Dr. Jay Bhattacharya’s Next Big Idea
Originally published at National ReviewThe emergence of Stanford epidemiologist Dr. Jay Bhattacharya as a public figure was one of the few salutary consequences of the Covid pandemic. Readers will recall that Bhattacharya is a coauthor of the Great Barrington Declaration that — among other assertions — challenged the shutdown of schools and urged that the most vulnerable receive “focused protection,” while the rest of society carry on, an approach intended to prevent the “cure” from being worse than the disease.
For their temerity, Bhattacharya and his Great Barrington colleagues were slandered in an email by NIH head Francis Collins as “fringe” doctors — which was obviously false as Bhattacharya alone had published more than 100 peer-reviewed professional articles and his colleagues taught at such “fringe” medical schools as Harvard and Oxford. Worse, Collins urged Anthony Fauci to actively discredit the Declaration with a “devastating takedown” rather than debate or discuss it, which would have been the proper scientific approach. The media loyally jumped to their command — while Stanford also made their own professor’s life miserable for daring to express a heterodox opinion. (To hear Bhattacharya’s take on that difficult experience, hit this link to our interview on the Humanize podcast.)
In the end, the Great Barrington Declaration was validated as probably a better approach than those promoted and/or mandated by our own public-health establishment. (The GBD recommendations were very similar to the approach taken by Sweden, which reaped a lower Covid death rate than most other countries.)
Now, Bhattacharya and colleagues are back with a new Covid-related campaign that they hope will help ensure that the catastrophic failings and consequential loss of trust in our public-health institutions are not repeated.
Known as the Norfolk Group, Bhattacharya and his coauthors hope to create a national commission to explore the official responses to Covid — itemize what went right and wrong — toward the end of planning a better public-health response if/when another pandemic threatens. From the Executive Summary:
In this document we list specific questions on specific topics related to COVID-19 pandemic responses in the United States. We believe these questions are vital for the nation to ask the White House, the CDC, the FDA, and other government officials, as well as state health departments, scientists, and the media. The public deserves answers to these questions so we can learn from our mistakes. Key issues include:
- What could have been done to better protect older high-risk Americans, so that fewer of them died or were hospitalized due to COVID-19?
- Why was there widespread questioning of infection-acquired immunity by government officials and some prominent scientists? How did this hinder our fight against the virus?
- Why were schools and universities closed despite early evidence about the enormous age-gradient in COVID-19 mortality, early data showing that schools were not major sources of spread, and early evidence that school closures would cause enormous collateral damage to the education and mental health of children and young adults?
- Why was there an almost exclusive focus on COVID-19 to the detriment of recognizing and mitigating collateral damage on other aspects of public health, including but not limited to, cancer screening and treatment, diabetes, cardio-vascular diseases, childhood vaccinations, and mental health?
- Why did the CDC fail to collect timely data to properly monitor and understand the pandemic? Why did we have to rely on studies from private initiatives and from other countries to understand the behavior of the virus and the effects of therapeutics, including vaccines?
- Why was there so much emphasis and trust in complex epidemiological models, which are by nature unreliable during the middle of an epidemic, with unknown input parameters and questionable assumptions?
- Could therapeutic trials have been run in a more timely manner? How was information on drug effectiveness and safety disseminated to doctors and clinicians? Were effective therapeutics easily accessible across the population? How did certain drugs become heavily politicized?
- Why did vaccine randomized trials not evaluate mortality, hospitalization, and transmission as primary endpoints? Why were they terminated early? Why were there so few studies from the highest-quality CDC and FDA vaccine safety systems?
- Why was the USA slow to approve and roll out critical COVID-19 testing capacity? Why was there more emphasis on testing young asymptomatic individuals than on testing to better protect older high-risk Americans? Why was so much effort spent on contact-tracing efforts?
- Why was there an emphasis on community masking and mask mandates, which had weak or no data to support them, at the expense of efficient and critical COVID-19 mitigation efforts? Why did the CDC or NIH not fund large randomized trials to evaluate the efficacy and potential harms of mask wearing? Why didn’t policy recommendations change after the publication of randomized trial data from Denmark and Bangladesh which showed no or minimal efficacy of mask wearing by the public?
These are important questions. But the U.S. government isn’t about to convene such a deep exploration without intense public pressure — too many literal and figurative buried skeletons, don’t you know.
Unfortunately, the Norfolk Group’s proposition has not received much attention. But the time may be ripe to build a political fire. The presidential campaign season is here. A first step would be for enterprising media members or debate moderators to ask every candidate — Republican, Democrat, and No Labels, if that middle approach comes to pass — whether they would support such a commission if elected, and, if not, why not.
The Covid debacle remains raw. If we are going to get past our deep divisions and find a proper approach going forward the next time a pandemic threatens, a dispassionate investigative commission — not a stacked deck in any direction — is a good place to start.