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Archive for Waste Fraud and Abuse

Mar
1

Year After Year, Medicare Keeps Flushing Perfectly Good Kidneys (and Dollars) Down the Drain

by Dr. Doug Perednia

As most of our readers know, Medicare is the government-sponsored health insurance program for the elderly and disabled.  What many Americans may not realize, however, is that Medicare has, by law, for many years been unusually and selectively dedicated to the care and feeding of kidney function.  This leads us to the question for today: when our elected leaders pass laws about the coverage of specific healthcare services, what logic (if any) dictates the services that will be provided?  Is common sense involved?  And most importantly, is healthcare policy formulated mostly in the brain, or mostly in the kidneys?

For those of you who may not be overly familiar with them, we should note that kidneys are certainly among the most amazing organs ever created.  Their functions include regulating the amount of water and salt in the body, balancing the amounts and proportions of sodium and potassium in the bloodstream, maintaining an appropriate blood pressure, helping to manage the production of red blood cells and various other tasks of great utility, such as detoxifying and/or eliminating potential poisons.    There is no question that anything we can do to mitigate the loss of kidney function is a useful social and medical endeavor.

Perhaps as a consequence of the kidney’s great importance in our lives, in 1972 Congress passed an amendment to the Medicare law that essentially made the federal government responsible for the cost of all care associated with end-stage renal disease (ESRD).  Since that time this has included both kidney dialysis (a process whereby the blood is filtered by a machine that amounts to an “artificial kidney” when it comes to eliminating excess salt, water and toxins in the bloodstream), and covering the cost of transplanting real kidneys from human donors into ESRD patients.  Medicare’s coverage is based upon Congress declaring that any American with ESRD would be declared to be “disabled” for Medicare purposes.

Of course all of this comes with a price.  As a recent review article in the New England Journal of Medicine recently documented, this has been considerable:

“In 2008, there were more than 112,000 new patients with ESRD in all eligibility categories (elderly, disabled, and ESRD-only). There were approximately 548,000 U.S. patients with ESRD (about 382,000 of whom were undergoing dialysis) at the end of 2008, but many of them were not covered by Medicare, either because they had not yet fulfilled the initial waiting period or because they had received transplants and their coverage had ceased after 3 years. Medicare expenditures for ESRD in 2008 were $26.8 billion for Parts A and B. Non-Medicare expenditures for ESRD (covered by employer-sponsored group health plans or paid directly by patients) added another $12.7 billion, for total national expenditures of $39.5 billion. According to an analysis by the U.S. Renal Data System, ESRD beneficiaries represented 1.3% of all Medicare beneficiaries and used 7.9% of Medicare expenditures.”

So it was with great pleasure that we met a patient just this week who had directly benefited from this program.  She is a middle-aged diabetic woman who had been on dialysis for several years before being able to find a compatible kidney donor.  The good news was that she was doing very well with her new kidney and was both pleased and relieved to have been able to discontinue the ritual and inconvenience of dialysis.  She felt better, looked better and felt that she could really enjoy life for the first time in years.  The bad news was that she was worried.  Very worried.  In spite of her new kidney she has not yet been able to find work – or at least find work with health insurance.  She was most worried about being able to keep using the drugs that were preventing rejection of her kidney.  But wasn’t she still covered by Medicare we asked?

“I am for a few more months,” she replied, “but Medicare benefits automatically terminate three years after a successful transplant.”  But won’t Medicare continue paying for her transplantation drugs and insulin even after that if she’s unable to find other insurance?  After all, if her diabetes rages out of control and she’s unable to take her transplantation medications, she’ll lose her kidney.

“I know.  That’s what I’m worried about.”  She gave a grim, twisted little smile.  “But at least if that happens I’ll qualify for Medicare again and we can start all over.”

In fact, she’s right about that.  It’s written in black and white, right here in this document that describes Medicare benefits for those with ESRD:

“If you have Medicare only because of ESRD, your Medicare coverage will end:

• 12 months after you stop dialysis; or

• 36 months after you have a kidney transplant and no longer need dialysis.

Your Medicare coverage will continue if:

• You start dialysis or you get a kidney transplant within 12 months after the month

you stopped getting dialysis; or

• You start or resume dialysis or get another kidney transplant within 36 months after the month you have a kidney transplant.

Your Medicare coverage will resume if:

• Your ESRD Medicare ends and you resume dialysis or get another transplant for kidney failure. Your Medicare can start right away without any waiting period.”

Now here is something strange.

