Dynamics of liver stiffness by transient elastography in patients with chronic hepatitis C virus infection receiving direct‐acting antiviral therapy—Results from the German Hepatitis C‐Registry

The impact of direct‐acting antiviral (DAA) therapies on fibrosis regression remains uncertain. In the current study, we prospectively evaluated dynamics of liver stiffness by transient elastography (TE) in patients with chronic HCV infection receiving DAA‐based treatment. Patients (260) were enroll...

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Veröffentlicht in:Journal of viral hepatitis 2020-07, Vol.27 (7), p.690-698
Hauptverfasser: Knop, Viola, Mauss, Stefan, Goeser, Tobias, Geier, Andreas, Zimmermann, Tim, Herzer, Kerstin, Postel, Nils, Friedrich‐Rust, Mireen, Hofmann, Wolf Peter, Ende, Katrin, Pathil, Anita, Bauer, Tilman, Zeuzem, Stefan, Berg, Thomas, Cornberg, Markus, Börner, Norbert, Ringelhan, Marc, Klinker, Hartwig, Schlenker, Thorsten, Lutz, Thomas, Heinzow, Hauke, Günther, Rainer, Busch, Heiner, Baumgarten, Axel, Buggisch, Peter, Roessle, Martin, Hüppe, Dietrich, Manns, Michael P., Niederau, Claus, Sarrazin, Christoph, Schirmacher, Peter, Simon, Karl‐Georg, Wedemeyer, Heiner
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Sprache:eng
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Zusammenfassung:The impact of direct‐acting antiviral (DAA) therapies on fibrosis regression remains uncertain. In the current study, we prospectively evaluated dynamics of liver stiffness by transient elastography (TE) in patients with chronic HCV infection receiving DAA‐based treatment. Patients (260) were enrolled in the German Hepatitis C‐Registry (DHC‐R), a national multicentre real‐world cohort. Liver stiffness (LS) was assessed at baseline, end of treatment (EOT) and 24 weeks after EOT (FU24) by TE. Biochemical, virological and clinical data were obtained in parallel. In patients with SVR, there was a significant improvement of LS between baseline (median [range], 8.6 [1.7‐73.5] kPa) and FU24 (7.9 [1.7‐75 kPa]; P 
ISSN:1352-0504
1365-2893
DOI:10.1111/jvh.13280