z-logo
open-access-imgOpen Access
Predictive factors of mortality in rheumatoid arthritis-associated interstitial lung disease analysed by modified HRCT classification of idiopathic pulmonary fibrosis according to the 2018 ATS/ERS/JRS/ALAT criteria
Author(s) -
Hideaki Yamakawa,
Shintaro Sato,
Emiri Tsumiyama,
Tomotaka Nishizawa,
Rie Kawabe,
Tomohiro Oba,
Teppei Kamikawa,
Masanobu Horikoshi,
Keiichi Akasaka,
Masako Amano,
Kazuyoshi Kuwano,
Hidekazu Matsushima
Publication year - 2019
Publication title -
journal of thoracic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.682
H-Index - 60
eISSN - 2077-6624
pISSN - 2072-1439
DOI - 10.21037/jtd.2019.11.73
Subject(s) - usual interstitial pneumonia , medicine , idiopathic pulmonary fibrosis , honeycombing , interstitial lung disease , high resolution computed tomography , exacerbation , radiology , asbestosis , pathology , lung
Interstitial lung disease (ILD) is associated with high morbidity and mortality in rheumatoid arthritis (RA). Although usual interstitial pneumonia (UIP) pattern was reported as a poor prognostic factor, in clinical practice, we often cannot classify high-resolution computed tomography (HRCT) patterns specifically as UIP or nonspecific interstitial pneumonia (NSIP). This study of RA-ILD aimed to elucidate prognosis by using our modified HRCT pattern classification according to the latest guideline on idiopathic pulmonary fibrosis (IPF).

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom