Literature DB >> 28244688

Determinants of exercise capacity in school-aged esophageal atresia patients.

Leontien C C Toussaint-Duyster1,2, Monique H M van der Cammen-van Zijp1,2, Marjolein Spoel1, Mhanfei Lam1, Rene M H Wijnen1, Johan C de Jongste3, Dick Tibboel1, Joost van Rosmalen4, Hanneke IJsselstijn1.   

Abstract

BACKGROUND AND AIMS: Data on long-term outcome of exercise capacity in school-aged children with esophageal atresia (EA) are scarce. We evaluated maximal exercise capacity and its relation to lung function. Moreover, we studied other possible determinants of exercise capacity and lung function.
METHODS: Exercise capacity of 63 children with EA born 1999-2007 was evaluated at the age of 8 years with the Bruce-protocol. Dynamic and static lung volumes, bronchodilator response and diffusion capacity were measured. Furthermore, perinatal characteristics, hospital admissions for lower respiratory tract infections (RTIs), RTIs treated with antibiotics in the past year, symptoms of gastroesophageal reflux, weight-for-height, and sports participation were evaluated as other potential determinants.
RESULTS: Exercise capacity was significantly below normal: mean (SD) SDS -0.91 (0.97); P < 0.001. All spirometric parameters were significantly below normal with significant reversibility of airflow obstruction in 13.5% of patients. Static lung volumes were significantly decreased (mean (SD) SDS TLChe -1.06 (1.29); P < 0.001). Diffusion capacity corrected for alveolar volume was normal (mean (SD) SDS KCO -0.12 (1.04)). Exercise capacity was positively associated with total lung capacity and negatively with SDS weight-for-height. Spirometric parameters were negatively associated with congenital cardiac malformation, duration of ventilation, and persistent respiratory morbidity.
CONCLUSION: Eight-year-old children with EA had reduced exercise capacity which was only associated with the reduction in TLChe and higher SDS weight-for-height. We speculate that diminished physical activity with recurrent respiratory tract infections may also play a role in reduced exercise capacity. This should be subject to further research to optimize appropriate intervention.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  congenital malformations; esophageal atresia; exercise capacity; pulmonary function testing; respiratory tract infections; school-aged children

Mesh:

Substances:

Year:  2017        PMID: 28244688     DOI: 10.1002/ppul.23687

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  4 in total

1.  Physical Fitness and Locomotor Skills in Children With Esophageal Atresia-A Case Control Pilot Study.

Authors:  Tatjana T König; Oliver J Muensterer
Journal:  Front Pediatr       Date:  2018-11-06       Impact factor: 3.418

2.  Pulmonary function in children and adolescents after esophageal atresia repair.

Authors:  Felipe Donoso; Hans Hedenström; Andrei Malinovschi; Helene E Lilja
Journal:  Pediatr Pulmonol       Date:  2019-09-18

3.  Cardiorespiratory performance capacity and airway microbiome in patients following primary repair of esophageal atresia.

Authors:  Christoph Arneitz; Jana Windhaber; Christoph Castellani; Bernhard Kienesberger; Ingeborg Klymiuk; Günter Fasching; Holger Till; Georg Singer
Journal:  Pediatr Res       Date:  2020-11-06       Impact factor: 3.756

4.  Cardiorespiratory performance and locomotor function of patients with anorectal malformations.

Authors:  Christoph Arneitz; Jana Windhaber; Christina Flucher; Paolo Gasparella; Eva Amerstorfer; Andrea Huber-Zeyringer; Christoph Castellani; Georg Singer; Holger Till
Journal:  Sci Rep       Date:  2021-09-23       Impact factor: 4.379

  4 in total

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