Literature DB >> 21129554

Long-term outcomes and the quality of life of Hirschsprung disease in adolescents who have reached 18 years or older--a 47-year single-institute experience.

Satoshi Ieiri1, Takanori Nakatsuji, Junko Akiyoshi, Mayumi Higashi, Makoto Hashizume, Sachiyo Suita, Tomoaki Taguchi.   

Abstract

BACKGROUND AND AIMS: Hirschsprung disease is considered to be curable when performing definitive surgery. However, the postoperative bowel function is not always satisfactory. The long-term postoperative function of bowel evacuation and the quality of life of such patients are considered to be important. In this study, we evaluated the general condition, bowel function, and social performance in adults who were older than 17 years who had suffered from Hirschsprung disease in childhood.
METHODS: From 1963 to 2009, 184 patients with Hirschsprung disease underwent definitive surgery, mostly Z-shaped anastomosis at Kyushu University Hospital. As a result, 146 (95.4%) of 153 of those patients survived and reached 17 years of age. Their present status and symptoms, anorectal functions, genitourinary functions, and social performance were evaluated during the clinical follow-up based on a questionnaire survey.
RESULTS: In our series, the evacuation score was rated as "excellent" (score of 7-8/8) in 66.7%, "good" (5-6/8) in 19.0%, "fair" (3-4/8) in 11.9%, and "poor" (0-2/8) in 2.4%. Therefore, 85.7% were considered to have a satisfactory bowel function. However, only 21.4% had a completely normal score of 8/8. Incontinence occurred in 16.7%, and soiling was present in 19.0% of the questionnaire respondents. The genitourinary function was considered to be within the reference range, and urinary problems were minimal. Among the respondents, 45.2% were married, and 68.4% of those married had children. The educational and professional careers of the respondents were successful.
CONCLUSIONS: In general, the bowel function was satisfactory. However, the ratio of patients with completely normal bowel function was low. Because incontinence and soiling impair the quality of life, pediatric surgeons should therefore continue trying to achieve a complete bowel function after definitive surgery for the treatment of Hirschsprung disease.
Copyright © 2010 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2010        PMID: 21129554     DOI: 10.1016/j.jpedsurg.2010.08.040

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


  19 in total

Review 1.  Redo pullthrough for Hirschsprung disease.

Authors:  Matthew W Ralls; Arnold G Coran; Daniel H Teitelbaum
Journal:  Pediatr Surg Int       Date:  2016-12-31       Impact factor: 1.827

2.  Transanal endorectal pull-through for Hirschsprung's disease using long cuff dissection and short V-shaped partially resected cuff anastomosis: early and late outcomes.

Authors:  Li Yang; Shao-Tao Tang; Guo-Qing Cao; Ying Yang; Shuai Li; Shi-Wang Li; Yong Wang; Yong-Zhong Mao; Qing-Lan Ruan; Guo-Bin Wang
Journal:  Pediatr Surg Int       Date:  2012-03-20       Impact factor: 1.827

3.  Effect of different surgical options on curative effect, nutrition, and health status of patients with slow transit constipation.

Authors:  Fan Li; Tao Fu; Weidong Tong; Anping Zhang; Chunxue Li; Yu Gao; Jin Song Wu; Baohua Liu
Journal:  Int J Colorectal Dis       Date:  2014-09-25       Impact factor: 2.571

4.  Migration and differentiation of transplanted enteric neural crest-derived cells in murine model of Hirschsprung's disease.

Authors:  Ryuhei Nishikawa; Ryo Hotta; Naoki Shimojima; Shinsuke Shibata; Narihito Nagoshi; Masaya Nakamura; Yumi Matsuzaki; Hirotaka J Okano; Tatsuo Kuroda; Hideyuki Okano; Yasuhide Morikawa
Journal:  Cytotechnology       Date:  2014-09-18       Impact factor: 2.058

5.  Isogenic enteric neural progenitor cells can replace missing neurons and glia in mice with Hirschsprung disease.

Authors:  R Hotta; L S Cheng; H K Graham; W Pan; N Nagy; J Belkind-Gerson; A M Goldstein
Journal:  Neurogastroenterol Motil       Date:  2015-12-20       Impact factor: 3.598

6.  Current status of Hirschsprung's disease: based on a nationwide survey of Japan.

Authors:  Tomoaki Taguchi; Satoshi Obata; Satoshi Ieiri
Journal:  Pediatr Surg Int       Date:  2017-01-05       Impact factor: 1.827

Review 7.  Stem cell-based therapy for hirschsprung disease, do we have the guts to treat?

Authors:  Ali Fouad Alhawaj
Journal:  Gene Ther       Date:  2021-06-14       Impact factor: 5.250

Review 8.  Long-term results of transanal pull-through for Hirschsprung's disease: a meta-analysis.

Authors:  J Zimmer; C Tomuschat; P Puri
Journal:  Pediatr Surg Int       Date:  2016-07-06       Impact factor: 1.827

9.  Postnatal human enteric neuronal progenitors can migrate, differentiate, and proliferate in embryonic and postnatal aganglionic gut environments.

Authors:  Lily S Cheng; Ryo Hotta; Hannah K Graham; Jaime Belkind-Gerson; Nandor Nagy; Allan M Goldstein
Journal:  Pediatr Res       Date:  2017-01-06       Impact factor: 3.756

10.  Disparities in the gut metabolome of post-operative Hirschsprung's disease patients.

Authors:  Vera Plekhova; Ellen De Paepe; Katrien Van Renterghem; Myriam Van Winckel; Lieselot Y Hemeryck; Lynn Vanhaecke
Journal:  Sci Rep       Date:  2021-08-09       Impact factor: 4.379

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.