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Archive for April 2011

Apr
26

Patients, Consumers, and the Krugman Commentary

by Dr. Doug Perednia

Just before Easter weekend, Paul Krugman – the Nobel Prize-winning economist employed as a commentator by The New York Times – published a piece entitled “Patients Are Not Consumers”.  We were so struck by the implications of this commentary that we intended to respond right away, but were unavoidably delayed.  As a result many others have already weighed in with their own commentaries.  A tip of the hat to Megan McArdle at The Atlantic, Jeffrey Grossman at JG, Caesarea,  Steven Spear at The High Velocity Edge, Aaron Carroll at The Incidental Economist and others.  But even after reading these we believe that the necessary analysis of Mr. Krugman’s commentary is still not complete.  Moreover, we believe that Mr. Krugman’s piece is, in the broad scope of things, even more important than even he might have realized.  More about that in a bit.

So let’s go ahead and visit the entire Krugman piece, and see if we can tease out the critical points.

“Last week, The New York Times reported on congressional backlash against the Independent Payment Advisory Board (IPAB), a key part of efforts to rein in health care costs.

 

 

But something struck me as I looked at Republican arguments against the board, which hinge on the notion that what we really need to do is to “make government health care programs more responsive to consumer choice.” 

 

 

How did it become normal to refer to medical patients as “consumers”? The relationship between patient and doctor used to be considered something special. Now politicians and supposed reformers talk about the act of receiving care as if it were no different from buying a car. What has gone wrong with us?” 

These three short paragraphs contain two separate thoughts.  The first is that it is somehow morally, ethically or socially reprehensible to think of patients, i.e, people who are ill, as being “consumers”.  Coming from an economist like Mr. Krugman, this seems a bit bizarre.  As Megan McArdle correctly observes:

“I found it very odd to see Paul Krugman complaining that “patients are not consumers” as if “consumer” were some sort of horrible, low-status role that should never taint the sacred realm of health care.  In my economics classes, “consumer” was not a value judgement; it was a descriptor.  A consumer is someone who consumes, just as a producer is someone who produces and a distributor is someone who distributes…  Patients consume health care resources.  Providers provide them. And the system through which labor and resources are allocated in our society remains money–an arrangement that I’m pretty sure that Paul Krugman doesn’t want to change.”

On its face it’s clearly ridiculous not to consider patients “consumers”, so to be fair Mr. Krugman must be using this language to mean something else.  The obvious implication then is that, although patients are “consumers” in the technical sense, they are also something more than that by virtue of their illness and vulnerability.  Perhaps something to be especially protected; to be given more options, opportunities and consideration than the average person might be.  This must be it because of Mr. Krugman’s next observation that: “The relationship between patient and doctor used to be considered something special.”  And indeed it was, and should be.  The historic purpose of the physician-patient relationship is to educate patients about their disease and guide them through the sometimes tough decisions that have to be made.  And, one might add, to specifically serve as an advocate for the patient when offering those choices and fighting, if necessary, with the patient’s insurer.

Just as clearly, Mr. Krugman believes that treating patients as people who must make consumption decisions for themselves based partly upon financial considerations is a bad idea.  There are two possible reasons for this.  The first is that they are vulnerable and somehow at risk for making bad decisions by virtue of their education, mental capacity or debilitating condition – thereby harming themselves.  The second is that they are likely to make bad decisions that will harm society or others.  Apparently both possibilities are of concern to Mr. Krugman, starting with the second one:

“About that advisory board: We have to do something about health care costs. We can’t maintain a system in which Medicare essentially pays for anything a doctor recommends. That’s especially true when that approach is combined with a system that gives doctors and hospitals a financial incentive to engage in excessive care.

 

 

Hence the advisory board, whose creation was mandated by last year’s health reform. The board, composed of health care experts, would be given a target rate of growth in Medicare spending. To keep spending at or below this target, the board would submit “fast-track” recommendations for cost control that would go into effect automatically unless overruled by Congress. 

 

 

Before you start yelling about “death panels,” bear in mind that we’re not talking about limits on what health care you’re allowed to buy with your own money. We’re talking only about what will be paid with taxpayers’ money.” 

Ah.  So the most important problem here is that patients will make decisions that are too costly, in part because they are given bad advice by doctors and hospitals who stand to benefit by urging them to choose more expensive options.  One should note that patients will be particularly indifferent to the cost of their care if these decisions have few or no financial consequences for them personally.  This is the case with Medicare Part D (whose “doughnut hole” was closed by ObamaCare), Medicaid, high-end insurance of the type given to many state and federal workers and union members, and many Medicare Advantage plans.

But let’s pause here.  We would be terribly negligent if we did not mention one out-and-out error or misconception that Mr. Krugman mentions in the last paragraph quoted.  The one about bearing in mind that “we’re not talking about limits on what health care you’re allowed to buy with your own money” when it comes to the decisions of the IPAB.  In fact, we are.  And the fact that many of our political and economic leaders do not appear to know this is both discouraging and a bit frightening.

