Scientific MOOCs follower. Author of Airpocalypse, a techno-medical thriller (Out Summer 2017)


Welcome to the digital era of biology (and to this modest blog I started in early 2005).

To cure many diseases, like cancer or cystic fibrosis, we will need to target genes (mutations, for ex.), not organs! I am convinced that the future of replacement medicine (organ transplant) is genomics (the science of the human genome). In 10 years we will be replacing (modifying) genes; not organs!


Anticipating the $100 genome era and the P4™ medicine revolution. P4 Medicine (Predictive, Personalized, Preventive, & Participatory): Catalyzing a Revolution from Reactive to Proactive Medicine.


I am an early adopter of scientific MOOCs. I've earned myself four MIT digital diplomas: 7.00x, 7.28x1, 7.28.x2 and 7QBWx. Instructor of 7.00x: Eric Lander PhD.

Upcoming books: Airpocalypse, a medical thriller (action taking place in Beijing) 2017; Jesus CRISPR Superstar, a sci-fi -- French title: La Passion du CRISPR (2018).

I love Genomics. Would you rather donate your data, or... your vital organs? Imagine all the people sharing their data...

Audio files on this blog are Windows files ; if you have a Mac, you might want to use VLC (http://www.videolan.org) to read them.

Concernant les fichiers son ou audio (audio files) sur ce blog : ce sont des fichiers Windows ; pour les lire sur Mac, il faut les ouvrir avec VLC (http://www.videolan.org).


International Brain-Dead Donor Ethics: Public Communication from French Transplant-Medicine Community Lacks Transparency and Effectiveness

Here is a translation of the article posted above
(dated September 2, 2005):


I.- Controversies and Updates in Organ Transplantation Ethics in France:

I am from France (Paris) and I'm trying to investigate about brain-dead donor ethics. In France, for the time being, transplantation Specialists defend the point of view that it is just out of the question to mention that brain death could be a questionable concept, especially when they are being asked this question by somebody from the public (closed-door medicine syndrom still striking in France, Doctors are suffering from it!). Nearly each and every French transplantation Specialist claims that a brain-dead donor is dead since brain death is death. There are just no other alternatives in their opinion. They justify their statement by referring to the August 2004 Amendment of the French Law of Bioethics. This Amendment is re-defining death as brain death. That is: the definition of death no longer includes the arrest of cardio-pulmonary functions: as of August 2004, brain death suffices. Brain death = death.

I am currently developing this Blog in order to show that the whole transplantation problematic involves issues, updates, controversies that are a great deal more complex than just the few explanations the non-specialist broad public is being (reluctantly?) provided with by the transplant-medicine community... Generally speaking, the transplant-medicine community points out that brain death is a concept allowing to legally state that a brain-dead patient is dead. Technically, however, this is another story: still breathing, with a working vascular system, the brain-dead patient seems sound asleep. By no means he seems to be dead. Says Dr.K. Ganapathy, Neurosurgeon, Apollo Hospitals, Chennai, India: "A dead brain in a body with a beating heart is one of the more macabre products of modern technology". And speaking of the effect of brain death on the family, he says: "Brain death has created a new class of dead people that does not conform to society’s expectations of normal death and dying. Brain death also causes great stress for the family and friends".



To download the recent scientific study: "Brain Death and Organ Donors", by Dr. K. Ganapathy, Neurosurgeon, Apollo Hospitals, Chennai, India, click here.
Source: Neurosurgery on the web.

My aim is to show that in other countries, like Japan, Germany, Denmark, a long-lasting debate has been involving the whole society, and in these countries (and others) it is acknowledged that the brain death concept has been plagued with some serious philosophical and biological inconsistencies.

I am referring to following "white papers", i.e. articles from the scientific press:

1.- "Role of Brain Death and the dead-donor rule in the ethics of organ transplantation". Article by RD Truog and WM Robinson, in: Critical Care Medicine N°31, September 2003, p.2391-2396.

2.- "Does it matter that organ donors are not dead ? Ethical and policy implications", in: Journal of Medical Ethics 2005, N°31, p.406-409.

3.- "A definition of human death should not be related to organ transplants". By C. Machado, President of the Cuban Commission for the Definition and Determination of Death, Institute of Neurology and Neurosurgery. In: Journal of Medical Ethics 2003; N°29: page 201-202.

4.- "Chronic 'brain death': meta-analysis and conceptual consequences". DA Shewmon, Department of Pediatrics, UCLA Medical School, Los Angeles, CA, USA. In: Neurology, Vol 51, Issue 6 1538-1545.

==> Read other scientific publications by Dr. Shewmon
("white papers" abstracts).

5.- "Brain Death: Reconciling Definitions, Criteria and Tests", by A. Halevy and B. Brody, in: Annals of Internal Medicine, 1993, N°119, p.519-525.

Of course this is a non-exhaustive list...

The Journal of Medical Ethics also provides with abstracts and some full text versions of articles regarding transplantation ethics. To read a selection of these articles, click here.

In Japan, the law allows people to choose between brain death and traditional death. Indeed, Japan could serve as an example, and France should at least listen to the lesson. Unfortunately, for the time being, we cannot seem to see this happening in France!

When asking in June 2005 a French Transplantation Coordinator (working in a Parisian suburb Hospital) about the arrested heart organ removal (non heart-beating donation), she told me it was too new a process to discuss it, especially with a person from the public, so she was not sure she could tell me much about it. Later, on August 2nd, 2005, Law Amendment N°2005-949, related to the procurement and graft of organs, tissues and cells, was published (Journal Officiel - French version) : kidney and liver removal, as well as the removal of some tissues and cells, shall also be performed on non heart-beating Donors. Before August 2nd, 2005, these organs, tissues and cells could be removed from brain-dead Donors (i.e. with functioning heart and lungs, thanks to artificial respiratory devices), or from living Donors (live kidney and liver removal). This new Law Amendment, including non heart-beating donation, should entail a raise in the number of organ Donors, especially with regards to kidney, liver, tissues and cells donation. In addition, the possibility to perform live Donor kidney removal using minimally invasive surgery (robotic surgery, French version) should also allow the organ donation to progress.

Generally speaking, I wish the French transplant medicine-community would take more into account what is happening in other countries, where debates involving the public opinion are taking place and have been doing so for a long time (again: Denmark, Japan, Germany...).
However, the new Law Amendment of August 2005 in France reminds of the already existing situation in Spain, where organs, tissues and cells procurement is working out better (increased number of Donors) thanks to the possibility of harvesting on non heart-beating Donors. It has been recently established that harvesting on non heart-beating Donors has allowed a 20 per cent-increase in organ donation in Spain.

For the time being, it is obviously impossible for a French person from the public (a non-specialist) to sort out the whole situation about the brain-death concept. The only thing French Doctors, Transplant Coordinators (nurses) and other transplantation specialists will ramble on and on about is: brain death is death... and conversely! I find this situation regrettable, even frustrating, and truly hope this Blog will help people from the public (like me!) find out whether they believe in the "traditional" concept/definition of death (i.e.: heart-lung functions arrested and brain destructed), or if they believe in the definition of death as "brain death" (i.e.: beating heart, functioning lungs, brain destructed). In the first case ("traditional death"), they are not likely to become a "brain-dead Donor", in the second case ("brain death"), they are likely to become a "brain-dead Donor".

You may ask: why ask all these questions?! If your brain is dead, then you're dead!!

