• The San Juan Daily Star

The search for a COVID test

People line up outside a COVID-19 test center in Coral Springs, Fla., on Sept. 10, 2021. Rapid at-home COVID-19 tests are widely available in some countries but are hard to find in the U.S. because the Food and Drug Administration has been slow to approve them.

By David Leonhardt

I tried to buy a rapid at-home COVID test yesterday, and the search did not go well.

My local CVS did not have any. On the CVS website, I found a store several miles away that claimed to have the tests in stock — but I discovered otherwise after driving there. On Amazon, I did find one available option: a box of 90 rapid tests. It cost $1,122.75.

When I told this tale of woe to my colleagues during our daily news meeting, one of them — Claire Moses, an editor based in London — offered to ship me some tests through trans-Atlantic mail. At-home tests are so widely available in Britain, Claire explained, that she could send a few to every member of The Morning’s editorial team.

I said no thanks, because I did not have an immediate need for a test. I was searching for one partly to see what the experience was like. I also assume that my family will want to have rapid tests on hand at some point.

If you wake up with a runny nose or scratchy throat, you should be able to grab a COVID-19 test from your bathroom shelf and find out the result within minutes. The tests exist. They are known as antigen tests and are widely available not only in Britain but also France, Germany and some other places. Rapid tests can identify roughly 98% of infectious COVID cases and have helped reduce the virus’ spread in Europe.

In the United States, by contrast, rapid tests are hard to find, because the Food and Drug Administration has been slow to approve them. FDA officials have defended their reluctance by saying that they need to make sure the tests work — which they certainly do. But many outside scientists have criticized the agency for blocking even those antigen tests with a demonstrated record of success in other countries.

The FDA has preferred a different kind of test, known as a PCR test, which is sensitive enough to identify many noninfectious cases (including some that are weeks old). But PCR tests come with a crucial downside: Many must be processed in a laboratory and take more than 24 hours to return results. In the meantime, a person with COVID may spread it to others.

Fortunately, though, today’s newsletter is not just another recounting of this country’s testing shortcomings. There has been some news this week. Soon, Americans will probably have better access to rapid tests than they now do.

More tests, soon

The FDA announced Monday that it would allow the sale of an antigen test known as Flowflex. The test has been available in Europe but not here, even though the company that makes it — Acon Laboratories — is based in San Diego.

The decision suggests that the FDA has become willing to approve other rapid tests too, Alex Tabarrok, an economist at George Mason University and an advocate of expanded testing, told me. Separately, the Biden administration plans to announce an expansion of rapid testing today, a White House official told me last night. It will be a $1 billion government purchase of tests, meant to accelerate their production, on top of other money the administration has already dedicated to rapid tests.

Together, these moves will quadruple the number of rapid tests available to Americans by early December, the official predicted. Some of the tests will be free (as many tests are in Europe, thanks to government subsidies), available at one of about 20,000 pharmacies or 10,000 community clinics nationwide. Others will be for sale at retailers.

Until now, antigen tests — like the ones CVS sells — have typically cost about $12 each in the United States. The coming influx of supply should cause the cost to fall, allowing antigen tests to become a bigger part of this country’s COVID response.

“There’s been a lot of spread of infection and a lot of disruption to people’s lives because we lack proper testing,” Dr. Amesh Adalja of Johns Hopkins University said on MSNBC yesterday. “If you can test rapidly and know your status, you can make an event very, very safe.”

As Tabarrok says, “If we are smart, we will replace masks with tests in the schools, workplaces and Thanksgiving celebrations.”

It is too late for rapid tests to do nearly as much good as they could have done last year, before vaccines were widely available. When future historians and scientists grade the U.S. response to the pandemic, testing is still likely to be counted as a major FDA failure, across both the Trump and Biden administrations. It has been a case study of how bureaucratic caution — and a refusal to get creative during a crisis — can do harm.

But it is not too late for rapid tests to improve day-to-day life. The Biden administration finally seems to be taking significant steps in that direction.

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