A protocol to determine valid in young cystic fibrosis patients
A protocol to determine valid in young cystic fibrosis patients
Objectives: measuring aerobic fitness (VO2max) via a maximal cardiopulmonary exercise test is an important clinical tool in cystic fibrosis. This study sought to establish: (1) the validity of traditional criteria to verify maximal efforts during a ramp cardiopulmonary exercise test; and (2) whether the VO2 measured during an exhaustive cardiopulmonary exercise test represents a valid VO2max in paediatric patients, using a subsequent exhaustive supramaximal (Smax) exercise test.
Design: cross-sectional.
Methods: fourteen patients (7–18 years; 10 males) completed an exhaustive ramp test to determine VO2max. Following 15-min recovery, Smax (110% ramp peak power output) was performed.
Results: ramp test VO2peak was significantly higher than VO2 documented at traditional endpoint criteria, including a RER of 1.00 (0.99 ± 0.47 L min−1 vs. 1.83 ± 0.78 L min−1, p < 0.001) and 1.10 (1.36 ± 0.59 L min−1 vs. 1.83 ± 0.78 L min−1, p < 0.001), despite 100% of patients satisfying these two criteria. Only 23% and 75% of patients satisfied the 95% age-predicted heart rate (HR) maximum and 180 b min−1 criteria. Whilst mean ramp and Smax VO2peak were not significantly different (1.83 ± 0.78 L min−1 vs. 1.82 ± 0.67 L min−1; p = 0.88), at the individual level Smax elicited a ‘meaningful’ (>9%) increase in VO2peak (range 9.9–38.3%) compared with VO2peak from the ramp test in 3 of 14 cases (21.4%).
Conclusions - Traditional criteria significantly underestimate VO2max in young cystic fibrosis patients. Conversely, Smax can confirm when ‘true’ VO2max is achieved. The use of Smax following cardiopulmonary exercise test represents an appropriate method to measure VO2max in young cystic fibrosis patients.
539-544
Saynor, Zoe L.
a4357c7d-db59-4fa5-b24f-58d2f7e74e39
Barker, Alan R.
a930df01-4fdb-44a9-8014-fe21e5ea3b04
Oades, Patrick J.
a75b6826-6d88-47a9-9656-f0f79a9b3a63
Williams, Craig A.
c96ddcec-3c7e-4686-b831-cbb4f004ccb0
1 November 2013
Saynor, Zoe L.
a4357c7d-db59-4fa5-b24f-58d2f7e74e39
Barker, Alan R.
a930df01-4fdb-44a9-8014-fe21e5ea3b04
Oades, Patrick J.
a75b6826-6d88-47a9-9656-f0f79a9b3a63
Williams, Craig A.
c96ddcec-3c7e-4686-b831-cbb4f004ccb0
Saynor, Zoe L., Barker, Alan R., Oades, Patrick J. and Williams, Craig A.
(2013)
A protocol to determine valid in young cystic fibrosis patients.
Journal of Science and Medicine in Sport, 16 (6), .
(doi:10.1016/j.jsams.2013.01.010).
Abstract
Objectives: measuring aerobic fitness (VO2max) via a maximal cardiopulmonary exercise test is an important clinical tool in cystic fibrosis. This study sought to establish: (1) the validity of traditional criteria to verify maximal efforts during a ramp cardiopulmonary exercise test; and (2) whether the VO2 measured during an exhaustive cardiopulmonary exercise test represents a valid VO2max in paediatric patients, using a subsequent exhaustive supramaximal (Smax) exercise test.
Design: cross-sectional.
Methods: fourteen patients (7–18 years; 10 males) completed an exhaustive ramp test to determine VO2max. Following 15-min recovery, Smax (110% ramp peak power output) was performed.
Results: ramp test VO2peak was significantly higher than VO2 documented at traditional endpoint criteria, including a RER of 1.00 (0.99 ± 0.47 L min−1 vs. 1.83 ± 0.78 L min−1, p < 0.001) and 1.10 (1.36 ± 0.59 L min−1 vs. 1.83 ± 0.78 L min−1, p < 0.001), despite 100% of patients satisfying these two criteria. Only 23% and 75% of patients satisfied the 95% age-predicted heart rate (HR) maximum and 180 b min−1 criteria. Whilst mean ramp and Smax VO2peak were not significantly different (1.83 ± 0.78 L min−1 vs. 1.82 ± 0.67 L min−1; p = 0.88), at the individual level Smax elicited a ‘meaningful’ (>9%) increase in VO2peak (range 9.9–38.3%) compared with VO2peak from the ramp test in 3 of 14 cases (21.4%).
Conclusions - Traditional criteria significantly underestimate VO2max in young cystic fibrosis patients. Conversely, Smax can confirm when ‘true’ VO2max is achieved. The use of Smax following cardiopulmonary exercise test represents an appropriate method to measure VO2max in young cystic fibrosis patients.
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Accepted/In Press date: 31 January 2013
e-pub ahead of print date: 18 March 2013
Published date: 1 November 2013
Identifiers
Local EPrints ID: 494041
URI: http://eprints.soton.ac.uk/id/eprint/494041
ISSN: 1440-2440
PURE UUID: 0b4807a3-733f-4909-a0c5-b148bf092d51
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Date deposited: 20 Sep 2024 16:33
Last modified: 21 Sep 2024 02:14
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Contributors
Author:
Zoe L. Saynor
Author:
Alan R. Barker
Author:
Patrick J. Oades
Author:
Craig A. Williams
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