Literature DB >> 27171573

Exercise responses are related to structural lung damage in CF pulmonary disease.

Elpis Hatziagorou1, Asterios Kampouras1, Vasiliki Avramidou1, Vasiliki Georgopoulou2, Fotis Kirvasilis1, Kalliopi Kontouli1, Helge Hebestreit3, John Tsanakas1.   

Abstract

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. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  HRCT; cardiopulmonary exercise testing; children; cystic fibrosis; spirometry

Mesh:

Year:  2016        PMID: 27171573     DOI: 10.1002/ppul.23474

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  3 in total

1.  Lung abnormalities do not influence aerobic capacity in school children born preterm.

Authors:  Christopher A O'Dea; Karla Logie; Andrew C Wilson; J Jane Pillow; Conor Murray; Georgia Banton; Shannon J Simpson; Graham L Hall; Andrew Maiorana
Journal:  Eur J Appl Physiol       Date:  2020-11-03       Impact factor: 3.078

2.  Does Pseudomonas aeruginosa Colonization Affect Exercise Capacity in CF?

Authors:  Asterios Kampouras; Elpis Hatziagorou; Vasiliki Avramidou; Vasiliki Georgopoulou; Fotios Kirvassilis; John Tsanakas
Journal:  Pulm Med       Date:  2019-12-09

Review 3.  Toward the Establishment of New Clinical Endpoints for Cystic Fibrosis: The Role of Lung Clearance Index and Cardiopulmonary Exercise Testing.

Authors:  Elpis Hatziagorou; Asterios Kampouras; Vasiliki Avramidou; Ilektra Toulia; Elisavet-Anna Chrysochoou; Maria Galogavrou; Fotios Kirvassilis; John Tsanakas
Journal:  Front Pediatr       Date:  2021-02-25       Impact factor: 3.418

  3 in total

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