Early ribavirin for hepatitis E virus infection in patients receiving immunosuppressive therapy: a retrospective, observational study

GND
1072851784
Affiliation
Department of Internal Medicine IV,Jena University Hospital , Friedrich Schiller University, Jena, Germany
Franz, Anika;
GND
140826882
ORCID
0000-0002-7696-475X
Affiliation
Department of Internal Medicine IV,Jena University Hospital , Friedrich Schiller University, Jena, Germany
Reuken, Philipp A;
GND
1323060723
Affiliation
Department of Internal Medicine IV,Jena University Hospital , Friedrich Schiller University, Jena, Germany
Guliyeva, Sura;
GND
1249109752
Affiliation
Department of Clinical Chemistry and Laboratory Medicine,Jena University Hospital , Jena, Germany
Rose, Michael;
GND
1141696290
Affiliation
Department of Clinical Chemistry and Laboratory Medicine,Jena University Hospital , Jena, Germany
Boden, Katharina;
GND
1116442140
Affiliation
Department of Internal Medicine IV,Jena University Hospital , Friedrich Schiller University, Jena, Germany
Stallmach, Andreas;
Affiliation
Department of Internal Medicine III, University Hospital RWTH Aachen, Aachen, Germany
Bruns, Tony

Objective Hepatitis E virus (HEV) infections are common, self-limiting causes of acute viral hepatitis. This study aimed to analyze hepatic injury, viremia, and chronicity rates in patients with acute HEV infection receiving immunosuppressive (IS) therapy taking into account ribavirin treatment. Methods In this retrospective, single-center, observational study, we analyzed the disease course of 25 non-cirrhotic patients receiving IS therapy who were diagnosed with acute HEV viremia. Forty-four patients with acute HEV viremia without IS therapy were controls. Results Demographics, symptoms at presentation, and extrahepatic manifestations were not different between patients with and without IS therapy, but liver injury at presentation was less severe in patients with IS therapy. Among the patients with IS therapy, 18 (72%) received ribavirin for a median of 56 days. Sustained viral clearance was observed in 21 patients with IS therapy, whereas 3 patients relapsed after ribavirin, and 1 patient had viral persistence. Among patients with sustained viral clearance, there was a longer duration of viremia in patients with IS therapy than in those without. Conclusions In this cohort of non-cirrhotic patient with IS, early treatment with ribavirin for acute HEV infection did not improve viral clearance rates, but may have shortened the duration of viremia.

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