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dc.contributor.authorO'Flaherty, N
dc.contributor.authorUshiro-Lumb, I
dc.contributor.authorPomeroy, L
dc.contributor.authorIjaz, S
dc.contributor.authorBoland, F
dc.contributor.authorDe Gascun, C
dc.contributor.authorFitzgerald, J
dc.contributor.authorO'Riordan, J
dc.date.accessioned2018-02-21T15:24:17Z
dc.date.available2018-02-21T15:24:17Z
dc.date.issued2018-02-14
dc.identifier.citationTransfusion-transmitted hepatitis B virus (HBV) infection from an individual-donation nucleic acid (ID-NAT) non-reactive donor. 2018 Vox Sang.en
dc.identifier.issn1423-0410
dc.identifier.pmid29441587
dc.identifier.doi10.1111/vox.12633
dc.identifier.urihttp://hdl.handle.net/10147/622806
dc.description.abstractLookback was initiated upon notification of an acute HBV infection in a repeat Irish donor, 108 days post-donation. The donation screened non-reactive by individual-donation nucleic acid testing (ID-NAT) using the Procleix Ultrio Elite multiplex assay and again when the archived sample was retested, but the discriminatory assay for HBV was reactive. The immunocompromised recipient of the implicated red cell component was tested 110 days post-transfusion, revealing a HBV DNA viral load of 470 IU/ml. Genotype C2 sequences identical across two regions of the HBV genome were found in samples from the donor and recipient.
dc.language.isoenen
dc.publisherVox sanguinisen
dc.rightsArchived with thanks to Vox sanguinisen
dc.titleTransfusion-transmitted hepatitis B virus (HBV) infection from an individual-donation nucleic acid (ID-NAT) non-reactive donor.en
dc.typeArticleen
dc.identifier.journalVox sanguinisen
refterms.dateFOA2018-08-28T01:45:02Z
html.description.abstractLookback was initiated upon notification of an acute HBV infection in a repeat Irish donor, 108 days post-donation. The donation screened non-reactive by individual-donation nucleic acid testing (ID-NAT) using the Procleix Ultrio Elite multiplex assay and again when the archived sample was retested, but the discriminatory assay for HBV was reactive. The immunocompromised recipient of the implicated red cell component was tested 110 days post-transfusion, revealing a HBV DNA viral load of 470 IU/ml. Genotype C2 sequences identical across two regions of the HBV genome were found in samples from the donor and recipient.


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