AbstractBackgroundDisease progression in cystic fibrosis (CF) is marked by worsening exercise tolerance. Further, maximal exercise capacity (VO2 peak) correlates with survival in CF, but maximal tests are uncomfortable and resource-intensive. A three-minute step test (STEP) has been validated in CF. Heart rate (HR) recovery after exercise correlates with all-cause mortality in adult non-CF populations. We compared HR recovery after the three-minute step test with VO2 peak in children with CF.Methods: Twenty-four children with CF performed STEP and a maximal exercise test. Correlation between the tests was assessed.Results: Maximum HR on STEP was lower than on the maximal test (140 vs. 190, p<0.01). Peak HR during STEP correlated inversely w...
Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause ...
This is the author accepted manuscript. The final version is available to members only from BASES vi...
Background: While exercise testing is increasingly used as a prognostic indicator in cystic fibrosis...
AbstractBackgroundDisease progression in cystic fibrosis (CF) is marked by worsening exercise tolera...
Clinical TrialJournal ArticleResearch Support, Non-U.S. Gov'tOBJECTIVES: Measuring aerobic fitness (...
International Journal of Exercise Science 14(3): 177-186, 2021. The purpose of the study was to asse...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
Objectives: Exercise testing in patients with cystic fibrosis (CF) has become an important tool in a...
BACKGROUND: We aimed to characterize the cardiopulmonary response during a 1-min sit-to-stand (STS) ...
Conference poster displayed at the Clinical Trials Symposium, RD&E Exeter, 5/11/15
Background: Regular assessment of exercise capacity in CF is a useful tool to facilitate exercise pr...
AbstractBackgroundThe reproducibility of cardiopulmonary exercise testing (CPET) has not been establ...
International Journal of Exercise Science 15(3): 1381-1394, 2022. The purpose of the study was to ev...
Background: Reduced exercise tolerance is a clear hallmark of cystic fibrosis (CF) and also an impor...
Author manuscript version of an article published in the Journal of Cystic Fibrosis. The definitive ...
Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause ...
This is the author accepted manuscript. The final version is available to members only from BASES vi...
Background: While exercise testing is increasingly used as a prognostic indicator in cystic fibrosis...
AbstractBackgroundDisease progression in cystic fibrosis (CF) is marked by worsening exercise tolera...
Clinical TrialJournal ArticleResearch Support, Non-U.S. Gov'tOBJECTIVES: Measuring aerobic fitness (...
International Journal of Exercise Science 14(3): 177-186, 2021. The purpose of the study was to asse...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
Objectives: Exercise testing in patients with cystic fibrosis (CF) has become an important tool in a...
BACKGROUND: We aimed to characterize the cardiopulmonary response during a 1-min sit-to-stand (STS) ...
Conference poster displayed at the Clinical Trials Symposium, RD&E Exeter, 5/11/15
Background: Regular assessment of exercise capacity in CF is a useful tool to facilitate exercise pr...
AbstractBackgroundThe reproducibility of cardiopulmonary exercise testing (CPET) has not been establ...
International Journal of Exercise Science 15(3): 1381-1394, 2022. The purpose of the study was to ev...
Background: Reduced exercise tolerance is a clear hallmark of cystic fibrosis (CF) and also an impor...
Author manuscript version of an article published in the Journal of Cystic Fibrosis. The definitive ...
Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause ...
This is the author accepted manuscript. The final version is available to members only from BASES vi...
Background: While exercise testing is increasingly used as a prognostic indicator in cystic fibrosis...