The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Chronic Hypersensitivity Pneumonitis: Differentiation from Idiopathic Pulmonary Fibrosis and Nonspecific Interstitial Pneumonia by Using Thin-Section CT
Abstract
PURPOSE: To retrospectively assess the accuracy of thin-section computed tomography (CT) in distinguishing chronic hypersensitivity pneumonitis (HP) from idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP), with histologic results as the reference standard. MATERIALS AND METHODS: This retrospective study was approved by the institutional research boards of the participating centers, and informed consent was waived. There was HIPAA compliance for all U.S. patients. The study included 66 patients (36 men, 30 women; mean age, 58.8 years +/- 10.9 [standard deviation]) with proved chronic HP (n = 18), IPF (n = 23), or NSIP (n = 25) who underwent CT. Two independent readers assessed the CT images, made a first-choice diagnosis, and noted the degree of confidence in the diagnosis. A general linear model was used to identify CT features that independently differentiated chronic HP from IPF and NSIP. Weighted kappa statistic was used to assess interobserver agreement. RESULTS: The CT features that best differentiated chronic HP were lobular areas with decreased attenuation and vascularity, centrilobular nodules, and absence of lower zone predominance of abnormalities (P < or = .008). The features that best differentiated NSIP were relative subpleural sparing, absence of lobular areas with decreased attenuation, and lack of honeycombing (P < or = .002). The features that best differentiated IPF were basal predominance of honeycombing, absence of relative subpleural sparing, and absence centrilobular nodules (P < or = .004). A confident diagnosis was made in 70 (53%) of 132 readings. This diagnosis was correct in 66 (94%) of 70 readings. The accuracy for the entire cohort was 80%. Interobserver agreement for confident diagnosis was good to excellent (kappa = 0.77-0.96). CONCLUSION: Characteristic CT features of chronic HP, IPF, and NSIP allow confident distinction between these entities in approximately 50% of patients.
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(2002) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.165.2.ats01 · Cited by 4,196
Statistical methods for assessing observer variability in clinical measures.
Brennan, P., & Silman, A. (1992) · BMJ · doi:10.1136/bmj.304.6840.1491 · Cited by 985
Austin, J. H., Müller, N. L., Friedman, P. J., Hansell, D. M., Naidich, D. P., Remy-Jardin, M., Webb, W. R., & Zerhouni, E. A. (1996) · Radiology · doi:10.1148/radiology.200.2.8685321 · Cited by 836
Self-citationClinical Diagnosis of Hypersensitivity Pneumonitis
Lacasse, Y., Selman, M., Costabel, U., Dalphin, J.-C., Ando, M., Morell, F., Erkinjuntti-Pekkanen, R., Müller, N., Colby, T. V., Schuyler, M., et al. (2003) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200301-137oc · Cited by 634
Self-citationClassification and Natural History of the Idiopathic Interstitial Pneumonias
Kim, D. S., Collard, H. R., & King, T. E. (2006) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200601-005tk · Cited by 431
Clinical Advances in the Diagnosis and Therapy of the Interstitial Lung Diseases
King, T. E. (2005) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200503-483oe · Cited by 330
Hunninghake, G. W., Lynch, D. A., Galvin, J. R., Gross, B. H., Mu¨ller, N., Schwartz, D. A., King, T. E., Lynch, J. P., Hegele, R., Waldron, J., et al. (2003) · Chest · doi:10.1378/chest.124.4.1215 · Cited by 317
Self-citationMacDonald, S. L. S., Rubens, M. B., Hansell, D. M., Copley, S. J., Desai, S. R., du Bois, R. M., Nicholson, A. G., Colby, T. V., & Wells, A. U. (2001) · Radiology · doi:10.1148/radiol.2213010158 · Cited by 310
Can CT distinguish hypersensitivity pneumonitis from idiopathic pulmonary fibrosis?
Lynch, D. A., Newell, J. D., Logan, P. M., King, T. E., & Müller, N. L. (1995) · American Journal of Roentgenology · doi:10.2214/ajr.165.4.7676971 · Cited by 236
Self-citationNon-Neoplastic Disorders of the Lower Respiratory Tract
Travis, W. D., Colby, T. V., Koss, M. N., Rosado-de-Christenson, M. L., Müller, N. L., & King, T. E. (2002) · doi:10.55418/1881041794 · Cited by 232
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Raghu, G., Collard, H. R., Egan, J. J., Martinez, F. J., Behr, J., Brown, K. K., Colby, T. V., Cordier, J.-F., Flaherty, K. R., Lasky, J. A., et al. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.2009-040gl · Cited by 7,186
Self-citationDiagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper
Lynch, D. A., Sverzellati, N., Travis, W. D., Brown, K. K., Colby, T. V., Galvin, J. R., Goldin, J. G., Hansell, D. M., Inoue, Y., Johkoh, T., et al. (2018) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(17)30433-2 · Cited by 1,030
Self-citationJavidan-Nejad, C., & Bhalla, S. (2009) · Radiologic clinics of North America · doi:10.1016/j.rcl.2008.11.006 · Cited by 49
Metadata
- Authors
- Silva, C. I. S., Müller, N. L., Lynch, D. A., Curran-Everett, D., Brown, K. K., Lee, K. S., Chung, M. P., & Churg, A.
- Venue
- Radiology
- Published
- 2008-01
- Volume
- 246
- Issue
- 1
- Pages
- 288-297
- ISSN
- 0033-8419 (ISSN-L)
- 1527-1315
- OpenAlex
- W2070365366
- Cited by
- 441
- References
- 17
- FWCI
- 17.25
- Type
- journal article
- Language
- en
- Open access
- closed
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