On Wed, 17 Sep 2008 12:52:18 -0400, Ed Huntress wrote:
Feel free to prune as you feel fit, if I think something important was
left out I'll reinsert it and not attribute ill intent on your part. You
are not a gunner, HH&C or Jerry...
"Curly Surmudgeon" wrote in message
. ..
On Wed, 17 Sep 2008 02:49:15 -0400, Ed Huntress wrote:
"Curly Surmudgeon" wrote in message
. ..
On Tue, 16 Sep 2008 17:33:16 -0400, Ed Huntress wrote:
snip
Yes, now I would. I just went through six sessions of laser eye
surgery for PDR. I don't want to do it again. I'll pay for the best
control I can get.
Physicians Desk Reference? Dunno "PDR." Most diabetics would opt for
injections when the pump is out of pocket, except for those in extreme
distress.
Sorry, you seemed to know about diabetes so I used the abbreviation for
proliferative diabetic retinopathy.
As for opting for injections, that's fine if you're lucky enough to
have A1c readings of less than 7.0. Some people's systems just won't
allow it, even if they do multiple blood-glucose tests and inject ten
times a day. I
test 5 times a day and inject 6 or more separate doses, but my A1c runs
around 7.2. The newest pumps should get someone like me down to
something under 6.8.
7.0 will carry you if you have good genes and haven't been diabetic for
more than 10 or 15 years. I have the right genes, but it's 35 years for
me. Until the eye problem I was the only Type 1 (juvenile) diabetic I
knew
with more than 30 years on the clock who had no major problems. Now I
have
one, but, thanks to advanced medical technology (laser surgery) I may
not have the problem again. Maybe.
I'll keep my fingers crossed for you but do not extrapolate your extreme
medical condition to the general populace.
Thanks, and I don't extrapolate. Type I diabetics make up just a fraction
of 1% of the population. I'm just a shining example d8-)
But considering that Type II (adult-onset) diabetics have similar problems
-- some of them worse, in fact, including the incidence of loss of limbs
-- and make up 23.1% of the US population over age 60 (and those are just
the ones that have been diagnosed), my situation is not really "extreme."
It's just that I got started earlier and serve as a kind of weathervane
for those who acquired the similar condition later in life. If you're in
your 50s or older, those 10-15 years of grace that 20-year-olds enjoy may
shrink to just a few years.
Note, I've designed medical instrumentation. One product is not too
dissimilar to your insulin pump, it took a blood sample from a drip
line and tested for lactate acid giving real time results. I am
very familiar with the industry.
Well, maybe I should interview you for an article I've had in the can
for a year. It's about medical-device manufacturing and meeting the
FDA and customer requirements. I have eight interviews done, but I'm
losing energy
for it.
Use my email in the header.
Thanks. I've put this message into the file in case I revive that
article. I have around 50 hours invested in it so I do want to finish
it.
snip
True but the root cause is that health care insurance is unavailable
at rational cost. Kaiser for my wife and I would be $1600/month in
the USA and is about $25 in Argentina.
So, Argentina has subsidized or government-run insurance. I'm all for
it.
Kinda, sorta both. Immigrants can buy into the state system but each
municipality has an open clinic where the costs are very cheap. A
front/side chest x-ray cost about $13, dental extraction of molar with
abscess cost a friend $6.70, etc. I've bought into private health
care at a local hospital chain. Ambulance service is free, I used it
two nights running when semi-conscious and unable to drive. Heh, I
had _chicken_pox_ at my age... Never knew it could be life
threatening...
Being in the seond or third economic tier can produce some wonderful
benefits for a country. For example, you don't have to invent or
develop much of anything. You just use the same stuff that was
developed in the leading countries.
You'll find that the companies selling that stuff can be very compliant
to your political needs. They'll set up an entirely separate accounting
system for dealing with you, one that doesn't have to account for any
upfront costs, because those are all paid for in the leading country.
Since your market is basically a gift to those companies, providing
unanticipated sales on otherwise idle production capacity, they'll be
happy to treat you as a source of marginal sales, and all that their
books will show as expense against their selling price in your country
is the marginal manufacturing costs and shipping. Something that costs
$100 in the leading country, where they're amortizing all of the
upfront costs, might cost $2 in your country. And it will appear on
their books as a profitable sale -- because it's a marginal sale.
Accounting can be a very creative thing. d8-) The problem with being a
second- or third-tier country in those circumstances is that your
economy basically don't exist outside of the orbit of the leading
countries. It creates quite a web of dependencies over which you have
no control. But it sure saves a hell of a lot of money.
