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Friday, April 26, 2024

Former Meta official releases documentary on Oct. 7 attack

 Former Meta executive Sheryl Sandberg’s new movie on sexual violence that occurred during Palestinian militant group Hamas’ Oct. 7 attack on Israel was released Friday, according to the film’s account on the social platform X.

“After October 7th, the reports were coming out about, not just mass murder, but mass sexual violence, and the usual people who should be speaking out were either ignoring it or denying it,” Sandberg said in an interview with Fox News’ Dana Perino Friday when asked about her motivation behind her participation in the movie, “Screams Before Silence,” in a clip highlighted by Mediaite.

“And, that’s not okay. And this documentary gives anyone a chance to hear directly from first responders,” Sandberg continued.

On an “about” section for the movie’s website, it states that “during the October 7 attacks on Israeli towns and at the Nova Music Festival, women and girls were raped, assaulted, and mutilated.”

“Released hostages have revealed that Israeli captives in Gaza have also been sexually assaulted,” the section reads. 

“Despite the indisputable evidence, these atrocities have received little scrutiny from human rights groups and international organizations,” the section continues. “Many leading figures in politics, academia, and media have attempted to minimize or even deny that they occurred. In Screams Before Silence, a 60-minute, presenter-led documentary film, Sheryl Sandberg, former [chief operating officer] of Meta and founder of LeanIn.org, interviews multiple eyewitnesses, released hostages, first responders, medical and forensic experts, and survivors of the Hamas massacres.”

A United Nations special group focused on sexual violence has found “clear and convincing information” that Hamas committed rape and sexualized torture during its deadly attack on Israel in October of last year. 

“Based on the information it gathered, the mission team found clear and convincing information that sexual violence, including rape, sexualized torture, cruel, inhuman and degrading treatment has been committed against hostages and has reasonable grounds to believe that such violence may be ongoing against those still held in captivity,” the U.N. special group said in a press release.

https://thehill.com/homenews/media/4625195-former-meta-official-releases-documentary-on-oct-7-attack/

'Google’s Plans to Combat Misinformation Ahead of the E.U. Elections'

 “We are all at risk of manipulation online right now.”

So begins a short animated video about a practice known as decontextualization and how it can be used to misinform people online. The video identifies signs to watch out for, including surprising or out of the ordinary content, seemingly unreliable sources, or video or audio that appear to have been manipulated or repurposed.


Though it may not look like it, this 50-second video is actually an election ad—one of three that Google will be rolling out across five European countries next month in advance of the European Union’s June parliamentary elections. But unlike traditional election ads that are designed to persuade people how to vote, these are seeking to educate voters about how they could be misled. It’s an initiative that Google describes as preventative debunking—or, more simply, “prebunking.”

“It works like a vaccine,” Beth Goldberg, the head of research at Google’s internal Jigsaw unit, which was founded in 2010 with a remit to address threats to open societies, tells TIME. By enabling prospective voters to recognize common manipulation techniques that could be used to mislead them—such as scapegoating or polarization—Goldberg says that prebunking “helps people to gain mental defenses proactively.”


Concerns about AI-generated disinformation and the impact it stands to have on contests around the world continues to dominate this year’s election megacycle. This is particularly true in the E.U., which recently passed a new law compelling tech firms to increase their efforts to clamp down on disinformation amid concerns that an uptick in Russian propaganda could distort the results.

Contrary to what one might expect, prebunking ads aren’t overtly political nor do they make any allusions to any specific candidates or parties. In the video about decontextualization, for example, viewers are shown a hypothetical scenario in which an AI-generated video of a lion set loose on a town square is used to stoke fear and panic. In another video, this time about scapegoating, they are shown an incident in which a community lays sole blame on another group (in this case, tourists) for the litter in their parks without exploring other possible causes. 

The beauty of this approach, Goldberg notes, is that it needn’t be specific. “It doesn’t have to be actual misinformation; you can just show someone how the manipulation works,” she says, noting that keeping the content general and focusing on manipulation strategies, rather than the misinformation itself, allows these campaigns to reach people regardless of their political persuasion.

