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Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial

During the first year of the COVID-19 pandemic, unauthorized drugs were widely used. Ivermectin and hydroxychloroquine are drugs that inhibit viral replication in vitro and that have been used in several medical centers. This clinical trial analyzes their efficacy in hospitalized patients with moder...

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Autores principales: Beltran Gonzalez, Jose Lenin, González Gámez, Mario, Mendoza Enciso, Emanuel Antonio, Esparza Maldonado, Ramiro Josue, Hernández Palacios, Daniel, Dueñas Campos, Samuel, Robles, Itzel Ovalle, Macías Guzmán, Mariana Jocelyn, García Díaz, Andrea Lucia, Gutiérrez Peña, César Mauricio, Martinez Medina, Lucila, Monroy Colin, Victor Antonio, Arreola Guerra, Jose Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938813/
https://www.ncbi.nlm.nih.gov/pubmed/35314650
http://dx.doi.org/10.3390/idr14020020
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author Beltran Gonzalez, Jose Lenin
González Gámez, Mario
Mendoza Enciso, Emanuel Antonio
Esparza Maldonado, Ramiro Josue
Hernández Palacios, Daniel
Dueñas Campos, Samuel
Robles, Itzel Ovalle
Macías Guzmán, Mariana Jocelyn
García Díaz, Andrea Lucia
Gutiérrez Peña, César Mauricio
Martinez Medina, Lucila
Monroy Colin, Victor Antonio
Arreola Guerra, Jose Manuel
author_facet Beltran Gonzalez, Jose Lenin
González Gámez, Mario
Mendoza Enciso, Emanuel Antonio
Esparza Maldonado, Ramiro Josue
Hernández Palacios, Daniel
Dueñas Campos, Samuel
Robles, Itzel Ovalle
Macías Guzmán, Mariana Jocelyn
García Díaz, Andrea Lucia
Gutiérrez Peña, César Mauricio
Martinez Medina, Lucila
Monroy Colin, Victor Antonio
Arreola Guerra, Jose Manuel
author_sort Beltran Gonzalez, Jose Lenin
collection PubMed
description During the first year of the COVID-19 pandemic, unauthorized drugs were widely used. Ivermectin and hydroxychloroquine are drugs that inhibit viral replication in vitro and that have been used in several medical centers. This clinical trial analyzes their efficacy in hospitalized patients with moderate COVID-19. Methods: This a controlled, clinical, randomized, double-blind trial that included hospitalized patients with COVID-19-induced pneumonia, without severe respiratory failure. Patients were randomized to one of three groups: Group 1—hydroxychloroquine, 400 mg every 12 h on the first day and, subsequently, 200 mg every 12 h for 4 days; Group 2—ivermectin, 12 mg or 18 mg, according to patient weight; and Group 3—placebo. At inclusion, blood samples for arterial blood gases and biochemical markers were obtained. The primary outcome was established as the length of stay due to patient improvement and the rate of respiratory deterioration or death. Results: During the month of August 2020, the admission of patients requiring hospitalization mostly encompassed cases with severe respiratory failure, so we ended the recruitment process and analyzed the data that was available at the time. One hundred and six (106) patients with an average age of 53 yrs (±16.9) were included, with a greater proportion of males (n = 66, 62.2%). Seventy-two percent (72%) (n = 76) had an associated comorbidity. Ninety percent (90%) of patients were discharged due to improvement (n = 96). The average duration of hospitalization was 6 days (IQR, 3–10). No difference in hospitalization duration was found between the treatment groups (Group1: 7 vs. Group 2: 6 vs. Group 3: 5, p = 0.43) nor in respiratory deterioration or death (Group 1: 18% vs. Group 2: 22.2% vs. Group 3: 24.3%, p = 0.83). Conclusions: In non-critical hospitalized patients with COVID-19 pneumonia, neither ivermectin nor hydroxychloroquine decreases the number of in-hospital days, respiratory deterioration, or deaths.
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spelling pubmed-89388132022-03-23 Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial Beltran Gonzalez, Jose Lenin González Gámez, Mario Mendoza Enciso, Emanuel Antonio Esparza Maldonado, Ramiro Josue Hernández Palacios, Daniel Dueñas Campos, Samuel Robles, Itzel Ovalle Macías Guzmán, Mariana Jocelyn García Díaz, Andrea Lucia Gutiérrez Peña, César Mauricio Martinez Medina, Lucila Monroy Colin, Victor Antonio Arreola Guerra, Jose Manuel Infect Dis Rep Article During the first year of the COVID-19 pandemic, unauthorized drugs were widely used. Ivermectin and hydroxychloroquine are drugs that inhibit viral replication in vitro and that have been used in several medical centers. This clinical trial analyzes their efficacy in hospitalized patients with moderate COVID-19. Methods: This a controlled, clinical, randomized, double-blind trial that included hospitalized patients with COVID-19-induced pneumonia, without severe respiratory failure. Patients were randomized to one of three groups: Group 1—hydroxychloroquine, 400 mg every 12 h on the first day and, subsequently, 200 mg every 12 h for 4 days; Group 2—ivermectin, 12 mg or 18 mg, according to patient weight; and Group 3—placebo. At inclusion, blood samples for arterial blood gases and biochemical markers were obtained. The primary outcome was established as the length of stay due to patient improvement and the rate of respiratory deterioration or death. Results: During the month of August 2020, the admission of patients requiring hospitalization mostly encompassed cases with severe respiratory failure, so we ended the recruitment process and analyzed the data that was available at the time. One hundred and six (106) patients with an average age of 53 yrs (±16.9) were included, with a greater proportion of males (n = 66, 62.2%). Seventy-two percent (72%) (n = 76) had an associated comorbidity. Ninety percent (90%) of patients were discharged due to improvement (n = 96). The average duration of hospitalization was 6 days (IQR, 3–10). No difference in hospitalization duration was found between the treatment groups (Group1: 7 vs. Group 2: 6 vs. Group 3: 5, p = 0.43) nor in respiratory deterioration or death (Group 1: 18% vs. Group 2: 22.2% vs. Group 3: 24.3%, p = 0.83). Conclusions: In non-critical hospitalized patients with COVID-19 pneumonia, neither ivermectin nor hydroxychloroquine decreases the number of in-hospital days, respiratory deterioration, or deaths. MDPI 2022-03-03 /pmc/articles/PMC8938813/ /pubmed/35314650 http://dx.doi.org/10.3390/idr14020020 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Beltran Gonzalez, Jose Lenin
González Gámez, Mario
Mendoza Enciso, Emanuel Antonio
Esparza Maldonado, Ramiro Josue
Hernández Palacios, Daniel
Dueñas Campos, Samuel
Robles, Itzel Ovalle
Macías Guzmán, Mariana Jocelyn
García Díaz, Andrea Lucia
Gutiérrez Peña, César Mauricio
Martinez Medina, Lucila
Monroy Colin, Victor Antonio
Arreola Guerra, Jose Manuel
Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial
title Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial
title_full Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial
title_fullStr Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial
title_full_unstemmed Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial
title_short Efficacy and Safety of Ivermectin and Hydroxychloroquine in Patients with Severe COVID-19: A Randomized Controlled Trial
title_sort efficacy and safety of ivermectin and hydroxychloroquine in patients with severe covid-19: a randomized controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938813/
https://www.ncbi.nlm.nih.gov/pubmed/35314650
http://dx.doi.org/10.3390/idr14020020
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