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      A new SARS-CoV-2 variant poorly detected by RT-PCR on nasopharyngeal samples, with high lethality: an observational study

      research-article
      , M.D. 1 , , , M.D. 2 , , P.D. 3 , , M.D. 4 , 5 , , M.D. 6 , , M.D 6 , , M.D 4 , , M.D 7 , , M.D 8 , , M.D 9 , , M.D 10 , , Ph.D. 3 , 11 , , M.D 5 , , M.D 5 , , M.D 12 , , M.D. 13 , , Ph.D. 14 , , Ph.D. 15 , , M.D. 16 , , M.D., Ph.D. 17 , , M.D. 17 , , M.D. 17 , , M.D., Ph.D. 18 , , Ph.D. 14 ,   , Ph.D. 19 , , M.D., Ph.D. 3 , # , , M.D., Ph.D. 20 , ∗∗ , # , , M.D. 1 , #
      Clinical Microbiology and Infection
      European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd.
      Coronavirus infections, COVID-19 / Epidemiology, SARS-CoV-2 variants, Severity of illness index / Virology

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          Abstract

          Objectives

          In early January 2021, an outbreak of nosocomial cases of COVID-19 emerged in Western France, with RT-PCR tests repeatedly negative on nasopharyngeal samples but positive on lower respiratory tract samples. Whole genome sequencing (WGS) revealed a new variant, currently defining a novel SARS-CoV-2 lineage: B.1.616. In March, WHO classified this variant as ‘under investigation’ (VUI). We analyzed the characteristics and outcomes of COVID-19 cases related to this new variant.

          Methods

          Clinical, virological, and radiological data were retrospectively collected from medical charts in the two hospitals involved. We enrolled inpatients with either: i) positive SARS-CoV-2 RT-PCR on a respiratory sample; ii) seroconversion with anti-SARS-CoV-2 IgG/IgM; iii) suggestive symptoms and typical features of COVID-19 on a chest CT scan. Cases were categorized as either: i) B.1.616; ii) variant of concern (VOC); iii) unknown.

          Results

          From January 1 st to March 24 th, 2021, 114 patients fulfilled inclusion criteria: B.1.616 (n=39), VOC (n=32), and unknown (n=43). B.1.616-related cases were older than VOC-related cases (81 years interquartile range [IQR] [73-88], vs 73 years IQR [67-82], P<0.05) and their first RT-PCR tests were rarely positive (6/39, 15% vs 31/32, 97%, P<0.05). B.1.616 variant was independently associated with severe disease (multivariable Cox model HR 4.0 95% CI [1.5-10.9]), and increased lethality: 28-day mortality 18/39 (46%) for B.1.616, vs. 5/32 (16%) for VOC, P=0.006.

          Conclusion

          We report a nosocomial outbreak of COVID-19 cases related to a new variant, B.1.616, poorly detected by RT-PCR on nasopharyngeal samples, with high lethality.

          Graphical abstract

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          Most cited references23

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          Dexamethasone in Hospitalized Patients with Covid-19 — Preliminary Report

          Abstract Background Coronavirus disease 2019 (Covid-19) is associated with diffuse lung damage. Glucocorticoids may modulate inflammation-mediated lung injury and thereby reduce progression to respiratory failure and death. Methods In this controlled, open-label trial comparing a range of possible treatments in patients who were hospitalized with Covid-19, we randomly assigned patients to receive oral or intravenous dexamethasone (at a dose of 6 mg once daily) for up to 10 days or to receive usual care alone. The primary outcome was 28-day mortality. Here, we report the preliminary results of this comparison. Results A total of 2104 patients were assigned to receive dexamethasone and 4321 to receive usual care. Overall, 482 patients (22.9%) in the dexamethasone group and 1110 patients (25.7%) in the usual care group died within 28 days after randomization (age-adjusted rate ratio, 0.83; 95% confidence interval [CI], 0.75 to 0.93; P<0.001). The proportional and absolute between-group differences in mortality varied considerably according to the level of respiratory support that the patients were receiving at the time of randomization. In the dexamethasone group, the incidence of death was lower than that in the usual care group among patients receiving invasive mechanical ventilation (29.3% vs. 41.4%; rate ratio, 0.64; 95% CI, 0.51 to 0.81) and among those receiving oxygen without invasive mechanical ventilation (23.3% vs. 26.2%; rate ratio, 0.82; 95% CI, 0.72 to 0.94) but not among those who were receiving no respiratory support at randomization (17.8% vs. 14.0%; rate ratio, 1.19; 95% CI, 0.91 to 1.55). Conclusions In patients hospitalized with Covid-19, the use of dexamethasone resulted in lower 28-day mortality among those who were receiving either invasive mechanical ventilation or oxygen alone at randomization but not among those receiving no respiratory support. (Funded by the Medical Research Council and National Institute for Health Research and others; RECOVERY ClinicalTrials.gov number, NCT04381936; ISRCTN number, 50189673.)
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            Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area

