Model update klaxon!! I’ve spent a while this weekend refitting my model to current data and trends, and as a result I’ve changed my mind on at least 3 things – and also got closer to a policy recommendation for Step 4 re-opening scheduled for 21st June. Thread follows: 1/n
First to note a few assumptions:
-Baseline controls and cautious behaviour (e.g. continued WFH) are assumed to continue after 21st June, until the end of 2021, and to reduce R by ~25%
-I’ve adjusted my vaccination schedules to more precisely match current supply estimates 2/n
– with thanks as always to @PaulMainwood for his insights on this.
-In particular, now that we have MHRA approval for 12-15 year olds to receive Pfizer, I’ve assumed that 12-17s get their first doses in September (& second doses in November) 3/n
-NB I haven’t modelled booster vaccinations for over-50s, nor any waning of immunity over time
-I’ve assumed the Delta variant has an effect of doubling the ratio of hospitalisations to infections in all age groups (as per PHE data, which also helps my model to match the 4/n
...current data – it was previously diverging by under-predicting hospital admissions)
-I have not changed my IFR estimates; so please note that if those extra hospitalisations feed through into extra deaths, my death figures could be understated by a factor of 2 or more. 5/n
-Since there remains some uncertainty as to exactly how transmissible Delta is (relative to Alpha), and how much of the apparent transmission gain is the effect of immunity escape, I’ve taken a scenario approach to this, with 4 main scenarios: 6/n
-Two scenarios have a significant immunity escape, which causes a 25% transmission gain, and the other two have a smaller escape, which causes only 12% gain
-On the other axis is the total transmission gain, which is 40% in two of the scenarios, and 70% in the other two. 7/n
The table below shows the R0 of the Delta variant which is assumed in each of these 4 scenarios – as you can see, it ranges from a bit above 5, to just over 7 – still quite a wide range of uncertainty: 8/n
In the two scenarios with lower (40%) total transmission gain, we have a moderately-sized exit wave, with peak hospitalisations of around 5000 per week, and total deaths of 5-10k (although note if my IFR estimates for Delta are wrong, that could be too low): 9/n
In the two scenarios with higher (70%) total transmission gain, we have a much larger exit wave, with peak hospitalisations of 20-30k per week (close to Jan 2021 levels), and total deaths in the 12-16k range – again note this could be under-estimated. 10/n
The first thing I’ve (partially) changed my mind on is the short-term dynamics. I was previously confident that R would fall away over the next 1-2 weeks, to around 1.1-1.2, before 21st June. That could still happen, if we’re in the 40% transmission scenarios, but... 11/n
…in the 70% transmission gain scenarios, R is more likely to stay in the 1.3-1.4 range over the next couple of weeks, as we still have some ‘damage’ from Delta to feed in (as it spreads into other regions), which will offset the benefits of vaccinations and warmer weather. 12/n
Unfortunately, distortions caused by half term and bank holidays to testing and infection patterns may confuse the picture over the next fortnight, making it harder to tell which of these scenarios is actually happening in real life. 13/n
The second thing I’ve changed my mind on is the impact of different lengths of delay to the Step 4 re-opening, scheduled for 21st June. I was previously arguing that a short (2-3 week) delay was unlikely to achieve much, except possibly to gain time to gather more data. 14/n
And that a longer delay (of 2-3 months, to late August or early September) would be more effective, as it would enable us to get more people double-vaxxed, before letting Delta run free. With more careful modelling, I now have reason to amend both of those views. 15/n
To illustrate this, I have taken the most severe of my 4 scenarios, with the higher (70%) transmission gain and the larger immunity escape, and plotted both the total deaths and peak hospitalisations for different dates of re-opening (Step 4): 16/n
This shows that, while short delays to re-opening don’t save many lives, they do have a big impact on predicted peak hospitalisations, bringing them down out of the “danger zone” to NHS capacity– effectively, the exit wave is being flattened out or split into smaller waves: 17/n
We can also note that delaying re-opening until September could make things worse, as it pushes the resulting exit wave into the winter. However I note that this situation could be improved by using booster vaccinations, or retaining baseline controls for longer into 2022. 18/n
The story is similar for my other high-transmission scenario (the one with the smaller vaccine escape) – except that here, the optimal point for re-opening looks to be a bit earlier e.g. in late July or early August, rather than in mid-August. 19/n
So, what’s my conclusion on Step 4? Well, I still want to gather more data before giving a final view. But if Matt Hancock’s reference today to a 40% transmission gain stands up (and assuming he was referring to the total gain, including the impact of immunity escape), 20/n
… then it may be that we could go ahead as planned on or close to 21st June. If however, the gain of 70% that we see in the genomics and case data (from @TWenseleers and @alexselby1770 analysis) persists, then we are facing a much larger exit wave, close to NHS capacity. 21/n
In those circumstances, I don’t think I could recommend proceeding with Step 4 as planned, if another NHS-threatening wave was on the horizon. And from the analysis shown above, I would (tentatively, at this stage) suggest a 5-6 week delay to late July/early August. 22/n
So, how can we work out which of those situations applies? Two main ways: firstly, new data to be published by PHE in the next Technical Briefing on vaccine effectiveness vs. Delta, on re-infection rates, and on Secondary Attack Rates. And secondly, the daily dashboard... 23/n
