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      Usefulness of Combined Renin-Angiotensin System Inhibitors and Diuretic Treatment In Patients Hospitalized with COVID-19

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          Abstract

          Antecedent use of renin-angiotensin system inhibitors (RASi) prevents clinical deterioration and protects against cardiovascular/thrombotic complications of COVID-19, for indicated patients. Uncertainty exists regarding treatment continuation throughout infection and doing so with concomitant medications. Hence, the purpose of this study is to evaluate the differential effect of RASi continuation in patients hospitalized with COVID-19 according to diuretic use. We used the Coracle registry, which contains data of hospitalized patients with COVID-19 from 4 regions of Italy. We used Firth logistic regression for adult (>50 years) cases with admission on/after February 22, 2020, with a known discharge status as of April 1, 2020. There were 286 patients in this analysis; 100 patients (35.0%) continued RASi and 186 (65%) discontinued. There were 98 patients treated with a diuretic; 51 (52%) of those continued RASi. The in-hospital mortality rates in patients treated with a diuretic and continued versus discontinued RASi were 8% versus 26% (p = 0.0179). There were 188 patients not treated with a diuretic; 49 (26%) of those continued RASi. The in-hospital mortality rates in patients not treated with a diuretic and continued versus discontinued RASi were 16% versus 9% (p = 0.1827). After accounting for age, cardiovascular disease, and laboratory values, continuing RASi decreased the risk of mortality by approximately 77% (odds ratio 0.23, 95% confidence interval 0.06 to 0.95, p = 0.0419) for patients treated with diuretics, but did not alter the risk in patients treated with RASi alone. Continuing RASi in patients concomitantly treated with diuretics was associated with reduced in-hospital mortality.

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          SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor

          Summary The recent emergence of the novel, pathogenic SARS-coronavirus 2 (SARS-CoV-2) in China and its rapid national and international spread pose a global health emergency. Cell entry of coronaviruses depends on binding of the viral spike (S) proteins to cellular receptors and on S protein priming by host cell proteases. Unravelling which cellular factors are used by SARS-CoV-2 for entry might provide insights into viral transmission and reveal therapeutic targets. Here, we demonstrate that SARS-CoV-2 uses the SARS-CoV receptor ACE2 for entry and the serine protease TMPRSS2 for S protein priming. A TMPRSS2 inhibitor approved for clinical use blocked entry and might constitute a treatment option. Finally, we show that the sera from convalescent SARS patients cross-neutralized SARS-2-S-driven entry. Our results reveal important commonalities between SARS-CoV-2 and SARS-CoV infection and identify a potential target for antiviral intervention.
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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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              Is Open Access

              Cardiovascular Implications of Fatal Outcomes of Patients With Coronavirus Disease 2019 (COVID-19)

              This case series study evaluates the association of underlying cardiovascular disease and myocardial injury on fatal outcomes in patients with coronavirus disease 2019 (COVID-19).
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                Author and article information

                Journal
                Am J Cardiol
                Am J Cardiol
                The American Journal of Cardiology
                Elsevier Inc.
                0002-9149
                1879-1913
                10 January 2022
                10 January 2022
                Affiliations
                [a ]Cardiovascular Diseases Unit, Department of Medical Sciences, AOUS Le Scotte Hospital University of Siena, Siena, Italy
                [b ]Baylor Heart and Vascular Institute, Baylor Scott & White Research Institute, Dallas, Texas
                [c ]Texas A&M University College of Medicine Health Science Center, Dallas, Texas
                [d ]Cardiovascular Diseases Unit, Department of Internal Medicine, University of Milan, Fondazione IRCCS Ca'Granda Ospedale Maggiore Policlinico Milan, Italy
                [e ]Cardiology, Department of Medical Sciences University of Turin, Le Molinette Hospital Turin, Italy
                [f ]Internal Internal Medicine ASST Nord Milano E. Bassini Hospital Cisanello Balsamo, Italy
                [g ]Interventional Cardiology and Cardiac Surgery Unit Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy
                [h ]Intensive Care University of Pavia, Fondazione IRCCS policlinico San Matteo, Pavia Italy
                [i ]Section of Electrophysiology and Cardiac Pacing, Azienda Ospedaliera Polo Universitario L Sacco, Milano Italy
                [j ]Department of Clinical Internal Anesthesiological and Cardiovascular Sciences, La Sapienza University Roma Italy
                [k ]Infectious Diseases Department of Medical Sciences, University of Torino, Città della Salute e della Scienza, Torino Italy
                [l ]Cardiorenal Society of America, Phoenix, AZ
                Author notes
                [* ]Corresponding author: Tel: +39577585363, +39577585461; fax: +39577233480.
                Article
                S0002-9149(21)01189-9
                10.1016/j.amjcard.2021.12.004
                8744009
                283ceb78-619b-48c3-9a86-4af806f81b0c
                © 2021 Elsevier Inc. 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
                : 31 August 2021
                : 29 November 2021
                Categories
                Article

                Cardiovascular Medicine
                Cardiovascular Medicine

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