SARS-CoV-2 infection and adverse outcomes in users of ACE inhibitors and angiotensin-receptor blockers: a nationwide case-control and cohort analysis
ObjectiveTo examine the impact of ACE inhibitor (ACE-I)/angiotensin receptor blocker (ARB) use on rate of SARS-CoV-2 infection and adverse outcomes.MethodsThis nationwide case-control and cohort study included all individuals in Denmark tested for SARS-CoV-2 RNA with PCR from 27 February 2020 to 26...
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Veröffentlicht in: | Thorax 2021-04, Vol.76 (4), p.370-379 |
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creator | Christiansen, Christian Fynbo Pottegård, Anton Heide-Jørgensen, Uffe Bodilsen, Jacob Søgaard, Ole Schmeltz Maeng, Michael Vistisen, Simon Tilma Schmidt, Morten Lund, Lars Christian Reilev, Mette Hallas, Jesper Voldstedlund, Marianne Husby, Anders Thomsen, Marianne Kragh Johansen, Nanna Borup Brun, Nikolai Constantin Thomsen, Reimar Wernich Bøtker, Hans Erik Sørensen, Henrik Toft |
description | ObjectiveTo examine the impact of ACE inhibitor (ACE-I)/angiotensin receptor blocker (ARB) use on rate of SARS-CoV-2 infection and adverse outcomes.MethodsThis nationwide case-control and cohort study included all individuals in Denmark tested for SARS-CoV-2 RNA with PCR from 27 February 2020 to 26 July 2020. We estimated confounder-adjusted ORs for a positive test among all SARS-CoV-2 tested, and inverse probability of treatment weighted 30-day risk and risk ratios (RRs) of hospitalisation, intensive care unit (ICU) admission and mortality comparing current ACE-I/ARB use with calcium channel blocker (CCB) use and with non-use.ResultsThe study included 13 501 SARS-CoV-2 PCR-positive and 1 088 695 PCR-negative individuals. Users of ACE-I/ARB had a marginally increased rate of a positive PCR when compared with CCB users (aOR 1.17, 95% CI 1.00 to 1.37), but not when compared with non-users (aOR 1.00 95% CI 0.92 to 1.09).Among PCR-positive individuals, 1466 (11%) were ACE-I/ARB users. The weighted risk of hospitalisation was 36.5% in ACE-I/ARB users and 43.3% in CCB users (RR 0.84, 95% CI 0.70 to 1.02). The risk of ICU admission was 6.3% in ACE-I/ARB users and 5.4% in CCB users (RR 1.17, 95% CI 0.64 to 2.16), while the 30-day mortality was 12.3% in ACE-I/ARB users and 13.9% in CCB users (RR 0.89, 95% CI 0.61 to 1.30). The associations were similar when ACE-I/ARB users were compared with non-users.ConclusionsACE-I/ARB use was associated neither with a consistently increased rate nor with adverse outcomes of SARS-CoV-2 infection. Our findings support the current recommendation of continuing use of ACE-Is/ARBs during the SARS-CoV-2 pandemic.Trial registration numberEUPAS34887 |
doi_str_mv | 10.1136/thoraxjnl-2020-215768 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7725106</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2501407829</sourcerecordid><originalsourceid>FETCH-LOGICAL-b522t-464b1067b17e07e297e1f82d3e13aa902dca24345c4a189470d5f0d766d39dd63</originalsourceid><addsrcrecordid>eNqNUVtvFCEUJsbGbld_gobEZyq3gRkfTDabekmaNGnVV8IA02WdhRWY1v4Q_69st131xfgEnO9yzuED4CXBp4Qw8aasYtI_1mFEFFOMKGmkaJ-AGeGiRYx24imYYcwxEkyKY3CS8xpj3BIin4FjVgmMym4Gfl4tLq_QMn5FFPowOFN8DFAHC7W9cSk7GKdi4sblCsMp1xKMA1wsz-p75XtfYq3c88O1j8WF7ANKzrhtRWA_RvOtat5CDYPeed9666DR2SETQ0lxvBebWNcp9arHu-zzc3A06DG7Fw_nHHx5f_Z5-RGdX3z4tFyco76htCAueE-wkD2RDktHO-nI0FLLHGFad5haoylnvDFck7bjEttmwFYKYVlnrWBz8G7vu536jbPG1Yn0qLbJb3S6U1F79TcS_EpdxxslJW1q52rw-sEgxe-Ty0Wt45TqFlnRBhOOZVt_eg6aPcukmHNyw6EDwWqXpjqkqXZpqn2aVffqz_EOqsf4KgHvCf1m_d-e5LfkMOy_Nb8AGeLAZQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2501407829</pqid></control><display><type>article</type><title>SARS-CoV-2 infection and adverse outcomes in users of ACE inhibitors and angiotensin-receptor blockers: a nationwide case-control and cohort