Deianova Nancy, Moonen Quincy, Sluis Sientje E, Niemarkt Hendrik J, de Jonge Wouter J, Benninga Marc A, de Boer Nanne K H, Tanger Helen L, van Weissenbruch Mirjam M, van Kaam Anton H, de Meij Tim G J, Koppen Ilan J N
Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Location AMC, Amsterdam, the Netherlands.
Department of Pediatric Gastroenterology, Amsterdam UMC Location University of Amsterdam. Amsterdam Reproduction & Development Research Institute, Amsterdam, the Netherlands.
Eur J Pediatr. 2023 Sep;182(9):3907-3915. doi: 10.1007/s00431-023-05035-8. Epub 2023 Jun 22.
Necrotizing enterocolitis (NEC) is associated with significant morbidity and mortality in preterm infants. Early recognition and treatment of NEC are critical to improving outcomes. Enteric nervous system (ENS) immaturity has been proposed as a key factor in NEC pathophysiology. Gastrointestinal dysmotility is associated with ENS immaturity and may serve as a predictive factor for the development of NEC. In this case-control study, preterm infants (gestational age (GA) < 30 weeks) were included in two level-IV neonatal intensive care units. Infants with NEC in the first month of life were 1:3 matched to controls based on GA (± 3 days). Odds ratios for NEC development were analyzed by logistic regression for time to first passage of meconium (TFPM), duration of meconial stool, and mean daily defecation frequency over the 72 h preceding clinical NEC onset (DF < T0). A total of 39 NEC cases and 117 matched controls (median GA 27 + 4 weeks) were included. Median TFPM was comparable in cases and controls (36 h [IQR 13-65] vs. 30 h [IQR 9-66], p = 0.83). In 21% of both cases and controls, TFPM was ≥ 72 h (p = 0.87). Duration of meconial stool and DF < T0 were comparable in the NEC and control group (median 4 and 3, resp. in both groups). Odds of NEC were not significantly associated with TFPM, duration of meconial stools, and DF < T0 (adjusted odds ratio [95% confidence interval]: 1.00 [0.99-1.03], 1.16 [0.86-1.55] and 0.97 [0.72-1.31], resp.).
In this cohort, no association was found between TFPM, duration of meconium stool, and DF < T0 and the development of NEC.
• Necrotizing enterocolitis (NEC) is a life-threatening acute intestinal inflammatory disease of the young preterm infant. Early clinical risk factors for NEC have been investigated in order to facilitate early diagnosis and treatment. • Signs of disrupted gastrointestinal mobility, such as gastric retention and paralytic ileus, have been established to support the diagnosis of NEC. Nevertheless, defecation patterns have insufficiently been studied in relation to the disease.
• Defecation patterns in the three days preceding NEC did not differ from gestational age-matched controls of corresponding postnatal age. Additionally, the first passage of meconium and the duration of meconium passage were comparable between cases and controls. Currently, defecation patterns are not useful as early warning signs for NEC. It remains to be elucidated whether these parameters are different based on the location of intestinal necrosis.
坏死性小肠结肠炎(NEC)与早产儿的高发病率和死亡率相关。NEC的早期识别和治疗对于改善预后至关重要。肠神经系统(ENS)不成熟被认为是NEC病理生理学的关键因素。胃肠动力障碍与ENS不成熟相关,可能是NEC发生的预测因素。在这项病例对照研究中,两个四级新生儿重症监护病房纳入了孕周(GA)<30周的早产儿。出生后第一个月内患NEC的婴儿与基于GA(±3天)的对照组按1:3进行匹配。通过逻辑回归分析NEC发生的比值比,分析胎粪首次排出时间(TFPM)、胎粪持续时间以及临床NEC发作前72小时内的平均每日排便频率(DF<T0)。共纳入39例NEC病例和117例匹配的对照(中位GA 27⁺⁴周)。病例组和对照组的中位TFPM相当(36小时[四分位间距13 - 65]对30小时[四分位间距9 - 66],p = 0.83)。病例组和对照组中均有21%的TFPM≥72小时(p = 0.87)。NEC组和对照组的胎粪持续时间以及DF<T0相当(两组中位值均为4和3)。NEC的发生几率与TFPM、胎粪持续时间以及DF<T0无显著关联(调整后的比值比[95%置信区间]分别为:1.00[0.99 - 1.03]、1.16[0.86 - 1.55]和0.97[0.72 - 1.31])。
在该队列中,未发现TFPM、胎粪持续时间以及DF<T0与NEC的发生之间存在关联。
• 坏死性小肠结肠炎(NEC)是危及生命的年轻早产儿急性肠道炎症性疾病。已对NEC的早期临床危险因素进行了研究,以促进早期诊断和治疗。
• 已确定胃肠蠕动紊乱的迹象,如胃潴留和麻痹性肠梗阻,以支持NEC的诊断。然而,关于疾病的排便模式研究不足。
• NEC前三天的排便模式与相应出生后年龄的孕周匹配对照组无差异。此外,病例组和对照组的胎粪首次排出时间和胎粪排出持续时间相当。目前,排便模式作为NEC的早期预警信号并无用处。基于肠道坏死部位,这些参数是否不同仍有待阐明。