Literature DB >> 9242738

High-resolution CT in the acute exacerbation of cystic fibrosis: evaluation of acute findings, reversibility of those findings, and clinical correlation.

R M Shah1, W Sexauer, B J Ostrum, S B Fiel, A C Friedman.   

Abstract

OBJECTIVE: The aims of this study were threefold: to compare high-resolution CT (HRCT) of adult patients with cystic fibrosis (CF) during acute exacerbations with asymptomatic patients with CF, to evaluate reversibility of HRCT abnormalities after exacerbations, and to correlate HRCT with clinical parameters. SUBJECTS AND METHODS: Nineteen symptomatic and eight asymptomatic patients were prospectively evaluated by HRCT and pulmonary function tests (PFTs). Symptomatic patients were reassessed 2 weeks after the exacerbation. Studies were independently reviewed by two radiologists using a modified Bhalla scoring system, noting the presence, extent, and severity of bronchiectasis, peribronchial thickening, mucus plugging, and atelectasis or consolidation. Modifications to the Bhalla system included evaluation of the presence and profusion of centrilobular nodules and air-fluid levels within bronchiectatic cavities. The highest possible score was 24 points. Higher scores indicated greater severity. Mosaic perfusion was noted but not included in the modified Bhalla HRCT score. Total modified Bhalla HRCT score and components of the HRCT score were correlated with corresponding PFT parameters.
RESULTS: Bronchiectasis, peribronchial thickening, mucus plugging, centrilobular nodules, and mosaic perfusion were identified in symptomatic and asymptomatic patients. Air-fluid levels in bronchiectatic cavities, identified in two patients, represented the only finding limited to acute exacerbation. Reversible findings included air-fluid levels (100%), centrilobular nodules (36%), mucus plugging (33%), and peribronchial thickening (11%). Total HRCT severity scores of symptomatic and asymptomatic patients correlated with forced vital capacity (FVC) (r = .44, p = .01) and forced expiratory volume at 1 sec (FEV1) (r = .34, p = .04). Severity of bronchiectasis correlated with FVC (r = .50, p = .004) and FEV1 (r = .40, p = .02). Mucus plugging and centrilobular nodules did not correlate with PFT parameters. In the symptomatic patients, improvement in HRCT score correlated with changes in FEV1/FVC (r = .39, p = .049).
CONCLUSION: Air-fluid levels in bronchiectatic cavities were the only parenchymal finding shown by HRCT that was limited to the acute exacerbation of CF in our study population. However, this finding was rare, being seen in two of 19 patients. Mucus plugging, centrilobular nodules, and peribronchial thickening were potentially reversible findings in symptomatic patients. HRCT accurately revealed disease severity in patients with CF. We also found that changes in HRCT scores correlated with clinical improvement as determined by PFTs.

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Year:  1997        PMID: 9242738     DOI: 10.2214/ajr.169.2.9242738

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  31 in total

1.  High resolution computed tomography of the chest in cystic fibrosis (CF): is simplification of scoring systems feasible?

Authors:  Anastasia Oikonomou; John Tsanakas; Elpis Hatziagorou; Fotios Kirvassilis; Stavros Efremidis; Panos Prassopoulos
Journal:  Eur Radiol       Date:  2007-11-27       Impact factor: 5.315

2.  Bronchus-associated lymphoid tissue (BALT) lymphoma of the lung showing mosaic pattern of inhomogeneous attenuation on thin-section CT: a case report.

Authors:  I J Lee; S H Kim; S H Koo; H B Kim; D H Hwang; K S Lee; Y Lee; K T Jang; D H Kim
Journal:  Korean J Radiol       Date:  2000 Jul-Sep       Impact factor: 3.500

3.  A semiquantitative MRI-Score can predict loss of lung function in patients with cystic fibrosis: Preliminary results.

Authors:  Juergen F Schaefer; Andreas Hector; Katharina Schmidt; Matthias Teufel; Sabrina Fleischer; Ute Graepler-Mainka; Joachim Riethmueller; Sergios Gatidis; Susanne Schaefer; Konstantin Nikolaou; Dominik Hartl; Ilias Tsiflikas
Journal:  Eur Radiol       Date:  2017-06-29       Impact factor: 5.315

4.  Automated CT scan scores of bronchiectasis and air trapping in cystic fibrosis.

Authors:  Emily M DeBoer; Waldemar Swiercz; Sonya L Heltshe; Margaret M Anthony; Paul Szefler; Rebecca Klein; John Strain; Alan S Brody; Scott D Sagel
Journal:  Chest       Date:  2014-03-01       Impact factor: 9.410

Review 5.  Cystic fibrosis lung disease: genetic influences, microbial interactions, and radiological assessment.

Authors:  Samuel M Moskowitz; Ronald L Gibson; Eric L Effmann
Journal:  Pediatr Radiol       Date:  2005-05-03

6.  Progression of lung disease on computed tomography and pulmonary function tests in children and adults with cystic fibrosis.

Authors:  P A de Jong; A Lindblad; L Rubin; W C J Hop; J C de Jongste; M Brink; H A W M Tiddens
Journal:  Thorax       Date:  2005-10-21       Impact factor: 9.139

Review 7.  [Thoracic findings in pediatric patients with cystic fibrosis].

Authors:  R Wunsch; C Wunsch
Journal:  Radiologe       Date:  2003-12       Impact factor: 0.635

Review 8.  Computed tomography and cystic fibrosis: promises and problems.

Authors:  Z A Aziz; J C Davies; E W Alton; A U Wells; D M Geddes; D M Hansell
Journal:  Thorax       Date:  2007-02       Impact factor: 9.139

9.  Alveolar recruitment of atelectasis under combined high-frequency jet ventilation: a computed tomography study.

Authors:  Paul Kraincuk; Günther Körmöczi; Mathias Prokop; Gerald Ihra; Alexander Aloy
Journal:  Intensive Care Med       Date:  2003-07-17       Impact factor: 17.440

10.  Development and validation of automated 2D-3D bronchial airway matching to track changes in regional bronchial morphology using serial low-dose chest CT scans in children with chronic lung disease.

Authors:  Pavithra Raman; Raghav Raman; Beverley Newman; Raman Venkatraman; Bhargav Raman; Terry E Robinson
Journal:  J Digit Imaging       Date:  2009-09-15       Impact factor: 4.056

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