The vast majority of healthcare providers who take care of Medicare patients do so “on assignment”.  This means that the clinician or other vendor agrees to take whatever Medicare will pay as payment in full for whatever goods and services are provided to the patient.  It is illegal for these providers to bill Medicare patients for any additional amounts, or in fact to charge patients anything for any good or service that Medicare itself covers as a benefit.  So what happens when a cost control organization such as the Independent Payment Advisory Board decides that they are going to cut costs by reducing the amount that they are going to pay clinicians for a specific healthcare good or service?  Well, if the reimbursement becomes so low that it is no longer economically feasible for the clinician to provide the service, (s)he has no choice but to tell the patient “sorry, I can’t do that for you”.  Can the patient then respond by using their own hard-earned dollars to pay that provider enough to cover the true cost of the service?  Nope. That would be illegal for any provider accepting assignment.  The patient’s money simply cannot be spent to purchase that service from that provider.  Medicare says so, and by manipulating prices the IPAB can effectively force many patients to forgo tests and treatments that they might otherwise desire and be willing to purchase with their own money.  Most Americans should know this, but they don’t.  Even a Nobel Prize winner like Mr. Krugman apparently doesn’t.

But let’s go on.  Back to Mr. Krugman’s original commentary:

“Now, what House Republicans propose is that the government simply push the problem of rising health care costs on to seniors; that is, that we replace Medicare with vouchers that can be applied to private insurance, and that we count on seniors and insurance companies to work it out somehow. This, they claim, would be superior to expert review because it would open health care to the wonders of “consumer choice.” What’s wrong with this idea (aside from the grossly inadequate value of the proposed vouchers)? One answer is that it wouldn’t work.

 

 

“Consumer-based” medicine has been a bust everywhere it has been tried. Medicare Advantage was supposed to save money; it ended up costing substantially more than traditional Medicare. America has the most “consumer-driven” health care system in the advanced world. It also has by far the highest costs yet provides a quality of care no better than far cheaper systems in other countries. 

 

 

But the fact that Republicans are demanding that we stake our health on a failed approach is only part of what’s wrong. As I said earlier, there’s something wrong with the whole notion of patients as “consumers” and health care as simply a financial transaction. 

 

 

Medical care, after all, is an area in which crucial decisions must be made. Yet making such decisions intelligently requires a vast amount of specialized knowledge. 

 

 

Furthermore, those decisions often must be made under conditions in which the patient is incapacitated, under severe stress or needs action immediately, with no time for discussion, let alone comparison shopping.” 

Here again in this selection, there are two separate ideas at work.  The first is that “consumer-based medicine” has actually been tried in the U.S. (and presumably elsewhere, although the author does not say where else “everywhere” might be), and did not work.  The second is the assertion that we mentioned previously that patients are incapable of making sound decisions about what which tests and treatments to select because they are rushed, incapacitated, ignorant or otherwise debilitated.  What Mr. Krugman really appears to be saying is not that patients are not consumers, but rather that they are lousy consumers.  Let’s look at both of these ideas; they are actually quite inter-related.

First let’s dispose of the time and incapacity issue.  It is a fact that the vast majority of healthcare goods and services are provided to patients (and their families) who are not mentally incapacitated or in an emergency situation, but instead seeking care for a problem that is not life-threatening, and often chronic in nature.  And where the patient herself is debilitated, their family generally isn’t.  So one should be hard-pressed to argue that severe stress or incapacity is the deciding factor (or even a deciding factor) in the majority of healthcare decisions made by patients and families in their capacity as consumers.  So what else could account for their poor and costly decision-making performance?

Well, to be a good, cost-effective consumer there are several pre-conditions.  The first one, as we mentioned previously, is that you absolutely must have your own financial skin in the game.  As an economist, Mr. Krugman should know this better than anyone.  How do we know?  Real world experience and common sense.  You’re a normal person. right?  Let’s say that we give you the option of getting whatever clothes you might need at either Target or Nieman-Marcus, all expenses paid.  You won’t have to contribute a dime.  Are you going to make any attempt to shop at Target, unless it’s substantially more convenient to do so?  Of course not.  If you have no personal financial liability, the actual cost of the clothes you choose will be immaterial to you.  Why should healthcare be any different?

What else does a consumer need in order to “be in charge”?  Three things: accurate prices, information about quality and performance, and “control”, (i.e., the ability to make the final decision about which course of action to take).  How do those stack up in the healthcare system we’ve known, and the one promised by the Affordable Care Act law?

Prices are the signals that the market sends to consumers and producers that tell them, other things equal, how eager they should be to buy or sell a given product or service.  If you don’t have accurate pricing, you’re not going to be in a position to judge the value of that good or service to you as an individual.  Yet it is practically impossible for any American patient to determine, in advance, the actual amount that both they and the insurance company will have to pay for nearly anything that is covered by insurance.  Just try it.  Their doctor won’t know.  There are so many combinations of coverage and co-pays and deductibles and write-offs that she’s not in any position to tell you.  Think your insurance company will tell you?  Try it.  Call them today and tell them you need a lumbar discectomy, and ask how much it will cost both you and them.  You’ll be on the phone for hours, and will almost certainly never find out.

