Abstract
There are needs to investigate the influencing factors of necrotizing enterocolitis (NEC) in low birth weight (LBW) newborns, to provide insights into the clinical management of NEC.
This study was a retrospective cohort study. Infants admitted to our hospital from January 1, 2019 to June 30, 2021 were selected. The clinical characteristics of NEC and no-NEC infants were evaluated. Logistic regression analyses were conducted to assess the risk factors of NEC in LBW infants.
A total of 192 LBW infants were included, the incidence of NEC in LBW infants was 35.42%. There were significant differences in the congenital heart disease, sepsis, breastfeeding, blood transfusion and probiotics feeding between NEC and no-NEC group (all P < .05), and there were no significant differences in birth weight, gestational age, mother's pregnancy-induced hypertension, premature rupture of fetal membrane, amniotic fluid pollution, fetal asphyxia, neonatal respiratory distress syndrome and mechanical ventilation between NEC and no-NEC group (all P > .05). Congenital heart disease (OR: 2.128, 95% CI: 1.103–3.511), sepsis (OR: 1.630, 95% CI: 1.022–2.549), and blood transfusion (OR: 1.451, 95% CI: 1.014–2.085) were the independent risk factors for NEC in LBW infants, and breastfeeding (OR: 0.494, 95% CI: 0.023–0.928), probiotics feeding (OR: 0.816, 95% CI: 0.782–0.982) were the protective factors for the NEC in LBW infants. The prognosis of NEC infants undergone surgery treatment was better than that of infants undergone conservative treatments (P = .043).
The incidence of NEC in LBW is high, which is affected by many factors, and comprehensive interventions targeted on the risk and protective factors should be made to improve the prognosis of LBW infants.
Keywords: infants, low birth weight, necrotizing enterocolitis, prevention, treatment
1. Introduction
Birth weight is an important indicator that reflects the fetal nutrition and growth and development in the mother's womb.[1] It is also an important indicator to measure the social development of a country and region and everyone's access to primary health care.[2] Low birth weight has become the leading cause of death for children under 5 years of age in China, seriously threatening children's life, health and intellectual development.[3] Improving the prognosis of low birth weight (LBW) infants and reducing the mortality of low birth weight infants are urgent and critical to the healthy career worldwide. With the advancement of medical technology, the survival rate of infants with low birth weight has much improved.[4] However, due to their weak metabolic and immune functions, they are susceptive to various complications. The incidence of necrotizing enterocolitis (NEC) in preterm infants is 2% to 7.5% as per national prospective surveillance study[5] and 5% to 22% in extremely low birth weight babies.[6] The prevention and treatment of complications associated with the low birth weight is vital to the prognosis of infants.
NEC is one of the common diseases that seriously threaten the life of newborns. The morbidity and mortality are higher in premature infants with LBW or gestational age less than 36 weeks.[7] In recent years, the rapid development of perinatal science and neonatal intensive care treatment technology have significantly improved the survival of low birth weight or premature infants.[8] Although the symptoms of NEC can be relieved through conservative treatments such as fasting, parenteral nutrition, fluid resuscitation, antibiotics, and maintaining acid-base balance, there are still a considerable number of children with NEC that require surgical treatment.[9,10] Therefore, it is necessary to further explore the clinical features and influencing factors of NEC in low birth weight infants, and provide evidence support for the prevention and treatment of clinical NEC.
2. Methods
In this study, all methods were performed in accordance with the relevant guidelines and regulations. This study was a retrospective cohort study. The study was approved by the institutional review boards of our hospital (approval number:1800102), and written informed consents had been obtained from the relatives of included infants.
2.1. Study population
This study selected LBW infants admitted to our hospital from January 1, 2019 to June 30, 2021 as the research population. The inclusion criteria of this study were: the birth weight of the newborn was 1500 to 2500 g; the case data were complete, and the relevant guardians had signed the informed consent. The exclusion criteria for this study were: incomplete data; infants who was diagnosed with congenital intestinal atresia, megacolon, malrotation, anal atresia; infants whose guardians did not agree to participate in this study.
