Eur J Pediatr Surg 2020; 30(05): 447-451
DOI: 10.1055/s-0039-1695789
Original Article

Multicenter Study of 342 Anorectal Malformation Patients: Age, Gender, Krickenbeck Subtypes, and Associated Anomalies

Tahmina Banu
1   Global Initiative for Children’s Surgery (GICS)
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
,
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
3   Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
,
Maryam Ghavami Adel
1   Global Initiative for Children’s Surgery (GICS)
4   Department of Pediatric Surgery, Tehran University of Medical Sciences, Tehran, Iran
,
Kokila Lakhoo
1   Global Initiative for Children’s Surgery (GICS)
5   Oxford Children's Hospital and University of Oxford, Oxford, United Kingdom
,
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
,
Arni Das
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
,
Nugayer Sharmeen
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
,
Benjamin Yapo
1   Global Initiative for Children’s Surgery (GICS)
6   National Department of Health, Mt Hagen Highlands Regional Hospital, Mount Hagen, Papua New Guinea
,
Kazi Md Noor-ul Ferdous
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
7   Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh
,
Kh Ahasanul Kabir
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
7   Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh
,
Mirza Kamrul Zahid
1   Global Initiative for Children’s Surgery (GICS)
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
8   Shaheed Suhrawardy Medical College and Hospital, Dhaka, Bangladesh
,
Kathryn Ford
1   Global Initiative for Children’s Surgery (GICS)
5   Oxford Children's Hospital and University of Oxford, Oxford, United Kingdom
,
Md Qumrul Ahsan
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
9   Department of Pediatric Surgery, Chattogram Ma O Shishu Hospital, Bangladesh
,
Mastura Akter
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
,
Md Afruzul Alam
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
,
Mozammel Hoque
2   Chittagong Research Institute for Children Surgery, Chittagong, Bangladesh
9   Department of Pediatric Surgery, Chattogram Ma O Shishu Hospital, Bangladesh
› Author Affiliations
Funding None.

Abstract

Introduction Published studies based on Krickenbeck classification of anorectal malformations (ARMs) are still insufficient to assess the global as well as regional relative incidence of different ARM subtypes, gender distribution, and associated anomalies. The primary purpose of this study was to provide an estimate of those in Global Initiative for Children's Surgery (GICS) research group.

Materials and Methods We collected ARM data prospectively for 1 year from four institutes of different geographic locations. A total of 342 patients were included in this study (195, 126, 11, and 10 from Bangladesh, Iran, Papua New Guinea, and Oxford, United Kingdom, respectively).

Results Overall male to female ratio was 1:1. The most frequent ARM subtype was perineal fistula (23.7% = 81/342). About 48.5% (166/342) patients had at least one associated anomaly. Cardiac and genitourinary systems were the most commonly affected systems, 31.6% (108/342) and 18.4% (63/342), respectively. These organ-systems were followed by anomalies of vertebral/spinal (9.9% = 34/342), musculoskeletal (4.4% = 15/342), and gastrointestinal/abdominal (3.2% = 11/342) systems. Rectovesical fistula had the highest percentage (96.4% = 27/28) of associated anomalies. About 18.1% (62/342) patients had multiple anomalies. ARMs (both isolated and with associated anomalies) occurred equally in males and females. Comparison between patients from Bangladesh and Iran showed differences in relative incidence in ARM subtypes. In addition, Iranian patient group had higher percentage of associated anomalies compared with Bangladeshi (73 vs. 35.4%).

Conclusion Our study provides important insights about ARM subtypes, gender distribution and associated anomalies based on Krickenbeck classification especially from Bangladesh and Iran.



Publication History

Received: 21 March 2019

Accepted: 14 July 2019

Article published online:
26 October 2019

© 2020. Thieme. All rights reserved.

Georg Thieme Verlag KG
Stuttgart · New York

 
  • References

  • 1 Wijers CH, van Rooij IA, Marcelis CL, Brunner HG, de Blaauw I, Roeleveld N. Genetic and nongenetic etiology of nonsyndromic anorectal malformations: a systematic review. Birth Defects Res C Embryo Today 2014; 102 (04) 382-400
  • 2 Levitt MA, Peña A. Anorectal malformations. Orphanet J Rare Dis 2007; 2: 33
  • 3 Zhang T, Tang XB, Wang LL. , et al. Mutations and down-regulation of CDX1 in children with anorectal malformations. Int J Med Sci 2013; 10 (02) 191-197
  • 4 Hsu JSJ, So M, Tang CSM. , et al. De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca. Hum Mol Genet 2018; 27 (02) 351-358
  • 5 Holschneider A, Hutson J, Peña A. , et al. Preliminary report on the International Conference for the Development of Standards for the Treatment of Anorectal Malformations. J Pediatr Surg 2005; 40 (10) 1521-1526
  • 6 Government of the People's Republic of Bangladesh. Ministry of Health and Family Welfare (MOHFW). Health bulletin 2017. Available at: http://www.dghs.gov.bd/images/docs/Publicaations/HealthBulletin2017Final13_01_2018.pdf . Accessed on 29.1.2019
  • 7 Solomon BD. VACTERL/VATER Association. Orphanet J Rare Dis 2011; 6: 56-56
  • 8 de Blaauw I, Wijers CH, Schmiedeke E. , et al. First results of a European multi-center registry of patients with anorectal malformations. J Pediatr Surg 2013; 48 (12) 2530-2535
  • 9 Minneci PC, Kabre RS, Mak GZ. , et al; Midwest Pediatric Surgery Consortium. Screening practices and associated anomalies in infants with anorectal malformations: results from the Midwest Pediatric Surgery Consortium. J Pediatr Surg 2018; 53 (06) 1163-1167
  • 10 Endo M, Hayashi A, Ishihara M. , et al; Steering Committee of Japanese Study Group of Anorectal Anomalies. Analysis of 1,992 patients with anorectal malformations over the past two decades in Japan. J Pediatr Surg 1999; 34 (03) 435-441
  • 11 van Rooij IA, Wijers CH, Rieu PN. , et al. Maternal and paternal risk factors for anorectal malformations: a Dutch case-control study. Birth Defects Res A Clin Mol Teratol 2010; 88 (03) 152-158
  • 12 Nah SA, Ong CC, Lakshmi NK, Yap TL, Jacobsen AS, Low Y. Anomalies associated with anorectal malformations according to the Krickenbeck anatomic classification. J Pediatr Surg 2012; 47 (12) 2273-2278
  • 13 Banu T, Chowdhury TK, Hoque M, Rahman MA. Cloacal malformation variants in male. Pediatr Surg Int 2013; 29 (07) 677-682
  • 14 Hofmann AD, Puri P. Association of Hirschsprung's disease and anorectal malformation: a systematic review. Pediatr Surg Int 2013; 29 (09) 913-917
  • 15 Karim A, Akter M, Aziz TT. , et al. Epidemiological characteristics of Hirschsprung's disease (HSCR): results of a case series of fifty patients from Bangladesh. J Pediatr Surg 2018; 53 (10) 1955-1959
  • 16 Theron AP, Brisighelli G, Theron AE, Leva E, Numanoglu A. Comparison in the incidence of anorectal malformations between a first- and third-world referral center. Pediatr Surg Int 2015; 31 (08) 759-764