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Transjugular Intrahepatic Portosystemic Shunt: A Possible Risk Factor for Direct-Acting Antiviral Treatment Failure in Patients With Hepatitis C?
Piecha, Felix; Gänßler, Jan-Michael; Jordan, Sabine; Ergen, Can; Ittrich, Harald; Kluwe, Johannes; Pischke, Sven; Lohse, Ansgar W; Schulze Zur Wiesch, Julian.
Affiliation
  • Piecha F; I. Department of Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Gänßler JM; I. Department of Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Jordan S; I. Department of Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Ergen C; I. Department of Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Ittrich H; Department of Diagnostic and Interventional Radiology and Nuclear Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Kluwe J; I. Department of Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Pischke S; I. Department of Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Lohse AW; I. Department of Medicine University Medical Center Hamburg-Eppendorf Hamburg Germany.
  • Schulze Zur Wiesch J; German Center for Infection Research Partner Site Hamburg-Lübeck-Borstel-Riems Germany.
Hepatol Commun ; 3(5): 614-619, 2019 May.
Article in En | MEDLINE | ID: mdl-31061950
ABSTRACT
Direct-acting antiviral (DAA) therapies have revolutionized the treatment of chronic hepatitis C virus infection, achieving sustained virological response (SVR) rates of >90% even in patients with advanced liver cirrhosis. Having observed an unusual case of repeated DAA therapy failures in a patient with a transjugular intrahepatic portosystemic shunt (TIPS), we assessed a possible association between prior TIPS placement and DAA failure. A structured search of our clinical database revealed 10 patients who had received DAA therapy after TIPS placement. At the time of therapy, most patients (8; 80%) presented with a Child-Pugh score B, and the following DAA regimens were used sofosbuvir/ledipasvir ± ribavirin (5 patients), sofosbuvir/daclatasvir ± ribavirin (3), sofosbuvir/velpatasvir (2), and sofosbuvir/velpatasvir/voxilaprevir (1). In total, 5 patients (50%) achieved an SVR, whereas a virological relapse occurred in the other half of the cases, including 2 patients with multiple relapses. In this patient cohort, SVR rates were unusually low for all regimens sofosbuvir/ledipasvir ± ribavirin, 3/5 (60%); sofosbuvir/daclatasvir ± ribavirin, 2/3 (66%); sofosbuvir/velpatasvir, 0/2 (0%); and sofosbuvir/velpatasvir/voxilaprevir, 0/1 (0%), and patients with a TIPS made up a relevant proportion of DAA failures in patients with cirrhosis at our center sofosbuvir/ledipasvir, 2/18 (11%); sofosbuvir/daclatasvir, 1/4 (25%); sofosbuvir/velpatasvir, 2/3 (66%); and sofosbuvir/velpatasvir/voxilaprevir, 1/1 (100%).

Conclusion:

We observed a high rate of virological relapse in patients with a TIPS who received DAA treatment and therefore postulate that TIPS placement may be a possible risk factor for DAA failure due to the profound hemodynamic changes evoked by the intervention. Longer treatment duration or addition of ribavirin might be warranted in these patients.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Risk_factors_studies Language: En Journal: Hepatol Commun Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Risk_factors_studies Language: En Journal: Hepatol Commun Year: 2019 Document type: Article