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Volume 72, Issue 2, Pages 278-283 (November 2009)


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Computer-assisted quantification of interstitial lung disease associated with rheumatoid arthritis: Preliminary technical validation

K. Martena, V. Dickend, C. Kneitzc, M. Hoehmannb, W. Kennb, D. Hahnb, C. EngelkeaCorresponding Author Informationemail address

Received 1 April 2008; received in revised form 6 July 2008; accepted 7 July 2008.

Abstract 

Purpose

To validate a threshold-based prototype software application (MeVis PULMO 3D) for quantification of chronic interstitial lung disease (ILD) in patients with rheumatoid arthritis (RA) using variable threshold settings for segmentation of diseased lung areas.

Methods

Twenty-two patients with rheumatoid arthritis were included and underwent thin-section CT (4×1.25mm collimation). CT scans were assessed by two observers for extent of ILD (EoILD), and twice by MeVis PULMO 3D for each protocol. MeVis PULMO 3D used four segmentation threshold (ST) settings (ST=−740, −780, −800 and −840HU). Pulmonary function tests were obtained in all patients. Statistical evaluation used 95% limits of agreement (LoA) and linear regression analysis.

Results

There was total concordance between the software measurements. Interobserver agreement was good (LoA=−28.36 to 17.58%). EoILD by readers correlated strongly with DLCO (r=−0.702, p<0.0001) and moderately with FVC (r=−0.523, p=0.018). There was close correlation between readers and MeVis PULMO 3D with best results for ST <780HU (EoILD vs. MeVis PULMO 3D: r=0.650 for ST=−800 and −840HU, respectively; p=0.002). MeVis PULMO 3D correlated best with DLCO at ST of −800HU (r=−0.44, −0.49, −0.58 and −0.57 for ST=−740, −780, −800 and −840, respectively; p=0.007–0.05) and moderately with FVC (r=−0.44, −0.51, −0.59 and −0.45 for ST=−740, −780, −800 and −840), respectively; p=0.007–0.05).

Conclusion

The MeVis PULMO 3D system used holds promise to become a valuable instrument for quantification of chronic ILD in patients with RA when using the threshold value of −800HU, with evidence of the closest correlations, both with human observers and physiologic impairment.

a Department of Radiology, Georg August University of Göttingen, Robert-Koch-Strasse 40, 37075 Göttingen, Germany

b Department of Radiology, University Hospital of Würzburg, Josef-Schneider-Strasse 2, 97080 Würzburg, Germany

c Department of Rheumatology and Clinical Immunology, Medizinische Klinik and Poliklinik, University Hospital of Würzburg, Klinikstrasse 6, 97070 Würzburg, Germany

d MeVis Research GmbH, Universitätsallee 29, 28359 Bremen, Germany

Corresponding Author InformationCorresponding author.

PII: S0720-048X(08)00388-4

doi:10.1016/j.ejrad.2008.07.008


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