To be honest, I happened to witness by chance, a couple of years ago, an organ removal (or harvesting) case on a brain-dead Donor (Donor was a 8-year-old child), and I find it hard to believe this kiddo was dead, as he was breathing and his heart was beating (of course thanks to the respiratory devices). The kid just seemed sound asleep!!

So I wanted to find out: if you happen to be a brain-dead Donor and if your organs are being removed (or harvested), is it 100 per cent sure you are not feeling any pain at all? I've asked this question to about 14 Transplantation Specialists (Physicians, Associations), and nearly all of them (about 95 per cent) answered: as a brain-dead Donor, you could not possibly feel any pain at all: you would be dead!! They were positive about that.
Yet some French physicians, nurses, and part of the French public opinion do question the viability of the brain-dead Donor concept (i.e. the Dead-Donor rule in the Organ Transplantation process): they are suspecting that, instead of being dead, the brain-dead patient would rather be dying. According to my experience, questioning and/or expressing concern about the viability of this (new) legal definition of death as Brain Death (since August 2004) is not politically correct in France.

Why? How's that expressing doubts about the brain death concept is not politically correct? Well, to start with, Physicians do need as many brain-dead donors as possible, to provide patients on waiting lists with organ(s), save their patients' life (waiting lists are breeding quickly, and so are technologies and knowledge related to transplantation, and last but not least, Physicians' reputation will be thriving on this transplant activity). Not to be forgotten the reputation of Health Centers (Clinics, Hospitals, etc) cutting-edge and state-of-the-art transplantation surgeon teams work in! A lot of money is at stake here, and a lot of people could potentially be saved! One brain-dead donor can potentially save the life of 7 to 8 people: two kidneys, one heart, valve, lung, liver, corneas, all sorts of things that can benefit living people!...

What I found out by inquiring for this Blog: considering the possibility, or probability, that death might be a process rather than an event, brain-dead donors might be "imminently dying" instead of dead.

A debate should be organized in France, involving public and political opinion(s). We should all be aware of the existing options. Presently, this is not the case: French Doctors are asking people: "-Are you willing to donate your organs or not?"; They do not ask them: "-Which death do you believe in? Brain death, or 'traditional death'?". By putting the emphasis on the organ donation instead of putting it on the sort of death people believe in, the question cannot be correctly answered. I would like to point out this lack of transparency and effectiveness in the communication from French Transplantation Specialists to French public opinion.

Let's try and wrap this up: dying or dead "brain-dead" patient?
"Brain death is not for diagnosing somebody who is dead. It's for creating a fiction for the determination of death, in order to get organs," says Dr. Paul Byrne, a Toledo, Ohio physician who has studied the subject of brain death for 20 years.

Says Dr. Andronikof, Ph.D., Head of Antoine Béclère Hospital Emergency Department (casualty ward), France:

"Nowadays, research scientists are working in fields which the major civilisations have always considered as sacrosanct: life, death and mankind. And consciences are accepting these exploits by adapting as fast as technology advances. In the book by J. Dauxois and Dr M. Andronikof, Casualty Ward Doctor, published by Editions du Rocher, January 2005, Marc Andronikov, doctor in charge of the casualty ward at Antoine Béclère Clamart hospital, who embodies all the enlightenment of Orthodox Christianity, effectively overturns all the weak consensus on scientific progress.

Have we any right to refuse?
Technically, anything can be done to mankind. It is possible… but do we not have a right to refuse? Do we not have the right to consider ourselves and to consider others as more than an assembly of interchangeable organs and tissues ? What treatment can one accept? Who is to decide what becomes of our bodies when consciousness is lost?… Is it admissible that a doctor in the casualty ward should be able to decide that a patent, who is condemned, must absolutely be revived using the full range of respiratory and circulatory machines… in order to be able to transplant his/her organs ? Since the 1976 Caillavet law, the consent of the patient is implicit and anyone who has not wilfully declared that they are opposed to the taking of their organs, is taken as accepting such practices. But who is aware of the fact?

'Death is not death'
Death is no longer defined as the ceasing of the three vital functions; nowadays, only cerebral death is considered in the scientific world and by the law as death but surely this definition which authorises the taking of organs from patients in irreversible coma must be a scientific mistake? It is claimed that the brain determines death because brain damage is currently irreversible whereas other organs, the heart, lungs can be replaced, by artificial means. Medical realities and the person as such are defined according to what is technically achievable today. Whereas death is a process, since all the functions do not cease at the same time... But the notion of cerebral death enables organs which are not affected to be taken before they are damaged.

Therefore 'the concept of equivalence between death and irreversible coma is based on three major errors: considering continuity as a point in time, considering a part as the whole, considering the foreseeable future as an event already achieved.' "

Source:
Genethique.org - Press Review, Monthly Letter N°62, February 2005.

According to Dr. Christopher De Giorgio, Professor of neurology and neurological surgery at the University of Southern California, "You can keep somebody on life support for a few days or a few weeks at the longest, but generally people do not survive past two weeks who are truly brain-dead." Dr. Paul Byrne, a Toledo, Ohio Physician who has studied the subject of brain death for 20 years, cites cases of brain-dead individuals who have survived for long periods of time, even years.

Assuming that the brain-dead patient is dying and not dead, that death is a process rather than the result of a process, means that "Brain Death" is a fiction, invented to allow Organ Donation. Which steps should be taken, in this case? I've came up with the following:

- tell the truth and no longer try and conceal it.

- Help people (public opinion + brain-dead patients' family) make the right choice. In my opinion, here's the alternative:

Alternative N°1)-I'm too afraid that somebody could possibly remove my organs when I would not be completely dead (I am too afraid that somebody would intrude in my dying process, I'd rather Physicians let me die in peace). Sorry, but I will not help save the life of up to 8 people thanks to my own death, I'm too afraid I would suffer in the process. In this case, I am objecting to donating my organs. Or: brain-dead patient's family are not giving their consent for patient's organs removal.

Alternative N°2)- The scenario is familiar: tragic accident, young victim, distraught family. Follow-up media coverage reports approvingly of the donation of the brain-dead victim's organs. The family expresses relief that some good has arisen from what could have been merely a senseless tragedy. In other words: I know that if I was to become brain-dead, therefore a potential organ donor, I could save the life of some people by donating my organs. Even if I could survive as a brain-dead patient for one more week, or two, or a few days, it doesn't matter. What's to be called life when you're brain-dead anyway? To me, brain-dead is dead. Living like a vegetable does not sound much like being alive. I prefer to help other people instead, no matter if that means somebody will intrude in my dying process, in order to remove my organs before I am totally dead. In this case, yes, I am an organ donor. Or: brain-dead patient's family are giving their consent for patient's organ removal.

I am quoting Dr. Alan Shewmon: "The Dead Donor Rule: Lessons from Linguistics"
Kennedy Institute of Ethics Journal - Volume 14, Number 3, September 2004, pp. 277-300, The Johns Hopkins University Press:

"American society traditionally has assumed a univocal notion of 'death,' largely because we have only one word for it and, until recently, have not needed a more nuanced notion. The reality of death-processes does not preclude the reality of death events. Linguistically, 'death' can be understood only as an event; there are other words for the process. Our death vocabulary should expand to reflect multiple events along the process from sickness to decomposition. Depending on context, some death-related events may constitute a more obvious discontinuity than others and more justifiably may be considered 'death' within that context. There is no reason to assume a priori that there must be an overarching, unitary concept of death from which all diagnostic criteria must derive.

Regarding organ transplantation, the relevant question is not 'Is the patient dead?' but rather 'Can organs X, Y, Z . . . be removed without causing or hastening death or harming the patient?'"


