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Arbidol combined with LPV/r versus LPV/r alone against Corona Virus Disease 2019: A retrospective cohort study

Identifieur interne : 001837 ( Pmc/Curation ); précédent : 001836; suivant : 001838

Arbidol combined with LPV/r versus LPV/r alone against Corona Virus Disease 2019: A retrospective cohort study

Auteurs : Lisi Deng [République populaire de Chine] ; Chunna Li [République populaire de Chine] ; Qi Zeng [République populaire de Chine] ; Xi Liu [République populaire de Chine] ; Xinghua Li [République populaire de Chine] ; Haitang Zhang [République populaire de Chine] ; Zhongsi Hong [République populaire de Chine] ; Jinyu Xia [République populaire de Chine]

Source :

RBID : PMC:7156152

Abstract

Highlights

Patients were given oral arbidol and LPV/r in the combination group and oral LPV/r only in the monotherapy group for 5–21 days.

Our study shows that oral arbidol and LPV/r in the combination group is associated with a significant elevated negative conversion rate of coronavirus’ test in 7-day and 14-day, compared with LPV/r only in the monotherapy group.

Combination therapy is associated with a significantly improved the chest CT scans in 7-day.

We suppose that reducing the viral load as soon as possible could benefit the delay of the progression of lung lesions.


