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Article: Lopinavir-ritonavir (LPV/r) for the Treatment of SARS-CoV-2 (COVID-19): A Systematic Review
Title | Lopinavir-ritonavir (LPV/r) for the Treatment of SARS-CoV-2 (COVID-19): A Systematic Review |
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Authors | |
Issue Date | 2020 |
Publisher | Research Open World. The Journal's web site is located at https://researchopenworld.com/category/journal-of-pharmacology-pharmaceutical-research/ |
Citation | Journal of Pharmacology & Pharmaceutical Research, 2020, v. 3 n. 2, p. 1-21 How to Cite? |
Abstract | Background: SARS-CoV-2 is the pathogenic agent of COVID-19, which has affected more than 200 countries; infected over 4 million people and declared a global pandemic. At the time of writing, no approved definitive therapeutic treatment for COVID-19 is available. Many studies are still on-going.
Lopinavir-ritonavir (LPV/r), or its combination has been advocated as a potential treatment. This study reviews the evidence of LPV/r usage in the treatment of SARS-CoV-2 infection.
Methods: A systematic review protocol was written based on the PRISMA Statement Article for review selected from electronic databases (PubMed, Embase and Medline). Inclusion criteria were: full English articles published between 2019 and 2020, accessible and peer-reviewed. The search keywords
were: Lopinavir, COVID, and SARS-CoV-2. Studies fulfilling the inclusion criteria were included, regardless of study designs. Data were extracted from published reports.
Findings: As of 9 May 2020, 243 manuscripts were identified. Thirteen studies were included with a total of 494 patients. These consisted of clinical trials (n=2), case reports (n=5), case series (n=3), and retrospective cohort studies (n=3). In the thirteen studies, the use of LPV/r shortened the PCR negativeconversion time for SARS-CoV-2, the earliest as being 5 days (Range: 5 to 28 days), and clinical improvement was expected as early as 2 days (Range: 2 to 28 days).
Interpretation: Our review shows that the use of LPV/r may be an effective treatment for non-severe COVID-19 patients, while only limited benefits were observed in severe COVID-19 patients. |
Persistent Identifier | http://hdl.handle.net/10722/286249 |
DC Field | Value | Language |
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dc.contributor.author | Yan, Z | - |
dc.contributor.author | Shum, KL | - |
dc.contributor.author | Lai, CL | - |
dc.date.accessioned | 2020-08-31T07:01:16Z | - |
dc.date.available | 2020-08-31T07:01:16Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Journal of Pharmacology & Pharmaceutical Research, 2020, v. 3 n. 2, p. 1-21 | - |
dc.identifier.uri | http://hdl.handle.net/10722/286249 | - |
dc.description.abstract | Background: SARS-CoV-2 is the pathogenic agent of COVID-19, which has affected more than 200 countries; infected over 4 million people and declared a global pandemic. At the time of writing, no approved definitive therapeutic treatment for COVID-19 is available. Many studies are still on-going. Lopinavir-ritonavir (LPV/r), or its combination has been advocated as a potential treatment. This study reviews the evidence of LPV/r usage in the treatment of SARS-CoV-2 infection. Methods: A systematic review protocol was written based on the PRISMA Statement Article for review selected from electronic databases (PubMed, Embase and Medline). Inclusion criteria were: full English articles published between 2019 and 2020, accessible and peer-reviewed. The search keywords were: Lopinavir, COVID, and SARS-CoV-2. Studies fulfilling the inclusion criteria were included, regardless of study designs. Data were extracted from published reports. Findings: As of 9 May 2020, 243 manuscripts were identified. Thirteen studies were included with a total of 494 patients. These consisted of clinical trials (n=2), case reports (n=5), case series (n=3), and retrospective cohort studies (n=3). In the thirteen studies, the use of LPV/r shortened the PCR negativeconversion time for SARS-CoV-2, the earliest as being 5 days (Range: 5 to 28 days), and clinical improvement was expected as early as 2 days (Range: 2 to 28 days). Interpretation: Our review shows that the use of LPV/r may be an effective treatment for non-severe COVID-19 patients, while only limited benefits were observed in severe COVID-19 patients. | - |
dc.language | eng | - |
dc.publisher | Research Open World. The Journal's web site is located at https://researchopenworld.com/category/journal-of-pharmacology-pharmaceutical-research/ | - |
dc.relation.ispartof | Journal of Pharmacology & Pharmaceutical Research | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Lopinavir-ritonavir (LPV/r) for the Treatment of SARS-CoV-2 (COVID-19): A Systematic Review | - |
dc.type | Article | - |
dc.identifier.email | Lai, CL: hrmelcl@hkucc.hku.hk | - |
dc.identifier.authority | Lai, CL=rp00314 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.hkuros | 313814 | - |
dc.identifier.volume | 3 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 1 | - |
dc.identifier.epage | 21 | - |
dc.publisher.place | United States | - |