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Erschienen in: Pediatric Surgery International 1/2023

01.12.2023 | Original Article

Functional outcome of Hirschsprung's disease in children: A single center study at The Children's Hospital Lahore

verfasst von: Muhammad Saleem, Jamaal Butt, Zubair Shaukat, Imran Hashim, Moeezah, Fatima Majeed, Muhammad Kamran, Umer Saleem

Erschienen in: Pediatric Surgery International | Ausgabe 1/2023

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Abstract

Aim

Hirschsprung’s disease (HD) is a congenital bowel disorder resulting in functional dysmotility. Advancement in surgical techniques has improved outcomes, but recent studies have identified problems having significant impact on patient's quality of life. The aim of this study is to analyze postoperative functional outcome after definitive surgery for Hirschsprung’s disease.

Method

A retrospective study was conducted at the Department of Pediatric Surgery, The Children's Hospital Lahore. The record of 64 patients was reviewed from the year 2009 to 2019. Parents were interviewed on phone calls and a predesigned questionnaire was filled. Degree of constipation, incontinence and voluntary bowel movements was analyzed according to Krickenbeck classification.

Results

Median age at initial presentation was 11 days, with male to female ratio of 3.9:1. Most common presentation was delayed passage of meconium (38%). Diagnosis was made on biopsy in 70.3%, but contrast enema and biopsy in 29.7%. Aganglionosis was limited to short segment in 81.3% and long segment in 14.5%. Decompressing enterostomy was made in 63% at a mean age of 191 days. Definitive surgery included Duhamel pull-through in 89.1%. Mean age at follow-up was 10.6 ± 4.19 years and alive patients were 95.4%. Postoperative enterocolitis was reported by 27%, while 35.5% reported fecal incontinence and 16.1% complained of constipation. 80% could voluntarily hold bowel movement, among which 5% had a feeling of urge and 15% had the capacity to verbalize. In 25% of the patients, fecal incontinence was a constant social problem and in 25% of these patients constipation was resistant to diet and laxatives.

