Clinical Improvement, Outcomes, Antiviral Activity, and Costs Associated With Early Treatment With Remdesivir for Patients With Coronavirus Disease 2019 (COVID-19)

Abstract Background Evidence remains inconclusive on any significant benefits of remdesivir in patients with mild-to-moderate COVID-19. This study explored the disease progression, various clinical outcomes, changes in viral load, and costs associated with early remdesivir treatment among COVID-19 p...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical infectious diseases 2022-04, Vol.74 (8), p.1450-1458
Hauptverfasser: Wong, Carlos K H, Lau, Kristy T K, Au, Ivan C H, Xiong, Xi, Lau, Eric H Y, Cowling, Benjamin J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1458
container_issue 8
container_start_page 1450
container_title Clinical infectious diseases
container_volume 74
creator Wong, Carlos K H
Lau, Kristy T K
Au, Ivan C H
Xiong, Xi
Lau, Eric H Y
Cowling, Benjamin J
description Abstract Background Evidence remains inconclusive on any significant benefits of remdesivir in patients with mild-to-moderate COVID-19. This study explored the disease progression, various clinical outcomes, changes in viral load, and costs associated with early remdesivir treatment among COVID-19 patients. Methods A territory-wide retrospective cohort of 10 419 patients with COVID-19 hospitalized from 21 January 2020 to 31 January 2021 in Hong Kong was identified. Early remdesivir users were matched with controls using propensity-score matching in a ratio ≤1:4. Study outcomes were time to clinical improvement of at least 1 point on WHO clinical progression scale, hospital discharge, recovery, viral clearance, low viral load, positive IgG antibody, in-hospital death, and composite outcomes of in-hospital death requiring invasive ventilation or intensive care. Results After multiple imputation and propensity-score matching, median follow-up was 14 days for both remdesivir (n = 352) and control (n = 1347) groups. Time to clinical improvement was significantly shorter in the remdesivir group than that of control (HR: 1.14; 95% CI: 1.01–1.29; P = .038), as well as for achieving low viral load (1.51; 1.24–1.83; P 
doi_str_mv 10.1093/cid/ciab631
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2552993620</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/cid/ciab631</oup_id><sourcerecordid>2552993620</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-aea857fe0c10a42b7be491e233039528e1fac5f132d1f44c36c318392e85ccb43</originalsourceid><addsrcrecordid>eNp9kc1q3DAUhUVpaX5X2RetSkLHqX4sj7UcnLQdCEwIabI0snxNFGxrqisH5nn6otXgaZddCF10Pr4LOoRccHbNmZZfrWvTMU0h-TtyzJVcZoXS_H2amSqzvJTlETlBfGWM85Kpj-RI5qJQTOXH5HfVu9FZ09P1sA3-DQYY44Jupmj9ALigqzG6NxcSsLL7Ke4W1IwtrTxGpCtEn3ZHaOmziy_01oR-Rx8DmLgXzY8PMLSAewvtfKD3JrqU4RxWPvjRpGxCeuMQDAIVjGt6WW2e1jcZ11dn5ENneoTzw31Kfn67fax-ZHeb7-tqdZdZqZYxM2BKteyAWc5MLpplA7nmIKRkUitRAu-MVR2XouVdnltZWMlLqQWUytoml6fkcvamj_g1AcZ6cGih780IfsJaKCW0loVgCf0yozZ4xABdvQ1uMGFXc1bvW6lTK_WhlUR_OoinZoD2H_u3hgR8ngE_bf9r-gOqopZ4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2552993620</pqid></control><display><type>article</type><title>Clinical Improvement, Outcomes, Antiviral Activity, and Costs Associated With Early Treatment With Remdesivir for Patients With Coronavirus Disease 2019 (COVID-19)</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Wong, Carlos K H ; Lau, Kristy T K ; Au, Ivan C H ; Xiong, Xi ; Lau, Eric H Y ; Cowling, Benjamin J</creator><creatorcontrib>Wong, Carlos K H ; Lau, Kristy T K ; Au, Ivan C H ; Xiong, Xi ; Lau, Eric H Y ; Cowling, Benjamin J</creatorcontrib><description>Abstract Background Evidence remains inconclusive on any significant benefits of remdesivir in patients with mild-to-moderate COVID-19. This study explored the disease progression, various clinical outcomes, changes in viral load, and costs associated with early remdesivir treatment among COVID-19 