So patients don’t have the price information they need to be good consumers.  How about information about the quality and performance of various different alternative treatments?  This is where a good doctor-patient relationship would come in handy.  Ideally your doctor will explain to you the purpose, nature, risks, benefits and alternatives for all of the different options that exist for your condition in a completely objective fashion.  He’d then answer any questions you might have and help you decide which alternative is best for you in your particular circumstances.

Unfortunately this is not the American healthcare system that we know, nor is it the one mandated by the ObamaCare law.  Clinicians in the U.S. are paid by the procedure, and the prices of those procedures are essentially fixed by the government.  So one potential source of bias is that doctors are given an incentive to recommend those tests and treatments they themselves perform and that the government has deemed to be most profitable.  But the problem hardly stops there.  Since the late 1980s, the government has decided that simply talking to patients will be one of the worst-paid and lowest margin services clinicians can offer.  As a direct result, talking and counseling time is a scarce commodity.  Still worse, insurance companies (including Medicare and Medicaid), have the final say about whether a given healthcare good or service will be paid for.  It is well established that doctors are reluctant to offer tests or treatments that they know are unlikely to be approved.  Therefore the information given to patients is highly likely to be skewed and incomplete.  And that’s well before we get to the issue of it being nearly impossible to find out which specific clinician or hospital is likely to be the best for a given patient’s particular medical condition.  The net result is patients are highly unlikely to have access to the unbiased and complete information that they are likely to need to make good consumption decisions.

This brings us to the final pre-condition for effective consumer choice: control.  As we’ve mentioned already, insurers are always the ones to have the final say about the options a given patient will have – and in the case of Medicare it may be impossible for them to spend their own hard-earned money to obtain the care that might be best for them.  This level of powerlessness is rarely encountered in any other aspect of the economy.  In healthcare it is an artifact of the system that the government and private insurers have been allowed, by law, to create.

Knowing all of this, let’s now return to Mr. Krugman’s dual claims that “consumer-driven healthcare” does not work, and that patients make lousy consumers.  What are we to make of them?

The first conclusion can only be that “consumer-driven” healthcare has never been tried in the United States on any large scale – especially for Medicare patients.  In fact, the only place where one might argue that American healthcare really is consumer-driven is in elective and cosmetic medicine, where patients pay cash for the goods and services rendered.  Contrary to Mr. Krugman’s assertion, the experience here has been quite promising.  Over the past ten years the real cost of cosmetic and elective procedures such as Lasik eye surgery, Botox, and laser treatments of the skin have steadily declined.  Prices are readily available, plenty of time is taken to explain things and clinicians and facilities market themselves based upon experience, convenience and a wide range of amenities.  In contrast, everywhere that insurance and government regulations have come between clinicians and patients the essential components of true “consumer choice” have been uniformly absent and prices have risen relentlessly.

The second conclusion is that perhaps Mr. Krugman is right about patients being lousy consumers, but it’s hardly their fault.  How are they supposed to make good and enlightened decisions if the healthcare system in general (and Medicare in particular), universally and systematically denies them the tools to do so?  Given the dysfunctional history of Medicare’s own rules and regulations to date, how is anyone supposed to have any faith that a new supremely powerful and self-funding IPAB is going to partner with the existing bureaucracy to make things better rather than even worse for individual patients?

We’ve spent a lot of digital ink on this analysis for good reason.  The relevance and importance of Mr. Krugman’s commentary goes well beyond his own credibility and that of The New York Times.  Many of the assertions that he’s made, and the arguments he uses, are that same ones that led to the creation of the IPAB by Congress and the Obama Administration.  If our political and economic leaders don’t understand the fundamentally flawed nature of the Mr. Krugman’s facts and analysis, our nation’s entire healthcare policy has been built on economic and medical quicksand.  The passage of the Affordable Care Act legislation ensures that inherently defective healthcare policies will be the law of the land for the foreseeable future.  The implications are truly chilling.

Which brings us to Mr. Krugman’s final paragraph:

“The idea that all this can be reduced to money — that doctors are just “providers” selling services to health care “consumers” — is, well, sickening. And the prevalence of this kind of language is a sign that something has gone very wrong not just with this discussion, but with our society’s values.”

We’d like to restate this paragraph in light of all that we’ve learned in this post:

The idea that this can all be reduced to money – that doctors are not neutral parties working solely on the behalf of patients, but paid agents acting according to a set of insurance and government-mandated incentives, rules and regulations about what healthcare patients may or may not know or be permitted access to in their capacity as self-interested consumers – is, well, sickening.  And the long history of support that so many of our economic and political leaders have lent to this situation is a sign that something has gone very wrong not just with this discussion, but with our society’s values.

What do you think?  Your comments are welcome.