analysis</title><source>Alma/SFX Local Collection</source><creator>Christiansen, Christian Fynbo ; Pottegård, Anton ; Heide-Jørgensen, Uffe ; Bodilsen, Jacob ; Søgaard, Ole Schmeltz ; Maeng, Michael ; Vistisen, Simon Tilma ; Schmidt, Morten ; Lund, Lars Christian ; Reilev, Mette ; Hallas, Jesper ; Voldstedlund, Marianne ; Husby, Anders ; Thomsen, Marianne Kragh ; Johansen, Nanna Borup ; Brun, Nikolai Constantin ; Thomsen, Reimar Wernich ; Bøtker, Hans Erik ; Sørensen, Henrik Toft</creator><creatorcontrib>Christiansen, Christian Fynbo ; Pottegård, Anton ; Heide-Jørgensen, Uffe ; Bodilsen, Jacob ; Søgaard, Ole Schmeltz ; Maeng, Michael ; Vistisen, Simon Tilma ; Schmidt, Morten ; Lund, Lars Christian ; Reilev, Mette ; Hallas, Jesper ; Voldstedlund, Marianne ; Husby, Anders ; Thomsen, Marianne Kragh ; Johansen, Nanna Borup ; Brun, Nikolai Constantin ; Thomsen, Reimar Wernich ; Bøtker, Hans Erik ; Sørensen, Henrik Toft</creatorcontrib><description>ObjectiveTo examine the impact of ACE inhibitor (ACE-I)/angiotensin receptor blocker (ARB) use on rate of SARS-CoV-2 infection and adverse outcomes.MethodsThis nationwide case-control and cohort study included all individuals in Denmark tested for SARS-CoV-2 RNA with PCR from 27 February 2020 to 26 July 2020. We estimated confounder-adjusted ORs for a positive test among all SARS-CoV-2 tested, and inverse probability of treatment weighted 30-day risk and risk ratios (RRs) of hospitalisation, intensive care unit (ICU) admission and mortality comparing current ACE-I/ARB use with calcium channel blocker (CCB) use and with non-use.ResultsThe study included 13 501 SARS-CoV-2 PCR-positive and 1 088 695 PCR-negative individuals. Users of ACE-I/ARB had a marginally increased rate of a positive PCR when compared with CCB users (aOR 1.17, 95% CI 1.00 to 1.37), but not when compared with non-users (aOR 1.00 95% CI 0.92 to 1.09).Among PCR-positive individuals, 1466 (11%) were ACE-I/ARB users. The weighted risk of hospitalisation was 36.5% in ACE-I/ARB users and 43.3% in CCB users (RR 0.84, 95% CI 0.70 to 1.02). The risk of ICU admission was 6.3% in ACE-I/ARB users and 5.4% in CCB users (RR 1.17, 95% CI 0.64 to 2.16), while the 30-day mortality was 12.3% in ACE-I/ARB users and 13.9% in CCB users (RR 0.89, 95% CI 0.61 to 1.30). The associations were similar when ACE-I/ARB users were compared with non-users.ConclusionsACE-I/ARB use was associated neither with a consistently increased rate nor with adverse outcomes of SARS-CoV-2 infection. Our findings support the current recommendation of continuing use of ACE-Is/ARBs during the SARS-CoV-2 pandemic.Trial registration numberEUPAS34887</description><identifier>ISSN: 0040-6376</identifier><identifier>EISSN: 1468-3296</identifier><identifier>DOI: 10.1136/thoraxjnl-2020-215768</identifier><identifier>PMID: 33293279</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and British Thoracic Society</publisher><subject>Antihypertensives ; Beta blockers ; clinical epidemiology ; Cohort analysis ; Coronaviruses ; COVID-19 ; critical care ; Ethnicity ; Infections ; Intensive care ; Patients ; Prescriptions ; Respiratory Infection ; Severe acute respiratory syndrome coronavirus 2 ; Ventilators ; viral infection</subject><ispartof>Thorax, 2021-04, Vol.76 (4), p.370-379</ispartof><rights>Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>This article is made freely available for use in accordance with BMJ’s website terms and conditions for the duration of the covid-19 pandemic or until otherwise determined by BMJ. You may use, download and print the article for any lawful, non-commercial purpose (including text and data mining) provided that all copyright notices and trade marks are