Iranian Society of Pediatric Surgeons
  • Register
  • Login

Iranian Journal of Pediatric Surgery

  • Home
  • About
    • About the Journal
    • Indexing & Abstracting
    • Submissions
    • Editorial Team
    • Privacy Statement
    • Contact
  • Current
  • Archives
Advanced Search
  1. Home
  2. Archives
  3. Vol. 10 No. 2 (2024): November
  4. Original Articles

Vol. 10 No. 2 (2024)

October 2024

Management of Hirschsprung's Associated Enterocolitis as a Post-Operative Complication: Single-Center Experience Management of Hirschsprung's Associated Enterocolitis as a Post-Operative Complication: Single-Center Experience

  • ahmed oshiba
  • Isooba safiyo ayub
  • Ahmed gabr khairi
  • Mohamed abdelazim abouheba

Iranian Journal of Pediatric Surgery, Vol. 10 No. 2 (2024), 30 October 2024 , Page 179-192
https://doi.org/10.22037/irjps.v10i2.45743 Published: 2024-10-15

  • View Article
  • Download
  • Cite
  • References
  • Statastics
  • Share

Abstract

Introduction: Enterocolitis is a potentially fatal consequence of Hirschsprung’s disease, it is characterized by fever, abdominal pain, foul-smelling diarrhea, and sepsis. Most neonatal morbidity and mortality are caused by Hirschsprung-associated enterocolitis (HAEC). Harald Hirschsprung initially discovered Hirschsprung's related enterocolitis in the 19th century and included it in his iconic description of megacolon. Trisomy 21, illness, familial history, and prior bouts of HAEC are risk factors for the condition. (3,4) According to Engun et al. patients who presented with a history of Hirschsprung's disease had a 35% incidence of HAEC, but those without such a history only had a 16% incidence. Similarly, HSD and trisomy 21 have a known association with 2.9 - 8.2% of HSD patients also having trisomy 21. This study aimed to evaluate HAEC as a postoperative complication in children who were admitted after pull-through surgery as regards the type of surgery, incidence, clinical presentation, sepsis workup, and management in Alexandria University Children’s Hospital.

Materials and Methods: This retrospective study included 30 patients with Hirschsprung disease who developed post-operative Hirschsprung-associated enterocolitis and were scheduled for surgical intervention from January 2021 to 2022.

Results:  In the studied group, the most commonly used pull-through procedure was the Soave (53.33%), followed by the Duhamel procedure (20%). Fewer subjects were operated using the Swenson and Rehbein methods, at 16.67% and 10% respectively. Most of our studied patients (26 patients) presented with signs and symptoms of Grade I HAEC, while 3 patients with Grade II and 1 patient with Grade III.

Conclusion:  Post-operative HAEC is a serious complication and needs to proper management to save the child either conservative treatment, repeated anal dilatation or surgical intervention in severe cases.

 

Keywords:
  • Hirschsprung-Associated Enterocolitis
  • Contrast Enema
  • Pull-Through
  • Megacolon
  • PDF

How to Cite

oshiba, ahmed, ayub, I. safiyo, khairi, A. gabr, & abouheba, M. abdelazim. (2024). Management of Hirschsprung’s Associated Enterocolitis as a Post-Operative Complication: Single-Center Experience: Management of Hirschsprung’s Associated Enterocolitis as a Post-Operative Complication: Single-Center Experience. Iranian Journal of Pediatric Surgery, 10(2), 179–192. https://doi.org/10.22037/irjps.v10i2.45743
  • ACM
  • ACS
  • APA
  • ABNT
  • Chicago
  • Harvard
  • IEEE
  • MLA
  • Turabian
  • Vancouver
  • Endnote/Zotero/Mendeley (RIS)
  • BibTeX

References

Scholfield DW, Ram AD: The importance of recording the first passage of meconium in neonates. BMJ. 2017 Mar 2;356.

Moore SW, Zaahl MG: A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling. Journal of pediatric surgery. 2008 Feb 1;43(2):325-9.