Categories : Liar Liar Pants on Fire Awards, Overhauling Healthcare, Personal Responsibility, Political Hellth, PPACA, Uncategorized
Apr
21

How to Sabotage A Healthcare System

by Dr. Doug Perednia

If you’ve ever been sick, especially with anything serious, you quickly realize that doctors, nurses and their ilk are an unusual and precious resource.  First you have to find smart people with personalities willing and able to put up with a lot of guff in the service of their fellow man.  Then they have to be willing to (usually borrow, and) spend tens or hundreds of thousands of dollars for medically-related schooling and training. They devote the prime years of their lives to this – typically completing residencies and fellowships between the ages of 28 and 35.  While their old school chums are partying and starting families and enjoying the blessings of youth, most of our doctors and nurses are locked up in hospitals and clinics with people who many other Americans would literally pay money to avoid: the infectious, those with draining wounds, dementia, or mental illness, people who are often neglected, smelly and dirty, gang members with gunshot wounds…the list goes on and on.  Of course our young clinicians aren’t alone in their misery.  Lots of people make truly amazing sacrifices in the course of their careers.  Our soldiers sleep outside in the elements, take great personal risks and see their comrades killed and wounded before their eyes.   Policeman, firemen, sailors and airmen, coal miners, rescue workers, all have it rough from time to time.  Even pig farmers don’t get off easily.  As the Discovery Channel has shown us, there are lots of people with “dirty jobs”.

So when you come right down to it, what makes doctors so special?  One thing:  “human capital”.

Having gone through so much time and training, these people are darned difficult, expensive and time-consuming to replace – especially after they’ve had the chance to gain some experience.  They don’t grow on trees.  So you’d be justified in thinking that, as a society, we ought to be nice to them.  Not necessarily doting, but decent.  Fair.  Honest.  And appreciative.  Not because they’re some sort of aristocracy, but because they valuable to us as human and economic resources.  It would not be a good idea if, for example, they all decided to quit tomorrow and open up cupcake shops, become computer programmers or go work on Wall Street.  After all, someone who is smart and hard-working enough to become a doctor or nurse is smart and energetic enough to go do something else if they become sufficiently fed up.  So let’s be nice to them, right?  As a matter of smart public policy if nothing else.

Someone might want to tell this to  the people at HHS and CMS who are responsible for nurturing America’s healthcare delivery systems .

Today’s lesson in public policy comes to us through the courtesy of a physician we’ll call Mark.  Mark is a medical internist and endocrinologist – one of those relatively few specialists standing in the way of an epidemic of diabetes that is sweeping the developed world.  Endocrinologists aren’t exactly a thick as bugs on a bumper.  The pay is not phenomenal, the patients can be complicated and relatively few endocrinologists are trained in the first place.  He is a classic example of the sort of provider you wouldn’t want to lose.

Mark also happens to be one of the fast-disappearing breed of physicians: those who are small businesspeople in solo practice.  Saddled with the same costs and business overhead of any small business with employees, modern solo practitioners also face two additional problems: declining insurance reimbursement and a crushing burden of administrative overhead caused by rules and regulations.  As a result it’s getting harder and harder for them to stay in business.  So Mark was understandably alarmed when he received an e-mail in February of 2011, entitled “”Claims Affected by the Affordable Care Act and 2010 Medicare Physician Fee Schedule Changes‏”.  Scrolling down farther, here is, in part, what it said:

“CMS ISSUES INSTRUCTIONS TO MEDICARE CONTRACTORS TO REPROCESS CLAIMS AFFECTED BY THE AFFORDABLE CARE ACT AND 2010 MEDICARE PHYSICIAN FEE SCHEDULE CHANGES

 

On March 23, 2010, President Obama signed into law the Affordable Care Act.  Various provisions of the new law were effective April 1, 2010, or earlier and, therefore, were implemented some time after their effective date.  In addition, corrections to the 2010 Medicare Physician Fee Schedule (MPFS) were implemented at the same time as the Affordable Care Act revisions to the MPFS, with an effective date retroactive to January 1, 2010.

 

Due to the retroactive effective dates of these provisions and the MPFS corrections, a large volume of Medicare fee-for-service claims will be reprocessed.  Given this large workload, the Centers for Medicare & Medicaid Services is taking steps to ensure that new claims coming into the Medicare program are processed timely and accurately, even as the retroactive adjustments are being made.  CMS will begin to reprocess these claims over the next several weeks.  CMS expects that this reprocessing effort will take some time and will vary depending upon the claim-type, the volume, and each individual Medicare claims administration contractor…

 

Medicare claims administration contractors will follow the normal process for handling any applicable underpayments or overpayments that occur while reprocessing your claims.  Underpayments will be included in your next regularly scheduled remittance after the adjustment.  Overpayments resulting from institutional provider (e.g., hospitals, inpatient rehabilitation facilities, etc.) claim adjustments will be offset immediately, regardless of the amount, unless there are insufficient funds to make the offset.  When these overpayments cannot be offset, the amounts will accumulate until a $25 threshold is reached.  At that time, a demand letter will be sent to the institutional provider.”

CMS is, of course, the Center for Medicare and Medicaid Services – the federal entity that controls Medicare.  In plain language what this letter means is that, when Congress passed the Affordable Care Act (aka “ObamaCare”) into law, they also retroactively changed the amount that they had agreed to pay doctors for seeing patients between January 1st and March 23rd, 2010.  For some things the amounts were going to go up, and for others they would go down.  But the changes in compensation were going to be made and applied not only after the doctor had already seen the patient, but after he or she had already been paid the previously agreed upon amount!  Of course, all doctors accepting Medicare patients during this time had seen the patient in good faith, and with a contract in hand for the period from January 1st to June 30th 2010 that said that they would be paid one amount.  Now Congress and Medicaid were saying that the original contract wasn’t worth the paper it was written on, and they were, in some cases, going to claw back some of the money that Mark and others had every right to believe that they had fairly and legitimately earned.  Sure, they would get paid more for some other things, but there is no guarantee that the amounts would magically balance out.