All true. On the other hand you are talking about providing cutting
edge technology to the general population and that's not a reasonable
expectation. Regrettably it's a path that will bankrupt the health care
system. Life sometimes sucks and if you are very poor you may not be
able to afford a life saving proceedure, that's what charity is for. On
the other hand those costs are outrageous and we must bring them down to
earth.
Well, that's all true, too. The healthcare issue as many people see it is
that everyone should have the same cutting-edge technology available to
them. That's a majority position in the US (as in most of the world) now,
as unrealistic as it may be. It will be the guiding idea behind health
care reforms.
The practical outcome will be different. The question is how much
different it will be, because health care reform is coming, whether the
conservative ideologues want it or not. It's a tsunami that's racing
across the seas from all directions.
Your program further inflates costs to the majority for the few, mine
chops the hell out of those costs for the majority at the expense of a
few. I believe that my program is the more humane by far.
If you follow the polls, you realize that yours is definitely a minority
position, and the trend is against you. It will lose, politically. It's
just a question of how soon it will come to a vote and move.
What will happen is that universal health care will be sold in a package
with efforts to cut medical costs. Some efforts will be successful. Others
will not. It will extend the delay to the crisis point for a while, maybe
for many years. And then we'll decide what we want and can have, once
again.
There's always a ready market for new drugs and new medical
technology.
True, and sometimes the costs are justified. But recognize that a
full 60% of new drugs are governmentally subsidized through
university research then turned over to pharmaceuticals for
manufacture and distribution with but a bare tithe to the
university while Abbott et. al. gains usuary profits on our own
tax dollar.
sigh I'm well aware of how that works. My last job in a medical
communication agency involved a drug on which Sanofi-Aventis had
paid something like $135 million in development costs, and $110
million in pre-approval marketing costs (which was paying my
salary). Then the FDA decided not to approve the drug. So my
company laid half of us off. d8-)
The basic research on that drug was not from a university, however.
I know that a lot of the basic research is done in universities.
What you may not know is that the testing that the pharma companies
have to go through after some basic-science lab makes a discovery
often costs ten times more than the basic research.
I'm familiar with the problem. The FDA should be an advisory, not
regulatory, agency. All the special interest groups like,
encourage, support, and fund that evil.
I completely disagree about having the FDA become an advisory agency,
We disagree then. I see the FDA as a self-serving bureaucracy
controlled by special interests. I do not like the idea of a
governmental agency telling me what medicines or treatments I can, and
can't, have.
The thing is, Curly, that you have no experience of buying or using
drugs in an environment that isn't dictated by the FDA and similar
agencies in other highly developed countries. So you're speculating
about how it would work out.
To the contrary, remember, I've lived in Argentina for about 3 years now
where I can buy just about any drug without a prescription and those
that do are drugs that I'm not interested in.
No, because Argentina's health care system, as I explained above, exists
in the shadow of the FDA and the European (and Japanese) equivalents of
our system. I don't know Argentina in particular but most countries are in
that situation. Argentina's health care system can only function because
it's parasitic on the systems of the major players, in terms of what drugs
are available, how they've been vetted, and what experience from those
more regulated countries tells the Argentinians about what works and what
doesn't.
They don't operate in a vacuum. A friend of mine who was the
Carter-Wallace rep for Africa, and who also repped throughout the
Caribbean, explained it in fine detail to me over a period of years. What
I learned from working for Big Pharma confirms the same thing. They're all
riding on information that comes from the drug development, testing,
approval process, and record-keeping of the major western countries. They
make their own decisions, but they don't have any significant amount of
their own information on which to base them. They can get all the
information they need from us, for free.
You can go online and collect the PIs (prescribing information) forms from
the FDA for 1,000 drugs in a couple of days; put a team of physicians and
other specialists together to review them; and develop a drug policy and
approvals for a medium-sized country in less than a month. And that's the
skeleton of how they actually do it.
How does that pertain to the cost of health care in the United States?
Simply because the USA pays too much isn't an indictment against others.
Those lower-tier economies have an office that sounds like FDA, but
it's usually an empty shell full of rubber stamps, giving supposed
approval to drugs and procedures that have gone through the approval
process of the FDA or the British, French, or German equivalents. And
the drugs they sell over-the-counter are mostly ones that have been
vetted, for prescription sale or otherwise, by the leading countries.
