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Article: Treatment of coronavirus disease 2019

TitleTreatment of coronavirus disease 2019
Authors
Keywordsantivirals
coronavirus disease 2019
severe acute respiratory syndrome coronavirus 2
treatment
Issue Date2020
PublisherLippincott Williams & Wilkins. The Journal's web site is located at http://www.co-hivandaids.com/
Citation
Current Opinion in HIV and AIDS, 2020, v. 15 n. 6, p. 336-340 How to Cite?
AbstractPurpose of review: Coronavirus disease 2019 (COVID-19) is a highly contagious and potentially lethal pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). No specific antiviral treatment is currently available. The purpose of this review is to highlight the main repurposed drug treatments with in-vitro or in-vivo efficacy against the SARS-CoV-2. Recent findings: Recent clinical trials suggested remdesivir, IFN-β-1b and favipiravir have potential clinical and/or virological benefits on patients with COVID-19. Short course of stress dose of corticosteroids might be used as adjunctive treatment to patients who are late presenters with cytokine storm. Convalescent plasma from recovered COVID-19 patients with high neutralizing antibody might also be beneficial in the treatment of severe disease. Summary: Early effective antiviral therapy in COVID-19 patients will suppress the SARS-CoV-2 viral load. Adjunctive therapy with corticosteroid and convalescent plasma might further ameliorate the cytokine response. Further randomized clinical trials of combination therapy are needed.
Persistent Identifierhttp://hdl.handle.net/10722/289389
ISSN
2021 Impact Factor: 4.061
2020 SCImago Journal Rankings: 1.901
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHung, IFN-
dc.date.accessioned2020-10-22T08:11:57Z-
dc.date.available2020-10-22T08:11:57Z-
dc.date.issued2020-
dc.identifier.citationCurrent Opinion in HIV and AIDS, 2020, v. 15 n. 6, p. 336-340-
dc.identifier.issn1746-630X-
dc.identifier.urihttp://hdl.handle.net/10722/289389-
dc.description.abstractPurpose of review: Coronavirus disease 2019 (COVID-19) is a highly contagious and potentially lethal pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). No specific antiviral treatment is currently available. The purpose of this review is to highlight the main repurposed drug treatments with in-vitro or in-vivo efficacy against the SARS-CoV-2. Recent findings: Recent clinical trials suggested remdesivir, IFN-β-1b and favipiravir have potential clinical and/or virological benefits on patients with COVID-19. Short course of stress dose of corticosteroids might be used as adjunctive treatment to patients who are late presenters with cytokine storm. Convalescent plasma from recovered COVID-19 patients with high neutralizing antibody might also be beneficial in the treatment of severe disease. Summary: Early effective antiviral therapy in COVID-19 patients will suppress the SARS-CoV-2 viral load. Adjunctive therapy with corticosteroid and convalescent plasma might further ameliorate the cytokine response. Further randomized clinical trials of combination therapy are needed.-
dc.languageeng-
dc.publisherLippincott Williams & Wilkins. The Journal's web site is located at http://www.co-hivandaids.com/-
dc.relation.ispartofCurrent Opinion in HIV and AIDS-
dc.rightsThis is a non-final version of an article published in final form in (provide complete journal citation)-
dc.subjectantivirals-
dc.subjectcoronavirus disease 2019-
dc.subjectsevere acute respiratory syndrome coronavirus 2-
dc.subjecttreatment-
dc.titleTreatment of coronavirus disease 2019-
dc.typeArticle-
dc.identifier.emailHung, IFN: ivanhung@hkucc.hku.hk-
dc.identifier.authorityHung, IFN=rp00508-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1097/COH.0000000000000652-
dc.identifier.pmid33002954-
dc.identifier.scopuseid_2-s2.0-85092514340-
dc.identifier.hkuros317183-
dc.identifier.volume15-
dc.identifier.issue6-
dc.identifier.spage336-
dc.identifier.epage340-
dc.identifier.isiWOS:000587785800003-
dc.publisher.placeUnited States-
dc.identifier.issnl1746-630X-

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