It’s a bit like you’d gone into a restaurant, eaten the food, and came back a few months later and demanded a partial refund, or you’d have your policeman friend close the restaurant and throw the proprietor in jail for retroactively “overcharging”.

Mark was understandably upset.  He wrote this at the time:

“What distinguishes a banana republic from a civilized country, primarily, is the rule of law. When you have your government changing the law and applying it retroactively, reaching into your pocket to get the money paid to you legitimately in the past, the rule of law is subverted.”

You have to admit, he has a bit of a point.  But the story hardly ends there.   One month later, the results of the claims reprocessing started to filter through the system in the form of revised “explanation of benefits” (EOB) forms.  Since he operates a small practice, Mark routinely looks at all of his EOBs.  On March 22nd he reported:

“I got the first 3 statements. Occasionally, there is a tiny fee increase (a few cents). Mostly a decrease, from about $0.40 to about $5 per visit/procedure.  In a busy multi-physician practice, this will amount to multiple thousands of dollars, with all the potential income and tax consequences.  Today, they deposited $0.26 to my account.”

As mentioned in the original e-mail, Medicare accumulated the decreased payments until they totaled at least $25.  And on April 6th, Mark received the first of what is likely to be a long series of letters from CMS asking for repayment of the amounts that Mark had “overcharged”.  It contained the following passage, apologizing for the request and asking that physicians be patient and understanding in a time of economic crisis for the nation, and signed by the Head of CMS, Dr. Donald Berwick:

“Dear Doctor,

 

As you know, Medicare is asking you to return a portion of certain insurance payments that were made to you for services rendered to Medicare patients between January 1 and April 1, 2011.  This request is being made as a result of provisions included in the Patient Protection and Affordable Care legislation passed by Congress and signed into law by President Obama last year.  This partial refund request is a direct result of retroactive provisions contained in the law, and does not in any way imply any error or wrongdoing on your part.

 

All of us here at Medicare greatly appreciate the work that you do on behalf of America’s seniors, and regret the inconvenience that this unexpected, retroactive change in federal law has caused.  We recognize that Medicare payments are already low relative to the cost of providing medical services, especially when the cost of complying with the necessary paperwork is taken into account.  We also realize that you rely on the integrity and predictability of the contracts that Medicare has made with you.  It is both unreasonable and a violation of the trust that you have placed in us to alter the terms of payment under these contracts retroactively.  I can assure you that we will work with Congress and the President to absolutely preclude any future regulations or legislation that would have an adverse impact on you or your practice.”

Just kidding!  We completely made that up.  Here is the corresponding passage from the actual letter that Medicare sent to Mark and hundreds of thousands of other physicians across the country:

“Dear Sir/Madam,

 

This is to let you know that you have received a Medicare payment in error which has resulted in an overpayment to you of $25.88.  The attached listing explains how this happened.

 

Why you are responsible:

 

You are responsible for being aware of correct claim filing procedures and must use care when billing and accepting payment.  In this situation, you billed and/or received payment for services you should have known you were not entitled to.  Therefore, you are not without fault and are responsible for repaying the overpayment amount.  If you dispute this determination please follow the appropriate appeals process listed below.

 

(Applicable authorities: Section 1870(b) of the Social Security Act; subsections 405.350 – 405.359 of Title 42, subsections 404.506 – 404.509, 404.510a and 404.512 of Title 20 of the United States Code of Federal Regulations.)”

The Actual Medicare “Overpayment” Letter

Of course the difference in these letters is one of both attitude and leadership.  Real healthcare leaders would look at healthcare providers as human capital; a scarce and valuable resource to be nurtured and treated fairly.  After all, neither the President nor Congress nor all of the people in CMS or the Department of Health and Human Services can take care of the medical needs of the elderly.  Only our country’s doctors and nurses can do that; and only if they stay in practice.  Unfortunately there are some early indications that the medical practice environment has become so poisoned that it’s no longer a desirable option for many doctors.  In a recent survey of several thousand physicians conducted by Merritt Hawkins, an astonishing 40% of doctors said that they intend to leave clinical practice within the next three years.  Even if half of them are bluffing, it’s still a staggering number.  But there’s an excellent chance they’re not.  The Massachusetts Medical Society Physician Practice Environment Index is at or near its lowest level since 1992.  Meanwhile, a record 45.5% of U.S. physicians are now over the age of 55.  Folks that old don’t tend to kid around much when it comes to whether their careers are making them miserable.  And anyone that age who can tolerate it financially is just aching to retire.

The other quality that we mentioned with regard to Medicare’s letter is attitude.  Are the leaders of our nation’s largest healthcare trying to pick a fight?  What right does any government official have to accuse doctors of somehow being at fault for this mess?  How can one best characterize the tone of the message?  Arrogance?  Intimidation?  Contempt?  Whatever it is, it’s hardly worthy of a government that is intended to serve the people rather than the other way around.  That’s not the America we know.

