Mittapalli Deepika, Sajjan Anil K, Charki Siddu, Patil Mallanagouda
Pediatrics, Shri B. M. Patil Medical College Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, IND.
Cureus. 2024 Sep 19;16(9):e69705. doi: 10.7759/cureus.69705. eCollection 2024 Sep.
Background Early initiation of enteral feeding in neonates on inotropic support may improve clinical outcomes compared to intravenous fluids, but the safety and optimal inotrope levels for enteral nutrition remain unclear. This study aims to assess the early initiation of enteral feeding versus intravenous fluids in newborns on inotrope support and to compare the clinical outcome in terms of hospital stay, morbidity, and mortality in neonates with enteral feed versus intravenous (IV) fluid group on inotropes. It also focuses on evaluating the safety of enteral nutrition in neonates with inotropic support and determining the cutoff levels of the inotropes at which enteral feed is well tolerated. Methodology A prospective cohort study was conducted at a tertiary care center in northern Karnataka from June 2022 to December 2023. Neonates born after 28 weeks or more of gestation or weighing more than 1000 grams with fluid nonresponsive shock were enrolled for the study. Neonates with gastrointestinal comorbidities or birth weight below 1000 grams, younger than 28 weeks of gestation, and with lethal congenital malformations were excluded. Eligible neonates were enrolled by the investigator into enteral and intravenous fluid groups at the clinical discretion of the treating neonatologist. Enteral feeding commenced with expressed breast milk or milk from milk bank after 6 hours of stable circulation while the intravenous fluid group received no feed initially. Inotropes were tapered upon stable circulation with feed volumes adjusted based on tolerance. The data obtained was entered into a Microsoft Excel sheet and statistical analyses were performed using IBM SPSS Statistics software, version 20. The results were presented as mean, standard deviation counts, percentages and diagrams. For normally distributed continuous variables between the two groups, they were compared using an independent sample t-test. For not normally distributed variables, the Mann-Whitney U test was used. Categorical variables between the two groups were compared using the chi-square test and Fisher's exact test and p<0.05 was considered statistically significant. Results The study included 142 neonates (71 per group). The enteral nutrition group had a higher percentage (62; 87.32%) of improved and discharged neonates than the intravenous fluid group (56; 78.87%). The mean time to reach full feeds was significantly lower in the enteral nutrition group (6.04 days) as compared to the intravenous fluid group (9.78 days), with a p-value of < 0.0001. Similarly, the duration of neonatal intensive care unit (NICU) stay was significantly shorter for enteral nutrition group (7.38 days) compared to intravenous fluid group (11.37 days), also with a p-value of < 0.0001. Three patients (4.22%) chose to get discharged against medical advice in the enteral nutrition group while five patients (7.04%) did the same in the intravenous fluid group. The death rate was also higher among intravenous fluid group (10; 10.08%) compared to enteral nutrition group (6; 8.45%). Independent samples t-test showed significant differences in time to reach full feed and duration of NICU stay between cases and controls. Conclusion Neonates receiving enteral feeds had significantly shorter NICU stays, suggesting improved clinical management. Adrenaline (0.1 mcg/kg) with dobutamine (10 mcg/kg) emerged as the optimal inotrope combination for feed tolerance.
背景 与静脉补液相比,对接受强心支持的新生儿早期开始肠内喂养可能改善临床结局,但肠内营养的安全性和最佳强心药物水平仍不明确。本研究旨在评估接受强心支持的新生儿早期开始肠内喂养与静脉补液的情况,并比较肠内喂养组与接受强心药物的静脉(IV)补液组新生儿在住院时间、发病率和死亡率方面的临床结局。研究还着重评估接受强心支持的新生儿肠内营养的安全性,并确定能良好耐受肠内喂养的强心药物临界水平。
方法 2022年6月至2023年12月在卡纳塔克邦北部的一家三级医疗中心进行了一项前瞻性队列研究。纳入妊娠28周或以上出生或体重超过1000克且对补液无反应性休克的新生儿。排除有胃肠道合并症、出生体重低于1000克、妊娠小于28周以及有致死性先天性畸形的新生儿。符合条件的新生儿由研究者根据新生儿治疗专家的临床判断纳入肠内和静脉补液组。循环稳定6小时后开始用挤出的母乳或母乳库的乳汁进行肠内喂养,而静脉补液组最初不进行喂养。循环稳定后逐渐减少强心药物用量,并根据耐受性调整喂养量。将获得的数据录入Microsoft Excel工作表,并使用IBM SPSS Statistics软件版本20进行统计分析。结果以均值、标准差计数、百分比和图表形式呈现。对于两组间呈正态分布的连续变量,使用独立样本t检验进行比较。对于非正态分布变量,使用曼-惠特尼U检验。两组间的分类变量使用卡方检验和费舍尔精确检验进行比较,p<0.05被认为具有统计学意义。
结果 该研究纳入了142例新生儿(每组71例)。与静脉补液组(56例;78.87%)相比,肠内营养组改善并出院的新生儿比例更高(62例;87.32%)。与静脉补液组(9.78天)相比,肠内营养组达到完全喂养的平均时间显著更短(6.04天),p值<0.0001。同样,与静脉补液组(11.37天)相比,肠内营养组新生儿重症监护病房(NICU)住院时间显著更短(7.38天),p值也<0.0001。肠内营养组有3例患者(4.22%)选择不听从医嘱出院,而静脉补液组有5例患者(7.04%)同样如此。静脉补液组死亡率(10例;10.08%)也高于肠内营养组(6例;8.45%)。独立样本t检验显示病例组和对照组在达到完全喂养的时间和NICU住院时间方面存在显著差异。
结论 接受肠内喂养的新生儿NICU住院时间显著更短,提示临床管理得到改善。肾上腺素(0.1微克/千克)与多巴酚丁胺(10微克/千克)是对喂养耐受性最佳的强心药物组合。