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Ribavirin Therapy in Immunodeficient Patients with Chronic Hepatitis E Virus Infection

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Hepatitis E virus (HEV) infection, usually self-limiting in immunocompetent individuals, may adopt a chronic course in immunodeficient patients. A low threshold for HEV screening in immunodeficient patients is advocated so early management can be initiated to minimise liver injury. This retrospective, observational study evaluated all cases (n=11) of chronic HEV diagnosed in immunodeficient patients in 2 university hospitals in Bristol, UK between February 2014 and October 2017. We report our experiences in the management of chronic HEV including ribavirin use. No patients achieved viral clearance spontaneously or with reduction of immunosuppression and so all were treated with ribavirin. The median time between chronic HEV diagnosis and initiation of ribavirin was 91 days (range, 1–293 days). The median ribavirin dose at initiation was 1000 mg/day (range 800-1200 mg/day) and at cessation was 900 mg/day (range 600–1200 mg/day), reduced due to anaemia. Different end points guided treatment cessation including negative HEV RNA PCR serology +/- negative stool HEV RNA PCR +/- biochemical remission at various time points. Following ribavirin therapy, HEV relapse occurred in 1 patient. The mean duration of ribavirin therapy, excluding the patient who was re-treated, was 4.6 months. One significant adverse event of severe anaemia requiring transfusion was observed. This case series supports the use of ribavirin monotherapy for chronic HEV in immunodeficient patients. Anaemia commonly developed prompting ribavirin dose reduction. We advocate 2 consecutive negative serum and stool HEV RNA PCR results sampled at 4 weekly intervals to guide ribavirin cessation.
Title: Ribavirin Therapy in Immunodeficient Patients with Chronic Hepatitis E Virus Infection
Description:
Hepatitis E virus (HEV) infection, usually self-limiting in immunocompetent individuals, may adopt a chronic course in immunodeficient patients.
A low threshold for HEV screening in immunodeficient patients is advocated so early management can be initiated to minimise liver injury.
This retrospective, observational study evaluated all cases (n=11) of chronic HEV diagnosed in immunodeficient patients in 2 university hospitals in Bristol, UK between February 2014 and October 2017.
We report our experiences in the management of chronic HEV including ribavirin use.
No patients achieved viral clearance spontaneously or with reduction of immunosuppression and so all were treated with ribavirin.
The median time between chronic HEV diagnosis and initiation of ribavirin was 91 days (range, 1–293 days).
The median ribavirin dose at initiation was 1000 mg/day (range 800-1200 mg/day) and at cessation was 900 mg/day (range 600–1200 mg/day), reduced due to anaemia.
Different end points guided treatment cessation including negative HEV RNA PCR serology +/- negative stool HEV RNA PCR +/- biochemical remission at various time points.
Following ribavirin therapy, HEV relapse occurred in 1 patient.
The mean duration of ribavirin therapy, excluding the patient who was re-treated, was 4.
6 months.
One significant adverse event of severe anaemia requiring transfusion was observed.
This case series supports the use of ribavirin monotherapy for chronic HEV in immunodeficient patients.
Anaemia commonly developed prompting ribavirin dose reduction.
We advocate 2 consecutive negative serum and stool HEV RNA PCR results sampled at 4 weekly intervals to guide ribavirin cessation.

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