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Feasibility of convalescent plasma therapy in severe COVID-19 patients with persistent SARS-CoV-2 viremia.
Camou, Fabrice; Tinevez, Claire; Beguet-Yachine, Mathilde; Bellecave, Pantxika; Ratiarison, Diana; Tumiotto, Camille; Lafarge, Xavier; Guisset, Olivier; Mourissoux, Gaëlle; Lafon, Marie-Edith; Bonnet, Fabrice; Issa, Nahéma.
  • Camou F; Department of Intensive Care and Infectious Diseases, Saint-Andre Hospital, CHU BORDEAUX, Bordeaux, France.
  • Tinevez C; Department of Intensive Care and Infectious Diseases, Saint-Andre Hospital, CHU BORDEAUX, Bordeaux, France.
  • Beguet-Yachine M; Etablissement Français du Sang Nouvelle Aquitaine, Bordeaux, France.
  • Bellecave P; Virology Laboratory, Pellegrin Hospital, CHU BORDEAUX, Bordeaux, France.
  • Ratiarison D; Etablissement Français du Sang Nouvelle Aquitaine, Bordeaux, France.
  • Tumiotto C; Virology Laboratory, Pellegrin Hospital, CHU BORDEAUX, Bordeaux, France.
  • Lafarge X; University of Bordeaux and CNRS UMR5234, Bordeaux, France.
  • Guisset O; Etablissement Français du Sang Nouvelle Aquitaine, Bordeaux, France.
  • Mourissoux G; INSERM U1035, University of Bordeaux, Bordeaux, France.
  • Lafon ME; Department of Intensive Care and Infectious Diseases, Saint-Andre Hospital, CHU BORDEAUX, Bordeaux, France.
  • Bonnet F; Department of Intensive Care and Infectious Diseases, Saint-Andre Hospital, CHU BORDEAUX, Bordeaux, France.
  • Issa N; Virology Laboratory, Pellegrin Hospital, CHU BORDEAUX, Bordeaux, France.
J Med Virol ; 93(9): 5594-5598, 2021 Sep.
Article in English | MEDLINE | ID: covidwho-1212757
ABSTRACT
This 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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: J Med Virol Year: 2021 Document Type: Article Affiliation country: Jmv.27032

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: J Med Virol Year: 2021 Document Type: Article Affiliation country: Jmv.27032