2.2. The diagnosis of NEC
The diagnosis of NEC was made in comply with the relevant diagnostic criteria.[11,12] The infants should have 2 or more of the following 4 characteristics and be diagnosed by X-ray examination:
-
1.
abdominal distension;
-
2.
blood in the stool;
-
3.
lethargy, apnea, low muscle tension;
-
4.
Gas in the intestinal wall.
And the diagnosis of NEC was made by 2 of experienced doctors in our departments.
2.3. Data collection
The 2 authors used self-designed forms to collect relevant clinical data of the children, including: birth weight, Gestational age, gender, whether the mother had pregnancy-induced hypertension, premature rupture of fetal membrane, amniotic fluid pollution, fetal asphyxia, congenital heart disease, neonatal respiratory distress syndrome, mechanical ventilation, sepsis, breastfeeding, blood transfusion, probiotics feeding.
2.4. Treatment
Infants with following conditions were treated with surgery, including pneumoperitoneum, positive abdominal puncture, or progressively worsening NEC symptoms and signs (such as signs of peritonitis, persistent blood in the stool, abdominal X-ray showing large amounts of ascites, fixed intestinal loop or continuous decrease in platelets, or continuous increase in white blood cells, etc.) the surgical methods were one-stage enterectomy, enterostomy, enterostomy, or abdominal drainage. Other NEC infants received conservative medical treatment.
2.5. Statistical methods
SPSS 23.0 statistical software was used for data analysis, measurement data was expressed as x ± s, and t test was used for data comparison between the 2 groups. The enumeration data was expressed as a percentage (%). For the analysis of clinical influencing factors in children with NEC, the NEC group and the no-NEC group were firstly subjected to univariate analysis, and then factors with statistically significant differences in the univariate analysis were included in the multivariate logistic regression analysis. Chi-Squared test or Fisher exact test were performed to evaluate the group difference. Please clarify. The test level α was 0.05, and the difference was statistically significant if P < .05.
3. Results
3.1. LBW infants
A total of 192 LBW infants were included in this present study, of whom 68 infants had been diagnosed as NEC, the incidence of NEC in LBW infants was 35.42%. As presented in Table 1, there were significant differences in the congenital heart disease, sepsis, breastfeeding, blood transfusion and probiotics feeding between NEC and no-NEC group (all P < .05), and there were no significant differences in birth weight, gestational age, mother's pregnancy-induced hypertension, premature rupture of fetal membrane, amniotic fluid pollution, fetal asphyxia, neonatal respiratory distress syndrome and mechanical ventilation between NEC and no-NEC group (all P > .05).
Table 1.
The characteristics of included LBW infants.
| Variables | NEC group (n = 68) | No-NEC group (n = 124) | t/χ2 | P |
| Birth weight (g) | 1838.12 ± 16.45 | 1840.22 ± 13.39 | 12.761 | .067 |
| Gestational age (weeks) | 30.54 ± 1.19 | 31.02 ± 2.24 | 2.197 | .061 |
| Male/female | 36/32 | 66/58 | 1.291 | .085 |
| Mother's pregnancy-induced hypertension | 12 (17.65%) | 20 (16.13%) | 1.744 | .092 |
| Premature rupture of fetal membrane | 19 (27.94%) | 32 (25.81%) | 1.602 | .077 |
| Amniotic fluid pollution | 30 (44.12%) | 55 (44.35%) | 1.812 | .075 |
| Fetal asphyxia | 10 (14.71%) | 15 (12.10%) | 1.097 | .056 |
| Congenital heart disease | 11 (16.18%) | 9 (7.26%) | 1.182 | .039 |
| NRDS | 10 (14.71%) | 16 (12.90%) | 1.201 | .066 |
| Mechanical ventilation | 18 (26.47%) | 28 (22.58%) | 1.102 | .053 |
| Sepsis | 16 (23.53%) | 10 (8.06%) | 1.614 | .008 |
| Breastfeeding | 32 (47.06%) | 105 (84.67%) | 1.126 | .012 |
| Blood transfusion | 12 (17.65%) | 7 (5.65%) | 1.229 | .005 |
| Probiotics feeding | 11 (16.18%) | 60 (48.38%) | 1.176 | .014 |
3.2. Risk factors of NEC in LBW infants
The variable assignments of multivariate logistic regression were showed in Table 2. As presented in Table 3, Logistic regression analyses indicated that congenital heart disease (OR: 2.128, 95% CI: 1.103–3.511), sepsis (OR: 1.630, 95% CI: 1.022–2.549), and blood transfusion (OR: 1.451, 95% CI: 1.014–2.085) were the independent risk factors for NEC in LBW infants, and breastfeeding (OR: 0.494, 95% CI: 0.023–0.928), probiotics feeding (OR: 0.816, 95% CI: 0.782–0.982) were the protective factors for the NEC in LBW infants.
