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Monday, March 18, 2024

Medicare’s Price-Setting Rules: An Alternative Perspective

 The growing financial burden from high commercial prices for medical services is fueling calls for reform. Private insurers already rely on Medicare’s coding architecture to adjudicate most claims, but they frequently provide large percentage add-ons to appease their affiliated networks. For instance, as documented in a series of recent studies, private insurers pay an average of as much as 231 percent of Medicare’s rates for inpatient hospital stays. Advocates for tighter price regulation see a ready opportunity to lower costs by extending the reach of Medicare’s limits to the private sector.


There is no question that capping commercial prices at an arbitrary percentage of Medicare, such as 150 percent, would lower overall costs, at least initially. Insurance premiums would fall, as would cost-sharing charges. If nothing else changed, the value to working-age households would outweigh the revenue losses for a health sector badly in need of more rigorous cost discipline.

But there are considerations beyond the convenience of using existing Medicare rules to regulate pricing throughout the health system. Relying almost exclusively on the government’s payment rules to control costs invites several questions: Are the data and methods underlying these regulations sound, and do they incentivize the right kind of care for patients, both now and in the future? Further, are there realistic alternatives that might deliver better results?

A review of the government’s current payment system catalog suggests room for improvement. The attraction is that Medicare’s rates, irrespective of how they have been derived, provide a level of control over pricing that is mostly non-existent in today’s highly compromised private market. But that is not the same thing as saying Medicare’s pricing rules -- built on a vast and entrenched fee-for-service coding and bill-paying system -- encourage efficiency, innovation, and high-value care.

Further, there is also one outlier model within Medicare that might be useful for stimulating new thinking about what is possible across more health care services.

Replacing ‘Cost-Plus’

Medicare did not always have its current reputation as a tightfisted payer. Indeed, today’s rules are a direct consequence of the program’s early history of ineffective cost control.

At enactment, Congress required the federal agency administering the program—originally the Social Security Administration and later the Health Care Financing Administration (which was eventually renamed the Centers for Medicare and Medicaid Services [CMS])—to operate as a passive purchaser, not a heavy-handed regulator. Hospitals and physicians tallied up their costs, and the government covered them, with some extra thrown in for acceptable “margins.” Few questions were asked.

Not surprisingly, this arrangement worked well for the industry but not taxpayers. From 1967 to 1980, Medicare spending per beneficiary grew at an average annual rate of 13 percent. Cost escalation was so rapid that by the late 1970s a political consensus had formed that something had to give.

In the early 1980s, Congress began a two-decade journey to jettison cost-plus reimbursement in favor of formula-based payments, which use cost reports and other sources for determining input expenses to calculate a fair “average” payment for itemized services. In most cases, the new systems were written so that the payments would be known by providers in advance of delivering care—that is, prospectively. Thus, the expenses incurred for individual patients became mostly irrelevant to what providers would be paid.

A major breakthrough came with congressional approval of the prospective payment system (PPS) for inpatient hospital care in 1983. The law’s successful and rapid implementation, and its acceptance as a relevant model for private insurers, encouraged policymakers to take up payment reforms for many other provider categories (see exhibit 1).

Exhibit 1. Partial List of CMS payment systems

Source: MedPAC 2023

Coding And Billing Drive Take-Up

An important source of CMS’s power is the fee-for-service coding systems that are the foundations for the various payment reforms enacted since 1983. In a complex and fragmented delivery system, insurers need a method for rapidly examining and adjudicating tens of millions of claims for payment. When Medicare built the infrastructure that allowed private insurers to drop cost-plus reimbursement, the entire industry moved swiftly to follow the government’s lead.

It was an understandable move. Building a claims and payment processing system for thousands of differing care scenarios is an expensive proposition. Hospitals, doctors, and the various other entities and clinicians seeking Medicare reimbursement had little choice but to gradually adopt the government’s standards. However, once they built systems incorporating Medicare rules, they were not eager to also build wholly separate systems for other payers. Additionally, private insurers did not want to invest the substantial capital required to separate themselves from the Medicare fee-for-service model.

The end result is that CMS’s rates and codes have become the industry standards for payment. Private insurers are free to modify their payment contracts in any way they find useful, but nearly all use Medicare’s current coding and payment systems act as their starting points. Selective modifications are then offered that cost private insurers far less to build and manage than it would cost them to build an entirely new model.

