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suPAR Cut-Offs for Risk Stratification in Patients With Symptoms of COVID-19
Objectives: Elevated soluble urokinase Plasminogen Activator Receptor (suPAR) is a biomarker associated with adverse outcomes. We aimed to investigate the associations between plasma suPAR levels (testing the cut-offs ⩽4, 4-6, and ⩾6 ng/mL) with risk of 14-day mortality, and with the risk of mechani...
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Published in: | Biomarker insights 2021, Vol.16, p.11772719211034685 |
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creator | Altintas, Izzet Eugen-Olsen, Jesper Seppälä, Santeri Tingleff, Jens Stauning, Marius Ahm El Caidi, Nora Olsen Elmajdoubi, Sanaá Gamst-Jensen, Hejdi Lindstrøm, Mette B Rasmussen, Line Jee Hartmann Kristiansen, Klaus Tjelle Rasmussen, Christian Nehlin, Jan O Kallemose, Thomas Hyppölä, Harri Andersen, Ove |
description | Objectives:
Elevated soluble urokinase Plasminogen Activator Receptor (suPAR) is a biomarker associated with adverse outcomes. We aimed to investigate the associations between plasma suPAR levels (testing the cut-offs ⩽4, 4-6, and ⩾6 ng/mL) with risk of 14-day mortality, and with the risk of mechanical ventilation in patients that tested positive for SARS-CoV-2.
Methods:
Observational cohort study of patients presenting with symptoms of COVID-19 at Department of Emergency Medicine, Amager and Hvidovre Hospital, Denmark from March 19th, 2020 to April 3rd, 2020. Plasma suPAR was measured using suPARnostic technologies. Patients were followed for development of mechanical ventilation and mortality for 14 days. Validation of our findings were carried out in a similar sized COVID-19 patient cohort from Mikkeli Central Hospital, Finland.
Results:
Among 386 patients with symptoms of COVID-19, the median (interquartile range) age was 64 years (46-77), 57% were women, median suPAR was 4.0 ng/mL (2.7-5.9). In total, 35 patients (9.1%) died during the 14 days follow-up. Patients with suPAR ⩽4 ng/mL (N = 196; 50.8%) had a low risk of mortality (N = 2; 1.0%; negative predictive value of 99.0%, specificity 55.3%, sensitivity 95.2%, positive predictive value 17.4%). Among patients with suPAR ⩾6 ng/mL (N = 92; 23.8%), 16 died (17.4%). About 99 patients (25.6%) tested positive for SARS CoV-2 and of those 12 (12.1%) developed need for mechanical ventilation. None of the SARS-CoV-2 positive patients with suPAR ⩽4 ng/mL (N = 28; 38.8%) needed mechanical ventilation or died. The Mikkeli Central Hospital validation cohort confirmed our findings concerning suPAR cut-offs for risk of development of mechanical ventilation and mortality.
Conclusions:
Patients with symptoms of COVID-19 and suPAR ⩽4 or ⩾6 ng/mL had low or high risk, respectively, concerning the need for mechanical ventilation or mortality. We suggest cut-offs for identification of risk groups in patients presenting to the ED with symptoms of or confirmed COVID-19. |
doi_str_mv | 10.1177/11772719211034685 |