One common theme in the great commotion about healthcare in America today is the concept of “waste, fraud and abuse”.  A second one – most common among intellectuals such as President Obama and former head of Medicare Dr. Donald Berwick – has to do with the need to institute and disseminate “best practices” in medicine.  And a third has to do with not delivering more care, but “smarter care”.  In light of all of these let’s consider the facts of this particular patient’s case.

A kidney transplant costs between $100,000 and $125,000.

A year of hemodialysis costs between $6,000 and $10,000 per month, or about $71,000 to $120,000 per year.

Put them together and you have the same amount of money that would place a taxpayer in the top 2% of annual income.  This is so much money that the President routinely lumps households like this into the general category of “millionaires” for tax purposes.

A month of immunosuppressant medications to prevent rejection of a transplanted kidney costs between $1,000 to $3,000 per month, less than one-third the cost of hemodialysis.

But even now, several years after the passage of the Affordable Care (“Obamacare”) Act, the federal government’s own health insurance program will pay for the entire cost of years of dialysis and a kidney transplant to get patients like this one off of dialysis, and then completely squander those investments by discontinuing coverage of the immunosuppressant drugs after 36 months, regardless of whether this will cause the patient to lose the kidney and go back on dialysis.

Lord knows we hate to be critical, but this is just plain stupid – even for a government agency whose healthcare policies routinely seem to be, er, ill-considered.  And clearly the patient we met this week is hardly an isolated case.  The briefest of Web searches on the topic uncovered this 2009 New York Times article about a patient on her second Medicare-funded transplanted kidney.  She lost the first one when she started stretching out her doses of immunosuppressant drugs due to cost considerations.

Perhaps what baffles us most about all of this is that so many people continue to place so much faith a single-payer healthcare system run by the federal government.  On what basis can they possibly believe that it will be efficient and/or well-run?  These are people who will appropriate and spend $17 billion to force physicians and hospitals to deploy expensive, inefficient and frequently despised and quite possibly even dangerous electronic medical record systems, but they can’t find the money to preserve organs they already paid to transplant once already?  Can’t this whole kidney program be considered a rather pure and special form of wasting and abusing taxpayers’ dollars?

Under these circumstances it’s hard to say which is in shorter supply: kidneys or common sense.

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Categories : Business and Law, Clinical Care, Economics, Ethics, Healthcare Policy, Politics, The Practice of Medicine, Waste Fraud and Abuse
Oct
13

Stealing The ER – Part II

by Dr. Doug Perednia

In our last post, we looked a new initiative devised by the Health Care Authority of the state of Washington, in which Medicaid patient who abused the Emergency Room would be punished by having their excess ER visits paid for by doctors, hospitals and those purchasing private health insurance.  It is a bold plan, and roughly the moral equivalent of tossing a pile of warm manure to your spouse while saying, “Here, hold this while I round up some more for you.”

Clearly this plan is nor a solution to the problem.  Why?  Because the underlying problem isn’t who needs to bear the financial responsibility for inappropriate behavior on the part of the patients involved, but how to stop the inappropriate behavior at the source, and/or mitigate its adverse consequences.  These particular patients could not care less about whether Medicaid picks up their tab, or doctors, hospitals and those with private insurance do.  What’s important is that they themselves don’t have to.

So if we really do wish to solve the problem, what are the options?

The real issue at stake here is theft: the undeserved and inappropriate taking of emergency room goods and services.  It doesn’t really matter whether the taking is intentional or not, (it clearly is in the case of drug seekers, but may not be in the case of people with chronic conditions or who don’t know any better), the point is that one personal is wrongly taking resources that belong to others.  Since healthcare discussions are often highly charged with emotion and cloudy thinking, let’s consider what might be done in a similar situation, but in a slightly different field.

Suppose we were to have a fairly well-defined population of people who regularly call in fire alarms every time they spot a fire.  They do this regardless of whether it’s the fire is a lit candle, a gas kitchen stove, well contained in a fireplace or a pile of burning leaves in someone’s yard.  Some of them even call in an alarm when no fire of any kind is present.  Each time they do, the fire department responds with a full complement of trucks, ambulances and other gear, only to find that their efforts are either unnecessary or ridiculous overkill.  Not only is this activity burning up millions of dollars in fuel, tires and manpower, but it’s dangerous.  Each time the fire department responds to a false alarm, there is an excellent chance that their response to a real emergency will be delayed.  How would we deal with this situation?  There is a wide range of responses that are far more appropriate than having the local fire district announce that, henceforth, the cost of these false alarms will simply be passed on to the miscreant’s neighbors.

