Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers

Detalhes bibliográficos
Autor(a) principal: Chahla, Rossana Elena
Data de Publicação: 2022
Outros Autores: Ruiz, Luis Medina, Mena, Teresa, Brepe, Yolanda, Terranova, Paola, Ortega, Eugenia Silvana, Barrenechea, Guillermo Gabriel, Goroso, Daniel Gustavo, Peral de Bruno, María de los Ángeles
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/30844
Resumo: Objective: to evaluate the therapeutic intervention with Ivermectin in outpatients with COVID-19 mild disease, to increase medical discharge and prevent the progression to moderate or severe disease. Methods: Randomized Trial, n= 254. The subjects were divided into experimental (EG: n= 110) and control groups (CG: n= 144). The EG received Ivermectin orally 0.6 mg/kg weight in two doses. All participants were by physical examination COVID-19 diagnosed with negative RT-PCR at the beginning and the end of protocol. Differences between the variables were determined using the Chi-square test (p<0.05). The contagion risk (Odds Ratio) was calculated using software STATA. Results: Both groups were similar in age, sex, and comorbidities. A significant reduction in the percentage of participants with symptoms (PPS) was observed in the EG and CG when the clinical evaluation of symptoms was performed from 5th to 9th day (p= 0.0005). When the clinical evaluation was performed from 10th to 14th day there was no significant difference. A higher proportion of medical discharge was observed in EG (98.2%) vs. CG (86.1%) (p= 0.0007). EG showed 8 times more chance of receiving medical discharge than CG (OR 8.71, 95% CI: 1·99 – 38.12, p= 0.004). The treatment effect with Ivermectin to obtain medical discharge from outpatient care was analyzed by logistic regression. Then, the chance to obtain medical discharge was independent of variables sex, age, and comorbidities. Conclusion: This work supports the potential efficacy of Ivermectin in outpatient care with mild COVID-19 as a potentially useful intervention of public health consideration.
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spelling Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centersEnsayos aleatorios - Reutilización de la Ivermectina para el tratamiento con COVID-19 de pacientes ambulatorios con enfermedad leve en centros de atención primariaEnsaio aleatório - Reutilização de Ivermectina para tratamento COVID-19 de pacientes ambulatórios com doença leve em centros primários de saúdeCOVID-19IvermectinaAtención ambulatoriaReposicionamiento de medicamentosAtención primaria de salud.COVID-19IvermectinDrug repurposingOutpatient carePrimary Health Care.COVID-19IvermectinaAssistência AmbulatorialReposicionamento de medicamentosAtenção Primária à Saúde.Objective: to evaluate the therapeutic intervention with Ivermectin in outpatients with COVID-19 mild disease, to increase medical discharge and prevent the progression to moderate or severe disease. Methods: Randomized Trial, n= 254. The subjects were divided into experimental (EG: n= 110) and control groups (CG: n= 144). The EG received Ivermectin orally 0.6 mg/kg weight in two doses. All participants were by physical examination COVID-19 diagnosed with negative RT-PCR at the beginning and the end of protocol. Differences between the variables were determined using the Chi-square test (p<0.05). The contagion risk (Odds Ratio) was calculated using software STATA. Results: Both groups were similar in age, sex, and comorbidities. A significant reduction in the percentage of participants with symptoms (PPS) was observed in the EG and CG when the clinical evaluation of symptoms was performed from 5th to 9th day (p= 0.0005). When the clinical evaluation was performed from 10th to 14th day there was no significant difference. A higher proportion of medical discharge was observed in EG (98.2%) vs. CG (86.1%) (p= 0.0007). EG showed 8 times more chance of receiving medical discharge than CG (OR 8.71, 95% CI: 1·99 – 38.12, p= 0.004). The treatment effect with Ivermectin to obtain medical discharge from outpatient care was analyzed by logistic regression. Then, the chance to obtain medical discharge was independent of variables sex, age, and comorbidities. Conclusion: This work supports the potential efficacy of Ivermectin in outpatient care with mild COVID-19 as a potentially useful intervention of public health consideration.Objetivo: evaluar la intervención terapéutica con Ivermectina en pacientes ambulatorios con enfermedad leve de COVID-19, para aumentar el alta médica y evitar la progresión a enfermedad moderada o grave. Métodos: Ensayo aleatorio, n= 254. Los