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Feeding disorders in children with oesophageal atresia: a cross-sectional study
Aurélie Pham1, Emmanuelle Ecochard-Dugelay2, Arnaud Bonnard3
1AP-HP, Department of Neonatology, Armand-Trousseau Childrens Hospital, Paris, France aurelie.pham@inserm.fr.
Insights
Paediatric feeding disorders (PFD) are common in children with oesophageal atresia (OA), affecting 42% of those studied. Early screening for PFD is crucial for improving growth and outcomes in these children.
Area of Science:
- Pediatric Surgery
- Neonatology
- Gastroenterology
- Developmental Pediatrics
Background:
- Survival rates for patients with oesophageal atresia (OA) have improved due to advancements in surgical and neonatal care.
- Despite improved survival, conditions associated with OA, such as feeding difficulties, remain a significant challenge.
- Paediatric feeding disorders (PFD) in children with OA are not well-described, impacting their development and growth.
Purpose of the Study:
- To describe the prevalence and characteristics of PFD in children born with OA using a standardized feeding scale.
- To identify conditions associated with the development of PFD in this patient population.
Main Methods:
- A national cohort study involving children with OA born between 2013 and 2016.
- Parents completed the French version of the Montreal Children's Hospital Feeding Scale.
- Data from 145 children were analyzed, with a focus on PFD and associated factors.
Main Results:
- 42% of the included children (n=145) developed PFD.
- Chronic respiratory symptoms were associated with an increased risk of PFD.
- 16% of children with PFD had no other complicating conditions besides OA.
Conclusions:
- PFD are highly prevalent in children with OA, necessitating systematic screening.
- There is no specific patient profile that predicts PFD risk, emphasizing the need for universal screening.
- Early identification and management of PFD can improve patient outcomes, particularly growth.
Introduction:
With advances in surgical and neonatal care, the survival of patients with oesophageal atresia (OA) has improved over time. Whereas a number of OA-related conditions (delayed primary anastomosis, anastomotic stricture and oesophageal dysmotility) may have an impact on feeding development and although children with OA experience several oral aversive events, paediatric feeding disorders (PFD) remain poorly described in this population. The primary aim of our study was to describe PFD in children born with OA, using a standardised scale. The secondary aim was to determine conditions associated with PFD.
Methods:
The Feeding Disorders in Children with Oesophageal Atresia Study is a national cohort study based on the OA registry from the French National Network. Parents of children born with OA between 2013 and 2016 in one of the 22 participating centres were asked to complete the French version of the Montreal Children's Hospital Feeding Scale.
Results:
Of the 248 eligible children, 145 children, with a median age of 2.3 years (Q1-Q3 1.8-2.9, min-max 1.1-4.0 years), were included. Sixty-one children (42%) developed PFD; 13% were tube-fed (n=19). Almost 40% of children with PFD failed to thrive (n=23). The presence of chronic respiratory symptoms was associated with the development of PFD. Ten children with PFD (16%) had no other condition or OA-related complication.
Conclusion:
PFD are common in children with OA, and there is no typical profile of patients at risk of PFD. Therefore, all children with OA require a systematic screening for PFD that could improve the care and outcomes of patients, especially in terms of growth.
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