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dc.contributor.authorErtesvåg, Nina Urke
dc.contributor.authorSakkestad, Sunniva Todnem
dc.contributor.authorZhou, Fan
dc.contributor.authorHoff, Ingrid
dc.contributor.authorKristiansen, Trygve
dc.contributor.authorJonassen, Trygve Müller
dc.contributor.authorFollesø, Elisabeth
dc.contributor.authorBrokstad, Karl Albert
dc.contributor.authorDyrhovden, Ruben
dc.contributor.authorMohn, Kristin Greve-Isdahl
dc.date.accessioned2023-03-22T12:53:35Z
dc.date.available2023-03-22T12:53:35Z
dc.date.created2022-10-19T10:53:06Z
dc.date.issued2022
dc.identifier.citationViruses. 2022, 14(8):1757.en_US
dc.identifier.issn1999-4915
dc.identifier.urihttps://hdl.handle.net/11250/3059870
dc.description.abstractBackground: Persistent fever after SARS-CoV-2 infection in rituximab-treated patients has been reported. Due to reduced sensitivity in conventional sampling methods and unspecific symptoms in these patients, distinguishing between low-grade viral replication or hyperinflammation is challenging. Antiviral treatment is recommended as prophylactic or early treatment in the at-risk population; however, no defined treatment approaches for protracted SARS-CoV-2 infection exist. Results: We present a case of 96 days of persistent fever and SARS-CoV-2 infection in a patient receiving B cell depletion therapy for multiple sclerosis. Migratory lung infiltrates and positive PCR tests from serum (day-58 post infection) and lower airways (day-90 post infection) confirmed continuous viral replication. The dominant symptoms were continuous high fever, dyspnea and mild to moderate hypoxemia, which never developed into severe respiratory failure. The patient was hospitalized three times, with transient improvement after late antiviral treatment and full recovery 6 months post-rituximab infusion. Conclusions: A strategy for securing samples from lower airways and serum should be a prioritization to strengthen diagnostic certainty in immunocompromised patients. B-cell-deprived patients could benefit from late treatment with SARS-CoV-2-specific monoclonal antibodies and antivirals. Importantly, increased intervals between immunosuppressive therapy should be considered where feasible.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titlePersistent Fever and Positive PCR 90 Days Post-SARS-CoV-2 Infection in a Rituximab-Treated Patient: A Case of Late Antiviral Treatmenten_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2022 by the authors.en_US
dc.source.volume14en_US
dc.source.journalVirusesen_US
dc.source.issue8en_US
dc.identifier.doi10.3390/v14081757
dc.identifier.cristin2062674
dc.source.articlenumber1757en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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