Being There
Kid: "He had it coming, right, Will?"
Munny: "We've all got it coming, Kid."
To understand health care reform, it is helpful to have faced Death. The near-death experience brings into sharper relief the reality underlying assorted canards surrounding reform.
My favorite is the notion, advanced by liberal and conservative alike, that the proper objective of reform is to control costs by eliminating treatments that are ineffective. This sounds reasonable unless you have faced Death. I have faced Death, admittedly through the eyes of another, but I think I know a couple of things. I am not claiming to be heroic. I am not asking for sympathy or trying to be emotionally manipulative. Just put yourself in these shoes for a second, as a dispassionate thought experiment.
In the matter of "ineffective," alternative interpretations are possible:
1. A treatment has zero chance of being effective, or a positive probability of being harmful.
2. A treatment has a positive but low chance of being effective, hence is disallowed by cost considerations.
3. A treatment is diseconomical: its costs outstrip its expected value. (Translation below.)
Nobody wants treatments that fall into category number one. That appears obvious. Unfortunately, whether a treatment deserves such a verdict may not be known with confidence. That fact that such a treatment exists suggests it would at least fall into category two. So let us say you are facing Death and have options in #2. Would you want an external authority -- public or private -- to make this decision for you? Probably not.
The cost factor in this particular context is irrelevant. In principle there could be insurance that finances "hail Mary" treatments, so one is not confronted in the actual event by the choice of a long-shot treatment combined with financial ruin. Then we could ask whether markets would provide such insurance, or whether there is some case for public involvement.
Before the fact, it can be difficult to gauge one's desire to have such insurance -- to be able to finance a hail-mary play. Having faced Death, I distrust professions of disinterest in long shots. Have you been there? If not, you might think differently in the actual event.
"Most health care expenditures take place in the last year of life." This expression badly deserves dissection. Those in the last year of their life often are uncertain it will be their last year, so remedial treatments may not be viewed as wasteful. Moreover, the last year is not the critical time period. Say you're in your last year, but a treatment gets you through another week. Is that treatment without merit? Have you been there? Again, cost is not necessarily at issue if insurance (public or private) is feasible.
What's another week? Have you been there? Another week could get you a conversation with a child about their college plans. An hour in a garden smelling the flowers. Not worth enough? Have you been there?
My other favorite bit of terminology is "heroic procedures." Believe me, if you are facing Death, you want a hero. All sorts of endeavors aim at great rewards resting on slim probabilities.
This brings us to the economists, the savants of category three. Ah. The fundamental theorem is as follows. A treatment has an average cost of $X. Sometimes it works, sometimes it doesn't. Its probability of working is Y/100. In other words, if you run it 100 times, it works Y times. It prolongs Life for w years. Life is worth $Z per year. So the expected benefit is Y/100 times w times $Z, or $YwZ. An august board of economical physicians -- who haven't been there -- compares X to YwZ. If YwZ is greater than X, the treatment is economical, hence permitted. If not, the patient is left to pay out-of-pocket, if she can, or go without, if she can't.
Economists know so much. They know how much your life is worth. They know that average costs and probabilities apply as much to you as to the population as a whole. They know how often a treatment works, and for how long.
Martin Feldstein made some of these points a few weeks ago, but they were lost in the brouhaha over his boogey-man rhetoric about single-payer.
The point is not that public control is unworkable. These decisions get made one way or another. The point is that we are getting crabbed notions of public health care management in the name of cost control by People Who Haven't Been There, who in fact won't be there because they live in the comfortable womb of good private insurance. Their trials will be of a different sort, because of course they too will eventually face Death. Meanwhile, cost concerns from both sides are driving reform into a ditch.
To fend off the taxaphobic enemies of reform, the Democrats seem to be trending to increasing restrictions on care, all in the name of enlightened governance and fiscal responsibility. Meanwhile the GOP is just pounding the table, trying to block any action at all.
Health care costs -- public and private -- grow much more rapidly than income. This is unsustainable in the long run. The problem becomes how to reduce the rate of growth. One source of growth is growing utilization per person; more drugs, more procedures, more surgeries, etc. The extent of treatment is diseconomical, but this is only clear after the fact, in aggregate. Before the fact, it is often not clear which treatments are undesirable. Until somebody has a way to make this decision, they should shut up about utilization growth.
Another source of high costs is high prices per procedure or treatment, compared to prices in other countries. A lot of time could be bought bringing down these prices, although this would upset providers. There are other useful measures in the realm of prevention, medical records, etc. But I would say the major choices are prices v. quantities. Restricting quantities is very dicey from the standpoint of somebody facing Death. Have you been there? Deflating prices is political difficult but less problematic from a consumer/patient perspective.
Once everyone is covered, public subsidies can be used to tighten the screws on prices. Quantity restrictions are tantamount to incomplete coverage. You're covered for some treatments but not for others. Insurance is most important for limiting the upside of catastrophic expenses, including for treatments that are "usually ineffective" or diseconomical in the analysis of People Who Haven't Been There. Because once you need that kind of treatment, you will want it. Health care costs are unsustainable in the long run, but facing Death is always a short-run thing.

















My favorite is "unnecessary tests". I can't tell you how many people I knew (note the past tense) whose doctor wouldn't do the "unnecessary test".
August 2, 2009 6:31 PM | Reply | Permalink
Thanks for your patience and sorry for the inconvenience!
Best regards, Mary, CEO of youtube to mp3
December 17, 2010 4:32 AM | Reply | Permalink
What youre saying is completely true. i agree with you.
children health
January 11, 2011 2:41 PM | Reply | Permalink
I do agree with all the ideas you have presented in your post. They’re very convincing and will definitely work. Still, the posts are very short for starters. Could you please extend them a bit from next time? Thanks for the post.by healthy families and child health plus
March 23, 2011 11:39 AM | Reply | Permalink
Well, I have been there, just as you have, since I have buried parents and friends, all of whom faced ailments that one could throw more money at. I think what you left out of your discussion is "quality of life".
At some point extending ones life means extending the period of time when the heart beats and air flows through the lungs, but the brain is "asleep", and not benefiting from the extension. At other times, extending ones life means continuing to experience a choice of brutal pain or a brain so fogged by drugs that wild dreams haunt you. And, at still other times, extending life just gives you some more days in a care facility, waiting for the inevitable appearance of the grim reaper.
Those times are not when economics dictates ones choice. Actually, economics is normally only a concern of the insurance company, and that entity will do just the calculations you mentioned, balancing their effect on profits, and bonuses, with rarely a thought for the human being discussed.
I don't think a government run health care system would change that aspect at all. The Civil Service people would still look at numbers and not people, and the numbers would rule.
Meanwhile, back to the debate over how to avoid bankrupting the entire population of this country with health care costs......
August 2, 2009 6:36 PM | Reply | Permalink
I've been there, too -- I lost my father just 3 months ago -- and I think I well understand what Rotwang is saying. I thought I was ready for that decision when the time came. But the truth is, when it's someone you love, it's the hardest thing in the world to say, "Let him go." I knew it was the right thing, but it was still almost impossible to bring myself to say it.
TV medical dramas do society a disservice. They lead us to expect miraculous outcomes as a matter of course. It would be preferable if they could give us a better sense of how very seldom heroic measures are successful, and if we had a better sense of that, we would be less likely to demand them.
August 3, 2009 2:21 AM | Reply | Permalink
In so many ways it is unfair to make policy based on the searing personal experiences of individual experience with death, and so you have my condolences.
You said, I think accurately, it is hard to let someone go, but my question is, what did your father want?
Many people are not in control of their own destiny at the end of life, so they really can't control how much effort is made to "save their life". Others make their wishes known ahead of time, formally or informally. Given the choice many people would rather choose a hospice than a hospital ICU.
August 3, 2009 1:33 PM | Reply | Permalink
Seconding hoppycalif2's observations. I watched my father die from pancreatic cancer a few years ago, and think it's worthwhile to contrast the expectations of different generations.
He looked around, talked to specialists, and investigated some experimental programs at a big state university medical center.
In the end, he decided that there wasn't enough of a chance of any reasonable outcome to offset the horrible nature of chemo and radiation. (My wife has had cancer three times, two times with these treatments, so I know a lot about what it does to a person. She survived all three times, thank God, but it was awful for her, and for those of us who had to watch.)
Back to Dad...
He went home, called Hospice and went on morphine to manage the pain, and died within a short time in his own bed, with my mother, brother and I there. Was it terrible to lose him? Sure. But the point is that he got to decide how he went out, and chose the most dignified path possible.
He was born in 1907, and lived most of his life without all of the amazing medical technology we take for granted now. Maybe that made a difference, as he and his generation were more familiar than are we with death and a certain kind of acceptance that comes with not having a lot of options, sometimes. I don't believe suffering is automatically enobling, but it is also part of life and death, and we ought to try to keep it real as much as possible.
They'd also gone through the Great Depression and WWII, and knew a lot about sacrifice and the things that make a life worth living. I think we've lost something important in that regard, with too many comforts and the expectation that our medical system is able to do just about anything. Maybe there are too many doctor shows on TV, with actors trying to look too heroic.
As to my wife's experience, we'll go the whole nine yards if there's a hope of success. What's one more time? But we've talked about this issue a lot, as you might imagine, and have decided that neither of us is going to assume that we're going to live forever, and that heroic measures to save us from the inevitable just aren't all that smart. Quality of life, and the dignity that comes from facing one's fate with a clear eye and some courage at the end, is worth more than all the high-tech futility around.
August 2, 2009 7:07 PM | Reply | Permalink
I agree with hoppy and goshen. Quality of life is important and heroic measures don't seem so worth it to those who have seen it done to others. My parents are simple working class folks, my mother never even graduated from high school. They were so horrified at the way my grandfather died that they both filled out living wills within a couple of years after his death to make sure it doesn't happen to them.
"Because once you need that kind of treatment, you will want it," may be how some deal with end of life issues but for others a peaceful, natural death is more desired than six more months of pain, suffering or near total disconnection from reality.
August 2, 2009 10:54 PM | Reply | Permalink
I appreciate the perspectives from happycalif2, Goshen, oceankat. Whatever happens between public health care and private insurance, those quality of life decisions should remain, as much as possible, in the domain of the patient and the patient's family and friends.
As to whether a public option would increase or decrease the patient/family decision-making power--well, I'm really wondering about that.
August 3, 2009 7:36 AM | Reply | Permalink
All medical decisions should be made jointly by patients and their doctors in my opinion.
The difficult fact is that most people are spending someone else's money at some point and so it's hard to prevent them from taking an interest in what you do.
