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10.1093/jac/dkaa331

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32812051!7529105!32812051
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suck abstract from ncbi


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pmid32812051      J+Antimicrob+Chemother 2020 ; 75 (11): 3366-3372
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  • The impact of sofosbuvir/daclatasvir or ribavirin in patients with severe COVID-19 #MMPMID32812051
  • Eslami G; Mousaviasl S; Radmanesh E; Jelvay S; Bitaraf S; Simmons B; Wentzel H; Hill A; Sadeghi A; Freeman J; Salmanzadeh S; Esmaeilian H; Mobarak M; Tabibi R; Jafari Kashi AH; Lotfi Z; Talebzadeh SM; Wickramatillake A; Momtazan M; Hajizadeh Farsani M; Marjani S; Mobarak S
  • J Antimicrob Chemother 2020[Nov]; 75 (11): 3366-3372 PMID32812051show ga
  • OBJECTIVES: Sofosbuvir and daclatasvir are direct-acting antivirals highly effective against hepatitis C virus. There is some in silico and in vitro evidence that suggests these agents may also be effective against SARS-CoV-2. This trial evaluated the effectiveness of sofosbuvir in combination with daclatasvir in treating patients with COVID-19. METHODS: Patients with a positive nasopharyngeal swab for SARS-CoV-2 on RT-PCR or bilateral multi-lobar ground-glass opacity on their chest CT and signs of severe COVID-19 were included. Subjects were divided into two arms with one arm receiving ribavirin and the other receiving sofosbuvir/daclatasvir. All participants also received the recommended national standard treatment which, at that time, was lopinavir/ritonavir and single-dose hydroxychloroquine. The primary endpoint was time from starting the medication until discharge from hospital with secondary endpoints of duration of ICU stay and mortality. RESULTS: Sixty-two subjects met the inclusion criteria, with 35 enrolled in the sofosbuvir/daclatasvir arm and 27 in the ribavirin arm. The median duration of stay was 5 days for the sofosbuvir/daclatasvir group and 9 days for the ribavirin group. The mortality in the sofosbuvir/daclatasvir group was 2/35 (6%) and 9/27 (33%) for the ribavirin group. The relative risk of death for patients treated with sofosbuvir/daclatasvir was 0.17 (95% CI 0.04-0.73, P = 0.02) and the number needed to treat for benefit was 3.6 (95% CI 2.1-12.1, P < 0.01). CONCLUSIONS: Given these encouraging initial results, and the current lack of treatments proven to decrease mortality in COVID-19, further investigation in larger-scale trials seems warranted.
  • |*Betacoronavirus[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |Antiviral Agents/*administration & dosage[MESH]
  • |COVID-19[MESH]
  • |Carbamates[MESH]
  • |Coronavirus Infections/*drug therapy/mortality[MESH]
  • |Drug Therapy, Combination[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Imidazoles/*administration & dosage[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy/mortality[MESH]
  • |Pyrrolidines[MESH]
  • |Ribavirin/*administration & dosage[MESH]
  • |SARS-CoV-2[MESH]
  • |Sofosbuvir/*administration & dosage[MESH]
  • |Treatment Outcome[MESH]


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