Literature DB >> 20006024

Clinical features of Hirschsprung's disease associated with Down syndrome: a 30-year retrospective nationwide survey in Japan.

Satoshi Ieiri1, Mayumi Higashi, Risa Teshiba, Isamu Saeki, Genshiro Esumi, Junko Akiyoshi, Takanori Nakatsuji, Tomoaki Taguchi.   

Abstract

PURPOSE: To identify the clinical features in diagnosis and treatment of Hirschsprung's disease (HD) associated with Down syndrome (DS), the authors retrospectively analyzed data for patients with DS from the past 3 nationwide surveys in Japan. This survey was already approved by the Japanese Society of Pediatric Surgeons.
METHODS: Patient data were collected in 3 phases-phase I (1978-1982), n = 47; phase II (1988-1992), n = 79; and phase III (1998-2002), n = 90. In total, data on 216 patients (5.6%) of 3852 were collected and analyzed.
RESULTS: The incidence of DS in patients with HD was 2.9%, 7.1%, and 8.2% in phases I, II, and III, respectively, with a corresponding male/female ratio of 5:1, 2.4:1, and 5:1. The ratio of the extent of aganglionosis was nearly consistent across all phases. In phases I, II, and III, the incidence of total colonic aganglionosis was 2.1%, 0%, and 2.2%; and that of cardiovascular anomalies, 36.1%, 45.6%, and 55.6%; and that of preoperative enterocolitis, 31.0%, 26.6%, and 24.4%. The 2 most common surgical procedures were the Soave procedure, including transanal endorectal pull-through, and Duhamel procedure including Z-shaped anastomosis. The mortality rate decreased over time, from 26.1% in phase I to 11.4% in phase II and 7.8% in phase III. Almost all mortality cases were associated with cardiovascular anomalies: 54.5%, 62.5%, and 85.7% in phases I, II, and III, respectively.
CONCLUSIONS: The incidence of HD with DS has increased over time. The number of male patients and cardiac anomalies has also increased in the last 10 years. Total colonic aganglionosis was rare. A marked decrease in the overall mortality rate was observed.

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Year:  2009        PMID: 20006024     DOI: 10.1016/j.jpedsurg.2009.07.055

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  8 in total

Review 1.  Advances in understanding the association between Down syndrome and Hirschsprung disease (DS-HSCR).

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2018-09-14       Impact factor: 1.827

Review 2.  Syndromic Hirschsprung's disease and associated congenital heart disease: a systematic review.

Authors:  Johannes W Duess; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-07-09       Impact factor: 1.827

3.  Epidemiology of Hirschsprung disease in California from 1995 to 2013.

Authors:  Jamie E Anderson; Melissa A Vanover; Payam Saadai; Rebecca A Stark; Jacob T Stephenson; Shinjiro Hirose
Journal:  Pediatr Surg Int       Date:  2018-10-15       Impact factor: 1.827

4.  Risk factors of enterostomy in neonates with Hirschsprung disease.

Authors:  Zhaozhou Liu; Yanan Zhang; Shuangshuang Li; Shen Yang; Jiawei Zhao; Ting Yang; Siqi Li; Yongwei Chen; Weihong Guo; Dawei Hou; Jingbin Du; Yingzi Li; Jinshi Huang
Journal:  Int J Colorectal Dis       Date:  2022-04-21       Impact factor: 2.571

Review 5.  Hirschsprung-associated enterocolitis: prevention and therapy.

Authors:  Philip K Frykman; Scott S Short
Journal:  Semin Pediatr Surg       Date:  2012-11       Impact factor: 2.754

6.  Hirschsprung's disease associated with Down syndrome: a meta-analysis of incidence, functional outcomes and mortality.

Authors:  Florian Friedmacher; Prem Puri
Journal:  Pediatr Surg Int       Date:  2013-09       Impact factor: 1.827

7.  Hirschsprung's Disease and Associated Congenital Heart Defects: A Prospective Observational Study from a Single Institution.

Authors:  Giulia Tuo; Alessio Pini Prato; Maria Derchi; Manuela Mosconi; Girolamo Mattioli; Maurizio Marasini
Journal:  Front Pediatr       Date:  2014-09-17       Impact factor: 3.418

8.  Stercoral ulcer after Hirschsprung's disease surgery.

Authors:  Toshihiko Kakiuchi; Atsuhisa Fukuta; Koichiro Yoshimaru; Yumeng Zhang; Ryo Shimoda; Muneaki Matsuo
Journal:  Clin Case Rep       Date:  2021-12-26
  8 in total

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