While Google’s prebunking campaign is relatively new, the tactic is not. Indeed, the concept dates back to the 1960s, when the social psychologist William McGuire sought to understand people’s susceptibility to propaganda during the Cold War and whether they could be defended against it. This culminated in what McGuire called “inoculation theory,” which rested on the premise that false narratives, like viruses, can be contagious and that by inoculating people with a dose of facts, they can become less susceptible. But it wasn’t until decades later that the theory began being applied to online information. In recent years, Jigsaw has conducted prebunking initiatives in Eastern Europe and Indonesia. Its forthcoming European campaign, which formally kicks off in May, will primarily be disseminated as short ads on YouTube and Meta platforms targeting voters in Belgium, France, Germany, Italy, and Poland. Afterwards, viewers will be invited to take a short, multiple-choice survey testing their ability to identify the manipulation technique featured in the ad.


Whereas prebunking doesn’t necessarily face as much resistance as more conventional forms of combating misinformation such as fact checking or content moderation, which some critics have likened to censorship, it isn’t a panacea either. Jon Roozenbeek, an assistant professor in psychology and security at King’s College London who has spent years working with Jigsaw on prebunking, tells TIME that one of the biggest challenges in these campaigns is ensuring that the videos are captivating enough to hold viewers’ attention. Even if they do, he adds, “You can’t really expect miracles in a sense that, all of a sudden after one of these videos, people begin to behave completely differently online.” he says. “It’s just way too much to expect from a psychological intervention that is as light touch as this.”

This isn’t to say that prebunking doesn’t have an impact. In previous campaigns, post-ad surveys showed that the share of individuals who could correctly identify a manipulation technique increased by as much as 5% after viewing a prebunking video. “We’re not doubtful that the effect is real; it’s just you can argue over whether it’s large enough,” Roozenbeek says. “That’s the main discussion that we’re having.”


While Jigsaw has led the way on prebunking efforts, they’re not the only ones utilizing this approach. In the U.S., the Biden administration has sought to counter Russian disinformation in part by declassifying intelligence forecasting the kinds of narratives that it anticipated the Kremlin would use, particularly in the run up to Moscow’s 2022 full-scale invasion of Ukraine. This practice has since extended to China (where the U.S. government used declassified materials to forecast potential Chinese provocations in the Taiwan Strait) and Iran (the U.S. declassified intelligence claiming that Tehran had transferred drones and cruise missiles to Houthi militants in Yemen that were being used to attack ships in the Red Sea). What the White House has billed as strategic declassification is just prebunking by another name.

Working with academics and civil society organizations across the E.U.’s 27 member states, Jigsaw’s latest prebunking campaign is set to be its biggest and most collaborative effort yet. And in an election that will see hundreds of millions of voters go to the polls to elect what polls project could be the most far-right European Parliament today, the stakes couldn’t be higher.


https://time.com/6970488/google-jigsaw-eu-elections-misinformation-prebunking/

California’s Single-Payer Health Insurance Dream Remains a Fantasy

 The state Assembly’s Health Committee advanced Assembly Bill 2200 this week. The bill would ban private health insurance and force all state residents into “CalCare,” a government-run health plan. Nine Democrats voted aye, four Republicans voted no, and three Democrats abstained. 

The measure now heads to the Appropriations Committee. But AB 2200’s odds of becoming law are still long. The state simply can’t afford the hundreds of billions of dollars it would cost each and every year. 

That’s a good thing, because single payer invariably results in long waits for subpar care.

Single payer has been a hobbyhorse of California Democrats for years. In 2017, the California Senate gave the thumbs-up to a similar single-payer bill. But then-Assembly Speaker Anthony Rendon refused to move it forward in his own chamber, because the law had no mechanism to cover its staggering $400 billion annual price tag. In 2022, another single-payer bill died in the Assembly before it could go to a vote. 

We’re experiencing déjà vu all over again. Assembly Speaker Robert Rivas recently expressed “concern” about the state’s ability to pay for AB 2200, especially given that California currently faces an estimated $73 billion budget deficit.  

The funding plan for AB 2200 is fantasy. The bill’s supporters are banking on a waiver from the federal government that would allow the state to divert all the money it uses for Medicare and Medicaid into this new “CalCare” scheme.

