Or do the increased cases lead to more hospitalizations than Delta?
Or do the increased cases lead to more hospitalizations than Delta?
It's probably better to have a 50% hospitalization rate and an R value of 0.8 than a 5% hospitalization rate and an R value of 2. After 3 'generations' of spreading the second situation already has more hospitalizations.
https://www.cdc.gov/coronavirus/2019-ncov/cases-updates/burd...
The Omicron variant R0 value appears to be somewhere in the 7 - 10 range.
https://www.thelancet.com/journals/lanres/article/PIIS2213-2...
Sure, but those aren’t the only choices. Over the last 30 days the daily case average has increased by 500%. During that same time the daily average hospitalized has risen 100%.
And the test positivity rate has increased to almost 30%, which implies an almost comical undercount in actual cases.
The contagiousness and severity are diverging in an extraordinary way. We’re likely undercounting cases by 1/5 or 1/10th.
Rapid tests are perfectly fine and should be counted by health departments.
Case in point. My family of 4 all tested positive on rapid tests. 3/4 of us had symptoms. None of us received PCR tests because the next available appointments (other than a 6 hour wait at a state run testing center) were a week away.
Thats 4 people not counted. And we were part of an outbreak that included 3 other families that all tested positive via rapid tests.
If the rising part of the S-curve is steep, that means people get infected within a shorter timespan and a corresponding higher load on hospital beds and healthcare personnel, which is what we are trying to avoid with the lockdowns.
What am I missing?
Also, calling exponential growth a 'conspiracy theory' seems unnecessary
So yes it's bad/dangerous in that hospitals may fill to overflowing and struggle to treat covid or non-covid patients, but not bad in that Omicron is directly killing more people than Delta et al.
https://news.sky.com/story/covid-news-latest-nhs-backlog-is-...
> Professor Andrew Hayward, of University College London, earlier told Sky News that it is unlikely there will be a variant more severe than Omicron.
He said: "This one will be hard to outcompete... given how successful it is."
Professor Hayward added that for a "variant to stick", it needs to have "some advantage over the existing variant and that advantage needs to be really in terms of increased transmissibility or escape from immunity".
He said: "There's no advantage to the virus itself becoming more severe."
I thought the virus doesn't care about becoming more or less sever since its transmission capability is all that matters to it and symptoms are hidden (thus increasing transmission between individuals) in the first days of infection and that's what evolution is driving him to be: more transmissible.
The fact symptoms appear sooner than delta seems to be a step backward for the virus in terms of efficacy and it's compensated by being way way way more virulent.
What am I getting wrong here ?
Also:
Omicron could as well have been more severe (and the jury is still out on long covid anyway). If there's another variant less virulent but compensated by hiding symptoms longer... then this would take over omicron and this variant could as well be more severe.
Is that totally out of the realm of possibilities ?
My regular joe thinking tells me that we can only be sure of the direction it's going to take when spring comes. 2021 had 5 vocs, it's only the first days of January.
https://www.vaccinestoday.eu/stories/what-is-r0/
Preliminary data on the Omicron variant indicates an R0 value in the 7 - 10 range. So SARS-CoV-2 might still have a little more room to evolve even higher contagiousness.
https://www.thelancet.com/journals/lanres/article/PIIS2213-2...
Something as infectious as Omicron but with better immune escape would presumably do very well, even once the Omicron waves pass.
https://coronavirus.data.gov.uk/
[bear in mind, the hospitalisation number is not quite what it seems. It is "people in hospital who happen to have Covid", not "people who got Covid so bad they need to be hospitalised". So if you have asymptomatic Covid and a broken leg, you count for this purpose. Still, you do require the whole Covid-safe theatre, medical staff in PPE so it's also not like "meh doesn't matter"]
https://coronavirus.data.gov.uk/details/healthcare?areaType=...
Just wanted to check that since (at at least one London hospital) they're on different wards (as in, even discounting that obviously you don't want 'broken leg with covid' on a general 'broken bones' ward with neg/query patients) so seems odd to me they'd report data like that vs. those needing treatment for it.
So there's at least three categories: people with really bad Covid, people with Covid bad enough they can't be at home, but not (at the time) awful, and people who don't suffer with Covid at all but could infect others, and something else is wrong with them.
I think they are all challenging to the healthcare system in different ways. Ultimately, if you project a complex situation onto R^1, it can't be too accurate.
> Ultimately, if you project a complex situation onto R^1, it can't be too accurate.
Absolutely, and it's all too easy to make 'obvious' armchair policy..! I was just a bit surprised since my assumption would be it counted the relevant wards (if it were up to me, I think that would be the first three; only not the isolation-but-there-for-something-else).
It very much looks like Omnicron is an upper respiratory infection vs previous variants that are lower respiratory infections.
Fewer % hospitalizations, but you have a much larger population getting it in a shorter amount of time.
When hospitals get oveerwhelmed you're going to get a knock down effect on non-covid issues where medical attention is needed but cannot be provided.
However it is important as the WHO recommends to do way more to export vaccines to countries that need it. Not just developed countries to prevent the chance of new variants.
My understanding is that in many of those countries, the vaccine is readily available, but people don't want to take it for various reasons.
why long? The EcoAlliance's gain-of-function (with the "Human Subjects Included" checked) NIH grant for Wuhan started in 2014, the human-specific DNA modifications of the virus were described in the EcoAlliance's 2018 DARPA grant proposal, and in the end of 2019 - voila!
With regard to omicron - we may be also witnessing the continuation of the same magic of the fast "gain-of-function" by the virus :
https://www.reuters.com/business/healthcare-pharmaceuticals/...
"By inserting this particular snippet into itself, Omicron might be making itself look "more human," which would help it evade attack by the human immune system, said Venky Soundararajan of Cambridge, Massachusetts-based data analytics firm nference, who led the study posted on Thursday on the website OSF Preprints.
This could mean the virus transmits more easily, while only causing mild or asymptomatic disease."
https://www.newsweek.com/how-dr-fauci-other-officials-withhe...
What's new to me though is how deep the involvement of US entities apparently was and how close to SARS-CoV-2 territory the whole endeavour came. So in this case, absence of evidence is definitely not evidence of absence.
Also that one of the drivers of shutting down the lab-leak theory was apparently commissioning the WIV to do GoF research! (Though I still wonder what all the other scientists supporting that editorial were doing.)
If those FOIA papers will be used for more investigations in the near future, thing should definitely become interesting.
If we're worried about Omicron mutating to become more deadly, why aren't we worried about the other human coronaviruses doing the same? 229E, NL63, OC43, HKU1 that have been around for ages?
There's nothing magic about Omicron, its just a repsiratory virus thats relatively new to humans so there's not so much population immunity. And looks like we're rapidly getting exposed to it, so its about to lose its advantage.
They can only insert themselves into specific cells (acidic ones in lungs, nose, throat, stomach) and thus are respiratory viruses.
SARS-Cov-2 can insert into most cells of your body and loves the organs like the heart, brain, testes, lungs, etc.
It is airborne like a cold but can damage your brain and heart where a cold cannot.
Many viruses can attack multiple organs in the body if the infection is bad enough and the viral load is big enough to spread that far - e.g. see https://www.healthline.com/health/viremia
The reason for this is Omicron replicates mainly in the upper respiratory areas and does not invade vital organs. This is also why its so contagious.