• 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

48例慢性肠道假性梗阻的病因及预后:一项10年回顾性病例系列研究

Causes and prognosis of chronic intestinal pseudo-obstruction in 48 subjects: A 10-year retrospective case series.

作者信息

Lu Wei, Xiao Yongtao, Huang Jianhu, Lu Lina, Tao Yiqing, Yan Weihui, Cao Yi, Cai Wei

机构信息

Department of Pediatric Surgery, Xin Hua Hospital, School of Medicine, Shanghai Jiao Tong University Shanghai Institute for Pediatric Research Shanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Shanghai, China.

出版信息

Medicine (Baltimore). 2018 Sep;97(36):e12150. doi: 10.1097/MD.0000000000012150.

DOI:10.1097/MD.0000000000012150
PMID:30200110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6133590/
Abstract

The aim of the study was to evaluate the prognosis and survival of pediatric subjects with chronic intestinal pseudo-obstruction (CIPO) and investigate the independent risk factors affecting their prognosis.This was a retrospective case series of all pediatric subjects suffering from CIPO and treated at the Pediatric Surgical ward of Xinhua Hospital between January 2006 and January 2016.The overall mortality was 19/48 (39.6%). Because of delayed CIPO diagnosis, many subjects underwent a variety of surgical procedures. The rate of additional surgical procedures was high (35/48, 72.9%), but the number of surgical procedures, parenteral nutrition, and megacystis did not affect mortality. Mycotic infection was significantly associated with mortality, while onset at <1 year and hypoganglionosis showed a tendency to be associated with mortality.Mycotic infection was associated with mortality of children with CIPO. Despite improving treatment approaches, the overall prognosis of CIPO remains poor. The choice of the surgical intervention could be based on standard criteria.

摘要

本研究旨在评估慢性肠假性梗阻(CIPO)患儿的预后和生存情况,并调查影响其预后的独立危险因素。这是一项对2006年1月至2016年1月期间在新华医院小儿外科病房接受治疗的所有CIPO患儿进行的回顾性病例系列研究。总死亡率为19/48(39.6%)。由于CIPO诊断延迟,许多患儿接受了各种手术。再次手术率很高(35/48,72.9%),但手术次数、肠外营养和巨膀胱并不影响死亡率。真菌感染与死亡率显著相关,而发病年龄<1岁和神经节减少症有与死亡率相关的趋势。真菌感染与CIPO患儿的死亡率相关。尽管治疗方法有所改进,但CIPO的总体预后仍然很差。手术干预的选择可基于标准标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/6133590/98b8ce49b579/medi-97-e12150-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/6133590/bb8a7fbabb9c/medi-97-e12150-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/6133590/64219bdcf417/medi-97-e12150-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/6133590/98b8ce49b579/medi-97-e12150-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/6133590/bb8a7fbabb9c/medi-97-e12150-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/6133590/64219bdcf417/medi-97-e12150-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/6133590/98b8ce49b579/medi-97-e12150-g006.jpg