The convenience and lower costs of building upon Medicare’s rules affect the design of Medicare Advantage (MA) plans, too, even as these optional coverage arrangements have reached enrollment parity with the traditional program. They have the flexibility under current rules to pay their affiliated providers on terms that differ from Medicare’s fee-for-service paradigm, but their usual approach is to accept Medicare’s coding systems as the starting point for payment with targeted modifications. Often, this means agreeing to pay a percentage add-on to Medicare’s rates, possibly with new conditions to prevent clinically questionable uses of certain services and to steer patients toward preferred providers.

It is an indication of the momentum behind Medicare’s payment rules that MA plans tend to use them as their launch points for payment. While large in total enrollment, none of the players in the MA market have the leverage to force terms onto the entire provider community in the way that Medicare can through its regulatory reach.

A Lumbering Regulator

Once in place, the series of payment reforms approved by Congress transformed HCFA (now CMS) into the regulatory powerhouse it is today. This is exactly what hospitals and doctors feared would occur when the program was launched.

The agency’s regular cadence of payment rule updates is now a year-round, must-watch enterprise. To keep up, the multi-trillion-dollar industry that CMS oversees (and directly and indirectly finances) employs an army of lawyers and lobbyists to comb through the rules and communicate publicly and privately with agency officials. The overall goal is to prevent surprises and secure terms that are as favorable as possible to stakeholder bottom lines.

The usual metric used to validate this state of affairs is continued access to care for beneficiaries with costs that are more under control than in the private market. The congressional agency tasked with monitoring the rules and suggesting changes—the Medicare Payment Advisory Commission (MedPAC)—regularly issues reports confirming the basic value of CMS’s rulemaking philosophy.

Of course, conjuring a persuasive and plausible counterfactual is difficult. Because of Medicare’s size—on average about one third of the market—most providers have only two realistic options: accept and work with the government’s rules, no matter how adverse the financial terms, or exit the market entirely. Not surprisingly, most choose to stay and then attempt to find ways to maximize their revenue while accepting what they cannot change.

While there is some logic and reasoning behind much of what CMS requires, the agency cannot escape certain tendencies that are typical when public authorities oversee complex sectors of the economy:

Stasis

The federal regulatory process is cumbersome and slow and exhibits substantial inertia. What already exists tends to continue unless loud and powerful voices go to Congress and demand change.

Part of the reason modifications tend to be incremental is that federal law governing the administrative process was written to protect the public from arbitrary rulemaking that could disrupt businesses and livelihoods. Federal agencies must provide notice of their planned changes, allow time for public input, respond to valid criticisms, and marshal supporting evidence before implementing disruptive changes. Falling short on any of these standards invites costly lawsuits.

Consequently, there are modifications every year to the major payment systems, but they tend to build gradually on what exists and are small compared to the vast architecture that lies beneath them. The government is also reluctant to pull back on its powers because of the awareness that reversing course and retaking control will be difficult. Thus, it is rare for payment rules to relax previously imposed requirements. The trend is toward the gradual accretion of power by CMS, not its dissipation.

Old And Questionable Data

Redetermining payments with new data is expensive, as the affected industries must collect what the government needs to update its formulas. It also invites controversy because—if the anticipated changes must be budget neutral, as is usually the case—there will be winners and losers, and the potential losers typically will activate their supporters in Congress to take up their cause. Because government agencies have strong self-preservation impulses, they tend to avoid conflicts that are not strictly necessary to fulfill their missions. For CMS, that means sticking with old data and methods as long as possible.

As an example, the starting point for the PPS for inpatient hospital care is a standardized per diem rate that has been indexed and modified continuously for four decades but nonetheless has its origins in 1981 cost data, which were used as the foundation for the first payment calculations.

For physician fees, the American Medical Association and its affiliated membership societies play an outsized role in maintaining the relative weights that are used to set fees for the various services provided by the members. The normal tool for determining the time and effort required for these services is a survey questionnaire sent to participating physicians. As documented by the Government Accountability Office, this approach suffers from exceptionally small sample sizes, poor response rates, and biased submissions.

The base rate for paying skilled nursing facilities is similarly suspect. Currently, it is tied to a sample of just 205 nursing homes dating back to 2006-2007. CMS sponsored an evaluation in these facilities of the time it took for staff to perform various services for patients and then constructed its prospective payment system based on the results. The final rule implementing the changes, which affects the entire industry, took more than a decade to implement.

Opacity

Each of the payment constructs administered by CMS is amended at regular (usually annual) intervals. Over many years and often decades, even such an incremental process can lead to substantial new layers of compliance. The overall effect is a system of rules characterized by complexity and heavy administrative processes.

