能减少和较低的成本,早产儿配方可能是更好的强化选择,特别是在资源有限的环境下。
印度临床试验注册中心,注册号:CTRI/2017/11/010593。