Julie Van Woensel, Jasenko Krdzalic, Tom de Jaegere, Marlou T H F Janssen, Sofia Ramiro, César Magro Checa, Robert B M Landewé, Rémy L M Mostard
{"title":"Radiological phenotypes in pulmonary sarcoidosis: a reliability study of newly defined high-resolution computer tomography phenotypes.","authors":"Julie Van Woensel, Jasenko Krdzalic, Tom de Jaegere, Marlou T H F Janssen, Sofia Ramiro, César Magro Checa, Robert B M Landewé, Rémy L M Mostard","doi":"10.1093/bjro/tzaf017","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>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.</p><p><strong>Methods: </strong>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 (K<sub>w</sub>) statistics.</p><p><strong>Results: </strong>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, <i>P</i> < .001). We observed a substantial inter-reader reliability between readers A and B (<i>K</i> <sub>w</sub> of 0.76), between readers B and C (K<sub>w</sub> of 0.66) and between readers A and C (<i>K</i> <sub>w</sub> of 0.66). For the scoring of the subgroups \"non-fibrotic\" vs. \"likely-to-be fibrotic,\" overall Fleiss' Kappa was substantial (<i>K</i> = 0.78, CI 0.607-0.944, <i>P</i> < .001). We observed a <i>K</i> <sub>w</sub> 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 (<i>K</i> <sub>w</sub> of 0.71) and it was almost perfect in scoring the subgroups (<i>K</i> <sub>w</sub> of 0.95). Intra-reader reliability was substantial between the scores of B in scoring the predominant phenotype (<i>K</i> <sub>w</sub> of 0.66) and subgroups (<i>K</i> <sub>w</sub> of 0.72).</p><p><strong>Conclusions: </strong>The inter- and intra-reader reliability of the newly proposed HRCT phenotypes obtained from the Delphi study is very acceptable.</p><p><strong>Advances in knowledge: </strong>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.</p>","PeriodicalId":72419,"journal":{"name":"BJR open","volume":"7 1","pages":"tzaf017"},"PeriodicalIF":2.1000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12255234/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BJR open","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/bjro/tzaf017","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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 (Kw of 0.76), between readers B and C (Kw of 0.66) and between readers A and C (Kw 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 Kw 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 (Kw of 0.71) and it was almost perfect in scoring the subgroups (Kw of 0.95). Intra-reader reliability was substantial between the scores of B in scoring the predominant phenotype (Kw of 0.66) and subgroups (Kw 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.