II.- International Controversies and Updates in Organ Transplantation Ethics

Source:
"THE DEFINITION OF DEATH: CONTEMPORARY CONTROVERSIES". Author: Bryan Jennett
Glasgow, UK. Published in: OXFORD JOURNALS. BRAIN – A Journal of Neurology
Brain, Vol. 123, No. 2, 408-411, February 2000, Oxford University Press.


"This book about brain death is as much to do with legal and philosophical considerations, public attitudes and public policy as with clinical aspects. It arose out of a conference in 1995, but is much more scholarly and coherent than a conference proceedings—with authors referring to each others' chapters and the Editors writing an introductory commentary to each group of chapters. Each chapter has its own reference list and all are well written, making the book as a whole a rewarding read. Its focus is on the US, but there are chapters on specific public policy problems in Denmark, Germany and Japan.

The Editors' introduction to the whole book raises the possibility that the public consensus following the report of the President's Commission might be about to deconstruct. The threat is from debates about whole brain, higher brain and brainstem definitions, and when death occurs, although they acknowledge that there has been little public interest in these academic controversies.

Reviewing the cultural context of the evolution of brain death, an historian details reactions to the 1968 Harvard criteria. A major aim was claimed to be the avoidance of prolonged futile life-support and promoting death with dignity, rather than to aid the harvesting of organs. But the media focused only on the transplant issue and there followed no fewer than 11 feature films on the theme of murders to provide donor organs. Initially, the AMA [American Medical Association] did not want doctors to be ruled by guidelines, and lawyers did not think doctors should decide on their own. However, the President's Commission in 1981 largely resolved these issues. Laws were passed recognizing brain death, but leaving doctors to devise and apply criteria. The concept was `sold' to the public on the basis of whole brain death, the President's Commission rejecting the alternative higher brain definition (declaring death once consciousness is permanently lost).

Those of us who were involved in the development of the UK Colleges' criteria in 1976 and in the furore over the BBC Panorama programme `Transplants—are the donors really dead?' in 1980 will find Plum's review of diagnostic criteria of particular interest. That TV programme in 1980 amounted to a challenge to the purely clinical criteria established in the UK, as contrasted with the use in many other places of confirmatory investigations, in particular the EEG. Plum points out that with increasing confidence in clinical guidelines many institutional codes in the US no longer require laboratory confirmation. According to the American Academic of Neurology in 1995 and the recent New York State guidelines detailed by Plum, EEG is not mandatory provided the clinical tests have been repeated with an interval of 6 hours. Indeed Plum tabulates six papers reporting EEG activity after brain death had been clinically evident, stating that none of these patients made any recovery, even to the vegetative state. He reviews alternative confirmatory tests, in particular stressing their unreliability. He notes that nonetheless some US hospitals still insist on them, as do some European countries. He concludes his review with a defence of the brainstem criteria, which in practice are those used by doctors who maintain that death of the whole brain is the basis of brain death. The Editors comment that `readers will judge whether Plum's conclusion is a savvy compromise or the beginning of a more widespread retreat from the notion of whole brain death'.

Pallis (the only British author) makes a more aggressive defence of the brainstem criteria, pointing out that these render irrelevant the anomalies that trouble those concerned to diagnose whole brain death. These include the persistence after brain death of EEG activity and of neurohumoral regulation of ADH secretion. Other neurologists here deal with this matter of how much of the brain must be dead by emphasizing that death is a process rather than an event, and that what matters for the whole brain definition is that there should no longer be any clinical evidence of critical or integrative brain function. This reiterates the assertion of the President's Commission that mere physiological activity, not discernible clinically, is irrelevant. In spite of these various doubts about the validity of the claim that the whole brain is dead, it is concluded that the criteria for brain death are probably the most reliable and valid in the whole of medical practice. That there is evidence that many doctors in the US do not always assiduously apply all of them does not make these criteria any less valid.

There is debate about the time of death—which functions have to have ceased and when it is known that cessation is irreversible? Several authors refer to the different purposes for which it has seemed necessary to define death, but one chapter is entitled the `Unimportance of Death'. This considers it unrealistic to expect the same criteria to define when it is appropriate to withdraw treatment, to harvest organs or to dispose of the body and assets of the deceased. Only for the last purpose is it necessary to define death, and for that the traditional cardiac criteria are required.

The demand for legislation about brain death in the US came largely from doctors seeking protection when harvesting organs, according to a leading academic lawyer who believes that if transplantation had evolved more slowly and gained gradual acceptance, no legislation would have been necessary. He and other contributors believe that doctors exaggerated the risk of litigation in these circumstances. Protection for doctors was supposedly gained by claiming that brain-dead organ donors were dead, but this insistence on the `dead donor rule' was an unexamined assumption. Indeed it has led to the offer also of a higher brain definition of death, which would declare vegetative patients dead in order to allow treatment to be withdrawn and organs taken. But treatment is regularly withdrawn from a wide range of patients for whom it is considered futile without any suggestion that they are already dead, and in the litigious climate in which medicine is practised in the US no doctor has ever been successfully prosecuted for such withholding or withdrawing of treatment. It would be better to accept criteria for treatment withdrawal and for organ removal without requiring the clinical and legal contortions needed to declare death. This could also allow donation from anencephalics without deciding that they are dead. It is ironic that the UK, one of the few countries where brain death legislation has been deemed unnecessary, is the only place that requires court approval before artificial nutrition and hydration can be withdrawn from patients in the persistent vegetative state.

The chapter titled `The conscience clause' notes that there have been formal objections to brain death from Orthodox Jews and some fundamentalists and Catholic pro-life campaigners. In some American states, the law is that death shall be pronounced when whole brain death criteria are satisfied, in others that death may be pronounced, leaving it to the doctor's discretion. Only in New Jersey is there specific provision for religious objectors, in an individual case, to insist on asystole before death is declared. Veatch argues that it is difficult to limit such choice to those with religious objections, and that all people might be given the choice to accept their own death being declared by cardiac, whole brain or higher brain criteria, via an advance directive or appointed surrogate. Whole brain death would be the default definition, if no opinion had been expressed.

The Editors' introduction to three chapters on public attitudes contrasts the absence of public discussion of brain death with the continuing interest in debating when life begins. The push for further redefinition of death comes from a small group of academics who seem concerned at the public's lack of concern. Surveying the empirical literature on attitudes there is much more debate about transplantation than specifically about brain death. The public remains confused about brain death, the vegetative state and coma and the possibility of recovery from each. The chapter on Christian fundamentalism comments on the tendency of adherents to be suspicious of technological advances and strong on the sanctity of life. Whilst against euthanasia and the higher brain definition of death, however, most groups accept whole brain criteria for death and are not opposed to transplantation. The chapter on Jewish attitudes accepts that many Jews do not follow the dictates of the Orthodox. The latter reject treatment withdrawal or refusal, with personal autonomy much less respected than by other religions. Transplantation is approved but there is still debate on whether the whole brain definition of death is acceptable—many Orthodox Jews would reject it.

The section on problems in three other countries illustrates, the Editors claim, concerns that exist under the surface in the US. Before Denmark passed a law accepting brain death in 1990, kidneys were taken from patients whose hearts had stopped but in whom it was usual to attempt to restart the heart by resuscitation before removing the organs. In 1985 a Committee on Transplantation recommended accepting brain death criteria and the Minister of Justice proposed a Bill in 1987, which met with surprising opposition in the media. A Council of Ethics was set up in 1988, with only three doctors among its 17 members; this was to deal with genetics and assisted reproduction, but it also took up the brain death debate. Its report in 1989 recommended taking organs once brain function had ceased during the death process, but that the time of death was when the heart later stopped. There followed an unprecedented public debate, actively promoted by the Council. It distributed 14 000 copies of its report across the country, set up more than 200 local debate meetings and sent a video film to more than 500 local groups. More than 1000 newspaper articles were written. Public opinion was 80% in favour of the minority on the council, who recommended declaring death when the brain death criteria were satisfied. The law passed in 1990 was virtually identical to that proposed in 1987 before the public debate.