One indication of this tendency toward impenetrability is the length of the annual payment rules, as published in the Federal Register. For instance, for the fiscal year that began on October 1, the new rule for hospital inpatient care is just short of 800 pages, with three columns of text for most of the published pages. The physician fee schedule and skilled nursing facilities rules for 2024 run 1227 and 147 pages, respectively.

Incumbency Privilege

As is observed in other heavily regulated industries, the expectation in Congress and within the industry is that CMS will administer payments in a manner that will be tight budgetarily but without jeopardizing the financial viability of large segments of the provider community. In other words, payments will be high enough to keep the doors open. This unstated premise means that the rules are constructed to meet the expectations of the existing provider community and not new entrants. Indeed, because of the complexity and start-up costs associated with compliance, it is exceptionally difficult and expensive for wholly new enterprises to enter these markets.

Prices From Suppliers

Medicare’s purchase prices for some durable medical equipment (DME) items offer a notable exception to the normal pattern. Instead of CMS calculating rates based on an administrative formula, the DME suppliers state their prices in a bidding process that is then used to determine what the government will pay.

CMS began paying for some DME based on competitive pricing in 2011, with subsequent rounds of bidding expanding the list of covered products and updating the reimbursement amounts. About half of all items included in Medicare’s DME coverage have had their fees determined at some point by the competitive pricing rules over the past decade, with the rest still paid pursuant to the terms of a fee schedule originally constructed based on the history of cost-plus charges from the suppliers.

Competitive bidding has delivered notable and consistent savings since 2011, with the program experiencing large and persistent reductions in the prices paid for the products covered by the new system. According to a study cited by MedPAC, the reduction in pricing from competitive bidding is expected to deliver $42 billion in total savings over a decade, including $17 billion in reduced out-of-pocket costs for Medicare beneficiaries. Exhibit 2 shows the effects of bidding on total DME spending and makes clear that requiring suppliers to specify their prices in a competitive market worked as planned to lower the cost burden for the program and its beneficiaries.

Exhibit 2. DME spending growth before and after competitive bidding

Source: Medicare Trustees Reports (2023 [pg. 143], 2018 [pg. 137], 2010 [pg. 179])

When Demand Is Price Sensitive

The dominant regulatory model employed by CMS today has become so entrenched and accepted by policymakers and the industry that it is rare for discussion to occur about potential alternative orientations. Indeed, as noted, the prevailing policy discussion currently is about extending Medicare’s regulatory reach further into the commercial market.

But one can imagine different possibilities. Indeed, it is not wishful thinking to seek absolute declines in prices for some services, not just stability, based on alternative models that would disrupt current market expectations. In particular, it is conceivable that, instead of relying exclusively on CMS to calculate what prices will be fair and reasonable, the providers of services could stipulate what prices they would like to charge—but only if the market were structured in a way that allowed for ready comparisons with competitors, and consequences based on the results.

To this end, reliance on bidding will only work when the demand for the services is price sensitive. In the case of DME, the consumer is the government, and the rules state that lower price offers are more likely to secure the government’s business.

For other services covered by Medicare, it would be more difficult, but not impossible, to rely on pricing from those providing the services. An essential requirement would be standardization of what is being priced to eliminate uncertainly around which suppliers are offering the lowest prices for the same set of clinical services.

For many (but not all) non-DME coverage, the beneficiaries, not the government, choose where to get care. Consequently, beneficiaries would be stepping into the role of price-sensitive consumers. That would have to be done carefully to ensure the bidding produces only savings and not higher costs.

There are several possibilities for beginning to test what would work:

High-Volume Imaging And Lab Services

Some categories of Medicare-covered services are similar to DME in that what is provided to patients is sufficiently replicable to lend itself to a bidding system. Lab services and medical imaging have accepted industry standards that should allow for apples-to-apples price comparisons even recognizing that quality and innovation cannot be sacrificed in exchange for maximizing cost reduction for the government.

High-Volume Surgical Procedures

CMS has been implementing a series of bundled payment initiatives over the past decade, including for total joint replacements, which emphasize pricing for all required services needed to complete the intervention. A redesigned initiative could establish standardized bundles for several high-volume interventions and then solicit bids in each market. With standardized bundles, patients would know precisely which goods and services would be included in bundle, allowing them to easily compare prices across the available options.

On the provider side, acceptable bids would have to be below the pricing that would occur under the current administered pricing models or clearly demonstrate superior quality for a higher price per procedure coupled with fewer complications and lower use of other services. Further, in order for the beneficiaries to have an incentive to migrate to lower-priced options, they would have to receive a share of the savings.