Table 2.
The variable assignment of multivariate logistic regression.
| Factors | Variables | Assignment |
| NEC | Y | Yes = 1, No = 2 |
| Congenital heart disease | X1 | Yes = 1, No = 2 |
| Sepsis | X2 | Yes = 1, No = 2 |
| Breastfeeding | X3 | Yes = 1, No = 2 |
| Blood transfusion | X4 | Yes = 1, No = 2 |
| Probiotics feeding | X5 | Yes = 1, No = 2 |
Table 3.
Logistic regression analysis on the risk factors of NEC in LBW infants.
| Variables | β | Wald | OR | 95% CI | P |
| Congenital heart disease | 0.118 | 6.163 | 2.128 | 1.103–3.511 | .041 |
| Sepsis | 0.122 | 2.199 | 1.630 | 1.022–2.549 | .026 |
| Breastfeeding | 0.108 | 2.507 | 0.494 | 0.023–0.928 | .021 |
| Blood transfusion | 0.167 | 3.949 | 1.451 | 1.014–2.085 | .014 |
| Probiotics feeding | 0.193 | 1.099 | 0.816 | 0.782–0.982 | .016 |
3.3. The prognosis of NEC treatment
Of the 68 LBW infants, 32 infants underwent surgical treatment. 20 underwent enterostomy, 9 infants underwent one-stage enterectomy, and 3 infants underwent abdominal drainage. Thirty-six patients underwent conservative treatments. As indicated in Table 4, the prognosis of NEC infants undergone surgery treatment was better than that of infants undergone conservative treatments (P = .043).
Table 4.
The prognosis of NEC treatments of LBW infants (n = 68).
| Death | |||||
| Treatment | Cases | Cure | Multiple organ failure | Severe sepsis | Give up |
| Surgery | 32 | 29 (90.63%) | 2 (6.25%) | 1 (3.12%) | 0 (0%) |
| Conservative treatments | 36 | 28 (77.78%) | 4 (11.11%) | 0 (0%) | 4 (11.11%) |
| χ2 | 1.127 | ||||
| P | .043 | ||||
4. Discussions
NEC is a common intestinal severe disease in the pediatric clinical setting. It mostly occurs in sick newborns or premature infants, and has a high mortality.[13] Studies[14,15] have reported that the mortality of NEC is about 25% to 30%. The incidence of neurodevelopmental abnormalities, gastrointestinal complications, and intestinal stenosis in survivors will also increase significantly.[16,17] Clinically, NEC-related influencing factors include intestinal infections, premature birth, local injury, and ischemia and hypoxia, which may destroy the intestinal mucosa and hinder its blood supply, leading to intestinal mucosal ischemia and hypoxia damage.[18] The occurrence of NEC in LBW infants is difficult to distinguish by clinical manifestations. Because of its poor specificity, blood in the stool, abdominal distension, and vomiting are rarely seen in the early stage.[19] Once it occurs, it is most likely to be late and it often accompanied by intestinal perforation.[20] Therefore, the treatment of NEC in children with low birth weight is more difficult and the prognosis is poor. Even through our study is a single center study experience, the results of our study have found that the incidence of NEC in LBW infants was 35.42%, and congenital heart disease, sepsis, and blood transfusion were the independent risk factors for NEC in LBW infants, and breastfeeding, probiotics feeding were the protective factors for the NEC in LBW infants, early preventions targeted on the risk factors are warranted.
