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Comparison of antiviral effect for mild-to-moderate COVID-19 cases between lopinavir/ritonavir versus hydroxychloroquine: A nationwide propensity score-matched cohort study.

Identifieur interne : 000921 ( Main/Corpus ); précédent : 000920; suivant : 000922

Comparison of antiviral effect for mild-to-moderate COVID-19 cases between lopinavir/ritonavir versus hydroxychloroquine: A nationwide propensity score-matched cohort study.

Auteurs : Min Joo Choi ; Minsun Kang ; So Youn Shin ; Ji Yun Noh ; Hee Jin Cheong ; Woo Joo Kim ; Jaehun Jung ; Joon Young Song

Source :

RBID : pubmed:33127507

English descriptors

Abstract

OBJECTIVES

We aimed to compare the antiviral effect of hydroxychloroquine (HCQ) and lopinavir/ritonavir (LPV/r) in patients with COVID-19.

METHODS

Nationwide retrospective case-control study was conducted to compare the effect of HCQ and LPV/r on viral shedding duration among patients with mild-to-moderate COVID-19 using the reimbursement data of National Health Insurance Service. After propensity score matching (PSM), multivariate analysis was conducted to determine statistically significant risk factors associated with prolonged viral shedding.

RESULTS

Overall, 4197 patients with mild-to-moderate COVID-19 were included. Patients were categorized into three groups: LPV/r (n = 1268), HCQ (n = 801), and standard care without HCQ or LPV/r (controls, n = 2128). The median viral shedding duration was 23 (IQR 17-32), 23 (IQR 16-32), and 18 (IQR 12-25) days in the LPV/r, HCQ, and control groups, respectively. Even after PSM, the viral shedding duration was not significantly different between LPV/r and HCQ groups: 23 (IQR, 17-32) days versus 23 (IQR, 16-32) days. On multivariate analysis, old age, malignancy, steroid use, and concomitant pneumonia were statistically significant risk factors for prolonged viral shedding.

CONCLUSION

The viral shedding duration was similar between HCQ and LPV/r treatment groups. There was no benefit in improving viral clearance compared to the control group.


DOI: 10.1016/j.ijid.2020.10.062
PubMed: 33127507
PubMed Central: PMC7590837

Links to Exploration step

pubmed:33127507

Le document en format XML

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<term>COVID-19 (virology)</term>
<term>Drug Therapy, Combination (MeSH)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Hydroxychloroquine (therapeutic use)</term>
<term>Lopinavir (administration & dosage)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Propensity Score (MeSH)</term>
<term>Retrospective Studies (MeSH)</term>
<term>Ritonavir (administration & dosage)</term>
<term>SARS-CoV-2 (MeSH)</term>
<term>Virus Shedding (drug effects)</term>
<term>Young Adult (MeSH)</term>
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<b>OBJECTIVES</b>
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<p>We aimed to compare the antiviral effect of hydroxychloroquine (HCQ) and lopinavir/ritonavir (LPV/r) in patients with COVID-19.</p>
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<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
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<p>Nationwide retrospective case-control study was conducted to compare the effect of HCQ and LPV/r on viral shedding duration among patients with mild-to-moderate COVID-19 using the reimbursement data of National Health Insurance Service. After propensity score matching (PSM), multivariate analysis was conducted to determine statistically significant risk factors associated with prolonged viral shedding.</p>
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<p>
<b>RESULTS</b>
</p>
<p>Overall, 4197 patients with mild-to-moderate COVID-19 were included. Patients were categorized into three groups: LPV/r (n = 1268), HCQ (n = 801), and standard care without HCQ or LPV/r (controls, n = 2128). The median viral shedding duration was 23 (IQR 17-32), 23 (IQR 16-32), and 18 (IQR 12-25) days in the LPV/r, HCQ, and control groups, respectively. Even after PSM, the viral shedding duration was not significantly different between LPV/r and HCQ groups: 23 (IQR, 17-32) days versus 23 (IQR, 16-32) days. On multivariate analysis, old age, malignancy, steroid use, and concomitant pneumonia were statistically significant risk factors for prolonged viral shedding.</p>
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<b>CONCLUSION</b>
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<p>The viral shedding duration was similar between HCQ and LPV/r treatment groups. There was no benefit in improving viral clearance compared to the control group.</p>
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