August 3, 2009 1:37 PM | Reply | Permalink
One of the interesting things about the reform package is that the costs of consultation/counseling required to make those end of life decisions rationally would be covered by the reform. I could make the decision fully informed, and were I incompetent, the person who was acting on my behalf could be fully informed. I won't want anyone to make those decisions on my behalf based on medical advertising, word of mouth, or any other alternative.
August 3, 2009 2:47 PM | Reply | Permalink
Well, there's one line I've seen that I can't quote exactly, but can paraphrase pretty closely. "I would rather that the bureaucrat who decides whether I get health care or not does not have a fiduciary responsibility to produce the greatest profit for his shareholders."
I find it troubling that "health insurance" companies categorize payment of medical bills as "losses," rather than the cost of doing business. I also find it troubling that "health insurance" companies spend so much on what they call "underwriting", which is the systematic denial of coverage and/or rescission of the policy you have been paying for years.
August 4, 2009 3:15 AM | Reply | Permalink
The best article I have seen on inflated health care costs was in The New Yorker Magazine. It deals with health costs whether or not one is near death, and how over treatment/surgeries/invasive tests can lead to complications and death.
The author noted the highest Medicare charges per person in the country was in one of the poorest counties, a city called McAllen, Texas.
The article reveals that the doctors in McAllen order every test they can get the government to pay for, and do unnecessary surgery that kills patients to fatten their pay checks. Some of the doctors admitted as much in interviews. They also operate under limits on lawsuits in Texas law.
This sort of medicine for the dollar and not for health of the patient is hard for either the patient or the payer to detect. The doctors involved all legally get a percentage of the dollars received for tests, and own the testing facilities in most cases.
The author compares McAllen with Grand Junction, CO, and finds the doctors there coordinate and evaluate care and have some of the lowest Medicare billings and best outcomes in the nation, with more conservative less invasive care.
August 2, 2009 7:29 PM | Reply | Permalink
You said: The best article I have seen on inflated health care costs was in The New Yorker Magazine. It deals with health costs whether or not one is near death, and how over treatment..
Sorry, but Atul Gawande's article was wrong on the merits. See a real analysis at this url:
http://tinyurl.com/lhewx6 McAllen: A tale of three counties
August 3, 2009 1:03 AM | Reply | Permalink
If you read the comments section of this article you will see the author of the article and Paul Krugman, as well as many others, agree rather than disagree with Gawande;
I do believe that the interaction of diabetes and heart disease explains much of the difference that is reported. I do not want to make this argument to obscure the value of Gawande's work - I think he is more right than he knows. I do not disagree with the need for a very thorough review of the incentive structures that physicians, hospitals and home health agencies are subject to (and creatively react against). Cost containment efforts for different provider types frequently work at cross-purposes and are in many cases counter-productive. I am concerned that the McAllen argument leads to a false conclusion that overly focuses on bad actors in specific locales as opposed to structural faults that are pervasive.
Posted by: Daniel Gilden | Jun 22, 2009 1:27:44 PM
Interestingly,this article actually proves Gawande is more right than he knows...adds more... disagreeing--physician are not only the bad actors driving the problem -- shows...actually, its multi layer, structural across providers and endemic...
Posted by: Paul Krugman | Jun 22, 2009 10:03:08 AM
August 3, 2009 8:52 AM | Reply | Permalink
McAllen and El Paso were used for the purpose of humanizing, or making more accessible, the fact that there is tremendous variation in Medicare spending depending on where you live. It has been carefully documented and analyzed by the researchers at the Dartmouth Atlas for 20 years. Any number of other cities could have been used.
Excess utilization due to excess supply as well as idiosyncratic medical practice (rather than evidence based medicine) are the chief culprits.
Read anything by John Wennberg, Eliott Fisher, Jon Skinner, or Shannon Brownlee.
August 3, 2009 1:44 PM | Reply | Permalink
Who is Daniel Gilden?
Is he the health care utilization wonk who runs Jen Associates?
If this is the guy some quick research indicates he means well, but the job of these guys is to get a piece of the pie, and the bigger the pie the bigger their portion. The doc's in McAllen would run circles around this wonk, similar to Tim Geithner vs. Wall Street
August 3, 2009 11:09 AM | Reply | Permalink
Rotwang - the vexing nature of this issue is illustrated by the fact that many thousands of pages have been devoted to it. For a sampling, visit the wikipedia article - http://en.wikipedia.org/wiki/Evidence-based_medicine - and some of its many links. One good one is the first external link - to the Institute of Medicine.
I would just make a few points.
1. No proposed reform would deny a treatment to anyone. What a reformed system would necessarily do is refrain from paying for all treatments in all circumstances. If reforms are adequate, however, the denials of payment will be fewer than currently.
2. In a world of limited resources, a decision to provide something for one person is a decision to deny something to someone else. No philosophy can circumvent that reality. Reform proposals that minimize ineffective interventions - whether totally ineffective or merely not very effective - can in some cases free up resources to provide interventions that do a better job. For some individuals, this will be a loss, but if reforms are prioritzed equitably, the overall result will be a net gain. Equally important, it may permit some individuals to receive treatment for an intervention that is vitally important, at the expense of another individual who then must either do without something less critical or pay for it out of pocket.
August 2, 2009 7:53 PM | Reply | Permalink
a decision to provide something for one person is a decision to deny something to someone else.
In McAllen, Texas, and other areas this is not a difficult decision under out current system.
You test those for whom the doctor can collect the highest reimbursement.
Fred may know if removing financial incentives for those providers ordering tests is part of some of the health care legislation.
August 2, 2009 8:24 PM | Reply | Permalink
HR3200 proposes pilot programs to determine how best to minimize unnecessary or duplicate programs and services. Nothing is mandatory at this point, but without some type of prioritization, American healthcare costs will be unsustainable. Failure to bite this bullet will ultimately endanger far more lives than even the current system puts at risk.
August 2, 2009 8:29 PM | Reply | Permalink
I think a better way to understand this is that currently your physician has very little idea how efficacious any of the possible treatments he or she could prescribe might be. Nor whether cheaper or less invasive treatment tend to dominate the more expensive, more invasive ones. They simply don't know. We would be much better off is every physician had an evidence based guide to what is most effective. You wouldn't need to restrict treatment, but you would need to educate.
The other point is that it makes no sense to have payment policies that provide incentives for providing more quantity of serves rather than the best quality service. Doctors have to decide to do what is best for their patient or to do what is best for their bottom line. In the absence of evidence, they can easily claim that they always act in the best interest of the patient, even when they really have no idea. The truth that is not well understood is that providing better quality health care is in fact cheaper then just doing what we are doing.
August 3, 2009 1:53 PM | Reply | Permalink
Great post, thank you for this.
My prediction is that everybody is going to overlook the key point: "..the major choices are prices v. quantities."
Most people are going to assume that "the last year of life" perfectly correlates to the person's actual age.
So, I expect to see a mad dash under the cover of "quality of life" in the coming month.
Great new argument to explain what the Health Benefits Committee is going to do: "OUR PANEL THINKS that YOUR QUALITY OF LIFE just doesn't make it worth the taxpayer money"
August 2, 2009 8:10 PM | Reply | Permalink
First, you should read some facts about this whole bill.
http://www.politifact.com/truth-o-meter/article/2009/jul/30/e-mail-analysis-health-bill-needs-check-/
Second, I may have insurance (and I have a pretty good plan through my employer), but none of us has assurance that, should something happen, that the insurance companies won't try to duck payment. I've worked in investigation of insurance fraud, and have come to loathe insurance adjusters. They're whole job is to stiff people who've paid premiums in the naive trust that when the time for paying a benefit comes that it'll happen. Too often, the private insurance system operates more like a shell game.
I hope you never have this experience, and any trust you have in the current system is never tested.
August 3, 2009 9:08 AM | Reply | Permalink
I have no doubt that you're right. But I think Rotwang makes a point here about understanding what the choices really are versus what they are claimed to be.
"Another source of high costs is high prices per procedure or treatment, compared to prices in other countries. A lot of time could be bought bringing down these prices, although this would upset providers. There are other useful measures in the realm of prevention, medical records, etc. But I would say the major choices are prices v. quantities. Restricting quantities is very dicey from the standpoint of somebody facing Death. Have you been there? Deflating prices is political difficult but less problematic from a consumer/patient perspective."
August 3, 2009 10:41 AM | Reply | Permalink
Very old patients have lower end of life care, in fact., because they tend to be healthier.
The choice between bringing down price or restricting quantity is a fallacy. If all you do is reduce the rate of payment then there is even greater incentive to increase the quantity if services to make up for it. Under a fee-for service payment system you are almost begging for it.
The other fallacy of this argument is the idea that the current supply of care is based on some sort of informed understanding of what is best for patients. It is not. The places who deliver the highest quality care the most efficiently do so by (1) deliver care in an organized way so care is not duplicated or worse exacerbated by multiple points of treatment, and (b) doing what the evidence shows them is the right thing to do, and then they do it the right way the first time.
August 3, 2009 2:01 PM | Reply | Permalink
I will not share my experiences, but feel qualified to say I have been there with death.
Rotwang seems to have a completely garbled message, partly, it would seem, because he is ignoring basic economics and partly because he seems not to realize how crappy private health insurance has become.
No one, let me repeat that no one lives "in the comfortable womb of good private insurance." No such thing exists any longer. Wealthy people can afford to pay out of pocket for an indefinitely long time and members of congress provide themselves luxurious health benefits, but the rest of us are already at risk, even those who have the semblance of "good private insurance."
The opponent is not the merciless economist (god how I hate to ever defend economists), it is the utilization review analyst, usually a nurse, who will deny your care for a poorly completed form as quickly as for the fact that it is quack quack quackery from Quacksville. Ironically, the UR analyst also has crappy health insurance.
This is not a new phenomenon to anticipate under a new government health plan (tightened to the bones by the anti-tax crowd), it is what we have had for 40+ years and it has been getting worse every year. When, 40 years ago, your doctor or your parent's doctor asked you to sign a form allowing him to receive assignment of your health insurance payment, you should have said "Hell no, I will pay you and deal with the insurance company myself." That would have delayed, if not blocked, the UR analyst development.
That water is way past under the bridge. And, THAT is why we need single payer. Single payer can free competent health care professionals to perform their services without the constant insolence of UR analysts, who should, collectively, be relegated to one of the lower rings of hell.
Now, having said that, that only scratches the surface of Rotwang's nonsense. As Rotwang well knows, societal decisions are based on allocation of scarce resources. The scarce resource in this instance is not health care, it is economic power, otherwise known as money. Despite our individual desire otherwise, there is a point where society cannot put more resources into health care. To do so takes resources away from other vital matters. I personally think we could easily take $1-200 billion a year out of the military budget, maybe more, and spend it on health care. But, I do not have the clout to make it happen.
