Exercise responses are related to structural lung damage in CF pulmonary disease
Summary Introduction Early detection of lung disease is a primary objective in monitoring patients with Cystic Fibrosis (CF); High‐Resolution‐Computed‐Tomography (HRCT) assesses structural damage. Spirometry and cardiopulmonary exercise testing are used for functional evaluation of CF lung disease....
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Published in | Pediatric pulmonology Vol. 51; no. 9; pp. 914 - 920 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.09.2016
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Summary
Introduction
Early detection of lung disease is a primary objective in monitoring patients with Cystic Fibrosis (CF); High‐Resolution‐Computed‐Tomography (HRCT) assesses structural damage. Spirometry and cardiopulmonary exercise testing are used for functional evaluation of CF lung disease.
Aim
To evaluate the deterioration of exercise testing parameters over a 2‐year period compared to the change of spirometry and HRCT parameters among CF patients.
Methods
Twenty‐eight CF patients were evaluated with HRCT, spirometry, and exercise testing; 15 had two assessments with an interval of 2 years. Correlation analyses between Bhalla score parameters and functional measures were performed.
Results
Twenty‐eight patients with CF (mean age 14.9 years, mean forced expiratory volume in 1 sec [FEV1] 83.2%) were evaluated. FEV1 was not found to change significantly in the 2‐year period (P = 0.612). Both mean Bhalla score and mean peak oxygen consumption (VO2 peak %) deteriorated significantly (P = 0.014 and P = 0.026, respectively). VO2 peak and respiratory equivalents for O2 and CO2 at peak exercise were found to be significant predictors of Bhalla score (r = −0.477, P = 0.010; r = 0.461, P = 0.018; r = 0.402; P = 0.042, respectively). Anaerobic threshold was associated with changes in Bhalla score over the following 2 years.
Conclusions
Exercise testing is more sensitive than spirometry to detect structural changes in CF lungs. Pediatr Pulmonol. 2016; 51:914–920. © 2016 Wiley Periodicals, Inc. |
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Bibliography: | none reported ArticleID:PPUL23474 ark:/67375/WNG-CHTX1QL3-H istex:60BE2492AA88473AF2B768284BCD5CC3017155BC |
ISSN: | 8755-6863 1099-0496 |
DOI: | 10.1002/ppul.23474 |