Eur J Pediatr Surg 2008; 18(1): 38-43
DOI: 10.1055/s-2008-1038325
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Quality of Life of Patients with Hirschsprung's Disease at 5 - 20 Years Post Pull-Through Operations

R. Niramis1 , 2 , S. Watanatittan1 , 2 , M. Anuntkosol1 , 2 , V. Buranakijcharoen1 , 2 , T. Rattanasuwan1 , 2 , A. Tongsin1 , 2 , W. Petlek1 , 2 , V. Mahatharadol1 , 2
  • 1Department of Surgery, Queen Sirikit National Institute of Child Health (Children's Hospital), Bangkok, Thailand
  • 2Faculty of Medicine, Rangsit University, Bangkok, Thailand
Further Information

Publication History

received November 22, 2006

accepted after revision February 14, 2007

Publication Date:
26 February 2008 (online)

Abstract

Purpose: The aim of this study was to evaluate the bowel habits and quality of life with respect to faecal continence of patients with Hirschsprung's disease (HD) who had undergone pull-through operations more than 5 years previously. Materials and Methods: Four hundred and sixty-seven patients who underwent pull-through operations for HD during the period of 1987 - 1999 were followed up for evaluation. A questionnaire including demographic data and a qualitative clinical scoring method as described by Holschneider was used for the evaluation of faecal continence. The scoring system did not require a physical examination. Outcomes of the 3 major procedures (Swenson, Duhamel and Soave technique) were analysed. The research was undertaken from October 2004 to September 2006. Patients with neurological defects and total colonic aganglionosis (TCA) were excluded from the analysis. Only patients with typical HD were evaluated, and they were divided into 3 groups based on the length of the period since surgery: 5 - 10 years in Group A; 10 - 15 years in Group B; and 15 - 20 years in Group C. Results: Only 204 patients (male to female ratio: 169 : 35) returned to the Queen Sirikit National Institute of Child Health for evaluation. Twenty-six patients were excluded because of TCA in 13, Down's syndrome in 9 and cerebral palsy in 4. The remaining 178 patients were evaluated and divided into Group A (n = 67), Group B (n = 75) and Group C (n = 36). Excellent results (14 points), good results (10 - 13 points) and fair results (5 - 9 points) were noted in Group A in 52.2 %, 34.3 % and 7.5 % of cases respectively, in Group B in 68 %, 28 % and 4 % of cases, respectively, and in Group C in 88.9 %, 11.1 % and 0 % of cases, respectively. Five cases (7.5 %) in Group A and 3 cases (4 %) in Group B with fair results still had problems such as constant soiling and an inability to hold back defecation. They experienced marked limitations in their social life because of their dependence on diapers and frustration because of teasing by their friends. Conclusion: Faecal incontinence still remains a problem in some patients with HD at 5 - 15 years after surgical correction. However, nearly all patients who were operated on more than 15 years previously had nearly normal faecal continence and a normal social life.