And it's wonderful. I needn't visit a doctor for simple drugs, I can
self-medicate, I can refill my one long term medication without being
molested by a self-interested bureaucracy. I can get immunizations and
injections at the pharmacy too. This is one major reason I live here,
I hate the "Big Brother" attitude.
It's only possible because there is a Big Brother who provides them with
all the information, for free. Then they make their own decisions, based
on their politics, their sense of responsibility to their people, their
legal structure, and their tolerance for a few unfortunate deaths
resulting from people who are medically ignorant making life-and-death
medical decisions. In the case of many countries, their willingness to
institute a system of controls -- that is, their willingness to pay for
such a system -- enters as a big factor.
The only direct comparison you can make is to the US before there was
an FDA. It was much harder to get a centralized, reliable count in
those days of how many people were winding up dead from taking the
drugs then available. But the number was substantial. We can tell now,
in a lot of cases, because those drugs have since been run through
large clinical trials in which the results have been measured.
That's an excellent foundation to convert the FDA upon too. That work
will not be lost, its the basis for evolving healthcare.
It won't be lost, but it's only available for drugs that are already
available. New ones need new studies and analysis.
Therefore only affecting new drugs, not the existing supply.
Focusing then on new products, do you believe that a half billion dollars
to release a new drug for, say, gout, is justified?
for
the same reason we got the FDA in the first place. Those greedy
corporate types you're complaining about wouldn't mind killing many
more people if they could get away with it. Testing on humans first
is the way to make more money.
That is not what I propose. Let the FDA provide online, honest, data
on drugs and let the buyer comment and beware.
You're proposing a system by which smart people save a few bucks, and
not-so-smart people make minor mistakes and drop dead. I don't really
like the sound of it.
"A few bucks"????? We're talking thousands and tens of thousands of
dollars per person! Do not extrapolate your health condition to the
population at large. Not-smart people do not "drop dead" they don't
medicate usually and if a few do "drop-dead" then that's life. Or
death.
Huh? Over 125,000 people die in the US each year from drug reactions and
mistakes alone. Misprescribing leads to some of the reactions; lack of
clinical-study information about drug interactions leads to most of
them. That's not "a few" who are dropping dead.
I'd have to see verification of that number before accepting it.
As for the "tens of thousands of dollars per person," the average
pharmaceutical bill in the US is $850/person. The way to cut that is
with some reforms in health care and the way the pharma industry is
regulated, not in deep-sixing the FDA, because it's the FDA that keeps
that 125,000 deaths from being a much larger number.
And the average health care cost is over $10,000 per person.
We pop a hell of a
lot of pills, and a lot of them are deadly if they're used ignorantly.
I will not pay for stupidity or ignorance. Tough luck but that's the way
the belly buttons. It's their life, if they don't do the homework that is
not a societal problem nor responsibility.
Note that I've actually been through the FDA approval process. Not
responsible but as an independent contractor responsible for
adhering to the requirements on glucose monitors, inhalation
dispensers and patient monitoring systems.
I should point out here that testing a medical device is NOTHING like
testing a drug. It's much simpler, and it's done with much smaller
cohorts, so it's vastly cheaper. You don't see $50 million studies for
devices, as you often do for drugs.
I think I mentioned elsewhere that a new drug requires roughly a half
billion dollars to become FDA certified. That is intolerable.
Half of that number is marketing. Cut the marketing, not the clinical
studies or drug regulations. I don't care how much the marketing people
get anymore. g
Again, I'd have to see some verification of that claim. Not that it makes
the FDA any less onerous, $250,000,000.00 is still intolerable.
Generics, Canadian, and other sources are often 90% cheaper.
Of course. Generics just ride on the research, testing,
post-marketing studies and marketing that was done for the
original drug. All they have to recover is manufacturing costs and
quality-control reporting. In Canada, they have price controls and
just refuse to allow the drug companies to amortize research and
development. The Canadians, and the French, and the Brits, and
everyone else knows that they can collect those costs in the US.
How long do you think a pharmaceutical should have a monopoly? Is
17 years not enough?
It depends on how you structure it. Some kind of regulated, extended
and mandatory licensing would reduce prices and keep up enough
income to fund big trials. And it's the big clinical trials that
cost most of the money in pharma. Patented medicines are too
expensive, but generics are too cheap.
Precisely why I want to change the FDA to an advisory agency. Today
it costs roughly half a billion dollars to bring a drug to market,
that is irrational and runs the prices up so that the general tax
fund must subsidize use.
