Sanitas
Revista arbitrada de ciencias de la salud
Vol. 2(2), 1-8, 2023
https://doi.org/10.5281/zenodo.10607357
1
Ivermectin for COVID-19 patients
Ivermectina para pacientes COVID-19
Carlos Vinicio Chiluisa-Guacho
ua.carloschiluisa@uniandes.edu.ec
Universidad Regional Autónoma de los Andes, Ambato, Tungurahua,
Ecuador
https://orcid.org/0000-0003-0233-6168
ABSTRACT
Objective: to analyse the efficacy of ivermectin as an alternative treatment for patients affected by
COVID-19. Methods: A descriptive literature review was conducted. Results and conclusion:
Patients randomised to receive ivermectin, placebo or another intervention suggest that a five-day
course of ivermectin was safe and showed some efficacy in the treatment of adult patients with mild
COVID-19. Although the rate of primary outcome events was slightly lower in the ivermectin group
compared to the placebo group, the difference did not reach statistical significance. Of note, adverse
events were not significantly different between the ivermectin and placebo groups. These findings are
promising but indicate the need for larger trials and further studies to confirm and deepen the
understanding of the efficacy and safety of ivermectin in the context of COVID-19.
Descriptors: ivermectin; covid-19; antibodies. (Source, DeCS).
RESUMEN
Objetivo: analizar la eficacia de la ivermectina como alternativa de tratamiento para pacientes
afectados por la COVID-19. Método: Se trabajó mediante una revisión descriptiva documental
bibliográfica. Resultados y conclusión: Los pacientes asignados aleatoriamente a recibir
ivermectina, placebo u otra intervención, sugieren que un tratamiento de cinco días con ivermectina
fue seguro y mostró cierta eficacia en el tratamiento de pacientes adultos con COVID-19 leve.
Aunque la tasa de eventos de resultado primario fue ligeramente menor en el grupo de ivermectina
en comparación con el grupo de placebo, la diferencia no alcanzó significancia estadística. Se
destaca que los eventos adversos no fueron significativamente diferentes entre los grupos de
ivermectina y placebo. Estos hallazgos son prometedores pero indican la necesidad de ensayos más
amplios y estudios adicionales para confirmar y profundizar en la comprensión de la eficacia y
seguridad de la ivermectina en el contexto de la COVID-19.
Descriptores: ivermectina; covid-19; anticuerpos antivirales. (Fuente, DeCS).
Received: 04/03/2023. Revised: 18/03/2023. Approved: 03/04/2023. Published: 01/05/2023.
Original in brief
Sanitas
Revista arbitrada de ciencias de la salud
Vol. 2(2), 1-8, 2023
Ivermectina para pacientes COVID-19
Ivermectin for COVID-19 patients
Carlos Vinicio Chiluisa-Guacho
2
INTRODUCTION
In the intricate scenario of the COVID-19 pandemic, the search for effective
treatments has brought attention to ivermectin, a drug known for its anti-parasitic
applications. This compound, which has travelled a significant path in medical care,
now takes centre stage as a potential treatment alternative for patients affected by
the virus.
1 2
Ivermectin, initially recognised for its efficacy in the control of parasitic diseases, has
attracted renewed interest due to its suspected ability to inhibit SARS-CoV-2 virus
replication. This possibility has sparked a scientific debate that seeks to understand
in depth how this drug may influence disease progression and severity.
3 4
Preliminary research suggests that ivermectin may have antiviral properties,
interfering with the ability of the virus to replicate. However, it is crucial to approach
these findings with caution and recognise the need for more robust clinical studies
to conclusively support the efficacy and safety of ivermectin in the context of COVID-
19.
5
Despite the attention and hope surrounding ivermectin, the scientific community
stresses the importance of following established protocols and relying on solid
evidence before considering its widespread implementation in the treatment of
patients with COVID-19. The complexity of the disease and the need for therapeutic
approaches supported by reliable clinical data are imperative to ensure the safety
and efficacy of any treatment.
6
In this fascinating chapter of medical research, ivermectin emerges as a promising
figure, but its ultimate role in the management of COVID-19 remains to be defined.
As science advances, it will be critical to maintain a balance between hope and
scientific rigour, ensuring that therapeutic decisions are backed by the strongest
available evidence.
Sanitas
Revista arbitrada de ciencias de la salud
Vol. 2(2), 1-8, 2023
Ivermectina para pacientes COVID-19
Ivermectin for COVID-19 patients
Carlos Vinicio Chiluisa-Guacho
3
We aim to examine the efficacy of ivermectin as a treatment alternative for patients
affected by COVID-19.
METHOD
A descriptive literature review was conducted. The meticulous approach involved an
exploration of 15 carefully selected articles from reliable sources such as PubMed,
Scielo and Scopus. This method allowed to comprehensively address the role of
ivermectin as a treatment alternative for patients affected by COVID-19.
The first stage consisted of a rigorous selection of articles specifically addressing the
relationship between ivermectin and COVID-19. Relevant publications were chosen,
considering methodological quality, timeliness of information and diversity of
perspectives.
The literature review became an essential compass, guiding us through the existing
contributions in the scientific literature. This process involved not only exploring the
results and conclusions of the studies, but also analysing the methods used in each
investigation to assess the effectiveness and safety of ivermectin.