Levin DN, Marcon MA, Rintala RJ, et al: Inflammatory bowel disease manifesting after surgical treatment for Hirschsprung disease. Journal of pediatric gastroenterology and nutrition. 2012 Sep 1;55(3):272-7

Suita S, Taguchi T, Ieiri S, et al: Hirschsprung's disease in Japan: analysis of 3852 patients based on a nationwide survey in 30 years. Journal of pediatric surgery. 2005 Jan 1;40(1):197-202.

Engum SA, Petrites M, Rescorla FJ, et al: Familial Hirschsprung's disease: 20 cases in 12 kindreds. Journal of pediatric surgery. 1993 Oct 1;28(10):1286-90.

Morabito A, Lall A, Gull S, et al: The impact of Down’s syndrome on the immediate and long-term outcomes of children with Hirschsprung’s disease. Pediatric surgery international. 2006 Feb; 22:179-81.

Heuckeroth RO: Hirschsprung disease—integrating basic science and clinical medicine to improve outcomes. Nature reviews Gastroenterology & hepatology. 2018 Mar;15(3):152-67.

Almetaher HA, Hassan HS, Elhalaby EA: Current management of Hirschsprung’s disease in Egypt: a survey of members of the Egyptian Pediatric Surgical Association. Annals of Pediatric Surgery. 2015;11(4):207-11.

Stockmann PT, Philippart AI: The Duhamel procedure for Hirschsprung's disease. In Seminars in Pediatric Surgery 1998 May 1 (Vol. 7, No. 2, pp. 89-95). WB Saunders.

Gao Y, Li G, Zhang X, et al: Primary transanal rectosigmoidectomy for Hirschsprung's disease: preliminary results in the initial 33 cases. Journal of pediatric surgery. 2001 Dec 1;36(12):1816-9.

Tiryaki T, Demirbag S, Atayurt H, et al: Topical nitric oxide treatment after pull through operations for Hirschsprung disease. Journal of pediatric gastroenterology and nutrition. 2005 Mar 1;40(3):390-2.

Gosain A, Brinkman AS: Hirschsprung’s associated enterocolitis. Current opinion in pediatrics. 2015 Jun;27(3):364.

Holschneider AM, Puri P, editors: Hirschsprung's disease and allied disorders. Berlin: Springer; 2008.;115-123

Surana R, Quinn FM, Puri P: Evaluation of risk factors in the development of enterocolitis complicating Hirschsprung's disease. Pediatric surgery international. 1994 Apr; 9:234-6.

Haricharan RN, Seo JM, Kelly DR, et al: Older age at diagnosis of Hirschsprung disease decreases risk of postoperative enterocolitis, but resection of additional ganglionated bowel does not. Journal of pediatric surgery. 2008 Jun 1;43(6):1115-23.

De Lorijn F, Kremer LC, Reitsma JB, et al: Diagnostic tests in Hirschsprung disease: a systematic review. Journal of pediatric gastroenterology and nutrition. 2006 May 1;42(5):496-505.

Parahita IG, Makhmudi A: Comparison of Hirschsprung-associated enterocolitis following Soave and Duhamel procedures. Journal of pediatric surgery. 2018 Jul 1;53(7):1351-4.

Tomuschat C, Zimmer J, Puri P: Laparoscopic-assisted pull-through operation for Hirschsprung’s disease: a systematic review and meta-analysis. Pediatric surgery international. 2016 Aug; 32:751-7.

Ambartsumyan L, Smith C, Kapur RP: Diagnosis of Hirschsprung disease. Pediatric and Developmental Pathology. 2020 Jan;23(1):8-22.

Green HL, Rizzolo D, Austin M: Surgical management for Hirschsprung disease: a review for primary care providers. JAAPA. 2016 Apr 1;29(4):24-9.

  • Abstract Viewed: 96 times
  • PDF Downloaded: 102 times

Download Statastics

  • Linkedin
  • Twitter
  • Facebook
  • Google Plus
  • Telegram

Developed By

Open Journal Systems
  • Home
  • Archives
  • Submissions
  • About the Journal
  • Editorial Team
  • Contact
Powered by OJSPlus