Fortunately for Medicare, most of its providers probably never saw this letter.  The vast majority probably don’t even know that the government is clawing back a portion of their income.  Most physicians are far too busy to look at all of their EOBs, especially if their billing is done off-site at a separate location.  Most of their medical billers probably saw the letter, and if they did they probably figured that they were somehow to blame; they felt lucky that they were not being accused of fraud or being charged a penalty.  Perhaps that was the intent of its wording all along.

But what about Mark?  What happened to him?  As a solo practitioner with large numbers of elderly patients, how did he react to all of this?  How seriously do doctors really take this sort of thing?

Pretty seriously.  Mark’s still in practice, but he no longer accepts Medicare.

 

Acknowledgements:

Many thanks to “Mark” for bringing this saga to my attention and the attention of many other physicians who had no idea that this was part of the Affordable Care Act (“Obamacare”) law.  Or that we needed to be checking our EOBs more closely.

Categories : Abuse of Power, Death By A Thousand Cuts, Political Hellth
Apr
19

BlogTalkRadio “The Art of Relating” Interviews Dr. Douglas Perednia

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Categories : Overhauling Healthcare
Apr
14

Who wants Socialized Medicine? Oregon Legislators Do! Seriously.

by Dr. Doug Perednia

Comedian Stephen Colbert is fond of calling Oregon “California’s Canada”.  That characterization will take on a whole new meaning if Democrats in the Oregon Legislature get their way and pass House Bill 3510.  This law would create the first completely socialized healthcare system in the United States.  In fact, the proposed “Affordable Health Care for All Oregon” (AHCAO) is so radical that “California’s Cuba” might be a more accurate label.

In an era when taxpayer-funded health plans like Medicare and Medicaid are facing bankruptcy and long-term deficits in the trillions, there is no question that the AHCAO plan is bold.  Private health insurance would be largely banned and replaced by comprehensive health insurance provided free of charge by the state.  Everyone living–or even just working–in the state would be fully covered, along with all immediate family members.  Care would be completely free, with no insurance premiums, deductibles or co-pays allowed.  Providers would be required to accept whatever reimbursement the plan might decide to give them as payment in full; balance billing would be prohibited.  Even drugs would be free as long as they’re on the AHCAO formulary.  And while there is no requirement that the benefits be gold-plated, they must include “comparable benefits” for those “who rely on spiritual means of healing”.

Socialism typically relies on central planning, and the AHCAO’s proposed healthcare revolution is no exception.  All decisions about coverage, eligibility, certificates of need, quality-of-care standards, contracting, ethical standards and everything else are to be made or approved by an unelected Board appointed by the governor.  Its decisions will be implemented by a brand-new state bureaucracy called The Oregon Health Authority (OHA).  The OHA is to be the state’s version of the Department of Health and Human Services, complete with its own insurance administrators, formularies, all-claims all-payers databases, guidelines of care and even its own version of the Agency for Healthcare Research and Quality.  That’s a tall order for a state of only 3.8 million people and a mixed record when it comes to managing complex healthcare programs.

Who will foot the bill for all of this?  The taxpayers of course, but not necessarily all taxpayers.  You might think that a state with no sales tax, the nation’s highest income and capital gains taxes, one of the highest unemployment rates, few large companies and a projected $3.5 billion budget shortfall would think twice about going back to the same few businesses and individuals to fund a huge new entitlement, but you’d be wrong.  One of the first duties of the AHCAO Board is to develop recommendations for a “system of dedicated, progressive taxes that are based on…ability to pay”.  It is to consider a progressive payroll tax, an even higher personal income tax, transaction taxes on stocks, bonds and other unearned income, a progressive surtax on those in higher income brackets and a progressive tax on gross business receipts divided by the number of full-time employees.  With financing like this, Oregon may need its own Mariel boatlift to ferry fleeing capital and businesses out of the state..

But the most remarkable thing about this initiative is not its considerable hubris or enormous scope, but how it manages to fly in the face of everything we’ve learned, or should have learned, about healthcare economics over the past fifty years.  Price controls implemented by Medicare and Medicaid have done nothing to control spending; but they have shifted costs to the private sector and reduced the number of providers who are willing and able to accept poor and elderly patients.  Completely isolating patients from the cost of their care invariably leads to overutilization.  And centralized “cost control” systems that place medical decision-making in the hands of insurers and bureaucrats now consume one-third of our healthcare dollars in the form of administrative overhead.  Ironically, a real healthcare revolution would denounce this dismal record and bury medical socialism once and for all.  Innovative use of free-market forces and widespread administrative simplification could easily save over $500 billion in healthcare costs each year; savings that could be used to pay down our debt, improve care or provide universal medical coverage.  Malpractice reform and re-thinking our expensive, counterproductive “top down” approach to medical information systems would save billions more.  Neither ObamaCare nor HB 3510 do any of these things.

Even in Left Coast Oregon, this particular legislation may not go very far this year.  Despite a Democratic governor and majority in the state senate, the election of 2010 saw Republicans picked up six new seats in the Oregon House to achieve a 30:30 tie.  But its mere introduction and initial hearing this month serves as a reminder that, no matter how badly managed the healthcare system is now, it’s always possible for well-meaning politicians, misguided laws and inept administration to make it even worse.