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fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_a372f7d0a4a547489c5b936a7c01e65f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_11772719211034685</sage_id><doaj_id>oai_doaj_org_article_a372f7d0a4a547489c5b936a7c01e65f</doaj_id><sourcerecordid>2613259612</sourcerecordid><originalsourceid>FETCH-LOGICAL-c499t-58db12ba8107b2cf4afd6fbe8e863c5cce6595e8dc37a6d1bb4f905a1bb444f93</originalsourceid><addsrcrecordid>eNp1kdtuEzEQhi0Eogd4AG6QJa639flwg1SFUiJFStVyuLS8Xjt1SNbB3q3Ut8dL2tIKcTP-Nf7nmxkNAO8wOsFYytMpEIk1wRhRJhR_AQ6nXDMlXz7RB-ColDVCXCiCXoMDyhjBRPNDsCjj5dkVnI1DswyhwJAyvIrlJ7wesh1iiK7G1MPYw8uqfD8U-CMON_D6brsb0rbAFOBs-X3-qcH6DXgV7Kb4t_fvMfj2-fzr7EuzWF7MZ2eLxjGth4arrsWktQoj2RIXmA2dCK1XXgnquHNecM296hyVVnS4bVnQiNtJsCrpMZjvuV2ya7PLcWvznUk2mj-JlFfG5iG6jTeWShJkhyyznEmmtOOtpsJKh3BtEyrr4561G9ut71zdMNvNM-jznz7emFW6NYpKLCmugA_3gJx-jb4MZp3G3Nf9DRGYEq4FJtWF9y6XUynZh8cOGJnpTuafY9aa909He6x4uF41nOwNxa7837b_J_4GRIWmMw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2613259612</pqid></control><display><type>article</type><title>suPAR Cut-Offs for Risk Stratification in Patients With Symptoms of COVID-19</title><source>Publicly Available Content Database</source><source>Sage Journals GOLD Open Access 2024</source><source>PubMed Central</source><source>Coronavirus Research Database</source><creator>Altintas, Izzet ; Eugen-Olsen, Jesper ; Seppälä, Santeri ; Tingleff, Jens ; Stauning, Marius Ahm ; El Caidi, Nora Olsen ; Elmajdoubi, Sanaá ; Gamst-Jensen, Hejdi ; Lindstrøm, Mette B ; Rasmussen, Line Jee Hartmann ; Kristiansen, Klaus Tjelle ; Rasmussen, Christian ; Nehlin, Jan O ; Kallemose, Thomas ; Hyppölä, Harri ; Andersen, Ove</creator><creatorcontrib>Altintas, Izzet ; Eugen-Olsen, Jesper ; Seppälä, Santeri ; Tingleff, Jens ; Stauning, Marius Ahm ; El Caidi, Nora Olsen ; Elmajdoubi, Sanaá ; Gamst-Jensen, Hejdi ; Lindstrøm, Mette B ; Rasmussen, Line Jee Hartmann ; Kristiansen, Klaus Tjelle ; Rasmussen, Christian ; Nehlin, Jan O ; Kallemose, Thomas ; Hyppölä, Harri ; Andersen, Ove</creatorcontrib><description>Objectives:
Elevated soluble urokinase Plasminogen Activator Receptor (suPAR) is a biomarker associated with adverse outcomes. We aimed to investigate the associations between plasma suPAR levels (testing the cut-offs ⩽4, 4-6, and ⩾6 ng/mL) with risk of 14-day mortality, and with the risk of mechanical ventilation in patients that tested positive for SARS-CoV-2.
Methods:
Observational cohort study of patients presenting with symptoms of COVID-19 at Department of Emergency Medicine, Amager and Hvidovre Hospital, Denmark from March 19th, 2020 to April 3rd, 2020. Plasma suPAR was measured using suPARnostic technologies. Patients were followed for development of mechanical ventilation and mortality for 14 days. Validation of our findings were carried out in a similar sized COVID-19 patient cohort from Mikkeli Central Hospital, Finland.
Results:
Among 386 patients with symptoms of COVID-19, the median (interquartile range) age was 64 years (46-77), 57% were women, median suPAR was 4.0 ng/mL (2.7-5.9). In total, 35 patients (9.1%) died during the 14 days follow-up. Patients with suPAR ⩽4 ng/mL (N = 196; 50.8%) had a low risk of mortality (N = 2; 1.0%; negative predictive value of 99.0%, specificity 55.3%, sensitivity 95.2%, positive predictive value 17.4%). Among patients with suPAR ⩾6 ng/mL (N = 92; 23.8%), 16 died (17.4%). About 99 patients (25.6%) tested positive for SARS CoV-2 and of those 12 (12.1%) developed need for mechanical ventilation. None of the SARS-CoV-2 positive patients with suPAR ⩽4 ng/mL (N = 28; 38.8%) needed mechanical ventilation or died. The Mikkeli Central Hospital validation cohort confirmed our findings concerning suPAR cut-offs for risk of development of mechanical ventilation and mortality.
