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Reproducibility of maximal cardiopulmonary exercise testing for young cystic fibrosis patients

Research output: Contribution to journalArticlepeer-review

  • Dr Zoe Saynor
  • Alan R. Barker
  • Patrick John Oades
  • Craig Anthony Williams
Background
The reproducibility of cardiopulmonary exercise testing (CPET) has not been established in young cystic fibrosis (CF) patients using a valid protocol.

Methods
Thirteen 7–18 year olds completed three CPETs, separated by 48 h and 4–6 weeks. CPET involved a ramp-incremental cycling test with supramaximal verification.

Results
Maximal oxygen uptake was repeatedly determined with no learning effect and typical errors expressed as a coefficient of variation (TECV%) of 9.3% (48 h) and 13.3% (4–6 weeks). The reproducibility of additional parameters of aerobic function [gas exchange threshold (TECV%: 11.2%, 16.8%); View the MathML sourceO2 mean response time (TECV%: 37.8%, 89.4%); View the MathML sourceO2 gain (TECV%: 17.4%, 24.5%)] and clinical utility [e.g. SaO2% (TECV%: 2.2%, 3.1%); ventilatory drive (View the MathML sourceE/View the MathML sourceCO2-slope) (TECV%: 7.8%, 17.7%)] was also established over the short- and the medium-term, respectively.

Conclusion
These results establish limits of variability to determine meaningful changes over the short- and the medium-term for CPET outcomes in young CF patients.
Original languageEnglish
Pages (from-to)644-650
JournalJournal of Cystic Fibrosis
Volume12
Issue number6
Early online date28 May 2013
DOIs
Publication statusPublished - Dec 2013

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