TY - JOUR
T1 - Persistent Hepatitis E virus infection across England and Wales 2009-2017
T2 - Demography, virology and outcomes
AU - the enhanced persistent HEV surveillance group
AU - Ankcorn, Michael
AU - Said, Bengü
AU - Morgan, Dilys
AU - Elsharkawy, Ahmed M.
AU - Maggs, James
AU - Ryder, Stephen
AU - Valliani, Talal
AU - Gordon, Fiona
AU - Abeysekera, Kushala
AU - Suri, Deepak
AU - McPherson, Stuart
AU - Galliford, Jack
AU - Smith, Belinda
AU - Pelosi, Emanuela
AU - Bansal, Sanjay
AU - Bethune, Claire
AU - Sheridan, David
AU - Vine, Louisa
AU - Tedder, Richard S.
AU - Ijaz, Samreen
AU - Riley, Unell
AU - Zuckerman, Mark
AU - Dalton, Harry
AU - Healy, Brendan
AU - Donati, Matthew
AU - Bicknell, Kelly
AU - Evans, Cariad
AU - Poller, Bozena
AU - Smit, Erasmus
AU - van Halsema, Clare
AU - Williams, Earl
AU - Raza, Mohammed
AU - McGann, Hugh
AU - Irving, Will
AU - Douthwaite, Sam
AU - Ch'ng, Chin Lye
AU - McCaughey, Conall
AU - Irish, Dianne
N1 - Publisher Copyright:
© 2020 John Wiley & Sons Ltd
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/2
Y1 - 2021/2
N2 - 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.
AB - 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.
KW - England
KW - Wales
KW - chronic
KW - hepatitis
KW - hepatitis E
KW - immunocompromised host
UR - http://www.scopus.com/inward/record.url?scp=85096914920&partnerID=8YFLogxK
U2 - 10.1111/jvh.13424
DO - 10.1111/jvh.13424
M3 - Article
C2 - 33073452
AN - SCOPUS:85096914920
SN - 1352-0504
VL - 28
SP - 420
EP - 430
JO - Journal of Viral Hepatitis
JF - Journal of Viral Hepatitis
IS - 2
ER -