Literature DB >> 33552793

The Prevalence and Clinical Profile of Hirschsprung's Disease at a Tertiary Hospital in Bahrain.

Alaa Ali1, Fayza Haider1, Saeed Alhindi1.   

Abstract

Background Hirschsprung's disease (HD) is a rare but important congenital pediatric disease of the colon, and its incidence varies widely between ethnic groups. Its incidence was first studied in Bahrain in 1980 using hospital-based data. Over a 16-month period, 10 cases were reported, representing a relatively high incidence rate: 1 per 4000 births. Even though the number of live births in Bahrain has increased dramatically over the last four decades (doubling from 10,000 to 20,000 per year), published studies about the incidence of HD are uncommon. In this research, we aimed to determine both the prevalence and the clinical characteristics of HD at a tertiary hospital in Bahrain. Methods This retrospective observational cross-sectional study included children diagnosed with HD at a tertiary hospital in Bahrain over the last seven years (2014-2020). Children over 10 years were excluded. Clinical data collected included gestational age, birth weight, gender, associated anomalies, clinical features at presentation, disease management, and complications. Results The prevalence of HD in Bahrain was found to be 1.3 per 10,000 live births, according to 18 patients qualified for inclusion in this study. The median age at diagnosis was 18 days; approximately 72% were males, and nearly 94% were Bahraini nationals. Three patients (16.7%) had associated anomalies including cardiac and urogenital malformations. Abdominal distention was the most common clinical presentation (83.3%) followed by constipation (77.8%). Half of the patients (50%) passed meconium within 48 hours of birth. Transanal full-thickness rectal biopsy was the method of diagnosis in most patients (83.3%). Seven patients (38.9%) were diagnosed comparatively late (beyond the neonatal period), at a mean age of 1-2 years. Significant associations between age at diagnosis and clinical presentation, initial management, or surgical intervention were not found. A total of 17 patients (94.4%) underwent the definitive surgery (transanal pull-through procedure). In this surgical group, initial colonic decompression was performed via rectal washout in six patients (35.3%) and via temporary stoma in three patients (17.8%). Laparotomy combined with the definitive surgery was necessary for six patients (35.3%). Most of the patients treated surgically had a short segment disease (70.5%). Conclusions The awareness of HD is highly important, especially with more than one-third of cases diagnosed outside the neonatal period and half of them passing meconium within 48 hours of birth. In addition, early detection of HD in the neonatal period would result in a less complicated course by reducing the number of patients requiring a multi-stage surgery and further laparotomies.
Copyright © 2021, Ali et al.

Entities:  

Keywords:  colonic aganglionosis; congenital megacolon; hirschsprung's disease; hirschsprung-associated enterocolitis; transanal pull-through procedure

Year:  2021        PMID: 33552793      PMCID: PMC7854313          DOI: 10.7759/cureus.12480

Source DB:  PubMed          Journal:  Cureus        ISSN: 2168-8184


  16 in total

1.  Embryonic development of the ganglion plexuses and the concentric layer structure of human gut: a topographical study.

Authors:  M Fu; P K H Tam; M H Sham; V C H Lui
Journal:  Anat Embryol (Berl)       Date:  2004-02-27

2.  Hirschsprung's disease prevalence in Europe: a register based study.

Authors:  Kate E Best; Marie-Claude Addor; Larraitz Arriola; Eszter Balku; Ingeborg Barisic; Fabrizio Bianchi; Elisa Calzolari; Rhonda Curran; Berenice Doray; Elizabeth Draper; Ester Garne; Miriam Gatt; Martin Haeusler; Jorieke Bergman; Babak Khoshnood; Kari Klungsoyr; Carmen Martos; Anna Materna-Kiryluk; Carlos Matias Dias; Bob McDonnell; Carmel Mullaney; Vera Nelen; Mary O'Mahony; Annette Queisser-Luft; Hanitra Randrianaivo; Anke Rissmann; Catherine Rounding; Antonin Sipek; Rosie Thompson; David Tucker; Diana Wellesley; Natalya Zymak-Zakutnia; Judith Rankin
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2014-07-26

3.  Hirschsprung's disease in the newborn.

Authors:  M D Klein; A G Coran; J R Wesley; R A Drongowski
Journal:  J Pediatr Surg       Date:  1984-08       Impact factor: 2.545

4.  Hirschsprung's disease in Japan: analysis of 3852 patients based on a nationwide survey in 30 years.

Authors:  Sachiyo Suita; Tomoaki Taguchi; Satoshi Ieiri; Takanori Nakatsuji
Journal:  J Pediatr Surg       Date:  2005-01       Impact factor: 2.545

5.  Maternal Risk Factors and Perinatal Characteristics for Hirschsprung Disease.

Authors:  Anna Löf Granström; Anna Svenningsson; Eva Hagel; Jenny Oddsberg; Agneta Nordenskjöld; Tomas Wester
Journal:  Pediatrics       Date:  2016-06-15       Impact factor: 7.124

6.  A comparison of suction and full-thickness rectal biopsy in children.

Authors:  Eleanor D Muise; Steven Hardee; Raffaella A Morotti; Robert A Cowles
Journal:  J Surg Res       Date:  2015-10-28       Impact factor: 2.192

Review 7.  Hirschsprung's disease: diagnosis and management.

Authors:  Jennifer Kessmann
Journal:  Am Fam Physician       Date:  2006-10-15       Impact factor: 3.292

Review 8.  Diagnosis of Hirschsprung's disease with particular emphasis on histopathology. A systematic review of current literature.

Authors:  Lukasz Szylberg; Andrzej Marszałek
Journal:  Prz Gastroenterol       Date:  2014-10-18

9.  Transanal endorectal pull-through procedure versus transabdominal surgery for Hirschsprung disease: A systematic review and meta-analysis.

Authors:  Bei-Lei Yan; Le-Wee Bi; Qian-Yu Yang; Xue-Si Wu; Hua-Lei Cui
Journal:  Medicine (Baltimore)       Date:  2019-08       Impact factor: 1.817

10.  Hirschsprung's disease in the UK and Ireland: incidence and anomalies.

Authors:  T J Bradnock; M Knight; S Kenny; M Nair; G M Walker
Journal:  Arch Dis Child       Date:  2017-03-09       Impact factor: 3.791

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