The first is education.  Since the population causing the problem is relatively small and well-defined and the cost of each false alarm is so high, one could easily spend a modest amount of money on a few employees whose full-time job is to meet each perpetrator, learn about their case, and attempt to directly influence their behavior.  Perhaps the individuals involved really don’t know what constitutes a real emergency.  Or maybe they’re too lazy to get their help from a local clinic during regular business hours.  It’s certainly important to know which it is.  It’s not clear whether Washington’s Health Care Authority tried this approach or not, but one can buy a great deal of training and social pressure for $35 million.  This certainly ought to be Plan A.  Logically, a second level of response would be applied to those who either will not, or cannot, respond to intensive education alone: reward and punishment.

Reward can be hazardous when inappropriate behavior is concerned.  The worst thing one can do is encourage everyone to behave badly.  But one systemic change that would be good for everyone is to convert all insurance – including Medicare and Medicaid – to high-deductible coverage tied to healthcare savings accounts (HSAs).  For those on Medicaid, the amount of the HSA would be provided by the government as part of the healthcare benefit; after all, the same amount of money almost certainly would have been spent anyway on conventional benefits.  But the most important part of these HSAs has to be that there is some reward or sweetener for not spending all of the money in them.  You get to use the interest earned to spend on anything you want, or to roll over the unspent amount into your retirement, or some other combination that provides each individual with a direct financial benefit in exchange for not spending the money on marginally beneficial healthcare goods and services.  The nature of human greed dictates that some portion of the insured population will respond by reducing their use of medical services.  But let’s not kid ourselves.  Simply utilizing HSAs won’t be enough to stop thousands of Medicaid patients who truly have no qualms about stealing the ER.  Some form of punishment will be needed.  The only real question is the form that it should take.

There is no greater challenge in healthcare than devising an appropriate punishment for those who abuse the system, but have nothing to lose.  You can’t bill them, for they can’t pay.  You can’t put liens on salaries they’re not earning, or houses they don’t own.  You can’t even seriously threaten to take away their Medicaid benefits, since they can always use point to the Emergency Medical Treatment and Active Labor Act (EMTALA) and show up at the nearest ER.  Even threatening them with jail time won’t necessarily do any good.  In the big picture incarceration is at least as expensive as healthcare; especially when one considers that prisoners are entitled to free food, lodging and healthcare.  No, in this case it’s not just that the punishment should fit the crime, but the punishment should prevent the crime.  There is only one way to accomplish this: to remove the reason these patients are going to the ER repeatedly for non-emergencies.

Simply don’t give them what they want.

Some might argue that 11,000 Washington Medicaid patients all want different things, but that’s only partly true.  Unless you’re a hospital buff, there are only two things a sane person could want in an emergency room – treatment or companionship.  (We’ll leave aside the issue of the mentally ill going to ERs.)  This makes the solution so easy that it can even be reduced to one of those guidelines of care that government agencies find so irresistible.

Step #1:  Medicaid ensures that it has a network of clinics available that agree to see Medicaid patients on an urgent care basis during regular business hours.  The goal of this network is to ensure that patients are not forced into the ER as a result of an unreasonable lack of access to routine care.

Step #2:   Medicaid maintains a secure, easy-to-use and easy-to-access and easy-to-search website in which ER staff may easily log the fact that a Medicaid patient presented for an ER visit, the diagnosis, and any treatment given.

Step #3:  Medicaid asks all hospital emergency rooms to kindly inform it whenever one of its beneficiaries presents for a condition, or in a manner, that the treating physician believes constitutes an abuse of the medical emergency treatment system.  The criteria for “system abuse” would be left entirely up to the treating provider.  (The website described in Step #2 will be especially useful for helping to identify drug seekers and other patients who are doctor-shopping or routinely abuse the ER.)

Step #4:  For any Medicaid patient seen in the emergency room who providers duly evaluate and judge to be presenting for a condition that does not constitute a true medical emergency, treatment is withheld or (in the case of conditions like asthma or diabetes) limited to that required to tide the patient over until urgent care clinics open on the following business day.  No narcotics may be given or prescribed on any such visit.  Instead, the patient is instructed to go to the nearest urgent care clinic in Medicaid’s network either immediately, or during the next business day.

Step #5:  Medicaid agrees to indemnify and hold harmless any healthcare provider and hospital following this policy in good faith against lawsuits or claims of negligence or improper withholding of care.

Step #6:  If Medicaid should be bold enough to try this approach, all we here at TRTH humbly ask is to receive a quarterly check for 1% of the money saved on ER visits.

Seriously, this is the sort of problem solving that our political and regulatory leaders are supposedly paid to do.  Yes, it’s easier and requires no thought to simply dump the problem on providers, hospitals and the private healthcare system, but thoughtlessness, complexity and spending other people’s money are exactly why we’re on the road to hellth rather than health.  We deserve far better policies than we’re getting.