            There is limited information describing the presenting characteristics and outcomes of US patients requiring hospitalization for coronavirus disease 2019 (COVID-19).
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              A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology

              The ongoing pandemic spread of a novel human coronavirus, SARS-COV-2, associated with severe pneumonia disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. We present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and de-labelling virus lineages that become unobserved and hence are likely inactive. By focusing on active virus lineages and those spreading to new locations this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2.
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                Author and article information

                Journal
                Clin Microbiol Infect
                Clin Microbiol Infect
                Clinical Microbiology and Infection
                European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd.
                1198-743X
                1469-0691
                7 October 2021
                7 October 2021
                Affiliations
                [1 ]Service de Réanimation polyvalente, CH de Saint-Brieuc, 10, rue Marcel Proust, 22000, Saint-Brieuc, France
                [2 ]Service de Biologie médicale, CH de Lannion, Centre Hospitalier Pierre-le-Damany, 22303, Lannion, France
                [3 ]National Reference Center for Respiratory Viruses, Molecular Genetics of RNA Viruses, CNRS-UMR 3569, University of Paris, Institut Pasteur, Paris, France
                [4 ]Service de Médecine Interne, CH de Lannion, Centre Hospitalier Pierre-le-Damany, 22303, Lannion, France
                [5 ]Service de Maladies Infectieuses, CH de Saint-Brieuc, 10 rue Marcel Proust, 22000, Saint-Brieuc, France
                [6 ]Service de Gériatrie, CH de Lannion, Centre Hospitalier Pierre-le-Damany, 22303 Lannion, France
                [7 ]Service d’Imagerie Médicale, CH de Lannion, Centre Hospitalier Pierre-le-Damany, 22303 Lannion, France
                [8 ]Service de Pneumologie, CH de Lannion, Centre Hospitalier Pierre-le-Damany, 22303 Lannion, France
                [9 ]Département d’informatique médicale, CH de Lannion, Centre Hospitalier Pierre-le-Damany, 22303 Lannion, France
                [10 ]Plateforme de surveillance continue, CH de Lannion, Centre Hospitalier Pierre-le-Damany, 22303 Lannion, France
                [11 ]Mutualized Platform of Microbiology, Pasteur International Bioresources Network, Institut Pasteur, Paris, France
                [12 ]Service de Biologie médicale, CH de Saint-Brieuc, 10, rue Marcel Proust 22000 Saint-Brieuc, France
                [13 ]Santé publique France, French national public health agency, Cellule Bretagne, Rennes, France
                [14 ]Evolutionary Genomics of RNA Viruses, Institut Pasteur, Paris, France
                [15 ]Unité Bioinformatique Evolutive & Hub de Bioinformatique et Biostatistique - Département Biologie computationnelle, USR3756 (C3BI/DBC), Institut Pasteur, Paris, France
                [16 ]Santé publique France, the French public health agency, Saint-Maurice, France
                [17 ]Service de Virologie, CHU de Rennes, 2, rue Henri le Guilloux¸35000, Rennes, France
                [18 ]Department of Infectious and Tropical Diseases, Assistance Publique-Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, Paris, France; Infections Antimicrobials Modelling Evolution (IAME) UMR 1137, University of Paris, Paris, France
                [19 ]Sorbonne Université, INSERM, Institut Pierre Louis d’Épidémiologie et de Santé Publique (IPLESP), Paris, France
                [20 ]Service de maladie infectieuse et de réanimation médicale, CHU de Rennes, 2, rue Henri le Guilloux, 35000, Rennes, France
                Author notes
                []Corresponding author. Service de Réanimation, CH de Saint-Brieuc, 10, rue Marcel Proust, 22000, Saint-Brieuc, France, , +33296017060.
                [∗∗ ]Corresponding author: Service de maladie infectieuse et de réanimation médicale, CHU de Rennes, 2, rue Henri le Guilloux35000, Rennes, France. , +33299284321.
                [#]

                These authors equally contributed to this manuscript.

                Article
                S1198-743X(21)00565-6
                10.1016/j.cmi.2021.09.035
                8496927
                6aed7f17-6e65-4bc1-8f8b-70b930b20157
                © 2021 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 12 July 2021
                : 25 September 2021
                : 29 September 2021
                Categories
                Original Article

                Microbiology & Virology
                coronavirus infections,covid-19 / epidemiology,sars-cov-2 variants,severity of illness index / virology

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