In Japan the story was quite different and much more fractious. The debate has been going on for 30 years but was partially resolved by a law passed only in 1997, many years after other countries, and 12 years after a Committee was set up by the Ministry of Health to consider the matter. Throughout this time one paediatric neurologist had organized steady opposition to brain death, which she saw as just an aid to transplantation. Several scandals involving transplant surgeons kept up a negative reaction to brain death, although by 1988 the Japanese Medical Association voted to accept the concept. But there were divisions between specialties; the association of neurologists and psychiatrists feared that the handicapped might become unwilling donors. In 1992 a cabinet committee was deeply divided, but a majority decision was in favour. However, this was rejected the next day by the Minister of Justice and the police. Some resistance rested on the traditional lack of good communication between Japanese doctors and their patients, leading to mistrust of the medical profession. There was, however, persistent search for public consensus, with support increasing from 29–55% between 1983 and 1995, as reflected in 15 national surveys. Although some of the resistance was based on traditional values the debate was largely secular with no participation by religious organizations. The recent law applies only to patients for whom permission has been given for organ donation.

In Germany there was early acceptance of brain death, and this practice went unchallenged for over 20 years, but then ran into trouble. Two months before the Harvard criteria, a German committee published similar criteria and further guidelines came in 1982. Both Protestant and Catholic churches accepted brain death and transplantation and there were few dissidents. However, the drafting of legislation in 1995 to legalize what had already become accepted practice stirred up opposition leading to public hearings for the Parliament. The Berliner Initiative against brain death comprised many doctors, theologians and others. However, medical associations and scientific societies supported the whole brain definition, and the churches did not retract their earlier support. Eventually the law was passed in 1997. The opposition arose partly from memories of the Nazi period, together with concern at the persisting paternalism of German doctors, limited public debate and the lack of organizations promoting patient rights.

These accounts of years of acrimonious dispute in three countries should make us grateful that our few months of debate in 1980/81 seemed to settle the matter quite quickly. But the lesson of Germany, where a peaceful consensus was challenged after many years, and the fears of the editors of this book that the same might happen in the US, should alert us to the need to maintain good practice in this sensitive field. This means ensuring not only that all involved are fully informed about the UK criteria, but that they apply them rigorously; also that they deal sensitively with the families involved.

The section on public policy faces the fact that public perception is more important than scientific reality, and this is reflected in how the law takes liberties with biology. For example, it treats adoptive parents as fully parents, and acknowledges change of sex although the chromosomes remain the same. Law is supposed to reflect the will of the public, raising in this area how much the public wants or needs to know about the ambiguities of the biology of death or can understand them. Can the public cope with death as a process and life as a transitional category? Would debate about the higher brain definition of death undermine confidence in whole brain or brainstem definitions of brain death? It is interesting that the three countries that have had the most heated debates over the issues have each in the end come to accept the concept of brain death.

The final section on `The future of death' acknowledges that in academic biological and philosophical circles there are challenges to the whole brain concept, but that only minority religious groups wants to return to the cardiac criteria. The need is to minimize harm from prolonged futile treatment or from premature organ removal. It seems better to decouple death from the sequence of perimortal actions and to allow free choice from a menu of alternative definitions of death.

The final chapter by a Yale law professor is a masterly summary. He considers that the calls for changes in definitions and the law are not persuasive, albeit accepting that the present criteria for brain death are conceptually incoherent. These criteria are clearly useful clinically, and if all were applied there would be few false positives. There is serious doubt whether changes would increase the availability of organs or reduce prolonged futile treatment and its cost in distress to families and in dollars. There is already choice regarding treatment refusal or withdrawal and the donation of organs. To impose choice about when death is declared would be ideologically polarizing, the danger of which is seen in the sometimes violent controversy about abortion. His soundbite is that the US needs another such divisive issue like it needs a second hurricane Andrew. Indeed, he admits that this might imply that the manuscript of this book might have been better burnt than published. Less cynically, he hopes that it will not provoke public controversy, but will rest quietly on library shelves so that `in 10 years we might reconvene to try to explain the persistence of the confusions we had identified' ".

==> Web Link to this Article

Organ transplantation: Worldwide News Blog - Transplantation d'organes : le Blog des News du monde entier

ACCESS THE ORGAN TRANSPLANTATION WORLDWIDE NEWS BLOG. Please note that this worldwide press review is bilingual (English and French).

ACCEDER AU BLOG DES NEWS CONCERNANT LES DONS ET GREFFES D'ORGANES.

A propos du Blog des News :

Cette revue de presse internationale est bilingue (français - anglais) !

====> Officiellement créée le 5 mai 2005 par décret dans le cadre de la loi de bioéthique du 6 août 2004, l'Agence de la Biomédecine a été inaugurée mardi 10 mai 2005. Elle marque une 'étape décisive en matière de bioéthique', a déclaré Philippe Douste-Blazy. Carine Camby prend la direction de l'Agence de la Biomédecine après avoir assuré celle de l'Etablissement Français des Greffes.

====> Quelles sont les positions actuellement défendues dans la presse publique et scientifique concernant les transplantations, dans le monde entier ?

Journal of Medical Ethics: scientific press (white papers) on organ transplantation ethics

The Journal of Medical Ethics (JME) is an international peer review journal for health professionals and researchers in medical ethics.

Aims and Scope:
Journal of Medical Ethics is a leading international journal that reflects the whole field of medical ethics. The journal seeks to promote ethical reflection and conduct in scientific research and medical practice. It features original articles on ethical aspects of health care, as well as case conferences, book reviews, editorials, correspondence, news and notes. To ensure international relevance JME has Editorial Board members from all around the world including the US, Europe, Australasia and Far East. JME is the official journal of the Institute of Medical Ethics.

You'll find below a selection of JME articles on transplantation ethics.
Source: JME Online.



1.-) "Defining death in non-heart beating organ donors", 2003, J. Med. Ethics N° 29, p. 182-185. Authors: N. Zamperetti, R. Bellomo, C. Ronco.

"Our proposal is that, for the time being, the definition of death should rest on the currently applied criterion of irreversible (however defined) asystole, with the open admission that it does not define 'death', but only a moment, in the process of dying where organ retrieval can be allowed."


2.-) "Death, dying and donation: organ transplantation and the diagnosis of death", Journal of Med. Ethics, 2002, N°28, p.89-94.
Authors:
H Kerridge 1, P Saul 2, M Lowe 3, J McPhee 4 and D Williams 5
1 Haematology Department, Bone Marrow Transplant Unit, Royal Free Hospital, Hampstead, London, UK
2 Intensive Care Unit, John Hunter Hospital, Newcastle, NSW, Australia
3 Faculty of Medicine, University of Fiji, Fiji
4 Clinical Unit in Ethics and Health Law, Faculty of Medicine and Health Sciences, University of Newcastle, NSW, Australia
5 Neurology Department, John Hunter Hospital, NSW, Australia

"Refusal of organ donation is common, and becoming more frequent. In Australia refusal by families occurred in 56% of cases in 1995 in New South Wales, and had risen to 82% in 1999, becoming the most important determinant of the country's very low organ donation rate (8.9/million in 1999).

