Literature DB >> 17006709

Long-term results of bowel function after treatment for Hirschsprung's disease: a 29-year review.

Maria Menezes1, Martin Corbally, Prem Puri.   

Abstract

Although various surgical procedures have been described to treat Hirschsprung's disease (HD), few studies have evaluated the long-term results of these children. The purpose of this study was to assess the long-term clinical outcome and bowel function of patients with HD. The hospital records of 259 consecutive patients with a confirmed histological diagnosis of HD during 1975-2003 were examined. Data was assessed for age at presentation, sex, clinical presentation, associated anomalies, level of aganglionosis, surgical procedures, complications and bowel function. Follow up was carried out by personal/telephone interviews with patients or their parents. Of the 259 patients with HD, 200 were males (77.2%) and 59 females (22.8%). Intestinal obstruction was the presenting feature in 147 patients (56.8%), intestinal perforation in 5 (1.9%), enterocolitis in 30 (11.6%) and constipation in 77 (29.7%). Thirty-nine patients (15.1%) had associated Down's syndrome. Two hundred and nine patients (80.7%) had rectosigmoid disease, 31 (12%) had long segment disease and 19 (7.3%) had total colonic aganglionosis. Forty-three patients (16.6%) had preoperative enterocolitis. Primary colostomy was performed in 160 patients and a primary pull through in 90. Seven patients had a sphincteromyectomy for ultrashort HD. Two patients died prior to treatment. Various pull through procedures were performed in these patients. Postoperative complications included: pelvic abcess in 2, rectal stricture in 10, perianal excoriation in 7, anastomotic leak in 8, intestinal obstruction in 3, wound dehiscence in 1, stomal prolapse/stenosis in 5, rectovesical fistula in 2 and enterocolitis in 56. Five patients underwent a redo pull through and 46 required a post pull through sphincterectomy. At the time of follow-up, 27 were lost to follow-up, 9 died, 18 had permanent stomas and 4 were too young to assess bowel function. Of the remaining 194 patients, bowel function was normal in 132 (68%). Twenty patients (10.3%) had soiling and 42 (21.7%) had constipation requiring laxatives or enemas. There was no difference in bowel function in relation to type of pull through operation. Only 34% of patients with Down's syndrome had normal continence. The majority of patients with HD continue to have disturbances of bowel function for many years before attaining normal continence.

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Year:  2006        PMID: 17006709     DOI: 10.1007/s00383-006-1783-8

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  20 in total

1.  Long-term clinical outcome in patients with Hirschsprung's disease and associated Down's syndrome.

Authors:  Maria Menezes; Prem Puri
Journal:  J Pediatr Surg       Date:  2005-05       Impact factor: 2.545

2.  Hirschsprung's disease. Evaluation of mortality and long-term function in 260 cases.

Authors:  F J Rescorla; A M Morrison; D Engles; K W West; J L Grosfeld
Journal:  Arch Surg       Date:  1992-08

3.  Long-term anorectal function after Duhamel operation for Hirschsprung's disease.

Authors:  H A Heij; X de Vries; I Bremer; S Ekkelkamp; A Vos
Journal:  J Pediatr Surg       Date:  1995-03       Impact factor: 2.545

4.  Long-term results of Swenson's operation for Hirschsprung's disease.

Authors:  P Puri; H H Nixon
Journal:  Prog Pediatr Surg       Date:  1977

5.  Management of Hirschsprung's disease in children with trisomy 21.

Authors:  D A Caniano; D H Teitelbaum; S J Qualman
Journal:  Am J Surg       Date:  1990-04       Impact factor: 2.565

6.  Short-pouch and low-anastomosis Duhamel procedure results in better fecal control and normal defecation pattern.

Authors:  B Antao; T Radhwan; M Samuel; E Kiely
Journal:  Dis Colon Rectum       Date:  2005-09       Impact factor: 4.585

7.  Clinical outcome and long-term quality of life after surgical correction of Hirschsprung's disease.

Authors:  S W Moore; R Albertyn; S Cywes
Journal:  J Pediatr Surg       Date:  1996-11       Impact factor: 2.545

8.  Management of Hirschsprung's disease: a comparison of Soave's and Duhamel's pull-through methods.

Authors:  Waleed Saleh; Khalid Rasheed; Mohammed Al Mohaidly; Hala Kfoury; Mohammad Tariq; Assia Al Rawaf
Journal:  Pediatr Surg Int       Date:  2004-08-11       Impact factor: 1.827

9.  Experience with primary laparoscopy-assisted endorectal pull-through for Hirschsprung's disease.

Authors:  Nien-Lu Wang; Hung-Chang Lee; Ming-Lun Yeh; Pei-Yeh Chang; Jin-Cherng Sheu
Journal:  Pediatr Surg Int       Date:  2004-01-24       Impact factor: 1.827

10.  The influence of trisomy 21 on outcome in children with Hirschsprung's disease.

Authors:  F M Quinn; R Surana; P Puri
Journal:  J Pediatr Surg       Date:  1994-06       Impact factor: 2.545

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  36 in total

1.  Rho-kinase expression in Hirschsprung's disease.

Authors:  David Coyle; Anne Marie O'Donnell; Nicolae Corcionivoschi; John Gillick; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-08-15       Impact factor: 1.827

2.  Developmental anomalies of the enteric nervous system in normoganglionic segments of bowel from rats with total colonic aganglionosis.

Authors:  Fumiko Horigome; Tatsunori Seki; Hiroyuki Kobayashi; Tsuyoshi Ozaki; Atsuyuki Yamataka
Journal:  Pediatr Surg Int       Date:  2007-10       Impact factor: 1.827

Review 3.  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

Review 4.  Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes.

Authors:  Robert O Heuckeroth
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2018-01-04       Impact factor: 46.802

5.  Surgical acquired aganglionosis: myth or reality?

Authors:  M J Bag; T Sáez; J Varas; H Vallejos; D Meléndez; S Salas; Y Quiroga; F Villagrán; S Montedonico
Journal:  Pediatr Surg Int       Date:  2014-07-15       Impact factor: 1.827

6.  Transplanted skin-derived precursor stem cells generate enteric ganglion-like structures in vivo.

Authors:  Justin P Wagner; Veronica F Sullins; James C Y Dunn
Journal:  J Pediatr Surg       Date:  2014-08       Impact factor: 2.545

7.  A durable model of Hirschsprung's colon.

Authors:  Justin P Wagner; Veronica F Sullins; Hassan A Khalil; James C Y Dunn
Journal:  J Pediatr Surg       Date:  2014-10-03       Impact factor: 2.545

8.  Decreased expression of TRAAK channels in Hirschsprung's disease: a possible cause of postoperative dysmotility.

Authors:  Anne-Marie O'Donnell; Hiroki Nakamura; Bina Parekh; Prem Puri
Journal:  Pediatr Surg Int       Date:  2019-09-21       Impact factor: 1.827

Review 9.  Total colonic aganglionosis: a systematic review and meta-analysis of long-term clinical outcome.

Authors:  Danielle Mc Laughlin; Florian Friedmacher; Prem Puri
Journal:  Pediatr Surg Int       Date:  2012-08       Impact factor: 1.827

Review 10.  The developmental etiology and pathogenesis of Hirschsprung disease.

Authors:  Naomi E Butler Tjaden; Paul A Trainor
Journal:  Transl Res       Date:  2013-03-22       Impact factor: 7.012

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