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1000 Titel
  • Systematic review of the efficacy and safety of antiretroviral drugs against SARS, MERS or COVID‐19: initial assessment
1000 Autor/in
  1. Ford, Nathan |
  2. Vitoria, Marco |
  3. Rangaraj, Ajay |
  4. Norris, Susan L |
  5. Calmy, Alexandra |
  6. Doherty, Meg |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-03-26
1000 Erschienen in
1000 Quellenangabe
  • 23(4):e25489
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1002/jia2.25489 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158851/ |
1000 Ergänzendes Material
  • https://onlinelibrary.wiley.com/doi/full/10.1002/jia2.25489#support-information-section |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • INTRODUCTION: Several antiretroviral drugs are being considered for the treatment of COVID‐19, the disease caused by a newly identified coronavirus, (SARS‐CoV‐2). We systematically reviewed the clinical outcomes of using antiretroviral drugs for the prevention and treatment of coronaviruses and planned clinical trials. METHODS: Three databases were screened from inception to 30 March 2020 for studies reporting clinical outcomes of patients with SARS, MERS or COVID‐19 treated with antiretrovirals. RESULTS: From an initial screen of 433 titles, two randomized trials and 24 observational studies provided clinical outcome data on the use of antiretroviral drugs; most studies reported outcomes using LPV/r as treatment. Of the 21 observational studies reporting treatment outcomes, there were three studies among patients with SARS, six studies among patients with MERS and 12 studies among patients with COVID‐19. In one randomized trial 99 patients with severe COVID‐19 illness were randomized to receive LPV/r (400/100 mg twice a day) and 100 patients to standard of care for 14 days: LPV/r was not associated with a statistically significant difference in time to clinical improvement, although LPV/r given within 12 days of symptoms was associated with shorter time to clinical improvement; 28 day mortality was numerically lower in the LPV/r group (14/99) compared to the control group (25/100), but this difference was not statistically significant. The second trial found no benefit. The certainty of the evidence for the randomized trials was low. In the observational studies 3 out of 361 patients who received LPV/r died; the certainty of evidence was very low. Three studies reported a possible protective effect of LPV/r as post‐exposure prophylaxis. Again, the certainty of the evidence was very low due to uncertainty due to limited sample size. CONCLUSIONS: On the basis of the available evidence it is uncertain whether LPV/r and other antiretrovirals improve clinical outcomes or prevent infection among patients at high risk of acquiring COVID‐19.
1000 Sacherschließung
gnd 1206347392 COVID-19
lokal MERS
lokal HIV
lokal SARS
lokal antiretroviral therapy
lokal coronavirus
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/Rm9yZCwgTmF0aGFu|https://frl.publisso.de/adhoc/uri/Vml0b3JpYSwgTWFyY28=|https://frl.publisso.de/adhoc/uri/UmFuZ2FyYWosIEFqYXk=|https://orcid.org/0000-0002-0042-2452|https://orcid.org/0000-0002-1137-6826|https://frl.publisso.de/adhoc/uri/RG9oZXJ0eSwgTWVn
1000 Label
1000 Förderer
  1. Bill and Melinda Gates Foundation |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Bill and Melinda Gates Foundation |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6424081.rdf
1000 Erstellt am 2020-11-06T20:54:53.032+0100
1000 Erstellt von 218
1000 beschreibt frl:6424081
1000 Bearbeitet von 25
1000 Zuletzt bearbeitet Mon Nov 09 08:44:51 CET 2020
1000 Objekt bearb. Mon Nov 09 08:44:40 CET 2020
1000 Vgl. frl:6424081
1000 Oai Id
  1. oai:frl.publisso.de:frl:6424081 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

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