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坏死性小肠结肠炎手术治疗后的长期随访:63例病例

Long-term follow-up after surgical management of necrotizing enterocolitis: sixty-three cases.

作者信息

Cikrit D, West K W, Schreiner R, Grosfeld J L

出版信息

J Pediatr Surg. 1986 Jun;21(6):533-5. doi: 10.1016/s0022-3468(86)80227-5.

DOI:10.1016/s0022-3468(86)80227-5
PMID:3723306
Abstract

One hundred twenty-five infants underwent surgical intervention for necrotizing enterocolitis between 1972 and 1984. Sixty-three infants, who survived more than 30 days postoperatively, were evaluated for long-term complications. There were 28 girls and 35 boys (mean birth weight 1,725 +/- 890 g; gestational age 32 +/- 4 weeks). Associated problems included hyaline membrane disease (43), cardiac anomalies (25), and trisomy 21(2). Thirty-six survivors required long-term ventilatory support. Fifty-nine infants underwent bowel resection and enterostomy, 3 decompressing enterostomies without resection, and 1, exploratory laparotomy only. Enterostomies were closed at four months. Twenty four had short bowel syndrome. Fifteen infants subsequently died for a late mortality rate of 23%. Mortality was related to sepsis (3), respiratory failure (5), cardiac anomalies (3), cardio-respiratory arrest (2), and TPN related liver failure (2), and was common with gestational age less than 31 weeks and birth weight less than 1,000 g. Medical problems included cholestasis (17), TPN induced cirrhosis (3), meningitis (3), seizures (8), and nutritional rickets (6). Significant developmental and intellectual delays were observed.

摘要

1972年至1984年间,125例患有坏死性小肠结肠炎的婴儿接受了手术治疗。对术后存活超过30天的63例婴儿进行了长期并发症评估。其中有28名女孩和35名男孩(平均出生体重1725±890克;胎龄32±4周)。相关问题包括透明膜病(43例)、心脏畸形(25例)和21三体综合征(2例)。36名幸存者需要长期通气支持。59例婴儿接受了肠切除和肠造口术,3例仅行减压性肠造口术而未行切除术,1例仅行剖腹探查术。肠造口术在四个月时关闭。24例患有短肠综合征。15例婴儿随后死亡,晚期死亡率为23%。死亡与败血症(3例)、呼吸衰竭(5例)、心脏畸形(3例)、心肺骤停(2例)和全胃肠外营养相关的肝功能衰竭(2例)有关,在胎龄小于31周和出生体重小于1000克的婴儿中较为常见。医学问题包括胆汁淤积(17例)、全胃肠外营养诱导的肝硬化(3例)、脑膜炎(3例)、癫痫发作(8例)和营养性佝偻病(6例)。观察到明显的发育和智力迟缓。

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Long-term follow-up after surgical management of necrotizing enterocolitis: sixty-three cases.坏死性小肠结肠炎手术治疗后的长期随访:63例病例
J Pediatr Surg. 1986 Jun;21(6):533-5. doi: 10.1016/s0022-3468(86)80227-5.
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High morbidity of enterostomy and its closure in premature infants with necrotizing enterocolitis.坏死性小肠结肠炎早产儿肠造口术及其关闭术的高发病率。
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Long-term follow-up after bowel resection for necrotizing enterocolitis: factors affecting outcome.坏死性小肠结肠炎肠切除术后的长期随访:影响预后的因素
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Surgical experience with neonatal necrotizing enterocolitis (NNE).新生儿坏死性小肠结肠炎(NNE)的手术经验。
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[Necrotizing enterocolitis--analysis of a case cohort].[坏死性小肠结肠炎——病例队列分析]
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Urinary I-FABP, L-FABP, TFF-3, and SAA Can Diagnose and Predict the Disease Course in Necrotizing Enterocolitis at the Early Stage of Disease.尿 I-FABP、L-FABP、TFF-3 和 SAA 可在疾病早期诊断和预测坏死性小肠结肠炎的病程。
J Immunol Res. 2020 Mar 3;2020:3074313. doi: 10.1155/2020/3074313. eCollection 2020.
2
Long term healthcare costs of infants who survived neonatal necrotizing enterocolitis: a retrospective longitudinal study among infants enrolled in Texas Medicaid.新生儿坏死性小肠结肠炎存活患儿的长期医疗费用:德克萨斯州医疗补助计划中纳入患儿的回顾性纵向研究。
BMC Pediatr. 2013 Aug 20;13:127. doi: 10.1186/1471-2431-13-127.
3
Does necrotizing enterocolitis affect growth and neurodevelopmental outcome in very low birth weight infants?
坏死性小肠结肠炎会影响极低出生体重儿的生长及神经发育结局吗?
Pediatr Surg Int. 2012 May;28(5):471-6. doi: 10.1007/s00383-012-3051-4. Epub 2012 Jan 25.
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Risk factors for intestinal failure in infants with necrotizing enterocolitis: a Glaser Pediatric Research Network study.坏死性小肠结肠炎婴儿发生肠衰竭的危险因素:一项 Glaser 儿科研究网络研究。
J Pediatr. 2010 Aug;157(2):203-208.e1. doi: 10.1016/j.jpeds.2010.02.023. Epub 2010 May 6.
5
Neonatal necrotizing enterocolitis: pathogenesis, classification, and spectrum of illness.新生儿坏死性小肠结肠炎:发病机制、分类及疾病谱
Curr Probl Pediatr. 1987 Apr;17(4):213-88. doi: 10.1016/0045-9380(87)90031-4.
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Neonatal necrotizing enterocolitis: experience with 100 consecutive surgical patients.新生儿坏死性小肠结肠炎:100例连续手术患者的经验
World J Surg. 1990 Sep-Oct;14(5):600-5. doi: 10.1007/BF01658800.
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A scoring system in predicting the risk of intestinal stricture in necrotizing enterocolitis.一种预测坏死性小肠结肠炎肠道狭窄风险的评分系统。
Eur J Pediatr. 1991 Sep;150(11):757-60. doi: 10.1007/BF02026705.