Categories : Political Hellth
Apr
7

Wasting Your Money Is As American As…Um, Medicare

by Dr. Doug Perednia
Insulin Pump

(Click on image to enlarge)

Having spent the last few posts discussing relatively lofty topics such as Medicare’s plans for ACOs and how human psychology influences the effectiveness of incentive programs, it’s time to write about something practical.  Something down-and-dirty.  Something that illustrates why America’s healthcare system is so complex and messed up.  How about looking at a stupid bureaucratic rule that drives knowledgeable healthcare providers nuts and wastes your Medicare tax dollars?

Oh, man.  So many choices, so little time.

Ah, here’s one.  Apparently the folks at Medicare do not trust your endocrinologist to know anything about diabetes, and they don’t actually know anything about it themselves.  So they’ve invented a rule that wastes money on pointless labs and often forces doctors to “game the system” so that their patients can receive appropriate care.  Will that do?  Sure it will.

So let’s talk about diabetes, one of the most important and expensive chronic medical conditions on Earth.  We know that diabetes is important to the federal government and the citizens of the United States because Secretary of Health and Human Services Kathleen Sebelius said so back in November of 2009:

“WASHINGTON – People with diabetes still carry some of the United State’s highest healthcare expenses, according to a report released by Health and Human Services Secretary Kathleen Sebelius.

 

‘Americans with diabetes are suffering in our current healthcare system,’ she said. ‘Health insurance reform will help ensure these Americans can get the prescription drugs and supplies they need and bring down premiums so all Americans can have high-quality, affordable health insurance.’

 

Affordable treatment remains inaccessible to many Americans suffering from chronic diseases. The report, ‘Preventing and Treating Diabetes: Health Insurance Reform and Diabetes in America,’ outlines the ways in which health insurance reform will lower costs and improve access to quality healthcare services for Americans with diabetes.”

For those of you who may not be medically inclined or diabetologists, we should first explain a little about diabetes.  This is a  disease in which there is too much sugar (aka, glucose) hanging around in the blood on a regular basis.  Normally blood sugar is regulated by having a special kind of pancreas cell called islet cells secrete the hormone insulin.  Insulin causes most other cells in the body to grab glucose from the blood stream and deposit it internally, thus lowering the level of sugar in the blood.  Having too much sugar in your blood over a prolonged period of time is unequivocally a bad thing.  Over time it damages the small blood vessels that supply oxygen and nutrients to virtually every important organ in your body, including the heart, kidneys, brain, eyes, skin and nerves.  This leads to serious and expensive complications like blindness, kidney failure, heart attacks, strokes, infections, skin sores, amputations and so on.  As a result, maintaining good control of blood sugar is something that every diabetic, physician and Medicare administrator should aspire to.

Another diabetes fact that is helpful to know for the purposes of this discussion is that there are two different types of diabetes, (creatively named  “Type 1” and Type 2”).

In Type 1 diabetes the islet cells in the pancreas have died off, leaving the body unable to make the insulin it needs to maintain healthy blood sugar levels.  Once you’re a Type 1 diabetic, you’re always going to be a Type 1 diabetic until researchers figure out a way to implant or re-grow pancreatic islet cells.  As a result, Type 1 diabetics are insulin-dependent; they must inject man-made insulin in order to regulate their diabetes.  In Type 2 diabetes the pancreas is still able to make insulin, but the other cells in the body tend to be resistant to it.  That is, it takes much higher levels of insulin than normal in order to get them to take up enough insulin to lower blood sugar to a safe level.  Type 2 diabetics may or may not require injections of insulin in order to keep their blood sugar under control.  Some Type 2 patients can be controlled with medications that increase insulin uptake by otherwise resistant cells, or simply flog the islet cells into making more insulin.  However every patient is different, and both Type 1 and Type 2 diabetics can be very complex and difficult to control.  That’s why many of them need to see endocrinologists; specialists who devote their entire lives to trying to figure out how to manage this and other hormone-related diseases properly.

How does one tell Type 1 and Type 2 diabetics apart?  One can usually, but not always, tell by the patient’s history and physical condition.  Young, thin people who suddenly become diabetic are almost always Type 1s, whereas older obese people are usually Type 2s.  If it’s really important to know which one you’re dealing with, you can check a couple of specific lab tests.  The first is to look for antibodies to the pancreatic islet cells (called “beta cells”) that make insulin.  These will be present in most Type 1 diabetics, but absent in Type 2s.  Unfortunately, at $429 a beta cell antibody panel isn’t cheap.  A second distinguishing test is called a C-peptide level.  C-peptide is a protein fragment that is made and released with insulin, and serves as a specific marker of insulin production.   As a result, most Type 1 diabetics will have low or absent levels of C-peptide, while most Type 2s will have normal or elevated levels, especially in the presence of high blood sugar levels.

We should also make one other very important point.  The vast majority of the risks and complications of both types of diabetes are almost exactly the same.  Both Type 1 and Type 2 diabetics can be have trouble with blood sugars that are too high, or too low.  Both can require injections of insulin to control adequately.  And both types of patients can develop blindness, heart attacks and all other manner of expensive, life-threatening complications.