Congenital heart disease can affect the blood flow of the intestinal tract. Due to the poor blood circulation, shock is prone to occur.[21] The abdominal aortic blood reflux occurs during diastole, resulting in insufficient intestinal blood flow and the mesentery in a hypoxic-ischemic state.[22] The high levels of TNF-α and IL-3 in children with congenital heart disease are also a factor that causes intestinal wall damage.[23,24] In this study, sepsis is a risk factor for NEC in infants with LBW, which is consistent with the results of previous related studies. However, it is been reported that sepsis due to other source of infection such as birth injury is a risk factor for NEC.[25] Newborns grow fast, and the expression of intestinal vascular growth factor is enhanced by the stimulation of sepsis.[26] When concentrated red blood cells are infused, it can cause blood redistribution in the body and change the blood supply of the mesentery.[27] The infused histocompatibility antigen can cause immune response and damage. In the intestinal mucosal barrier, large amounts of oxygen free radicals can also cause reperfusion injury.[28,29] This study has found that breastfeeding is a protective factor for NEC, which is consistent with the results of previous related studies.[23,30] Breast milk contains high secretory IgA, lactoferrin, peroxidase and anti-inflammatory factors, which can enhance the immunity of newborns and promote the proliferation of intestinal bifidobacteria.[31,32] Probiotics can regulate the balance of intestinal flora, neutralize intestinal toxins, and promote the decline of harmful bacterial enzyme activities, activate the immune function of macrophages, neutrophils and natural killer cells, and promote the repair and enhancement of intestinal mucosal epithelial cells function, thereby reducing the occurrence of neonatal NEC.[33–35]
Sepsis can cause large-scale growth and reproduction of many kinds of bacteria in the blood, and produce a large amount of toxins that enter the intestine through the blood circulation and destroy the body's negative feedback function, leading to intestinal mucosal necrosis.[36,37] The results of multiple studies have shown that sepsis is a risk factor for neonatal NEC. Breastfeeding is a protective factor in the occurrence of NEC in LBW infants. The nutritional value of breast milk is more in line with the needs of newborns.[33] The protective ingredients in breast milk can effectively improve the intestinal flora, promote the growth of beneficial bacteria, and significantly reduce the occurrence of NEC.[38,39] It is been reported that infants are prone to NEC within 24 hours of blood transfusion, because blood transfusion therapy can change the blood distribution, resulting in a significant increase in intestinal free radicals and causing reperfusion injury.[40] The results of this study indicate that interventions should be made as soon as possible for NEC in LBW infants to improve the prognosis.
Anti-inflammatory, antispasmodic and other medical treatments are difficult to achieve satisfactory results for children with NEC who have full-thickness mucosal pathological changes and hardening of the intestinal wall.[41] At this time, children with intestinal inflammation may further involve normal adjacent tissues, and surgical treatment should be performed in time.[42] The principle of surgical treatment is to carry out timely surgical intervention as far as possible before the intestinal ischemic necrosis of the infants has not been perforated. The timing of surgery associated with NEC is difficult for clinicians to grasp in clinical NEC diagnosis and treatment. At present, it has been believed that the absolute indication for surgery is a plain radiograph of the abdomen that prompts "pneumoperitoneum, X-rays suggest that portal vein gas and thrombocytopenia, severe acidosis and shock and other progressive clinical symptoms and signs are also relative surgical indications.[43–45] For infants with free air under the diaphragm found in plain radiographs of the abdomen, unstable hemodynamics and aggravated abdominal distension, surgical treatment should be performed in a timely manner to improve the prognosis of the infants.[46]
5. Conclusions
To sum up, we have found that the NEC in LBW infants is very common, and congenital heart disease, sepsis, and blood transfusion were the independent risk factors for NEC in LBW infants, and breastfeeding, probiotics feeding were the protective factors for the NEC in LBW infants. It is necessary to actively intervene against congenital heart disease, sepsis and blood transfusions as risk factors for NEC. Besides, breastfeeding should be highly advocated, and probiotics are given to children to adjust the balance of intestinal flora.[47] Limited by small sample size, future studies with larger sample size and rigorous design are needed to further elucidate the potential risk factors of NEC in infants, to provide reliable evidences to the clinical prevention and treatment of NEC.
Author contributions
Conceptualization: Xuerong Tan.
Data curation: Xuerong Tan.
Formal analysis: Xuerong Tan.
Investigation: Xuerong Tan, Yunxia Zhou, Li Zhang, Jiaying Wang.