Conclusion

On long-term follow-up, fecal incontinence was more worrisome, affecting quality of life and requiring help of the bowel management program. Such patients need close follow-up after definitive procedure, so that they have normal stooling habits in their adulthood and lead a normal life.
Literatur
1.
2.
Zurück zum Zitat Granéli C, Dahlin E, Börjesson A, Arnbjörnsson E, Stenström P (2017) Diagnosis, symptoms, and outcomes of Hirschsprung’s disease from the perspective of gender. Surg Res Pract 2017:1–8CrossRef Granéli C, Dahlin E, Börjesson A, Arnbjörnsson E, Stenström P (2017) Diagnosis, symptoms, and outcomes of Hirschsprung’s disease from the perspective of gender. Surg Res Pract 2017:1–8CrossRef
3.
Zurück zum Zitat Dai Y, Deng Y, Lin Y, Ouyang R, Li L (2020) Long-term outcomes and quality of life of patients with Hirschsprung disease: a systematic review and meta-analysis. BMC Gastroenterol 20(1):67CrossRefPubMed Dai Y, Deng Y, Lin Y, Ouyang R, Li L (2020) Long-term outcomes and quality of life of patients with Hirschsprung disease: a systematic review and meta-analysis. BMC Gastroenterol 20(1):67CrossRefPubMed
4.
Zurück zum Zitat Reding R, de Ville GJ, Gosseye S, Clapuyt P, Sokal E, Buts JP et al (1997) Hirschsprung’s disease: a 20-year experience. J Pediatr Surg 32(8):1221–1225CrossRefPubMed Reding R, de Ville GJ, Gosseye S, Clapuyt P, Sokal E, Buts JP et al (1997) Hirschsprung’s disease: a 20-year experience. J Pediatr Surg 32(8):1221–1225CrossRefPubMed
5.
Zurück zum Zitat Rintala RJ, Pakarinen MP (2012) Long-term outcomes of Hirschsprung’s disease. Semin Pediatr Surg 21(4):336–343CrossRefPubMed Rintala RJ, Pakarinen MP (2012) Long-term outcomes of Hirschsprung’s disease. Semin Pediatr Surg 21(4):336–343CrossRefPubMed
6.
Zurück zum Zitat Niramis R, Watanatittan S, Anuntkosol M, Buranakijcharoen V, Rattanasuwan T, Tongsin A et al (2008) Quality of life of patients with Hirschsprung’s disease at 5–20 years post pull-through operations. Eur J Pediatr Surg 18(1):38–43CrossRefPubMed Niramis R, Watanatittan S, Anuntkosol M, Buranakijcharoen V, Rattanasuwan T, Tongsin A et al (2008) Quality of life of patients with Hirschsprung’s disease at 5–20 years post pull-through operations. Eur J Pediatr Surg 18(1):38–43CrossRefPubMed
7.
Zurück zum Zitat Nasr A, Grandpierre V, Sullivan KJ, Wong CA, Benchimol EI (2021) Long-term outcomes of patients surgically treated for Hirschsprung disease. J Can Assoc Gastroenterol 4(5):201–206CrossRefPubMed Nasr A, Grandpierre V, Sullivan KJ, Wong CA, Benchimol EI (2021) Long-term outcomes of patients surgically treated for Hirschsprung disease. J Can Assoc Gastroenterol 4(5):201–206CrossRefPubMed
8.
Zurück zum Zitat Engum SA, Grosfeld JL (2004) Long-term results of treatment of Hirschsprung’s disease. Semin Pediatr Surg 13(4):273–285CrossRefPubMed Engum SA, Grosfeld JL (2004) Long-term results of treatment of Hirschsprung’s disease. Semin Pediatr Surg 13(4):273–285CrossRefPubMed
9.
Zurück zum Zitat Bischoff A, Bealer J, Peña A (2016) Critical analysis of fecal incontinence scores. Pediatr Surg Int 32(8):737–741CrossRefPubMed Bischoff A, Bealer J, Peña A (2016) Critical analysis of fecal incontinence scores. Pediatr Surg Int 32(8):737–741CrossRefPubMed
10.
Zurück zum Zitat Yanchar NL, Soucy P (1999) Long-term outcome after Hirschsprung’s disease: patients’ perspectives. J Pediatr Surg 34(7):1152–1160CrossRefPubMed Yanchar NL, Soucy P (1999) Long-term outcome after Hirschsprung’s disease: patients’ perspectives. J Pediatr Surg 34(7):1152–1160CrossRefPubMed
11.
Zurück zum Zitat Khademi G, Khazdouz M, Sezavar M, Imani B, Akhavan H, Babapour A (2015) Clinical outcome and bowel function after surgical treatment in Hirschsprung′s disease. Afr J Paediatr Surg 12(2):143CrossRefPubMed Khademi G, Khazdouz M, Sezavar M, Imani B, Akhavan H, Babapour A (2015) Clinical outcome and bowel function after surgical treatment in Hirschsprung′s disease. Afr J Paediatr Surg 12(2):143CrossRefPubMed
12.
Zurück zum Zitat Fortuna RS (1996) Critical analysis of the operative treatment of Hirschsprung’s disease. Arch Surg 131(5):520CrossRefPubMed Fortuna RS (1996) Critical analysis of the operative treatment of Hirschsprung’s disease. Arch Surg 131(5):520CrossRefPubMed
13.
Zurück zum Zitat Menezes M, Puri P (2006) Long-term outcome of patients with enterocolitis complicating Hirschsprung’s disease. Pediatr Surg Int 22(4):316–318CrossRefPubMed Menezes M, Puri P (2006) Long-term outcome of patients with enterocolitis complicating Hirschsprung’s disease. Pediatr Surg Int 22(4):316–318CrossRefPubMed
14.
Zurück zum Zitat Hagens J, Reinshagen K, Tomuschat C (2022) Prevalence of Hirschsprung-associated enterocolitis in patients with Hirschsprung disease. Pediatr Surg Int 38(1):3–24CrossRefPubMed Hagens J, Reinshagen K, Tomuschat C (2022) Prevalence of Hirschsprung-associated enterocolitis in patients with Hirschsprung disease. Pediatr Surg Int 38(1):3–24CrossRefPubMed
Metadaten
Titel
Functional outcome of Hirschsprung's disease in children: A single center study at The Children's Hospital Lahore
verfasst von
Muhammad Saleem
Jamaal Butt
Zubair Shaukat
Imran Hashim
Moeezah
Fatima Majeed
Muhammad Kamran
Umer Saleem
Publikationsdatum
01.12.2023
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Surgery International / Ausgabe 1/2023
Print ISSN: 0179-0358
Elektronische ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-023-05451-9

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