X-Message-Number: 2329 Date: 07 Jul 93 03:03:11 EDT From: "Steven B. Harris" <> Subject: CRYONICS: The Wrong Stuff Dear Cryonet: I too, like so many people, have been following the bleach/perfusate incident in various ways, and have considered all of the various postings and articles. This incident is a long way from being over, but I do want to say a couple of things now, since some very strange things have been said so far, and some corrections and clarifications are needed. First, this is, of course, a serious matter. Hypochlorite is toxic stuff, and is extremely damaging to tissues. I am quite sure that it is damaging to tissues in concentrations much smaller than 0.1 meq/liter, so at this point the finding of lithium concentrations below this value do not rule out the occurrence of a big problem. Tests for blood lithium were developed to monitor lithium administration to manic depressive people, not monitor hypochlorite administration to suspension patients, and the lithium test is no more sensitive than it needs to be for its clinical use. Since hypochlorite is a lot more toxic than lithium, it ought to be obvious that we labor under a limitation here trying to make one test do completely for the other. Thus, I'm happy the blood levels were below the relatively crude cut-off for standard clinical conditions as regards lithium, but this is NOT enough to clear up the hypo- chlorite issue. Second, Hugh Hixon's reported finding that perfusate neutralizes hypochlorite within ten seconds does not clear up the issue, either. At minimum we need more information, which I assume is forthcoming. Hypochlorite is an oxidant which, in the presence of acid (for instance, in an acidic ischemic patient at the beginning of perfusion) would be expected to disproportionate into chloride and free chlorine, the last of which is also nasty stuff. Presumably, some or all of this might be prevented by reductants (such as reduced glutathione) in the perfusate, but we need to know how Hugh made the determination that this is happening. At what pH was this done, and how do we know this was the pH of the patient? Did Hugh do the neutralization measurement at near ice temps? If actual crystals of hypo- chlorite penetrated the circuit, does it not follow that crystals may have been perfused? How does perfusate do vs. undissolved crystals of hypochlorite at ice temps? Since 10 seconds is also on the order of the circulation time from heat exchanger to brain, how can we be confident that no crystals reached the brain? There are so many questions remaining that it is prema- ture (to say the least) to call Mike Darwin's (or anyone else's) concerns in this matter overblown. To put it simply: it seems still possible that was significant damage to this patient. Enough hypochlorite got into the patient to turn his blood dark, remember, which means that much hemoglobin (at the very least) was oxidized by the bleach. We hope this all happened in the vicinity of the heat exchanger, but we still do not yet know for sure. To really begin to have some confidence that damage was done entirely to blood heme proteins and not brain heme proteins, we need to do a more sensitive lithium test, and then subject an experimental animal to similar conditions, and similar concentrations of lithium hypochlorite during an ice temp perfusion (such as a canine total body washout). If we can recover the animal alive after that, we can rest easy. If we cannot, at least we will know that brain damage has been done. I realize, of course, that the suggestion of animal research at this point is a politically sensitive one, since it appears that with the loss of Mike, Jerry, and a few other technical people from the Alcor advisory staff that Alcor has now lost the ability to recover live animals from a cold perfusion. In fact, if the last patient is any index, Alcor has now lost even the ability to do routine blood gas measurements during perfusions. In this context, it is a little chilling (forgive me) to be reading discussion on the net about whether or not Alcor can do perfusions without Mike Darwin. Of course they can. If the truth were told, just about anyone with an embalming pump, a lot of ice, and some guts can do a cryonic perfusion. In fact, if you do a bad perfusion, the results look pretty much the same as a good one, and the fewer tests you do, the less difference there is. It's depressing as Hell, but I think there may be a sort of Gresham's Law of Cryonics: bad suspensions drive out good ones. They're certainly cheaper and easier and less stressful to all involved. Furthermore, the differences are not always readily apparent (in the future, folks, if you add half a pound of the wrong chemical, the blood won't always turn color to warn you). At this point, with the loss of Mike and Jerry and basic research capability, I'm afraid that Alcor is not only at the point where it cannot tell if it is doing good suspensions or not, but it is at a point where it is now unable even to approach the problem of how to tell one from the other. It's a long way back from there. Steve Harris Rate This Message: http://www.cryonet.org/cgi-bin/rate.cgi?msg=2329