• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

食管闭锁和先天性膈疝幸存者持续性呼吸道疾病的前瞻性对比评估

A prospective comparative evaluation of persistent respiratory morbidity in esophageal atresia and congenital diaphragmatic hernia survivors.

作者信息

Gischler Saskia J, van der Cammen-van Zijp Monique H M, Mazer Petra, Madern Gerard C, Bax Nikolaas M A, de Jongste Johan C, van Dijk Monique, Tibboel Dick, Ijsselstijn Hanneke

机构信息

Department of Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, Erasmus University Medical Center, 3000 CA Rotterdam, The Netherlands.

出版信息

J Pediatr Surg. 2009 Sep;44(9):1683-90. doi: 10.1016/j.jpedsurg.2008.12.019.

DOI:10.1016/j.jpedsurg.2008.12.019
PMID:19735809
Abstract

PURPOSE

The aim of the study was to compare long-term respiratory morbidity in children after repair of esophageal atresia (EA) or congenital diaphragmatic hernia (CDH).

PATIENTS AND METHODS

Children were seen at 6, 12, and 24 months and 5 years within a prospective longitudinal follow-up program in a tertiary children's hospital. Respiratory morbidity and physical condition were evaluated at all moments. At age 5 years, pulmonary function and maximal exercise performance were tested.

RESULTS

In 3 of 23 atresia patients and 10 of 20 hernia patients, bronchopulmonary dysplasia was developed. Seventeen atresia and 11 hernia patients had recurrent respiratory tract infections mainly in the first years of life. At age 5, 25% of EA and CDH patients measured showed reduced forced expiratory volume in 1 second (z-score < -2). Both atresia and hernia patients showed impaired growth, with catch-up growth at 5 years in patients with EA but not in those with hernia. Maximal exercise performance was significantly below normal for both groups.

CONCLUSIONS

Esophageal atresia and CDH are associated with equal risk of long-term respiratory morbidity, growth impairment, and disturbed maximal exercise performance. Prospective follow-up of EA patients aimed at identifying respiratory problems other than tracheomalacia should be an integral part of interdisciplinary follow-up programs.

摘要

目的

本研究旨在比较食管闭锁(EA)或先天性膈疝(CDH)修复术后儿童的长期呼吸系统发病率。

患者与方法

在一家三级儿童医院的前瞻性纵向随访项目中,于6个月、12个月、24个月及5岁时对儿童进行观察。在各个时间点评估呼吸系统发病率和身体状况。在5岁时,测试肺功能和最大运动能力。

结果

23例闭锁患者中有3例、20例疝患者中有10例发生支气管肺发育不良。17例闭锁患者和11例疝患者主要在生命的头几年反复发生呼吸道感染。在5岁时,测量的EA和CDH患者中有25%的1秒用力呼气量降低(z评分<-2)。闭锁患者和疝患者均出现生长发育受损,EA患者在5岁时出现追赶生长,而疝患者则未出现。两组的最大运动能力均显著低于正常水平。

结论

食管闭锁和CDH与长期呼吸系统发病率、生长发育受损及最大运动能力受干扰的风险相当。针对EA患者进行旨在识别除气管软化以外的呼吸问题的前瞻性随访,应成为跨学科随访项目的一个组成部分。