The bundle definitions now used by CMS could be the starting point for initiating a bidding model, but these terms could be modified over time to become broader. This would open up more opportunities for the participating providers and health systems to reengineer their care protocols and processes to reduce expenses while improving patient outcomes.

A bidding model also could be a first step toward bundles established around patient conditions (e.g., osteoarthritis), where a single, risk-adjusted price based on the bids could cover the care needed to improve patient health. This method would accommodate considerations around the potential complications associated with various options (whether surgical or not) into patient care decisions.

Primary And Chronic Care Management

Currently, physicians providing primary care to, and managing chronic diseases for, Medicare patients send claims to Medicare for each service they provide. As an alternative, these physicians could be paid a risk-adjusted monthly fee in return for a commitment to provide a defined set of services to the patients who select them. For instance, participating practices could be asked to submit a bid for the monthly charge they would request to cover a certain number of in-person visits, routine tests, and video and audio communication.

Beneficiaries could select any primary care or chronic care management practice that they find attractive, but they would pay more or less based on the submitted monthly charge bids from the practices. Further, unlike the current ACO models, beneficiaries would pay higher cost-sharing if they elected to receive services covered by this initiative from providers not included in their initial designations. The initiative also differs from MA in that the beneficiary would select only a provider for routine primary and care management services and not a full network for all of their potential health care needs.

Eliminating payment claims for the tens of millions of services submitted by primary care physicians would dramatically reduce the administrative burden on doctors’ offices, the government, and patients.

These reforms would be embedded within traditional Medicare, but the objective would be to set new pricing terms that would lower costs for private coverage, too. As with the current payment rules, if Medicare incorporated price comparisons into its reimbursement models, and the results were positive, there is not much doubt that the private sector would move in this direction, too. The effect would be to amplify the potential for genuine price competition to occur throughout the industry, and for the savings to multiply.

The Goal Is Value

The power of Medicare’s payment rules is not in dispute. The formulas the government uses have become the accepted norms for the industry. Hospitals, physician practices, and other providers of health-related services build their business plans around them.

Some proponents of Medicare’s existing processes would like to take the next step toward an all-payer system based on the government’s rulemaking power. Costs in the private sector would come down, at least for a time, but this approach would lock in place today’s inefficiencies and mediocrity. 

It is not fanciful to believe better is possible. Market pricing, while challenging, would reward efficiency, productivity improvement, and value-enhancing innovation. These are the key ingredients for breakthrough improvements and should not be written off as unachievable.

Authors’ Note

David Bernstein reports personal fees from: 1) Harvard Business School; 2) National Academy of Medicine; 3) The Heritage Foundation; 4) Mass General Brigham – Population Health Management; 5) Children’s Orthopaedic Surgical Foundation (COSF); 6) CapaDev (value-based health care consulting firm); 7) Value In Health (value-based health care “think tank” in the Kingdom of Saudi Arabia). He also reports support for attending meetings and/or travel from PROMIS Health Organization (PHO) and grants from: 1) AOFAS (American Orthopaedic Foot & Ankle Society); 2) AFSH (American Foundation for Surgery of the Hand); 3) CSRS (Cervical Spine Research Society). He reports editorial roles, including: 1) Associate Editor at Clinical Orthopaedics and Related Research; 2) Social Media Editor at Spine; 3) Editorial Board Member at Journal of Orthopaedic Experience & Innovation

James Capretta serves on the Advisory Board of the National Institute for Health Care Management Foundation.

https://medicare-price-setting-rules.tiiny.co/

White House Wants to Double Dip on Drug Rebates

 As part of its "Strike Force on Unfair and Illegal Pricing," the White House just doubled down on a December plan to allow the federal government to tear up exclusive patent agreements between innovative drug companies and research universities.

The White House says such action would reduce drug prices – and claims it has the authority to do this on patented medicines that benefited, at their earliest stages, from federal research grants.

The plan could be finalized any day.

Many legal experts have argued that the "march-in" process the government is citing for this supposed authority is of dubious legality. But ultimately, the policy rests the argument that when the government funds some of the research that underpins a drug, it should receive a rebate, of sorts, on that investment. 

The White House defends this proposal by citing the fact that "taxpayers have spent hundreds of billions of dollars on research catalyzing the discovery and development of new prescription drugs."

This ignores how federal research funding works and what it is designed for – and also ignores the fact that the government already reaps benefits, and tax revenue, from the increased public health improvements and economic activity caused by drug innovation. Evidently that's not enough, and the government wants to double-dip.