It’s highly unlikely Washington would accede to such a request. Even if it did, AB 2200 would still require a raft of tax hikes on businesses and households across the state. Prior efforts to impose single payer have proposed new gross receipts taxes on business revenues, payroll taxes on employers, and much higher marginal tax rates on households. 

Two years ago, the projection was that state tax revenue would have to double — and the average household’s taxes would soar by $12,250.

According to a new study from my Pacific Research Institute colleague Wayne Winegarden, such tax increases would have dire economic ramifications. Just five years after implementation, single payer would cause California’s economy to be nearly 3% smaller and have 332,000 fewer jobs than otherwise expected. Average household incomes would be $1,200 lower.

Democratic Assemblywoman Pilar Schiavo commented during the hearing that it’s really not debatable today that single payer saves money. She apparently has some reading to do.

Then there’s the devastating impact single payer would have on patients. One need only look to Canada and the United Kingdom to see what government-dominated health care looks like in practice. 

The median wait in Canada for specialist treatment following referral by a general practitioner is more than six months. As of January, nearly 7.6 million people in England were on waiting lists to see a doctor. 

To keep a lid on costs, CalCare would slash reimbursement rates for physicians. That would prompt doctors to flee to other states. Democratic Assemblywoman Akilah Weber, a medical doctor, expressed concern that the bill’s payment rates would not be sufficient to keep doctors in California — or attract new ones. “We already have a provider shortage, and if we don’t do this correctly, we’ll just worsen that,” Weber said.

Speaker Rivas seems to understand all this. He’s called single payer a “tough, tough sell, especially in a budget climate that we are experiencing now.” 

The Assembly Appropriations Committee will eventually have to acknowledge that math. So the political conventional wisdom is that the Appropriations Committee will be the end of the line for single payer this time.

Under this scenario, AB 2200’s progressive supporters will still get to crow that they are fighting for single payer. Establishment Democrats — including Gov. Gavin Newsom — won’t have to take a position on a controversial bill during an election year. 

The losers, of course, are ordinary Californians, who can be forgiven for wondering why their elected officials are wasting time on pipe dreams like single payer — rather than addressing things that actually affect their lives, like the state’s high cost of living and lack of affordable housing.

Sally C. Pipes is president, CEO, and Thomas W. Smith Fellow in Health Care Policy at the Pacific Research Institute. Her latest book is False Premise, False Promise: The Disastrous Reality of Medicare for All (Encounter 2020). 

https://timesofsandiego.com/opinion/2024/04/25/californias-single-payer-health-insurance-fantasy-is-turning-to-ashes/

How to Discipline Health Care Costs

 Health care presents unique challenges to elected officials. Without some public regulation, market failures will lead to consequences many voters would find unacceptable, as Kenneth Arrow explained long ago in a seminal essay. Among the problems that inevitably arise is the collision of risk aversion among consumers, which leads them to seek insurance protection against expensive medical services, with the ability of insurers to steer clear of potential customers who can be identified as high risks because of their health conditions. Without governmental intervention, the market will drift toward restricted access to care for the very sick. Public regulation and subsidies are the tools all countries use, including the US, to address this unavoidable problem.

But these challenges in the market do not mean that the only viable system is one based on full governmental control, which itself carries risks owing to the predictable failings of regulations written and overseen by politically sensitive officials. Advanced economies have tended toward strong centralization but many are not monolithic. There is room in some of them, such as in Germany and Switzerland, for non-governmental institutions to play significant roles too.

The US occupies a unique position on this policy spectrum. None of its peer countries allow as much space as the US for private insurance and privately-owned systems of care provision to engage directly with consumers and patients beyond the reach of full public regulation. Even so, the US does not have a “free market” for medical services, as critics so often state incorrectly. There is substantial regulation, and hefty public subsidization too. The result is best seen as an unruly public-private non-system with requirements written based on changing historical conditions and no overall plan guiding their evolution.

