Effectiveness of various surgical methods in treatment of Hirschsprung’s disease in children

  • Marija Lukac Faculty of Medicine University of Belgrade University Children's Hospital
  • Sanja Sindjic Antunovic Faculty of Medicine University of Belgrade, University Children's Hospital
  • Dragana Vujovic Department of Pediatric Surgery, Belgrade, Serbia
  • Ivana Petronic Faculty of Medicine University of Belgrade University Children's Hospital
  • Dejan Nikolic University Children's Hospital
  • Vladimir Radlovic University Children's Hospital
  • Tamara Krstajic University Children's Hospital
  • Zoran Krstic Faculty of Medicine University of Belgrade University Children's Hospital
Keywords: hirschsprung disease, surgical procedures, operative, postoperative complications, reoperation, child,

Abstract


Background/Aim. Hirschsprung’s disease is the most common identifiable developmental disorder of the enteric nervous system, characterized by a failure of its formation in a variable segment of distal bowel. Currently available surgical therapies for Hirschsprung’s disease, although lifesaving, are associated with numerous complications. The aim of our study was to evaluate the effectiveness of different surgical methods and the incidence of serious complications after radical surgery of rectosigmoid Hirschsprung’s disease. Methods. A retrospective analysis, from June 1997 until May 2012 was carried out on 84 patients operated for Hirschsprung’s disease of rectosigmoid colon. Transanal endorectal pull-through was performed in 30 (35.7%) patients (group I), while 54 (64.3%) patients were operated by other (Soave, Duhamel or Swenson) procedures (group II). The age at operation, the incidence and severity of postoperative complications, the need for previous colostomy and the number of reoperations are countered in order to evaluate the efficacy of surgical procedures. Results. In the group I, the mean age at operation was 9.41 ± 6.37 months and in the group II the mean age at operation was 16.8 ± 13.9 months which was significantly higher (p < 0.01). In the group I there were only 3 (10%) patients with complications, one (3%) of them was prone to only one redo procedure (1.00 ± 0.00) and there was no need for previous colostomy in all patients (100%). In the group II there were 16 (30%) patients with significantly frequent complications (p < 0.05), about 2 reoperations on the average (1.94 ± 1.84) in 4 of them (25%) and 22 (41%) redo procedures, which was, in total, significantly higher than in the group I (p < 0.01). Only Soave’s procedure was performed without previous colostomy in 20 (37%) patients. Conclusion. Transanal endorectal pull-through in surgical treatment of patients with Hirschsprung’s disease is more effective than other procedures concerning earlier onset, low incidence and less severe complications, which would require further operations, and no scars.

 

References

Butler TN, Trainor PA. The developmental etiology and patho-genesis of Hirschsprung disease. Transl Res 2013; 162(1): 1−15.

Teitelbaum DH, Cilley RE, Sherman NJ, Bliss D, Uitvlugt ND, Renaud EJ, et al. A decade of experience with the primary pull-through for hirschsprung disease in the newborn period: a multicenter analysis of outcomes. Ann Surg 2000; 232(3): 372−80.

Puri P. Hirschsprung's disease. In: Oldham TO, Colombani PM, Foglia RP, editors. Surgery of infants and children: Scientific principles and practice. New York: Lippincott-Raven; 1997. p. 1277−99.

de la Torre L, Ortega A. Transanal versus open endorectal pull-through for Hirschsprung's disease. J Pediatr Surg 2000; 35(11): 1630−2.

Goldstein AM, Hofstra RM, Burns AJ. Building a brain in the gut: development of the enteric nervous system. Clin Genet 2013; 83(4): 307−16.

Peña A, Elicevik M, Levitt MA. Reoperations in Hirschsprung disease. J Pediatr Surg 2007; 42(6): 1008−13.

Langer JC. Hirschsprung disease. Curr Opin Pediatr 2013; 25(3): 368−74.

Tannuri AC, Tannuri U, Romão RL. Transanal endorectal pull-through in children with Hirschsprung's disease--technical refinements and comparison of results with the Duhamel procedure. J Pediatr Surg 2009; 44(4): 767−72.

Aslan MK, Karaman I, Karaman A, Erdoğan D, Cavuşoğlu YH, Cakmak O. Our experience with transanal endorectal pull-through in Hirschsprung's disease. Eur J Pediatr Surg 2007; 17(5): 335−9.

Sheng Q, Lv Z, Xiao X. Re-operation for Hirschsprung’s dis-ease: experience in 24 patients from China. Pediatr Surg Int 2012; 28(5): 501−6.

Dutta HK. Clinical experience with a new modified transanal endorectal pull-through for Hirschsprung's disease. Pediatr Surg Int 2010; 26(7): 747−51.

Frykman PK, Short SS. Hirschsprung-associated enterocolitis: prevention and therapy. Semin Pediatr Surg 2012; 21(4): 328−35.

Ruttenstock E, Puri P. Systematic review and meta-analysis of enterocolitis after one-stage transanal pull-through procedure for Hirschsprung's disease. Pediatr Surg Int 2010; 26(11): 1101−5.

Luis LA, Encinas JL, Avila LF, Andrés AM, Burgos L, Fernández A, et al. Hirschsprung disease: lessons learned from the last 100 cases. Cir Pediatr 2006; 19(3): 177−81.

Langer JC, Seifert M, Minkes RK. One-stage Soave pull-through for Hirschsprung's disease: a comparison of the transanal and open approaches. J Pediatr Surg 2000; 35(6): 820−2.

Chatoorgoon K, Pena A, Lawal TA, Levitt M. The problematic Duhamel pouch in Hirschsprung's disease: manifestations and treatment. Eur J Pediatr Surg 2011; 21(6): 366−9.

Bischoff A, Levitt MA, Lawal TA, Peña A. Colostomy closure: how to avoid complications. Pediatr Surg Int 2010; 26(11): 1087−92.

Pena A, Migotto-Krieger M, Levitt MA. Colostomy in anorectal malformations: a procedure with serious but preventable com-plications. J Pediatr Surg 2006; 41(4): 748−56.

Rintala RJ. Transanal coloanal pull-through with a short mus-cular cuff for classic Hirschsprung's disease. Eur J Pediatr Surg 2003; 13(3): 181−6.

Zhang S, Wang W, Bai Y, Wang W. Evaluation of anorectal function after transanal one-stage endorectal pull through op-eration in children with Hirschsprung's disease. Zhongguo Dang Dai Er Ke Za Zhi 2007; 9(3): 188−92.

Published
2017/01/24
Section
Original Paper