No other investors, whether public or private, are entitled to such rebates. (Surely the White House wouldn't propose that all investors who have some of their 401(k) plans in Apple receive coupons to use at the local Apple Store.)

But let's assume, for the sake of argument, that the government is entitled to discounts. How large should they be?

We can quantify that by looking at the current drug-development ecosystem.

The primary source of public research funding comes via grants from the National Institutes of Health and National Science Foundation. Such funding, which generally advances early stage, basic science, is socially useful – and best described as laying the groundwork for "scientific infrastructure." Scientists rely on this research to innovate.

Some federally backed research breakthroughs are transformed into patentable inventions. Thanks to the Bayh-Dole Act of 1980, universities can patent their researchers' inventions and license those patents to companies that then endeavor to commercialize them. Prior to Bayh-Dole, the government retained the patent rights on inventions that stemmed from federally funded research – and licensed fewer than 5% of them.

Because university patents generally involve very early-stage research – and because the likelihood of successful commercialization is very rare – the licensing revenue tends to be very modest.

Indeed, the aggregate revenue of all technology transfer offices was around $3 billion in 2018, compared to $100 billion in federal funding across all fields of research, not just biotech, that year. In other words, for every $100 invested in basic research, there's typically just $3 of potentially marketable discoveries. Public funding for basic research is important, but very few products come out of that funding. 

Companies, by contrast, spent around $83 billion on pharmaceutical R&D in 2019 – and took in hundreds of billions in revenue.

We can conservatively assume that half of all university licensing revenue comes from deals inked between universities and biotech companies. That equates to $1.5 billion in annual licensing fees from early-stage medical research.

So even if we assume the government "deserves" all $1.5 billion, that's still just 1.8% of total private-sector, life-science R&D spending – and a fraction of 1% of drug industry revenues.

Plus, the government already demands steep discounts on the drugs it purchases. Medicaid, for example, purchases drugs at a mandated rebate that is at least 23% below what other insurers pay. This rebate is on top of the sales, corporate, and other taxes that the government already claws back from drug companies.

In other words, even if the government controlled the licensing rights to every patent developed with federal funding (as was the status quo before the Bayh-Dole Act) and was able to license those technologies to the private sector for commercialization (which it was incapable of doing in the decades before Bayh Dole), the government is already getting a much bigger discount than any licensing deal would ever yield.

The drug development ecosystem is complex. The government helpfully bankrolls some basic research. But it's the private industry that funds development. This development can cost upwards of $3 billion per successful drug, after accounting for the costs of the roughly 88% of experimental drugs that enter clinical trials but don't make it through the FDA approval process.

In fact, a 2022 analysis from Vital Transformation found that for every $1 in public funding for approved drugs that relied at least in part on a patent developed with government funding, private industry spends about $66 to bring a drug to the market.

The White House premised its march-in proposal on the idea that patients and insurers overpay for medicines that benefited from basic research investments. But the  government already enjoys the best of both worlds -- robust economic growth from innovation, tax revenues from those innovations, a healthier populace, and preferential regulations that give it discounted prices.

Disrupting this delicate balance would make patients, workers, and taxpayers all worse off. 

Tomas Philipson is an economist at the University of Chicago who served on the White House Council of Economic Advisers as a member and acting chairman, 2017-20.

https://www.realclearhealth.com/blog/2024/03/15/the_white_house_wants_to_double_dip_on_drug_rebates_1018720.html

Sens. Scott, Rubio Call For Plan To Handle Influx Of Haitian Migrants

 Florida Republican Sens. Rick Scott and Marco Rubio have called on the Biden administration to produce a plan to deal with a potential influx of Haitian migrants into the United States as political and social unrest intensifies in the Caribbean country.

In a Friday letter to Biden, the senators suggested that the administration's current open-border policy could lead to mass migration from Haiti into the United States, and have a "direct negative impact on American families."

"Floridians and the rest of the American public will not tolerate your administration again opening the floodgates for countless, unvetted foreign nationals to stream into our country, putting our national security at grave risk and creating untold public safety threats for our communities," Scott and Rubio wrote. "We must consider this danger due to the numerous reports of gangs committing jailbreaks in Haiti and releasing thousands of dangerous criminals."

Earlier this month, Haiti fell into chaos and a state of emergency was declared amid fighting between criminal gangs and government forces - with Haitian Prime Minister Ariel Henry stealing away to Kenya to negotiate a deal for a long-delayed UN-backed security mission (to 'secure the children,' we're sure).

