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by bsder 2996 days ago
You are defending the position that we should let someone die because they don't have enough money to pay for medical treatment.

Are you really sure you want to go there?

Now, if you want to argue I would argue that why is this CEO letting a "friend" go without healthcare when CoveredCA has platinum plans at about $7000/year for an individual?

3 comments

> You are defending the position that we should let someone die because they don't have enough money to pay for medical treatment.

> Are you really sure you want to go there?

Yes, I absolutely am. Grown-ups in the adult world have to make choices. We have limited resources and time, and yes, sometimes that means that we can't give life saving treatments to every person that needs it.

Assuming they were limited, but what if they weren't ? Some drugs/treatments cost more just because a greedy murderer was allowed to rack the price.
Occasionally that is true, but often if you look more deeply into the pricing of these things, that's really not the case. Pharmaceutical companies are businesses, and they invested hundreds of millions, sometimes billions of dollars of their own money to discover these treatments. They have to be able to recoup that cost in the market place. If you do not allow them to do that, they simply won't invest in finding the treatments anymore.

There are alternative funding models, of course. We could have the government fund all pharmaceutical research. But that has a whole host of other problems. It's really actually a difficult problem without a simple solution. You might say "well, maybe we should do a mixed public/private model of some kind", and if you said that, you'd probably arrive at about what we have now in the US.

> Pharmaceutical companies ... invested hundreds of millions, ... to discover these treatments.

Some purchased the rights only to rack up the prices. Just because they are a business doesn't mean they should be allowed.

Yes, that is true, but irrelevant. A purchasing entity can price the drug fairly, and an entity doing original research can price the drug unfairly. Whether or not the IP was bought and sold is a non-sequitur.

What actually matters is that we have two problems:

1. How do we incentivize drug discovery?

2. How do we treat all the people that need treatment?

Right now our answer to #1 is that we allow people to charge the people that need treatment, for a limited time. This system works ok, but there may be better ones. If you have any, i'd love to hear them.

One approach would be to place an upper limit on the price of each drug or medical procedure based on the expected gain in Quality Adjusted Life Years (QALY) for an average patient. Although it's uncomfortable to discuss, we already place a dollar value on human life in civil wrongful death lawsuits. So we know roughly what an extra year of life is worth. And that value can be adjusted based on whether the patient is able to live a normal life or will still be bedridden (or other limitations) even with the treatment.
This article might be interesting reading: http://levine.sscnet.ucla.edu/papers/ip.ch.9.m1004.pdf

Skimming it, it doesn't really explain the means by which pharmaceutical companies succeed under weak or absent patent laws, it just says that they do. It seems to leave open the explanation, "Chemical and pharmaceutical companies in countries with weak or no patent laws make most of their money by selling into countries that have such laws." I haven't read it too carefully, though. It does say that they exaggerate their costs (presumably so as to argue for patent laws); that lots of those costs are perverse (e.g. bribing doctors); and that the patent laws inhibit innovation in lots of ways.

Meanwhile, I vaguely remember reading someone's proposal: Health insurance companies, at least in theory, basically make a bet that their customers will have good health. Let's suppose a health insurance company has 100k customers, and it's expected that 0.1% of them (let's say there's no way to tell who) will develop disease X sometime during the term of their insurance plan, and the treatment for disease X costs $50k. Then the expected total cost per customer is .001 * $50k = $50. The insurance company would therefore be fine agreeing to cover all costs of treating X for any insurance premium exceeding $50 over the term of the plan. Let's say they charge $70 to cover that particular item, and risk-averse customers agree to it. This is the classical notion of health insurance (I think in practice it's diverged significantly from that).

Once these plans are agreed to, the insurance company stands to bear an expected $50 * 100k = $5m of costs (for $7m in revenue). Now, if the insurance company has some way of, say, spending $2m to fund medical research that cuts the cost of treating X from $50k to $25k, then that would save them $2.5m in costs. (Making no reference to patenting or even selling the drug.)

Now, research is almost never guaranteed to produce the results you expect (arguably it wouldn't be called "research", merely "implementation"), and furthermore it takes time, perhaps longer than the term of the insurance plans. The uncertainty might be handled with a research consultant who makes "educated guesses" as to the expected value of different research paths. As for the time taken, (a) you could project how many insurance plans of this type you expect to have at the time the research completes, and (b) you could work something out with other insurance companies that provide similar plans. Which brings me to the biggest point:

I chose the figure of 100k customers. What if we imagine either a very large health insurance provider, or a joint effort by multiple insurance companies? Company A expects to have 5m insurance plans covering disease X when the research completes; company B expects 10m; company A will contribute $z and B will contribute $2z, or perhaps they'll just commit to funding the research and then find out how many plans they have when the research completes and divide the costs at that point. With a total of 15m customers, the research is now profitable if it costs anything less than 15m * $25 = $375m. The wider the consortium can be, the wider the range of treatments it will now become profitable to research.

This sounds extremely weird when you read it in Europe.
We in Europe have the same choices to face. For example,

" In June, Nice said the £48,000 per year price tag of the drug, which could benefit 450 women a year, could not be justified."

https://www.telegraph.co.uk/news/health/11785840/NICE-refuse...

Doesn't to me. Deploying limited resources effectively is critical to all care-giving. There is no "costs don't matter" in Europe.

The US aspect that is weird is when the discussion is not really about maximising value, its actually about maximising profits.

No it does not. There are treatments that are deemed to expensive and will not be provided. Typically it will be a trade off between how effective the treatment is and how expensive it is. European healtcare systems does not have infinite money.
Are you really sure you want to go there?

This is just bullying, regardless of how disagreeable you find someone's position.

And she is defending that effectively tax money should pay for medical treatment. ANY medical treatment, with the only limitation that it prolongs life.

It is already the case that millions people lost ~20% of their disposable income because of insurance increases. In many cases it is lower a LOT of people who would normally be comfortably above the poverty line back down to the poverty line (those are the people losing the most in the individual mandate and subsidy system). And we all know that anything less than 2x the poverty line definitely feels like poverty and already cannot be escaped through savings and/or good financial sense.

So there is a choice to be made. A choice between the cost of the individual mandate and coverage on families and the fact that we want everyone to be "saved" from health problems.

This is further complicated by the fact that anyone saved from a health problem increases healthcare demands both linearly (very few health treatment really fixes things, so future demands on healthcare by the same patient will on average be higher), and exponential (a LOT of health problems are inheritable), because people demand the genetics of their kids be "respected" even when known problems exist. Afterwards, of course, it is unfair to blame the kids or the parents, even in entirely predictable problem cases. And then you have 5 kid families, where the parents were warned long before anything happened, which all have severe genetic problems resulting in brain defects. 2 cannot survive a single day without medical care and only 1 will ever live independently. But 3 would like to marry and have kids themselves (I don't blame the kids, however the parents should have known better, also we need to figure out the very sane policy of 100% refund of fertility treatments for couples without fertility problems for this reason) ... At what point is it not reasonable anymore ?

Insurance premium increases were increasing and erasing real wage growth for years before the ACA was passed.