Ivermectin to prevent hospitalizations in patients with COVID-19 (IVERCOR-COVID19) a randomized, double-blind, placebo-controlled trial

被引:66
|
作者
Vallejos, Julio [1 ]
Zoni, Rodrigo [1 ]
Bangher, Maria [1 ]
Villamandos, Silvina [1 ]
Bobadilla, Angelina [2 ]
Plano, Fabian [3 ]
Campias, Claudia [2 ]
Chaparro Campias, Evangelina [4 ]
Fernanda Medina, Maria [1 ]
Achinelli, Fernando [3 ]
Andres Guglielmone, Hector [4 ]
Ojeda, Jorge [3 ]
Farizano Salazar, Diego [3 ]
Andino, Gerardo [4 ]
Kawerin, Pablo [4 ]
Dellamea, Silvana [3 ]
Cristina Aquino, Antonia [3 ]
Flores, Victor [3 ]
Martemucci, Carolina N. [4 ]
Maria Martinez, Silvina [4 ]
Emanuel Segovia, Juan [2 ]
Itati Reynoso, Paola [1 ]
Carolina Sosa, Noelia [1 ]
Elizabeth Robledo, Mariana [1 ]
Maria Guarrochena, Joaquina
Mercedes Vernengo, Maria [2 ]
Ruiz Diaz, Natalia [4 ]
Meza, Elba [2 ]
Gabriela Aguirre, Maria [1 ]
机构
[1] Inst Cardiol Corrientes, Bolivar 1334, RA-3400 Corrientes, Argentina
[2] Minist Salud Publ Prov Corrientes, Epidemiol, Corrientes, Argentina
[3] Minist Salud Publ Prov Corrientes, Minist Salud Publ Corrientes, Hosp Campana, Corrientes, Argentina
[4] Minist Salud Publ Prov Corrientes, Corrientes, Argentina
关键词
INHIBITOR;
D O I
10.1186/s12879-021-06348-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) has changed our lives. The scientific community has been investigating re-purposed treatments to prevent disease progression in coronavirus disease (COVID-19) patients. Objective: To determine whether ivermectin treatment can prevent hospitalization in individuals with early COVID-19. Design, setting and participants: A randomized, double-blind, placebo-controlled study was conducted in non-hospitalized individuals with COVID-19 in Corrientes, Argentina. Patients with SARS-CoV-2 positive nasal swabs were contacted within 48 h by telephone to invite them to participate. The trial randomized 501 patients between August 19th 2020 and February 22nd 2021. Intervention: Patients were randomized to ivermectin (N = 250) or placebo (N = 251) arms in a staggered dose, according to the patient's weight, for 2 days. Main outcomes and measures: The efficacy of ivermectin to prevent hospitalizations was evaluated as primary outcome. We evaluated secondary outcomes in relationship to safety and other efficacy end points. Results: The mean age was 42 years (SD +/- 15.5) and the median time since symptom onset to the inclusion was 4 days [interquartile range 3-6]. The primary outcome of hospitalization was met in 14/250 (5.6%) individuals in ivermectin group and 21/251 (8.4%) in placebo group (odds ratio 0.65; 95% confidence interval, 0.32-1.31; p = 0.227). Time to hospitalization was not statistically different between groups. The mean time from study enrollment to invasive mechanical ventilatory support (MVS) was 5.25 days (SD +/- 1.71) in ivermectin group and 10 days (SD +/- 2) in placebo group, (p = 0.019). There were no statistically significant differences in the other secondary outcomes including polymerase chain reaction test negativity and safety outcomes. Limitations: Low percentage of hospitalization events, dose of ivermectin and not including only high-risk population. Conclusion: Ivermectin had no significant effect on preventing hospitalization of patients with COVID-19. Patients who received ivermectin required invasive MVS earlier in their treatment. No significant differences were observed in any of the other secondary outcomes.
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页数:11
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