retained. https://bmj.com/coronavirus/usage</rights><rights>Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b522t-464b1067b17e07e297e1f82d3e13aa902dca24345c4a189470d5f0d766d39dd63</citedby><cites>FETCH-LOGICAL-b522t-464b1067b17e07e297e1f82d3e13aa902dca24345c4a189470d5f0d766d39dd63</cites><orcidid>0000-0001-9135-3474 ; 0000-0002-0727-953X ; 0000-0003-1241-4385 ; 0000-0002-7398-814X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33293279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Christiansen, Christian Fynbo</creatorcontrib><creatorcontrib>Pottegård, Anton</creatorcontrib><creatorcontrib>Heide-Jørgensen, Uffe</creatorcontrib><creatorcontrib>Bodilsen, Jacob</creatorcontrib><creatorcontrib>Søgaard, Ole Schmeltz</creatorcontrib><creatorcontrib>Maeng, Michael</creatorcontrib><creatorcontrib>Vistisen, Simon Tilma</creatorcontrib><creatorcontrib>Schmidt, Morten</creatorcontrib><creatorcontrib>Lund, Lars Christian</creatorcontrib><creatorcontrib>Reilev, Mette</creatorcontrib><creatorcontrib>Hallas, Jesper</creatorcontrib><creatorcontrib>Voldstedlund, Marianne</creatorcontrib><creatorcontrib>Husby, Anders</creatorcontrib><creatorcontrib>Thomsen, Marianne Kragh</creatorcontrib><creatorcontrib>Johansen, Nanna Borup</creatorcontrib><creatorcontrib>Brun, Nikolai Constantin</creatorcontrib><creatorcontrib>Thomsen, Reimar Wernich</creatorcontrib><creatorcontrib>Bøtker, Hans Erik</creatorcontrib><creatorcontrib>Sørensen, Henrik Toft</creatorcontrib><title>SARS-CoV-2 infection and adverse outcomes in users of ACE inhibitors and angiotensin-receptor blockers: a nationwide case-control and cohort analysis</title><title>Thorax</title><addtitle>Thorax</addtitle><addtitle>Thorax</addtitle><description>ObjectiveTo examine the impact of ACE inhibitor (ACE-I)/angiotensin receptor blocker (ARB) use on rate of SARS-CoV-2 infection and adverse outcomes.MethodsThis nationwide case-control and cohort study included all individuals in Denmark tested for SARS-CoV-2 RNA with PCR from 27 February 2020 to 26 July 2020. We estimated confounder-adjusted ORs for a positive test among all SARS-CoV-2 tested, and inverse probability of treatment weighted 30-day risk and risk ratios (RRs) of hospitalisation, intensive care unit (ICU) admission and mortality comparing current ACE-I/ARB use with calcium channel blocker (CCB) use and with non-use.ResultsThe study included 13 501 SARS-CoV-2 PCR-positive and 1 088 695 PCR-negative individuals. Users of ACE-I/ARB had a marginally increased rate of a positive PCR when compared with CCB users (aOR 1.17, 95% CI 1.00 to 1.37), but not when compared with non-users (aOR 1.00 95% CI 0.92 to 1.09).Among PCR-positive individuals, 1466 (11%) were ACE-I/ARB users. The weighted risk of hospitalisation was 36.5% in ACE-I/ARB users and 43.3% in CCB users (RR 0.84, 95% CI 0.70 to 1.02). The risk of ICU admission was 6.3% in ACE-I/ARB users and 5.4% in CCB users (RR 1.17, 95% CI 0.64 to 2.16), while the 30-day mortality was 12.3% in ACE-I/ARB users and 13.9% in CCB users (RR 0.89, 95% CI 0.61 to 1.30). The associations were similar when ACE-I/ARB users were compared with non-users.ConclusionsACE-I/ARB use was associated neither with a consistently increased rate nor with adverse outcomes of SARS-CoV-2 infection. Our findings support the current recommendation of continuing use of ACE-Is/ARBs during the SARS-CoV-2 pandemic.Trial registration numberEUPAS34887</description><subject>Antihypertensives</subject><subject>Beta blockers</subject><subject>clinical epidemiology</subject><subject>Cohort analysis</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>critical care</subject><subject>Ethnicity</subject><subject>Infections</subject><subject>Intensive care</subject><subject>Patients</subject><subject>Prescriptions</subject><subject>Respiratory Infection</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Ventilators</subject><subject>viral