Pfizer’s oral antiviral drug (a combination of nirmatrelvir and ritonavir tablets) is strongly recommended for patients with non-severe COVID-19 who are at highest risk of hospitalization, such as unvaccinated, older, or immunosuppressed patients, with lack of vaccination as an additional risk factor to consider, says a WHO Guideline Development Group of international experts in The BMJ today.
The experts explain that nirmatrelvir/ritonavir likely represents a superior choice for these patients because it may prevent more hospitalizations than the alternatives, has fewer potential harms than the antiviral drug molnupiravir, and is easier to administer than intravenous options such as remdesivir and antibody treatments.
However, they recommend against its use in patients at lower risk, as the benefits are trivial. And they make no recommendation for patients with severe or critical COVID-19, as there are currently no trial data on nirmatrelvir/ritonavir for this group.
Their recommendation is based on new data from two randomized controlled trials involving 3,100 patients.
In these trials, moderate certainty evidence showed that nirmatrelvir/ritonavir reduced hospital admission (84 fewer admissions per 1,000 patients), low certainty evidence suggested no important difference in mortality, and high certainty evidence suggested little or no risk of adverse effects leading to drug discontinuation.
In the same guideline update, WHO also makes a conditional (weak) recommendation to use the antiviral drug remdesivir for patients with non-severe COVID-19 at highest risk of hospitalization.
This is based on new data from five randomized controlled trials involving 2,700 patients and replaces a previous recommendation against treatment with remdesivir in all patients with COVID-19 regardless of disease severity.
The panel noted that antiviral drugs should be administered as early as possible in the course of the disease, and acknowledged some cost and resource implications which may make access to low and middle income countries challenging, noting, also, that the access to these drugs is tied to the access to SARS-CoV-2 diagnostic tests, especially for those targeting the early phase of disease.
There also remains uncertainty regarding risk of emergence of resistance, they add.
Today’s recommendations are part of a living guideline, developed by the World Health Organization with the methodological support of MAGIC Evidence Ecosystem Foundation, to provide trustworthy guidance on the management of COVID-19 and help doctors make better decisions with their patients.
Living guidelines allow researchers to update previously vetted and peer reviewed evidence summaries as new information becomes available.
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