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Friday, October 7, 2022

FedEx Features AditxtScore™ Immune Monitoring Center and its Service in Richmond, VA

 Aditxt, Inc.’s (NASDAQ: ADTX) ("Aditxt", or the "Company") AditxtScore™ is featured by FedEx in a video presentation that showcases the various ways in which both companies are playing critical roles in a challenging environment that includes the nation’s response to COVID-19.

In the clip, the Aditxt team provides a virtual tour of its AditxtScore™ Center, while describing how the Company works with scientists and technicians to process samples from around the country to help physicians and health care professionals identify and understand their patients’ immune status.

Blood specimens from physicians, clinics, and hospitals are delivered by FedEx in a system that relies on speed, precision, and attention to detail. AditxtScore chose to work with FedEx based upon a track record of timely delivery, since maintaining the stability of each sample is critical to the Company’s business.

Aditxt then processes the samples using proprietary technologies and generates a personalized profile of the individual’s level of immune response to the COVID-19 virus or vaccine.

https://finance.yahoo.com/news/fedex-features-aditxtscore-immune-monitoring-130000264.html

Biden’s Medicaid plans will send the program completely off the rails

 Medicaid is on the verge of becoming the most broken welfare program in American history. President Joe Biden is moving forward with three dangerous policies that will further undermine its already-shaky integrity and even expand it into housing, food and climate change. State leaders and Congress must fight to restore Medicaid to its mission of protecting the health and well-being of the truly needy.

The most immediate threat comes from Biden’s three-month extension of the COVID public-health emergency, which was set to expire Oct. 13. So long as the emergency is in effect, states receive added Medicaid funding on the condition they don’t cut ineligible recipients from the rolls.

As I show in a new paper, Medicaid could swell to 100 million enrollees by January, or nearly a third of America’s population. Yet at least 21 million are ineligible, and that number will only rise. Taxpayers are spending $16 billion per month on ineligible recipients, a high cost that grows higher by the day.

The emergency is set to expire in January, but it’s possible if not probable Biden will extend it again to keep as many people on Medicaid as possible. (He’s already extended it several times, despite stating early this year that normal life could resume and saying last month, “The pandemic is over.”)

Even if he lets the emergency end, his administration wants states to take well over a year to remove ineligible enrollees. In all likelihood, the president will keep finding ways to keep people on Medicaid who shouldn’t be.

Which leads to the second policy Biden is pushing. In August, his administration proposed a rule that in the name of improving “retention” would make it much harder to identify ineligible enrollees. The Centers for Medicare and Medicaid Services wants to ban states from conducting in-person interviews to determine program eligibility. States rely on these interviews precisely because they make it easier to identify waste and fraud. The Biden administration also wants to limit the information states can request from Medicaid recipients, making it more difficult to discover if they’re ineligible while reducing the frequency of eligibility reviews.

What’s more, Team Biden is trying to force states to help ineligible enrollees find different coverage before removing them from Medicaid. That will add such an intense administrative burden to cash-strapped state governments that they’ll likely avoid the hassle of removing ineligible people altogether. (Hilariously, the rule claims to help reduce “administrative burden.”) If this rule moves forward, the Biden administration will end any serious attempt at program integrity, even though Medicaid is already rife with abuse and on the fast track to insolvency.

Finally, the Biden administration is pushing Medicaid far beyond its purpose. Last month, the Centers for Medicare and Medicaid Services approved unprecedented waivers for Massachusetts and Oregon. Both states can now use scarce Medicaid dollars to pay for enrollees’ food and housing, on the grounds that such issues influence health outcomes. That’s not what Congress created Medicaid to cover.

The situation is laughably bad in Oregon. The federal government is letting the state spend Medicaid money on things like air conditioners and air filters. Why? Because those items help residents deal with climate change, and climate change purportedly affects individual health.

These waivers are all the more extraordinary since the Biden administration refuses to grant state waivers that get Medicaid recipients into work and eventually off the program. This White House would rather use Medicaid to address “extreme weather” than promote employment, which has proven health benefits, from mental health to lower mortality.

