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WPCNR THE LETTER TICKER. By Dr. Katelyn Jetelina [email protected] May 18, 2022: We are clearly in the middle of an infection surge in the U.S. Hospitalizations are increasing but not reflecting case acceleration, and deaths are nearing pandemic lows. The individual risk of severe disease continues to decline thanks to immunity and treatments. This changing dynamic has sparked an intense tug-of-war among scientists, leaders, and the public—a push towards “normalcy” from some and push back towards “urgency” from others. Where one lands on this spectrum is centered around the answer to one question: Are we in a public health emergency? Challenging answer This debate will ultimately decide if, when, and how we differentiate a country-wide emergency (epidemic) from a manageable situation (a middle phase) until we reach a predictable, static state of disease (endemic). Essentially we’re collectively deciding where we place SARS-CoV-2 in our repertoire of threats. This isn’t something the U.S. has navigated in the modern day with a novel respiratory virus. In reality, our collective answer isn’t purely epidemiological, but also physiological, cultural, political, and moral. I think this is difficult, particularly in the U.S., for four reasons: No goal.  The CDC defines an epidemic as “an increase, often sudden, in the number of cases of a disease above what is normally expected in that population in that area.” For the past two years, there’s no doubt we experienced a country-wide epidemic—it was novel and, by definition, above normally expected—causing a public health disaster of over 1 million deaths. Because we know SARS-CoV-2 will be with us in the foreseeable future, what is now an “unexpected increase” in disease? For example, U.S. deaths are starting to plummet which looks relatively great, but how low is low enough?   One group suggested that an “acceptable” endemic level of SARS-CoV-2 would be to keep peak COVID-19 deaths in a surge below the peak of a bad flu season. As I charted below, we are far from the flu threshold. The worst flu season was in 2017-2018 where 61,000 deaths were recorded. In the first 5 months of 2022, we already surpassed this number more than 2-fold. This lands SARS-CoV-2 as the third leading cause of death. Is this truly an “acceptable” level for the U.S.?   Unpredictability.  If we are not in an epidemic, then we are floating in a weird middle-ground because we’re not in an endemic either. Transmission is not stable or predictable, the virus is changing quickly, and we have no idea what it will do next: Will Omicron continue to mutate in a ladder-like fashion or will it mutate to an entirely different Variant of Concern and throw us for a loop, like Omicron did after Delta? We have no idea. If we do get an Omicron-like event, when will it happen? We have models suggesting it will be in 1.5 years or 10 years. In other words, we have no idea. Will the virus mutate to become less severe or more severe? Unfortunately, viruses mutate randomly. We don’t know the next move.This means that if we’re not in an emergency today, we may be in one tomorrow. The dynamic nature of the virus is also changing the meaning of “emergency” over time. For example, during the Delta wave and before vaccines, the emergency was mortality. But during Omicron, the emergency was hospital capacity (and mortality). Some have argued that the next emergency is already in the works: morbidity due to long COVID. Our definition of an emergency will change, making it even more difficult for us to collectively define the “end” of an emergency. Fatigue.  In a series of polls, it’s clear that about half the country would like to move on from this virus. In one poll, 55% of voters think COVID-19 should be “treated as an endemic disease that will never fully go away” while 38% say it should be “treated as a public health emergency.” Pandemic fatigue is real. People are losing hope. And, individual-level risk is low, so the population-level threat feels distant. The collective, national-level psyche plays a huge role in defining our collective threshold of concern about SARS-CoV-2. No safety net or trust.  During the Omicron peak, Denmark boldly declared the emergency over. I was not surprised given their high vaccination rate, ability to track the virus with comprehensive data, and wide safety net of universal healthcare coverage, paid time off, etc. More than 90% of Danes approved ending the state of emergency, too. In Australia, public trust enabled them to dodge death until the vast majority of the population was vaccinated. But safety nets and trust are in short supply in the U.S. Because of this, the decision to end a public health emergency in the U.S. is particularly difficult, as it’s a question of leaving people behind and trusting institutions. This is really important to get right Practically speaking, defining an emergency is really important for funding and thus our capacity to fight. The current public health emergency declaration, for example, goes until July 15, 2022. The Biden Administration promised states 60 days notice before the declaration expires, which would have been two days ago. I would be very surprised if they let the emergency expire in the middle of a surge, but as I outlined above, the answer isn’t clear. As the Kaiser Family Foundation clearly laid out, if the emergency declaration goes away, it will be a big deal. We will see changes in almost every aspect of this pandemic response as outlined below. Together it will be more difficult to fight the virus and easier to accept the current state of affairs as “normal.”   Concurrently, the White House is also trying to push two pandemic preparedness funding packages. These need to go through, but it’s unclear whether the public will prioritize pandemic preparedness if we’re not in an emergency (we tend to have short term memory loss). If pandemic preparedness is not funded, the U.S. public health system will continue the deadly and exhausting cycle of neglect and panic that we’ve experienced for decades. But is this reason alone sufficient to declare an emergency? Bottom line We are in a strange phase of the pandemic—caught somewhere between epidemic of emergency and endemic of manageable disease, determined by the push and pull of epidemiology, culture, politics, and psychology. We haven’t clearly defined our end goal, so it’s incredibly confusing to know what to think, who to listen to, or what to do. And we are tired of trying to figure it out. We, as a nation, will ultimately decide what we accept from SARS-CoV-2 based on national-level decisions (Do we fund public health to improve data systems, discover the next generation of vaccines, and support testing for Medicaid and Medicare?), institutional-level decisions (Do businesses improve ventilation and filtration? Can we build trust with the public again?), and individual-level decisions (Do we use antigen tests to break transmission chains? Do we wear masks when surging? Do we get vaccinated?). Every day we unconsciously (or consciously) inch towards the collective answer. The decision is up to us. This week we got more tools to help:You can now order 8 more antigen tests to be delivered to your home. Go to the USPS website now. The FDA approved age 5-11 boosters, but the CDC needs to approve. They meet Thursday and should approve it quickly thereafter. On June 8, 21, and 22, the FDA meets to discuss the under 5 vaccine. The FDA approved a 3-in-1 Labcorp test that can detect COVID, the flu, and RSV. Specimens have to be mailed for testing (questioning broad feasibility), but this is a step in the right direction. “Your Local Epidemiologist (YLE)” is written by Dr. Katelyn Jetelina, MPH PhD—an epidemiologist, biostatistician, wife, and mom of two little girls. During the day she works at a nonpartisan health policy think tank, and at night she writes this newsletter. Her main goal is to “translate” the ever-evolving public health science so that people will be well equipped to make evidence-based decisions. This newsletter is free thanks to the generous support of fellow YLE community members. To support the effort, please subscribe here:Subscribe nowLikeCommentShare Thanks for subscribing to Your Local Epidemiologist. This post is public, so feel free to share it.Share© 2022 Your Local Epidemiologist Unsubscribe 548 Market Street PMB 72296, San Francisco, CA 94104

