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dc.rights.licenseopenen_US
hal.structure.identifierCHU Bordeaux
dc.contributor.authorCAMOU, Fabrice
hal.structure.identifierCHU Bordeaux
dc.contributor.authorTINEVEZ, Claire
hal.structure.identifierEtablissement Français du Sang Nouvelle Aquitaine [Bordeaux] [EFS Bordeaux Nouvelle Aquitaine]
dc.contributor.authorBEGUET-YACHINE, Mathilde
hal.structure.identifierCHU Bordeaux
dc.contributor.authorBELLECAVE, Pantxika
hal.structure.identifierEtablissement Français du Sang Nouvelle Aquitaine [Bordeaux] [EFS Bordeaux Nouvelle Aquitaine]
dc.contributor.authorRATIARISON, Diana
hal.structure.identifierCHU Bordeaux
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorTUMIOTTO, Camille
hal.structure.identifierBiothérapies des maladies génétiques et cancers
hal.structure.identifierEtablissement Français du Sang Nouvelle Aquitaine [Bordeaux] [EFS Bordeaux Nouvelle Aquitaine]
dc.contributor.authorLAFARGE, Xavier
hal.structure.identifierCHU Bordeaux
dc.contributor.authorGUISSET, Olivier
hal.structure.identifierCHU Bordeaux
dc.contributor.authorMOURISSOUX, Gaelle
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorLAFON, Marie-Edith
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBONNET, Fabrice
hal.structure.identifierCHU Bordeaux
dc.contributor.authorISSA, Nahema
dc.date.accessioned2023-05-23T09:34:51Z
dc.date.available2023-05-23T09:34:51Z
dc.date.issued2021-05-03
dc.identifier.issn0146-6615en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/182256
dc.description.abstractEnThis study aims to assess the efficacy and safety of convalescent plasma therapy (CPT) in COVID-19 critically ill patients with protracted severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNAemia. A retrospective cohort study was conducted in intensive care unit (ICU). All patients with severe COVID-19 pneumonia for whom RNAemia remained positive more than 14 days after onset of the infection were included and given CPT. The primary objective was to evaluate SARS-CoV-2 RNAemia 7 days (D7) after CPT. A total of 14 patients were included and they received a median CPT volume of 828 ml (range: 817-960). CPT was administered in a median time of 14 days after ICU admission. At D7, 13/14 patients had negative SARS-CoV-2 blood PCR and one patient had negative blood PCR 11 days after CPT. At D7 and at D14, the clinical status was improved in 7/14 and 11/14 patients, respectively. The 28-day mortality rate was 14%. No CPT-related adverse effects had been reported. CPT is safe and may be efficient in patients with protracted RNAemia admitted in ICU for severe COVID-19 pneumonia. Randomized controlled trials are needed to confirm these results.
dc.language.isoENen_US
dc.subject.enCombination therapy
dc.subject.enDisease control
dc.subject.enGeneralized infection
dc.subject.enPathogenesis
dc.subject.enSARS coronavirus
dc.subject.enVirus classification
dc.title.enFeasibility of convalescent plasma therapy in severe COVID-19 patients with persistent SARS-CoV-2 viremia
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/jmv.27032en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
bordeaux.journalJournal of Medical Virologyen_US
bordeaux.pageOnline ahead of printen_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.institutionCNRSen_US
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionINSERM
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-03278001
hal.version1
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
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