Literature DB >> 9269974

Hirschsprung's disease: a 20-year experience.

R Reding1, J de Ville de Goyet, S Gosseye, P Clapuyt, E Sokal, J P Buts, P Gibbs, J B Otte.   

Abstract

During the period from 1972 to 1992, 59 children received surgical treatment at the University of Louvain Medical School for biopsy-proven Hirschsprung's disease (HD). The extent of aganglionosis was as follows: short segment restricted to the rectosigmoid or descending colon (n = 44, 75%); long segment (n = 9,15%); ultra-short segment (n = 3, 5%); unknown length because of death without autopsy (n = 3, 5%). The median age at operation was 7 months for short-segment disease compared with 14 months for those with long-segment disease. Surgical procedures used for short-segment disease were Swenson with colostomy (n = 16), Swenson-Pellerin without colostomy (n = 27), Duhamel (n = 1), and for long-segment disease were Martin (n = 3), Swenson-Deloyers (n = 2), Swenson-Boley (n = 2) and ileostomy only in = 2). Lynn's sphincteromyotomy was performed in the three ultra-short cases. There were six deaths (10%) at a median age of 86 days (range, 28 to 1545 days), three had long-segment disease, and the others were not classified because of death before curative surgery. Enterocolitis (EC) was the most common cause of death (five cases) and was also the major source of morbidity after curative surgery (12 of 44, 27%) in short-segment patients, three of seven (43%) in long-segment patients. The functional success of the procedure was evaluated in 70% of the surviving patients (37 of 53; mean follow-up, 8.7 years; range, 1.2 to 21.5), using a novel semiquantitative scoring system, specifically designed for children who have HD. This system assesses normal stool evacuation, abdominal distention, soiling, and severe incontinence. The results were compared with those from a population of 39 healthy children and adolescents and demonstrated progressive improvement in function during childhood and adolescence (P = .04) for patients treated for short-segment disease. However, function was found to be consistently poorer in all age groups when compared with healthy controls (5 to 10 years, P < .01; 10 to 15 years, P < .05; > 15 years, P < .01).

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Year:  1997        PMID: 9269974     DOI: 10.1016/s0022-3468(97)90686-2

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


  20 in total

1.  Rectal suction biopsy in the workup of childhood chronic constipation: indications and diagnostic value.

Authors:  Alessio Pini-Prato; Stefano Avanzini; Valerio Gentilino; Giuseppe Martucciello; Girolamo Mattioli; Cristina Coccia; Stefano Parodi; Giovanni Maria Bisio; Vincenzo Jasonni
Journal:  Pediatr Surg Int       Date:  2006-12-14       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

Review 3.  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

Review 4.  Familial Hirschsprung's disease: a systematic review.

Authors:  Danielle Mc Laughlin; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-07-16       Impact factor: 1.827

Review 5.  Hirschsprung's disease: what about mortality?

Authors:  Alessio Pini Prato; Valentina Rossi; Stefano Avanzini; Girolamo Mattioli; Nicola Disma; Vincenzo Jasonni
Journal:  Pediatr Surg Int       Date:  2011-05       Impact factor: 1.827

6.  Botulinium toxin, as bridge to transanal pullthrough in neonate with Hirschsprungs disease.

Authors:  S M V Hosseini; H R Foroutan; S Zeraatian; B Sabet
Journal:  J Indian Assoc Pediatr Surg       Date:  2008-04

7.  Long-term outcomes and quality of life after subtotal colectomy combined with modified Duhamel procedure for adult Hirschsprung's disease.

Authors:  Lin Wang; Qi He; Jun Jiang; Ning Li
Journal:  Pediatr Surg Int       Date:  2014-01       Impact factor: 1.827

8.  Hirschsprung's disease: 13 years' experience in 112 patients from a single institution.

Authors:  Alessio Pini Prato; Valerio Gentilino; Camilla Giunta; Stefano Avanzini; Stefano Parodi; Girolamo Mattioli; Giuseppe Martucciello; Vincenzo Jasonni
Journal:  Pediatr Surg Int       Date:  2007-12-01       Impact factor: 1.827

Review 9.  Hirschsprung-associated enterocolitis: prevention and therapy.

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

Review 10.  Hirschsprung Disease beyond Infancy.

Authors:  Casey M Calkins
Journal:  Clin Colon Rectal Surg       Date:  2018-02-25
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