Dr. Alexander Wong Profile picture
Feb 20 20 tweets 9 min read
"Hi Alex, what's BA.2? Is it a little bad or is it REALLY bad?"

BA.2 is a sub-lineage of Omicron. The 'original' lineage of Omicron is designated as BA.1 & remains the dominant strain circulating in most parts of Canada currently.

A brief 🧵 of what we know thus far. /1
BA.1 & BA.2 are both classified by @WHO as Omicron, but are distinct viruses. See the phylogenetic diagram below (thx @kallmemeg).

BA.2 has over 25 mutations that differentiate it vs BA.1.

Many questions still exist around how similar BA.1 & BA.2 are clinically. /2
Danish pre-print data comparing transmission of BA.1 vs BA.2 in household settings suggests BA.2 IS more transmissible than BA.1.

BA.2 also LIKELY possess more immune-evasive properties vs BA.1 that could reduce vaccine efficacy. /3

medrxiv.org/content/10.110…
Recent @UKHSA report from Feb 16 also suggests BOTH transmissibility AND immune-evasiveness properties that drive the growth of BA.2 vs. BA.1.

Nice summary below @kallmemeg.

So STRONG evidence to support overall growth advantage of BA.2 over BA.1. /4

Because of these growth advantages over BA.1, BA.2 WILL quickly become the dominant variant just as Omicron dominated Delta worldwide.

Graph courtesy @JeffGeeChartz below shows how BA.2 now dominates in many countries including India, Denmark, etc. /5
BA.2 has been reported across Canada, including Saskatchewan. None of this is surprising. We fully expect BA.2 to eventually dominate BA.1 across Canada.

Wastewater analysis throughout January 2022 has identified BA.2 in multiple #SK communities. /6

cbc.ca/news/canada/sa…
BA.1 was ALREADY super transmissible. BA.2 looks to be even more so. Not great.

Here are BIG clinical questions re: BA.2.

- How do vaccines protect against BA.2?
- If you've recovered from BA.1, are you protected vs BA.2?
- Does BA.2 cause MORE severe illness than BA.1?

/7
The caveat with all things #COVID19 is that data & our understanding continues to rapidly evolve.

What we think is right today, could be wrong tomorrow.

That said, right now data looks REASSURING that BA.2 is NOT worse than BA.2 clinically. /8
Recent @UKHSA data showed that serum from triple-vaccinated persons DID neutralize BOTH BA.1 & BA.2 equally well.

Also, NO difference in most recent real-world vaccine effectiveness analysis from UK for BA.1 vs. BA.2. Early times, though. /9

Evidence base for BA.2 is very immature, so need to take this in the appropriate context, but so far UK data has shown ZERO persons infected with BA.1 who then acquired BA.2.

All reinfections w/ BA.2 occurred in persons with Alpha, Delta, or original SARS-CoV-2 strain. /10
A recent Japanese preprint on BA.2's pathogenicity in hamsters suggests possibly increased virulence vs BA.1, as well as decreased vaccine efficacy.

How this translates clinically in humans, difficult to know.

IMO, not reason for mad panic. /11

biorxiv.org/content/10.110…
Recent preprint data from South Africa provides the first CLINICAL evidence that BA.2 DOES NOT cause more severe illness vs. BA.1.

Caveats again with regards to comparing South Africa's epidemiology vs that of other settings.

Still, encouraging. /12

What about protection vs BA.2 *if* you're triple vaccinated? Or is different than protection vs BA.1?

Limited preprint data encouraging.

Neutralizing antibody responses w/ 3 doses in BA.2 were only ~1.4 times lower than BA.1, but still protective. /13

medrxiv.org/content/10.110…
Same preprint. 6 persons w/ 2 or 3 doses of mRNA & recovered from BA.1 developed neutralizing Ab responses vs BA.2 ~1.3 times lower vs BA.1, but STILL protective.

This suggests reinfection risk w/ BA.2 is VERY LOW if you have 2 or 3 doses *AND* recovery w/ BA.1.

Phew. /14
The problem is that we know that protection vs. Omicron infection wanes quickly, more so than with past variants.

Here is recent UK data showing how protection w/ 3 mRNA doses wanes vs Omicron infection over time (h/t @AdamJKucharski). /15

Similarly, protection w/ 3 doses vs. severe illness & hospitalizations w/ Omicron also wanes over time, though not as significantly compared to infection.

Here is recent UK data that shows this trend vs. hospitalization.

h/t @AdamJKucharski. /16

So, to summarize, BA.2:

- IS more transmissible & immune evasive vs BA.1, meaning BA.2 WILL inevitably dominate BA.1 worldwide.
- Doesn't clearly cause more severe illness vs BA.1, but data is immature.
- 3 doses +/- BA.1 recovery DOES provide significant protection vs BA.2

/17
Much credit once again goes to the superb work from South Africa (@Tuliodna & @nicd_sa) along with excellent UK surveillance for informing the world regarding BA.2 thus far.

Ongoing worldwide surveillance remains critical via PCR testing & analysis. /18

In our local context, is BA.2 something to worry about in Saskatchewan? I'd say "maybe".

It's MORE transmissible than BA.1. With masking & other protections out the window & hospitals / ICUs still struggling, we'll likely see a prolongation OR new spike when BA.2 hits. /19
How do you protect yourself & loved ones from BA.2? Nothing new.