When we max out on our willingness to pay, all other health care finance decisions are zero-sum between health care beneficiaries and vendors. For example, in my long ago job in public health finance, we were concerned that fast growing costs for certain elderly would be spent in the opportunity cost of immunizations and other relatively inexpensive but very effective health care for children.
The low hanging fruit in the health care pie is the excessive overhead of insurance companies (including all those UR analysts). The next, not quite as easy to get at amount is the profiteering by nursing homes, hospitals, pharmaceutical manufacturing companies, medical appliance companies, and others in the health care production function. Yes, that includes physicians who, understandably, make up the most bizarre excuses possible for their extraordinary pay relative to other similarly skilled professionals. Then, there is the matter of what to do with momma (or pop), the very existence of the entire nursing home industry reflects a disgraceful failure of the family.
All of that comes before deliberate rationing. I say deliberate, because we have had de facto rationing for quite some time.
I hope Rotwang does not repeat this sort of column. I have long been a fan of his, but scare mongering is no more attractive among progressives than it is among the right.
August 2, 2009 8:32 PM | Reply | Permalink
I agree that "the comfortable womb of good private insurance" does not really exists except for Wall Street Masters and in the imagination of healthy 30somethings.
But how does that affect the medical choices offered those facing death in the last month and weeks when care costs the most? Those without insurance may not even get to the point where those choices are possible. That is where rationing happens now and where reform will be expensive if everyone is covered.
But if they end up in an ICU in a teaching hospital like I worked at I never was able to see any difference in the choices presented whether they were destitute or wealthy. Yes, the wealthy always had the option of a second opinion from the Mayo Clinic. But in that ICU I saw no difference in care wether it was paid for by insurance, medicare, medicaid or state aid.
Rotwang seems to think reform will restrict those choices but I don't see that changing either no matter what happens. Doctors will be paid less if they aren't paid fee for service. That is where money will be saved but that won't restrict the patients choices.
August 2, 2009 10:30 PM | Reply | Permalink
And why would you think I am in disagreement with you? I agreed that aggregate health budget must stop growing, but I pointed at other places for it to stop.
August 3, 2009 10:24 AM | Reply | Permalink
Oh, I see, you think that I am saying docs de facto ration at the ICU. No such thing. The rationing is going on at the admittance office and in the emergency room.
August 3, 2009 10:35 AM | Reply | Permalink
"Oh, I see, you think that I am saying docs de facto ration at the ICU. No such thing. The rationing is going on at the admittance office and in the emergency room."
No, I wasn't disagreeing with you and I don't think you were saying that docs ration care in the ICU. I was clumsily trying to focus your points on Rotwang's concern about the "last week of care".
August 3, 2009 3:19 PM | Reply | Permalink
My two cents anecdotals, large non-profit hospitals in a medium-sized city. I had a close family member in ICU in life/death situation for several months, very expensive, 15 years ago, @ 63 years old. And 3 months in ICU at the end 2 years ago. Quite a few regular hospitalizations inbetween for complications/infections, and other expensive care, but overall pretty good quality of life inbetween.
The doctors 15 years ago seemed to be stronger advocates of life. Somehow over the intevening 13 years many of them have been won over to the "hospice uber alles" movement, that anyone with acute illness or of Medicare age doesn't deserve an old college try or the expense of much sophisticated intervention. So much so that I found it appalling at times, it came from things that were said to me personally but also from discussing with other families in the ICU as one ends up doing in that situation. I can't tell you how many families had stories of one doctor saying it's over, send them to hospice, and other cases just like mine, where they got another opinion and another good decade or more of life.
I agree with you in that I never saw any, not a smidgen, of profit-motivation in any of this, nor consideration of who was paying. It doesn't have to do with insurance companies. It's not as simple as how the individual patient is paying. (Part of the reason is how hospitals are paid by Medicare and Medicaid already, it really does not apply to even think of individual payments.) They don't think like that, but they do think about rationing now much more than they ever did, and they often do it very cruelly and also some do it ineptly. They are really playing God. Often. I saw so much more evidence of it in the 2 years ago episode than the 15 years ago one.
In a way, I think it really would be better if there were government protocols, because from my anedotals, many are now rationing by personal decision on whether they think the patient's life is worth it, really appallingly in some cases. It would save a lot of mental suffering by family members.
Think about this...what a doctor might value in quality of life is simply not the same as a patient that is not a doctor ...not everyone thinks golfing is so cool, for example...matter of fact, I happen to have had lots of doctors as clients in the past and I didn't envy their lives one bit, nor did I all of them were contributing much to society, hah.
August 3, 2009 2:01 PM | Reply | Permalink
Are you saying that at this hospital all of the doctors were rationing care on the basis of their personal evaluation of the patient's potential quality of life regardless of the patient's and family's wishes? So it was a matter of the culture of this hospital or group of doctors?
As I understand the proposal for "best practice protocols" these protocols would not be binding. But it would be a public and political (approved by congress on a regular basis) document that families could use in the situation you describe to challenge the options that physicians offer.
And those same protocols could also be used in the opposite case where physicians may end up prolonging the suffering with endless and futile procedures. Yes that happens too as others in this thread have confirmed. One family member suffers for months on life support and then the whole family decides to make out living wills to prevent that in their own case.
The wingnuts will say Obama is trying to kill Granny but they may end up using the same protocols to make sure Granny gets the best care possible.
August 3, 2009 4:05 PM | Reply | Permalink
I was saying that over time I've seen a lot of evidence of a lot of doctors in ICU care in two hospitals get much more comfortable with telling patients "it's over and there's nothing we can do for him/her" when that wasn't true. Literally not true, as in, they found another doctor and it wasn't over and it wasn't poor quality of life, either. More and more it seems, they won't do high risk, they feel like they are wasting their time on those with iffy chances, seems they would rather give their services to the easier cases with a better upside chance. Example, something like a person that's 60, lost a leg to diabetes, has had a lot of years of drug treatment meaning might have failing kidneys sooner rather than later...they say no to a heart valve replacement necessary to prevent infectious that all of a sudden have been happening because of that problem, tell the family it's not possible, that the patient should just get "comfort care," i.e., wait for imminent death through stroke or blood poisoning. Said patient finds another doctor, gets the operation, lives another 10 years with same quality of life as previous and without the complicating infections. I heard three stories of patient's families tracking down the doctors who told them to let their family members with such type situations in order to inform them of the life that they had been enjoying after finding someone willing to take a chance. What I am saying is that in my experience, pushing of hospice over intervention with a relatively high risk of failure is becoming increasingly popular among doctors. And yes, that's contrary to what you are reading in the media, where everyone is saying everyone with insurance is getting all possible care. I saw evidence that doctors in ICU type care are already cutting way down on trying to save lives that are already compromised, i.e., if you weren't 100% healthy before the current problem, they tend to think of rationing what they do for you, they make calculations about how valuable your life and years are, calculations they wouldn't make if, for example, you were the leader of a big country or the pope or someone of similar importance.
August 3, 2009 4:36 PM | Reply | Permalink
"Doctors will be paid less if they aren't paid fee for service. That is where money will be saved but that won't restrict the patients choices."
Bad doctors should be paid less, and better doctors should be paid more. Doctors who are wasting resources should be paid less, doctors using resources effectively for the benefit of the paitient should be paid more.
August 3, 2009 2:05 PM | Reply | Permalink
August 3, 2009 2:04 AM | Reply | Permalink
The rumors of fraud in Medicaid and Medicare are greatly exaggerated. And the expense of rendering any program, public or private, fraud-free is, as Rotwang calls it, diseconomical.
August 3, 2009 10:22 AM | Reply | Permalink
It's not about fraud, it is about eliminating waste in a system where you are paid for each service whether it is wasteful or not.
Most physicians really have very little idea whether they are wasting resources or not.
August 3, 2009 2:09 PM | Reply | Permalink
What makes you think there is any less fraud and abuse in private insurance? Many years ago, I worked for an insurance company, and you bet we had a department whose job it was to root out fraud and abuse. However, we didn't report any statistics about F&A in regards to our private plans (we also did some Medicare Part B, and CHAMPUS, which we did have to report). To the best of my knowledge, most of the fraud cases in the private plans were settled out of court with the doctor. Medicare fraud would have been referred to the appropriate US Attorney. Also, if a doctor is convicted of Medicare fraud, at the very least they are generally barred from any further Medicare billing. If I had to guess, I'd guess that there was actually less fraud in the Medicare system, simply due to the fact that it was more publicized.
August 3, 2009 11:50 AM | Reply | Permalink
I find some similarity between death-penalty arguments and the current "effective medicine" questions. A good reason to not settle a criminal case by disposing of one suspect is that it precludes possibly finding the real culprit. Eliminating appeals can eliminate truth.
Why does Mayo Clinic have a better track record than McAllen, Texas' hospital? It's not that it did fewer tests and procedures, it's that the different emphasis at Mayo does not answer too quickly by resorting to tests and procedures. That the staff doctors can spend more time on a case doesn't mean worse care, even though it is less costly overall.
I doubt that any patients of Mayo doctors feel they did not get adequate care. Its reputation comes from results. This is the kind of cost control in question, not the patient-shedding or procedure-denying insurance model.
A colleague who shares my high-quality health insurance, and makes an easy six figures salary, went to Mayo for problems with his playing caused by focal dystonia. He went there for the results, not the cost savings.
August 2, 2009 9:22 PM | Reply | Permalink
You are exactly right.
We could add the name of another dozen integrated providers/multi-specialty practice groups that provide more cost effective care precisely because they are so focused on providing the highest quality patient-centered care.
August 3, 2009 2:12 PM | Reply | Permalink
As someone who has been there and worked in an ICU I can tell you that there are three huge variables in the "last week"; the individual, the immediate family and the attending physician and the choices of treatments that they choose to present.
To grossly oversimplify it, if the patient wants to push the limits then they will get the 1% choice, if not they will get the 5% choice. But it also depends on the attending. Is she participating in research in a 1% choice or did he recently have a horrible experience last week with the 10% choice? The biggest variable may simply be on how the physician presents the choices to the patient. But there is always always a bias towards trying everything if the patient or the family insist on it.
I don't see reform changing any of those dynamics in terms of what choices are offered unless hospitals put increased restrictions on physicians when insurance doesn't cover it and doctors would fight that tooth and nail. "Hail Mary" and long shot treatments are often the leading edge of medical practice and yesterday's long shot is often tomorrow’s standard. Hospitals who limit that loose doctors and patients.
But there is one aspect of reform that does have the potential to cut costs in the last week in a major way. If the fee for service model is changed to a team oriented salary model for physicians then the cost of that last week would be greatly reduced at the physician’s expense. I don’t think that would alter the choices of treatments for the most part but it may change the type of physician who would choose to be an intensivist or hospitalist.
