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Serial CT analysis in idiopathic pulmonary fibrosis: comparison of visual features that determine patient outcome

Serial CT analysis in idiopathic pulmonary fibrosis: comparison of visual features that determine patient outcome
Serial CT analysis in idiopathic pulmonary fibrosis: comparison of visual features that determine patient outcome
Aims Patients with idiopathic pulmonary fibrosis (IPF) receiving antifibrotic medication and patients with non-IPF fibrosing lung disease often demonstrate rates of annualised forced vital capacity (FVC) decline within the range of measurement variation (5.0%–9.9%). We examined whether change in visual CT variables could help confirm whether marginal FVC declines represented genuine clinical deterioration rather than measurement noise.

Methods In two IPF cohorts (cohort 1: n=103, cohort 2: n=108), separate pairs of radiologists scored paired volumetric CTs (acquired between 6 and 24 months from baseline). Change in interstitial lung disease, honeycombing, reticulation, ground-glass opacity extents and traction bronchiectasis severity was evaluated using a 5-point scale, with mortality prediction analysed using univariable and multivariable Cox regression analyses. Both IPF populations were then combined to determine whether change in CT variables could predict mortality in patients with marginal FVC declines.

Results On univariate analysis, change in all CT variables except ground-glass opacity predicted mortality in both cohorts. On multivariate analysis adjusted for patient age, gender, antifibrotic use and baseline disease severity (diffusing capacity for carbon monoxide), change in traction bronchiectasis severity predicted mortality independent of FVC decline. Change in traction bronchiectasis severity demonstrated good interobserver agreement among both scorer pairs. Across all study patients with marginal FVC declines, change in traction bronchiectasis severity independently predicted mortality and identified more patients with deterioration than change in honeycombing extent.

Conclusions Change in traction bronchiectasis severity is a measure of disease progression that could be used to help resolve the clinical importance of marginal FVC declines.
0040-6376
648-654
Jacob, Joseph
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Aksman, Leon
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Procter, Alex
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Gholipour, Bahareh
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Cross, Gary
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Barnett, Joseph
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Brereton, Christopher J.
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Jones, Mark G.
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van Moorsel, Coline
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van Es, Hendrik
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van Beek, Frouke T.
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Veltkamp, Marcel
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Desai, Sujal
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Judge, Eoin P.
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Burd, Teresa
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Kokosi, Maria
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Savas, Recep
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Bayraktaroglu, Selen
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Mogulkoc, Nesrin
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Altmann, Andre
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Wells, Athol U.
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Jacob, Joseph
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Aksman, Leon
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Procter, Alex
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Gholipour, Bahareh
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Cross, Gary
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Barnett, Joseph
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Brereton, Christopher J.
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Jones, Mark G.
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van Moorsel, Coline
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van Es, Hendrik
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van Beek, Frouke T.
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Veltkamp, Marcel
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Desai, Sujal
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Judge, Eoin P.
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Burd, Teresa
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Kokosi, Maria
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Savas, Recep
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Bayraktaroglu, Selen
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Mogulkoc, Nesrin
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Altmann, Andre
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Wells, Athol U.
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Jacob, Joseph, Aksman, Leon, Procter, Alex, Gholipour, Bahareh, Cross, Gary, Barnett, Joseph, Brereton, Christopher J., Jones, Mark G., van Moorsel, Coline, van Es, Hendrik, van Beek, Frouke T., Veltkamp, Marcel, Desai, Sujal, Judge, Eoin P., Burd, Teresa, Kokosi, Maria, Savas, Recep, Bayraktaroglu, Selen, Mogulkoc, Nesrin, Altmann, Andre and Wells, Athol U. (2020) Serial CT analysis in idiopathic pulmonary fibrosis: comparison of visual features that determine patient outcome. Thorax, 75 (8), 648-654. (doi:10.1136/thoraxjnl-2019-213865).

Record type: Article

Abstract

Aims Patients with idiopathic pulmonary fibrosis (IPF) receiving antifibrotic medication and patients with non-IPF fibrosing lung disease often demonstrate rates of annualised forced vital capacity (FVC) decline within the range of measurement variation (5.0%–9.9%). We examined whether change in visual CT variables could help confirm whether marginal FVC declines represented genuine clinical deterioration rather than measurement noise.

Methods In two IPF cohorts (cohort 1: n=103, cohort 2: n=108), separate pairs of radiologists scored paired volumetric CTs (acquired between 6 and 24 months from baseline). Change in interstitial lung disease, honeycombing, reticulation, ground-glass opacity extents and traction bronchiectasis severity was evaluated using a 5-point scale, with mortality prediction analysed using univariable and multivariable Cox regression analyses. Both IPF populations were then combined to determine whether change in CT variables could predict mortality in patients with marginal FVC declines.

Results On univariate analysis, change in all CT variables except ground-glass opacity predicted mortality in both cohorts. On multivariate analysis adjusted for patient age, gender, antifibrotic use and baseline disease severity (diffusing capacity for carbon monoxide), change in traction bronchiectasis severity predicted mortality independent of FVC decline. Change in traction bronchiectasis severity demonstrated good interobserver agreement among both scorer pairs. Across all study patients with marginal FVC declines, change in traction bronchiectasis severity independently predicted mortality and identified more patients with deterioration than change in honeycombing extent.

Conclusions Change in traction bronchiectasis severity is a measure of disease progression that could be used to help resolve the clinical importance of marginal FVC declines.

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Serial visual IPF analysis - Accepted Manuscript
Available under License Creative Commons Attribution.
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Accepted/In Press date: 20 December 2019
e-pub ahead of print date: 28 April 2020
Published date: 15 July 2020

Identifiers

Local EPrints ID: 437924
URI: http://eprints.soton.ac.uk/id/eprint/437924
ISSN: 0040-6376
PURE UUID: 4efe6696-4a85-4154-9344-a499d8eeaf41
ORCID for Mark G. Jones: ORCID iD orcid.org/0000-0001-6308-6014

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Date deposited: 24 Feb 2020 17:30
Last modified: 17 Mar 2024 03:11

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Contributors

Author: Joseph Jacob
Author: Leon Aksman
Author: Alex Procter
Author: Bahareh Gholipour
Author: Gary Cross
Author: Joseph Barnett
Author: Christopher J. Brereton
Author: Mark G. Jones ORCID iD
Author: Coline van Moorsel
Author: Hendrik van Es
Author: Frouke T. van Beek
Author: Marcel Veltkamp
Author: Sujal Desai
Author: Eoin P. Judge
Author: Teresa Burd
Author: Maria Kokosi
Author: Recep Savas
Author: Selen Bayraktaroglu
Author: Nesrin Mogulkoc
Author: Andre Altmann
Author: Athol U. Wells

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