Comparison between cardiopulmonary exercise testing parameters and computed tomography findings in patients with thoracic sarcoidosis
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Lung
Abstract
Cardiopulmonary exercise testing (CPET) is
a safe and clinically useful method to assess functional
capacity and to follow disease progression and the response
to treatment in several clinical conditions.
Aim We set out to determine the relationship between
outcome measures of CPET and high-resolution computed
tomography (HRCT) findings in thoracic sarcoidosis.
Methods A cross-sectional study was carried out in which
42 nonsmoking outpatients (22 females; median age =
46.5 years) were evaluated. All the patients underwent
pulmonary function tests (PFTs) and CPET. By using
CPET, the most probable causes of exercise limitation were
separated into respiratory mechanics (n = 25) and cardio vascular (n = 17). By using HRCT, the following patterns
were recorded: predominant nodules (n = 18), predomi nant ground-glass opacity (n = 10), and predominant
traction bronchiectasis and honeycombing (n = 14).
Results Although significant differences have been
shown for both PFT parameters and CPET results, only the
latter were able to distinguish between patients with
ground-glass opacity and patients with traction bronchiec tasis and honeycombing on HRCT. A statistically signifi cant difference was found for peak VO2, breathing reserve,
and P(A-a)O2 when patients with predominant traction
bronchiectasis and honeycombing were compared to
patients with other HRCT patterns (p\0.0001). There was
no statistical difference among the patterns with abnormal
CPET and the patterns of abnormalities on HRCT
(p[0.05).
Conclusion The functional capacity assessed by CPET
was strongly influenced by HRCT patterns in sarcoidosis.
Patients with traction bronchiectasis and honeycombing
have lower exercise capacity measured by CPET.
Description
p. 425–431.: il. p&b.
Citation
LOPES, Agnaldo José et al. Comparison between cardiopulmonary exercise testing parameters and computed tomography findings in patients with thoracic sarcoidosis. Lung, v. 189, p. 425–431, 2011.