The essence of the analysis lay in the application of a synthetic-analytical method.
This approach involved not only summarising the individual findings of each study,
but also synthesising the information to identify patterns, convergences and
divergences in the results. The connection between the various studies was explored
to reveal a more complete picture of the current research landscape on ivermectin
and COVID-19.
Each article was subjected to a critical appraisal, considering the internal validity of
the studies, the consistency of the results and the practical relevance of the
conclusions. This evaluation contributed to the generation of a coherent and reliable
analysis.
The information obtained was synthesised to provide a comprehensive view of the
efficacy and safety of ivermectin in the treatment of patients with COVID-19. This
Sanitas
Revista arbitrada de ciencias de la salud
Vol. 2(2), 1-8, 2023
Ivermectina para pacientes COVID-19
Ivermectin for COVID-19 patients
Carlos Vinicio Chiluisa-Guacho
4
process involved identifying trends, comparing divergent results and formulating
conclusions that could guide future research and clinical decisions.
RESULTS
Despite initial speculation about the efficacy of ivermectin in the treatment of patients
with COVID-19, the documentary findings provide clarity. In a comprehensive
analysis, an exceptional more than 5000-fold reduction in viral RNA was observed
in both the supernatant and cell pellets of samples treated with ivermectin at a
concentration of 5 μM at 48 hours. This significant reduction reached 99.98% in viral
RNA in these samples, with no toxicity detected at any of the concentrations tested.
7 8 9
By exploring various literature sources, an encouraging picture emerges about the
ability of ivermectin to inhibit SARS-CoV-2 viral replication. In particular, it is noted
that a dose of 150 mcg/kg/day orally for 3 days was effective in controlling viral
replication within 24-48 hours, with no relevant side effects in our system. This
phenomenon suggests that early administration of ivermectin, during the initial
phase of infection (viral replication), could be crucial to limit viral load, prevent severe
disease progression and reduce person-to-person transmission.
The convergence of various literature sources, supported by more than 40 years of
experience in the use of ivermectin in various pathologies, reinforces the conclusion
that a specific dosage of 150 mcg/kg/day orally for 3 days has the potential to control
viral replication in a short period of time, without relevant side effects in our system.
10 11 This analysis, supported by the established safety profile, suggests that
ivermectin deserves further consideration as a viable antiviral option against SARS-
CoV-2.
Based on the current evidence, characterised by very low to low certainty, the
efficacy and safety of ivermectin in the treatment or prevention of COVID-19 is
uncertain. Existing studies are limited in size and few meet standards considered to
be of high quality. Multiple ongoing investigations may provide clearer answers in
Sanitas
Revista arbitrada de ciencias de la salud
Vol. 2(2), 1-8, 2023
Ivermectina para pacientes COVID-19
Ivermectin for COVID-19 patients
Carlos Vinicio Chiluisa-Guacho
5
future review updates. Overall, the available reliable evidence does not support the
use of ivermectin to treat or prevent COVID-19, unless conducted in the context of
well-designed randomised trials.
12
While treatment with ivermectin for five days has been identified as safe and effective
in the management of adult patients with mild COVID-19. However, larger trials are
required to validate these initial results.
13
A total of 3,515 patients were randomly assigned to three groups: those receiving
ivermectin (679 patients), placebo (679 patients) or another intervention (2,157
patients). These findings remained consistent in both a modified intention-to-treat
analysis, which included only patients who received at least one dose of ivermectin
or placebo (relative risk, 0.89; 95% Bayesian credible interval, 0.69 to 1.15), and a
per-protocol analysis, which included only patients with 100% compliance with the
assigned regimen (relative risk, 0.94; 95% Bayesian credible interval, 0.67 to 1.35).
No significant effects of ivermectin use on secondary outcomes were observed and
no significant adverse events were recorded.
14 15
CONCLUSION
The results of this study, which included 3,515 patients randomised to receive
ivermectin, placebo or another intervention, suggest that a five-day course of
ivermectin was safe and showed some efficacy in the treatment of adult patients with
mild COVID-19. Although the rate of primary outcome events was slightly lower in
the ivermectin group compared to the placebo group, the difference did not reach
statistical significance. Of note, adverse events were not significantly different
between the ivermectin and placebo groups. These findings are promising but
indicate the need for larger trials and further studies to confirm and deepen the
understanding of the efficacy and safety of ivermectin in the context of COVID-19.
Sanitas
Revista arbitrada de ciencias de la salud
Vol. 2(2), 1-8, 2023
Ivermectina para pacientes COVID-19
Ivermectin for COVID-19 patients
Carlos Vinicio Chiluisa-Guacho
6
FUNDING
Non-monetary
CONFLICT OF INTEREST
There is no conflict of interest with individuals or institutions involved in the research.
ACKNOWLEDGEMENTS
To the frontline health personnel during the COVID-19 pandemic.
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Sanitas
Revista arbitrada de ciencias de la salud
Vol. 2(2), 1-8, 2023
Ivermectina para pacientes COVID-19
Ivermectin for COVID-19 patients
Carlos Vinicio Chiluisa-Guacho
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