sujetos se dividieron en grupos, experimental (GE: n= 110) y control (GC: n= 144). El GE recibió Ivermectina vía oral 0,6 mg/kg de peso en dos dosis. Los participantes fueron diagnosticados por examen físico COVID-19 y RT-PCR negativa al principio y al final del protocolo. Las diferencias entre variables se determinaron mediante prueba de Chi-cuadrado (p<0,05). El riesgo de contagio (Odds Ratio) se calculó utilizando el software STATA. Resultados: Ambos grupos fueron similares en edad, sexo y comorbilidades. Se observó una reducción significativa del porcentaje de participantes con síntomas (PPS) en ambos grupos cuando la evaluación clínica de los síntomas se realizó del 5º al 9º día (p= 0,0005). Cuando la evaluación clínica se realizó del 10º al 14º día no hubo diferencias significativas. Se observó una mayor proporción de altas médicas en el GE (98,2%) frente al GC (86,1%) (p= 0,0007). El GE mostró 8 veces más chances de recibir alta médica que el GC (OR 8,71, IC 95%: 1-99 - 38,12, p= 0,004). El efecto del tratamiento con Ivermectina para obtener alta médica de atención ambulatoria se analizó mediante regresión logística. La chance de obtener alta médica fue independiente de las variables sexo, edad y comorbilidades. Conclusiones: Este trabajo apoya la potencial eficacia de la Ivermectina en la atención ambulatoria con COVID-19 leve como una intervención de consideración en salud pública.Objetivo: avaliar a intervenção terapêutica com Ivermectina em pacientes ambulatoriais com doença leve de COVID-19, para aumentar a alta médica e prevenir a progressão para doença moderada ou grave.  Métodos: Ensaio Randomizado, n= 254. Os sujeitos foram divididos em grupo experimental (GE: n= 110) e grupo controle (GC: n= 144).  O GE recebeu Ivermectina oral 0,6 mg/kg de peso em duas doses.  Todos os participantes realizarão exame físico COVID-19 e diagnosticados com RT-PCR negativo no início e no final do protocolo.  As diferenças entre as variáveis ​​foram determinadas pelo teste Qui-quadrado (p<0,05).  O risco de contágio (Odds Ratio) foi calculado por meio do software STATA.  Resultados: Ambos os grupos foram semelhantes em idade, sexo e comorbidades.  Uma redução significativa no percentual de participantes com sintomas (PPS) foi observada no GE e GC quando a avaliação clínica dos sintomas foi realizada do 5º ao 9º (p= 0,0005).  Quando a avaliação clínica foi realizada do 10º ao 14º dia não houve diferença significativa.  Foi observada Maior proporção de alta médica no GE (98,2%) vs. GC (86,1%) (p= 0,0007).  O GE apresentou 8 vezes mais chance de receber alta médica do que o GC (OR 8,71, IC 95%: 1,99 – 38,12, p= 0,004).  O efeito do tratamento com Ivermectina para obter alta médica da assistência ambulatorial foi analisado pela regressão logística.  Então, a chance de obter alta médica foi independente das variáveis ​​sexo, idade e comorbidades.  Conclusão: Este trabalho apoia a eficácia potencial da Ivermectina na assistência ambulatorial com COVID-19 leve como uma intervenção potencialmente útil de saúde pública.Research, Society and Development2022-06-21info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/3084410.33448/rsd-v11i8.30844Research, Society and Development; Vol. 11 No. 8; e35511830844Research, Society and Development; Vol. 11 Núm. 8; e35511830844Research, Society and Development; v. 11 n. 8; e355118308442525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/30844/26582Copyright (c) 2022 Rossana Elena Chahla; Luis Medina Ruiz; Teresa Mena; Yolanda Brepe; Paola Terranova; Eugenia Silvana Ortega; Guillermo Gabriel Barrenechea; Daniel Gustavo Goroso; María de los Ángeles Peral de Brunohttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessChahla, Rossana ElenaRuiz, Luis Medina Mena, Teresa Brepe, YolandaTerranova, PaolaOrtega, Eugenia SilvanaBarrenechea, Guillermo GabrielGoroso, Daniel GustavoPeral de Bruno, María de los Ángeles2022-07-01T13:34:06Zoai:ojs.pkp.sfu.ca:article/30844Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:47:27.003195Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
Ensayos aleatorios - Reutilización de la Ivermectina para el tratamiento con COVID-19 de pacientes ambulatorios con enfermedad leve en centros de atención primaria
Ensaio aleatório - Reutilização de Ivermectina para tratamento COVID-19 de pacientes ambulatórios com doença leve em centros primários de saúde
title Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
spellingShingle Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
Chahla, Rossana Elena
COVID-19
Ivermectina
Atención ambulatoria
Reposicionamiento de medicamentos
Atención primaria de salud.
