Esophageal atresia is the most common congenital anomaly of the esophagus and is caused by abnormal development of the esophagus during intrauterine life. In children with esophageal atresia, structural abnormalities due to congenital anomalies and tracheoesophageal fistula, tracheomalacia, respiratory problems, recurrent respiratory tract infections, structural abnormalities, surgical interventions for repair and treatment, and decreased physical activity levels may negatively affect pulmonary function, effective coughing, muscle strength, exercise capacity, posture, motor function, and quality of life. This study aims to compare physical characteristics, body composition, pulmonary function and muscle strength, peak cough flow, posture assessment, peripheral muscle strength test, motor function, exercise capacity, physical activity level, fatigue, frailty and quality of life between children with esophageal atresia and their healthy peers.
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Forced vital capacity
Timeframe: 1st day
Forced expiratory volume in one second
Timeframe: 1st day
Forced expiratory volume in one second/forced vital capacity ratio
Timeframe: 1st day
Peak expiratory flow
Timeframe: 1st day
Forced mid-expiratory flow
Timeframe: 1st day
Body composition
Timeframe: 1st day
Maximal inspiratory pressure
Timeframe: 1st day
Maximal expiratory pressure
Timeframe: 1st day
Peak cough flow
Timeframe: 1st day
Hand grip strength
Timeframe: 1st day
Knee extensor muscle strength
Timeframe: 1st day
Shoulder abductor muscle strength
Timeframe: 1st day
Motor function
Timeframe: 1st day
Functional exercise capacity
Timeframe: 1st day
Physical activity level
Timeframe: 1st day
Exercise capacity
Timeframe: 1 week after other assessments
Frailty
Timeframe: 1st day