None of Biden’s Medicaid policies should be allowed to stand. Medicaid already dominates state budgets, with nearly $1 out of $3 spent going to the program. To remove ineligible enrollees and protect taxpayers, governors should immediately opt out of the extra funding provided under the public-health emergency. Doing so will allow states to begin cleaning up their Medicaid rolls instead of waiting, potentially indefinitely, for the federal government to untie their hands.

Meanwhile, Republicans and sane Democrats in Congress should push for policies that prevent the Biden administration from gutting state eligibility reviews. They should also seek to restrict state Medicaid waivers to direct health issues. Such measures should make their way into must-pass laws, thereby overcoming the threat of a Biden veto.

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The alternative is to let Medicaid break to the point of irreparability. It’s already too close.

Sam Adolphsen, a former chief operating officer at the Maine Department of Health and Human Services, is policy director at the Foundation for Government Accountability.

https://nypost.com/2022/10/06/bidens-medicaid-plans-will-send-the-program-completely-off-the-rails/

Electric vehicles catching fire in Florida after Hurricane Ian

 Electric car owners have seen their rides catch fire after becoming waterlogged during Hurricane Ian and it can take hours to put the conflagrations out, a top Florida official warned Thursday.

As the Sunshine State recovers from the punishing Category 4 storm that made landfall last week, first responders have faced further destruction from electric vehicles that were submerged in water from the extensive flooding and later caught fire, Jimmy Patronis, Florida’s chief financial officer and state fire marshal, said on Twitter.

“There’s a ton of EVs disabled from Ian,” he tweeted. “As those batteries corrode, fires start.

“That’s a new challenge that our firefighters haven’t faced before. At least on this kind of scale.”

Firefighters are shown extinguishing a fire on a white Tesla.
Electric vehicles could catch fire after Ian devestated Florida, a top official said.
JimmyPatronis/Twitter
The car fire took hours to put out, officials said.
The car fire took hours to put out, officials said.
JimmyPatronis/Twitter

In his tweet, Patronis posted a video of firefighters with the North Collier Fire Rescue District in Naples putting an electric vehicle fire out as a bystander is heard saying it’s taken thousands of gallons of water to extinguish it.

“It takes special training and understanding of EVs to ensure these fires are put out quickly and safely,” Patronis tweeted.

Additional footage of the same vehicle fire posted on Facebook by the North Collier Fire Rescue District shows firefighters dousing the car’s top and underbelly with water to eliminate any sparks.

The rescue district said firefighters received the call while Patronis and state Rep. Bob Rommel visited the area. The two state officials were brought to the incident so they could see the difficulty of putting EV fires out and said it took firefighters hours to ensure the blaze was extinguished.

“This is an issue many fire departments across [southwest] Florida are experiencing right now,” the district wrote on Facebook. “These vehicles have been submerged in salt water; they have extensive damage and can potentially be serious fire hazards.”

Florida is only behind California for most electric vehicles on the road at more than 95,000 registered in the state, according to the US Department of Energy. 

Rebuilding from Hurricane Ian is expected to cost billions of dollars, officials have said.

https://nypost.com/2022/10/06/electric-vehicles-catching-fire-in-florida-after-hurricane-ian/

Thursday, October 6, 2022

Rite Aid may place all store items in showcases due to theft in NYC

 Rite Aid is contemplating placing all merchandise in showcases in New York City in an effort to curb retail theft, according to Fox 5 New York. 

In late September, executives at Rite Aid cited "shrink," a term that retailers use to describe theft, as an issue the pharmacy chain is dealing with during the company's quarterly earnings call.  

CEO Heyward Donigan said Rite Aid experienced "unexpected headwinds" from shrink, "particularly in our New York urban stores." 

Company Chief Retail Officer Andre Persaud said the "headline here is the environment that we operate in, particularly in New York City, is not conducive to reducing shrink just based upon everything you read and see on social media and the news in the city."

Rite Aid posted a $331.3 million net loss for the third quarter of fiscal 2022, up from $100.3 million a year prior. Matt Schroeder, Rite Aid's CFO, said during the earnings call that Rite Aid's front-end gross profit was "impacted by a $5 million increase in shrink."

During the earnings call, Persaud noted that Rite Aid has made progress on "improving our product protection, improving our organized retail client program" and stated the drug store chain's goal is to "stay in the communities." 

