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Upper Gastrointestinal Endoscopy with biopsy in paediatric feeding disorders
Robyn Robinson1, Nicholas Placone2, Mitchell Katz1,3
1CHOC Children's, Orange, CA, USA.
Insights
Children with persistent feeding problems show higher rates of eosinophilic esophagitis (EoE) compared to controls. Upper endoscopy may be warranted for unresolved pediatric feeding disorders.
Area of Science:
- Pediatric Gastroenterology
- Digestive Endoscopy
- Esophageal Disorders
Background:
- Persistent feeding problems in children are a common concern.
- Upper gastrointestinal (GI) pathology can contribute to feeding difficulties.
- The role of endoscopy in evaluating pediatric feeding disorders requires further investigation.
Purpose of the Study:
- To compare upper GI pathology found during endoscopy in children with feeding problems versus controls.
- To determine the prevalence of esophagitis, including eosinophilic esophagitis (EoE), in these groups.
Main Methods:
- Esophagogastroduodenoscopy (EGD) biopsy results were analyzed.
- Two age-matched cohorts were studied: 86 children in a feeding clinic and 86 controls referred for other reasons.
- Biopsy findings were statistically compared between the feeding and control groups.
Main Results:
- Abnormal endoscopy biopsies were found in 57% of the feeding cohort and 53% of controls.
- Microscopic esophagitis was present in 30% of the feeding group and 26% of controls (p=0.98).
- Eosinophilic esophagitis (EoE) was diagnosed in 15.1% of the feeding group and 8% of controls (p=0.15), a significant increase.
Conclusions:
- While abnormal biopsies and microscopic esophagitis rates were similar, EoE incidence was notably higher in children with feeding disorders.
- The tripling of EoE incidence in the feeding group compared to previous reports warrants attention.
- Persistent pediatric feeding disorders may necessitate upper endoscopy evaluation.
Aim:
Our aim was to evaluate upper GI pathology found endoscopically among children seen in a GI feeding clinic for persistent feeding problems compared with controls.
Methods:
Esophagogastroduodenoscopy biopsy results were examined among two cohorts of children. The first group included 86 children evaluated in a gastroenterology feeding clinic for paediatric feeding disorders. A comparison was made with an age-matched control group of 86 children referred for endoscopy for conditions other than disordered feeding.
Results:
In the feeding cohort, 57% had abnormal endoscopy biopsies. These included 30% with microscopic esophagitis and 15.1% with eosinophilic esophagitis (EoE). Among the controls, 53% had abnormal biopsies, which included 26% with microscopic esophagitis and 8% with eosinophilic esophagitis. The statistical comparison between groups included p = 0.98 for microscopic esophagitis and p = 0.15 for eosinophilic esophagitis.
Conclusion:
Results demonstrated similar prevalence of abnormal endoscopy biopsies and microscopic esophagitis in both groups. The incidence of eosinophilic esophagitis in the feeding group triples that of previous reports and nearly doubles controls. Our findings suggest paediatric feeding disorders which do not resolve may warrant investigation by upper endoscopy.
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