Life-threatening COVID-19 is associated with strong inflammation, where an IL-6-driven cytokine storm appears to be a cornerstone for enhanced pathology. Nonetheless, the specific inhibition of such pathway has shown mixed outcomes. This could be due to variations in the dose of tocilizumab used, the stage in which the drug is administered or the severity of disease presentation. Thus, we performed a retrospective multicentric study in 140 patients with moderate to critical COVID-19, 79 of which received tocilizumab in variable standard doses (< 400 mg, 400–800 mg or > 800 mg), either at the viral (1–7 days post-symptom onset), early inflammatory (8–15) or late inflammatory (16 or more) stages, and compared it with standard treated patients. Mortality, reduced respiratory support requirements and pathology markers were measured. Tocilizumab significantly reduced the respiratory support requirements (OR 2.71, CI 1.37–4.85 at 95%) and inflammatory markers (OR 4.82, CI 1.4–15.8) of all patients, but mortality was only reduced (4.1% vs 25.7%, p = 0.03) when the drug was administered at the early inflammatory stage and in doses ranging 400–800 mg in severely-ill patients. Despite the apparent inability of Tocilizumab to prevent the progression of COVID-19 into a critical presentation, severely-ill patients may be benefited by its use in the early inflammatory stage and moderate doses.
The off-label use of antiviral and antimalarial drugs has been considered by many researchers as a fast and relatively safe alternative to provide therapeutic options to treat COVID-19, but the assessment of such drug-specific effectiveness in this regard is far from complete. Especially, the current body of knowledge about COVID-19 therapeutics needs more data regarding drug effectiveness and safety in the severely ill patients with comorbidities. In the present article, we retrospectively analyze data from 61 patients that received treatment with chloroquine, lopinavir/ritonavir, both drugs administered together, or a standard treatment with no antiviral drugs, and the study was carried in severely ill patients. We found that either drug is ineffective at treating COVID-19, as they are not able to reduce hospitalization length, mortality, C-reactive protein (CRP), lactate dehydrogenase (LDH), d-Dimer, or ferritin, or to enhance gasometric parameters, lymphocytes, total leukocytes, and neutrophil levels, whereas both drugs administered together decrease circulating lymphocytes, increase LDH and ferritin levels, and more importantly, enhance mortality. In this way, our results show that both drugs are ineffective and even potentially harmful alternatives against SARS-CoV-2.
The emergency situation of the COVID-19 pandemics requires immediate action. As happens with emerging pathogens, there are no specific treatments for this threat, so that the most logical answer in order to find safe and effective candidates seems to be drug repurposing. The main efforts in finding a specific treatment for this disease have been directed to finding antiviral agents, nonetheless, COVID-19 also involves lung and systemic inflammation, coupled with ineffective immunity; bacterial and fungal coinfections; respiratory dysfunction; and coagulopathy. These additional pathophysiologic axes also require a set of treatments, and in this review we will analyze such adjunctive therapies.
The emergency situation of the COVID-19 pandemics requires immediate action. As happens with emerging pathogens, there are no specific treatments for this threat, so that the most logical answer in order to find safe and effective candidates seems to be drug repurposing. The main efforts in finding a specific treatment for this disease have been directed to finding antiviral agents, nonetheless, COVID-19 also involves lung and systemic inflammation, coupled with ineffective immunity; bacterial and fungal coinfections; respiratory dysfunction; and coagulopathy. These additional pathophysiologic axes also require a set of treatments, and in this review we will analyze such adjunctive therapies.
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