The repeatability of submaximal endurance exercise testing in cystic fibrosis

Submaximal endurance cycle ergometer exercise tests are used to measure the efficacy of an exercise intervention, but the repeatability of these tests in patients with cystic fibrosis (CF) has not been established. The purpose of this study was to examine the repeatability of submaximal endurance te...

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Bibliographic Details
Published inPediatric pulmonology Vol. 42; no. 1; pp. 75 - 82
Main Authors Barry, Sinead C., Gallagher, Charles G.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.01.2007
Wiley-Liss
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Summary:Submaximal endurance cycle ergometer exercise tests are used to measure the efficacy of an exercise intervention, but the repeatability of these tests in patients with cystic fibrosis (CF) has not been established. The purpose of this study was to examine the repeatability of submaximal endurance testing in stable CF. Fifteen adults with CF underwent two submaximal endurance tests carried out over a 7‐day period. A subset of six subjects returned 28 days later for a third submaximal endurance test. Workload was set at 80% of maximum workload and exercise was performed to exhaustion. Oxygen consumption, minute ventilation, tidal volume, carbon dioxide output, respiratory rate, heart rate, and oxygen saturation were measured at rest, at end exercise and at four matched times during the submaximal endurance tests (20, 40, 60, and 80% of exercise duration calculated from the first endurance test). Submaximal endurance test time was highly repeatable with no significant learning effect identified on multiple testing. Submaximal endurance exercise time demonstrated a variability of 5.7% which is consistent with high levels of repeatability. Metabolic, ventilatory and cardiac variables were all also highly reproducible between test days. Submaximal endurance testing is repeatable in stable CF, confirming that submaximal endurance tests are a reliable tool for assessment of therapeutic benefit in patients with CF. Pediatr Pulmonol. 2007; 42:75–82. © 2006 Wiley‐Liss, Inc.
Bibliography:ark:/67375/WNG-CXGRMR8G-X
ArticleID:PPUL20547
This work was performed at Department of Respiratory Medicine, St. Vincent's University Hospital, Elm Park, Dublin 4, Ireland.
National Rehabilitation Board
istex:7618F7FE4060EBDBA613B8920B65A594FBEC06BD
Health Research Board
Cystic Fibrosis Research Trust
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:8755-6863
1099-0496
DOI:10.1002/ppul.20547