At the center of this complex mix of federal and state programs and regulations is a vast network of hospitals, physician practices, nursing homes, and other institutions that are both highly skilled and technically competent and thus capable of world-class care. But its fragmentation and complexity also lead to excessively burdensome costs, paid through high premiums and expensive public programs. For years, the US has spent far more on health care than any other high-income country, as documented by data compiled by the Organization for Economic Cooperation and Development (OECD). In 2022, the US spent 56 percent more than the next highest-spending country—Switzerland.

The heavy burden these costs impose is the principal failing of the US system and the one that still needs to be addressed in a coordinated fashion. The challenge is to create new structures that inject durable cost discipline into the provision of medical services without eroding their quality and timeliness. That should be possible as studies show that much of the high-cost burden is associated with irrational pricing in some settings, frequent occasions when services are rendered to patients despite scant empirical evidence of their efficacy, and heavy administrative overhead and maddening levels of paperwork.

There is an opportunity here for proponents of a market-oriented solution to show they have a plan for attacking this problem, but they need to frame the debate properly in order to win it. What’s needed is not one-off ideas but a system change that incentivizes continuous productivity and quality improvement in the processes governing patient care. Market proponents must convince voters such a system change is more likely to occur with their ideas and not with more centralized government control. It is a tall challenge, but not an impossible one.

What’s at Stake?

The provision of medical services to patients in the US is conducted mostly by privately-run hospitals, physician practices, labs, clinics, and diagnostic centers. It is an uncoordinated system operating without the guidance of a coherent overarching plan. While its default setting is to deliver high-quality care, exorbitant bills are also the norm, as fees are set without any apparent connection to the marginal costs of providing the services, as would be the expectation in a functioning market. Patients are also on the receiving end of substandard care in far too many instances, owing to gaps in coordination among those providing services and the inaccessibility of care in some circumstances.

Despite a plethora of potential targets for cost-cutting, easing this burden has proved elusive. A major obstacle is the difficulty of separating what is wasteful and expendable from the essential. Without processes capable of making such careful distinctions, cost-cutting risks eroding the quality of care provided to patients.

An additional problem is the misidentification of the core challenge. Some opponents of a stronger governmental role believe the solution is the easing of rules that would allow healthier individuals to buy less expensive insurance. Lowering their premiums, however, often means higher costs for those with pre-existing conditions, not a lowering of the overall bill. While some steps in insurance deregulation might be helpful, the primary forces driving high costs are the expenses incurred by major health systems delivering services to patients. To put a real dent in costs, these mega-systems must become more efficient on a continuous basis. As in other markets, innovations that lead to new ways of providing services at less cost would deliver substantial societal benefits by lowering the total cost burden without harming the quality of care provided to patients.

The primary mission for policymakers is thus devising reforms that lead to a continuous search for more efficiency and higher productivity in the provision of services to patients. Market interventions that lead to such improvements are not the strong suit of government regulators. Consequently, there is an opportunity here for market advocates to make their case.

The Government’s Options

Over the past decade, the imperative to improve the efficiency of the nation’s entire network of medical care institutions has led the government to attempt a re-engineering of the system based on a vision the government itself developed.

Falling under the heading of “value-based” payment reforms, the federal government has encouraged hospitals and physician groups to form new entities dubbed “accountable care organizations,” or ACOs, which are said to have the potential to deliver better care at less cost by eliminating unnecessary expenses.

The exact channel for the efficiency improvements of ACOs has been harder to pinpoint but the idea is that the government can incentivize a transformation by using its regulatory powers to reward those ACOs capable of meeting the government’s cost and quality objectives. Successful ACOs get bonus payments. The government is also running a series of experiments to test other cost-cutting models.

After a decade of experimentation, the evidence is thin to non-existent that the government has found the right formula. As is often the case with regulatory initiatives, it is hard to write nationwide rules that work in all markets, or which are nimble and flexible enough to provide room for entrepreneurial initiative. Some ACOs show promise, but most exist to help hospitals and physician groups maximize their revenues without fundamentally changing their business plans. Further, the rules tend to cater to incumbents and the protection of their financial viability at the expense of truly innovative but also disruptive competitors.

