Persistent Hepatitis E virus infection across England and Wales 2009-2017: Demography, virology and outcomes.


Journal

Journal of viral hepatitis
ISSN: 1365-2893
Titre abrégé: J Viral Hepat
Pays: England
ID NLM: 9435672

Informations de publication

Date de publication:
02 2021
Historique:
received: 15 06 2020
revised: 20 09 2020
accepted: 02 10 2020
pubmed: 20 10 2020
medline: 1 9 2021
entrez: 19 10 2020
Statut: ppublish

Résumé

The first clinical case of persistent HEV infection in England was reported in 2009. We describe the demography, virology and outcomes of patients identified with persistent HEV infection in England and Wales between 2009 and 2017. A series of 94 patients with persistent HEV infection, defined by HEV viraemia of more than 12 weeks, was identified through routine reference laboratory testing. Virology, serology and clinical data were recorded through an approved PHE Enhanced Surveillance System. Sixty-six cases (70.2%) were transplant recipients, 16 (17.0%) had an underlying haematological malignancy without stem cell transplantation, six (6.4%) had advanced HIV infection, five (5.3%) were otherwise immunosuppressed, and one patient (1.1%) had no identified immunosuppression. Retrospective analysis of 46 patients demonstrated a median 38 weeks of viraemia before diagnostic HEV testing. At initial diagnosis, 16 patients (17.0%) had no detectable anti-HEV serological response. Of 65 patients treated with ribavirin monotherapy, 11 (16.9%) suffered virological relapse despite undetectable RNA in plasma or stool at treatment cessation. Persistent HEV infection remains a rare diagnosis, but we demonstrate that a broad range of immunocompromised patients are susceptible. Both lack of awareness and the pauci-symptomatic nature of persistent HEV infection likely contribute to significant delays in diagnosis. Diagnosis should rely on molecular testing since anti-HEV serology is insufficient to exclude persistent HEV infection. Finally, despite treatment with ribavirin, relapses occur even after cessation of detectable faecal shedding of HEV RNA, further emphasising the requirement to demonstrate sustained virological responses to treatment.

Identifiants

pubmed: 33073452
doi: 10.1111/jvh.13424
doi:

Substances chimiques

RNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

420-430

Investigateurs

Unell Riley (U)
Mark Zuckerman (M)
Harry Dalton (H)
Brendan Healy (B)
Matthew Donati (M)
Kelly Bicknell (K)
Cariad Evans (C)
Bozena Poller (B)
Erasmus Smit (E)
Clare van Halsema (C)
Earl Williams (E)
Mohammed Raza (M)
Hugh McGann (H)
Will Irving (W)
Sam Douthwaite (S)
Chin Lye Ch'ng (CL)
Conall McCaughey (C)
Dianne Irish (D)

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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Auteurs

Michael Ankcorn (M)

Blood Borne Virus Unit, Virus Reference Department, National Infection Service, Public Health England, London, UK.
Transfusion Microbiology, National Health Service Blood and Transplant, London, UK.

Bengü Said (B)

Emerging Infections and Zoonoses, National Infection Service, Public Health England, London, UK.

Dilys Morgan (D)

Emerging Infections and Zoonoses, National Infection Service, Public Health England, London, UK.

Ahmed M Elsharkawy (AM)

The Liver Unit, University Hospitals Birmingham, Birmingham, UK.

James Maggs (J)

Department of Gastroenterology, Buckinghamshire Healthcare NHS Trust, Buckinghamshire, UK.

Stephen Ryder (S)

Department of Hepatology, Nottingham University Hospitals NHS Trust, Nottingham, UK.

Talal Valliani (T)

North Bristol Liver Unit, North Bristol NHS Trust, Southmead Hospital, Bristol, UK.

Fiona Gordon (F)

Department of Hepatology, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.

Kushala Abeysekera (K)

Department of Hepatology, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.

Deepak Suri (D)

Department of Hepatology, University College London Hospitals, London, UK.

Stuart McPherson (S)

Liver Unit, Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, & Institute of Cellular Medicine, Newcastle University, Newcastle, UK.

Jack Galliford (J)

Department of Nephrology, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Belinda Smith (B)

Department of Hepatology, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Emanuela Pelosi (E)

Department of Infection, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Sanjay Bansal (S)

Department of Paediatric Hepatology, Gastroenterology & Nutrition Center, King's College Hospital NHS Foundation Trust, London, UK.

Claire Bethune (C)

Department of Immunology and Allergy, University Hospitals Plymouth NHS Trust, Plymouth, UK.

David Sheridan (D)

South West Liver Unit, University Hospitals Plymouth NHS Trust, Plymouth, UK.

Louisa Vine (L)

South West Liver Unit, University Hospitals Plymouth NHS Trust, Plymouth, UK.

Richard S Tedder (RS)

Blood Borne Virus Unit, Virus Reference Department, National Infection Service, Public Health England, London, UK.
Transfusion Microbiology, National Health Service Blood and Transplant, London, UK.
Department of Medicine, Imperial College London, London, UK.

Samreen Ijaz (S)

Blood Borne Virus Unit, Virus Reference Department, National Infection Service, Public Health England, London, UK.

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