Methodology: Xuerong Tan, Jiaying Wang, Wenqiong Yang.
Project administration: Lan Xu, Wenqiong Yang.
Resources: Xuerong Tan, Lan Xu, Wenqiong Yang.
Software: Yunxia Zhou, Lan Xu.
Supervision: Yunxia Zhou, Jiaying Wang.
Validation: Xuerong Tan, Yunxia Zhou, Li Zhang.
Visualization: Xuerong Tan, Li Zhang.
Writing – original draft: Xuerong Tan, Li Zhang.
Writing – review & editing: Xuerong Tan.
Footnotes
Abbreviations: LBW = low birth weight, NEC = necrotizing enterocolitis.
How to cite this article: Tan X, Zhou Y, Xu L, Zhang L, Wang J, Yang W. The predictors of necrotizing enterocolitis in newborns with low birth weight: a retrospective analysis. Medicine. 2022;101:7(e28789).
XT and YZ contributed equally to this work.
In this study, all methods were performed in accordance with the relevant guidelines and regulations. The study was approved by the institutional review boards of our hospital (approval number:1800102), and written informed consents had been obtained from the relatives of included infants.
The authors have no funding and conflicts of interests to disclose.
All data generated or analyzed during this study are included in this published article [and its supplementary information files].
References
- [1].Kheirouri S, Alizadeh M. Maternal dietary diversity during pregnancy and risk of low birth weight in newborns: a systematic review. Public Health Nutr 2021;11:01–32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [2].Wang H, Zhang Z, Liu Y, et al. Pre-pregnancy body mass index in mothers, birth weight and the risk of type I diabetes in their offspring: a dose-response meta-analysis of cohort studies. J Gynecol Obstet Hum Reprod 2021;50:08–14. [DOI] [PubMed] [Google Scholar]
- [3].Liu Y, Xu J, Chen D, Sun P, Ma X. The association between air pollution and preterm birth and low birth weight in Guangdong, China. BMC Public Health 2019;19:01–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [4].Yu F, Cao B, Wen Z, Li M, Chen H, Xie G. Is donated breast milk better than formula for feeding very low birth weight infants? A systematic review and meta-analysis. Worldviews Evid Based Nurs 2019;16:485–94. [DOI] [PubMed] [Google Scholar]
- [5].Rees CM, Eaton S, Pierro A. National prospective surveillance study of necrotizing enterocolitis in neonatal intensive care units. J Pediatr Surg 2010;45:1391–7. [DOI] [PubMed] [Google Scholar]
- [6].Battersby C, Santhalingam T, Costeloe K, Modi N. Incidence of neonatal necrotising enterocolitis in high-income countries: a systematic review. Arch Dis Child Fetal Neonatal Ed 2018;103:F182–9. [DOI] [PubMed] [Google Scholar]
- [7].Chen S, Wang XQ, Hu XY, et al. Meconium-stained amniotic fluid as a risk factor for necrotizing enterocolitis in very low-birth weight preterm infants: a retrospective cohort study. J Matern Fetal Neonatal Med 2020;33:4102–7. [DOI] [PubMed] [Google Scholar]
- [8].Sato R, Malai S, Razmjouy B. Necrotizing enterocolitis reduction using an exclusive human-milk diet and probiotic supplementation in infants with 1000-1499 gram birth weight. Nutr Clin Pract 2020;35:331–4. [DOI] [PubMed] [Google Scholar]
- [9].McNelis K, Goddard G, Jenkins T, et al. Delay in achieving enteral autonomy and growth outcomes in very low birth weight infants with surgical necrotizing enterocolitis. J Perinatol 2021;41:150–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [10].Buhrer C, Fischer HS, Wellmann S. Nutritional interventions to reduce rates of infection, necrotizing enterocolitis and mortality in very preterm infants. Pediatr Res 2020;87:371–7. [DOI] [PubMed] [Google Scholar]
- [11].Chun S, Shan Z. Evidence-based medicine interpretation of the prevention and surgical management of necrotizing enterocolitis in very low birth weight infants. Chin J Pediatr Surg 2015;19:88–91. [Google Scholar]
