2013
DOI: 10.1111/tid.12096
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Hepatitis E virus infection in a liver transplant recipient: delayed diagnosis due to variable performance of serologic assays

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Cited by 21 publications
(14 citation statements)
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“…Importantly, none of these anti-HEV-assays has been approved by the Food and Drug Administration (FDA), while in Europe and Asia, many different assays are used. In the US, testing for HEV is limited to few specialized centers, and thus diagnosis of HEV infections in the US can be delayed [51]. …”
Section: Diagnosis Of Acute Hev Infectionmentioning
confidence: 99%
“…Importantly, none of these anti-HEV-assays has been approved by the Food and Drug Administration (FDA), while in Europe and Asia, many different assays are used. In the US, testing for HEV is limited to few specialized centers, and thus diagnosis of HEV infections in the US can be delayed [51]. …”
Section: Diagnosis Of Acute Hev Infectionmentioning
confidence: 99%
“…Recently, Yoo et al. reported a case in which an HEV infection was missed in an adult SOT recipient because of the poor sensitivity of a commercial HEV serologic assay.…”
Section: Discussionmentioning
confidence: 99%
“…Barriers to diagnosis include low clinical suspicion, lack of epidemiological risk factors and population prevalence estimates among North American SOT recipients, and paucity of commercially available, reliable, and accurate testing for HEV markers of infection. The lack of a US Food and Drug Administration (FDA)‐approved diagnostic test, and the variability in the performance characteristics of commercially available serologic assays, make testing for HEV infection especially challenging .…”
mentioning
confidence: 99%
“…As these studies suggest, the limited reliability of available tests may well delay a patient's HEV diagnosis . Additionally, HEV infection can be misdiagnosed or entirely missed through a failure to consider this virus as a possibility.…”
Section: Diagnosismentioning
confidence: 99%