infection</subject><issn>0040-6376</issn><issn>1468-3296</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqNUVtvFCEUJsbGbld_gobEZyq3gRkfTDabekmaNGnVV8IA02WdhRWY1v4Q_69st131xfgEnO9yzuED4CXBp4Qw8aasYtI_1mFEFFOMKGmkaJ-AGeGiRYx24imYYcwxEkyKY3CS8xpj3BIin4FjVgmMym4Gfl4tLq_QMn5FFPowOFN8DFAHC7W9cSk7GKdi4sblCsMp1xKMA1wsz-p75XtfYq3c88O1j8WF7ANKzrhtRWA_RvOtat5CDYPeed9666DR2SETQ0lxvBebWNcp9arHu-zzc3A06DG7Fw_nHHx5f_Z5-RGdX3z4tFyco76htCAueE-wkD2RDktHO-nI0FLLHGFad5haoylnvDFck7bjEttmwFYKYVlnrWBz8G7vu536jbPG1Yn0qLbJb3S6U1F79TcS_EpdxxslJW1q52rw-sEgxe-Ty0Wt45TqFlnRBhOOZVt_eg6aPcukmHNyw6EDwWqXpjqkqXZpqn2aVffqz_EOqsf4KgHvCf1m_d-e5LfkMOy_Nb8AGeLAZQ</recordid><startdate>20210401</startdate><enddate>20210401</enddate><creator>Christiansen, Christian Fynbo</creator><creator>Pottegård, Anton</creator><creator>Heide-Jørgensen, Uffe</creator><creator>Bodilsen, Jacob</creator><creator>Søgaard, Ole Schmeltz</creator><creator>Maeng, Michael</creator><creator>Vistisen, Simon Tilma</creator><creator>Schmidt, Morten</creator><creator>Lund, Lars Christian</creator><creator>Reilev, Mette</creator><creator>Hallas, Jesper</creator><creator>Voldstedlund, Marianne</creator><creator>Husby, Anders</creator><creator>Thomsen, Marianne Kragh</creator><creator>Johansen, Nanna Borup</creator><creator>Brun, Nikolai Constantin</creator><creator>Thomsen, Reimar Wernich</creator><creator>Bøtker, Hans Erik</creator><creator>Sørensen, Henrik Toft</creator><general>BMJ Publishing Group Ltd and British Thoracic Society</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9135-3474</orcidid><orcidid>https://orcid.org/0000-0002-0727-953X</orcidid><orcidid>https://orcid.org/0000-0003-1241-4385</orcidid><orcidid>https://orcid.org/0000-0002-7398-814X</orcidid></search><sort><creationdate>20210401</creationdate><title>SARS-CoV-2 infection and adverse outcomes in users of ACE inhibitors and angiotensin-receptor blockers: a nationwide case-control and cohort analysis</title><author>Christiansen, Christian Fynbo ; Pottegård, Anton ; Heide-Jørgensen, Uffe ; Bodilsen, Jacob ; Søgaard, Ole Schmeltz ; Maeng, Michael ; Vistisen, Simon Tilma ; Schmidt, Morten ; Lund, Lars Christian ; Reilev, Mette ; Hallas, Jesper ; Voldstedlund, Marianne ; Husby, Anders ; Thomsen, Marianne Kragh ; Johansen, Nanna Borup ; Brun, Nikolai Constantin ; Thomsen, Reimar Wernich ; Bøtker, Hans Erik ; Sørensen, Henrik Toft</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b522t-464b1067b17e07e297e1f82d3e13aa902dca24345c4a189470d5f0d766d39dd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antihypertensives</topic><topic>Beta blockers</topic><topic>clinical epidemiology</topic><topic>Cohort analysis</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>critical care</topic><topic>Ethnicity</topic><topic>Infections</topic><topic>Intensive care</topic><topic>Patients</topic><topic>Prescriptions</topic><topic>Respiratory Infection</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Ventilators</topic><topic>viral infection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Christiansen, Christian Fynbo</creatorcontrib><creatorcontrib>Pottegård, Anton</creatorcontrib><creatorcontrib>Heide-Jørgensen, Uffe</creatorcontrib><creatorcontrib>Bodilsen, Jacob</creatorcontrib><creatorcontrib>Søgaard, Ole Schmeltz</creatorcontrib><creatorcontrib>Maeng, Michael</creatorcontrib><creatorcontrib>Vistisen, Simon Tilma</creatorcontrib><creatorcontrib>Schmidt, Morten</creatorcontrib><creatorcontrib>Lund, Lars Christian</creatorcontrib><creatorcontrib>Reilev, Mette</creatorcontrib><creatorcontrib>Hallas, Jesper</creatorcontrib><creatorcontrib>Voldstedlund, Marianne</creatorcontrib><creatorcontrib>Husby, Anders</creatorcontrib><creatorcontrib>Thomsen, Marianne Kragh</creatorcontrib><creatorcontrib>Johansen, Nanna Borup</creatorcontrib><creatorcontrib>Brun, Nikolai Constantin</creatorcontrib><creatorcontrib>Thomsen, Reimar