The diagnostic accuracy of chest Xray screening for silicosis: a systematic review, meta-analysis and modelling study
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Author(s)
Howlett, Patrick
Durairaj, Ashwin
Lesosky, Maia
Feary, Johanna
Type
Journal Article
Abstract
Chest X-ray (CXR) is widely used for silicosis diagnosis, despite concerns regarding sensitivity. We investigated the diagnostic accuracy of CXR for silicosis screening compared with CT, high-resolution CT (HRCT) and autopsy, and modelled the relationship between CXR sensitivity and disease severity.
Medline, Embase, Scopus and Web of Science databases were searched on 2 July 2024 (PROSPERO registration: CRD42024513830). Meta-analyses were performed by reference standard and at increasing reference test severity cut-offs. The Quality Assessment of Diagnostic Accuracy Studies-2 tool assessed risk of bias. In scenarios of fixed and relative sensitivity, according to disease severity, we estimated missed silicosis cases and the number needed to screen (NNS) in hypothetical populations of low (5%), medium (15%) and high (30%) silicosis prevalence.
Twenty studies included 2156 participants and 1105 silicosis cases. CXR had moderate sensitivity (0.76; 95% CI 0.63 to 0.86, I2=84%) and high specificity (0.89, 95% CI 0.77 to 0.95, I2=57%) compared with HRCT in 12 studies, and low sensitivity (0.50, 95% CI 0.45 to 0.55, I2=0%) and high specificity (0.91, 95% CI 0.87 to 0.93, I2=20%) compared with autopsy in two studies. CXR sensitivity increased with higher reference test severity cut-offs. Clinically relevant numbers of cases were missed in fixed and relative sensitivity scenarios; increased prevalence and less severe disease resulted in more missed cases and a lower NNS.
Silicosis severity and reference test type both plausibly influence CXR sensitivity. Assuming either fixed or relative sensitivity results in missed silicosis cases. Judicious HRCT screening is likely to improve case detection.
Medline, Embase, Scopus and Web of Science databases were searched on 2 July 2024 (PROSPERO registration: CRD42024513830). Meta-analyses were performed by reference standard and at increasing reference test severity cut-offs. The Quality Assessment of Diagnostic Accuracy Studies-2 tool assessed risk of bias. In scenarios of fixed and relative sensitivity, according to disease severity, we estimated missed silicosis cases and the number needed to screen (NNS) in hypothetical populations of low (5%), medium (15%) and high (30%) silicosis prevalence.
Twenty studies included 2156 participants and 1105 silicosis cases. CXR had moderate sensitivity (0.76; 95% CI 0.63 to 0.86, I2=84%) and high specificity (0.89, 95% CI 0.77 to 0.95, I2=57%) compared with HRCT in 12 studies, and low sensitivity (0.50, 95% CI 0.45 to 0.55, I2=0%) and high specificity (0.91, 95% CI 0.87 to 0.93, I2=20%) compared with autopsy in two studies. CXR sensitivity increased with higher reference test severity cut-offs. Clinically relevant numbers of cases were missed in fixed and relative sensitivity scenarios; increased prevalence and less severe disease resulted in more missed cases and a lower NNS.
Silicosis severity and reference test type both plausibly influence CXR sensitivity. Assuming either fixed or relative sensitivity results in missed silicosis cases. Judicious HRCT screening is likely to improve case detection.
Date Issued
2026-02-12
Date Acceptance
2025-06-11
Citation
Occupational and Environmental Medicine, 2026, 82 (12), pp.614-620
ISSN
1351-0711
Publisher
BMJ Publishing Group
Start Page
614
End Page
620
Journal / Book Title
Occupational and Environmental Medicine
Volume
82
Issue
12
Copyright Statement
© Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY. Published by BMJ Group. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
License URL
Identifier
10.1136/oemed-2024-110000
Publication Status
Published
Article Number
ARTN 620
Date Publish Online
2026-01-12