patients. Methods A territory-wide retrospective cohort of 10 419 patients with COVID-19 hospitalized from 21 January 2020 to 31 January 2021 in Hong Kong was identified. Early remdesivir users were matched with controls using propensity-score matching in a ratio ≤1:4. Study outcomes were time to clinical improvement of at least 1 point on WHO clinical progression scale, hospital discharge, recovery, viral clearance, low viral load, positive IgG antibody, in-hospital death, and composite outcomes of in-hospital death requiring invasive ventilation or intensive care. Results After multiple imputation and propensity-score matching, median follow-up was 14 days for both remdesivir (n = 352) and control (n = 1347) groups. Time to clinical improvement was significantly shorter in the remdesivir group than that of control (HR: 1.14; 95% CI: 1.01–1.29; P = .038), as well as for achieving low viral load (1.51; 1.24–1.83; P &lt; .001) and positive IgG antibody (1.50; 1.31–1.70; P &lt; .001). Early remdesivir treatment was associated with lower risk of in-hospital death (HR: .58; 95% CI: .34–.99; P = .045), in addition to a significantly shorter length of hospital stay (difference: −2.56 days; 95% CI: −4.86 to −.26; P = .029), without increasing risks of composite outcomes for clinical deterioration. Conclusions Early remdesivir treatment could be extended to hospitalized patients with moderate COVID-19 not requiring oxygen therapy on admission. Among hospitalized patients with moderate COVID-19, early initiation of remdesivir was associated with significantly shorter time to clinical improvement, low viral load and positive IgG (immunoglobulin G) antibody, a shorter length of hospital stay, and a significantly lower risk of in-hospital death.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciab631</identifier><identifier>PMID: 34265054</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adenosine Monophosphate - analogs &amp; derivatives ; Alanine - analogs &amp; derivatives ; Antiviral Agents ; COVID-19 - drug therapy ; Hospital Mortality ; Humans ; Immunoglobulin G ; Retrospective Studies ; SARS-CoV-2</subject><ispartof>Clinical infectious diseases, 2022-04, Vol.74 (8), p.1450-1458</ispartof><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-aea857fe0c10a42b7be491e233039528e1fac5f132d1f44c36c318392e85ccb43</citedby><cites>FETCH-LOGICAL-c357t-aea857fe0c10a42b7be491e233039528e1fac5f132d1f44c36c318392e85ccb43</cites><orcidid>0000-0002-6895-6071</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34265054$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wong, Carlos K H</creatorcontrib><creatorcontrib>Lau, Kristy T K</creatorcontrib><creatorcontrib>Au, Ivan C H</creatorcontrib><creatorcontrib>Xiong, Xi</creatorcontrib><creatorcontrib>Lau, Eric H Y</creatorcontrib><creatorcontrib>Cowling, Benjamin J</creatorcontrib><title>Clinical Improvement, Outcomes, Antiviral Activity, and Costs Associated With Early Treatment With Remdesivir for Patients With Coronavirus Disease 2019 (COVID-19)</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Abstract Background Evidence remains inconclusive on any significant benefits of remdesivir in patients with mild-to-moderate COVID-19. This study explored the disease progression, various clinical outcomes, changes in viral load, and costs associated with early remdesivir treatment among COVID-19 patients. Methods A territory-wide retrospective cohort of 10 419 patients with COVID-19 hospitalized from 21 January 2020 to 31 January 2021 in Hong Kong was identified. Early remdesivir users were matched with controls using propensity-score matching in a ratio ≤1:4. Study outcomes were time to clinical improvement of at least 1 point on WHO clinical progression scale, hospital discharge, recovery, viral clearance, low viral load, positive IgG antibody, in-hospital death, and composite outcomes of in-hospital