- [12].Xuguang Z, Junli Z, Lixia Z. Analysis of pathogenic bacteria and surgical treatment of neonatal necrotizing enterocolitis. Chin J Nosocomiol 2020;22:24–8. [Google Scholar]
- [13].Oddie SJ, Young L, McGuire W. Slow advancement of enteral feed volumes to prevent necrotising enterocolitis in very low birth weight infants. Cochrane Database Syst Rev 2017;8:20–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [14].Pengjun S, Gengfeng J, Qi Q. Analysis of clinical features of necrotizing enterocolitis in premature twins. Chin J Pract Pediatr 2021;36:04–7. [Google Scholar]
- [15].Huifang D, Xiaoli Z, Wenli L. Analysis of the clinical characteristics of small-for-gestational age and suitable for gestational-age neonates with necrotizing enterocolitis. China J Child Health 2020;18:11–4. [Google Scholar]
- [16].Qian T, Zhang R, Zhu L, et al. Necrotizing enterocolitis in low birth weight infants in China: Mortality risk factors expressed by birth weight categories. Pediatr Neonatol 2017;58:509–15. [DOI] [PubMed] [Google Scholar]
- [17].Murthy S, Parker PR, Gross SJ. Low rate of necrotizing enterocolitis in extremely low birth weight infants using a hospital-based preterm milk bank. J Perinatol 2019;39:108–14. [DOI] [PubMed] [Google Scholar]
- [18].Bazacliu C, Neu J. Necrotizing enterocolitis: long term complications. Curr Pediatr Rev 2019;15:115–24. [DOI] [PubMed] [Google Scholar]
- [19].Kane AF, Bhatia AD, Denning PW, Shane AL, Patel RM. Routine supplementation of lactobacillus rhamnosus GG and risk of necrotizing enterocolitis in very low birth weight infants. J Pediatr 2018;195:73–9. e72. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [20].Hong CR, Fullerton BS, Mercier CE, et al. Growth morbidity in extremely low birth weight survivors of necrotizing enterocolitis at discharge and two-year follow-up. J Pediatr Surg 2018;53:1197–202. [DOI] [PubMed] [Google Scholar]
- [21].Lin H, Mao S, Shi L, Tou J, Du L. Clinical characteristic comparison of low birth weight and very low birth weight preterm infants with neonatal necrotizing enterocolitis: a single tertiary center experience from eastern China. Pediatr Surg Int 2018;34:1201–7. [DOI] [PubMed] [Google Scholar]
- [22].Jammeh ML, Adibe OO, Tracy ET, et al. Racial/ethnic differences in necrotizing enterocolitis incidence and outcomes in premature very low birth weight infants. J Perinatol 2018;38:1386–90. [DOI] [PubMed] [Google Scholar]
- [23].Lin HY, Chang JH, Chung MY, Lin HC. Prevention of necrotizing enterocolitis in preterm very low birth weight infants: is it feasible? J Formos Med Assoc 2014;113:490–7. [DOI] [PubMed] [Google Scholar]
- [24].Perrone S, Tataranno ML, Santacroce A, Negro S, Buonocore G. The role of oxidative stress on necrotizing enterocolitis in very low birth weight infants. Curr Pediatr Rev 2014;10:202–7. [PubMed] [Google Scholar]
- [25].Pinpin W, Nannan H, Guangzhou W. High-risk factors and coping analysis of necrotizing enterocolitis in premature infants. Chin Clin Res 2020;28:02–6. [Google Scholar]
- [26].Jiaxin T, Jing M, Yanwei S. The role of macrophage polarization in the pathogenesis of necrotizing enterocolitis. China Pediatr Emerg Med 2021;28:1047–53. [Google Scholar]
- [27].Fengning Z. Research progress on the pathogenesis of neonatal necrotizing enterocolitis. Int J Pediatr 2020;47:04–6. [Google Scholar]
- [28].Wang K, Tao G, Sylvester KG. Recent advances in prevention and therapies for clinical or experimental necrotizing enterocolitis. Dig Dis Sci 2019;64:3078–85. [DOI] [PubMed] [Google Scholar]
- [29].Raffaeli G, Ghirardello S, Passera S, Mosca F, Cavallaro G. Oxidative stress and neonatal respiratory extracorporeal membrane oxygenation. Front Physiol 2018;9:04–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [30].Walsh V, McGuire W. Immunonutrition for preterm infants. Neonatology 2019;115:398–405. [DOI] [PubMed] [Google Scholar]