I have worked with both types and I want my doctor on a salary, if he’s in it for the money let him go into plastic surgery or to Wall Street.
August 2, 2009 9:46 PM | Reply | Permalink
BobFred2 - Although a salary model works well in the VA system, I doubt that it's politically viable on a national scale. An alternative will be to replace "fee for service" with "fee for value", in essence attempting to substitute quality for quantity. Needless to say, defining "value" will not be easy, but criteria already exist is some areas - e.g., blood pressure control, blood sugar levels in diabetes, smoking cessation, etc.
August 2, 2009 10:10 PM | Reply | Permalink
Kaiser pays their doctors a salary, not based on tests, surgeries, treatments, etc., just a salary. It works very well, as far as I can see, and I have been in the Kaiser plan for many years, off and on, currently on. My current primary physician, the best one I have ever had, is a lady from Pakistan, whom I gladly trust my life with. And, I am equally pleased with the many specialists I have had to use there. Given how well the Kaiser model works, I can't understand why that model, along with the Mayo Clinic model, isn't used more often.
August 3, 2009 12:37 AM | Reply | Permalink
Many companies offer Kaiser and a PPO. Most people choose a PPO even if they have to pay more.
August 3, 2009 2:10 AM | Reply | Permalink
Kaiser? Ah Yes...
Hey Hoppy . . .
Here's a little background on our health plan over at Bill Moyer's Journal blog (scroll down to "On an end note" ...
27 years ...
Years ago, my dad often referred to Kaiser as a communist idea. I tried to explain to him, yes it is socialized health care but not communist, but it's very good. He asked what's the difference. He felt that way until he needed help at the local VA after having a stroke. When he was feeling better and up and about, I asked how he felt about the VA care. He said it was top-notch and it saved his life. I said, that's what socialized health care can do. He never said another bad word about me and my family being members of Kaiser. God rest his soul.
Oh sure there's horror stories about Kaiser. Why hell, there's horror stories about all kinds of health care systems. We do not live in a perfect world.
~OGD~
August 3, 2009 3:17 AM | Reply | Permalink
What a story OGD. One of thousands that need to be told. And of course you are telling the story so well in so many blogs.
I just mean the personal aspect. Like Miguel, Like Bwak....
Thank you.
August 3, 2009 3:59 AM | Reply | Permalink
I agree, that's a story indicative of what we're dealing with here, and quite humorous as well.
August 3, 2009 8:04 AM | Reply | Permalink
August 3, 2009 2:33 AM | Reply | Permalink
Fee for value doesn't require favorable outcomes when they are not possible, but rather the best results achievable in terms of illness avoidance, comfort, quality of life, reduction of suffering, and when possible, disease cure or optimal amelioration. It's not always easy to define in every circumstance, but there's already sufficient experience to show it's achievable, and better than what we have now.
August 3, 2009 10:29 AM | Reply | Permalink
How and how will decide in each and every case what is the best results achievable? We still haven't figured out how to reward a teacher or a school for the the best results achievable. Don't you think that health care is a little more complicated?
August 3, 2009 10:50 AM | Reply | Permalink
What you are saying amounts to acknowledging you are lost and insisting that the only choice of finding your way is straight ahead.
Lots' of places are working on this and have viable options. Your own ignorance is a poor excuse for continuing the stupid path we are on.
August 3, 2009 2:17 PM | Reply | Permalink
Why don't we start with education? Let's figure out how to reward a teacher or a school for a good work.
THis will be a prove of concept.
August 3, 2009 2:56 PM | Reply | Permalink
Um, that would be "proof" of concept.
August 4, 2009 1:03 PM | Reply | Permalink
I agree, and I think physicians themselves could go a long way toward curbing end-of-life costs if they would help the patient's family come to a most difficult decision by simply saying, "We would recommend not going ahead with further measures at this point." Or something along that line. My own experience leads me to believe that in at least some instances, the family just needs to be reassured that it's OK to say "No more," that it's not likely that further extraordinary measures will change the outcome. There can be a huge gap between what the layman knows in his head and what he feels in his heart, and the professionals need to help them bridge that gap.
August 3, 2009 2:38 AM | Reply | Permalink
You assume the doctors actually know. The lack of systematic evidence is, I think you will find, somewhat shocking. That last thing you want is your physician saying "in my experience..." when data are available to shed light on actual prognoses.
You should look into the "shared decision-making" model.
August 3, 2009 2:21 PM | Reply | Permalink
However, they are entitled to pay themselves directly or by buying a private insurance.
You seems to advocate something that we have today in K-12 education: Mediocre overcrowded public schools with low paying teachers, rigid rules and regulations and many levels of bureaucracy without any choice for customers versus private schools with small classes and high quality teachers.
August 3, 2009 2:52 AM | Reply | Permalink
My mother died of a form of leukemia. There were treatments to prolong her life for years (mainly blood transfusions) and she had good insurance.
She chose not to wish for a hero. She was tired of being medically messed with. She was tired of feeling really crappy for a large percent of her time. And on and on. Family-members tried to do it for her, but she more and more steadfastly resisted treatment. And that's pretty much how it ended.
I only mention this as an alternative to the scenario that Rotwang depicted.
August 2, 2009 10:11 PM | Reply | Permalink
I've been there too.
Single payer advocates, however, are not touting cost control primarily from things like unnecessary tests. Single payer advocate are touting cost controls through economies of scale and elimination of the for profit healthcare insurers who charge way too much for their own profit and for exhorbitant and unnecessary administrative costs. That's where the biggest long term savings are realized and ought to be. Cost savings on things like "unnecessary tests" are at best marginal savings and won't make any big difference in the overall cost of care. Unifying the system nationally as we have done with Medicare, economies of scale and elimination of profit are all within our grasp and perfectly reasonable if and only if we quit farting around with the half measures and ineffective "reforms". We need a radical transformation of our healthcare system which will only come when the profit is taken out of it and some form of single payer funding is established.
August 2, 2009 10:24 PM | Reply | Permalink
Why, under the same single payer Medicare system for similar patients with the same prognosis, do we spend twice as much on a patient in New York as in Salt Lake City?
Answer it largely has to do with the amount of care being delivered.
There is ample evidence that delivering care more effectively can reduce costs dramatically. What happens if we change who pays for it is mostly speculation.
August 3, 2009 2:25 PM | Reply | Permalink
This leaves the impression that private insurance is not 100% driven by the metrics of option #3. To pretend that "rationing" by the government will be more brutal than what the market-based private insurance industry does today is a fallacy. With the system we have today, if you need serious health care and the insurance company is called on to provide it, you (and your employer, family, etc.) are very likely to lose coverage.
In a past life, I made an awful lot of money writing software to help accomplish their goals. And as a small family business, saw the other side after my father had bypass surgery and suddenly we and our employees were faced with tripled premiums. They won't write policies lasting longer than a year for a reason. Only the largest pools can absorb even a single bypass surgery without a significant re-rate.
Watch the recent Bill Moyers interview with one of our former clients. You will never get a more accurate description of how care is rationed every day by an insurance industry that flat-out lies to the public.
There is no way a government run system could ever match the Darwinistic brutality of the private insurance industry. Period. Their reward structure is based on how many people they can allow to die by denying coverage. Anyone who asserts differently does not know what they are talking about (or are lying).
August 2, 2009 10:53 PM | Reply | Permalink
I've seen the same thing with my employer. It is a small business by the textbook definition (less than 500 employees) but it is not small: ~250 employees and $45 million in revenues.
In 2003 we had two medical 'events' among employees and their dependents. One guy's wife became pregnant with twins. She spent several weeks before their birth in the hospital herself, and the twins were born prematurely. The twins spent 2 weeks in NICU, and a total of 10 weeks in the hospital.
About three months later an employee survived a brain aneurysm. He had neurosurgery, spent several weeks in the hospital, and had months of physical therapy afterward.
Fast forward 6 months to the annual renewal of our health plan and the company we were with sought a 40% increase in premiums. I don't think it was a coincidence. And, just for context, this was after several years of the company eating annual increases of 10%-15%.
If we had paid the 40% it would have represented about 10% of the company's total annual profits. We looked for another plan instead. We shopped every plan in the state and the best deal we could get was a 30% increase, coupled with switching to a high deductible plan. The company used to be able to offer great benefits but when it comes to health insurance we have been on the treadmill of paying more for less every year of the past decade.
August 3, 2009 12:43 AM | Reply | Permalink
Joe Bob, what you have written is the best point I've seen yet for the public option. I could almost say that I hadn't yet made up my mind about the issue until I just read your comment.
The scenario illustrates well the core of our problem, and implicitly directs us toward a public alternative.
August 3, 2009 8:16 AM | Reply | Permalink
Sure sounds like a public option, paired with changing the incentives for doctors from fee-for-service (and avoiding medical malpractice costs) to one that pays them an outstanding salary for the service they give to society and devalues excessive and unnecessary tests, is an outcome that would mitigate most of the problems with the current private insurance nightmare.
August 3, 2009 9:23 AM | Reply | Permalink
Some additional costs in the current system are:
- the employer's costs for researching, regotiating, and administering an employee health plan;
- the cost for HR consultancies who assist employers in this process; and
- the sales, marketing and adminstrative costs of the insurance companies for dealing with employers.
These may not be significant for big companies, but they add up for small companies.
August 3, 2009 10:19 AM | Reply | Permalink
I think this post is brilliant and that it's a shame that what Rotwang is talking about here isn't part of the debate.
The problems we have with our health care system in America can't all be summarized as problems of cost. The cost of health care and health insurance is too high but you can only say that something costs too much in relation to... what you get.
If health care in America costs too much then the corollary is also true -- we get too little for what we pay.
The focus of this debate has been about bringing costs down. That's a mistake. We should be talking about making more and more generous service available.
As Rotwang illustrates quite well... this notion of expenditures in the last year of life is all bunk. Heck, up until the point that the patient agrees to hospice and end of life pain mitigation, the medical establishment should be spending huge amounts to set the patient back to healthy. We should be doing more and thus paying more when the patient is in trouble. That's... um... the point.
Health care doesn't "cost too much." The problem is that we pay and we get too little.
August 3, 2009 1:11 AM | Reply | Permalink
I think you have the right attitude, destor. The JFK of "we'll put a man on the moon in 10 years" would be proud of you. Not to mention, the whining about how expensive the care of people that aren't of the most profitable age demographic is getting quite tiresome, and is not very pretty coming from people that call themselves "progressive." It's good to see someone argue "we can do this, and we can do it better than everyone else" instead. (And after all, as anyone who watches late night televsion knows, there's money and jobs in producing things like personal mobility devices with which the disabled can be as nasty and aggressive as the more able bodied. :-))
August 3, 2009 2:13 PM | Reply | Permalink
No, actually the debate has largely been about how to cover everyone and how to pay for it. The only sense that we are talking about cost is how to lower the Federal on-budget cost of the subsidies needed to provide universal coverage.