WPCNR WESTCHESTER CRITICAL. By John F. Bailey. May 18, 2022:

Last Sunday, as America became aware of the formula crisis when the Food & Drug Administration announced it to everyone’s surprise.

One, just one public leader in the entire state immediately suggested a way to do it, Paul Feiner, Town Supervisor of Greenburgh came up with an idea to “find that formula,” in a letter to the public, which WPCNR printed:

“Many parents with babies are stressed because they are having a difficult time getting the formula they need for their child. I would like to help. If you are having difficulty finding a formula your child needs please e mail me at [email protected]. I will be asking student interns and volunteers  to help you find the formula and will also connect you to resourrces that we become familiar. There are formula finder sites  on social media. Will also reach out to medical professionals, other parents and find out if there are substitute formulas that your child can use.”

Two days since that letter appeared, I contacted Mr. Feiner this morning and asked him how the Formula Finding operation has started.

He issued this statement Wednesday morning to WPCNR:

“I have helped a few residents so far -100% success.

In each of the cases I have posted on social media requests for bottles/cans of formula and residents have donated unopened or unused formulas. 

I thought more people would contact me. Have also been posting on the town website advisories on what parents can do if they need a formula. 

Some student interns are working in my office – preparing a fact sheet –listing social media sites parents can access for help.

Also people can contact Amazon Canada and get formulas.

The students are going to interview doctors, nutritionists, host a cable TV show highlighting their findings.  Working on this. Will share their fact sheet when it’s completed.”

For perspective, WPCNR has seen no news conferences on formula availability locally, no information from the state, the county, any Department of Health, doctors organizations, hospitals, or any other towns, pharmacies, food chains in the county, or local stores in either White Plains or any city for that matter, on the state of formula supply in the county.

Where is the urgent information on breast feeding how to get women who are delivering today can use their own breast milk to keep their babies alive, and prepare to do so?

Now I am not a doctor, or even pretend to make medical decisions, but the mothers scheduled to deliver babies in the next two months need to be briefed by their hospitals, delivering doctors and pediatricians (if not already which I automatically assume the moms-about-to-deliver have been briefed) on the need to be able to breast feed their babies for at least 2 months.

Or 3 months because the Food & Drug Administration has given Abbott, the manufacturer of formula 8 weeks to clean up their plant that they closed after the contamination was found.

Reuters Explainer reported Tuesday that once the FDA approves that “initial” requirements have been metanufacturing could begin in two weeks. Peter Pitts of the Center for Medicine in the Public Interest, a former FDA commissioner said after the 2-weeks to reopening, full plant capacity could happen in 4 to 6 weeks.

Peter Pitts, president of the Center for Medicine in the Public Interest and former FDA associate commissioner, said Abbott should be able to meet its two weeks target for re-opening the facility, and expects it to be fully operational in another four-to-six weeks.

No explanation from the NY Times press report Tuesday on why Abbott Laboratories did not start cleaning out the Sturgis, Michigan plant when they closed it in February which manufactures Abbott baby formula, because cronobacter bacteria, from which 4 babies (according to Reuters Explainer yesterday) who had consumed Abbot formula sickened and two died.

Abbot Laboratories has denied that that the cronobacter bacteria was in the formulas the 4 babies consumed, Reuters Explainer chronicled the possible connection that started the recall of Abbott products Similac, Alimentum and EleCare powdered formulas. A specialty liquid formula called Similac PM 60/40 was added at the end of February. Of the four infants found sick, three had cronobacter sakazakii infections, and one Salmonella newport

Consumers reported four infants who were sick, including three with Cronobacter sakazakii infections and one with Salmonella newport, who had been fed formula products made at the Sturgis plant. A fourth infant with cronobacter sakazakii was later added.

Cronobacter sakazakii can cause life threatening sepsis infections or meningitis and may have contributed to the death of two of the infants, the U.S. Food and Drug Administration has said.

Abbott says there is no evidence to link its formulas to these illnesses.

The FDA and the CDC has not put out any information that connects the illnesses and the plant. FDA officials said that the investigation was impeded by having only two of the four sickened babies’ clinical samples.

The CDC analyzed clinical samples from two of the infants and did not find a genetic match to the environmental strains found at the plant. It also said the bacteria from the patient samples were not closely related to one another.

The FDA and Abbott tested environmental and product samples at the plant. They found five environmental samples containing Cronobacter sakazakii. The product samples tested negative.

At this writing there have not yet been reports of such infections or deaths of babies from the Cronobactor sakazakii from products shipped overseas