Use of an antiviral mouthwash as a barrier measure in the SARS-CoV-2 transmission in adults with asymptomatic to mild COVID-19: a multicentre, randomized, double-blind controlled trial

被引:33
作者
Carrouel, Florence [1 ]
Valette, Martine [2 ]
Gadea, Emilie [3 ,4 ]
Esparcieux, Aurelie [5 ]
Illes, Gabriela [6 ]
Langlois, Marie Elodie [7 ]
Perrier, Herve [8 ]
Dussart, Claude [1 ]
Tramini, Paul [9 ]
Ribaud, Melina [10 ]
Bouscambert-Duchamp, Maude [2 ]
Bourgeois, Denis [1 ]
机构
[1] Univ Claude Bernard Lyon 1, Univ Lyon, EA4129, Lab Syst Hlth Care, Lyon, France
[2] Hosp Civils Lyon, Croix Rousse Hosp, Natl Ctr Virus Resp Infect, Virol Lab,Inst Infect Agents, Lyon, France
[3] Univ Jean Monnet, EA4607, Equipe SNA EPIS, St Etienne, France
[4] Emile Roux Hosp Ctr, Clin Res Unit, Le Puy En Velay, France
[5] Protestant Infirm, Dept Internal Med & Infect Dis, Caluire Et Cuire, France
[6] Intercommunal Hosp Ctr Mt de Marsan & Pays Source, Dept Internal Med & Infect Dis, Mt de Marsan, France
[7] St Joseph St Luc Hosp, Dept Internal Med & Infect Dis, Lyon, France
[8] Protestant Infirm, Clin Res Unit, Lyon, France
[9] Univ Montpellier, Fac Dent Med, Dept Publ Hlth, Montpellier, France
[10] Natl Inst Agron Res INRAE, BioSP, UR546, Avignon, France
关键词
beta-cyclodextrin; Citrox; Coronavirus disease 2019; Mouthwash; Saliva; Severe acute respiratory syndrome coronavirus 2; Viral load; INFECTION;
D O I
10.1016/j.cmi.2021.05.028
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To determine if commercially available mouthwash with beta-cyclodextrin and citrox (bioflavonoids) (CDCM) could decrease the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) salivary viral load. Methods: In this randomized controlled trial, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) PCR-positive patients aged 18-85 years with asymptomatic to mild coronavirus disease 2019 (COVID-19) symptoms for <8 days were recruited. A total of 176 eligible patients were randomly assigned (1:1) to CDCM or placebo. Three rinses daily were performed for 7 days. Saliva sampling was performed on day 1 at 09.00 (T1), 13.00 (T2) and 18.00 (T3). On the following 6 days, one sample was taken at 15.00. Quantitative RT-PCR was used to detect SARS-CoV-2. Results: The intention-to-treat analysis demonstrated that, over the course of 1 day, CDCM was significantly more effective than placebo 4 hours after the first dose (p 0.036), with a median percentage (log(10) copies/mL) decrease T1-T2 of-12.58% (IQR-29.55% to-0.16%). The second dose maintained the low median value for the CDCM (3.08 log(10) copies/mL; IQR 0-4.19), compared with placebo (3.31 log(10) copies/mL; IQR 1.18-4.75). At day 7, there was still a greater median percentage (log(10) copies/mL) decrease in salivary viral load over time in the CDCM group (-58.62%; IQR-100% to-34.36%) compared with the placebo group (-50.62%; IQR-100% to-27.66%). These results were confirmed by the per-protocol analysis. Conclusions: This trial supports the relevance of using CDCM on day 1 (4 hours after the initial dose) to reduce the SARS-CoV-2 viral load in saliva. For long-term effect (7 days), CDMC appears to provide a modest benefit compared with placebo in reducing viral load in saliva. (C) 2021 The Author(s). Published by Elsevier Ltd on behalf of European Society of Clinical Microbiology and Infectious Diseases.
引用
收藏
页码:1494 / 1501
页数:8
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