We calibrated a model used in a lot of @cmmid_lshtm COVID-19 work to the South African outbreak & interventions. In this model, to explain the increasing epidemic, 501Y.V2 needs to be either more transmissible or evading cross-protection.
NB: NOT PEER REVIEWED
If there is cross-protection against 501Y.V2, it's roughly 50% more transmissible. If it has the same transmissibility, then prior infection only confers 80% protection against 501Y.V2.
Both of these are big public health problems!
NB: NOT PEER REVIEWED
We also saw indications of increased severity, but many potential explanations there.
Both increased transmissibility and severity call for urgency in vaccination and continued vigilance in other measures, and continuing analysis of new variants.
Submitted (finally) revisions to this analysis of using the test-negative study design in the presence of public health measures. Some new thoughts, in light of pandemic!
Work w/ @rozeggo, @TJHladish, & John Edmunds.
When criteria for testing vary systematically, the design can be biased. In outbreak & pandemic response, testing happens passively (e.g. you're sick => seek care => get tested) & actively (e.g. co-worker is test+ => contact-tracing => you get tested).
NB: NOT PEER REVIEWED
These represent diff risks and thus differ in thresholds for testing. e.g. in passive route, generic risk => testing conditional on symptoms, but for active scenario => high exposure risk => unconditional testing (e.g. COVID19 TTI protocols).
We forecast dates that African countries would *report* 1K and 10K cases. We used very sparse data (first 25 or fewer cases prior to 23 March), w/ deliberately low-detail method (branching processes), assuming global epi estimates & discounting any potential interventions.
That very simple approach worked well for countries that couldn't (or didn't) respond to early warnings like ours. My previous tweets about this report are from 27 March; since then 12 countries have reported >1K cases: who.int/docs/default-s…