death requiring invasive ventilation or intensive care. Results After multiple imputation and propensity-score matching, median follow-up was 14 days for both remdesivir (n = 352) and control (n = 1347) groups. Time to clinical improvement was significantly shorter in the remdesivir group than that of control (HR: 1.14; 95% CI: 1.01–1.29; P = .038), as well as for achieving low viral load (1.51; 1.24–1.83; P &lt; .001) and positive IgG antibody (1.50; 1.31–1.70; P &lt; .001). Early remdesivir treatment was associated with lower risk of in-hospital death (HR: .58; 95% CI: .34–.99; P = .045), in addition to a significantly shorter length of hospital stay (difference: −2.56 days; 95% CI: −4.86 to −.26; P = .029), without increasing risks of composite outcomes for clinical deterioration. Conclusions Early remdesivir treatment could be extended to hospitalized patients with moderate COVID-19 not requiring oxygen therapy on admission. Among hospitalized patients with moderate COVID-19, early initiation of remdesivir was associated with significantly shorter time to clinical improvement, low viral load and positive IgG (immunoglobulin G) antibody, a shorter length of hospital stay, and a significantly lower risk of in-hospital death.</description><subject>Adenosine Monophosphate - analogs &amp; derivatives</subject><subject>Alanine - analogs &amp; derivatives</subject><subject>Antiviral Agents</subject><subject>COVID-19 - drug therapy</subject><subject>Hospital Mortality</subject><subject>Humans</subject><subject>Immunoglobulin G</subject><subject>Retrospective Studies</subject><subject>SARS-CoV-2</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1q3DAUhUVpaX5X2RetSkLHqX4sj7UcnLQdCEwIabI0snxNFGxrqisH5nn6otXgaZddCF10Pr4LOoRccHbNmZZfrWvTMU0h-TtyzJVcZoXS_H2amSqzvJTlETlBfGWM85Kpj-RI5qJQTOXH5HfVu9FZ09P1sA3-DQYY44Jupmj9ALigqzG6NxcSsLL7Ke4W1IwtrTxGpCtEn3ZHaOmziy_01oR-Rx8DmLgXzY8PMLSAewvtfKD3JrqU4RxWPvjRpGxCeuMQDAIVjGt6WW2e1jcZ11dn5ENneoTzw31Kfn67fax-ZHeb7-tqdZdZqZYxM2BKteyAWc5MLpplA7nmIKRkUitRAu-MVR2XouVdnltZWMlLqQWUytoml6fkcvamj_g1AcZ6cGih780IfsJaKCW0loVgCf0yozZ4xABdvQ1uMGFXc1bvW6lTK_WhlUR_OoinZoD2H_u3hgR8ngE_bf9r-gOqopZ4</recordid><startdate>20220428</startdate><enddate>20220428</enddate><creator>Wong, Carlos K H</creator><creator>Lau, Kristy T K</creator><creator>Au, Ivan C H</creator><creator>Xiong, Xi</creator><creator>Lau, Eric H Y</creator><creator>Cowling, Benjamin J</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6895-6071</orcidid></search><sort><creationdate>20220428</creationdate><title>Clinical Improvement, Outcomes, Antiviral Activity, and Costs Associated With Early Treatment With Remdesivir for Patients With Coronavirus Disease 2019 (COVID-19)</title><author>Wong, Carlos K H ; Lau, Kristy T K ; Au, Ivan C H ; Xiong, Xi ; Lau, Eric H Y ; Cowling, Benjamin J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-aea857fe0c10a42b7be491e233039528e1fac5f132d1f44c36c318392e85ccb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adenosine Monophosphate - analogs &amp; derivatives</topic><topic>Alanine - analogs &amp; derivatives</topic><topic>Antiviral Agents</topic><topic>COVID-19 - drug therapy</topic><topic>Hospital Mortality</topic><topic>Humans</topic><topic>Immunoglobulin G</topic><topic>Retrospective Studies</topic><topic>SARS-CoV-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wong, Carlos K H</creatorcontrib><creatorcontrib>Lau, Kristy T K</creatorcontrib><creatorcontrib>Au, Ivan C H</creatorcontrib><creatorcontrib>Xiong, Xi</creatorcontrib><creatorcontrib>Lau, Eric H Y</creatorcontrib><creatorcontrib>Cowling, Benjamin J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wong, Carlos K H</au><au>Lau, Kristy T K</au><au>Au, Ivan C H</au><au>Xiong, Xi</au><au>Lau, Eric H Y</au><au>Cowling, Benjamin J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Improvement, Outcomes, Antiviral Activity, and Costs Associated With Early