"We're looking at literally putting everything behind showcases to ensure the product's there for customers who want to buy it," he said.

Other actions Rite Aid has considered include operating a "pharmacy only and as a pharmacy prescription-only format in some of the communities," he said. The company has also placed off-duty police officers in some stores. 

Rite Aid closed locations in New York's Hell's Kitchen and Upper East Side neighborhoods earlier in the year. 

New York Post reporter spotted an instance of alleged shoplifting in January at the Hell’s Kitchen location, where "store sources" told the outlet people have stolen over $200,000 in items over a couple of months. 

Actor and comedian Michael Rapaport said he was at the Upper East Side store in January when he watched someone load a pair of bags full of allegedly stolen items. Video captured by Rapaport showed the alleged thief passing a store security guard as he left holding the bags.

TickerSecurityLastChangeChange %
RADRITE AID CORP.5.22-0.17-3.24%

The stores were closing "for a number of reasons" based on months-long reviews that were carried out "across the full footprint of 2,500 stores," a Rite Aid spokesperson previously told FOX Business. Rite Aid's store closing plan meant the shuttering of over 60 locations across the country. 

https://www.foxbusiness.com/markets/rite-aid-may-put-all-items-showcases-due-theft-new-york-city

Be Alert for Ebola, CDC Says

 While there are no suspected U.S. cases of Ebola, the country needs to be ready for early identification and testing for patients who present with symptoms and have recently traveled to Uganda, where there is an ongoing outbreak, the CDC said on Thursday.

In a Health Alert Network advisory, the agency recommended that clinicians be prepared to consider Ebola virus disease as a differential diagnosis if a patient presents with the symptoms of the disease or viral hemorrhagic fever. Symptoms can include fever, headache, muscle and joint pain, fatigue, loss of appetite, gastrointestinal symptoms, and unexplained bleeding.

If a patient presents with those symptoms, the CDC recommended that clinicians immediately take a travel history and move the patient to a private room for any further clinical evaluation. Clinicians should also contact their local or state health department if a patient is suspected to have the disease, the CDC said.

The agency noted that early recognition and identification of a patient suspected to have Ebola virus disease is critical. This is in part because there is not an FDA-approved vaccine or treatment for the strain of Ebola virus causing the outbreak in Uganda, which is known as the Sudan strain. Ervebo, the only Ebola vaccine approved in the U.S., is indicated for the Zaire strain and is not expected to offer protection from the Sudan strain, according to the CDC.

Clinicians need to be aware of how the disease is transmitted, the agency said. For example, a person is not contagious until symptoms appear. The Sudan virus is not spread through airborne transmission but spreads through direct contact with the body fluids of a person who is sick with or has died from the disease.

Since 2000, there have been five Ebola outbreaks involving the Sudan strain in Uganda, including the current outbreak.

Uganda's latest outbreak was officially declared by its Ministry of Health on September 20. The first confirmed case was in a 25-year-old man who was diagnosed with viral hemorrhagic fever and died the day prior -- his blood tested positive for the Sudan strain of the Ebola virus.

The patient's death prompted an investigation that revealed "a cluster of unexplained deaths" over the previous month in the nearby community. So far, the CDC said, there are 44 confirmed cases of Ebola in total in Uganda, and 10 confirmed deaths along with 20 probable deaths.

As of October 6, no suspected cases of Ebola related to this outbreak have occurred outside of Uganda, where the outbreak is limited to regions away from Kampala, Uganda's capital, and the travel hub of Entebbe.

The CDC noted that Thursday's alert and recommendations were issued as a precaution, and that the agency is communicating with U.S. public health departments, laboratories, and healthcare workers to raise awareness of this outbreak.

Even though there are not direct flights between the two countries, the U.S. embassy in Uganda announced that all U.S.-bound travelers who have been to Uganda in the previous 3 weeks would be redirected for enhanced screening to one of five designated U.S. airports: John F. Kennedy International Airport in New York City; Newark Liberty International Airport in New Jersey; Hartsfield-Jackson Atlanta International Airport; Chicago O'Hare International Airport; or Dulles International Airport in Washington, D.C.

https://www.medpagetoday.com/infectiousdisease/ebola/101101

Experts Grapple With New Reality: Polio May Never Be Eradicated

 The global endgame for polio has long been eradication, but recent events in the U.S. and around the world have raised questions about whether that lofty goal can be achieved, poliovirus experts say.

