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. 2021 Feb 1;72(2):239-243.
doi: 10.1097/MPG.0000000000002921.

One-year Outcomes of Congenital Duodenal Obstruction: A Population-based Study

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One-year Outcomes of Congenital Duodenal Obstruction: A Population-based Study

George S Bethell et al. J Pediatr Gastroenterol Nutr. .

Abstract

Objectives: Congenital duodenal obstruction (CDO) occurs in 1.2 per 10,000 live births and is frequently associated with other anomalies, most commonly cardiac. The aim of this study was to report important outcomes to 1 year following surgical repair.

Methods: This was a prospective population-based study using the British Association of Paediatric Surgeons Congenital Anomaly Surveillance System. Cases were identified at specialist pediatric surgical centres in the United Kingdom during a 12-month period starting in March 2016. Outcomes were recorded at 1 year following surgical repair.

Results: There were 100 infants with possible follow-up at 1 year and follow-up was achieved in 80 of these (80%) of whom 76 were alive at 1 year. The remainder had been discharged home, although one remained on parenteral nutrition. Five (6.1%) infants underwent repeat surgery for reasons related to CDO and overall 23 (23%) experienced at least 1 central venous catheter-related complication within 1 year. Overall mortality either before repair or within 1 year following surgical repair was 8.4% (95% CI 2.5%-14.4%), no deaths were related to CDO.

Conclusions: One year outcomes for CDO are generally very good with poor outcomes typically related to comorbidities. These data are useful for national benchmarking and parental counselling.

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Conflict of interest statement

The authors report no conflicts of interest.

References

    1. Bethell GS, Long AM, Knight M, et al. BAPS-CASS. Congenital duodenal obstruction in the UK: a population-based study. Arch Dis Child Fetal Neonatal Ed 2020; 105:178–183.
    1. Singh MV, Richards C, Bowen JC. Does Down syndrome affect the outcome of congenital duodenal obstruction? Pediatr Surg Int 2004; 20:586–589.
    1. Mustafawi AR, Hassan ME. Congenital duodenal obstruction in children: a decade's experience. Eur J Pediatr Surg 2008; 18:93–97.
    1. Gfroerer S, Theilen TM, Fiegel HC, et al. Comparison of outcomes between complete and incomplete congenital duodenal obstruction. World J Gastroenterol 2019; 25:3787–3797.
    1. Escobar MA, Ladd AP, Grosfeld JL, et al. Duodenal atresia and stenosis: long-term follow-up over 30 years. J Pediatr Surg 2004; 39:867–871.

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