- [31].Miller J, Tonkin E, Damarell RA, et al. A systematic review and meta-analysis of human milk feeding and morbidity in very low birth weight infants. Nutrients 2018;10:10–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [32].Ford SL, Lohmann P, Preidis GA, et al. Improved feeding tolerance and growth are linked to increased gut microbial community diversity in very-low-birth-weight infants fed mother's own milk compared with donor breast milk. Am J Clin Nutr 2019;109:1088–97. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [33].Aceti A, Maggio L, Beghetti I, et al. Probiotics prevent late-onset sepsis in human milk-fed, very low birth weight preterm infants: systematic review and meta-analysis. Nutrients 2017;9:35–44. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [34].Jiao X, Fu MD, Wang YY, Xue J, Zhang Y. Bifidobacterium and Lactobacillus for preventing necrotizing enterocolitis in very-low-birth-weight preterm infants: a systematic review and meta-analysis. World J Pediatr 2020;16:135–42. [DOI] [PubMed] [Google Scholar]
- [35].Hagen PC, Skelley JW. Efficacy of bifidobacterium species in prevention of necrotizing enterocolitis in very-low birth weight infants. A systematic review. J Pediatr Pharmacol Ther 2019;24:10–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [36].Ting JY, Synnes A, Roberts A, et al. Association between antibiotic use and neonatal mortality and morbidities in very low-birth-weight infants without culture-proven sepsis or necrotizing enterocolitis. JAMA Pediatr 2016;170:1181–7. [DOI] [PubMed] [Google Scholar]
- [37].Pammi M, Suresh G. Enteral lactoferrin supplementation for prevention of sepsis and necrotizing enterocolitis in preterm infants. Cochrane Database Syst Rev 2017;6:14–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [38].Kelley L. Increasing the consumption of breast milk in low-birth-weight infants: can it have an impact on necrotizing enterocolitis? Adv Neonatal Care 2012;12:267–72. [DOI] [PubMed] [Google Scholar]
- [39].Luquan L, Lu G, Zhongyao Z. Advances in the diagnosis and medical treatment of neonatal necrotizing enterocolitis. Chin J Pract Pediatr 2020;35:05–9. [Google Scholar]
- [40].Janjindamai W, Prapruettrong A, Thatrimontrichai A, Dissaneevate S, Maneenil G, Geater A. Risk of necrotizing enterocolitis following packed red blood cell transfusion in very low birth weight infants. Indian J Pediatr 2019;86:347–53. [DOI] [PubMed] [Google Scholar]
- [41].Howarth C, Banerjee J, Aladangady N. Red blood cell transfusion in preterm infants: current evidence and controversies. Neonatology 2018;114:07–16. [DOI] [PubMed] [Google Scholar]
- [42].Robinson JR, Rellinger EJ, Hatch LD, et al. Surgical necrotizing enterocolitis. Semin Perinatol 2017;41:70–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [43].Knell J, Han SM, Jaksic T, Modi BP. Current status of necrotizing enterocolitis. Curr Probl Surg 2019;56:11–38. [DOI] [PubMed] [Google Scholar]
- [44].Shulhan J, Dicken B, Hartling L, Larsen BM. Current knowledge of necrotizing enterocolitis in preterm infants and the impact of different types of enteral nutrition products. Adv Nutr 2017;8:80–91. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [45].Yali G, Song P. The value of abdominal X-ray examination in the classification and prognosis of neonatal necrotizing enterocolitis. China Med Imaging Technol 2020;36:44–7. [Google Scholar]
- [46].Fujiang Y, Bo H. Surgical diagnosis and treatment of neonatal necrotizing enterocolitis. Chin J Clin 2020;48:04–9. [Google Scholar]
- [47].Zhongtang L, Nan X, Han L. Pathogen characteristics of necrotizing enterocolitis in premature infants and analysis of probiotic intervention effects and prognostic factors in Nanjing area. Chin J Microecol 2020;32:05–10. [Google Scholar]