In 1988, the World Health Organization (WHO) adopted a resolution for global eradication of poliomyelitis, the disease caused by both wild type and, in rare cases, vaccine-derived poliovirus (VDPV). The goal was to do so by 2000, and early reports from the CDC suggested that public health workers were making quick progress. Globally, the number of reported cases of poliomyelitis dropped by 70% from 1988 through 1993 -- and the driving force of success was the oral poliovirus vaccine (OPV).

Yet, 22 years after that target date, poliovirus is still showing up in communities around the world. In July, the CDC confirmed a well-documented case of polio paralysis in an unvaccinated man in New York state. There have also been several instances of detection of VDPV in wastewater in New York and the U.K.

And wild poliovirus -- once thought to be isolated in Pakistan and Afghanistan -- was detected in Mozambique and Malawi earlier this year, two countries in a global region that was certified as polio-free as recently as 2020.

This global resurgence has experts grappling with a new reality, one where countries all over the world must maintain high rates of vaccination and hope that VDPV does not result in the rare case of paralysis, according to Vincent Racaniello, PhD, a virologist at Columbia University in New York City.

"We can eradicate polio, the disease, as long as we keep immunizing, and achieve greater than 90% immunization rates," Racaniello told MedPage Today. "Note that the original goal of eradicating polio was linked to cessation of polio vaccination. However, as long as strains of poliovirus circulate in any country, it is not possible to stop immunizing."

Oral Polio Vaccine Paradox

Paradoxically, eradication has remained out of reach for the same reason that rates of poliomyelitis have decreased -- because of OPV.

"I doubt that poliovirus can be eradicated," Racaniello said. "As long as we keep using OPV in some countries, OPV-derived viruses will continue to circulate and pose a threat to any unvaccinated people."

While OPV was pivotal in the early efforts to eliminate poliomyelitis, it has now become one of the primary reasons experts like Racaniello say vaccination efforts against polio can't be eased. OPV contains a live, attenuated poliovirus that is designed to live harmlessly in a person's intestinal tract, but this strain can mutate and revert to a version of the virus (VDPV) that can cause poliomyelitis in individuals who are not vaccinated. While this mutation occurs as rarely as once in approximately 3 million cases, it presents enough of a risk that polio vaccination can never be eased while it is in use.

This OPV paradox is one reason that the U.S. has exclusively used the injectable poliovirus vaccine (IPV) since 2000, which only contains the inactivated poliovirus. Concern over the limitations of OPV have led many experts, including those at the WHO, to recommend a switch to IPV globally.

"The U.S. would certainly be able to help expand the use of IPV globally," Racaniello said. "It is not easy. Not only would production need to be ramped up, but sterile needles would need to be supplied as well as trained healthcare workers to use them. It is my understanding that WHO would like to globally switch to IPV after 2026."

The turn to IPV has not been a panacea for poliovirus in the U.S., though. IPV is made up of three poliovirus serotypes. It provides protection against paralysis in individuals, but it does not prevent infection in the intestines. While any infection would be harmless to someone who's been vaccinated with IPV, the vaccine doesn't prevent further transmission of the poliovirus, according to the CDC.

This means that even after a global switch to IPV, poliovirus will still be capable of circulating through the global population, which will pose a threat of paralysis to unvaccinated individuals.

This is one reason that the CDC also said that immunization efforts must remain the core tool in the push to limit and eradicate poliovirus despite several challenges to those efforts, including low rates of vaccine compliance, difficulty reaching certain communities, geopolitical instability, supply-chain issues, and more recently the COVID-19 pandemic.

"Although challenges remain, it is important to emphasize that the number of polio cases has been reduced by 99.9% in the last three decades thanks to the commitment of frontline staff, affected communities, governments, donors, and partners," a CDC spokesperson told MedPage Today.

Regardless of which vaccine is used, the primary dilemma is still the ability of poliovirus to continue circulating -- but there is a new potential weapon in the this fight to eliminate poliovirus.

