Literature DB >> 26436668

Validating chest MRI to detect and monitor cystic fibrosis lung disease in a pediatric cohort.

Leonie A Tepper1,2, Pierluigi Ciet1,2, Daan Caudri1, Alexandra L Quittner3, Elisabeth M W J Utens4, Harm A W M Tiddens1,2.   

Abstract

BACKGROUND: Computed Tomography (CT) is the gold standard to assess bronchiectasis and trapped air in cystic fibrosis (CF) lung disease, but has the disadvantage of radiation exposure. Magnetic Resonance Imaging (MRI) is a radiation free alternative.
OBJECTIVE: To validate MRI as outcome measure by: correlating MRI scores for bronchiectasis and trapped air with clinical parameters, and by comparing those MRI scores with CT scores.
METHODS: In patients with CF (aged 5.6-17.4 years), MRI and CT were alternated annually during routine annual check-ups between July 2007 and January 2010. Twenty-three children had an MRI performed 1 year prior to CT, 34 children had a CT 1 year prior to MRI. Bronchiectasis and trapped air were scored using the CF-MRI and CF-CT scoring system. CF-MRI scores were correlated with clinical parameters: FEV1 , Pseudomonas aeruginosa, pulmonary exacerbations and patient-reported respiratory symptoms measured on the Cystic Fibrosis Questionnaire-Revised (CFQ-R), using Spearman's correlation coefficient. MRI and CT scores were compared using intra-class correlation coefficients (ICC) and Bland-Altman plots.
RESULTS: Fifty-seven patients who had an MRI, CT and CFQ-R during the study period were included. CF-MRI bronchiectasis correlated with FEV1 , Pseudomonas aeruginosa, pulmonary exacerbations and patient-reported respiratory symptoms. CF-MRI trapped air only correlated with FEV1 and Pseudomonas aeruginosa. ICCs between MRI and CT bronchiectasis and trapped air were 0.41 and 0.35 respectively. MRI tended to overestimate bronchiectasis compared to CT.
CONCLUSION: The associations between CF-MRI scores and several important clinical parameters further contributes to the validation of MRI. MRI provides different information than CT.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  cystic fibrosis (CF); imaging

Mesh:

Year:  2015        PMID: 26436668     DOI: 10.1002/ppul.23328

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


  11 in total

1.  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

2.  Changes in magnetic resonance imaging scores and ventilation inhomogeneity in children with cystic fibrosis pulmonary exacerbations.

Authors:  Hartmut Grasemann; Pierluigi Ciet; Reshma Amin; Nancy McDonald; Michelle Klingel; Harm A W M Tiddens; Felix Ratjen; Lars Grosse-Wortmann
Journal:  Eur Respir J       Date:  2017-08-24       Impact factor: 16.671

3.  Diffusion weighted imaging in cystic fibrosis disease: beyond morphological imaging.

Authors:  Pierluigi Ciet; Goffredo Serra; Eleni Rosalina Andrinopoulou; Silvia Bertolo; Mirco Ros; Carlo Catalano; Stefano Colagrande; Harm A W M Tiddens; Giovanni Morana
Journal:  Eur Radiol       Date:  2016-02-12       Impact factor: 5.315

4.  New severity assessment in cystic fibrosis: signal intensity and lung volume compared to LCI and FEV1: preliminary results.

Authors:  Sabrina Fleischer; Mareen Sarah Kraus; Sergios Gatidis; Winfried Baden; Andreas Hector; Dominik Hartl; Ilias Tsiflikas; Juergen Frank Schaefer
Journal:  Eur Radiol       Date:  2019-11-14       Impact factor: 5.315

5.  Ultrashort Echo-Time Magnetic Resonance Imaging Is a Sensitive Method for the Evaluation of Early Cystic Fibrosis Lung Disease.

Authors:  David J Roach; Yannick Crémillieux; Robert J Fleck; Alan S Brody; Suraj D Serai; Rhonda D Szczesniak; Stephanie Kerlakian; John P Clancy; Jason C Woods
Journal:  Ann Am Thorac Soc       Date:  2016-11

6.  Agreement between magnetic resonance imaging and computed tomography in the postnatal evaluation of congenital lung malformations: a pilot study.

Authors:  Salvatore Zirpoli; Alice Marianna Munari; Alessandra Primolevo; Marco Scarabello; Sara Costanzo; Andrea Farolfi; Gianluca Lista; Elena Zoia; Gian Vincenzo Zuccotti; Giovanna Riccipetitoni; Andrea Righini
Journal:  Eur Radiol       Date:  2019-02-22       Impact factor: 5.315

Review 7.  Lung and large airway imaging: magnetic resonance imaging versus computed tomography.

Authors:  Mark C Liszewski; Pierluigi Ciet; Abbey J Winant; Edward Y Lee
Journal:  Pediatr Radiol       Date:  2022-05-16

8.  Quantitative chest computerized tomography and FEV1 equally identify pulmonary exacerbation risk in children with cystic fibrosis.

Authors:  Don B Sanders; Zhanhai Li; Katelyn Parker-McGill; Philip Farrell; Alan S Brody
Journal:  Pediatr Pulmonol       Date:  2018-08-29

9.  Lung morphology assessment of cystic fibrosis using MRI with ultra-short echo time at submillimeter spatial resolution.

Authors:  Gaël Dournes; Fanny Menut; Julie Macey; Michaël Fayon; Jean-François Chateil; Marjorie Salel; Olivier Corneloup; Michel Montaudon; Patrick Berger; François Laurent
Journal:  Eur Radiol       Date:  2016-02-02       Impact factor: 5.315

10.  Cross-sectional analysis of follow-up chest MRI and chest CT scans in patients previously affected by COVID-19.

Authors:  Martina Pecoraro; Stefano Cipollari; Livia Marchitelli; Emanuele Messina; Maurizio Del Monte; Nicola Galea; Maria Rosa Ciardi; Marco Francone; Carlo Catalano; Valeria Panebianco
Journal:  Radiol Med       Date:  2021-07-12       Impact factor: 3.469

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.