If I recall correctly, SA charges CI members $60,000 for field standby, stabilization, and transport. SA does approximately one or two cases per year, apparently using contract perfusionists and surgeons when available for the blood washout phase of procedures. The alternative for CI members is simple packing in ice some unspecified period after legal death, and shipment by a local mortician; no cardiopulmonary support, no associated rapid cooling, no blood washout.
As I understand it, Maxim makes two claims:
SA underdelivers and overcharges for services, (“incompetence”) while representing itself in a disingenuous and probably legally prohibited way.
The industry SA operates in should be regulated because of claim 1.
If so, she is apparently saying that government regulations be put in place to force an organization with ~ $100K in annual revenues to spend up to $470K on salaries (recently computed elsewhere on Less Wrong) for a full-time certified perfusionist and a cardiovascular surgeon (how they would maintain skills is unspecified), or nobody should be allowed to attempt to provide any cryonics field service other than simple packing in ice. And the government should provide this consumer protection for two citizens per year even though nearly every medical expert, politician, regulator, inspector, and enforcement official will believe that these enforced medical standards are cargo cult science applied to dead bodies who could not possibly be revived because (a) they are already dead, and (b) the later cryopreservation itself is certainly fatal.
Why isn’t there concern that by prematurely requiring highly credentialed people, by law, to do cryonics stabilizations that the government itself wouldn’t be misleading people about the legitimacy of cryonics? The way things are now, people don’t look to the government to evaluate cryonics procedures. (Nor should they for a field as small and misunderstood as cryonics.) People have to kick the tires themselves. They have to know how limited present cryopreservation procedures are. They have to read the case reports, know that mistakes happen, and decide for themselves whether $60,000 is likely to be worth more than simple packing in ice. They have to know what they are getting into.
The reason, in a nutshell, why I’m concerned about government regulation in the present state of development of cryonics is that by not understanding cryonics, not really caring about it, not actually valuing it, they will almost certainly get the regulation wrong. The extreme political hostility that has traditionally motivated calls for cryonics regulation also helps insure this. Good regulation requires good dialog, not name-calling.
Why isn’t there concern that by prematurely requiring highly credentialed people, by law, to do cryonics stabilizations that the government itself wouldn’t be misleading people about the legitimacy of cryonics?
I agree this is a major concern. What’s the standard procedure in medicine for experimental treatments? As far as I’m aware (and I am not a doctor), subjects generally don’t pay for them (I do know a lot of drug trials occur in Texas because you can compensate the subjects, so apparently the cash flow is in the opposite direction for at least one other field).
And so the most appropriate model for cryonics right now might be “if you want to volunteer your body at death, we’d like to try to get better at preserving people.” That strikes me as a lot more honest than charging people for a service, and make it a lot clearer what’s going on. In efficient markets, prices convey information- and so a pretty common bias is to consider price a good proxy of quality.
And so the most appropriate model for cryonics right now might be “if you want to volunteer your body at death, we’d like to try to get better at preserving people.” That strikes me as a lot more honest than charging people for a service, and make it a lot clearer what’s going on. In efficient markets, prices convey information- and so a pretty common bias is to consider price a good proxy of quality.
Does anyone have a realistic commercial interest in developing cryonics based treatments?
If I recall correctly, SA charges CI members $60,000 for field standby, stabilization, and transport. SA does approximately one or two cases per year, apparently using contract perfusionists and surgeons when available for the blood washout phase of procedures. The alternative for CI members is simple packing in ice some unspecified period after legal death, and shipment by a local mortician; no cardiopulmonary support, no associated rapid cooling, no blood washout.
If so, she is apparently saying that government regulations be put in place to force an organization with ~ $100K in annual revenues to spend up to $470K on salaries (recently computed elsewhere on Less Wrong) for a full-time certified perfusionist and a cardiovascular surgeon (how they would maintain skills is unspecified), or nobody should be allowed to attempt to provide any cryonics field service other than simple packing in ice. And the government should provide this consumer protection for two citizens per year even though nearly every medical expert, politician, regulator, inspector, and enforcement official will believe that these enforced medical standards are cargo cult science applied to dead bodies who could not possibly be revived because (a) they are already dead, and (b) the later cryopreservation itself is certainly fatal.
Why isn’t there concern that by prematurely requiring highly credentialed people, by law, to do cryonics stabilizations that the government itself wouldn’t be misleading people about the legitimacy of cryonics? The way things are now, people don’t look to the government to evaluate cryonics procedures. (Nor should they for a field as small and misunderstood as cryonics.) People have to kick the tires themselves. They have to know how limited present cryopreservation procedures are. They have to read the case reports, know that mistakes happen, and decide for themselves whether $60,000 is likely to be worth more than simple packing in ice. They have to know what they are getting into.
The reason, in a nutshell, why I’m concerned about government regulation in the present state of development of cryonics is that by not understanding cryonics, not really caring about it, not actually valuing it, they will almost certainly get the regulation wrong. The extreme political hostility that has traditionally motivated calls for cryonics regulation also helps insure this. Good regulation requires good dialog, not name-calling.
I agree this is a major concern. What’s the standard procedure in medicine for experimental treatments? As far as I’m aware (and I am not a doctor), subjects generally don’t pay for them (I do know a lot of drug trials occur in Texas because you can compensate the subjects, so apparently the cash flow is in the opposite direction for at least one other field).
And so the most appropriate model for cryonics right now might be “if you want to volunteer your body at death, we’d like to try to get better at preserving people.” That strikes me as a lot more honest than charging people for a service, and make it a lot clearer what’s going on. In efficient markets, prices convey information- and so a pretty common bias is to consider price a good proxy of quality.
Does anyone have a realistic commercial interest in developing cryonics based treatments?