Leading causes of refusal, identified in many studies, include the lack of understanding by families of brain death and its implications, and subsequent reluctance to relegate the body to purely instrumental status. It is an interesting paradox that surveys of the public continue to show considerable support for organ donation programmes—in theory we will, in practice we won't (and don't).

In this paper we propose that the Australian community may, for good reason, distrust the concept of and criteria for 'whole brain death', and the equation of this new concept with death of the human being. We suggest that irreversible loss of circulation should be reinstated as the major defining characteristic of death, but that brain-dead, heart-beating entities remain suitable organ donors despite being alive by this criterion. This presents a major challenge to the 'dead donor rule', and would require review of current transplantation legislation. Brain dead entities are suitable donors because of irreversible loss of personhood, accurately and robustly defined by the current brain stem criteria."


3.-) "An antidote to the emerging two tier organ donation policy in Canada: the Public Cadaveric Organ Donation Program", Journal of Med. Ethics 2005, N° 31, p.188-191. Author: Stephen Giles, Toronto General Hospital, Canada.

"In Canada, as in many other countries, there exists an organ procurement/donation crisis. This paper reviews some of the most common kidney procurement and allocation programmes, analyses them in terms of public and private administration, and argues that privately administered living donor models are an inequitable stopgap measure, the good intentions of which are misplaced and opportunistic. Focusing on how to improve the publicly administered equitable cadaveric donation programme, and at the same time offering one possible explanation for its current failure, it is suggested that the simple moral principle of 'give and you shall receive', already considered by some, be extended further. This would allow for those who are willing to sign up to be a public cadaveric donor be given a priority for receiving an organ donation should they ever require it. It is argued that this priority may provide the motivation to give that is so far lacking in Canada. This model is called the Public Cadaveric Organ Donation Program."


4.-) "It is immoral to require consent for cadaver organ donation", Journal of Med. Ethics 2003, N°29, p.125-127. Author: H E Emson.

This article defends the opinion that a dead body is a republic. Hence consent should not be required for cadaver donation.

"In my opinion any concept of property in the human body either during life or after death is biologically inaccurate and morally wrong. The body should be regarded as on loan to the individual from the biomass, to which the cadaver will inevitably return. Development of immunosuppressive drugs has resulted in the cadaver becoming a unique and invaluable resource to those who will benefit from organ donation. Faced with the biological reality, the moral error of any concept of property in the body, and the quantitative failure of voluntary organ donation, I believe that the right of control over the cadaver should be vested in the state as representative of those who may benefit from organ donation.

How one regards the dead human body, the cadaver, is in part governed by one’s familiarity with it. At the present time, very few people ever see a cadaver which has not in some way been altered after death, and even fewer touch, handle, deal in any way with the dead human body. In developed countries, death itself most frequently occurs away from the home, in an institution, under the supervision of professional caregivers. For most people, ideas concerning the cadaver, its nature, the proper way to deal with it, are formed under these conditions.

As a pathologist specialising in forensic pathology, for 50 years I have been at the other end of the spectrum of experience. In my daily work I have been privileged to examine the cadaver in all its stages after death from the immediate postmortem moments through all the stages of decomposition to bare bones. Working in a relatively small community, I have sometimes been charged with examining the body of someone I have known in life, which is never an easy task. These experiences have moulded my ideas as to what the cadaver is, what it represents, and how it should be treated. My beliefs are by no means unique, but I believe the experience which has formed them is unusual and because of this, important. Reading the works of ethicists who pronounce upon these matters, I wonder how many of them have ever viewed and touched a human cadaver, or seen a decomposing body.

Out of all this I have become what I understand is termed a dichotomist, one who believes that the body and soul are separate, different entities. I use the term "soul" for want of a better, not knowing a word which does not in some way carry implications of the soul’s origin, nature, value, and destination. I wish to imply none of these, nor to intrude here my own religious beliefs. For the purposes of this discussion, the soul to me is a non-physical, immaterial entity which animates the body and gives it what we know as life. In knowing and experiencing a person, we cannot separate body and soul, because we always know them together. From the moment of birth until that of death they are inseparable and intertwined to form the person, the human being. At death the soul departs from the body—I have watched this occur—and here I express no beliefs whatsoever as to what happens to it at that point; where it goes, if anywhere, what its future is, if any. What is clear to me is, that without the soul, the body is not and can never again be a part of the person. The cadaver is not, what the body has been.

The body, on the other hand, is more easily defined and described. This, the physical entity animated by the soul, is formed of chemical elements and compounds, organised into tissues and organs, combined in a marvellous complexity and with the soul, it is the human person. In this combined state, the person is alive; without the soul, the body is dead, with all that implies. From the moment of conception the component parts of the body are formed from material drawn from the external physical world, in active interchange and dynamic equilibrium with the biomass, the sum total of living organisms on the planet, and with some of its inorganic matter. We study the human person from its earliest beginnings, through growth, differentiation, maturity, decline, disease, and death. The life of the metazoan animal Homo sapiens, as we know it—and this is only one of the ways of considering the human being—is finite; senescence starts with the zygote, and corporeal death is its inevitable end.

After death the human body decays, a process with which few are familiar and which excites revulsion which is both instinctive and learned. The instinctive part of this revulsion I think is easily explained, as an inherited reflex acquired by ancestral experience that rotten meat is not good to eat. Embedded very deeply in the nature of humanity there is another element to this, a belief that death is not the end of the soul and that the life of the body can somehow persist or be restored. This was expressed in the burial practices of the earliest humans, in the staining of bones of the deceased with red pigment as a symbol of continuing or resurgent life. Such practices have been elaborated by many different cultures, as in preservation and veneration of the bones of ancestors; burial with grave goods, food, slaughtered animals, and slaves, and mummification and embalming, to retain a simulacrum of continuing life, the last a common practice in many contemporary societies including our own. All these seek in some manner to deny the fact of death, or at the very least to delay its acceptance, to spread this as a process over a period of time, and to come to admit it gradually rather than as an instant blow at a single temporal point. Such practices often contrast oddly an expressed belief in an afterlife in a better world, with profound reluctance to leave this one. Many religions express belief in some form of "the resurrection of the body" but so far as I am aware, at the present time, this is only rarely interpreted as a strict physical reconstitution of its elements as at the moment of death. There is too much practical human experience for this, and however belief in a resurrection is interpreted, an element of symbolism is for most people inescapable.

However acceptance of death is denied or delayed, the human body is inexorably destined to decay as the beginning of a recycling process. Its constituent components are broken down by various means into simpler forms, and these in turn are recycled into the bodies of later generations of living things. We die and decay—or are burned—to come up again as wheat or roses, which in turn may form the bodies of future generations of people. Were this not so I would not be alive to write this, nor you to read it; the elements which might have formed us would all have been locked up in the indestructible physical remains of the first generation of living organisms. Decay is the inevitable and necesssary consequence of finite corporeal mortal life.

Viewed from this point, the human body can only legitimately be regarded as on extended loan from the biomass, to the individual of which it forms a part, and any view of it as property which can be owned and disposed of must be examined very seriously, questioned, and modified. Our culture accepts as a fundamental principle that while the body is animated by the soul, the person resulting from this union has a right to the preserved integrity of the body which is a necessary part of his or her total being. This is expressed in law, in our society, by prohibitions against killing, wounding, or even such minimal assault as threatening to touch the body without the person’s consent. But how we should view the cadaver after death is a very different and much more questionable matter.

