Performance of two‐dimensional shear wave elastography and transient elastography compared to liver biopsy for staging of liver fibrosis

Author:

Kovatsch Audrey1,Honcharova‐Biletska Hanna2,Segna Daniel13,Steigmiller Klaus4,Blümel Sena1,Deibel Rudolf A.1,Kühlewindt Tobias1,Leinenkugel Georg1,Müller Sandra1,Furrer Eva4,Schawkat Khoschy56,Reiner Cäcilia S.6,Weber Achim2,Müllhaupt Beat1,Scharl Michael1,Gubler Christoph17,Jüngst Christoph18ORCID

Affiliation:

1. Department of Gastroenterology and Hepatology University Hospital Zurich Zurich Switzerland

2. Department of Pathology University Hospital Zurich Zurich Switzerland

3. Department of Visceral Surgery and Medicine Inselspital, Bern University Hospital, University of Bern Bern Switzerland

4. Institute of Epidemiology, Biostatistics and Prevention University of Zurich Zurich Switzerland

5. Department of Radiology Brigham and Women's Hospital and Harvard Medical School Boston Massachusetts USA

6. Institute of Diagnostic and Interventional Radiology University Hospital Zurich Zurich Switzerland

7. Division of Gastroenterology &Hepatology Triemli Hospital Zurich Switzerland

8. Department of Medicine II Saarland University Medical Center, Saarland University Homburg Germany

Abstract

AbstractBackgroundStaging of liver fibrosis traditionally relied on liver histology; however, transient elastography (TE) and more recently two‐dimensional shear wave elastography (2D‐SWE) evolved to noninvasive alternatives. Hence, we evaluated the diagnostic accuracy of 2D‐SWE assessed by the Canon Aplio i800 ultrasound system using liver biopsy as reference and compared the performance to TE.MethodsIn total, 108 adult patients with chronic liver disease undergoing liver biopsy, 2D‐SWE and TE were enrolled prospectively at the University Hospital Zurich. Diagnostic accuracies were evaluated using the area under the receiver operating characteristic (AUROC) analysis, and optimal cut‐off values by Youden's index.ResultsDiagnostic accuracy of 2D‐SWE was good for significant (≥F2; AUROC 85.2%, 95% confidence interval (95%CI):76.2–91.2%) as well as severe fibrosis (≥F3; AUROC 86.8%, 95%CI: 78.1–92.4%) and excellent for cirrhosis (AUROC 95.6%, 95%CI: 89.9–98.1%), compared to histology. TE performed equally well (significant fibrosis: 87.5%, 95%CI: 77.7–93.3%; severe fibrosis: 89.7%, 95%CI: 82.0–94.3%; cirrhosis: 96%, 95%CI: 90.4–98.4%), and accuracy was not statistically different to 2D‐SWE. 2D‐SWE optimal cut‐off values were 6.5, 9.8 and 13.1 kPa for significant fibrosis, severe fibrosis and cirrhosis, respectively.ConclusionsPerformance of 2D‐SWE was good to excellent and well comparable with TE, supporting the application of this 2D‐SWE system in the diagnostic workup of chronic liver disease.

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

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