- Get fully vaccinated / boosted!!
- Mask appropriately indoors (ideally w/ respirator)
- Use RATs before indoor gatherings
- Upgrade ventilation / filtration
- Stay home & test if symptomatic

Be safe, all.

/end

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More from @awong37

Feb 22
Saskatchewan #COVID19 wastewater data released today for 4 #SK communities.

Both Saskatoon & Regina showing significant INCREASES in viral load week over week. Discouraging.

Reasons for increase unclear at this time. BA.2 driven?

Brief 🧵 to review #SK wastewater data. /1
Let's start with Regina.

@UofRegina wastewater analysis shows rebounding viral load levels week-over-week, suggestive of ongoing high rates of viral transmission in community.

BA.1 remains dominant but 18% BA.2 reported too. We expect BA.2 to dominate in coming days. /2 Image
Also, note that @UofRegina plot is time-lagged by 13 days, as the most recent analysis comes from the time period b/w Feb 6-12 inclusive.

So presumably proportion of BA.2 in Regina is higher now, just don't know how much higher. /3
Read 11 tweets
Feb 11
Great @SaskHealth Town Hall last PM re: #COVID19 in Saskatchewan. Key points:

- Community MAY have peaked w/ Omicron.
- Non-ICU/ICU numbers STILL rising
- #SK non-ICU system capacity MAXED OUT.
- Relaxed public health measures in #SK = LONGER & MORE SEVERE Omicron wave

🧵 /1
Let's start w/ cases, non-ICU & ICU COVID patients, & deaths.

CASES (blue line) are falling. This may be artificial to degree given limited PCR testing in #SK.

HOSPITALIZED (non-ICU) patients (light green 'shade') are at HIGHEST LEVELS of pandemic, now exceeding Delta. /2
ICU patients (dark green 'shade') are rising but nowhere near levels seen w/ Delta when #SK had to fly patients to Ontario.

DEATHS (red line) are rising gradually with Omicron but remain considerably lower than #SK's Delta peak. /3
Read 21 tweets
Feb 1
Yesterday, Premier Moe said #COVID19 cases in Saskatchewan are more frequent in the vaccinated vs. those who aren't.

THUS, vaccines DON'T prevent infection with or transmission of Omicron.

The Premier's conclusions are INCORRECT. But why?

It's complicated. Here we go.

🧵 /1
The Premier's incorrect conclusion stems from a simplistic interpretation of the data. 'Base rate fallacy' is one problem, but there are MANY other factors at play.

We explained 'base rate fallacy' with cases & vax status back in August. See below. /2

For 'base rate fallacy' & #COVID19 & hospitalizations, this is the diagram EVERYONE uses (thx @MarcRummy).

MANY more people are fully vaccinated now, so even though a small proportion of them go to hospital, the absolute numbers are the same as those unvaccinated. See below. /3
Read 25 tweets
Jan 30
"Hi Alex. I have #COVID19 infection. Should I try to get Paxlovid? What is it? Will it help me?"

Short answer: YES, you should.

BUT, there's LOT of things to know about it, and your eligibility for it will depend on where you live + many other things, too.

Explainer 🧵. /1
Paxlovid's generic name is nermatrelvir/ritonavir. It's a combination of 3 pills taken twice daily for 5 days.

Nermatrelvir is a "protease inhibitor". It works by blocking an enzyme ("protease") that the virus needs to manufacture new copies of itself. /2
In this situation, Ritonavir acts as what we call a "booster drug".

It inactivates an enzyme in our bodies called CYP3A4 that plays an important role in metabolizing and removing many medications from our bodies.

This allows nermatrelvir to exist longer in our bodies. /3
Read 15 tweets
Jan 29
Earlier today, @PremierScottMoe posted a letter. In it, he stated:

- Being vaccinated DOES NOT prevent one from contracting #COVID19
- Vaccines are NOT reducing transmission of #COVID19

Both statements are FALSE & should be corrected ASAP for the record. Thank you.

🧵 (/1) ImageImage
Many studies show 3 doses of mRNA vaccine (Pfizer or Moderna) provides 60-70% protection (vaccine effectiveness, VE) vs Omicron infection.

If you don't get infected, then you don't transmit the virus. Simple.

So being vaccinated, esp. w/ 3 doses, makes a HUGE difference. (/2)
Here is a recent pre-print from Moderna showing ~68% VE against Omicron infection with 3 doses of vaccine.

Also, VE to prevent hospitalization w/ Omicron following 3 doses was >99%. That's HUGE. (/3)

medrxiv.org/content/10.110…
Read 13 tweets
Jan 21
On January 18, @PremierScottMoe posted a graphic comparing "real-time" QC / ON / MB hospitalizations / ICU admissions vs. SK.

Problem: SK is ~3 weeks behind those provinces w/ our Omicron surge.

We MUST be careful interpreting this data. We're NOT OK, Saskatchewan.

🧵👇 (1/n)
A more reasonable and appropriate comparison would be to look at where MB/QC/ON were at ~3 weeks from Jan 18 to create a more fair "apples vs apples" graphic.

For those 3 provinces, that would take us to about Dec 28. Let's see what the data shows us. (2/n)
We have #QC data from Dec 28 & Jan 18 in the graphics below courtesy @sante_qc:

Dec 28: 804 in hospital (including ICU), 128 in ICU
Jan 18: 3425 in hospital (including ICU), 285 in ICU

(3/n)
Read 11 tweets

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