COVID-19
Ivermectin
Drug repurposing
Outpatient care
Primary Health Care.
COVID-19
Ivermectina
Assistência Ambulatorial
Reposicionamento de medicamentos
Atenção Primária à Saúde.
title_short Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
title_full Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
title_fullStr Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
title_full_unstemmed Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
title_sort Randomized trials - Ivermectin repurposing for COVID-19 treatment of outpatients with mild disease in primary health care centers
author Chahla, Rossana Elena
author_facet Chahla, Rossana Elena
Ruiz, Luis Medina
Mena, Teresa
Brepe, Yolanda
Terranova, Paola
Ortega, Eugenia Silvana
Barrenechea, Guillermo Gabriel
Goroso, Daniel Gustavo
Peral de Bruno, María de los Ángeles
author_role author
author2 Ruiz, Luis Medina
Mena, Teresa
Brepe, Yolanda
Terranova, Paola
Ortega, Eugenia Silvana
Barrenechea, Guillermo Gabriel
Goroso, Daniel Gustavo
Peral de Bruno, María de los Ángeles
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Chahla, Rossana Elena
Ruiz, Luis Medina
Mena, Teresa
Brepe, Yolanda
Terranova, Paola
Ortega, Eugenia Silvana
Barrenechea, Guillermo Gabriel
Goroso, Daniel Gustavo
Peral de Bruno, María de los Ángeles
dc.subject.por.fl_str_mv COVID-19
Ivermectina
Atención ambulatoria
Reposicionamiento de medicamentos
Atención primaria de salud.
COVID-19
Ivermectin
Drug repurposing
Outpatient care
Primary Health Care.
COVID-19
Ivermectina
Assistência Ambulatorial
Reposicionamento de medicamentos
Atenção Primária à Saúde.
topic COVID-19
Ivermectina
Atención ambulatoria
Reposicionamiento de medicamentos
Atención primaria de salud.
COVID-19
Ivermectin
Drug repurposing
Outpatient care
Primary Health Care.
COVID-19
Ivermectina
Assistência Ambulatorial
Reposicionamento de medicamentos
Atenção Primária à Saúde.
description Objective: to evaluate the therapeutic intervention with Ivermectin in outpatients with COVID-19 mild disease, to increase medical discharge and prevent the progression to moderate or severe disease. Methods: Randomized Trial, n= 254. The subjects were divided into experimental (EG: n= 110) and control groups (CG: n= 144). The EG received Ivermectin orally 0.6 mg/kg weight in two doses. All participants were by physical examination COVID-19 diagnosed with negative RT-PCR at the beginning and the end of protocol. Differences between the variables were determined using the Chi-square test (p<0.05). The contagion risk (Odds Ratio) was calculated using software STATA. Results: Both groups were similar in age, sex, and comorbidities. A significant reduction in the percentage of participants with symptoms (PPS) was observed in the EG and CG when the clinical evaluation of symptoms was performed from 5th to 9th day (p= 0.0005). When the clinical evaluation was performed from 10th to 14th day there was no significant difference. A higher proportion of medical discharge was observed in EG (98.2%) vs. CG (86.1%) (p= 0.0007). EG showed 8 times more chance of receiving medical discharge than CG (OR 8.71, 95% CI: 1·99 – 38.12, p= 0.004). The treatment effect with Ivermectin to obtain medical discharge from outpatient care was analyzed by logistic regression. Then, the chance to obtain medical discharge was independent of variables sex, age, and comorbidities. Conclusion: This work supports the potential efficacy of Ivermectin in outpatient care with mild COVID-19 as a potentially useful intervention of public health consideration.
publishDate 2022
dc.date.none.fl_str_mv 2022-06-21
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/30844
10.33448/rsd-v11i8.30844
url https://rsdjournal.org/index.php/rsd/article/view/30844
identifier_str_mv 10.33448/rsd-v11i8.30844
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/30844/26582
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 11 No. 8; e35511830844
Research, Society and Development; Vol. 11 Núm. 8; e35511830844
Research, Society and Development; v. 11 n. 8; e35511830844
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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