Url:
DOI: 10.1016/j.jinf.2020.03.002
PubMed: 32171872
PubMed Central: 7156152

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PMC:7156152

Le document en format XML

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<p id="para0002">Patients were given oral arbidol and LPV/r in the combination group and oral LPV/r only in the monotherapy group for 5–21 days.</p>
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<p id="para0003">Our study shows that oral arbidol and LPV/r in the combination group is associated with a significant elevated negative conversion rate of coronavirus’ test in 7-day and 14-day, compared with LPV/r only in the monotherapy group.</p>
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</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">J Infect</journal-id>
<journal-id journal-id-type="iso-abbrev">J. Infect</journal-id>
<journal-title-group>
<journal-title>The Journal of Infection</journal-title>
</journal-title-group>
<issn pub-type="ppub">0163-4453</issn>
<issn pub-type="epub">1532-2742</issn>
<publisher>
<publisher-name>The British Infection Association. Published by Elsevier Ltd.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">32171872</article-id>
<article-id pub-id-type="pmc">7156152</article-id>
<article-id pub-id-type="publisher-id">S0163-4453(20)30113-4</article-id>
<article-id pub-id-type="doi">10.1016/j.jinf.2020.03.002</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Arbidol combined with LPV/r versus LPV/r alone against Corona Virus Disease 2019: A retrospective cohort study</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" id="au0001">
<name>
<surname>Deng</surname>
<given-names>Lisi</given-names>
</name>
<xref rid="aff0001" ref-type="aff">a</xref>
<xref rid="fn1" ref-type="fn">1</xref>
</contrib>
<contrib contrib-type="author" id="au0002">
<name>
<surname>Li</surname>
<given-names>Chunna</given-names>
</name>
<xref rid="aff0001" ref-type="aff">a</xref>
<xref rid="fn1" ref-type="fn">1</xref>
</contrib>
<contrib contrib-type="author" id="au0003">
<name>
<surname>Zeng</surname>
<given-names>Qi</given-names>
</name>
<xref rid="aff0002" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author" id="au0004">
<name>
<surname>Liu</surname>
<given-names>Xi</given-names>
</name>
<xref rid="aff0001" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author" id="au0005">
<name>
<surname>Li</surname>
<given-names>Xinghua</given-names>
</name>
<xref rid="aff0001" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author" id="au0006">
<name>
<surname>Zhang</surname>
<given-names>Haitang</given-names>
</name>
<xref rid="aff0001" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author" id="au0007">
<name>
<surname>Hong</surname>
<given-names>Zhongsi</given-names>
</name>
<email>hongzhs@mail.sysu.edu.cn</email>
<xref rid="aff0001" ref-type="aff">a</xref>
<xref rid="cor0001" ref-type="corresp"></xref>
</contrib>
<contrib contrib-type="author" id="au0008">
<name>
<surname>Xia</surname>
<given-names>Jinyu</given-names>
</name>
<email>xiajinyu@mail.sysu.edu.cn</email>
<xref rid="aff0001" ref-type="aff">a</xref>
<xref rid="cor0001" ref-type="corresp"></xref>
</contrib>
</contrib-group>
<aff id="aff0001">
<label>a</label>
Department of Infectious Diseases, the Fifth Affiliated Hospital, Sun Yat-sen University, 52 East Meihua Road, Zhuhai 519000, Guangdong Province, China</aff>
<aff id="aff0002">
<label>b</label>
Cancer Center, the Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, Guangdong Province, China</aff>
<author-notes>
<corresp id="cor0001">
<label></label>
Corresponding authors.
<email>hongzhs@mail.sysu.edu.cn</email>
<email>xiajinyu@mail.sysu.edu.cn</email>
</corresp>
<fn id="fn1">
<label>1</label>
<p id="notep0001">Equal contribution.</p>
</fn>
</author-notes>
<pub-date pub-type="pmc-release">
<day>11</day>
<month>3</month>
<year>2020</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="epub">
<day>11</day>
<month>3</month>
<year>2020</year>
</pub-date>
<history>
<date date-type="accepted">
<day>6</day>
<month>3</month>
<year>2020</year>
</date>
</history>
<permissions>
<copyright-statement>© 2020 The British Infection Association. Published by Elsevier Ltd. All rights reserved.</copyright-statement>
<copyright-year>2020</copyright-year>
<copyright-holder></copyright-holder>
<license>
<license-p>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.</license-p>
</license>
</permissions>
<abstract abstract-type="author-highlights" id="abs0001">
<title>Highlights</title>
<p>
<list list-type="simple" id="celist0001">
<list-item id="celistitem0001">
<label></label>
<p id="para0002">Patients were given oral arbidol and LPV/r in the combination group and oral LPV/r only in the monotherapy group for 5–21 days.</p>
</list-item>
<list-item id="celistitem0002">
<label></label>
<p id="para0003">Our study shows that oral arbidol and LPV/r in the combination group is associated with a significant elevated negative conversion rate of coronavirus’ test in 7-day and 14-day, compared with LPV/r only in the monotherapy group.</p>
</list-item>
<list-item id="celistitem0003">
<label></label>
<p id="para0004">Combination therapy is associated with a significantly improved the chest CT scans in 7-day.</p>
</list-item>
<list-item id="celistitem0004">
<label></label>
<p id="para0005">We suppose that reducing the viral load as soon as possible could benefit the delay of the progression of lung lesions.</p>
</list-item>
</list>
</p>
</abstract>
<abstract id="abs0002">
<title>Summary</title>
<sec>
<title>Background</title>
<p>Corona Virus Disease 2019 (COVID-19) due to the 2019 novel coronavirus (SARS-CoV-2) emerged in Wuhan city and rapidly spread throughout China. We aimed to compare arbidol and lopinavir/ritonavir(LPV/r) treatment for patients with COVID-19 with LPV/r only.</p>
</sec>
<sec>
<title>Methods</title>
<p>In this retrospective cohort study, we included adults (age≥18years) with laboratory-confirmed COVID-19 without Invasive ventilation, diagnosed between Jan 17, 2020, and Feb 13, 2020. Patients, diagnosed after Jan 17, 2020, were given oral arbidol and LPV/r in the combination group and oral LPV/r only in the monotherapy group for 5–21 days. The primary endpoint was a negative conversion rate of coronavirus from the date of COVID-19 diagnosis(day7, day14), and assessed whether the pneumonia was progressing or improving by chest CT (day7).</p>
</sec>
<sec>
<title>Results</title>
<p>We analyzed 16 patients who received oral arbidol and LPV/r in the combination group and 17 who oral LPV/r only in the monotherapy group, and both initiated after diagnosis. Baseline clinical, laboratory, and chest CT characteristics were similar between groups. The SARS-CoV-2 could not be detected for 12(75%) of 16 patients’ nasopharyngeal specimens in the combination group after seven days, compared with 6 (35%) of 17 in the monotherapy group (
<italic>p</italic>
< 0·05). After 14 days, 15 (94%) of 16 and 9 (52·9%) of 17, respectively, SARS-CoV-2 could not be detected (
<italic>p</italic>
< 0·05). The chest CT scans were improving for 11(69%) of 16 patients in the combination group after seven days, compared with 5(29%) of 17 in the monotherapy group (
<italic>p</italic>
< 0·05).</p>
</sec>
<sec>
<title>Conclusion</title>
<p>In patients with COVID-19, the apparent favorable clinical response with arbidol and LPV/r supports further LPV/r only.</p>
</sec>
</abstract>
<kwd-group id="keys0001">
<title>Keywords</title>
<kwd>Corona Virus Disease 2019</kwd>
<kwd>Arbidol</kwd>
<kwd>Lopinavir/ritonavir</kwd>
<kwd>Antiviral intervention</kwd>
<kwd>Combination therapy</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

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