The new warning is based on preliminary studies by the National Institutes of Health’s Rapid Acceleration of Diagnostics initiative.
Covid-19 antigen tests may be less capable of detecting the fast-spreading Omicron variant, the Food and Drug Administration cautioned on Tuesday.
The new warning is based on preliminary studies by the National Institutes of Health’s Rapid Acceleration of Diagnostics initiative using patient samples with live virus — analysis that “represents the best way to evaluate true test performance in the short-term,” according to FDA.
“Early data suggests that antigen tests do detect the Omicron variant but may have reduced sensitivity,” the FDA said on Tuesday.
Many popular at-home antigen tests are intended to be used serially — meaning people should take two tests on separate days — to ensure more accurate results.
FDA reemphasized its recommendation that the public “closely follow the tests’ instructions,” adding that if people test negative on an antigen test but have symptoms of Covid-19 or have a “high likelihood of infection due to exposure,” they should seek out a molecular test to confirm the result.
“Although the data is preliminary, the FDA believes it is important to share with the public,” FDA spokesperson Stephanie Caccomo told POLITICO. “We will continue to keep the public informed if additional information comes to light.”
The new NIH data comes less than a week after a different NIH study of heat-inactivated Omicron samples found antigen tests were able to detect the Omicron “with similar performance” to other variants.
The Biden administration recently announced it intends to purchase 500 million at-home tests and begin distributing them in January. But it is unclear how much supply of the popular rapid tests will be available immediately: the government’s solicitation for the tests was posted last week and U.S. manufacturing levels remain limited.