Airflow limitation following cardiopulmonary exercise testing and heavy-intensity intermittent exercise in children with cystic fibrosis.

2.50
Hdl Handle:
http://hdl.handle.net/11287/607445
Title:
Airflow limitation following cardiopulmonary exercise testing and heavy-intensity intermittent exercise in children with cystic fibrosis.
Authors:
Stevens, D.; Oades, Patrick ( 0000-0001-5265-6923 ) ; Williams, Craig A.
Abstract:
The clinical importance of exercise testing and training in the healthcare management of young patients with cystic fibrosis (CF) is growing. The aim of the present study was to determine the incidence of airflow limitation following cardiopulmonary exercise testing (CPET) and heavy-intensity intermittent exercise (HIIE) in young patients with CF. Nineteen young patients with CF and respective paired-matched controls performed CPET and HIIE on separate days. Forced expiratory volume in one second (FEV1) was measured pre- and post each exercise modality. A fall in FEV1 of 10 % or greater was used to define airflow limitation. The incidence of airflow limitation was significantly greater in the CF group than in the controls following CPET (32 vs. 5 %; p = 0.03); however, no significant difference in the incidence of airflow limitation was shown following HIIE between the CF group and controls (11 vs. 16 %; p = 0.64).
Citation:
Airflow limitation following cardiopulmonary exercise testing and heavy-intensity intermittent exercise in children with cystic fibrosis. 2015, 174 (2):251-7 Eur. J. Pediatr.
Publisher:
Springer
Journal:
European journal of pediatrics
Issue Date:
Feb-2015
URI:
http://hdl.handle.net/11287/607445
DOI:
10.1007/s00431-014-2387-2
PubMed ID:
25119817
Additional Links:
http://dx.doi.org/10.1007/s00431-014-2387-2
Type:
Journal Article; Research Support, Non-U.S. Gov't
Language:
en
ISSN:
1432-1076
Appears in Collections:
2015 RD&E publications; Paediatrics; Honorary contracts publications

Full metadata record

DC FieldValue Language
dc.contributor.authorStevens, D.en
dc.contributor.authorOades, Patricken
dc.contributor.authorWilliams, Craig A.en
dc.date.accessioned2016-04-29T15:13:51Zen
dc.date.available2016-04-29T15:13:51Zen
dc.date.issued2015-02en
dc.identifier.citationAirflow limitation following cardiopulmonary exercise testing and heavy-intensity intermittent exercise in children with cystic fibrosis. 2015, 174 (2):251-7 Eur. J. Pediatr.en
dc.identifier.issn1432-1076en
dc.identifier.pmid25119817en
dc.identifier.doi10.1007/s00431-014-2387-2en
dc.identifier.urihttp://hdl.handle.net/11287/607445en
dc.description.abstractThe clinical importance of exercise testing and training in the healthcare management of young patients with cystic fibrosis (CF) is growing. The aim of the present study was to determine the incidence of airflow limitation following cardiopulmonary exercise testing (CPET) and heavy-intensity intermittent exercise (HIIE) in young patients with CF. Nineteen young patients with CF and respective paired-matched controls performed CPET and HIIE on separate days. Forced expiratory volume in one second (FEV1) was measured pre- and post each exercise modality. A fall in FEV1 of 10 % or greater was used to define airflow limitation. The incidence of airflow limitation was significantly greater in the CF group than in the controls following CPET (32 vs. 5 %; p = 0.03); however, no significant difference in the incidence of airflow limitation was shown following HIIE between the CF group and controls (11 vs. 16 %; p = 0.64).en
dc.language.isoenen
dc.publisherSpringeren
dc.relation.urlhttp://dx.doi.org/10.1007/s00431-014-2387-2en
dc.rightsArchived with thanks to European journal of pediatricsen
dc.subjectWessex Classification Subject Headings::Paediatricsen
dc.titleAirflow limitation following cardiopulmonary exercise testing and heavy-intensity intermittent exercise in children with cystic fibrosis.en
dc.typeJournal Articleen
dc.typeResearch Support, Non-U.S. Gov'ten
dc.identifier.journalEuropean journal of pediatricsen
dc.type.versionPublisheden

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