Literature DB >> 8863241

Maximal oxygen consumption and stress performance in children operated on for congenital diaphragmatic hernia.

A Zaccara1, A Turchetta, A Calzolari, B Iacobelli, A Nahom, M C Lucchetti, P Bagolan, M Rivosecchi, A G Coran.   

Abstract

The long-term follow-up of patients operated on for congenital diaphragmatic hernia (CDH) at birth has been extensively evaluated, both clinically and with respect to respiratory function. However, little is known about the sports practice and stress performance of these subjects. Fifteen of 107 patients operated on for CDH underwent exercise stress testing with a stepwise increase in workload. A questionnaire was provided, which requested information on sports practice and lifestyle. Maximal oxygen consumption [Vo2 max] was measured along with dynamic lung volumes. Clinical examination included a whole-body assessment (height, weight, skinfolds) and vital parameters (heart rate and blood pressure). Fifteen healthy children who practiced regular physical activity (2 to 4 hours/week) served as controls. All the CDH patients experienced a good lifestyle, but only 8 of them were participating in sports. Exercise duration and Vo2 max were significantly lower for the CDH patients, and were lowest for the sedentary patients. Therefore, the reduced Vo2 max of these otherwise healthy children most likely represents a lower degree of physical fitness rather than decreased respiratory function. Fitness is an expression of well-being; thus, there is evidence that these patients could safely participate in competitive motor activities.

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Year:  1996        PMID: 8863241     DOI: 10.1016/s0022-3468(96)90094-9

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  6 in total

Review 1.  Adult outcome of congenital lower respiratory tract malformations.

Authors:  M S Zach; E Eber
Journal:  Thorax       Date:  2001-01       Impact factor: 9.139

2.  Pulmonary function, exercise performance, and growth in survivors of congenital diaphragmatic hernia.

Authors:  S S Marven; C M Smith; D Claxton; J Chapman; H A Davies; R A Primhak; C V Powell
Journal:  Arch Dis Child       Date:  1998-02       Impact factor: 3.791

3.  Mid- and long-term effects on pulmonary perfusion, anatomy and diaphragmatic motility in survivors of congenital diaphragmatic hernia.

Authors:  Francesco Arena; Sergio Baldari; Antonio Centorrino; Maria Pia Calabrò; Giovanni Pajno; Giovanni Pajino; Salvatore Arena; Filippo Andò; Biagio Zuccarello; Giuseppe Romeo
Journal:  Pediatr Surg Int       Date:  2005-10-21       Impact factor: 1.827

Review 4.  The long-term follow-up of patients with a congenital diaphragmatic hernia: a broad spectrum of morbidity.

Authors:  M G Peetsold; H A Heij; C M F Kneepkens; A F Nagelkerke; J Huisman; R J B J Gemke
Journal:  Pediatr Surg Int       Date:  2008-10-08       Impact factor: 1.827

5.  Lung volumes, ventricular function and pulmonary arterial flow in children operated on for left-sided congenital diaphragmatic hernia: long-term results.

Authors:  Nasreddin Abolmaali; Arne Koch; Knut Götzelt; Gabriele Hahn; Guido Fitze; Christian Vogelberg
Journal:  Eur Radiol       Date:  2010-02-18       Impact factor: 5.315

6.  Congenital diaphragmatic hernia and exercise capacity, a longitudinal evaluation.

Authors:  Leontien C C Toussaint-Duyster; Monique H M van der Cammen-van Zijp; Johan C de Jongste; Dick Tibboel; Rene M H Wijnen; Saskia J Gischler; Joost van Rosmalen; Hanneke IJsselstijn
Journal:  Pediatr Pulmonol       Date:  2019-02-11
  6 in total

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