In that part of the ethics of our society which is expressed in law, there is no concept of the cadaver as property which may be disposed of for gain. The law, formed over a period of time before the possibility of transplantation existed, at present charges someone with the responsibility to dispose of the cadaver in accordance with society’s customary practice and the requirements of public health, and gives this person powers to do so, but the cadaver is not his or her property. Until very recently there was no significant value in a human cadaver, and no legitimate use for it save its quantitatively very minor utilisation in dissection as a part of the training of physicians and surgeons. All this changed, recently, suddenly and dramatically, with the invention of immunosuppressive drugs which block the bodily rejection of transplanted organs and tissues, and make organ transplantation possible as a practical and effective treatment of human disease. The change is tremendous, unprecedented, unparalleled in our experience. The difference—for example, between chronic haemodialysis and kidney transplantation for the treatment of renal failure, is the difference between existence and life. From the strictly practical viewpoint, from being an object without intrinsic value destined only for disposal, the cadaver became at one leap a vital resource, something quite new in human experience. This quantum jump in technological capability brought with it, as all such advances inevitably do, totally new ethical problems. These in their turn can and must be tackled, and possibly solved, and faced with the unprecedented, it can only be done by fundamental examination of our basic beliefs, and their reconciliation with immutable physical facts.

One thing which must be considered at the very beginning, is the problem of immediacy. To be effective, an organ for transplantation must be removed as soon after death as possible. But it may be very difficult for relatives to accept that their loved one’s body, maintained in a semblence of life by artificial respiration, is in fact dead and will obviously be so when the respirator is turned off. Added to this, there is acceptance of death as a process, not as an event; a fact which those close to the deceased come to accept gradually and which in its fullness may take years. Some progress towards reconciling these facts—for human emotions are facts with which we must deal—and resolving this dilemma, can be made when the death of an individual is known to be inevitable but can be postponed for a short time during which the family can come to terms with it. A great deal more could be done by the more gradual and diffuse processes of public education, but while the problem can be lessened, it inevitably will remain.

The cadaver has now become, to those who may receive its organs as replacement for their own which have failed, quite literally a source of continued life restored to something close to its fullness, and qualitatively different from existence maintained by mechanical means. In discussing this I shall limit myself to kidney transplantation, the commonest procedure which has become routine. Again, one wonders if some of the ethicists who pronounce on this, have ever met with and talked to patients who have experienced both existence maintained by haemodialysis, and life restored by transplantation. There is this real difference. This situation requires re-examination of basic beliefs; to whom does the cadaver "belong", and who should morally have rights to determine its disposal? To the deceased, it is something that has been a vital component of the person but now is no longer and is no more needed. To the bereaved family, it is a remaining part of the beloved deceased person, emotionally tremendously evocative, hallowed by individual experience and by centuries of belief and tradition. To the potential recipient of its donated organs, it is the very new hope of restored life.

I do not think that the concept of ownership or property in the human body is an accurate, defensible, or moral one, and I believe that the body should be regarded morally as on loan from the biomass to the individual of whom it is, during life, a part. Previously a matter of only academic interest, this is now of immense practical importance. I have no problem with the right of the individual to bodily inviolability during life; integrity of the body is a necessary part of integrity of the person, together with the individual freedoms that are commonly stated in charters of rights and the like. I am deeply concerned with the right of the person to govern disposal of their body after death, when separation of body and soul is irrevocably complete, and the individual is incapable of reconstitution. The person no longer exists, the soul has departed, and the individual who was but is no longer has no further use for the body which has been part of him or her during life. The concept of the right of a person to determine before death, the disposal of their body after death, made sense only when there was no continuing use for that body; it makes neither practical nor moral sense now, when the body for which the dead person no longer has any use, is quite literally a vital resource, a potential source of life for others. Another way of looking at the cadaver, is to liken it to a dress or a suit of clothes hanging in a closet, worn by the person during life, evocative of pleasant experiences and happy times, but now no longer needed by the one who has died and useful only as a memorial by the bereaved. If it can help to keep the living warm, should not this be done? Is this not both practically and morally, its right utilisation?

If this argument is correct, then it is even more morally unacceptable for the relatives of the deceased to deny utilisation of the cadaver as a source of transplantable organs. Their only claim upon it is as a temporary memorial of a loved one, inevitably destined to decay or be burned in a very short time. To me, any such claim cannot morally be sustained in the face of what I regard as the overwhelming and pre-emptive need of the potential recipient. It is particularly unacceptable when the deceased has during life expressed consent for cadaver organ donation, and still unacceptable if he or she has expressed no opinion. The need of the potential recipient, the benefit which may accrue to him or her, to me trumps and surpasses all other considerations. The proportionate benefit is too great to be subordinate to anything else. This can be expressed in a simple parable. A rich man has a loaf which he does not need, which he cannot eat, for which he has no use. To a poor man, starving, the gift of this loaf would be the gift of life itself. But the rich man says: "I will not give you this loaf; I will drop it on the dunghill to decay, or fling it in the fire to burn". This is to me a specific analogy of the denial of organ donation, of the conscious refusal to grant it. In many instances the denial is not conscious, a positive act, but a negative omission, a failure to consider and decide upon the possibility before it becomes real. It is commonplace that there is a great gap between the proportion of people in a society who favour organ donation, and the much smaller proportion who do anything about it.

In my opinion the human cadaver, at the point at which life departs, should become a resource for those who may benefit from donation of its organs. Our society has conspicuously failed to achieve this by voluntary means, and the increasing length of the queues for donated organs testifies eloquently to this failure. On the other hand, a majority of the community express their belief that cadaver organs should be used for transplantation. Faced with this contradiction and the dilemma so caused, it appears to be morally and practically necessary for society to act to overcome this failure, and this could best be done by making the human cadaver the charge and responsibility of the state, to determine its best disposition. Without going into detail, it might be done by establishing an organisation for this purpose, under the authority of the state but at "arm’s length", very strictly separated from government and politics. The rights and responsibilities of disposal of the cadaver should be vested in this organisation. When the cadaver has been used, if possible, as a source of transplantable organs it may, if the family wishes, be reconsigned to their care, for such religious and social observances as they desire. Practically, this might be welcomed by many, as removing the necessity for an agonising decision by the family. Also practically, it is impossible for the family, in such circumstances, to be able to tell what has been done; after routine autopsy the body is reconstituted so that there is no outward sign, to ordinary observation such as that at an open coffin funeral or memorial service, that any examination has been performed. Legally, this might be regarded as an extension of the doctrine of Parens patriae, the assumption by the state of parental responsibility when this is necessary, on behalf of the persons benefiting from organ donation and transplantation. Morally, I regard the rights of the potential recipient, because of the benefits accruing, to be pre-emptive over all others.

In this situation, the idea of consent and its corollary, refusal are not morally applicable. One may be able to give or refuse consent to a procedure which affects oneself, but organ donation affects no one physically; no human person is involved as donor. To grant the right and power of consent to an individual who may be affected emotionally, is to elevate the possible emotional affect of one person, as more important than the physical life of another. The imbalance of benefit is too great to permit of this, and I find it morally unacceptable. To require consent for cadaver organ donation from the one of whose person in life the body is a part, is unacceptably to extend control of that body beyond legitimate limits. To require consent from the relatives of a previously living person is unacceptably to extend their control over matters where the good of others should be the predominant concern. The concept of consent in this situation is morally incorrect.

