How do we measure how well the flu vaccine works every year? We use an observational study called the "test negative design." A few tweets on how it works, and why it will be a big part of ongoing COVID-19 vaccine evaluation. 1/8

Figure source: Fukushima et al. (2017) Vaccine
In the test negative design, individuals with disease symptoms seek healthcare and testing. If they test positive, they are TEST POSITIVE CASES. If they test negative (and their symptoms are caused by something else), they are TEST NEGATIVE CONTROLS. 2/8
We can then look back and see how many of the test positive cases were vaccinated, and how many of the test negative controls were unvaccinated. Where the vaccine works well, there won't be many vaccinated people testing positive. 3/8
On the other hand, a flu vaccine doesn't protect against other respiratory viruses, so we would expect a mix of vaccinated and unvaccinated controls, reflecting vaccination coverage in the underlying population. We can estimate vaccine effectiveness as 1 minus the odds ratio. 4/8
Test negative designs are valuable because they are inexpensive. They can be integrated into existing surveillance systems. They are far cheaper than a cohort study where you have to follow many thousands of people to observe a small number of cases. 5/8
They also reduce a certain type of bias that can occur because the type of people who go to their doctor when they feel sick may also be the type of people who get vaccinated. But this study restricts to these "care seeking" individuals (and those who can access testing). 6/8
This will be a vital study design for evaluating COVID-19 vaccines. While randomized trials are the gold standard, they are increasingly difficult to do, as they may be unethical or people may not consent to participate. Observational study designs will fill in the gaps. 7/8
So it is critical that these study designs are of high quality, because we will use them to determine how durable vaccines are, how well different vaccines work against new variants, and so on. I hope this primer helps! 8/8
science.sciencemag.org/content/370/65…

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More from @nataliexdean

17 Feb
THINK LIKE AN EPIDEMIOLOGIST: Lately I have been asked why we are seeing a dramatic turnaround in cases in the US. Is it vaccines? Herd immunity? An artifact due to a drop in testing? Behavior change? Weather?? A few tweets about how I step through this question. 1/6 Image
To start, I look to see whether the drop is an artifact. While testing has dropped somewhat, it's not enough to explain the rapid drop in cases. A drop in testing would also not explain the drop in hospitalizations that is consistent across regions. 2/6
covidtracking.com/data/charts ImageImage
I then consider the similarity of the drop across locations, looking by subregion and by state. The similar patterns seen are relevant because different places have different vaccination coverage, levels of acquired immunity, and weather. Why the turnaround at a similar time? 3/6 ImageImage
Read 7 tweets
8 Feb
Warning - some in-the-weeds tweets about vaccine efficacy trials, new strains, and decision making under uncertainty. I offer more questions than answers, but hopefully it can generate some discussion...
1/6
For COVID vaccine studies, we can imagine two goals:
(1) We aim to measure efficacy precisely (minimize uncertainty, regardless of the true efficacy), or
(2) We simplify our goal and try to measure if the vaccine is doing well enough - is efficacy above our success threshold? 2/6
This is relevant for discussions about how well vaccines are performing against different variants. For those who are already vaccinated, we want to know how well the vaccine works against a new strain. What is the efficacy, even if it is lower? This is like the first goal. 3/6
Read 6 tweets
3 Feb
Oxford/AZ reports overall reduction in PCR positivity of 54.1%, but only 2% "vaccine efficacy against asymptomatic infection."

Confused?

Allow me to explain with crudely drawn pictures why the overall findings are still quite positive. 1/8
Let's start by imagining the base case (no vaccine). SARS-CoV-2 infections fall into a range of categories: severe, moderate, mild, or asymptomatic.
(Categories not perfectly to scale for all of this, don't @ me). 2/8
Vaccines protect against disease in two major ways.
- They can prevent infection entirely.
- Or they may not prevent infection, but they prep your immune system so that you don't develop symptoms. Usually it is some combination of the two. 3/8
Read 9 tweets
29 Jan
With Novavax results, a welcome addition of another efficacious vaccine. The more, the merrier. Though the observed lower efficacy in South Africa is discouraging (and exactly how much lower is hard to tell given uncertainty), I’m glad we have these data in hand. 1/5
Well-conducted placebo controlled trials can give us the clearest read on how these vaccines are working against different variants. It was fortuitous to have these two trials in the UK and South Africa that we can compare in this way. We want to know what we’re dealing with. 2/5
Fortunately the vaccine is working well against the UK variant. But as we see in South Africa (and in laboratory studies with other vaccines), we cannot assume that vaccines are equally effective against all variants. We will need to continually monitor their effectiveness. 3/5
Read 5 tweets
13 Jan
A few tweets on a topic that keeps coming up in discussion. There are many different types of vaccine efficacy - efficacy against infection, against transmission, against disease, and against severe disease - and these can vary for a single vaccine. How are they related? 1/5
Efficacy against infection will by necessity be lowest, because if a vaccine protects you from infection, it also protects you from transmitting to others and getting symptoms. We have a little data on this from Moderna and Oxford, but will get more from antibody testing. 2/5
Even if a vaccine does not prevent infection, it could make you less infectious by reducing viral load, reducing duration of infectiousness, or by preventing symptoms like coughing/sneezing. This effect is hard to measure without contact tracing or cluster randomized studies. 3/5
Read 5 tweets
29 Dec 20
Our group's household secondary attack rate meta-analysis has gained traction, but not for the reasons I'd hoped for. We did not conclude "no asymptomatic or pre-symptomatic spread" of SARS-CoV-2. A short explanation of what we did observe. 1/7
jamanetwork.com/journals/jaman…
Using only the household studies included in our main analysis, we conducted a sub-analysis breaking out index cases designated as symptomatic versus asymptomatic/pre-symptomatic. We observe lower transmission from this latter group, though there was much less data. 2/7
Since we are relying upon other studies in the literature, we were unable to separate out fully asymptomatic index cases (never develop symptoms) from pre-symptomatic index cases. But others have tackled this problem directly. Their conclusions below. 3/7
medrxiv.org/content/10.110…
Read 7 tweets

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