PropertyValue
?:abstract
  • Background: COVID-19 is highly contagious, potentially deadly current pandemic with no evidence-based cure or vaccines The efficacy and safety of transfusion plasma of recovered patients were tested to treat patients with severe infection Method: In this preliminary, controlled study, 30 patients were allocated to one of two groups: Standard therapy group (control, n = 15) and recovered COVID-19 plasma group (RCP, n = 15) Control group, received standard therapy alone, while patients allocated to RCP group, were given a single dose,250 ml, of plasma of recovered COVID-19 individuals, plus standard COVID-19 therapy Neutralizing antibodies and severe COVID-19 serum biomarkers e g C-reactive protein, ferritin and d-dimer were measured in all patients before and after transfusion Our primary outcome was reduction of two or more of a four-category illness-severity scale over 5 days study period: Respiratory frequency ≥24/min, blood oxygen saturation ≤ 93% on room air, partial pressure of arterial oxygen to fraction of inspired oxygen ratio 50% of both lungs Results: Plasma of recovered COVID-19 resulted in improvement of laboratory and radiological findings In RCP group, there was statistically significant improvement of clinical parameters, as well as serum ferritin, D-dimer, c-reactive protein, and the size of lung lesion compared to control group (P ≤ 0 05) COVID-19 neutralizing antibodies appeared in serum of RCV patients, but failed to show in the control group patients during 5 days study period Conclusion: Plasma of recovered COVID-19 individuals is safe and effective therapeutic modality that significantly accelerated clinical improvement in patients with severe COVID-19 infection © 2020 The Author(s) Published by Informa UK Limited, trading as Taylor & Francis Group
is ?:annotates of
?:creator
?:journal
  • Egyptian_Journal_of_Anaesthesia
?:license
  • unk
?:publication_isRelatedTo_Disease
?:source
  • WHO
?:title
  • Efficacy and safety of transfusing plasma from COVID-19 survivors to COVID-19 victims with severe illness. A double-blinded controlled preliminary study
?:type
?:who_covidence_id
  • #915828
?:year
  • 2020

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