The Senators' letter slams Biden for the ongoing crisis at the Southern border, the Epoch Times reports.

"Since you took office, your administration has allowed more than 8 million people to pour across our southern border, including untold numbers of foreign nationals that you have released into the interior of the country," they wrote.

"You create a magnet for illegal immigration here, appease evil regimes, and put the American people at risk, while further expecting taxpayers to pay for the unrest, humanitarian crises and mass border crossings that result."

The letter cites FBI Director Christopher Wray's March 11 comments before the Senate Intelligence Committee in which he raised the alarm about risks to Americans thanks to the Biden administration's open-border policies.

According to Wray, the surge in illegal crossings at the southern border threatens the safety of Americans.

"From an FBI perspective, we are seeing a wide array of very dangerous threats that emanate from the border," said Wray, who added that the FBI is "very concerned" about a specific human smuggling operation with ties to ISIS.

The letter then turns to the potential for mass migration from Haiti, and whether the Biden administration conducts vetting and background checks on Haitians arriving in the US.

Rep. Matt Gaetz (R-FL) also raised concerns during a House Armed Services Committee meeting on March 12th, in which he predicted that the current 'trickle' of people leaving Haiti will "accelerate" in the coming weeks - for which south Broward and Palm Beach Counties have been prime destinations for people from the island nation. According to Gaetz "they don’t disperse throughout the country; they stay in southeast Florida."

Meanwhile, a top Pentagon official on March 12 said during testimony that the US has no plans to send troops to Haiti, nor activate the Coast Guard and Navy's ability to interdict illegal immigrant flotillas and return them to their point of origin or a port in a 3rd nation.

Guantanamo Bay?

On March 14, during a press call, White House national security spokesman John F. Kirby said the Biden administration is considering using a naval facility at Guantanamo Bay to process and repatriate illegal immigrants coming from Haiti.

The naval station at Guantanamo Bay has been used in the past for processing and repatriating illegal Haitian immigrants, and it “remains an option” for the future if maritime migration trends continue to worsen, according to Mr. Kirby. -Epoch Times

On March 7, the Coast Guard interdicted a vessel carrying 65 Haitian immigrants near Inagua, Bahamas, before repatriating them back to Haiti.

https://www.zerohedge.com/markets/sens-scott-rubio-call-plan-handle-influx-haitian-migrants

'New Kind of Hospital Is Coming to Rural America'

 As rural hospitals continue to struggle financially

opens in a new tab or window, a new type of hospital is slowly taking root, especially in the Southeast.

Rural emergency hospitals receive more than $3 million in federal funding a year and higher Medicare reimbursements in exchange for closing all inpatient beds and providing 24/7 emergency care. While that makes it easier for a hospital to keep its doors openopens in a new tab or window, experts say it doesn't solve all of the challengesopens in a new tab or window facing rural healthcare.

People might have to travel further for treatments for illnesses that require inpatient stays, like pneumonia or COVID-19. In some of the communities where hospitals have converted to the new designation, residents are confused about what kind of care they can receive. Plus, rural hospitals are hesitant to make the switch, because there's no margin of error.

"It's ironic" that the facilities that might need the most help can't afford to take the risk, said Carrie Cochran-McClain, chief policy officer at the National Rural Health Association. She pointed to having to give up certain services and benefits, such as a federal discount program for prescription drugs.

The government, which classifies hospitals by type, rolled out the rural emergency option in January 2023. Only 19 hospitals across the U.S. received rural emergency hospital status last year, according to the University of North Carolina's Sheps Center for Health Services Research.

The majority are in the South, with some in the Midwest, and hospitals in Nebraska and Florida recently started to explore the option.

The designation is aimed at a very specific population, said George Pink, PhD, deputy director of the Sheps Center's Rural Health Research Program, and that's rural hospitals on the brink of closure with few people getting inpatient care already.

Saving Rural Care

That was the case for Irwin County Hospital in Ocilla, Georgia, which was the second rural emergency hospital established in the U.S.

Weeks prior to converting, the hospital received at least $1 million in credit from the county so it could pay employees -- money that county board of supervisors chairman Scott Carver doubted he'd see returned.

"We operate on a $6 million budget for the county, so to extend that kind of line of credit was dangerous on our part to some degree," he said. "But ... we felt like we had to try."

Irwin County Hospital became a rural emergency hospital on Feb. 1, 2023. Quentin Whitwell, the hospital's CEO, said it was an ideal candidate.