Disappointment with existing results is leading to renewed interest in policy levers that are more clearly within the government’s competence—price controls. Beginning in the 1980s, the federal agency running the Medicare program developed regulations for various categories of services that set payments based on numerous sources of data, such as historical costs and other measures of expected expenses for the inputs of patient care. Providers of covered services are required to accept these payments in full when agreeing to be participants in the Medicare program.

Proponents of a strong federal role in cost control want to extend the reach of these payment rules to the commercial setting, and thereby dramatically lower the cost burden in private insurance. It is well documented that many commercial insurance plans pay rates for services are far above what Medicare pays for its enrollees. For instance, several recent studies have shown that commercial insurance plans pay, on average, more than double what Medicare does for inpatient hospital care.

What’s more, price setting by the government polls extremely well, with large bipartisan majorities expressing support for aggressive action by Congress. If the federal government were to step in and cap what hospitals can charge, it would meet with little resistance among the patients needing these services.

The allure of public price-setting beyond Medicare is what animates the drive to set up a new “public option” health insurance plan to compete with private offerings. Several states—including Washington and Colorado—are experimenting with tying certain private plans with publicly-determined rates for services and calling it a public option.

Of course, hospitals fiercely object to having all of their rates capped by government rules, as do physicians who would face cutbacks similar to those that would occur for hospitals if Medicare’s fees were extended to all commercial insurance. Further, the regulations required to make public option plans viable risk driving away private insurers that are attentive to their bottom lines. Opposition from these industries and other providers of services is the principal reason public option plans are still not approved in most states and have not been approved by Congress either.

While government-determined price caps are guaranteed to lower costs for consumers, it does not necessarily follow that they will lead to the more efficient provision of care. For instance, providers of services might respond to price caps by simply reducing their expenses on an indiscriminate basis so as to not offend their internal constituencies. Rethinking their workflows to cut unnecessary outlays is harder work than across-the-board cuts and the added effort does not necessarily lead to better market outcomes because total revenue for these entities will be determined more by government rules than by consumer preferences.

Further, once in place, government price caps become tempting targets for further budgetary savings. In Medicare, physician fees have been cut repeatedly for three decades in response to budget pressures, to the point that they are now 40 percent below the average fees paid by commercial plans. It is easier politically to cut fees for providers of medical services than it is to raise taxes or ask patients to pay more for the care they receive.

The cumulative effects of such cuts in fees can lead to access problems for patients, as has been observed in many other countries with fully nationalized systems. The wait lists in the UK are a direct consequence of running the entire budget for the health system through a political process. The same problem manifests itself in Canada too even though the providers of services are not owned and staffed by the central government. It is an unavoidable reality of price setting that the supply of the affected services tends to fall when the revenue for the industry comes under the full control of the government.

A Structured Market

The alternative to stricter payment controls enforced by the government is a market with rules designed to incentivize the reengineering of care processes to eliminate unnecessary expenses. The providers most successful at improving their productivity would be able to offer lower prices to customers, which, with the right rules, could lead to growth in their market shares.

There are two key considerations when structuring these markets: standardization of the products and services, and strong financial incentives for consumers to select lower-priced options. Neither condition exists in the US today.

Standardization is critical because health care is so complex that variation obscures pricing differences. For instance, a consumer will find it nearly impossible to identify the lowest-priced option for a surgical procedure if the prices cited by the competing surgeons vary by whether or not the anesthesia and radiological services are included or excluded from them. With standardized bundles set by government rules, providers would have to disclose what they would charge for their services in a market that would allow consumers to compare the offerings on an apples-to-apples basis. The highest-priced providers would have trouble explaining why they are outliers.

The other crucial ingredient is an incentive for the consumer to want to use lower-priced providers of services. For instance, if a surgeon charges $1000 less than a competitor in the same market, patients must share in the savings when they opt for the lower-priced provider. Otherwise, there would be no incentive for the affected surgeons to offer competitive prices as doing so may or may not lead to higher volume and more revenue.

The benefits of writing such rules for the market are not mysterious or unknown, as they have been revealed by various targeted experiments over the years. When a large California-based purchasing system imposed standardized pricing requirements on surgeons offering joint replacement procedures, and then also built strong consumer incentives into the model to encourage migration to lower-priced options, the savings were immediate and dramatic, with patient volume dropping at high-priced providers by more than a third and rising at lower-priced alternatives by more than 20 percent.