A New Tool to Fight Poliovirus

The CDC spokesperson said global immunization campaigns are still "the most effective way to end outbreaks and prevent the emergence of new ones within a community or across borders. When high-quality immunization campaigns and surveillance are coupled with strong government, civil society, and community commitment, we can eradicate polio."

To that end, the agency has been monitoring a new tool that has the potential to untangle the OPV paradox -- the novel OPV2 vaccine (nOPV2), which was designed to be more genetically stable than previous versions of OPV and ideally resistant to reverting to the more transmissible and dangerous VDPV.

It's the latest version in a series of updates to the OPV vaccine that includes the type-2 version of OPV, which the CDC reported was responsible for "approximately 90% of all cVDPV [circulating vaccine-derived poliovirus] outbreaks."

In November 2020, the WHO granted nOPV2 an emergency use listing to be used in response to outbreaks in 2021. According to the CDC, this novel vaccine demonstrated immunization efficacy without leading to mutations that might result in circulating VDPV.

"Based on promising results from clinical trials of nOPV2 and the initial use in the field, the vaccine should prove as immunogenic and more genetically stable than mOPV2 [type-2 monovalent OPV], and therefore be less likely to result in new emergence of variant type-2 polioviruses in under-immunized communities," the CDC spokesperson said.

According to the CDC, over 100 millions doses of nOPV2 have already been administered globally. The CDC also noted that early data suggest that nOPV2 is indeed genetically stable in real-world settings, and therefore might be the solution to limiting much of the VDPV transmission seen around the world.

"At this point, 6 years after the OPV switch to remove Sabin-strain poliovirus type 2, use of nOPV2 is essential to stopping all transmission of vaccine-derived poliovirus type 2 as well as strengthening the effectiveness of nOPV2 campaigns," the CDC spokesperson said.

But experts warn that production and manufacturing challenges have been a hindrance to global vaccination programs, even before the approval of a novel vaccine that can help limit the circulation of VDPV. (See this sidebar on supply-side challenges.)

Polio Endgame Interrupted

Given the nature of earlier vaccines and the evolution of VDPV, global eradication of poliovirus has been challenged from the start. Even the consistent use of IPV for 22 years has not protected the U.S. from poliomyelitis completely, Racaniello said.

"Currently, many people in the U.S. are likely infected with poliovirus, but they have no signs of disease," he said. "We can keep immunizing with IPV and as long as greater than 90% of the U.S. is immunized, we will not have polio the disease, but the virus will still be here."

The CDC maintains that ongoing immunization campaigns will continue to protect the U.S. from outbreaks, and the WHO has begun to push for use of IPV in more counties, according to Racaniello.

Still, he noted that even global adoption of IPV would not necessarily lead to the eradication of poliovirus because people immunized with IPV could still spread VDPV. Even with worldwide use of IPV, Racaniello said, "no one can predict whether these viruses would circulate indefinitely or not."

The inability of current vaccines to eradicate the virus has led the public health community to start considering a new endgame. A review article in The Lancet noted that the "recent surge of polio cases urgently calls for a reassessment of the programme's current strategy and a new design for the way forward."

The authors proposed a plan of "sustainable protection" that focuses on "maintaining high rates of population immunity indefinitely."

This article echoes the language that appears in a WHO paper on the 2018 status of poliomyelitis and the poliovirus, which called for awareness of "the urgent need to accelerate globally activities to implement and certify containment of polioviruses" and to focus on the containment of all polioviruses to "ensure the long-term sustainability of the eradication of poliomyelitis."

Eradicating poliovirus is not the language used by global health leaders. The focus is on containing the poliovirus to prevent the occurrence of paralysis. As Racaniello noted, the reason for this change is the realization that past public health efforts overestimated the ability of both IPV and OPV to achieve eradication.

"Even if all three wild poliovirus serotypes are eradicated, we will still have circulation of vaccine-derived strains of poliovirus in humans," Racaniello said. "We will have simply replaced wild polioviruses with vaccine-derived polioviruses. Therefore, to protect the world's population against paralysis caused by vaccine-derived polioviruses, immunization must continue indefinitely."

https://www.medpagetoday.com/special-reports/exclusives/101054

HHS Outlines Timeline for Medicare Drug Benefits in the Inflation Reduction Act

 The Inflation Reduction Act has a lot of moving parts when it comes to healthcare, but Medicare beneficiaries will start seeing some benefits from it as early as next year, HHS officials said Thursday.