相似文献

1
Causes and prognosis of chronic intestinal pseudo-obstruction in 48 subjects: A 10-year retrospective case series.48例慢性肠道假性梗阻的病因及预后:一项10年回顾性病例系列研究
Medicine (Baltimore). 2018 Sep;97(36):e12150. doi: 10.1097/MD.0000000000012150.
2
Long-term outcome of chronic intestinal pseudo-obstruction adult patients requiring home parenteral nutrition.需要家庭肠外营养的慢性肠假性梗阻成年患者的长期预后。
Am J Gastroenterol. 2009 May;104(5):1262-70. doi: 10.1038/ajg.2009.58. Epub 2009 Apr 14.
3
Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstruction.慢性肠道假性梗阻患者线粒体缺陷的发生率
Gastroenterology. 2009 Jul;137(1):101-9. doi: 10.1053/j.gastro.2009.03.054. Epub 2009 Apr 1.
4
Surgical treatment and prognosis of chronic intestinal pseudo-obstruction in children.儿童慢性假性肠梗阻的外科治疗与预后
J Pediatr Surg. 2005 Nov;40(11):1753-9. doi: 10.1016/j.jpedsurg.2005.07.046.
5
Pediatric chronic intestinal pseudo-obstruction is a rare, serious, and intractable disease: a report of a nationwide survey in Japan.小儿慢性假性肠梗阻是一种罕见、严重且难治的疾病:日本全国性调查的报告
J Pediatr Surg. 2014 Dec;49(12):1799-803. doi: 10.1016/j.jpedsurg.2014.09.025. Epub 2014 Nov 6.
6
Chronic intestinal pseudo-obstruction due to adult-onset acquired isolated hypoganglionosis with muscular atrophy in the small intestine: a case report and review of literature.成人获得性孤立性小肠运动神经元病致慢性假性肠梗阻:病例报告及文献复习。
Clin J Gastroenterol. 2024 Apr;17(2):244-252. doi: 10.1007/s12328-023-01902-x. Epub 2024 Jan 9.
7
Chronic intestinal pseudo-obstruction.慢性肠道假性梗阻
Best Pract Res Clin Gastroenterol. 2007;21(4):657-69. doi: 10.1016/j.bpg.2007.03.002.
8
Pediatric Intestinal Pseudo-obstruction in the Era of Genetic Sequencing.基因测序时代的小儿肠道假性梗阻
Curr Gastroenterol Rep. 2019 Dec 17;21(12):70. doi: 10.1007/s11894-019-0737-y.
9
The chronic intestinal pseudo-obstruction subtype has prognostic significance in patients with severe gastrointestinal dysmotility related intestinal failure.慢性肠道假性梗阻亚型对严重胃肠动力障碍相关肠衰竭患者具有预后意义。
Clin Nutr. 2018 Dec;37(6 Pt A):1967-1975. doi: 10.1016/j.clnu.2018.09.008. Epub 2018 Sep 22.
10
Chronic intestinal pseudo-obstruction: a rare first manifestation of systemic lupus erythematosus.慢性肠道假性梗阻:系统性红斑狼疮的罕见首发表现。
Lupus. 2013 Aug;22(9):957-60. doi: 10.1177/0961203313492873. Epub 2013 Jun 12.

引用本文的文献

1
Incidence, diagnostics, therapeutic management and outcomes of paediatric intestinal pseudo-obstruction in the Netherlands: A 20-year retrospective cohort study.荷兰儿童肠道假性梗阻的发病率、诊断、治疗管理及预后:一项20年回顾性队列研究
J Pediatr Gastroenterol Nutr. 2025 Jan;80(1):34-45. doi: 10.1002/jpn3.12400. Epub 2024 Nov 1.
2
Association between Red Blood Cell Distribution Width and Short-Term Mortality in Patients with Paralytic Intestinal Obstruction: Retrospective Data Analysis Based on the MIMIC-III Database.麻痹性肠梗阻患者红细胞分布宽度与短期死亡率的关联:基于MIMIC-III数据库的回顾性数据分析
Emerg Med Int. 2023 Oct 23;2023:6739136. doi: 10.1155/2023/6739136. eCollection 2023.
3