"We're still finding out what some of the impacts are, given that it's a new thing," said Whitwell, who through his company Progressive Health Systems owns and manages six hospitals in the Southeast, most of which are rural emergency hospitals or have applied for the designation. "But the change to a rural emergency hospital has transformed this hospital."

A combination of state programs and tax credits, plus the new designation, means the hospital has $4 million in the bank, Carver said. Simply put, the work was worth it to him.

Traci Harper, a longtime Ocilla resident, isn't so sure. About a year ago, she rushed her son to the hospital for emergency care for spinal meningitis.

Because the new designation requires the hospital to transfer patients to larger hospitals within 24 hours, Harper's son was sent to another in-state facility and 3 days later ended up getting the care he needed in a hospital in Jacksonville, Florida.

"That's 2 hours away," she said. "The whole time I could have taken him there myself, but nobody told me that."

'Barely Surviving'

Nebraska's first rural emergency hospital opened in February in a city called Friend.

Warren Memorial Hospital had reached a breaking point: Federal pandemic relief money had dried up. The city, which owns the hospital, had to start extending lines of credit so hospital employees could get paid. A major street repair project was even delayed, said Jared Chaffin, the hospital's chief financial officer and one of three co-CEOs.

"Back in the summer, we were barely surviving," said Amy Thimm, RN, the hospital's vice president of clinical services and quality and co-CEO.

Though residents expressed concerns at a September town hall about closing inpatient services, the importance of having emergency care outweighed other worries.

"We have farmers and ranchers and people who don't have the time to drive an hour to get care, so they'll just go without," said Ron Te Brink, co-CEO and chief information officer. "Rural health care is so extremely important to a lot of Nebraska communities like ours."

The first federal payment, about $270,000, arrived March 5. Chaffin projects the hospital's revenue will be $6 million this year -- more than it's ever made.

"That's just insane, especially for our little hospital here," he said. "We still have Mount Everest to climb, and we still have so much work ahead of us. The designation alone is not a savior for the hospital -- it's a lifeline."

Rural Troubles

That lifeline has proven difficult to hold onto for Alliance Healthcare System in Holly Springs, Mississippi, another one of Whitwell's hospitals and the fourth facility in the country to convert.

Months after being approved as a rural emergency hospital in March 2023, CMS reneged on its decision.

Hospital CEO Kenneth Williams, MD, told the Associated Press that the government said the hospital isn't rural because it is less than an hour away from Memphis. A CMS spokesperson said the facility was "inadvertently certified."

The hospital has until April to transition back to full service, but many in the community of largely retirees believe the hospital has closed, Williams said. Patient volume is at a record low. If the federal payments stop coming, Williams isn't sure the hospital will survive.

"We might have been closed if we hadn't [become a rural emergency hospital], so ... something had to be done," he said. "Do I regret all of the issues that for some reason we've incurred that the other [hospitals] have not? I don't know."

Though Alliance appears to be one of few facilities that have been negatively impacted by converting to a rural emergency hospital, Pink said it's too soon to know if the federal designation is a success.

"If my intuition is correct, it will probably work well for some communities and it may not work well for others," he said.

Cochran-McClain said her organization is trying to work with Congress to change regulations that have been a barrier for rural facilities, like closing inpatient behavioral health beds that are already scarceopens in a new tab or window.

Brock Slabach, the National Rural Health Association's chief operations officer, told the Associated Press that upwards of 30 facilities are interested in converting to rural emergency hospitals this year.

As Whitwell sees it: "As this program evolves, there will be more people that I think will understand the value."

https://www.medpagetoday.com/hospitalbasedmedicine/generalhospitalpractice/109222

Why are our leaders pushing to deregulate pot and other drugs research shows are dangerous?

 As the medical and scientific study of cannabis and psychedelics intensifies in the search for therapeutic uses, the inherent dangers are also becoming more and more apparent.

So why are many of our officials leading the charge for laxity in our federal regulations and increased access to dangerous drugs for all of us, including our teens?

Vice President Kamala Harris even hosted a White House roundtable Friday on removing marijuana restrictions.

I am one physician who believes the science points in the opposite direction, toward more caution rather than increased recreational usage.

Let’s start with marijuana.

A study of more than 400,000 Americans just published in the Journal of the American Heart Association revealed a 42% increase in stroke and a 25% increase in heart attacks associated with regular marijuana use over a four-year period. 

This is no surprise considering previous studies have shown the tar in marijuana is toxic to both the lungs and the heart, and THC itself (the psychoactive chemical in pot) can cause an increase in heart rate and blood pressure.