References

  • 1 Bourdelat D, Vrsansky P, Pages R, Duhamel B. Duhamel operation 40 years after: a multicentric study.  Eur J Pediatr Surg. 1997;  7 377-380
  • 2 Caniano D A, Teitelbaum D H, Qualman S J. Management of Hirschsprung's disease in children with trisomy 21.  Am J Surg. 1990;  159 402-404
  • 3 Catto-Smith A G, Coffey C MM, Nolan T M. et al . Fecal incontinence after the surgical treatment of Hirschsprung's disease.  J Pediatr. 1995;  127 954-957
  • 4 Ciley R, Statter M, Coran A. A definitive treatment of Hirschsprung's disease in the newborn with a one-stage procedure.  Surgery. 1994;  115 551-556
  • 5 Fortuna R S, Weber T R, Tracy T F. et al . Critical analysis of the operative treatment of Hirschsprung's disease.  Arch Surg. 1996;  131 520-525
  • 6 Heij H A, de Vries X, Bremer I. et al . Long-term anorectal function after Duhamel operation for Hirschsprung's disease.  J Pediatr Surg. 1995;  30 430-432
  • 7 Heikkinen M, Rintala R J, Louhimo I. Bowel function and quality of life in adult patients with operated Hirschsprung's disease.  Pediatr Surg Int. 1995;  10 342-344
  • 8 Holschneider A M. Elektromanometrie des Enddarmes. 2nd ed. München, Wien, Baltimore; Urban & Schwarzenberg 1982: 213-218
  • 9 Holschneider A M. Hirschsprung's Disease. Stuttgart; Hippokrates, Thieme-Stratton 1982
  • 10 Hung W. Treatment of Hirschsprung's disease with a modified Duhamel-Grob-Martin operation.  J Pediatr Surg. 1991;  26 849-852
  • 11 Ikeda K, Goto S. Total colonic aganglionosis with or without small bowel involvement: an analysis of 137 patients.  J Pediatr Surg. 1986;  21 319-322
  • 12 Jasonni V, Martuciello G. Soave's extramucosal endorectal pull-through procedure. Holschneider AM, Puri P Hirschsprung's Disease and Allied Disorders. London; Harwood Academic Publishers 2000: 336-351
  • 13 Joosten K FM, Festen C, van de Staak F HJM. Is Rehbein's operation an obsolete method of treating Hirschsprung's disease?.  Pediatr Surg Int. 1988;  3 204-207
  • 14 Kleinhaus S, Boley S J, Sheran M. et al . Hirschsprung's disease: a survey of the members of the Surgical Section of the American Academy of Pediatrics.  J Pediatr Surg. 1979;  14 588-597
  • 15 Livaditis A. Hirschsprung's disease: long-term results of the original Duhamel operation.  J Pediatr Surg. 1981;  16 484-486
  • 16 Marty Tl, Seo T, Matlak M E. et al . Gastrointestinal function after surgical correction of Hirschsprung's disease: long-term follow-up in 135 patients.  J Pediatr Surg. 1995;  30 655-658
  • 17 Mishalany H G, Wooley M M. Postoperative functional and manometric evaluation of patients with Hirschsprung's disease.  J Pediatr Surg. 1987;  22 443-446
  • 18 Moore S W, Albertyn R, Cywes S. Clinical outcome and long-term quality of life after surgical correction of Hirschsprung's disease.  J Pediatr Surg. 1996;  31 1496-1502
  • 19 Moore S W, Johnson A G. Hirschsprung's disease: genetic and functional associations of Down's and Waardenburg syndromes.  Semin Pediatr Surg. 1998;  17 156-161
  • 20 N-Fekete C, Ricour C, Martelli H. et al . Total colonic aganglionosis (with or without ileal involvement): a review of 27 cases.  J Pediatr Surg. 1986;  21 251-254
  • 21 Nixon H H. Hirschsprung's disease: progress in management and diagnosis.  World J Surg. 1985;  9 189-202
  • 22 Polley T Z, Coran A G, Wesley J R. A ten-year experience with ninety-two cases of Hirschsprung's disease.  Ann Surg. 1985;  202 349-355
  • 23 Quinn F MJ, Surana R, Puri P. The influence of trisomy 21 on outcome in children with Hirschsprung's disease.  J Pediatr Surg. 1994;  29 781-783
  • 24 Rassouli R, Holschneider A M, Bolkenius M. et al . Long-term results of Rehbein's procedure: a retrospective study in German-speaking countries.  Eur J Pediatr Surg. 2003;  13 187-194
  • 25 Rescorla F J, Morrison A M, Engles D. et al . Hirschsprung's disease: evaluation of mortality and long-term function in 260 cases.  Arch Surg. 1992;  127 934-942
  • 26 Sherman J O, Snyder M E, Weitzman J J. et al . A 40-year multinational retrospective study of 880 Swenson procedures.  J Pediatr Surg. 1989;  24 233-238
  • 27 Shono K, Hutson J M. The treatment and postoperative complications of Hirschsprung's disease: a 10-year experience.  Pediatr Surg Int. 1994;  9 362-365
  • 28 Swenson O, Sherman J O, Fischer J H. et al . The treatment and postoperative complications of congenital megacolon.  Ann Surg. 1975;  182 266-273
  • 29 Teitelbaum D H, Qualman S J, Caniano D A. Hirschsprung's disease: identification of risk factors for enterocolitis.  Ann Surg. 1988;  207 240-244
  • 30 Yanchar N L, Soucy P. Long-term outcome after Hirschsprung's disease: patients' perspective.  J Pediatr Surg. 1999;  31 1152-1160

M.D. Rangsan Niramis

Department of Surgery
Queen Sirikit National Institute of Child Health (Children's Hospital)

420/8 Rajavithi Road

Bangkok 10400

Thailand

Email: rniramis@childrenhospital.go.th

    >