If we were really talking about how to reduce cost of care then you would understand how huge a fallacy it is to assume that more care for an individual is better. It is not.
Generosity has little to do with anything. It is effectiveness and quality that matter.
Most other developed countries get just as good outcomes as we do for half the cost. Getting to where they are is not a matter of more dollars.
August 3, 2009 2:34 PM | Reply | Permalink
The questions are reasonable and the answers hard, but, ultimately, they are misdirected. The point is not simply to see how the proposed system handles the tough questions, but how it's treatment compares to the current one. And kgb999 got it exactly right--it's not like the private insurance companies ignore option (3).
I had the same question the very first time I heard Obama proclaim, during the campaign last year, that the reform will include a database of effective treatments. The problem with such a database is not what's in it, but what's excluded. Every insurance company has a list of standard treatments that it covers, and another list of treatments that are not covered, irrespectively of the probability--or, for that matter, the economy--of a positive outcome.
The point is that an insurance company has an incentive to qualify perfectly accepted procedures as experimental, because it makes economic sense--they don't have to pay for "experimental" treatments. Appeals are irrelevant--the only thing that they are afraid of are court cases. That is, a patient--or, more likely, the estate and the survivors--must sue the insurance company for denial of life-saving treatment, Rainmaker style. If they lose, not only are they on the hook for the award money, but they can no longer claim the treatment as experimental (other companies may try, but would have a hard time justifying doing so if dragged to court).
So, at least in some sense, this keeps the industry honest--they have to factor in costs of litigation and probability of loss (fairly low, especially with the likelihood of a fairly low value settlement) and, at some point, decide that it's cheaper to allow some expensive treatments.
Note that these decisions are purely economic and very similar to option (3). On one side, the cost of treatment multiplied by the frequency of requests for treatment multiplied by the probability of effectiveness. On the other side, you have the cost of litigation (>> cost of treatment) multiplied by the probability of litigation (
This is how private insurance companies do risk assessment. At first glance, it is hard to make it worse. On one hand, the companies delay recognition of life-saving procedures as long as possible, on the other--they can always resort to recision to avoid the responsibility. And organ transplants (among other things) are not exactly emergency procedures, so they are not likely to be picked up on the public nickel under the current regime (except, perhaps, with Medicare and VA).
But, the good thing about it is that doctors are persistent and innovative. Ability of doctors to document their experimentation has improved tremendously over the course of the last century and effectiveness of treatment can be--eventually--objectively demonstrated.
There are two ways to make this situation worse. First, a public database of effective treatments with a hard edge--allow it if it's in, disallow it if it's not--would effectively stifle experimentation. Right now, new procedures--aside from pharmaceutical and medical devices companies doing their own research--are developed in public hospitals which find ways to at least partially cover the costs. Sometimes this is covered by self-paying patients who have nothing to lose and sometimes it is covered by the state, as long as doctors can justify the procedure. There is a good probability that under the reform regime this incentive for innovation will be gone. If the public option removes experimentation and it is already not in the interest of private insurers to provide research backing to new procedures, there will be no new procedures. The US is likely to go from a leading medical research and medical technology nation to an also-ran. Sure, we'll still have to accept the procedures developed in other countries that are proven to be effective, but that just guarantees that we are not at the tail end of the medical world.
The second problem is that the public bureaucracy that handles these decisions is very likely to end up being immune from prosecution (and other court challenges). The worst we can say about private insurers is that they are semi-immune--the initial costs and legal obstacles are so high, that only a handful of cases are likely to make it through. But, if the public bureaucracy is completely immune (as it is in virtually every other sphere, including environmental protection), it will also protect the private insurers--they can always point fingers at the public database and claim, "It ain't in there!" That would mean that the public option is also likely to remove the last economic check on the anti-consumer decision-making by the insurers.
Now, it is fairly easy to come up with good statutory language that would protect the reform from these two failures. But, given the nutty nature of congressional negotiation and complete ignorance of virtually 99% of congressmen on these issues, the probability of this happening is essentially nil.
This does not mean, to me, at least, that we should back away from the public option. But we should be aware of the pitfalls. And always remember that great is the enemy of good. What we really don't need is the mediocre bill that half-heartedly allows a crippled version of the public option but, at the same time, eliminates the meagre handful of protections that we now have against private insurers' overreach. And given the prostitution nature of the swing votes, I am very concerned that this is exactly what will happen.
August 3, 2009 1:18 AM | Reply | Permalink
Perhaps the point of trying to figure out what treatments work is to actually inform doctors of the consequences of their decisions. If they knew, they could adopt the best practices without anyone telling them what they can or cannot do. No one forces Mayo, Intermountain, Geisinger, Billings, Cleveland, Marshfield to look at their own data to continuously improve the quality of care they deliver. You have to ask why it is that the rest of the health care industry gets away without doing that.
It's shocking how little people understand that the delivery of care today is not nearly as scientific as they imagine.
August 3, 2009 2:42 PM | Reply | Permalink
I reject the idea that you can't have an opinion unless you have faced death. It reminds me of a conservative friend who said all pro choice people are hypocrites because they weren't aborted as fetuses. I may change my mind as I face death, but I just may be more rational now.
Society has limited resources and no obligation to provide heroic (i.e. far beyond standard) health care. It is an oversimplification, but every million dollars spent on heroic health care in the last years of life is a million that can't be spent on child nutritional programs. I'm not insensitive, but I was appalled when my wife got into an argument with a surgeon about performing a total mastectomy on her 90 year old grandmother. The surgeon won. The operation was successful, the surgeon no doubt chalked it up as a "win", but she did not have another coherent day in the remaining year of her life.
August 3, 2009 1:30 AM | Reply | Permalink
But... you don't know it's the last year of a patient's life until they die. So you can only look back later and say "look at what we spent int he last year" and so that's a weird and arbitrary way to judge things.
As for limited resources and "heroic care" just come on... we should take all those cost savings from cutting the F-22 and put them into healthcare and we'll be fine. Or... put at much into healthcare right now as we've spent on Iraq. We're not penniless.
August 3, 2009 1:55 AM | Reply | Permalink
How much is reasonable to spend on a premature born baby?
August 3, 2009 1:56 AM | Reply | Permalink
72 times as much as for a 72 year old.
August 3, 2009 2:44 PM | Reply | Permalink
Can you be more specific? How much we should spend on 5 year old, 10 year old, 50 year old 65 year old?
August 3, 2009 2:52 PM | Reply | Permalink
We spend 20 times on a 5 year old as on a 100 year old, which would be three times as much as on a 15 year old but only 20 percent more than on a 4 year old. We should spend on a 65 year old 1/13 as much as on a 5 year old but 2/3 less than a 43 year old. A 50 year old, we should not pay for at all, and even less fro a 49 year old. Spend three time on a 25 year old what you spend on a 75 year old but only half as much as on a 50 year old.
August 3, 2009 4:19 PM | Reply | Permalink
Yes, I have been there.
That out of the way, I'm trying to understand what the post is trying to say about managed health care. Are you implying that everyone should have a right to whatever treatment they want because life is precious? I'm sorry to break it to you but that is never going to happen, it's just not possible.
We don't have the capability to give everyone every possible treatment no matter what - it's not happening now, can we agree on that? The USA is far from "the best health care in the world" in cost or in effectiveness. On the contrary treatments today are routinely denied on the basis of profit, terms of coverage, fine print, and sometimes whatever insurance companies can get away with - if you're covered at all. Treatments are being denied today that are not terribly expensive and not experimental just because a policy doesn't cover it. I am lucky not to have been in this particular situation, and my heart goes out to those who were.
No matter what we choose, we can't do everything for everyone. We're surely not doing it now, and we won't do it later.
I do understand that reformed health care, if done right (read single payer or government option) will make more care available to more people more often.
That's it.
We have universal health care to decide. It's not a triage ethics panel.
August 3, 2009 1:47 AM | Reply | Permalink
If 40 years ago we had single payer or government option, we would have today Universal Tylenol care and nothing else. To add insult to the injury this care would be very expensive.
Can you imagine if 30 years ago we created Universal single payer computer care, How much would an IBM mainframe would cost today, how long would you have to wait to get an access to the terminal. We would talk about cost control, merit pay for programmers and so on.
August 3, 2009 2:22 AM | Reply | Permalink
This is probably the single dumbest comment that I've seen on TPMCafe in a long time.
August 3, 2009 3:17 AM | Reply | Permalink
Don't count on it. The author of this comment is good at it.
August 3, 2009 10:42 AM | Reply | Permalink
It's pretty close though.
Too bad everyone on Medicare only gets Tylenol. I never knew they couldn't choose Advil.
August 3, 2009 2:46 PM | Reply | Permalink
Today everyone on Medicare can choose Tylenol or Advil. However, Advil is a me-too drug. In the future the development of me-too drugs will be discouraged, so everyone only gets Tylenol.
August 3, 2009 3:08 PM | Reply | Permalink
Oh, bullshit. Codswallop, from beginning to end.
No, you don't have to have been there. When my mother was dying, we all, including her, made the same decisions we said we would when she was healthy. In the end, she looked at the quality of life she had to look forward to, stopped dialysis and died peacefully.
Moreover, just because someone wants some hugely expensive treatment doesn't mean they are entitled to have someone else pay for it. They need to deal with the fact that they, like everyone else, are going to die of something someday. Maybe people WOULD want another week to smell the roses even if it cost 100,000 poor children their dental care. Tough shit. People need to grow up.
August 3, 2009 2:33 AM | Reply | Permalink
However, if someone wants some hugely expensive treatment they are entitled to pay for it.
You seems to advocate something that we have today in K-12 education: Mediocre overcrowded public schools with low paying teachers, rigid rules and regulations and many levels of bureaucracy without any choice for customers versus private schools wit small classes and high quality teachers.
August 3, 2009 3:06 AM | Reply | Permalink
I stand corrected--it was not a single comment. It's a pair of ignorant, uninformed, lame opinions.
August 3, 2009 3:19 AM | Reply | Permalink
These are nothing. You should have seen AnnaA during the primaries.
August 3, 2009 7:43 AM | Reply | Permalink
What in the world are you talking about?
August 3, 2009 5:40 AM | Reply | Permalink
You are all very smart people. You are capable of a thought experiment. Why don't you try to imagine what would happen to any industry if rules proposed for health care would apply to that industry?
