The authors evaluated a number of different tests against PCR positive and culture positive specimens. (Culture positive is generally appreciated as representing likely transmissible virus).
They find a large disparity across different tests...
2/
Against culturable virus, they find that the Abbott PanBio Test and the SD Biosensor (Neither available in the US right now) perform very well. An additional 3 tests were evaluated 2, also looked quoted good but the rapigen performed quite poorly.
3/
Overall, this data fits the expectations (best performance against transmissible virus - versus sensitivity against any-time PCR+ samples, many of which no longer have viable virus).
I expect that this is just the beginning of these types of data and these types of tests!
• • •
Missing some Tweet in this thread? You can try to
force a refresh
NEW! research shows rapid antigen tests can work in a real world setting - with asymptomatic and symptomatic people. The rapid "paper-strip" antigen test called the BinaxNOW detected >90% of people with high viral loads who are likely to be infectious nytimes.com/2020/10/15/hea…
1/
I've written about the BinaxNOW from @AbbottNews before and why these types of tests can be 'game changers' for our ability to combat this virus
Can we create a brand new metric to know if #COVID19 is increasing/decreasing without staring at case counts & fractions positive - both greatly obscured by test practices.
In this incredible Tweet thread 👆 @jameshay218 describes the new work - we hope will lay new groundwork for public health authorities to track this/future viruses & if control strategies are working
One piece that is so cool about this method is we do NOT need a time series of case data to create a trajectory (those little bars on @nytimes website or google that we’ve all stared at for the past 9 months to see trend up vs down in cases). We can do it from a single day!
3/
Re-exposures are essential to build our immune system. This is not in question. They are like training.
But like anything, when enough people get a re-exposure, there are going to be rare cases here and there that go awry and someone gets more sick the second time.
2/
But this is rare and should NOT be interpreted as people will not build protective immunity and that vaccines will not work.
The take away from this piece should be “In a rare event, a person in the US gets a severe second infection with SARS-CoV-2”
The most important point of deployable rapid tests are that they can be used by many people, frequently!
But should not be used as confirmatory testing of -ve PCRs. This doesn’t make sense and WH use for this confuses how these tests are most appropriately used.
2/
These tests should be to screen ppl (frequently) for +ve results to identify people likely needing to be isolated
In this case @POTUS has had numerous PCR tests and is the president! He can get a viral culture test if he wants to go out w confidence he is not contagious
3/
It's said to be poor w very low sensitivity - the news, @US_FDA and many others say so
But this is a mistake. It's a very good rapid test
I explain here at ~3:30
(Just found link from an old talk)
The short story is the main study from NYU that led to the low sensitivity claims used an extremely skewed sample set
If you remove from the paper just the +ve samples with a Ct value >40 (incredibly miniscule RNA loads), the sensitivity of the test jumps from 60% --> 90%!
If you take only samples with Ct values <38 (still on par w almost any other PCR test), then sensitivity jumps from 60% --> 95%!!
So the problem wasn't the test, it was the samples evaluated. 30% of them were at the very limit of detection of a SLIGHTLY better test