The @AnnalsofIM study included all cases in those age 5-39 y (overall incidence was 1 per 30 000 - 200 000 doses), but via U.S. (active) VSD & (passive) VAERS reporting systems.
However, in the U.S., short doses intervals have been used (e.g. 3 wks for Pfizer 1-2)
(3/)
The new @CircAHA study instead looked at data from England, with data for those 13+ years.
Apart from the BNT162b2 (Pfizer) and mRNA-1273 (Moderna) vaccines, they also had data for ChAdOx1 (AstraZeneca)
(4/)
As one can see from their supplement the risk of hospital admission or death was ⬆️ from SARSCoV2-induced myocarditis — in #unvaccinated — than from the vaccine, both overall, and in the <40 year old group.
(again ⬆️ w/ Moderna dose 2, but many countries only give it to >30y) 4/
However, note that interval between doses impacts the incidence – the recommended interval between doses has been short in e.g. the U.S. and Israel (corona.health.gov.il/en/vaccine-for…).
This is also how the trials were done (e.g. 3-week interval between Pfizer doses 1 and 2)
(5/)
Indeed, a Canadian study (n=19,740,741 doses) found that the interval was a modulating risk factor:
For the group 12-17 yo, myocarditis incidence ⬇️ with interval:
⦿ ~1/10 000 doses @ ≤30 day-interval
⦿ 1 per 18000-27000 at interval @ 30+ days jamanetwork.com/journals/jaman…
(6/)
For the Nordic countries, a study found the incidence of myocarditis to be highest in the 16-to-24-year olds:
Excess incidence with the Pfizer vaccine was 5.6 extra cases per 100 000 doses — so, ~1/18 000 doses, similar to the Canadian data.
In the Nordic data, they found no deaths of myocarditis below the age of 40, with similar (overall good) outcomes as observed in the U.S. data (jamanetwork.com/journals/jama/…)
Overall, deaths were otherwise ⬆️ (.8%) from unvaccinated SARSCoV2 myocarditis vs. from Pfizer's (.2%)
(7/)
The CDC also has some slides on myocarditis in their June 2022 ACIP update:
Here's a great comparison of the risk & course of myocarditis associated with the vaccine, with those from the virus itself:
Apart from overall more serious myocarditis, #SARSCoV2 can indeed ⬆️ the risk of multiple cardiac & non-cardiac conditions:
An 8-month trial in mostly females (17/18) with #obesity & type 2 #diabetes, shows that those randomized to an *intensive* #lifestyle intervention (n=10) e.g. had:
⦿ Preliminärt ger 3 vaccindoser ~70-75% skydd mot symptomatisk #COVID19 orsakad av Omicron
- åtminstone ~2 veckor efter dos 3 & hos yngre
Därmed antas vaccinskyddet mot svår C19 vara än högre
Trista nyheter-> 🧵
2/ Trista nyheter:
I jämförelse med smittsamma Delta tycks Omicron, *preliminärt*:
⬆️ Reinfektionsrisken 5x (3.4-7.8x) för de med tidigare COVID-19
⬆️ ~2 ggr oddsratio att föra smittan vidare till nära kontakter
⬆️ ~3 ggr oddsratio att föra smittan vidare till hushållskontakter
3/ Trista nyheter:
*preliminära*
⦿ ~22% kontra tidigare 11% risk att en hushållskontakt smittas (secondary attack rate; SAR)
⦿ Smittan växer nu med dubblering var 2.5:e dag i Storbritannien – beräknas kunna ta över (dvs. majoritet av fallen) om någon vecka i Storbritannien.
2/ Reinfektioner är som regel - ej alltid - mildare.
"Reinfections had 90% lower odds of resulting in hospitalization or death than primary infections"
- Omicrons effekter ännu oklar, men ⬆️ reinfektionsrisken
-Vaccinering därmed viktigt för denna grupp nejm.org/doi/full/10.10…
3/ Att reinfektioner (~2a exponering) ger mildare förlopp är jämförbart med hur vaccinen - fast via säker 1:a exponering för virusprotein - sänker risken för allvarlig COVID-19.
Oklart: Vissa tror att 2, särskilt 3 vaccindoser, kan ge hyfsat skydd mot allvarlig C19 av Omicron
->
Pulmonary #embolism (lung blood clot) was >10 times more common after #SARSCoV2 infection (COVID19; ~15x over background rate), vs after getting #Pfizer's or #AstraZeneca's vaccine (~1.2x> background)
2) First of all – as the authors note – in those #vaccinated against COVID-19, "thrombosis, thrombocytopenia, and thrombosis with thrombocytopenia were very rare events."
3) Data from 1.9 Million (M) recipients of AstraZeneca, ~1.7 M of Pfizer, and ~300k COVID-19 cases (few old) – compared with ~2.3 M in the general population.
These cohorts were used to calculate the observed incidence vs. background (SIR) or observed vs. expected # of cases.