Armed with this information, we can now get back to our story.

Mr. Overton is a 65 year-old Type 1 diabetic who recently had to switch to Medicare because, as the courts have ruled, older Americans are not allowed to collect social security unless they also drop their private insurance and sign up for Medicare.  He had been on an insulin pump for many years.  An insulin pump is a $4,000-$5,000 device that can be programmed to deliver both a steady continuous dose of insulin as well as larger amounts to be delivered as needed at specific times.  Insulin pumps are particularly useful in managing blood sugars in Type 1 and Type 2 diabetics, like Mr. Overton, whose diabetes is difficult to control.  Just prior to signing up for Medicare his insulin pump broke.  Therefore one of the first orders of business after the insurance changeover was to get it replaced.

Most private health insurers will pay for insulin pumps based upon the need to manage the patient’s clinical condition, regardless of whether the patient is Type 1 or Type 2.  For example, you might have a Type 2 patient who does hard physical labor.  While he is working his muscles readily take up glucose and his blood sugar levels are pretty good, but when he stops for the day his blood sugars will suddenly run very high.  This type of patient is not a great candidate for long-acting insulin, but a pump can be used to rapidly change his insulin dosage based upon both the time of day and his level of physical activity.  Other good candidates for pumps include patients who get very low blood sugars in the middle of the night (a phenomenon known as “nocturnal hypoglycemia”), patients who suffer from the “dawn phenomenon” (in which their blood sugars skyrocket in the early morning), women whose diabetes becomes difficult to control due to pregnancy, those with wide fluctuations in their blood sugars throughout the day, and patients with multiple emergency room visits for severe hypoglycemia.  All that an endocrinologist needs to do in order to get a pump approved in cases like these is document that these sorts of problems are occurring despite their best efforts to manage them without a pump.

But despite Ms. Sebelius’ obvious concern about the quality of care that Americans with diabetes receive, the federal government has a very different perspective on how to distribute insulin pumps.  As Mr. Overton found out, when it comes to Medicare, even the most deserving patient isn’t going to get an insulin pump without first spending at least $80 on unnecessary tests.

Medicare’s written policy on paying for insulin pumps can be found on page 123 of the Medicare National Coverage Determinations Manual, Chapter 1, Part 4, Section 280.14.  Like most private insurers, Medicare will only provide a pump if it is clinically indicated by virtue of diabetes that is otherwise difficult to control, and/or if the patient had an insulin pump prior to their enrollment in Medicare.   But for reasons of its own, CMS added another requirement: it will only pay for a pump if the patient has a positive beta cell autoantibody test, or BOTH a low fasting C-peptide level and a concurrently obtained fasting blood glucose level that is less than or equal to 225mg/dL.

The first question that doctors, patients and taxpayers ought be asking themselves is “why”?  By adding the lab test requirement, Medicare’s official policy is to only pay for insulin pumps for patients with Type 1 diabetes.  But as we’ve seen, when it comes to both managing the disease and developing potentially expensive or fatal complications, there is no real difference between hard-to-control Type 1 and Type 2 diabetics.  They both have problems that can be helped by insulin pumps, and they can both cost Medicare a fortune if their diabetes is not well controlled.  So why does Medicare insist upon discriminating against patients with Type 2 disease?

The second more technical question that one might ask of an agency headed by a quality guru like Dr. Donald Berwick is, “why doesn’t your C-peptide testing requirement make any clinical sense?”  I’ve asked several distinguished endocrinologists about this myself, and they have no idea.  You see, for the vast majority of diabetics, the higher the blood sugar level goes the more insulin they will be trying to produce.  So if you want to verify that someone’s C-peptide level really is low, it really shouldn’t matter if their blood glucose level is greater than 225.  In fact, with higher blood sugar levels you can be pretty darned certain that they really can’t produce adequate levels of insulin.  But the way Medicare’s requirement is written, if a patient’s blood sugar level is 226 mg/dL at the time the C-peptide level is drawn, they magically no longer qualify for an insulin pump.  Who the heck thought that up?

The result is predictable, and happened in Mr. Overton’s case.   His endocrinologist ordered the fasting C-peptide test and blood glucose.  The results came back with a low C-peptide and a fasting glucose of 247 mg/dL.  Total cost: $80 spent for nothing.  Since he obviously needs the insulin pump, his physician re-ordered the tests but had him inject some regular insulin shortly before drawing his blood.  The result: C-peptide still low, but the blood sugar was now less than 225.  Same patient, same disease, the pump is approved, but Medicare has now spent $160 of your tax dollars for no reason at all.

How can we possibly trust the government to “reform healthcare” if this is how they approach the management of one of the most common and expensive chronic diseases in the world?  And if we were to adopt a government-run “single-payer” system, what’s to keep our single-payer from wasting money like this on every diabetic instead of just those over the age of 65?  How is it that Medicare and Medicaid have the temerity to reward and punish physicians based upon “best practices” and “guidelines of care”, when their own insurance coverage criteria are irrational, medically defective and economically wasteful?

If you know the answers, please share them.  We’re stumped.

Categories : Bureaucracy Run Amok, Quality Questions, Stupid Guideline Tricks, Waste Fraud and Abuse
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