This having been said, in a society which places predominant value in autonomy, it may not be possible to enact in law what is morally correct. Should this matter ever attain the status of a legislative proposal, as it has in some countries, it might be a practical necessity to extend the principle of autonomy to a right to refusal of cadaver organ donation, to a living individual—to legitimise, in effect, the attitude of the rich man in my parable. To me this would be immoral, but it might be necessary to condone this limited immorality, commonly expressed as the right to opt out, or to refuse, to the individual. It would be a limited sacrifice to the much greater good."


5.-) "Is the body a republic?", Journal of Medical Ethics 2005 N°31, p.470-475. Author: Simona Giordano, Institute of Medicine, Law and Bioethics (IMLAB), School of Law, University of Manchester, UK.

"The ethics of post-mortem organ retention and use is widely debated in bioethics and law. However, the fundamental ethical issues have often been inadequately treated. According to one argument, dead bodies are no longer "persons". Given the great benefits dead bodies offer to human kind, they should be automatically treated as public property: when the person dies, the body becomes a public thing (a res publica, a republic). This paper articulates the ethical issues involved in organ and tissue retention and use, both in the case in which the deceased’s wishes are known and in the case in which the wishes are not known. It contends that a dead body is not a republic. The state should maximise availability of organs and tissues by inviting or requiring citizens to make an informed and responsible choice on the matter."


Role of brain death and the dead-donor rule in the ethics of organ transplantation

Abstract:
The "dead-donor rule" requires patients to be declared dead before the removal of life-sustaining organs for transplantation. The concept of brain death was developed, in part, to allow patients with devastating neurologic injury to be declared dead before the occurrence of cardiopulmonary arrest. Brain death is essential to current practices of organ retrieval because it legitimates organ removal from bodies that continue to have circulation and respiration, thereby avoiding ischemic injury to the organs.



The concept of brain death has long been recognized, however, to be plagued with serious inconsistencies and contradictions.

Indeed, the concept fails to correspond to any coherent biological or philosophical understanding of death. We review the evidence and arguments that expose these problems and present an alternative ethical framework to guide the procurement of transplantable organs. This alternative is based not on brain death and the dead-donor rule, but on the ethical principles of nonmaleficence (the duty not to harm, or primum non nocere) and respect for persons. We propose that individuals who desire to donate their organs and who are either neurologically devastated or imminently dying should be allowed to donate their organs, without first being declared dead. Advantages of this approach are that (unlike the dead-donor rule) it focuses on the most salient ethical issues at stake, and (unlike the concept of brain death) it avoids conceptual confusion and inconsistencies. Finally, we point out parallel developments, both domestically and abroad, that reflect both implicit and explicit support for our proposal.

© 2003 Lippincott Williams & Wilkins, Inc.

Source:
Critical Care Medicine. 31(9):2391-2396, September 2003.
Truog, Robert D. MD, FCCM; Robinson, Walter M. MD, MPH
Copyright © 2005, Society of Critical Care Medicine. All rights reserved.
Published by Lippincott Williams & Wilkins.

Does it matter that organ donors are not dead? Ethical and policy implications

LAW, ETHICS, AND MEDICINE

ABSTRACT
The "standard position" on organ donation is that the donor must be dead in order for vital organs to be removed, a position with which we agree. Recently, Robert Truog and Walter Robinson have argued that (1) brain death is not death, and (2) even though "brain dead" patients are not dead, it is morally acceptable to remove vital organs from those patients. We accept and defend their claim that brain death is not death,



and we argue against both the US "whole brain" criterion and the UK "brain stem" criterion. Then we answer their arguments in favour of removing vital organs from "brain dead" and other classes of comatose patients. We dispute their claim that the removal of vital organs is morally equivalent to "letting nature take its course", arguing that, unlike "allowing to die", it is the removal of vital organs that kills the patient, not his or her disease or injury. Then, we argue that removing vital organs from living patients is immoral and contrary to the nature of medical practice. Finally, we offer practical suggestions for changing public policy on organ transplantation.

--------------------------------------------------------------------------------

Abbreviations: EEG, electroencephalogram; UDDA, uniform determination of death act

Source :
J Med Ethics 2005;31:406-409 © 2005 BMJ Publishing Group Ltd & Institute of Medical Ethics

M Potts2 and D W Evans1
1 Queens’ College, Cambridge, Cambridge, UK
2 Philosophy and Religion Department, Methodist College, 5400 Ramsey Street, Fayetteville, NC 28311-1498, USA

Correspondence to:
Professor M Potts
5400 Ramsey Street, Fayetteville, NC 28311 – 1498, USA;
gratiaetnatura@yahoo.com

Brain death is not death

The Nasty Side of Organ Transplanting:

Dr David Wainwright Evans, Cardiologist, Queens College, Cambridge, United Kingdom, suggests that organ donors diagnosed "brain dead" may still be alive:

"There were never sound scientific or philosophical grounds for a redefinition of death based on the loss of testable brain function while the body remains alive 1. Pressure for a viable heart for transplantation nevertheless resulted in a diagnosis of death on some such basis in Cape Town 2, in 1967. There followed “a euphoric, uncontrolled epidemic of heart transplantation around the world”3. This, together with demand for other organs which, to be viable in recipients, required that they be perfused until their removal, necessitated “the production of a set of legal and philosophical justifications”2 for procedures which would otherwise be seen as assault.



The story of how the Harvard Brain Death Committee produced, in 1968, a facilitating redefinition of death based on “irreversible coma” with “no discernible central nervous system activity” makes interesting reading4. The ease with which their novel redefinition of death became incorporated into American law, and subsequently accepted in many other countries, gave food for thought. It seemed to resist attacks upon its inconsistencies and contradictions because of its utility - indeed its perceived necessity to some transplant practices.

That is, until last year [2003]. Fittingly, the paper formally admitting that the concept of brain death - as this new form of death became widely known - “fails to correspond to any coherent biological or philosophical understanding of death” came from the Harvard Medical School too 5.

While the philosophical arguments about concepts of death may be for others, the possibility of diagnosing - with the necessary certainty - the “irreversible cessation of all functions of the entire brain, including the brain stem”, while the rest of the body remains alive, has always been the concern of the doctor. That “whole brain” definition was the requirement stipulated in the quaintly named Uniform Determination of Death Act (1981) if death were to be certified on other than the universally accepted cardiorespiratory basis. The Harvard tests - essentially of brainstem mediated reflexes and ventilator dependence, with or without EEG, in patients whose coma was believed irremediable - clearly lacked the power to make that diagnosis. The many protocols in use worldwide failed similarly. Indeed, their very number6 proclaimed the fact that the syndromes they diagnosed could not be one and the same entity7. And prominent among the variations was the apnoea test, which might lead to the misdiagnosis of respiratory centre failure if inadequately stimulating. If stringent, it might prove lethal 8.

Truog and Robinson acknowledge that many patients currently diagnosed “brain dead” do not, as a matter of fact, meet the American legal requirements governing that practice. They say that many of them retain demonstrable brain function - and that this knowledge, which should be uncomfortable to those certifying death on the basis that there is none, is set aside on the premise that it is not “significant”. That practice is reminiscent of the stance assumed by those who foisted “brain death” upon us here in the UK in 1979. They simply promulgated a set of prognostic criteria, first published in 1976, with a directive that they were to be used thenceforth as criteria for the diagnosis of death9 . The illogicality of that change of use was pointed out in 1980 10. The diagnosis (of “brain death”) was crucially dependent upon the absence of specified brainstem reflexes. Other persisting brainstem function, such as blood pressure control, was to be ignored. EEG activity was not to be sought. If demonstrated, it was to be set aside as of no “significance”. Such was the pretence to knowledge of our marvellous brain’s function which did not, and still does not, exist.

