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Exercise performance and quality of life in children with cystic fibrosis and mildly impaired lung function: relation with antibiotic treatments and hospitalization.
Vandekerckhove, Kristof; Keyzer, Michiel; Cornette, Jasper; Coomans, Ilse; Pyl, Filip; De Baets, Frans; Schelstraete, Petra; Haerynck, Filomeen; De Wolf, Daniel; Van Daele, Sabine; Boone, Jan.
Afiliação
  • Vandekerckhove K; Department of Pediatric Cardiology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium. Kristof.vandekerckhove@uzgent.be.
  • Keyzer M; Department of Pediatric Cardiology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium.
  • Cornette J; Department of Pediatric Cardiology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium.
  • Coomans I; Department of Pediatric Cardiology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium.
  • Pyl F; Department of Paediatric Pulmonology, Ghent University Belgium, Ghent, Belgium.
  • De Baets F; Department of Paediatric Pulmonology, Ghent University Belgium, Ghent, Belgium.
  • Schelstraete P; Department of Paediatric Pulmonology, Ghent University Belgium, Ghent, Belgium.
  • Haerynck F; Department of Paediatric Pulmonology, Ghent University Belgium, Ghent, Belgium.
  • De Wolf D; Department of Pediatric Cardiology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium.
  • Van Daele S; Department of Paediatric Pulmonology, Ghent University Belgium, Ghent, Belgium.
  • Boone J; Department of Movement and Sport Sciences, Ghent University, Ghent, Belgium.
Eur J Pediatr ; 176(12): 1689-1696, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28965267
ABSTRACT
This study evaluates the impact of antibiotic treatments and hospitalization on exercise performance and health-related quality of life (QOL) in children with mild cystic fibrosis (CF) lung disease. Forty-seven children between 7 and 17 years with mild CF underwent a maximal exercise test including spiro-ergometry and filled out a QOL-questionnaire (PedsQL™). Amount of antibiotic treatments (AB) and hospitalization days in the last 3 years were reviewed. FEV1% was mildly decreased (91.7 ± 17.9 L/min, p = 0.02). Maximal oxygen consumption (VO2max), test duration and anaerobic threshold were lower compared to a control population (VO2max% 94 ± 15 vs 103 ± 13, p = 0.009). FEV1% correlated with AB and hospitalization episodes in the last year and 3 years before testing, VO2max% only correlated with AB in the last 3 years. Domains of school functioning and emotional functioning were low. Children with higher VO2max% and less AB in the last 3 years had better physical health. Physical health and school functioning were negatively correlated with hospitalization days in the last year.

CONCLUSION:

Patients with mild CF lung disease have good exercise performance although still lower than the normal population. VO2max% is affected by number of antibiotic treatments over a longer period. There is an impact of hospitalization days on quality of life. What is Known • Children with CF have lower exercise performance; there is an association between hospitalization frequency and exercise performance • Quality of life is diminished in children with CF and influenced by respiratory infections What is New • Even patients with mild CF lung disease have lower maximal exercise performance (VO 2 max) and a lower anaerobic threshold; VO 2 max is lower in children who had more antibiotic treatments in the last 3 years • School and emotional functioning are diminished in children with mild CF lung disease; hospitalization is negatively correlated with school functioning and physical functioning.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Tolerância ao Exercício / Fibrose Cística / Hospitalização Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Eur J Pediatr Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Tolerância ao Exercício / Fibrose Cística / Hospitalização Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Eur J Pediatr Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Bélgica