These same principles also work when consumers are selecting insurance plans. With standard offerings, and incentives to migrate to lower-premium plans, insurers would have strong incentives to build provider networks that offer high-quality services with the lowest possible prices.

Making the Case

The provision of medical care to patients now accounts for about 20 percent of the US economy. One way or another, the financial burdens this sector imposes on consumers need to be disciplined so that scarce resources that could be used for other purposes, such as housing or educational advancement, are not wasted on over-priced and low-value health care.

The only question is what intervention will be chosen to bring about this discipline.

For many decades, there has been a steady movement toward federal control of the US health system. Public subsidies have grown, as have the rules restricting what is and is not allowable among those providing services to patients. It is not hard to imagine Congress taking the final steps toward full price regulation of the entire system, by extending the rules already embedded in Medicare to the commercial market. Once Congress makes such a choice, it will not be reversed quickly or easily or perhaps ever.

For those who might be concerned about the US adopting a health system under full federal control, they must coalesce around a viable alternative. Market discipline is possible but only with rules that make it clear to all concerned who is offering the best value to patients, and who is not, and then rewarding those providers who have done the hard work to become more productive and efficient over time.

Without the presentation of such an alternative, the endpoint for US health care is clear. The only uncertainty is how long it will take to get there.

James C. Capretta is a senior fellow at the American Enterprise Institute and the author of US Health Policy and Market Reforms: An Introduction, published by AEI Press in 2022.

https://lawliberty.org/how-to-discipline-health-care-costs/

H5N1 update: We have to do better, faster

 H5N1—also known as bird flu—continues to spread among animals and, for the first time, is spreading among cows. Thankfully, the risk to the public is low, but the more the virus spreads, the more chances it has to mutate and jump species to spread among humans. Given H5N1’s high mortality rate, we don’t want this to happen.

This outbreak is concerning; unfortunately, communication and data transparency have been profoundly lacking. We must do better and faster — repeating the same communication mistakes that fueled confusion, distrust, and misinformation during Covid-19 is inexcusable. 

Here’s what we do and don’t know about H5N1.

This post builds off previous YLE updates of the current cow outbreak. To get up to speed, start here.

H5N1 continues to spread among animals

H5N1 been detected among 33 dairy cattle herds in 8 states. The virus is spreading through multiple known pathways: wild bird → cow; cow → cow; cow → poultry, and once from cow → human. Thankfully, there is currently no evidence of human-to-human transmission.

How big is the “true” outbreak? We don’t know. Symptomatic testing of animals and humans is voluntary, and asymptomatic testing is not happening (likely due to industry pressure), which means we are flying blind. It’s been reported that more workers have symptoms — such as fever, cough, and lethargy — but are unwilling to test. We could have more human cases. Among the tests conducted, it’s unclear how many have been done, how many were positive, and how many humans have been exposed.

Two positive updates:

  • There is a federal rule for moving cows now. As of yesterday, the federal government requires testing all lactating cows before moving across states. Finally! Unfortunately, it’s likely too late to contain transmission.

  • Pigs have been testing negative. This is good news. Pigs are dangerous hosts for H5N1 because they have avian and human receptors. They are known as “mixing vessels” for influenza viruses.

The outbreak is much larger and started earlier than we thought.

We don’t know how big the outbreak is from physically swabbing animals and humans, but two clues suggest this has been spreading under our noses for a while: 

  1. Clue #1: The FDA found H5N1 fragments in the milk supply. This was surprising because milk from known infected cows was not going to the market. This confirms that the cow outbreak is bigger than previously known.

    Thankfully, milk pasteurization should deactivate any bird flu that makes it into the milk supply. Scientists confirmed this yesterday: they could not grow active virus from the milk samples. This means the virus fragments detected in milk were broken pieces that cannot replicate and, thus, cannot harm humans. The FDA is testing more samples just in case. Thus far, the public has seen no data.