本文引用的文献

1
Chronic Intestinal Pseudo-obstruction: Clinical and Manometric Characteristics in the Chilean Population.慢性肠道假性梗阻:智利人群的临床和测压特征
J Neurogastroenterol Motil. 2017 Apr 30;23(2):273-280. doi: 10.5056/jnm16101.
2
New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome).胎儿巨膀胱遗传学的新见解:ACTG2突变,其在巨膀胱-小结肠-肠蠕动不良综合征(伯登综合征)中编码γ-2平滑肌肌动蛋白
Fetal Diagn Ther. 2015;38(4):296-306. doi: 10.1159/000381638. Epub 2015 May 13.
3
Pediatric chronic intestinal pseudo-obstruction is a rare, serious, and intractable disease: a report of a nationwide survey in Japan.
The Potential Role of Microorganisms on Enteric Nervous System Development and Disease.
微生物在肠神经系统发育和疾病中的潜在作用。
Biomolecules. 2023 Feb 27;13(3):447. doi: 10.3390/biom13030447.
4
Dynamic integration of enteric neural stem cells in ex vivo organotypic colon cultures.肠神经干细胞在离体器官型结肠培养中的动态整合。
Sci Rep. 2021 Aug 5;11(1):15889. doi: 10.1038/s41598-021-95434-4.
5
Initial Presentation of a Pediatric Intestinal Pseudo-Obstruction Episode After SARS-CoV-2 Virus (COVID-19) Infection.新型冠状病毒(COVID-19)感染后小儿肠道假性梗阻发作的初始表现
JPGN Rep. 2021 Apr 12;2(2):e059. doi: 10.1097/PG9.0000000000000059. eCollection 2021 May.
6
Clinical Outcomes of Pediatric Chronic Intestinal Pseudo-Obstruction.小儿慢性假性肠梗阻的临床结局
J Clin Med. 2021 May 28;10(11):2376. doi: 10.3390/jcm10112376.
7
Anti-CV2/CRMP5 antibody-positive paraneoplastic neurological syndromes with chronic intestinal pseudo-obstruction in a small-cell lung cancer patient: a case report and literature review.抗 CV2/CRMP5 抗体阳性小细胞肺癌伴慢性假性肠梗阻的副肿瘤性神经系统综合征:病例报告及文献复习。
J Int Med Res. 2020 Dec;48(12):300060520974466. doi: 10.1177/0300060520974466.
8
A Rare Case of Chronic Small Bowel Pseudo-Obstruction.慢性小肠假性梗阻一例罕见病例
Cureus. 2020 May 7;12(5):e8003. doi: 10.7759/cureus.8003.
9
Acquired segmental sigmoid hypoganglionosis: A case report.获得性节段性乙状结肠神经节减少症:一例报告。
Medicine (Baltimore). 2020 Jan;99(4):e18803. doi: 10.1097/MD.0000000000018803.
10
Pediatric Intestinal Pseudo-obstruction in the Era of Genetic Sequencing.基因测序时代的小儿肠道假性梗阻
Curr Gastroenterol Rep. 2019 Dec 17;21(12):70. doi: 10.1007/s11894-019-0737-y.
小儿慢性假性肠梗阻是一种罕见、严重且难治的疾病:日本全国性调查的报告
J Pediatr Surg. 2014 Dec;49(12):1799-803. doi: 10.1016/j.jpedsurg.2014.09.025. Epub 2014 Nov 6.
4
Dysmotility disorders: a nutritional approach.动力障碍性疾病:一种营养治疗方法。
Curr Opin Clin Nutr Metab Care. 2014 Sep;17(5):483-8. doi: 10.1097/MCO.0000000000000095.
5
Advancement in the clinical management of intestinal pseudo-obstruction.肠道假性梗阻临床管理的进展
Expert Rev Gastroenterol Hepatol. 2015 Feb;9(2):197-208. doi: 10.1586/17474124.2014.940317. Epub 2014 Jul 14.
6
In vivo transplantation of neurosphere-like bodies derived from the human postnatal and adult enteric nervous system: a pilot study.源自人类出生后及成人肠神经系统的类神经球体的体内移植:一项初步研究。
PLoS One. 2014 Apr 3;9(4):e93605. doi: 10.1371/journal.pone.0093605. eCollection 2014.
7
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome.平滑肌肌动蛋白(ACTG2)基因的杂合性新生突变和遗传突变是巨膀胱-小结肠-肠蠕动不良综合征的病因。
PLoS Genet. 2014 Mar 27;10(3):e1004258. doi: 10.1371/journal.pgen.1004258. eCollection 2014 Mar.
8
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.新生 ACTG2 突变导致先天性膀胱扩张、小结肠和肠蠕动不足。
Hum Genet. 2014 Jun;133(6):737-42. doi: 10.1007/s00439-013-1406-0. Epub 2013 Dec 13.
9
A practical guide for the diagnosis of primary enteric nervous system disorders.原发性肠道神经系统疾病诊断实用指南。
J Pediatr Gastroenterol Nutr. 2013 Nov;57(5):677-86. doi: 10.1097/MPG.0b013e3182a8bb50.
10
Isolated hypoganglionosis: results of a nationwide survey in Japan.孤立性神经节减少症:日本全国性调查结果
Pediatr Surg Int. 2013 Nov;29(11):1127-30. doi: 10.1007/s00383-013-3378-5.