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Updated: Sep 15, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Radiological phenotypes in pulmonary sarcoidosis: a reliability study of newly defined high-resolution computer
Julie Van Woensel1, Jasenko Krdzalic2, Tom de Jaegere2
1Department of Respiratory Medicine, Zuyderland Medical Centre, Heerlen, Limburg, 6419PC, The Netherlands.
Objectives:
An accurate morphological classification of distinct pulmonary phenotypes in sarcoidosis is lacking. Recently, a multinational Delphi study was conducted to reach a consensus on recognizable high-resolution computer tomography (HRCT) phenotypes in pulmonary sarcoidosis as a basis for a more distinctive classification. The reliability of these phenotypes has not yet been evaluated.
Methods:
HRCT scans of adult sarcoidosis patients from the pulmonology department of a single sarcoidosis referral center were scored by three blinded independent readers. Seven phenotypes were distinguished as described in the Delphi study. They were divided into two subgroups: "non-fibrotic" and "likely-to-be fibrotic". Intra- and inter-reader reliability for scoring the predominant phenotype and the subgroup was assessed using weighted Kappa (Kw) statistics.
Results:
Forty-five patients (mean age, 47 years ± 12, 28 men) were included. For the scoring of the predominant phenotype, inter-reader reliability between all readers was substantial with an overall Fleiss' kappa of 0.69 (CI 0.622-0.765, P < .001). We observed a substantial inter-reader reliability between readers A and B (K w of 0.76), between readers B and C (Kw of 0.66) and between readers A and C (K w of 0.66). For the scoring of the subgroups "non-fibrotic" vs. "likely-to-be fibrotic," overall Fleiss' Kappa was substantial (K = 0.78, CI 0.607-0.944, P < .001). We observed a K w score of 0.76 between readers A and B; 0.81 between readers A and C; 0.76 between readers B and C. Intra-reader reliability was substantial between the scores of A in scoring the predominant phenotypes (K w of 0.71) and it was almost perfect in scoring the subgroups (K w of 0.95). Intra-reader reliability was substantial between the scores of B in scoring the predominant phenotype (K w of 0.66) and subgroups (K w of 0.72).
Conclusions:
The inter- and intra-reader reliability of the newly proposed HRCT phenotypes obtained from the Delphi study is very acceptable.
Advances In Knowledge:
This study is the first to assess the reliability of these HRCT phenotypes and supports the use of them for classification purposes in future clinical and pathogenetic studies.
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