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At-home defense: why widespread rapid antigen testing is key to curbing the pandemic

By
Yasmin Tayag
Yasmin Tayag
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By
Yasmin Tayag
Yasmin Tayag
Down Arrow Button Icon
December 9, 2021, 5:06 PM ET

Much like in 2020, holiday travel this year is riddled with uncertainty—and the unanswered questions about Omicron don’t make planning any easier. This year, however, one difference could help make travel slightly less fraught: Rapid at-home COVID tests are finally available.

The accessibility—and reliability—of at-home tests have come a long way since the early days of the pandemic, when those available on the market were largely unregulated by the Food and Drug Administration. In December 2020, the agency issued its first emergency use authorization for an over-the-counter at-home antigen test—the Ellume COVID-19 Home Test—and has since approved a handful more, including Quidel’s QuickVue, Abbott’s BinaxNOW, and ACON Laboratories’ Flowflex.

These tests, said Harvard epidemiologist Stephen Kissler, will be useful in light of the recent changes to the CDC’s guidelines for international travel, which require people to have a negative test result within 24 hours of flying into the US. “I think the rapid antigen tests are very good for that,” he said.

He added that they’d be useful as a “screening method” before any large gathering, like a holiday party or family dinner. “I would encourage everyone who’s attending to take a rapid antigen test beforehand,” he said. While PCR tests remain the gold standard for accuracy, often by the time the results come back, enough time has passed that a person may have become newly infected or an infection that previously went under the radar may have become detectable. “For the rapid tests,” he said, “test as close as you can to the thing that you’re testing for.”

Unlike PCR testing, which amplifies the virus’ genetic material so it can detect even tiny amounts, antigen tests look for proteins on the virus surface. One upside of this is that these tests give results more quickly than PCR tests—often in less than an hour—but a downside is that they’re not as sensitive, which means they are more likely to turn up a false negative result. However, as the New York Times noted, antigen tests are “excellent at flagging people who have high viral loads—and who are thus most likely to be actively transmitting the virus to others.”

The rapid tests that are currently available have “pretty comparable sensitivity and specificity,” Kissler said. (Specificity, a test’s ability to tell whether a person is negative for a disease, is similarly high in both antigen and PCR tests.) The major differences between brands are ease of use and the amount of time it takes to turn around a result, he said.

Some public health experts have been calling for widespread at-home rapid testing since the beginning of the pandemic, arguing that they were the key to reopening society. Now, these tests are available in many stores and pharmacies, but there’s still a lot of room for improvement: Tests are often in short supply, and both authorization and manufacturing of additional tests has been sluggish, despite the Biden administration’s September injection of $3 billion in funding into the effort to scale up at-home testing. The administration recently laid out a plan to make tests free to citizens—they generally range from $15 to $35—but the plan drew criticism because it requires people to submit their receipts to private insurers for reimbursement.

Despite the caveats, at-home rapid tests are an important tool for curbing the pandemic. This holiday season, test often and before going to large events, if you can. Doing so can help you avoid unwittingly spreading the coronavirus to large groups of people. “That’s really the fuel of the fire for this pandemic,” said Kissler. Antigen tests “don’t bring the risk of bringing infection to a gathering down to zero, but they do reduce the odds by an awful lot.”

Thanks for reading, and please reach out if you have any questions or comments—I’d love to hear from you.

Stay safe out there,

Yasmin

@yeahyeahyasmin

DIGITAL HEALTH

Suki, a voice-based clinical assistant company, banks $55 million in funding. The California-based startup—already a major player in the healthcare virtual assistant market with a Google partnership under its belt—completed a round of series C funding that brings its valuation up to $400 million. Framed as tools to alleviate physician burnout by helping them avoid administrative tasks like dictation, coding, and record retrieval, voice-based digital assistants are a growing market, estimated to grow to $6 billion in 2026 up from $1.1 billion in 2021. Other key players include Microsoft, which acquired the speech-to-text company Nuance Communications this year, and Amazon, which has already embedded Alexa in a number of clinical settings. (Fierce Healthcare)

INDICATIONS

AstraZeneca’s COVID drug gets FDA go-ahead. On Wednesday, the FDA issued emergency use authorization for AztraZeneca’s monoclonal antibody treatment Evusheld to prevent COVID-19 in some people with immune problems, including people taking immunosuppressive medications and those who can’t get vaccinated for certain health reasons. The drug, which is classified as “long-acting,” could provide protection for those people for up to six months. It isn’t, however, “a substitute for vaccination in individuals for whom COVID-19 vaccination is recommended,”said the FDA.

Pfizer boosters hold up against Omicron. Laboratory datareleased by Pfizer and BioNTech on Wednesday show that people who have had three doses of their vaccine can neutralize the Omicron variant. Two doses, meanwhile, seem to provide much lower protection against Omicron compared to other variants, like Delta. While the companies only looked at 39 samples, this early data seems to emphasize theimportance of getting a booster shot. It bears reminding, however, that being fully vaccinated isstill expected to protect against severe disease and death from COVID, regardless of the variant.

THE BIG PICTURE

The youth mental health crisis is getting worse. A 53-pageadvisory report released Wednesday from U.S. Surgeon General Vivek Murthy warned of the impact that the pandemic is having on youth mental health, which was already worsening before COVID-19. For example, U.S. emergency room visits due to suspected suicide attempts were 51% higher for adolescent girls and 4% for boys in early 2021 compared to early 2019; globally, some 25% of youth have experienced depressive symptoms and 20% have experienced anxiety symptoms. In addition to the stresses of COVID, other challenges affecting youth mental health in the past year according to the report include “the national reckoning over the deaths of Black Americans at the hands of police officers, including the murder of George Floyd; COVID-related violence against Asian Americans; gun violence; an increasingly polarized political dialogue; growing concerns about climate change; and emotionally-charged misinformation”.

REQUIRED READING

COVID-19 may hide in fat cells, increasing the risk of severe disease and long-COVID among overweight and obese patientsby Grady McGregor

We’re ‘dangerously unprepared’ for future pandemics even after COVID, global study warnsby Chris Morris

Australia finds a new ‘Omicron-like’ COVID strain that’s harder to track through typical screeningby Matthew Burgess and Bloomberg

This is the web version of The Capsule, a weekly newsletter monitoring advances in healthcare and biopharma. Sign up to get it delivered free to your inbox.

About the Author
By Yasmin Tayag
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