  1. Clue #2: Genomic surveillance can tell us how, where, and when H5N1 mutates. After being reluctant to share genetic data, USDA finally shared 239 viral sequences from animal infections. However, the data was incomplete—the date and location of the sample collection were not included, making it difficult to answer key questions about how the virus has changed over time and, therefore, predict where it might end up. 

    Also, there was no mention of what USDA scientists found with this data internally. We’ve relied on scientists on social media to walk through what they found after analyzing the raw data, which suggests an estimated spillover to dairy cows starting in December.

Wastewater is spiking. Is it H5N1?  

Some on social media discovered wastewater spiking in some places with infected herds. For example, in Amarillo, Texas, wastewater is skyrocketing for flu A while the rest of the state remains low. 

Could this be H5N1? Yes, but we don’t know for sure; the government has not officially shared anything about wastewater. This is incredibly disappointing, given this is the perfect use case for wastewater monitoring.

While we don’t have a wastewater test for H5N1 yet, it has many similarities to flu strain A. Some wastewater systems include human wastewater and stormwater. Given that Amarillo has stockyards, this strengthens the possibility that it’s H5N1, especially since we aren’t seeing it in other parts of the state. The most likely scenario? The spike is from milk dumping or animal sewage. We need more data.

The tools work, but…

The U.S. government has confirmed that Tamiflu and the stockpiled H5N1 vaccines are predicted to have efficacy if this does move to humans. This is great news. And I agree there shouldn’t be panic. But I caution leaders against the “we’re fine, we have vaccines” attitude.

  • What about manufacturing and supply?

  • What about the rest of the globe?

  • What about vaccine hesitancy?

  • And decline in trust?

  • And access problems?

Of course, fully relying on vaccines and overconfidence were among the big mistakes of the Covid-19 emergency. As one of our colleagues wrote, “It’s best to face these threats with humility and determination.”

A communication void will be filled with confusion, mistrust, and misinformation

Information from the response has not been easy to find, has not been complete, and has not been backed with data, leaving many of us to piece together a fuzzy picture. 

This is a big problem for many reasons:

  1. Misinformation brews in information voids. People, rightfully so, have questions and can’t find answers.

  2. Trusted messengers don’t know what’s going on. During an outbreak, top-down, credible, and consistent communication is necessary. Equally important is actively equipping trusted messengers—mass media, scientists, physicians, and community leaders—so they can communicate from the bottom up.

  3. Tools could be at risk. For example, wastewater surveillance is one of the only tools that wasn’t weaponized during Covid-19 emergency. My biggest concern is that if we aren’t transparent—walking the public through what we are and are not doing with wastewater—people will become hesitant about this surveillance.

  4. Chips away at credibility. Although brilliant scientists are within each agency, their expertise isn’t shining through.

  5. Harming global capacity to respond. This is an emerging global pandemic threat. Other countries need to know, for example, if they should start testing their cows. If they should be looking for mutations, and where. 

We need a coordinated response from our government. Yes, there are multiple players involved. And yes, they have their own priorities, legal authorities, agility, experience, and politics. However, honest, frequent, direct communication earns the public’s trust and confidence. If not, communities are starved for good information during outbreaks or emergencies, leading to unnecessary anxiety, confusion, and frustration. 

After much pressure, government agencies finally hosted a live briefing for the media yesterday. This is a positive step in the right direction and, I hope, a sign that the winds are changing.

Bottom line 

Responses need to get better faster. H5N1 is a dangerous disease that can affect our economy, food security, and animal and human health. This response has been incredibly difficult to watch on the heels of Covid-19 (and mpox and other emergencies like the East Palestine train accident). We get just so many “practice runs” before it starts costing lives again.

Love, YLE and Dr. P


“Your Local Epidemiologist (YLE)” is written and founded by Dr. Katelyn Jetelina, M.P.H. Ph.D.—an epidemiologist, wife, and mom of two little girls. During the day, she is a senior scientific consultant to several organizations, including CDC. At night, she writes this newsletter. Her main goal is to “translate” the ever-evolving public health world so that people will be well-equipped to make evidence-based decisions. 


https://yourlocalepidemiologist.substack.com/p/h5n1-update-we-have-to-do-better