But what's the basis on which the FDA would "advise"? The last drug I
worked on as an employee (rimonabant) was being sold in France,
Germany, the UK, and parts of South America before three long-term
studies ordered by the FDA turned up the problems with it. The
Europeans got egg on their faces -- and some dead citizens -- because
they didn't require the long-term studies. Now they're pulling back
and black-boxing those drugs. But they never would have known the
problems without those huge studies, which cost something like $100
million in total to run.
There you go, publish those data, update as more data becomes
available. Caveat emptor.
That's precisely what they do. It's all available to the public, once
it's submitted for FDA approval. I read around 360 studies related to
the marketing for one drug, alone. Regarding "caveat emptor," how many
do you have time to read? They run around 8 or 10 pages each, on the
average, and they're not very entertaining.
If my life is dependent upon the results I'll read every last one in
detail.
I've read thousands of clinical studies but I'll do the emptoring, and
let the FDA do my caveating, thank you. d8-)
That should be your option too but not my obligation to subsidize.
Who pays for that if the FDA doesn't impose it as a requirement for
approval? You're talking about going back to the dark ages of the drug
business, when people died from taking drugs and no one knew the drug
was involved in the deaths. Hell, no one even knew that the people who
died had been taking the drugs.
Statistical review can pull that data from the noise. People died in
the example you offered even with testing.
Many die even with the testing we have now. Many more would die without
it.
So? I'm not belittling your point, in fact I'll submit that it is true,
but artificially extending a dying persons life simply isn't worth the
cost in most cases.
Not only test subjects but
subjects who were denied the new medications but might have been
helped. That's life. And death. **** happens, no one life is worth the
cost of FDA regulations.
FDA fast-tracks cancer drugs and many other critical drugs now. You
might want to make the track faster. I think it's about right.
It can be argued that limiting drugs as the FDA does costs lives too.
I've read the arguments. The data is available. You'll find it with a
good search on PubMed.
snip
You are one of the lucky, many cannot get insurance because they
are under employed, unemployed, homeless.
Yeah, we know. I'm very lucky. The year before last I paid insurance
out of my pocket for six months, and it cost me almost $7,000.
How would you change that inequity?
Universal health care, with a single-payer system and optional
supplemental insurance. Take the European and Canadian systems,
analyze the good and the bad in each, and design a better one based on
those experiences.
You'll have to re-engineer a lot of the health care business to do it.
Tort reform, reducing redundancies in testing facilities, etc. Very
socialist-sounding. Very politically incorrect. But the only way to
reduce costs and provide health care for everyone at the same time.
The danger with it is not so much a case of limiting coverage (that
will happen no matter what system you use, including our present
free-for-all system), but rather limiting innovation. That part will
require very careful work.
Since the US is the last country of any substance without universal
health care, this is where most of the innovation happens. The
Europeans and others are tuned to our drum; they adjust their systems
so they don't look too bad in the innovation department, given our
example. It's hard to say how that would work if there was no
free-for-all system like the US against which to compare oneself. It
is a concern, if every major country has a controlled system. It's
easy to become complacent if there is nothing against which to compare
your results.
I don't expect a universal system to work really well. I just expect
it to produce a better result than we have now, in terms of health
statistics. There is no way that it will produce as much innovation.
You pay your money and take your choice. My choice is universal
coverage.
Mandated health insurance, right? What about those who do not want
mandate health care?
Screw 'em.
And the opposition feels the same about your program. In fact there is
more justification on the liberty side than the mandatory side given that
we are a nation based upon individual liberties.
As it is, they're winding up in the ER and taxpayers are footing the bill.
Not a justification, stop doing that at the same time we cut the burden
and make health care affordable. That argument is self justifying.
This isn't Zimbabwe or the Sudan so we aren't going to
just let them die, so ram health care coverage down their throats, for
the same reason we don't let people drive without liability insurance.
I'll fight you on using coercion every time.
What you propose violates my freedom and monopolizes the health care
industry.
Yup. When your "freedom" becomes my tax bill, because you can't or won't
cover your own ass, you've just forfeited some of your freedom, IMO. Or
you can move out. That's your freedom.
It's your tax bill because you voluntarily assume the costs, a self
serving argument. Stop doing that and your justification evaporates.
It is also a license to steal and further empowers the FDA monopoly.
What's your gripe with the FDA? I can see bitching about Big Pharma, or
hospitals, or doctors, but the FDA does a pretty good job, IMO. What is
it you think they do?
