The clinical use of lung MRI in cystic fibrosis: what, now, how?

Abstract:

:To assess airway and lung parenchymal damage non-invasively in cystic fibrosis (CF), chest MRI has been historically out of the scope of routine clinical imaging due to technical difficulties such as the low proton density and respiratory and cardiac motion. However, technological breakthroughs have recently emerged to dramatically improve lung MRI quality (including signal-to-noise ratio, resolution, speed, contrast). At the same time, novel treatments have changed the landscape of CF clinical care. In this contemporary context, there is a recent consensus that lung MRI can be used clinically to assess CF in a radiation-free manner and enable quantification of lung disease severity. MRI can now achieve 3-dimensional, high-resolution morphological imaging, and beyond this morphological information, MRI may offer the ability to differentiate active inflammation versus scarring tissue sensitively. MRI could also characterize various forms of inflammation for early guidance of treatment. Moreover, functional information from MRI can assess regional, small airway disease with sensitivity to detect small changes even in patients with mild CF. Finally, automated quantification methods have emerged to support the conventional visual analyses for more objective and reproducible assessment of the disease severity. This manuscript aims to review the most recent developments of lung MRI, with a focus on practical application and clinical value in CF, and the perspectives on how these modern techniques may converge and impact patient care soon.

journal_name

Chest

journal_title

Chest

authors

Dournes G,Walkup LL,Benlala I,Willmering MM,Macey J,Bui S,Laurent F,Woods JC

doi

10.1016/j.chest.2020.12.008

subject

Has Abstract

pub_date

2020-12-17 00:00:00

eissn

0012-3692

issn

1931-3543

pii

S0012-3692(20)35453-2

pub_type

杂志文章,评审

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