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Several specific high-resolution computed tomography patterns correlate with survival in patients with idiopathic pulmonary fibrosis

Minna Mononen, Hannu-Pekka Kettunen, Sanna-Katja Suoranta, Miia Kärkkäinen, Tuomas Selander, Minna Purokivi, Riitta Kaarteenaho

2021Journal of Thoracic Disease15 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Evidence of honeycombing in high-resolution computed tomography (HRCT) is a recognized risk factor for shortened survival in patients with idiopathic pulmonary fibrosis (IPF), but few studies have evaluated the feasibility of exploiting other specific patterns for predicting survival. The aim of this study was to examine the extent of specific HRCT patterns in IPF and determine whether they correlate with clinical features, pulmonary function tests (PFT), and survival. METHODS: Both the presence and extent of specific HRCT patterns, such as traction bronchiectasis, honeycombing, architectural distortion, reticulation, emphysema, and ground glass opacity, in 129 HRCT examinations were scored semi-quantitatively in three zones of each lung. HRCT examinations were also re-classified according to the 2011 and 2018 international statements. Correlations were calculated between the scores of specific HRCT patterns, clinical features, PFT, and patient survival. RESULTS: 37 months, P=0.026). The extents of traction bronchiectasis, honeycombing, and architectural distortion displayed an inverse correlation with all PFT values at the time of diagnosis. There were few differences between the radiological classifications of the 2011 and 2018 international statements. CONCLUSIONS: We conclude that several specific HRCT patterns displayed a correlation with shortened survival in IPF; these may help in evaluating the risk of death in IPF patients.

Topics & Concepts

HoneycombingMedicineHigh-resolution computed tomographyIdiopathic pulmonary fibrosisUsual interstitial pneumoniaRadiologyPulmonary function testingBronchiectasisGround-glass opacityInternal medicineLungComputed tomographyCancerAdenocarcinomaInterstitial Lung Diseases and Idiopathic Pulmonary FibrosisChronic Obstructive Pulmonary Disease (COPD) ResearchCystic Fibrosis Research Advances