Treatment With Remdesivir for Patients With Coronavirus Disease 2019 (COVID-19)</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2022-04-28</date><risdate>2022</risdate><volume>74</volume><issue>8</issue><spage>1450</spage><epage>1458</epage><pages>1450-1458</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Abstract Background Evidence remains inconclusive on any significant benefits of remdesivir in patients with mild-to-moderate COVID-19. This study explored the disease progression, various clinical outcomes, changes in viral load, and costs associated with early remdesivir treatment among COVID-19 patients. Methods A territory-wide retrospective cohort of 10 419 patients with COVID-19 hospitalized from 21 January 2020 to 31 January 2021 in Hong Kong was identified. Early remdesivir users were matched with controls using propensity-score matching in a ratio ≤1:4. Study outcomes were time to clinical improvement of at least 1 point on WHO clinical progression scale, hospital discharge, recovery, viral clearance, low viral load, positive IgG antibody, in-hospital death, and composite outcomes of in-hospital death requiring invasive ventilation or intensive care. Results After multiple imputation and propensity-score matching, median follow-up was 14 days for both remdesivir (n = 352) and control (n = 1347) groups. Time to clinical improvement was significantly shorter in the remdesivir group than that of control (HR: 1.14; 95% CI: 1.01–1.29; P = .038), as well as for achieving low viral load (1.51; 1.24–1.83; P &lt; .001) and positive IgG antibody (1.50; 1.31–1.70; P &lt; .001). Early remdesivir treatment was associated with lower risk of in-hospital death (HR: .58; 95% CI: .34–.99; P = .045), in addition to a significantly shorter length of hospital stay (difference: −2.56 days; 95% CI: −4.86 to −.26; P = .029), without increasing risks of composite outcomes for clinical deterioration. Conclusions Early remdesivir treatment could be extended to hospitalized patients with moderate COVID-19 not requiring oxygen therapy on admission. Among hospitalized patients with moderate COVID-19, early initiation of remdesivir was associated with significantly shorter time to clinical improvement, low viral load and positive IgG (immunoglobulin G) antibody, a shorter length of hospital stay, and a significantly lower risk of in-hospital death.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>34265054</pmid><doi>10.1093/cid/ciab631</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6895-6071</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1058-4838
ispartof Clinical infectious diseases, 2022-04, Vol.74 (8), p.1450-1458
issn 1058-4838
1537-6591
language eng
recordid cdi_proquest_miscellaneous_2552993620
source Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adenosine Monophosphate - analogs & derivatives
Alanine - analogs & derivatives
Antiviral Agents
COVID-19 - drug therapy
Hospital Mortality
Humans
Immunoglobulin G
Retrospective Studies
SARS-CoV-2
title Clinical Improvement, Outcomes, Antiviral Activity, and Costs Associated With Early Treatment With Remdesivir for Patients With Coronavirus Disease 2019 (COVID-19)
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T05%3A19%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Clinical%20Improvement,%20Outcomes,%20Antiviral%20Activity,%20and%20Costs%20Associated%20With%20Early%20Treatment%20With%20Remdesivir%20for%20Patients%20With%20Coronavirus%20Disease%202019%20(COVID-19)&rft.jtitle=Clinical%20infectious%20diseases&rft.au=Wong,%20Carlos%20K%20H&rft.date=2022-04-28&rft.volume=74&rft.issue=8&rft.spage=1450&rft.epage=1458&rft.pages=1450-1458&rft.issn=1058-4838&rft.eissn=1537-6591&rft_id=info:doi/10.1093/cid/ciab631&rft_dat=%3Cproquest_cross%3E2552993620%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2552993620&rft_id=info:pmid/34265054&rft_oup_id=10.1093/cid/ciab631&rfr_iscdi=true