On January 1, 2023, the $35 cap for a month's supply of a covered insulin product in Part D, and the $0 out-of-pocket copay for recommended vaccines goes into effect, Meena Seshamani, MD, PhD, director of the Center for Medicare, told MedPage Today at a press briefing at HHS headquarters here.

That vaccine provision will be a real "game-changer" for beneficiaries who would otherwise have to pay out of pocket for expensive vaccines such as the shingles vaccine, said CMS Administrator Chiquita Brooks-LaSure. "A couple of weeks ago I was with beneficiaries, talking and hearing about what a difference that will make."

On Sept. 1, 2023, Medicare will announce the first 10 drugs whose prices it will negotiate under the Medicare drug price negotiation provision of the new law, Seshamani continued. A year later, in September 2024, HHS will publish the maximum fair price that has been negotiated for the 10 drugs, and in 2025, the $2,000 out-of-pocket cap for beneficiaries' drug costs in Medicare Part D and Medicare Advantage will take effect. Finally, in 2026, the negotiated price for the first 10 drugs will actually be implemented.

When it comes to the drug price negotiations, "We want to be as transparent as possible," HHS Secretary Xavier Becerra said at the briefing. "We want people to look at this process, and at the end of the day, we want to see it grow, because right now it's limited to Medicare ... We want to prove it can be done, and transparency will be one of the pillars of the program."

The IRA's drug price negotiation provisions set out very specific criteria for which drugs Medicare will be able to negotiate prices for. For example, the list includes single-source small-molecule drugs with no generic competition -- but only if the drug was approved more than 7 years ago. Similarly, Medicare also may negotiate prices for biologics with no marketed biosimilar, but only if the biologic was approved more than 11 years ago. Asked by MedPage Today whether HHS had concerns about the strictness of the criteria, Becerra said only: "We're always happy when Congress gives us more work and lets us do something we've been wanting to do."

Drug companies that refuse to accept the price negotiated by Medicare have a choice: Pay an excise tax on sales of all of their products -- not just those they sell to Medicare beneficiaries -- that starts at 65% and increases to 95% depending on how long they don't comply with the negotiated price. Or, they can withdraw all of their products from both the Medicare and Medicaid programs.

Becerra was asked about a comment by Sen. Mike Lee (R-Utah) that this sort of "price control" could lead to drug shortages. "First, this isn't price control," Becerra said. "Secondly, I think we understand that the [first 10] drugs that would probably be covered are drugs that are not only important to the Medicare recipient, but to the industry that produces them. So what I think we're going to find is true competition in the pricing of those medications that are used by Medicare recipients. What it should do is help drive down the cost of these drugs ... There's no reason why we should see a shortage of a drug when, in fact, it's already being sold for less in other parts of the world."

The secretary was also asked whether the price negotiation provision would result in new drugs being put on the market at very high prices, such as a recently approved amyotrophic lateral sclerosis drug that will cost an estimated $150,000 per year. "I think Americans are accustomed to having new drugs come in at very high prices," said Becerra. "And that may be the best reason to have the ability for 65 million people to say, 'Let's get the best price.' In other parts of the world, they're getting a better price, so there's no reason why we shouldn't try to get a better price as well."

He suggested it was up to the pharmaceutical firms to explain why their drugs are often priced so high initially.

Even with new tools like price negotiation and a requirement for drugmakers to pay Medicare a rebate if their prices rise higher than inflation, "does anyone believe that a drugmaker wants to leave the American market?" he asked. "Does anyone believe that a sure payment that comes out of Medicare is something that any vendor wants to give up? If there's a more reliable market, more lucrative market, please point it out to me."

"I don't think you're going to see a whole bunch of folks abandoning the American market when it comes to drugs, because we're good payers," he added. "We have a pretty solid track record of paying our bills. And at the same time, we probably utilize prescription medication at a higher rate than most. So it's just a matter of making sure we get it right."

https://www.medpagetoday.com/publichealthpolicy/medicare/101102