August 3, 2009 10:45 AM | Reply | Permalink
The whole point is that health-care isn't just any other industry. It's a system of social welfare with both public and private components. In the 1980s, a bunch of Republican "visionaries" got together and tried to figure out how they can squeeze more private money out of the public sector. They identified two large swaths of regulated social entitlements as ripe for privatization--these were healthcare and education. The attempt to take over education started with A Nation at Risk. But the take over of healthcare proceeded much faster, starting with complete privatization (and "profitization") of the medical insurance industry (yes, Blue Cross Blue Shield used to be a system of non-profits). We've been paying for it ever since.
The rest of civilized world recognizes the importance of healthcare as a part of the social welfare system. And it coexists peacefully with private outfits while most of the public is covered by the "public option", just like public education coexists with private education. Both appear to prevent at least some of those who want access to the private system from getting in, but, in exchange, it provides access to the public system for all.
August 3, 2009 12:19 PM | Reply | Permalink
August 3, 2009 2:18 PM | Reply | Permalink
rofl
August 3, 2009 2:51 PM | Reply | Permalink
I would like to be sympathetic, but I completely agree with this comment.
I have been there. Granted my experience was rushed-the doctor told me he had to operate immediately-without any anesthetic- or I would die. And damn straight I was scared to death and would have done anything he said. No matter how expensive.
But that isn't the point, life or death fear is not a fair position to make rational judgments in, and of course survival takes over. The point is that death naturally happens and that our culture needs to learn to accept that. Maybe you won't get to have that last conversation. Maybe you will. Who knows. But maybe its also okay to die peacefully without bankrupting the world so you could have 5 more minutes.
Most cultures throughout the world have ways of respectfully leaving it. Where we die with honor and our loved ones. It would be nice if we did as well.
August 3, 2009 3:11 AM | Reply | Permalink
If you say so.
You are definitely asserting moral authority, however.
Just like everyone else.
That's not an inherently bad thing.
It just gets us nowhere.
August 3, 2009 7:50 AM | Reply | Permalink
Aren't the insurance companies already making these decisions about what treatments they will and will not cover? And who they will and will not cover?
Healthcare reform is not about making every single experimental treatment available at no charge for anybody who wants it. My understanding is that it is about making basic doctor's appointments, tests, treatments, prescriptions and hospital treatment available to more people, and at a more affordable cost.
Nobody is saying that you can't have these experimental treatments....you just have to pay for them yourself. And I don't think that there is anything wrong with that.
We seem to want everything but we don't want to pay higher taxes in order for it to happen.
I agree with some of the posters too about end of life care......I've been there w/ family members and friends. We aren't meant to live forever, and the way our society tries to prolong life sometimes robs the patient of a dignified death and sometimes creates more pain for the person dying. It's a very personal issue. Again, nobody is saying that you can't keep someone alive on a machine.........you just might have to pay for it after a certain amount of time. And if the insurance companies, who profit from cutting off care, are not setting that time limit, you may actually get more coverage.
August 3, 2009 8:05 AM | Reply | Permalink
"My understanding is that it is about making basic doctor's appointments, tests, treatments, prescriptions and hospital treatment available to more people, and at a more affordable cost."
Well said. In a recent Charlie Rose interview with Dr. Frist and Dr. Dean, it was said that the goal was to treat high blood pressure successfully instead of skipping that step and giving everyone a heart transplant. That comment came from Dr. Frist--and Dr. Dean agreed.
August 3, 2009 9:21 AM | Reply | Permalink
Good summary of the lies and the facts about the bill(s). Not saying the current plans are perfect, but it would be so refreshing if the opponents weren't so utterly shameless.
Spread it around....
http://www.politifact.com/truth-o-meter/article/2009/jul/30/e-mail-analysis-health-bill-needs-check-/
August 3, 2009 9:11 AM | Reply | Permalink
Medicare's estimated costs for 2009 is $420 billion. Approx. 70% of Medicare costs are spent in the last 30 days of life. Nearly $300 billion will be spent this year alone for the last 30 days of life for just the Medicare population.
Note that these numbers represent the last 30 days of life, i.e. the costs may have extended the patient's life for a maximum of 30 days. These data do not reflect costs incurred to lengthen life by 31 days, or 60 days, or a year. And obviously the numbers don't reflect successful treatments that extended life indefinitely.
With 50 million unisured today, that's $6000 spent this year alone for every man, woman and child who is not insured during the last 30 days of life for Medicare recipients.
Yes, I've been there with parents.
PEACE
August 3, 2009 9:23 AM | Reply | Permalink
I'm puzzled. The United States government was able to contain International Communism. So why can it not contain the costs of health insurance?
August 3, 2009 9:30 AM | Reply | Permalink
"You are definitely asserting moral authority, however.
Just like everyone else.
That's not an inherently bad thing.
It just gets us nowhere."
On the contrary. It gets us everywhere. It's the absence of moral authority that leads to nowhere. That is why the post that started this discussion is so valuable. I want to thank that poster for starting what I regard as very likely the best dialogue about anything I've ever read on this page.
August 3, 2009 9:59 AM | Reply | Permalink
Er, every form of insurance has 'bureaucrats' who 'decide' treatment on this basis and others, like 'pre-existing exclusions'. This is the famous 'rationing' argument. My grandmother is received Alzheimers drugs that are considered only occaisionally useful, are about $2k/month, and seem to be slowing the progression of the disease. They are not allowed on the UK system as being too expensive.
It is simple to me, this becomes the competitive landscape. In other words, if an insurance company wants to either offer riders to other policies, or wants to extend a higher level of care, then so be it.
As for the 'end of life' problem, that's kind of a no brainer, you need a lot of medical care when you are dying! What constitutes 'heroic measures will be a troubling discussion no matter where the healthcare is coming from. Likewise, defensive medicine where extraordinary measures are regularly prescribed probably costs some other more likely surviving person of life, assuming, as they are, that resources are limited.
August 3, 2009 10:15 AM | Reply | Permalink
Here in Europe, statistically, we are at least as healthy as Americans are but spend only half of what Americans spend per head.
August 3, 2009 10:24 AM | Reply | Permalink
People will be justifiably wary of any new method of managing health care. Politically, it will very easy to garner opposition to any new arrangement that withholds treatment -- even if it withholds treatment less often that the current system does. Morally, I don't see how anyone can justify a health care system that withholds treatment.
If you want people to support a new system, that new system will have to give everyone complete freedom in their medical decisions. It is going to have to pay for the riskiest, most experimental treatments for everyone's kid, spouse, or parent. If it won't do that, then people will hate it just like they hate private insurers now.
There is really no difference between an insurance company letting a loved one die in order to save money and the government letting a loved one die in order to save money.
August 3, 2009 10:44 AM | Reply | Permalink
Did anyone else find this blog post offensive? It begins as if it's using economic logic to analyze the issue, but quickly veers into arguments appealing solely to emotion. In particular, the refrain of "have you been there?" suggests two things:
1) People who have seen end-of-life situations firsthand ("faced Death") have a more valid perspective on spending on end-of-life treatments and tests for life-threatening conditions. Faced with a policy argument, simply say, "Have you been there?" and, if the answer is no, presumably, argument over.
We should all acknowledge there are strong, deeply personal emotions and stories in the health-care debate. Using them as rhetorical clubs to beat those who have different opinions cheapens everybody.
2) The author seems to assume that everyone who has "faced Death" will agree that there's no treatment not worth trying. In fact, as many comments have pointed out, that is not the case.
My grandmother, who passed away last month at the age of 87, made it abundantly clear repeatedly that she did not want treatments that would extend her life if it meant she could not live independently. "Call Dr. Kevorkian!" was her repeated refrain. (In fact, she died of sudden deteriorative brain function that lasted about 6 months and for which doctors could do very little.)
Of course these intensely personal decisions need to stay with patients and families, in consultation with their doctors. Still, this is something we need to talk about when discussing health care reform. IT seems that sometimes those who want to preserve the status quo argue as if mentioning that these difficult situations exist is the end of the discussion. It's not, and we need to acknowledge the difficulty and sensitivity and move forward with the discussion.
Argument that appeal primarily to emotions must be treated with caution.
M.
August 3, 2009 10:46 AM | Reply | Permalink
Yes I agree. The post doesn't frame its own argument in terms of what it is trying to say. It implies that nothing is too expensive to try when you are dying, and anyone who isn't dying isn't qualified to weigh in on the debate. Both of these arguments are BS.
Right now, before even getting to the question of expensive or experimental treatments, people are dying because they are denied standard treatments that their current coverage or their complete lack of insurance does not provide for them.
Let's fix that first.
August 3, 2009 11:05 AM | Reply | Permalink
Agreed. I'm sympathetic to those "facing death" but, when it comes to my own care, I'd rather forgo expensive and likely futile treatments so that others may receive effective care. I'd rather see 100, 50 or even 1 child get regular pediatric care than see the system spend hundreds of thousands of dollars on one procedure that has a 5% chance of prolonging my life a few more years.
It's not a question of being a bean counter. My own sense of morality tells me that there's a point at which the greater good will be better-served by not pursuing that "hail mary" procedure. It's a sad reality that we cannot provide every medical procedure to every person all the time but it is a reality at this point in time.
Take a step back and think about the others around you. Like death itself, we must come to terms with the hard decisions medical care presents us with and not insist upon impractical solutions that deprive others because of the emotions involved. Depriving the many for the benefit of the few is the height of immorality.
August 3, 2009 12:36 PM | Reply | Permalink
I was a hospice nurse for 15 years starting in 1983 and have stood with many patients in the aftermath of futile treatments that had for all practical purposes been imposed by MDs. I say imposed, perhaps a little unfairly, because far too often the patients and their families natural desire to avoid death combined with some doctor's discomfort with death or with giving bad news or with feeling helpless to offer a significantly helpful treatment, suppressed a frank conversation about what was realistic to expect from any of the treatment options available and often there was never any discussion of the option of palliation only.
In the early days of hospice the lion's share of our patients had come to conclusion that they wanted to forgo treatment on their own, often against resistance from their medical providers. Upon admission, pts would be told that hospice wasn't for everyone and that it wasn't the place for those still seeking curative treatment. It was not unusual for pts to have to actually change doctors in order to get a referral for hospice care.
Over time, as medicare, private insurers, etc. caught on to the economic advantages of forgoing expensive treatments in futile situations and awareness of the ethics of offering futile treatments came more to the fore in the medical field, more pts were steered into hospice who still desired to be aggressively treated. Was a good thing, a bad thing, or just a thing?