Conclusions:
Patients with symptoms of COVID-19 and suPAR ⩽4 or ⩾6 ng/mL had low or high risk, respectively, concerning the need for mechanical ventilation or mortality. We suggest cut-offs for identification of risk groups in patients presenting to the ED with symptoms of or confirmed COVID-19.</description><identifier>ISSN: 1177-2719</identifier><identifier>EISSN: 1177-2719</identifier><identifier>DOI: 10.1177/11772719211034685</identifier><identifier>PMID: 34421295</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Coronaviruses ; COVID-19 ; Emergency medical care ; Mechanical ventilation ; Mortality ; Original Research ; Patients ; Risk groups ; Severe acute respiratory syndrome coronavirus 2 ; U-Plasminogen activator ; Ventilation</subject><ispartof>Biomarker insights, 2021, Vol.16, p.11772719211034685</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021.</rights><rights>The Author(s) 2021. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021 2021 SAGE Publications Ltd unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-58db12ba8107b2cf4afd6fbe8e863c5cce6595e8dc37a6d1bb4f905a1bb444f93</citedby><cites>FETCH-LOGICAL-c499t-58db12ba8107b2cf4afd6fbe8e863c5cce6595e8dc37a6d1bb4f905a1bb444f93</cites><orcidid>0000-0001-6790-2218 ; 0000-0002-5027-4435 ; 0000-0001-6038-5027</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371731/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2613259612?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,21966,25753,27853,27923,27924,27925,37012,38516,43895,44590,44945,45333,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34421295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Altintas, Izzet</creatorcontrib><creatorcontrib>Eugen-Olsen, Jesper</creatorcontrib><creatorcontrib>Seppälä, Santeri</creatorcontrib><creatorcontrib>Tingleff, Jens</creatorcontrib><creatorcontrib>Stauning, Marius Ahm</creatorcontrib><creatorcontrib>El Caidi, Nora Olsen</creatorcontrib><creatorcontrib>Elmajdoubi, Sanaá</creatorcontrib><creatorcontrib>Gamst-Jensen, Hejdi</creatorcontrib><creatorcontrib>Lindstrøm, Mette B</creatorcontrib><creatorcontrib>Rasmussen, Line Jee Hartmann</creatorcontrib><creatorcontrib>Kristiansen, Klaus Tjelle</creatorcontrib><creatorcontrib>Rasmussen, Christian</creatorcontrib><creatorcontrib>Nehlin, Jan O</creatorcontrib><creatorcontrib>Kallemose, Thomas</creatorcontrib><creatorcontrib>Hyppölä, Harri</creatorcontrib><creatorcontrib>Andersen, Ove</creatorcontrib><title>suPAR Cut-Offs for Risk Stratification in Patients With Symptoms of COVID-19</title><title>Biomarker insights</title><addtitle>Biomark Insights</addtitle><description>Objectives:
Elevated soluble urokinase Plasminogen Activator Receptor (suPAR) is a biomarker associated with adverse outcomes. We aimed to investigate the associations between plasma suPAR levels (testing the cut-offs ⩽4, 4-6, and ⩾6 ng/mL) with risk of 14-day mortality, and with the risk of mechanical ventilation in patients that tested positive for SARS-CoV-2.
Methods:
Observational cohort study of patients presenting with symptoms of COVID-19 at Department of Emergency Medicine, Amager and Hvidovre Hospital, Denmark from March 19th, 2020 to April 3rd, 2020. Plasma suPAR was measured using suPARnostic technologies. Patients were followed for development of mechanical ventilation and mortality for 14 days. Validation of our findings were carried out in a similar sized COVID-19 patient cohort from Mikkeli Central Hospital, Finland.
Results:
Among 386 patients with symptoms of COVID-19, the median (interquartile range) age was 64 years (46-77), 57% were women, median suPAR was 4.0 ng/mL (2.7-5.9). In total, 35 patients (9.1%) died during the 14 days follow-up. Patients with suPAR ⩽4 ng/mL (N = 196; 50.8%) had a low risk of mortality (N = 2; 1.0%; negative predictive value of 99.0%, specificity 55.3%, sensitivity 95.2%, positive predictive value 17.4%). Among patients with suPAR ⩾6 ng/mL (N = 92; 23.8%), 16 died (17.4%). About 99 patients (25.6%) tested positive for SARS CoV-2 and of those 12 (12.1%) developed need for mechanical ventilation. None of the SARS-CoV-2 positive patients with suPAR ⩽4 ng/mL (N = 28; 38.8%) needed mechanical ventilation or died. The Mikkeli Central Hospital validation cohort confirmed our findings concerning suPAR cut-offs for risk of development of mechanical ventilation and mortality.
