Literature DB >> 33027836

Parent-Reported Feeding Difficulties among Children Born with Esophageal Atresia: Prevalence and Early Risk Factors.

Sofie Örnö Ax1, Kate Abrahamsson2, Vladimir Gatzinsky2, Linus Jönsson2, Michaela Dellenmark-Blom3.   

Abstract

INTRODUCTION: We aimed to describe the prevalence of observable feeding difficulties during mealtimes among children with repaired esophageal atresia (EA) and to determine their early predictors.
MATERIALS AND METHODS: A survey, based on parents' reports and concerning difficulties in EA children's nutritional intake, was performed with the help of 114 families of 2 to 17-year-old EA patients. Neonatal and clinical/surgical data were collected from medical records. Comparisons were made of the prevalence n (%) of feeding difficulties between children in three age groups (2 to 7 years, 8 to 12 years, or 13 to 17 years of age) using the Mantel-Haenszel chi-square test. Logistic regression identified outcome predictors (odds ratio: 95% confidence interval). Predictors with p ≤ 0.1 in the univariable analysis were included in multiple regression analysis (p < 0.05).
RESULTS: Seventy-five percent of the young children aged 2 to 7, (median number of feeding difficulties: 2), 61% of school-aged children aged 8 to 12 (median number of feeding difficulties: 1), and 60% patients in the teenage group, aged 13 to 17, (median number of feeding difficulties: 1), reported feeding difficulties. Surgical complications after EA repair independently predicted children having a gastrostomy (p ≤ 0.01), using a food infusion pump (p ≤ 0.01), taking small portions to facilitate eating (p = 0.01), and needing >30 minutes to finish a main meal (p = 0.02). Congenital independent predictors were VACTERL, low birth weight, and preterm birth.
CONCLUSION: Parentally observed feeding difficulties were commonly reported during early childhood, although prevalence decreases in older age groups. Several congenital and surgical factors were identified as independent predictors of complicated nutritional intake patterns. Thieme. All rights reserved.

Entities:  

Year:  2020        PMID: 33027836     DOI: 10.1055/s-0040-1716880

Source DB:  PubMed          Journal:  Eur J Pediatr Surg        ISSN: 0939-7248            Impact factor:   2.191


  3 in total

1.  Postoperative morbidity and health-related quality of life in children with delayed reconstruction of esophageal atresia: a nationwide Swedish study.

Authors:  Michaela Dellenmark-Blom; Sofie Örnö Ax; Elin Öst; Jan F Svensson; Ann-Marie Kassa; Linus Jönsson; Kate Abrahamsson; Vladimir Gatzinsky; Pernilla Stenström; AnnaMaria Tollne; Erik Omling; Helene Engstrand Lilja
Journal:  Orphanet J Rare Dis       Date:  2022-06-20       Impact factor: 4.303

2.  Factors of family impact in a Swedish-German cohort of children born with esophageal atresia.

Authors:  John E Chaplin; Julia H Quitmann; Michaela Dellenmark-Blom; Kate Abrahamsson; Jens Dingemann; Stefanie Witt; Carmen Dingemann; Linus Jönsson; Vladimir Gatzinsky; Monika Bullinger; Benno M Ure
Journal:  Orphanet J Rare Dis       Date:  2022-05-21       Impact factor: 4.303

3.  Family mealtime behaviors in children who are tube fed and preparing to transition to oral eating: A comparison to other pediatric populations.

Authors:  Andrea M Garcia; Marshall T Beauchamp; Susana R Patton; Sarah Edwards; Meredith L Dreyer Gillette; Ann M Davis
Journal:  J Health Psychol       Date:  2020-12-18
  3 in total

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