Literature DB >> 16793982

Thin-section CT in patients with cystic fibrosis: correlation with peak exercise capacity and body mass index.

Jonathan D Dodd1, Sinead C Barry, Rupert B M Barry, Charles G Gallagher, Stephen J Skehan, James B Masterson.   

Abstract

PURPOSE: To evaluate whether thin-section chest computed tomographic (CT) findings correlate with exercise capacity, body mass index (BMI), dyspnea, and leg discomfort in patients with cystic fibrosis (CF).
MATERIALS AND METHODS: Institutional ethics committee approval was obtained, and patients provided written informed consent. Twenty-two patients (13 male and nine female patients; mean age, 22 years +/- 5.9; age range, 17-41 years) with stable CF underwent thin-section CT and exercise testing on a cycle ergometer. Three radiologists blinded to the clinical severity of disease and the spirometric findings of all patients independently and randomly scored all scans with a modified Bhalla scoring system. The primary measurement of the outcome of exercise testing was percentage of predicted peak O2 uptake. Univariate (Spearman rank correlation) and multivariate analyses were used to compare thin-section CT, clinical (age, sex, spirometric data, and BMI), and exercise measurements.
RESULTS: The correlation between total thin-section CT score and percentage of predicted peak O2 uptake was stronger than the correlation between the percentage of predicted peak O2 uptake and any clinical measurement (R = -0.60, P < .01). The thin-section CT structural abnormalities that had the strongest correlation with percentage of predicted peak O2 uptake were severity of bronchiectasis and presence of sacculations or abscesses (R = -0.70 and -0.71, respectively; P < .01). Multivariate analysis showed total thin-section CT score to be the only significant predictor of exercise capacity, accounting for 42% of the variance in percentage of predicted peak O2 uptake.
CONCLUSION: In patients with CF, the correlation between thin-section CT score and exercise limitation is stronger than that between spirometry results or BMI and exercise limitation. RSNA, 2006

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Year:  2006        PMID: 16793982     DOI: 10.1148/radiol.2401050502

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  3 in total

1.  Respiratory therapy: a problem among children and adolescents with cystic fibrosis.

Authors:  Taiane Dos Santos Feiten; Josani Silva Flores; Bruna Luciano Farias; Paula Maria Eidt Rovedder; Eunice Gus Camargo; Paulo de Tarso Roth Dalcin; Bruna Ziegler
Journal:  J Bras Pneumol       Date:  2016 Jan-Feb       Impact factor: 2.624

2.  Exercise capacity in patients with cystic fibrosis vs. non-cystic fibrosis bronchiectasis.

Authors:  Ronen Bar-Yoseph; Anat Ilivitzki; Dan M Cooper; Michal Gur; Gur Mainzer; Fahed Hakim; Galit Livnat; Zeev Schnapp; George Shalloufeh; Merav Zucker-Toledano; Yael Subar; Lea Bentur
Journal:  PLoS One       Date:  2019-06-13       Impact factor: 3.240

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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