Perhaps the question asked of voters in next year’s upcoming elections should be: “How’re those politically controlled, heavily regulated, idiotically complex, thoughtless, passing-the-buck and spending-other-people’s-money healthcare laws and policies workin’ out for ya?”

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Categories : Business and Law, Economics, Ethics, Healthcare Policy, Hospitals and Health Systems, Politics, Waste Fraud and Abuse
Oct
10

Stealing The ER – Part 1

by Dr. Doug Perednia

Recently the state of Washington announced that it had had it with paying for the Emergency Room (ER) abuses of its Medicaid patients.

“The state Health Care Authority sent letters to patients on Medicaid, the federal-state health insurance for the poor, warning them the government wouldn’t pay for their nonemergency treatment after three visits.

The agency is trying to save an estimated $72 million in federal and state Medicaid spending, as directed by state lawmakers who tried this spring to crack down on emergency room misuse…

…Many patients who are poor make the emergency room their first stop.

More than 46,000 times in fiscal year 2010, Washington ERs treated the conditions listed as non-emergencies for Medicaid patients who already had come in for three, four or even more similar visits that year, state officials say. One person visited 125 times.

That kind of repeated use is far from the norm – just 3 percent of Medicaid ER patients seek emergency care more than three times for those conditions – but when it happens, taxpayers or hospitals foot the bill.

‘What we’re talking about here is people that go to the emergency room 10, 20, 30 times,’ said Dr. Jeff Thompson, the state Medicaid program’s chief medical officer. ‘I do not have to do an (electrocardiogram) every time … because I know that this is a subjective, ill-defined chest pain.’”

To provide guidance with respect to what Washington’s Health Care Authority considers a true emergency, the state published a list of over 700 diagnoses that it believes should be addressed electively on an out-patient basis rather than in the Emergency Room.  Controversy has arisen because some of these are arguably difficult to distinguish from other conditions that most people would agree do constitute emergencies.  Some of these “grey area” diagnoses include shortness of breath, hypoglycemic coma, “non-specific” chest and abdominal pain, food poisoning, bacteria-caused infections such as salmonella enteritis and shigellosis, sprains, gall stones, “hemorrhage (i.e., bleeding) not otherwise specified”, “syncope (i.e., fainting) and collapse” and abdominal pain in the left-lower quadrant.  You can appreciate the problem immediately posed by emergency room physicians.  Since left-lower quadrant pain is one of the most popular presentations of acute appendicitis, how is the average schnook supposed to know that it’s not appendicitis (which even the folks at Washington Medicaid agree really is a true emergency) unless one is evaluated by a real live doctor?  After all, even the most malingering malingerer is perfectly capable of developing real and serious disease at some point in their life.

It seems that Washington’s doctors object to this “innovation” for two reasons.  The first is out of concern for the fate of patients who might be discouraged from coming into the Emergency Room when they really did have a medical emergency.  This is no surprise; most doctors tend to feel strongly about that sort of thing.  The second reason was out of a very rational concern that Medicaid’s “frequent flier” beneficiaries might not stop coming to the ER with non-emergencies just because the state refuses to pay for the extra visits.  After all, if the state wasn’t going to pay for these visits, the hospitals and the ER physician groups seeing these folks will have to foot the bill themselves for patients whom they are required to see by law.

(We forget.  What is it called when you’re unwillingly forced by other people to do work for them without any form of payment?  Never mind…it’ll come to us eventually.)

So the docs did what every re-blooded American is taught to do from the age when they can first understand television commercials: they filed a lawsuit.

“The lawsuit, which asks the court for an injunction, says the state did not follow proper rule-making procedures, ignored lawmakers’ directions and is violating state and federal Medicaid laws, including “prudent layperson” standards governing the coverage of ER visits.”

One of the big objections cited by the physician groups is that their ideas and suggestions were essentially ignored in the process of coming up with this scheme.  Even the state’s medical director for Medicaid, Dr. Jeff Thompson conceded that the entire process was the result of a one-sided and single-minded need on Medicaid’s part to cut $35 million from its ER budget.  Moreover, there is really no question that many of these visits were clear and unadulterated abuses of the system.

“Only a small minority — about 3 percent of Medicaid patients who use ERs in a year, or about 11,000 patients — seek care in ERs more than three times a year. Those patients have been specifically notified by Medicaid about the changes, Thompson said.

A few patients visit ERs 20, 30 or more times a year, he said. In 2005, the top Medicaid ER user, a 27-year-old woman, visited ERs 172 times, mostly with migraine and headache complaints, according to DSHS.