The problem is marijuana is not what it was even a decade ago — the THC content is now soaring well over 30% in all cannabis products from weed to vapes to edible “gummies.”

This leads to more anxiety, more cognitive problems, more cannabis-induced psychosis (especially in those who have underlying mental-health problems) and more developmental delay in young children who are exposed to it in the womb when pregnant women foolishly use it to combat morning sickness.

There are more emergency-room visits from vomiting disorders, overdoses and car accidents, especially when cannabis products are laced with fentanyl or amphetamines or combined with alcohol.

Some politicians say legalization for recreational use in 24 states with more to follow will lead to less illicit use.

In fact the opposite has been true, as shadow gray- and black-market industries spring up, hiding behind the legal dispensaries.

In the 38 states where so-called medical marijuana use is legal, the category is too often an excuse for easy access for an unproven use like countering insomnia.

And a loophole in the 2018 farm bill allows hemp-derived delta-8 THC, which can be half as powerful as what’s found in marijuana and is becoming more popular with teens.

The problem is not just with marijuana.

It extends to psychedelic substances, from magic mushrooms (psilocybin) to ketamine to the plant-brew ayahuasca and even to the African iboga plant, despite the fact ibogaine leads to a prolonged nightmarish experience that increases your risk of heart arrhythmias.

Ibogaine is being touted for use for post-traumatic stress disorder and opioid withdrawal — notwithstanding its cardiac risks and the fact it’s illegal across the United States and remains a Schedule I controlled substance, meaning it doesn’t have any medical use and is a highly addictive substance.

This category is a wise precaution without the science to prove otherwise.

Many prominent psychiatric researchers are searching for substances that may have similar effects as the psychedelics but without the dangerous hallucinatory results.

This is a smart pursuit, but we certainly aren’t there yet.

In the meantime, the idea of “microdosing” psychedelics, which has become so popular among celebrities and their followers, has not been medically studied or found to have any therapeutic benefit. 

That’s a major problem with so-called medical uses of or self-treatment with psychoactive substances.

Physicians and scientists who are carefully studying a powerful substance but have not come to any verifiable conclusions should not be used as an excuse for reckless recreational use of a drug. 

Once again politicians attempting to garner votes or back a growing industry may hijack and misrepresent science by obscuring the risks and dangers of hallucinatory chemicals.

Marc Siegel, MD, is a clinical professor of medicine and medical director of Doctor Radio at NYU Langone Health and a Fox News medical analyst.

https://nypost.com/2024/03/17/opinion/why-are-our-leaders-pushing-to-deregulate-pot-and-other-drugs-research-shows-are-dangerous/

'Exercise pill’ could replace physical benefits of working out: study

 Tired of working out? There may soon be a pill for that.

A new “exercise pill” could potentially replace some — not all — of the benefits of working out, according to a new study.

Scientists from the Washington University School of Medicine in St. Louis spent 10 years creating new compounds that seem to be able to mimic the physical benefits of a workout — at least in rodent cells — that could become ingredients for a future supplement.

Athletic man with a naked torso holding pills in his hand. Vitamins and doping. Healthy lifestyle and diet. Medicine Concept
The findings could result in a new way to treat muscle atrophy and other medical conditions.alones – stock.adobe.com

The team of researchers, who presented their findings at the spring meeting of the American Chemical Society (ACS), hope to replicate the physical effects of exercise, specifically the ability to enhance metabolism and growth, as well as improved muscle performance.

“We cannot replace exercise; exercise is important on all levels,” Bahaa Elgendy, a professor of anesthesiology and the project’s principal investigator, said in a media release. “If I can exercise, I should go ahead and get the physical activity. But there are so many cases in which a substitute is needed.”

However, the findings could result in a new way to treat muscle atrophy and other medical conditions, including heart failure and neurodegenerative disease.

If the drug could mimic the physical effects of exercise, it could help offset the weakness in a person’s muscles that occur naturally as people age or for those affected by cancer, certain genetic conditions or any other reason a person may be unable to do regular physical activity.

Elgendy added that the “exercise pill” could potentially counter the loss of both muscle and fat caused by other drugs, such as new weight-loss medications.

When the scientists tested on mice, they found that the compound increased a fatigue-resistant muscle fiber, which in turn improved the rodents’ endurance when running on a treadmill.

But more testing needs to be done before the pill can be available for human use. The scientists will be testing the compound in other animals as the next step in the research process.

https://nypost.com/2024/03/18/lifestyle/new-exercise-pill-could-replace-working-out-study/