相似文献

1
A prospective comparative evaluation of persistent respiratory morbidity in esophageal atresia and congenital diaphragmatic hernia survivors.食管闭锁和先天性膈疝幸存者持续性呼吸道疾病的前瞻性对比评估
J Pediatr Surg. 2009 Sep;44(9):1683-90. doi: 10.1016/j.jpedsurg.2008.12.019.
2
Pulmonary morbidity in 100 survivors of congenital diaphragmatic hernia monitored in a multidisciplinary clinic.在一家多学科诊所对100名先天性膈疝幸存者的肺部发病率进行监测。
J Pediatr Surg. 2001 Jan;36(1):133-40. doi: 10.1053/jpsu.2001.20031.
3
Impaired somatic growth and delayed lung development in infants with congenital diaphragmatic hernia--evidence from a 10-year, single center prospective follow-up study.先天性膈疝患儿的躯体生长受损及肺发育延迟——来自一项为期10年的单中心前瞻性随访研究的证据
J Pediatr Surg. 2009 Jul;44(7):1309-14. doi: 10.1016/j.jpedsurg.2008.10.047.
4
Survival of severe congenital diaphragmatic hernia has morbid consequences.严重先天性膈疝的存活会带来不良后果。
J Pediatr Surg. 2005 Jan;40(1):36-45; discussion 45-6. doi: 10.1016/j.jpedsurg.2004.09.037.
5
Prospective longitudinal evaluation of lung function during the first year of life after repair of congenital diaphragmatic hernia.先天性膈疝修补术后 1 年内肺功能的前瞻性纵向评估。
Pediatr Crit Care Med. 2012 May;13(3):e133-9. doi: 10.1097/PCC.0b013e3182231872.
6
Long term respiratory outcomes of congenital diaphragmatic hernia, esophageal atresia, and cardiovascular anomalies.先天性膈疝、食管闭锁和心血管畸形的长期呼吸系统结局。
Semin Fetal Neonatal Med. 2012 Apr;17(2):105-11. doi: 10.1016/j.siny.2012.01.008. Epub 2012 Jan 31.
7
Pulmonary function and exercise testing in adult survivors of congenital diaphragmatic hernia.先天性膈疝成年幸存者的肺功能和运动测试
Pediatr Pulmonol. 2007 Apr;42(4):325-31. doi: 10.1002/ppul.20579.
8
Reflux in esophageal atresia, tracheoesophageal cleft, and esophagocoloplasty: Bianchi's procedure as an alternative approach.食管闭锁、气管食管瘘及食管结肠成形术中的反流:比安基手术作为一种替代方法
J Pediatr Surg. 2005 Apr;40(4):666-9. doi: 10.1016/j.jpedsurg.2005.01.004.
9
Congenital diaphragmatic hernia associated with esophageal atresia: incidence, outcomes, and determinants of mortality.先天性膈疝合并食管闭锁:发病率、结局和死亡率的决定因素。
J Am Coll Surg. 2013 Jan;216(1):90-95.e2. doi: 10.1016/j.jamcollsurg.2012.09.014. Epub 2012 Nov 21.
10
Long-term pulmonary morbidity in survivors of congenital diaphragmatic hernia.先天性膈疝幸存者的长期肺部发病率
Pediatr Pulmonol. 2005 May;39(5):433-9. doi: 10.1002/ppul.20193.

引用本文的文献

1
Long-term pulmonary outcome of children with congenital diaphragmatic hernia: functional lung MRI using matrix-pencil decomposition enables side-specific assessment of lung function.先天性膈疝患儿的长期肺部预后:使用矩阵分解的功能肺部 MRI 能够进行特定于侧别的肺部功能评估。
Eur Radiol. 2024 Jun;34(6):3773-3785. doi: 10.1007/s00330-023-10395-8. Epub 2023 Nov 20.
2
Cardiorespiratory performance and locomotor function of patients with anorectal malformations.肛肠畸形患者的心肺功能和运动功能。
Sci Rep. 2021 Sep 23;11(1):18919. doi: 10.1038/s41598-021-98368-z.
3
Neurodevelopmental outcome of patients with congenital gastrointestinal malformations: a systematic review and meta-analysis.
先天性胃肠道畸形患者的神经发育结局:系统评价和荟萃分析。
Arch Dis Child Fetal Neonatal Ed. 2021 Nov;106(6):635-642. doi: 10.1136/archdischild-2021-322158. Epub 2021 Jun 10.
4
Congenital malformations potentially affecting respiratory function: multidisciplinary approach and follow-up.先天性畸形可能影响呼吸功能:多学科方法和随访。
Acta Biomed. 2020 Sep 4;92(1):e2021069. doi: 10.23750/abm.v92i1.10591.
5
Volatile Organic Compounds, Bacterial Airway Microbiome, Spirometry and Exercise Performance of Patients after Surgical Repair of Congenital Diaphragmatic Hernia.先天性膈疝修补术后患者的挥发性有机化合物、气道细菌微生物组、肺量测定和运动表现。
Molecules. 2021 Jan 26;26(3):645. doi: 10.3390/molecules26030645.
6
Esophageal Atresia: Nutritional Status and Energy Metabolism to Maximize Growth Outcome.食管闭锁:营养状况与能量代谢以实现最佳生长结局
Children (Basel). 2020 Nov 14;7(11):228. doi: 10.3390/children7110228.
7
Cardiorespiratory performance capacity and airway microbiome in patients following primary repair of esophageal atresia.心肺功能表现能力和气道微生物组在食管闭锁患者初次修复术后。
Pediatr Res. 2021 Jul;90(1):66-73. doi: 10.1038/s41390-020-01222-7. Epub 2020 Nov 6.
8
Oesophageal atresia: The growth gap.食管闭锁:生长差距。
World J Gastroenterol. 2020 Mar 28;26(12):1262-1272. doi: 10.3748/wjg.v26.i12.1262.
9
A parent-reported standardised checklist is not sensitive to screen for motor problems at school age following neonatal critical illness.家长报告的标准化检查表对筛查新生儿危重症后学龄期的运动问题并不敏感。
Acta Paediatr. 2020 Sep;109(9):1801-1806. doi: 10.1111/apa.15192. Epub 2020 Feb 22.
10
Pulmonary function in children and adolescents after esophageal atresia repair.儿童和青少年食管闭锁修复术后的肺功能。
Pediatr Pulmonol. 2020 Jan;55(1):206-213. doi: 10.1002/ppul.24517. Epub 2019 Sep 18.