Pfizer’s Paxlovid antiviral medication lowers long-COVID risk: Study

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Pfizer Inc.’s blockbuster Paxlovid antiviral that lowers rates of illness and death in people infected with the coronavirus also cuts the risk of some symptoms of disabling long COVID, a study found.

Taking the oral medication within five days of testing positive for a SARS-CoV-2 infection was linked to a 26 percent lower risk of lingering post-viral complications, researchers with the Veterans Affairs St. Louis Health Care System said in the study. That equates to 2.3 fewer cases of long COVID within three months of infection for every 100 patients treated, according to the findings released Saturday on the medRxiv server ahead of publication in a peer-reviewed journal.

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The research, based on an analysis of electronic health records in databases maintained by the Department of Veterans Affairs, suggests that wider use of Paxlovid won’t just stave off critical disease during the acute phase of infection, but will limit patients’ likelihood of longer-term problems. Long COVID is estimated to afflict almost 150 million people worldwide and predicted to cost $3.7 trillion in the US alone.

The condition is of “profound urgency,” according to Anthony Fauci, US President Joe Biden’s top medical adviser. “This is a very troublesome virus -- not only in its acute effects, but in the not-yet-fully appreciated potential long-term effects,” Fauci said September 26 in an interview.

No one knows yet what causes the constellation of long-haul symptoms that the US National Institutes of Health calls post-acute sequelae of COVID-19, or PASC. The NIH is funding a late-stage trial in early 2023 that will test whether Paxlovid, given twice a day for 15 days, can relieve long COVID symptoms.

Paxlovid is authorized by the US Food and Drug Administration for treatment of acute COVID-19 illness in people with one or more risk factors for progression to severe disease.

Broad benefits

The latest study analyzed electronic health records of users of the VA system, the largest integrated health-care system in the US. Researchers compared 9,217 COVID-19 patients treated with Paxlovid against 47,123 patients who didn’t get the antiviral or antibody treatment within the first month of a SARS-CoV-2 infection.

Patients in the study caught COVID-19 in the second quarter of 2022 and were followed until August 31. They were mostly white males, which might limit how generalizable the study’s findings are to other groups, the authors said.

The researchers found that taking Paxlovid for five days at the start of a SARS-CoV-2 infection reduced the risk of some PASC symptoms, including heartbeat and blood clotting abnormalities, fatigue, muscle pain, neurocognitive impairment, and shortness of breath. Not all long COVID symptoms were prevented, and the authors reasoned that different conditions may be driven by different biological mechanisms, including some that are attenuated by antiviral therapy.

It’s not yet clear whether a longer course of treatment, a stronger dose, or both, may reduce the long-COVID risk even more, the authors said.

A five-day course was also associated with a 48 percent lower risk of dying and a 30 percent decreased risk of being hospitalized 30 to 90 days after a positive COVID-19 test.

The benefits were seen across individuals who were unvaccinated, vaccinated, and boosted, and in people who were treated for either a first or subsequent COVID-19 infection.

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