The FDA violates my right to choose and treats me like a child. I do not
like being patronized by anyone, especially my government.
Redirecting the FDA to an advisory agency would immediately chop off at
least half the cost of health.
Baloney. It would just speed up the casket business.
Probably both.
Remove the AMA
monopoly and another quarter might be saved.
Great. We'll let anybody put out a shingle. I told my wife, after
studying endocrinology for some of my work, that maybe I should go into
the business and start prescribing hormones. It would be a great
experiment and fun, too. d8-)
No prescriptions required, remember? Along with advising buyers on drugs
the FDA must keep open records for health care providers, both the
positives and negatives. If you like a provider then rate them, kind of
like what Ebay does. Bad providers, snake oil salesmen, and charlatans
are subject to fraud laws and would soon be out of business.
FDA advisories should include herbs, vitamins and minerals too. There are
many herbs that can be life threatening. I do not want them regulated
either, I want my government to _inform_ me to the risks and allow me the
liberty of self medication.
Cutting health care costs by
75% would be easy and making care available to those who now cannot
afford your care would save more lives than are now being lost.
Hey, you aren't in the market for a Bridge to Nowhere by any chance, are
you?
Nope, I'm not a Trojan Moose.
What we now have are a number of state protected monopolies which
prevent competitive forces to rein in health care costs. I cannot/will
not vote for that.
Significant competitive forces don't exist in health care; never did,
and never will. You don't shop around when you're having a heart attack.
That is why health care is so expensive, no competition. $1,800 taxi
rides (ambulance) for 1.5 miles and no alternative, intolerable.
This transitions into the quality of care issue too. Another
factor we've not discussed is the costs caused by AMA monopoly of
providers. Midwives and alternative treatments have essentially
been banned to create a monopoly. Then there is the FDA making
many drugs prescription only. In fact some years ago the FDA
stated that they would have made many current over the counter
drugs a prescription item if they had it to do over. They are now
trying to rectify that by regulating vitamins, minerals and even
tobacco.
We Americans have an aversion to reading about dead people who took
drugs they were told were OK.
**** happens. Life is not guaranteed safe. The government is only
permitted to regulate fraud and crime, not what we ingest.
I think the law disagrees with you on that. g
You realize that I have a very low opinion of laws which violate my
liberty, don't you? We have no obligation to obey anti-constitutional
laws.
shrug The Founding Fathers didn't anticipate CT scans and open-heart
surgery. They were lucky to get leeches.
The FDA wants to regulate the medicinal use of leeches too.
Your ideas concerning
pharma are ideological, abstract, and unreal based on what we know
about drugs, Curly. You're laying out a prescription for ignorance and
death. No one would know what drugs are causing what side effects and
adverse outcomes; all you'd have is a collection of rumors, marketing
claims, and guesswork.
That is an unsupportable assertion and one that I disagree with deeply.
Well, fine. Spend four or five years studying and writing about
pharmaceuticals and health insurance, and we'll have another talk.
When market forces are unleashed we also need to revamp fraud laws to
keep the manufacturers honest but all major diseases have drug
treatment now so the number of new drugs coming onto the market is
smaller. And hideously more costly given the current FDA regulations.
We cannot permit an industry to blackmail us for health care.
You tell 'em.
No, I pretty much ignore them but those still in the USA do not have my
options. They are saddled with monopolies which rape, pillage, and
destroy the economy, leave many with unacceptable or no health care, and
enrichen the few at the expense of the many.
That is not what America is about.
We've gone beyond that and hardly anyone who knows the issues would
want to go back. Your reactionary approach would result in a meaner
and riskier health care system for everyone. It would be cheap, but it
would leave a lot of bodies and maimed lives in its wake.
Nope, all the current drug treatment programs would continue, no risk
involved. Only new drugs coming onto the market might risk, advise the
patient rather than burden the health care of every other individual on
earth. This is where the FDA would come in, monitor the use of new
drugs and provide statistical analysis of the effects for advising
other users in the future.
That's what they do now. Then they regulate the ones that would kill us
off the market. That's about it.
I do not want the FDA to "regulate" anything, I want the FDA to "advise"
on much more than drugs. They should assist us in selection
practitioners, herbs, minerals, vitamins, exercise programs, maternal
care, infant care, all health related data.
Governmental treatment as infants is not the American way. Nor is
coercion, punishment, or regulation.
--
Regards, Curly
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