In terms of my personal self interest as a nurse who thrived on working with patients who were actively engaged in a process of reaching a state of acceptance of their mortality, there was less time for that kind of interpersonal work and more time spent running around like a 911 service for symptoms that in a more resolved patient could have been handled over the phone. The fear level of these new types of patient/families required more hands on care but was less focused on the work of accepting death and working through the developmental tasks of the dying.
However, my own interest aside, I can't say whether this development was good or bad. There are so many interests involved, patients, their loved ones, society and their ability to pay for aggressive and often futile care, the caregivers, etc. Still, there are a few things I know.
1. There are limits to everything, medicine's ability to heal, society's ability to pay for care, patient's abilities to investigate and pursue the wisest course of treatment for themselves at a time they are under great physical and psychological stress, etc. These limitations can't be legislated away ever.
It's easier to rail about rationing than to acknowledge that it already happens of necessity and apply rational thought to how to most fairly and compassionately manage it. The latter approach is wiser in my eyes.
2. Our knowledge of which treatments work the best all across the medical field is pretty dismal.
Obviously I could write all day on this but I have to run so I'll just conclude by saying its silly to blame any one group for this very complicated human situation in which we find ourselves. It's laughable to blame UR nurses, MD's and even insurance companies (considering we've created a system based on a profit motive). We need to understand better what treatments actually work best before we can offer meaningful choices to patients. The reforms related to studying the efficacy of various treatments are vital to improving the situation. It would also be a help if the profit motive were removed from the equation but that's not even on the table.
August 3, 2009 10:47 AM | Reply | Permalink
I take the UR nurse comment to be a response to me, so I will counter-respond. UR (outside of a very limited instantiation within medical facilities) exists only within the role of health care payers and serves solely for health care payers to second guess first order medical professionals who would provide services in order to avoid "unnecessary" payment. Were health care payment divorced from service usage (single payer hmo models, or physician-on-staff models), almost all UR would immediately become pointless, which is what it is now.
August 3, 2009 11:11 AM | Reply | Permalink
"UR (outside of a very limited instantiation within medical facilities) exists only within the role of health care payers and serves solely for health care payers to second guess first order medical professionals who would provide services in order to avoid "unnecessary" payment."
I've had my battles with UR folks over the years as an advocate for others and myself so I hesitate to come off as an apologist for them. I also don't disagree that putting Docs on a salary would be a good idea. However, its just too simple to say that would make UR unnecessary. Even within the boundaries of what is acceptable to UR personnel, there are unnecessary and futile treatments being offered.
For example, a new and mild case of rosacea might be managed just fine by an ointment that comes in two strengths 0.75% & 1%. The milder strength is available in generic and the stronger was patented when the patent ran out on the lesser strength. If the 1% ointment is ordered here both the insurance company and the patient pay considerably more for the drug without much added effectiveness considering the mildness of the case. UR shouldn't have a role here? Are doctors never to be questioned? I don't see how having docs on salary solves this. I wouldn't blame the doc here, the 1% stuff has a recognizable name she/he's been prescribing for years. Extrapolate across the entire population of newly diagnosed rosacea suffers with mild cases and this amounts to more than a few bucks.
Okay, that's a skin condition and not a cancer and I wouldn't doubt the prescriber was acting in good faith. It's not probably practical for a UR person to examine things in such detail for a minor condition once a treatment is ordered. However, I have no problem once the question of effectiveness has been scientifically resolved through proper studies [and perhaps in this case they have been done - this is merely an illustration]with requiring the weaker strength under certain circumstances. That's why my prior comments addressed our lack of knowledge about the comparative effectiveness of various treatments.
How much money is wasted across the entire spectrum of conditions by well meaning practitioners?
I think there is both a need and a potential for mischief for UR regardless of how docs get paid.
I can believe you may have a valid point in your head about all this but you're expressing it in such simplistic terms that it sounds silly, as I said.
August 3, 2009 2:56 PM | Reply | Permalink
No, UR should not have a role there. You are now in the area of diseconomic behavior; when you get down to nickle-and-dime decisions in health care, UR analysts cost more than they produce. They are financially productive for payers because (1) they engage in more than nickle-and-dime decisions (transplants, "experimental" treatment, etc.), (2) they delay expenditures and (3) they create such a hassle factor that medical providers evade them by just not prescribing what they think they might bring them in contact with UR analysts. I know that one of my own regular medical providers does exactly that; he talks about it.
When worrying about other people's care, we have a remarkable ability to expect health care to be delivered at the frictionless zero-waste level. Yet we buy all sort of retail goods that are produced in non-zero-waste environments, and I dare anyone to say that he or she performs in a zero waste work environment. I expect physicians to make some less than perfect economic decisions. It would be good to expel the corrupt factors that contribute to these decisions; such as the unbridled access pharmaceutical representatives have to physicians or their tendency to given physicians all manner of gifts. But, even after removing the corruption, I do not expect physicians to be any more perfect than anyone else. The constant presence of pre-auditors (UR analysts)is not, thereby, justified.
August 3, 2009 5:16 PM | Reply | Permalink
To quote myself:
"It's not probably practical for a UR person to examine things in such detail for a minor condition once a treatment is ordered."
So is it your position then that medical providers should have no one reviewing their decisions with an eye towards efficacy and expense?
We all are aware of the way many insurers wrongly use their UR personnel at their customers expense. What I find faulty in your words is the assumption that there is no legitimate role for UR outside of hospitals.
And to quote you:
"they create such a hassle factor that medical providers evade them by just not prescribing what they think they might bring them in contact with UR analysts. I know that one of my own regular medical providers does exactly that; he talks about it."
I don't know. If one of my providers was unwilling to go the mat for me on a treatment he/she felt was clearly in my best interest, I'd be looking for a new provider.
August 3, 2009 9:31 PM | Reply | Permalink
The problem with this argument is that it doesn't examine the premise that "cost containment" means limiting treatment for existing illness.
In fact, true "cost containment" comes about by implementing preventive measures. A healthcare system that funds preventive measures reduces the illnesses for which expensive treatments are required. The current "for profit," "fee for service" system is actually providing broad-based disincentives for preventive measures that improve health, because all the profit is in providing treatment.
I refer you to the example of Singapore, which has mandatory insurance (HSA's, actually) and a public option. Singapore has the lowest infant mortality in the world and the fourth longest life expectancy. Those ought to be the measures of a healthcare system's effectiveness. Oh, and in Singapore, per capita spending on healthcare is about 1/7th what it is in the United States. That's "cost containment" with a vengeance.
Thanks.
mp
August 3, 2009 10:49 AM | Reply | Permalink
I wish you would post more often, Michael.
August 3, 2009 11:50 AM | Reply | Permalink
1. A treatment has zero chance of being effective, or a positive probability of being harmful.
The assertion that there are no such treatments is certainly wrong. The Fen-Phen diet pills is one recent example, but there are a myriad more out there.
If the statement is changed slighly, to include treatments that are less effective than alternative treatments, there is a strong case to be made that many treatments would fall in the less effective category.
For example, there are studies that show that heart bypass, stents, and drugs are equivalent in outcomes, but that bypass is far more expensive than stents, which are more expensive than the drug therapy.
August 3, 2009 10:53 AM | Reply | Permalink
There is actually a good reason for built-in economic checks on treatment choices. A good example is Nexxium. There are two ways for pharma companies to maintain profits--to find new treatments for common illnesses and to tweak existing treatments to extend patents. The latter is particularly unsound economically--this why we have the FDA, in part. If the new treatment is not particularly more effective than its predecessor (or alternative) and either 1) is more expensive or 2) is potentially more harmful, there is an economic disincentive from allowing it.
This is not the same as creating a "last resort" treatment--there is a reason for some obscure expensive alternatives in cases where more traditional treatments don't work (think MRSA). These are both more expensive and more harmful--both with side effects and potential complications--but are also necessary. This model need not be limited to pharma. If research shows that a particular treatment is merely a more expensive alternative, there is no reason to allow it. But if it is shown that it is a more expensive and riskier alternative that has a chance to help where the traditional treatment does not, that should be sufficient reason for allowing it (but, of course, with restrictions). What we don't want is the Pharma-Rep approach--it's new, it's expensive, it must work better.
August 3, 2009 12:38 PM | Reply | Permalink
Another reason why an expensive treatment for MRSA is warranted is that the patient would typically recover well and lead a normal, productive life thereafter. In the past, infectious diseases like this routinely killed people in the prime of life. A great-grandfather died of "blood poisoning".
However, most medical expenses are devoted to treatment of end-of-life diseases, to chronic diseases which are essentially incurable, and to extreme neonatal care which leaves the patient alive, but impaired for life. The case for really expensive treatments in these cases is less clear.
Most end-of-life treatments are already paid for by Medicare. In many cases, at the end of life the heart fails. I would suggest that the life of most patients could be extended for up to a week by putting these patients on heart-lung machines. This would be extremely expensive, but it would extend life.
Clearly, we don't do this even though heart-lung machines do exist and are capable of extending life in this manner.
In treatments for chronic conditions, the case is murkier. Statin drugs are used to control cholesterol levels. There is no reason to use expensive Lipitor (still on patent) if cheap Zocor (off patent as simvastatin) controls the patient's cholesterol level and is tolerated well.
A secondary consideration is that there is no evidence for the proposition that taking a cholesterol lowering drug extends the life or health of a person who has not had a heart attack. In fact, the mechanisms by which statins presumably "work" are not that well understood, and it may be that they actually benefit the patient through an anti-inflammatory action, rather than cholesterol lowering.
Other, less expensive drugs and supplements may achieve the anti-inflammatory effect just as well.
August 3, 2009 3:40 PM | Reply | Permalink
I've always said that a little extra time wouldn't be worth it if it came at the expense of my family.
That is, if it meant more than just bankrupting me -- if it meant severely affecting the financial fortunes of my children -- would it be worth it?
To be consistent in my thinking, it seems that I should also apply this belief more broadly. What if my last ditch treatment affects children in general?
I think we can all agree that there are only so many resources on this planet.
If having a little extra time -- perhaps just days? -- means I'm using finite resources that could really make a difference for, say, a toddler who would then live decades, is it moral to use those resources?
It seems as if this post is arguing that anyone who's "been there" would. I wonder.
August 3, 2009 12:45 PM | Reply | Permalink
You are making an assumption that it's a zero-sum game. Where in the world did you get that idea?
August 3, 2009 3:19 PM | Reply | Permalink
Aaargh, while giving thanks to Rotwang for making important points, I feel the need to rant.
It always amazes me what happens with this topic on liberal blogs. So many pat flippant stories lauding the noble "he/she died with dignity" example, With nary a recognition how offensive and scary they might sound to others.
Just like in the movies, the noble Eskimo elder, no longer able to hunt or gather or skin a seal, going off to starve on the ice floe in order to save valuable resources for the next generation, is the great hero to be admired.
