Journal of the College of Physicians and Surgeons Pakistan
ISSN: 1022-386X (PRINT)
ISSN: 1681-7168 (ONLINE)
Affiliations
doi: 10.29271/jcpsp.2022.02.274
Sir,
Ivermectin, a FDA-approved and popular anti-parasitic agent, has been used against mild novel coronavirus disease 2019 (COVID-19). It has demonstrated efficacy in the prophylaxis and treatment of COVID-19 patients. The evidence, so far, is based on in-vitro studies. The literature found is in pre-print form. Ivermectin is a cheap agent with safe side effect profile. It prevents viral and hosts proteins from entering into the host cell nuclei.1
Reported data has shown convincing evidence of ability of ivermectin in reducing viral load in patients of COVID-19. Early administration of ivermectin was shown to be effective in early viral clearance and reduced duration of symptoms in patients with mild COVID-19. It was found as inhibitor of SARS-CoV-2 replication in the laboratory.1
Ivermectin has been in use for both parasitic and bacterial infections in the developing countries; and is effective and affordable. The 5-day course of ivermectin costs US $1.80 1,2 and is readily available; hence, it may be considered an attractive alternative for COVID-19 treatment.
Investigators at the University of Navarra Clinic and Barcelona Institute of Global Health published a pilot study, which showed efficacy of drug in reducing viral load, disease duration, and in stopping its transmission.2 It also deliberated on a fact that despite two proven vaccines, protecting people globally to stop viral spread, will take at least two years; hence, treatment options are needed focusing on COVID-19 infection. Ivermectin was studied as an agent reducing viral transmission, when given within the first five days of symptom onset.3,4 Another study from Bangladesh, a randomised, double blind, placebo controlled trial, conducted to find out rapid viral clearance with the use of ivermectin, showed early viral clearance in the 5-day ivermectin treatment arm.5 A retrospective study in 2020 found that ivermectin reduced mortality when compared with azithromycin and hydroxychloroquine.5
Ivermectin is being used in Latin-American countries, despite lack of convincing evidence of its efficacy.3-5 The study subjects were given one single dose of ivermectin or placebo to 24 patients with confirmed mild symptoms within first 72 hours. No difference was found in the PCR-positive patients. The mean viral load in the ivermectin-treated group was three times lower at 4 days and 18 times lower at 7 days after treatment.3 The difference found was not statistically significant. Reduced duration of symptoms, such as loss of smell and taste and cough, was found.
Another study conducted at Pasteur Institute observed similar findings in terms of reduced viral loads, symptom duration, and antibody levels; and warranted larger studies with patient diversity.4 Robust randomised controlled clinical trials of ivermectin in COVID-19 treatment are needed to validate these important findings.
CONFLICT OF INTEREST:
The author declared no conflict of interest.
AUTHOR’S CONTRIBUTION:
SS: Solely drafted and edited the manuscript.
REFERENCES