Wernich</creatorcontrib><creatorcontrib>Bøtker, Hans Erik</creatorcontrib><creatorcontrib>Sørensen, Henrik Toft</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Thorax</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Christiansen, Christian Fynbo</au><au>Pottegård, Anton</au><au>Heide-Jørgensen, Uffe</au><au>Bodilsen, Jacob</au><au>Søgaard, Ole Schmeltz</au><au>Maeng, Michael</au><au>Vistisen, Simon Tilma</au><au>Schmidt, Morten</au><au>Lund, Lars Christian</au><au>Reilev, Mette</au><au>Hallas, Jesper</au><au>Voldstedlund, Marianne</au><au>Husby, Anders</au><au>Thomsen, Marianne Kragh</au><au>Johansen, Nanna Borup</au><au>Brun, Nikolai Constantin</au><au>Thomsen, Reimar Wernich</au><au>Bøtker, Hans Erik</au><au>Sørensen, Henrik Toft</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SARS-CoV-2 infection and adverse outcomes in users of ACE inhibitors and angiotensin-receptor blockers: a nationwide case-control and cohort analysis</atitle><jtitle>Thorax</jtitle><stitle>Thorax</stitle><addtitle>Thorax</addtitle><date>2021-04-01</date><risdate>2021</risdate><volume>76</volume><issue>4</issue><spage>370</spage><epage>379</epage><pages>370-379</pages><issn>0040-6376</issn><eissn>1468-3296</eissn><abstract>ObjectiveTo examine the impact of ACE inhibitor (ACE-I)/angiotensin receptor blocker (ARB) use on rate of SARS-CoV-2 infection and adverse outcomes.MethodsThis nationwide case-control and cohort study included all individuals in Denmark tested for SARS-CoV-2 RNA with PCR from 27 February 2020 to 26 July 2020. We estimated confounder-adjusted ORs for a positive test among all SARS-CoV-2 tested, and inverse probability of treatment weighted 30-day risk and risk ratios (RRs) of hospitalisation, intensive care unit (ICU) admission and mortality comparing current ACE-I/ARB use with calcium channel blocker (CCB) use and with non-use.ResultsThe study included 13 501 SARS-CoV-2 PCR-positive and 1 088 695 PCR-negative individuals. Users of ACE-I/ARB had a marginally increased rate of a positive PCR when compared with CCB users (aOR 1.17, 95% CI 1.00 to 1.37), but not when compared with non-users (aOR 1.00 95% CI 0.92 to 1.09).Among PCR-positive individuals, 1466 (11%) were ACE-I/ARB users. The weighted risk of hospitalisation was 36.5% in ACE-I/ARB users and 43.3% in CCB users (RR 0.84, 95% CI 0.70 to 1.02). The risk of ICU admission was 6.3% in ACE-I/ARB users and 5.4% in CCB users (RR 1.17, 95% CI 0.64 to 2.16), while the 30-day mortality was 12.3% in ACE-I/ARB users and 13.9% in CCB users (RR 0.89, 95% CI 0.61 to 1.30). The associations were similar when ACE-I/ARB users were compared with non-users.ConclusionsACE-I/ARB use was associated neither with a consistently increased rate nor with adverse outcomes of SARS-CoV-2 infection. Our findings support the current recommendation of continuing use of ACE-Is/ARBs during the SARS-CoV-2 pandemic.Trial registration numberEUPAS34887</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and British Thoracic Society</pub><pmid>33293279</pmid><doi>10.1136/thoraxjnl-2020-215768</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9135-3474</orcidid><orcidid>https://orcid.org/0000-0002-0727-953X</orcidid><orcidid>https://orcid.org/0000-0003-1241-4385</orcidid><orcidid>https://orcid.org/0000-0002-7398-814X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antihypertensives Beta blockers clinical epidemiology Cohort analysis Coronaviruses COVID-19 critical care Ethnicity Infections Intensive care Patients Prescriptions Respiratory Infection Severe acute respiratory syndrome coronavirus 2 Ventilators viral infection |
title | SARS-CoV-2 infection and adverse outcomes in users of ACE inhibitors and angiotensin-receptor blockers: a nationwide case-control and cohort analysis |
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