Influence of Early Total Enteral Feeding in Preterm Infants with Respiratory Distress Syndrome.

Neonatology Pub Date : 2024-07-17 DOI:10.1159/000539544
Rohit Anand, Sushma Nangia
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Abstract

Introduction: Providing adequate nutrition in the management of preterm infants has been challenging. The objective of this secondary analysis of data from the randomized trial comparing "less invasive surfactant therapy (LISA) with InSurE method of surfactant administration" is to demonstrate the feasibility of early total enteral feeding (ETEF) in hemodynamically stable preterm neonates on respiratory support and to examine the factors associated with failure of ETEF.

Methods: Secondary analysis of a randomized controlled trial comparing "LISA versus InSurE among preterm infants between 26 and 34 weeks of gestation" enrolled 150 infants with 117 being hemodynamically stable. ETEF without any parenteral supplementation was started on day 1 of life using the mother's own milk (MoM) or donor human milk (<32 weeks of GA) and MoM or preterm formula (33-34 weeks of GA). The data were analyzed to assess the proportion of babies developing feed intolerance and/or necrotizing enterocolitis (NEC) and factors associated with failure of ETEF. All Infants were assessed for the day of attainment of full enteral feeding defined as receiving and tolerating 150 mL/kg of enteral feeds per day.

Results: Out of these 117 babies, 102 tolerated ETEF, and 15 had one or more episodes of FI requiring total parenteral nutrition, but none developed NEC till discharge or death. On the assessment of possible factors associated with ETEF failure, there were no differences in baseline characteristics but statistically significantly increased incidence of culture-positive sepsis as well as the requirement of antibiotic therapy for possible sepsis (early as well as late-onset sepsis) in babies with failure of ETEF. The babies who tolerated ETEF achieved full enteral feeding (150 mL/kg/day) significantly earlier (5.48 ± 1.1 days) compared to those with ETEF failure (7 ± 3.4 days) (p 0.001). The time to regain birth weight was earlier in the ETEF group without significant differences in growth parameters. There was also a reduction in the duration of hospital stay in babies who tolerated ETEF, but both these results were not statistically significant.

Conclusion: ETEF is feasible in preterm neonates with respiratory distress syndrome who are on respiratory support. It resulted in earlier attainment of full enteral feeds and decreased the incidence of sepsis with reduced antibiotic usage.

早产儿呼吸窘迫综合征早期全肠内喂养的影响
简介为早产儿提供充足的营养一直是一项挑战。本研究对 "微创表面活性疗法(LISA)与 InSurE 表面活性给药法 "随机试验数据进行二次分析,目的是证明对接受呼吸支持、血流动力学稳定的早产新生儿进行早期全肠内喂养(ETEF)的可行性,并研究与 ETEF 失败相关的因素:一项随机对照试验的二次分析比较了 "LISA 与 InSurE 在妊娠 26 至 34 周早产儿中的应用",该试验共招募了 150 名婴儿,其中 117 名血液动力学稳定。婴儿出生后第 1 天开始使用母乳(MoM)或供体母乳(孕 32 周)以及母乳或早产儿配方奶粉(孕 33-34 周),ETEF 无需任何肠外补充剂。对数据进行了分析,以评估出现饲料不耐受和/或坏死性小肠结肠炎(NEC)的婴儿比例,以及与 ETEF 失败相关的因素。所有婴儿都接受了完全肠内喂养日的评估,完全肠内喂养是指每天接受并耐受 150 毫升/千克的肠内喂养:结果:在这 117 名婴儿中,102 名能够耐受 ETEF,15 名出现一次或多次 FI,需要全肠外营养,但直到出院或死亡都没有出现 NEC。在评估与 ETEF 失败相关的可能因素时,发现 ETEF 失败的婴儿在基线特征方面没有差异,但培养阳性败血症的发生率以及因可能发生败血症(早期和晚期败血症)而需要抗生素治疗的比例却有显著统计学差异。与 ETEF 失败的婴儿(7 ± 3.4 天)相比,耐受 ETEF 的婴儿实现完全肠内喂养(150 毫升/千克/天)的时间明显更早(5.48 ± 1.1 天)(P 0.001)。ETEF 组婴儿恢复出生体重的时间更早,但生长参数无明显差异。耐受 ETEF 的婴儿住院时间也有所缩短,但这两项结果均无统计学意义:结论:对于患有呼吸窘迫综合征、需要呼吸支持的早产新生儿来说,ETEF 是可行的。ETEF 能让新生儿更早地获得完全的肠内喂养,并能减少抗生素的使用,从而降低败血症的发病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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