Conclusions:
Patients with symptoms of COVID-19 and suPAR ⩽4 or ⩾6 ng/mL had low or high risk, respectively, concerning the need for mechanical ventilation or mortality. We suggest cut-offs for identification of risk groups in patients presenting to the ED with symptoms of or confirmed COVID-19.</description><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Emergency medical care</subject><subject>Mechanical ventilation</subject><subject>Mortality</subject><subject>Original Research</subject><subject>Patients</subject><subject>Risk groups</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>U-Plasminogen activator</subject><subject>Ventilation</subject><issn>1177-2719</issn><issn>1177-2719</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kdtuEzEQhi0Eogd4AG6QJa639flwg1SFUiJFStVyuLS8Xjt1SNbB3q3Ut8dL2tIKcTP-Nf7nmxkNAO8wOsFYytMpEIk1wRhRJhR_AQ6nXDMlXz7RB-ColDVCXCiCXoMDyhjBRPNDsCjj5dkVnI1DswyhwJAyvIrlJ7wesh1iiK7G1MPYw8uqfD8U-CMON_D6brsb0rbAFOBs-X3-qcH6DXgV7Kb4t_fvMfj2-fzr7EuzWF7MZ2eLxjGth4arrsWktQoj2RIXmA2dCK1XXgnquHNecM296hyVVnS4bVnQiNtJsCrpMZjvuV2ya7PLcWvznUk2mj-JlFfG5iG6jTeWShJkhyyznEmmtOOtpsJKh3BtEyrr4561G9ut71zdMNvNM-jznz7emFW6NYpKLCmugA_3gJx-jb4MZp3G3Nf9DRGYEq4FJtWF9y6XUynZh8cOGJnpTuafY9aa909He6x4uF41nOwNxa7837b_J_4GRIWmMw</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Altintas, Izzet</creator><creator>Eugen-Olsen, Jesper</creator><creator>Seppälä, Santeri</creator><creator>Tingleff, Jens</creator><creator>Stauning, Marius Ahm</creator><creator>El Caidi, Nora Olsen</creator><creator>Elmajdoubi, Sanaá</creator><creator>Gamst-Jensen, Hejdi</creator><creator>Lindstrøm, Mette B</creator><creator>Rasmussen, Line Jee Hartmann</creator><creator>Kristiansen, Klaus Tjelle</creator><creator>Rasmussen, Christian</creator><creator>Nehlin, Jan O</creator><creator>Kallemose, Thomas</creator><creator>Hyppölä, Harri</creator><creator>Andersen, Ove</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AYAGU</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6790-2218</orcidid><orcidid>https://orcid.org/0000-0002-5027-4435</orcidid><orcidid>https://orcid.org/0000-0001-6038-5027</orcidid></search><sort><creationdate>2021</creationdate><title>suPAR Cut-Offs for Risk Stratification in Patients With Symptoms of COVID-19</title><author>Altintas, Izzet ; Eugen-Olsen, Jesper ; Seppälä, Santeri ; Tingleff, Jens ; Stauning, Marius Ahm ; El Caidi, Nora Olsen ; Elmajdoubi, Sanaá ; Gamst-Jensen, Hejdi ; Lindstrøm, Mette B ; Rasmussen, Line Jee Hartmann ; Kristiansen, Klaus Tjelle ; Rasmussen, Christian ; Nehlin, Jan O ; Kallemose, Thomas ; Hyppölä, Harri ; Andersen, Ove</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-58db12ba8107b2cf4afd6fbe8e863c5cce6595e8dc37a6d1bb4f905a1bb444f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Emergency medical care</topic><topic>Mechanical ventilation</topic><topic>Mortality</topic><topic>Original Research</topic><topic>Patients</topic><topic>Risk groups</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>U-Plasminogen activator</topic><topic>Ventilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Altintas, Izzet</creatorcontrib><creatorcontrib>Eugen-Olsen, Jesper</creatorcontrib><creatorcontrib>Seppälä, Santeri</creatorcontrib><creatorcontrib>Tingleff, Jens</creatorcontrib><creatorcontrib>Stauning, Marius Ahm</creatorcontrib><creatorcontrib>El Caidi, Nora Olsen</creatorcontrib><creatorcontrib>Elmajdoubi, Sanaá</creatorcontrib><creatorcontrib>Gamst-Jensen, Hejdi</creatorcontrib><creatorcontrib>Lindstrøm, Mette B</creatorcontrib><creatorcontrib>Rasmussen, Line Jee Hartmann</creatorcontrib><creatorcontrib>Kristiansen, Klaus Tjelle</creatorcontrib><creatorcontrib>Rasmussen, Christian</creatorcontrib><creatorcontrib>Nehlin, Jan O</creatorcontrib><creatorcontrib>Kallemose, Thomas</creatorcontrib><creatorcontrib>Hyppölä, Harri</creatorcontrib><creatorcontrib>Andersen, Ove</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Australia & New Zealand Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Publicly Available Content 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><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biomarker insights</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Altintas, Izzet</au><au>Eugen-Olsen, Jesper</au><au>Seppälä, Santeri</au><au>Tingleff, Jens</au><au>Stauning, Marius Ahm</au><au>El Caidi, Nora Olsen</au><au>Elmajdoubi, Sanaá</au><au>Gamst-Jensen, Hejdi</au><au>Lindstrøm, Mette B</au><au>Rasmussen, Line Jee Hartmann</au><au>Kristiansen, Klaus Tjelle</au><au>Rasmussen, Christian</au><au>Nehlin, Jan O</au><au>Kallemose, Thomas</au><au>Hyppölä, Harri</au><au>Andersen, Ove</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>suPAR Cut-Offs for Risk Stratification in Patients With Symptoms of COVID-19</atitle><jtitle>Biomarker insights</jtitle><addtitle>Biomark Insights</addtitle><date>2021</date><risdate>2021</risdate><volume>16</volume><spage>11772719211034685</spage><pages>11772719211034685-</pages><issn>1177-2719</issn><eissn>1177-2719</eissn><abstract>Objectives:
Elevated soluble urokinase Plasminogen Activator Receptor (suPAR) is a biomarker associated with adverse outcomes. We aimed to investigate the associations between plasma suPAR levels (testing the cut-offs ⩽4, 4-6, and ⩾6 ng/mL) with risk of 14-day mortality, and with the risk of mechanical ventilation in patients that tested positive for SARS-CoV-2.
Methods:
Observational cohort study of patients presenting with symptoms of COVID-19 at Department of Emergency Medicine, Amager and Hvidovre Hospital, Denmark from March 19th, 2020 to April 3rd, 2020. Plasma suPAR was measured using suPARnostic technologies. Patients were followed for development of mechanical ventilation and mortality for 14 days. Validation of our findings were carried out in a similar sized COVID-19 patient cohort from Mikkeli Central Hospital, Finland.
Results:
Among 386 patients with symptoms of COVID-19, the median (interquartile range) age was 64 years (46-77), 57% were women, median suPAR was 4.0 ng/mL (2.7-5.9). In total, 35 patients (9.1%) died during the 14 days follow-up. Patients with suPAR ⩽4 ng/mL (N = 196; 50.8%) had a low risk of mortality (N = 2; 1.0%; negative predictive value of 99.0%, specificity 55.3%, sensitivity 95.2%, positive predictive value 17.4%). Among patients with suPAR ⩾6 ng/mL (N = 92; 23.8%), 16 died (17.4%). About 99 patients (25.6%) tested positive for SARS CoV-2 and of those 12 (12.1%) developed need for mechanical ventilation. None of the SARS-CoV-2 positive patients with suPAR ⩽4 ng/mL (N = 28; 38.8%) needed mechanical ventilation or died. The Mikkeli Central Hospital validation cohort confirmed our findings concerning suPAR cut-offs for risk of development of mechanical ventilation and mortality.
Conclusions:
Patients with symptoms of COVID-19 and suPAR ⩽4 or ⩾6 ng/mL had low or high risk, respectively, concerning the need for mechanical ventilation or mortality. We suggest cut-offs for identification of risk groups in patients presenting to the ED with symptoms of or confirmed COVID-19.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>34421295</pmid><doi>10.1177/11772719211034685</doi><orcidid>https://orcid.org/0000-0001-6790-2218</orcidid><orcidid>https://orcid.org/0000-0002-5027-4435</orcidid><orcidid>https://orcid.org/0000-0001-6038-5027</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Coronaviruses COVID-19 Emergency medical care Mechanical ventilation Mortality Original Research Patients Risk groups Severe acute respiratory syndrome coronavirus 2 U-Plasminogen activator Ventilation |
title | suPAR Cut-Offs for Risk Stratification in Patients With Symptoms of COVID-19 |
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