Literature DB >> 23510652

A protocol to determine valid V˙O2max in young cystic fibrosis patients.

Zoe L Saynor1, Alan R Barker, Patrick J Oades, Craig A Williams.   

Abstract

OBJECTIVES: Measuring aerobic fitness (V˙O2max) 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 V˙O2 measured during an exhaustive cardiopulmonary exercise test represents a valid V˙O2max 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 V˙O2max. Following 15-min recovery, Smax (110% ramp peak power output) was performed.
RESULTS: Ramp test V˙O2peak was significantly higher than V˙O2 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 V˙O2peak 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 V˙O2peak (range 9.9-38.3%) compared with V˙O2peak from the ramp test in 3 of 14 cases (21.4%).
CONCLUSIONS: Traditional criteria significantly underestimate V˙O2max in young cystic fibrosis patients. Conversely, Smax can confirm when 'true' V˙O2max is achieved. The use of Smax following cardiopulmonary exercise test represents an appropriate method to measure V˙O2max in young cystic fibrosis patients.
Copyright © 2013 Sports Medicine Australia. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; Exercise test; Lungs; Paediatric physician; Physical fitness; Supramaximal verification

Mesh:

Year:  2013        PMID: 23510652     DOI: 10.1016/j.jsams.2013.01.010

Source DB:  PubMed          Journal:  J Sci Med Sport        ISSN: 1878-1861            Impact factor:   4.319


  10 in total

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2.  Overall and differentiated sensory responses to cardiopulmonary exercise test in patients with cystic fibrosis: kinetics and ability to predict peak oxygen uptake.

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4.  The Effect of Dysglycaemia on Changes in Pulmonary and Aerobic Function in Cystic Fibrosis.

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5.  Ventilatory response to exercise in adolescents with cystic fibrosis and mild-to-moderate airway obstruction.

Authors:  Bart C Bongers; Maarten S Werkman; Tim Takken; Erik H J Hulzebos
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6.  Exercise capacity following a percutaneous endoscopic gastrostomy in a young female with cystic fibrosis: a case report.

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7.  The Coupling of Peripheral Blood Pressure and Ventilatory Responses during Exercise in Young Adults with Cystic Fibrosis.

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8.  Cardiopulmonary responses to maximal aerobic exercise in patients with cystic fibrosis.

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Review 9.  The Maximal Oxygen Uptake Verification Phase: a Light at the End of the Tunnel?

Authors:  Gustavo Z Schaun
Journal:  Sports Med Open       Date:  2017-12-08

10.  Analysis of oxygen uptake efficiency parameters in young people with cystic fibrosis.

Authors:  Owen W Tomlinson; Alan R Barker; Lucy V Chubbock; Daniel Stevens; Zoe L Saynor; Patrick J Oades; Craig A Williams
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  10 in total

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