So much cluelessness, so flippant, so many seem to have absolutely no recognition how much their "please older people, die with dignity like this other person did" stories have in common with those who would like all women who get pregnant to accept nature as it comes, to follow through with what nature wants for them.
Nor do I see any recognition how frightening it might sound to someone like a 30-year old cerebal palsy victim to read the "please die with dignity" advocacy, things like lauding those who chose to forgo dialysis as someone to be admired and also thereby inferring that those who chose to partake of it, especially past a certain age, are parasited on society. The cerebal palsy victim reading must think: geez, my medical care is far more expensive than dialysis and my life is far more limited than the lives of those on dialysis, so what must these people want of me? What age do they think I should have given up the ghost at and quietly gone off on the ice floe? And what quality of life is good enough for them? Do I have to go through some testing to prove that I am having quality of life to meet their standards?
Seems to me it's as if people who talk like this haven't gotten around very much, haven't gotten outside their own Eskimo tribe as it were. Don't realize that there are other kinds of people out there, many of them, people who have an incredible drive to live as long as possible, even in pain, even with severe illness and handicap. And it was people like them that cause life expectancy to raise over the centuries. (BTW, I don't happen to consider myself one of them, sometimes my midlife aches pains and problems seem to be too much for me already. But at least I acknowledge that there are others out there who love life far more than I do and would put up with far more to keep just a sliver of it.)
Here's the thing, gang: all this "die with dignity" talk is REAL COUNTERPRODUCTIVE to health care reform. It scares a lot of folks out there, folks who think people like you might end up in charge of what health care they are allowed, maybe you will even someday limit what they can pay for our of pocket. The way some of these "die when it's your time" stories are just plain scary. Just like some of those right wingers scare the bejesus out of you when you think they might be in charge of who can get an abortion.
Not only that, I wonder what happened to twist some supporters of "progressivism," as in progress, scientific progress (with results like raising life expectancy levels,) into negativity as to life extension. Ya know, it wasn't so long ago that heart bypass was a risky, expensive operation available only to a few. So shouldn't you have been advocating all along against heart bypasses and for "dying with dignity" instead before it became a common thing and before they all could continue to collect Medicare and Social Security, thereby saving the rest of us a lot of dough? If you had, maybe we wouldn't have all these seniors with heart bypasses playing cards, reading, doing crosswords, surfing the internet, and watching TV, with visits to the heart specialist for checkups, leeching our scarce resources with their Medicare payments for walkers, oxygen tanks and meals on wheels? They are not productive members of society, after all, comrades, right? Work and produce or die, is that the rule?
One suggestion to all who like to laud "dying with dignity" stories: preface your story with the word "choice," just like you would do with the abortion issue. (Unless you are the type who likes to make the point that abortions or even sterilization for poor women are good mainly because they save society money in the long run, and lower the number of "useless" lives, if that's the case, carry on.)
I find myself more sympathetic to the "expatjourno2" version of the argument upthread, i.e., "get real, grow up, society can't afford to pay for everything for everybody and if you want some things, you are going to have to pay for them yourself." But implicit in that argument is that the rich will always be able to pay for the experimental, that some of them will be just as into living as long as possible as many less rich, and that we shouldn't prohibit them from doing that, nor laud others for refusing to do it even if they could. Because maybe something will come of it that will benefit all. We didn't all used to have indoor plumbing, you know. Quality of life, it's real relative.
Finally, I am anxious to see what side many of those pushing the "death with dignity" theme will be on the first the new medical review board labels Ted Kennedy's current treatment as experimental for an "ordinary" person. Are you willing to accept a Ted Kennedy allowed a year more than someone else? Are you ready to disparage him as not dying dignified, too? Or will you go the socialist route and say everyone with brain cancer should get it and we should all pay for it?
August 3, 2009 1:31 PM | Reply | Permalink
We often spend a million dollars to save premature babies, often minorities. Should we let them die with dignity?
August 3, 2009 2:02 PM | Reply | Permalink
Geez, what the hell does "minorities" have to do with this discussion?
August 3, 2009 3:11 PM | Reply | Permalink
Turning "give people the autonomy to make this choice" into "please die with dignity already I have an appointment to make" is BS. You should run for Congress, or write for the Weekly Standard with chops like that.
August 3, 2009 4:28 PM | Reply | Permalink
Well you can see it as political talking points if you wish, doesn't phase me a bit, because I know what I feel and it comes from the heart, there's nothing I feel more strongly about. It comes from personal experience and a lot of pretty hellish stress, nervous breakdown type stress when it came to several family members involved, including me.
I'm with Rotwang: "Have you been there?
My whole extended family had a pretty nightmarish 2007, it wasn't just one family member dealing with major hospital dramas (and not just one too early funeral, but several, BTW.) As he said:
What's another week? Have you been there? Another week could get you a conversation with a child about their college plans. An hour in a garden smelling the flowers. Not worth enough? Have you been there?
My other favorite bit of terminology is "heroic procedures." Believe me, if you are facing Death, you want a hero. All sorts of endeavors aim at great rewards resting on slim probabilities.
People tell these noble die-with-dignity stories but many of them ring super-simplified to me, like they are second hand--I can't believe they were involved in the hard decions making or the extended bedside duty--simplified the stories are turned into easy lessons and nostrums--often sounds to me they weren't sitting there through the whole thing. More often than not, it doesn't usually work out like an easy life/death choice that many seem to like to present, it goes step by step, and each step is a hard and complicated decision. Dying with dignity vs. hellish intervention is not a real picture of what usually really happens. But it certainly is the case that some providers try to make it look like that, especially if you're totally trusting of our medical system and don't do your research, they'll draw a real simple picture for you that isn't the truth.
August 3, 2009 4:58 PM | Reply | Permalink
Let me ask you this, Rotwang: have you ever been an uninsured worker who must work through a bad back or severe chest pain because you can't afford surgery? In the U.S., we force uninsured workers to work through severe chest pain or a bad back so we can give an 88-year-old Medicare recipient a $400,000 surgery to entend his/her life another six months. Does this sound like justice to you?
[And for the record, I have been there. I watched my Uncle, who had type II diabetes, congestive heart failure, who had severe depression, and more, die at 53. I watched him throughout his life refuse to eat a single vegetable, refuse to take his medication for depression, refused to exercise regularly, etc. When my always altruistic mother volunteered to give my uncle a kidney transplant, my father and I told my mother, "over my dead body." We just did not want my mother giving a transplant to a person who had no record of keeping himself healthy -- even if it was her own brother.]
August 3, 2009 1:59 PM | Reply | Permalink
Nobody has to work through a bad back or severe chest pain because he can't afford surgery. It a myth.
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If the patient lacks, or has inadequate, insurance, and meets certain low- and moderate-income requirements, the patient may qualify for discounted payment or charity care.
August 3, 2009 2:24 PM | Reply | Permalink
Most hospitals have a similar policy for what amounts to a write-off. The trouble is this is an area severely abused by many (if not all) healthcare organizations. The providers rarely, if ever, volunteer the information--yes, it's available on the net, in hospital manuals, etc., but you must know it's there to look for it. Then you have to go through the process of applying for it, which is, quite frequently, not the most convenient. On top of it, federal rules provide that once the charge is billed as bad it cannot be re-written as free-care. So, instead of reclassifying the debt and waving it, hospitals send the bills to collections. And, if all that was not bad enough, the qualifications are highly restrictive. One may think that this would at least work for those with incomes below the poverty line--never mind the question as to whether those just above the poverty line may afford it and when, if ever, the charges become affordable. But even this would not be true. Even to qualify for state assistance (with federal funds), one must have no assets exceeding $6000 for a family. So if you have a fairly reliable car, you're shit out of luck. Much of this regulation--not coincidentally--dates to 1993/4, the same time that Hilarycare reform failed.
Over the past decade, the free-care allotment at major nonprofit hospital chains across the country went down from 6-7% of the budget to 1.5-2%, in some instances close to 0.5%. This has lead a number of organizations to question the validity of their non-profit mission--and, in fact, the IRS is in the process of revising tax exemption guidelines for health-care organizations. Of course, they've been revising for the past three years, so one has to question the commitment, but it's better than nothing.
August 3, 2009 3:41 PM | Reply | Permalink
Indeed. Been there and done that myself. I had to drop out of school and move to another state to qualify, bartered rent for housecleaning for my landlord, and lived on a minimal diet of rice and beans (bought in bulk, I couldn't afford canned) and the occasional orange and whatever green stuff was cheapest. No movies or beers or books or new clothes or nights out... basically missed my young adult years entirely. Even with that discount I was spending most of my money on paying for my cancer follow-up visits, and I had the absolute best case scenario, staying in clinical remission, no serious treatment-related health issues (at the time) and needing no extra tests or treatments.
Still, some of the charges were "accidentally" billed to me without discounts and were on my account years later, in spite of doing everything I could to straighten things out. Eventually I had to settle those charges - some of those I ended up paying twice, first at the 50% discount and then later at full cost - so that I could continue to receive care, but by that time I had married into an insurance policy so was able to save up and pay them off.
Young adults are the only age group in which the survival rates for cancer have not improved over time. Insurance issues are big part of the reason for that.
August 3, 2009 4:27 PM | Reply | Permalink
You are very lucky that we didn't move to a single payer health care system 40 years ago. It's very unlikely that drugs that helped you to survive cancer and get through you cancer treatment would be developed under single payer health care and profit-less small pharma.
August 4, 2009 3:02 AM | Reply | Permalink
Nonsense AnnaA.
Pharma companies spend their research funds on things that patients will require for years and years...preferably rich patients. Think Viagra.
Chemo drugs either work or they don't...either way the patient only takes them for a few months. They get developed with public funded research....which we'd have more, not less, of under a single payer plan.
Put docs on salary, and more of them will being doing the research they'd like to be doing instead of overpopulating the specialties that currently pay the big bucks.
August 4, 2009 12:12 PM | Reply | Permalink
There is nothing wrong with Viagra. If people want cars, Ipods, yachts, computers, shoes, or Viagra capitalism will produce what people want. This is great. We all should applaud Pharma companies for creating high paying jobs and satisfying customer demands.
However you are totally clueless about cancer and what does it takes to go through Chemo for several months and how many drugs are needed to help patients to survive Chemo.
August 4, 2009 2:16 PM | Reply | Permalink
Quick ...
Someone open the drain ... The gene pool has been infected by a microorganism from beyond the asteroid belt...
~OGD~
August 4, 2009 2:45 PM | Reply | Permalink
This information is very useful! Thanks!
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March 28, 2011 3:37 AM | Reply | Permalink
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April 27, 2011 7:51 AM | Reply | Permalink