As many as half the high-use ER patients are seeking drugs, Thompson says, and because ERs are so crowded, patients with true emergencies may not get the attention they need.”

For the purposes of thinking about this whole affair logically, let’s restate the basic problem:

There are about 11,000 out of roughly 367,000 Washington Medicaid patients who appear to be repeatedly abusing the state’s ERs.  They’re costing Medicaid tens of millions of dollars in probably unjustified expense each year, so one of our single-payer government insurers decided to do what they do best: simply dump the cost and the problem onto the private sector in the form of an unfunded mandate to see these patients anyway.  Who will ultimately pay for this?  Why everyone with private insurance or who pays for healthcare out-of-pocket, of course!  Anyone who thinks that you can simply bill these patients for the amounts Medicaid won’t cover is dreaming.  The vast majority of them are unemployed, and drug-seekers are notoriously unreliable bill-payers.  Unless the doctors and hospitals are to go out of business, they’ll have to raise their rates to private insurers.  With its single-payer monopsony on services delivered to old folks and the disabled, Medicare won’t contribute a cent.  (In fact, both the ObamaCare legislation and the recent budget ceiling agreement call for Medicare to cut payments to providers by nearly three-quarters of a trillion dollars over the next ten years.)  So as a direct result of government regulation, its single-payer insurance coverage practices and the “Affordable” Care Act, business, employees and individuals – and that probably includes you – will see health insurance premiums become even more unaffordable in 2012, after a 9% increase in 2011.

Too bad they’re the same taxpayers who are already paying for Medicare and Medicaid in the first place.  This isn’t a solution to the problem of inappropriate spending; it’s just putting the purchase on a different credit card.  Of course with innovative thinking like this, other states are already looking to follow suit.  Just as no good deed goes unpunished, in healthcare no bad idea goes un-imitated.

Let’s try to apply some common sense and come up with a better solution, shall we?  That’ll be the topic of our next post.

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Categories : Business and Law, Economics, Ethics, Healthcare Policy, Hospitals and Health Systems, Politics, Waste Fraud and Abuse
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.

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Categories : Bureaucracy Run Amok, Quality Questions, Stupid Guideline Tricks, Waste Fraud and Abuse
Jan
24

Violate A “Guideline”, Go to Jail?

by Dr. Doug Perednia

The digital ink was barely dry on our last post about the sometimes questionable and largely non-evidence-based nature of clinical guidelines, when the Justice Department decided to weigh in on the topic.  As if to underscore Dr. Rich’s assertion that “guidelines are no longer guidelines”, the Federal government has raised the prospect of fining your doctor and/or sending her to prison for the crime of not strictly following guidelines of care.  As reported by MedPage Today:

“Federal prosecutors are looking into physicians’ prescribing practices relating to implantable cardioverter defibrillators (ICDs), the Heart Rhythm Society has told its members.

 

In a mailing sent to HRS members, the group said it had been contacted by the Department of Justice to assist in a probe of ICD prescribing.

 

“[HRS] has agreed to assist in an advisory role to lend expertise concerning proper guidelines for clinical decision making,” according to a copy of the notice posted by two members on the Internet.

 

The notice indicated that the society was prohibited from commenting further on its role in the investigation. Justice Department officials could not be reached for comment.

 

It was therefore unclear whether the probe is related directly to a report in the Journal of the American Medical Association earlier this month indicating that ICDs are often prescribed for patients who don’t qualify for the devices under published guidelines…

 

The HRS notice appears to raise the possibility that the Justice Department may be considering prosecution of individual clinicians, in addition to its already disclosed investigation into alleged payola schemes by ICD manufacturers.”

If the Justice Department investigation is, in fact, going to target clinicians based upon their adherence to guidelines, the American healthcare system is headed down a very slippery slope.  Government regulators and prosecutors will, of course, contend that they’re simply looking for “waste, fraud and abuse”, and that looking for non-adherence to guidelines is a reasonable screening tool when looking for criminals.  But let’s not kid around.  Any such policy is going to have a chilling effect on treating patients as individuals rather than statistically average widgets.  You may need a test or procedure as a part of good medical care, but your doctor is going to be too scared to order it if her record of “guideline compliance” is at stake.

Think about it.  For the first time your doctor may have a real choice to make if your medical condition doesn’t happen to fit neatly into some academic cookbook.  Adhere to the guideline and commit malpractice, or violate the guidelines and risk jail time.

Using guidelines in this way is unscientific, unethical and just plain wrong.

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Categories : Abuse of Power, Stupid Guideline Tricks, Waste Fraud and Abuse
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