This article captures so well the difficulty, persistence and personal toll it’s taken to help the US (and elsewhere) have the crucial tools we all need to keep society going through this pandemic.
I can’t say I succeeded. If I had, we wouldn’t have long lines and empty shelves. I truly did everything possible and imaginable to me to try to ensure we didn’t end up right here, right now. Blind in the face of a much more infectious virus that is sweeping the globe.
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A year ago, @hannaskrueger profiled a series of epidemiologists & public health leaders. That, in my view, was a remarkable portrayal of just how difficult the virus had been on many front line workers.
I wish I could say it got better. But 2021 was immensely more difficult
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At what point did the science of rapid tests get lost??
FREQUENCY • ACCESSIBILITY • SPEED are most important aspects of a test for public health
Talking about tests not detecting in the 1st 24 hours of contagiousness assumes people are testing in those hours. Most don’t.
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Most of the time that someone is contagious is not spent in the first 24 hrs of being contagious. Obviously.
Frequent rapid testing for public health has always been about the sensitivity and EFFECTIVENESS of the testing REGIMEN.
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If a test fails to turn pos on d 1 but someone wasn’t using the test that day, then it doesn’t matter
It’s MORE likely ppl use a test sometime in days 2,3,4,5,6 or 7 than day 1. Public health testing also must consider the days it DOES detect - not just the days it doesn’t.
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Today - in midst of Omicron - millions of Americans are begging for access to rapid tests, thousands dying daily.
Get this:
many manufacturers with very high quality rapid tests are begging To ship 100’s of millions of tests to US
But can’t.
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These are some of the largest companies in the world that make diagnostic tests.
Their rapid tests have been used the world around in this pandemic with research paper after research paper showing their benefit and quality.
But FDA has them in a holding pattern for months
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Why?
Bc despite tremendous amount of data from real world use in millions of ppl - FDA demands the companies check off onerous but remarkably useless check boxes designed for evaluating medical devices.
FDA formally does not recognize that public health testing exists
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“we found that Liverpool city region’s early rollout of community rapid testing was associated with a 32% fall in Covid-19 hospital admissions after careful matching to other parts of the country in a similar position to Liverpool but without rapid testing”
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“We also found that daily lateral flow testing as an alternative to quarantine for people who had been in close contact with a known infected person enabled emergency services to keep key teams such as fire crews in work, underpinning public safety.”
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