…data on cases and hospitalisations may enable us to refine our view of R, and hence the transmission gain we are seeing in practice. (although as noted above, distortions caused by half term and bank holidays may cloud this picture somewhat). 24/n
I’m hopeful that the combination of those two data sources may enable us to get to a clearer view before decisions need to be made on the 14th June. If not, there may still be a case for a short (e.g. 2 week) delay to enable the data to settle down a bit. 25/n
I would stress that there is still a wide funnel of uncertainty, and my model doesn’t capture all of the dynamics that may be important. For example, stronger seasonality than I’ve allowed for, or heterogeneity effects in immunity acquisition, could make things better. 26/n
But on the other hand, waning of immunity over time, and differences in immunity and natural R between different regions and age groups, could cause things to evolve in less favourable directions. The SPI-M models will capture some of these dynamics better than mine does. 27/n
You may recall I’d said I’d changed my mind on 3 things, and I’ve so far only mentioned 2. So what’s the third? Vaccination of teenagers. I was previously promoting this as a helpful step towards the herd-immunity threshold, and was keen to get it done ASAP e.g. in July. 28/n
But looking at the models now, it doesn’t make much difference. Why is this? Partly because of Delta’s escape on the 1st dose, which makes it less effective, and also because the exit wave is now starting earlier (in June), so vaccinating in July is already too late. 29/n
Hence the impact is marginal, and so it’s hard to justify doing it (vs. sending the vaccine to help older people in other countries). There may still be arguments for vaccinating UK teenagers at a later stage, but right now this analysis suggests it shouldn’t be a priority. 30/n
I think that’s enough changes of mind for one day, so will leave it there for now – I’ll update again if & when we get more data from PHE. And apologies I won't be around much to answer questions today - I need to get back to work! /end.
• • •
Missing some Tweet in this thread? You can try to
force a refresh
thanks to the person who pointed me towards this report: assets.publishing.service.gov.uk/government/upl… (you know who you are!) - lots of interesting data. In particular it does support the anecdotal evidence that average length of stay in hospital is shorter in recent admissions: see this chart 1/3
...and compare to the older data in the chart below. So after 10 days, about 75% have been discharged in the recent data, compared to 40% in the older data. (but note deaths are lower in the recent data, which slightly offsets the benefits for hospital bed occupancy). 2/3
what's not entirely clear to me is whether this is just the result of a lower average age of patients being admitted - see below- (and would reverse if more older cases arrived), or whether it says something more fundamental about the progression of covid disease with Delta. 3/3
I think the age dynamics of the current case growth are interesting, particularly as they have shifted in the last week or two. Growth is now very clearly dominated by the 20-30s, while growth in school-age children has tailed off: 1/6
If we look more closely e.g. at 5-9 year olds, we can see that tailing off of growth. I’m not 100% sure why this has happened, it seems slightly early for a half term effect, so maybe local PH efforts and bubble closures are having an impact? &/or parents being vaxxed?? 2/6
Meanwhile the growth in 20-24s is pretty dramatic, doubling in just under a week, and now back to levels not seen since February: 3/6
A few thoughts on yesterday’s PHE data: overall, the report is a bit of a mixed bag. Of the three significant bits of news, one is positive, one negative, and the other neutral. But you might not get that impression from the reaction here on Twitter or in the media. 1/n
Let’s take the negative first: we now have data suggesting that the new variant (Delta) is more likely to lead to people being admitted to hospital – perhaps 2.5 times more likely than when infected with the old Alpha variant. 2/n
That’s clearly bad news, and will have an impact on model projections for Step 4. But it’s not necessarily a complete disaster: if we can control the spread of the virus, then it doesn’t matter what the hospitalisation ratio is, because very few people will be catching it. 3/n
Some thoughts on where we are, in the form of a “zigzag” thread where I offer alternating good and bad news, and end on a question mark. Let’s start with some bad news: 1/11
This morning’s threads from @alexselby1770 and @TWenseleers, as well as last week's PHE data on secondary attack rates , are all pointing towards ~70% higher transmission for the Delta variant (B.1.617.2) vs Alpha (B.1.1.7) 2/11
BUT (good news) my previous analysis showed 55-60% higher R0 wasn’t a disaster, and could be kept under control with a combination of baseline controls and cautious behaviour (eg. continued WFH). A quick model run suggests 70% isn't very different. 3/11
I’ve been away for a few days, and have come back today with a fresh eye. A couple of observations: 1. What was a handful of hotspots before, now looks like more broadly-based growth 2. Whereas growth last week was led by the u20s, it’s now the 20-30s leading the way. 1/5
To evidence the latter, look at the growth rates by age category last week: 2/5
It’s even better than that: it’s brilliant news. By my calcs, Hancock’s statistic (10% of people in hospital have had 2 doses of vaccine) implies the vaccine is having at least a 95% protective effect – and probably more like 98%, or maybe even higher. Let me explain… 1/n
To start with, we have to recognise that for this calculation, not all people are equal – some have more hospitalisation risk than others. So vaxxing those people will have more of an effect. Fortunately, we have targeted our vaccines on those with highest risk. 2/n
By applying some broad weighting factors to different JCVI categories, I can estimate that c. 71% of the (pre-vaccine) hospitalisation risk is in people who have now had a second dose of the vaccine, and a further 22% is in people who have had a first dose. 3/n