The term “brain death” was formally abandoned, in this country [the UK], in 1995 11. But comatose, ventilator-dependent patients are still being certified “dead” for transplant purposes using similar tests. These are now held to diagnose the irreversible loss of the capacity for consciousness, although no sound scientific evidence has been advanced to support that claim.

Nor, since these patients are not exposed to the anoxic drive stimulus, do they have the power to diagnose the irreversible loss of the capacity to breathe. That being so, the merits and demerits of the new conceptual basis for certifying these patients dead should be of no practical concern to the doctors who care for them.

Where requests for the organs of such patients are concerned, Truog and Robinson (like others12,13) propose the abandonment of all obfuscation about their status in the dying process. They suggest that people should be allowed to donate their organs when they become “neurologically devastated or imminently dying”, without first being declared dead. This refreshing call to face the facts has implications for the validity of the “consent” given by those led to believe that their offer of organs will not be taken up until after their death. But it may be that more will be prepared to register as prospective donors on the proposed new basis if it is fully and frankly explained - and the necessary legislation enacted after open debate."


Source:
Article by Dr. David W Evans - Retired Physician (sometime Consultant Cardiologist at Papworth Hospital)
27 Gough Way, Cambridge, CB3 9LN - and Queens’ College, CB3 9ET (DWEvansMD@tinyworld.co.uk)

Competing interests : None

References

1. Beyond Brain Death : the Case Against Brain Based Criteria for Human Death. Eds. Potts M,
Byrne PA, Nilges RG. Kluwer Academic Publishers, Dordrecht, 2000

2. Hoffenberg R. Christiaan Barnard : his first transplants and their impact on concepts of death.
BMJ 2001;323:1478-80 (and see bmj.com ‘Rapid responses’ to this article)

3. Smith T. Clinical freedom. BMJ 1987;295:1583

4. Singer P. Is the sanctity of life ethics terminally ill? In: Brain Death, Ed. Machado C. Elsevier Science B.V. 1995, 231-243

5. Truog RD, Robinson WM. Role of brain death and the dead-donor rule in the ethics of organ transplantation. Crit Care Med 2003;31:2391-96

6. Wijdicks EFM. Brain death worldwide : accepted fact but no global consensus in diagnostic criteria.
NEUROLOGY 2002; 58:20-25

7. Evans DW. ‘Open letter to Professor Wijdicks’, bmj.com ‘Rapid responses’ 11 Dec 2002

8. Coimbra CG. Implications of ischemic penumbra for the diagnosis of brain death. Braz J Med Biol Res 1999;32:1479-87

9. Conference of Medical Royal Colleges and their Faculties in the UK. Memorandum on the diagnosis
of death. BMJ 1979;I:332

10. Evans DW, Lum LC. Brain death. Lancet 1980 (November 8th):1022

11. Working Group convened by the Royal College of Physicians and endorsed by the Conference of
Medical Royal Colleges and their Faculties in the United Kingdom. Criteria for the diagnosis of brain stem death. J Roy Coll Physns Lond 1995;29:381-2

12. Kerridge IH, Saul P, Lowe M, McPhee J, Williams D. Death, dying and donation : organ transplantation and the diagnosis of death. J Med Ethics 2002;28:89-94

13. Woodcock TE. New act regulating human organ transplantation could facilitate organ donation.
BMJ 2002;324:1099

La mort encéphalique : la position des neuro-psychiatres en Allemagne

Quelle est la situation en Allemagne ?
Le site internet PubMed, qui répertorie des résumés de publications scientifiques récentes, dans différents pays (langue de ce site : anglais essentiellement, mais aussi espagnol, allemand et quelques traductions de résumés en français), permet de mener une recherche très précise concernant la mort encéphalique en vue du prélèvement des organes. Des points de vue scientifiques sur la question sont exposés, commentés, débattus. La situation n'est pas identique pour chaque pays, et le consensus n'est pas encore atteint.



Voici un point récent sur la situation en Allemagne, du point de vue de deux neuro-psychiatres, diplômés de l'Université de Cologne, département de Neurologie :

"The diagnosis of brain death: medical and legal aspects with special reference to the German Transplantation Law (TPG):"

"The diagnosis of brain death following total and irreversible cessation of all cerebral functions is based on anthropological assumptions and conventions as well as on the exact medical diagnosis of total loss of brain function. The question whether individual life ends after cerebral function is irreversibly lost cannot be answered by medical definition alone. Clear and unrefutable legal definitions of death and the cessation of the rights of the individual must be provided before organs may be harvested from brain dead individuals. Acceptance of these definitions by the general population is of paramount importance for the practice of organ donation. In the first part of this article, the legal definition of death and the provisions of the German transplantation law are critically reviewed. The legal statements deal with the question of the definition of death and how death can be detected. The provisions of the German transplantation law are referenced with special attention to the provision of prior consent to the removal of organs following after the diagnosis of brain death. The provisions of the German constitution with respect to the preservation of the personal rights of the individual are discussed in the light of organ harvesting. The second part deals with the medical procedure of determining brain death in adults. The medical statements pertain to the diagnostic steps to be taken in the diagnosis and determination of brain death. The prerequisites for entering the diagnostic procedure to determine brain death are described. The clinical signs of total and irreversible cessation of brain function are listed, and the technical examinations to corroborate the clinical signs of brain death as accepted in Germany are delineated. In the perspective of the authors, individuals having suffered brain death still possess the protection of their personal human rights according to the German constitution since it cannot be conclusively demonstrated that total loss of brain function alone constitutes the cessation of life in the sense of the German constitution."


Source :
Haupt WF, Hofling W, Klinik und Poliklinik fur Neurologie der Universität zu Koln, Germany.
Fortschr. Neurol. Psychiatr. 2002 Nov; 70(11):583-90.


La mort cérébrale : résoudre les contradictions de la déclaration éthique de la mort

Voici un article scientifique traitant des contradictions de la déclaration éthique de la mort :

Canadian Journal of Anesthesia 50:725-731 (2003)
© Canadian Anesthesiologists' Society, 2003
Neuroanesthesia and Intensive Care

[Brain death: resolving inconsistencies in the ethical declaration of death:]

La mort cérébrale : résoudre les contradictions de la déclaration éthique de la mort :



"Objectif : Les premiers critères de mort cérébrale ont été formulés en 1968 pour répondre, en partie, aux inquiétudes soulevées par la recherche d’organes pour les greffes. Malgré 30 ans d’application, un certain doute subsiste chez les professionnels et le public sur la validité de la notion théorique à l’origine de cette façon de déterminer la mort. Notre revue aborde les perspectives historiques de la formulation des critères de mort cérébrale et des contradictions des critères cliniques actuels.

Méthode : La revue descriptive provient de la consultation de références dans MEDLINE et d’autres sources publiées.

Constatations principales : Le principal concept de la détermination de la mort est l’arrêt irréversible de la fonction cardio-pulmonaire ou neurologique. Cependant, il y a des contradictions dans les critères neurologiques de la mort entre les pays, entre les populations de patients et dans l’usage des tests de confirmation. Ces contradictions peuvent inquiéter le public et la profession médicale sur la validité de la détermination de la mort par des critères neurologiques.

Conclusion : La greffe d’organes est fondée sur l’acceptation publique et professionnelle du fait que le donneur soit décédé. Étant donné que les critères de mort cérébrale, ou de leur application, demeurent variables, nous croyons qu’il est raisonnable d’envisager la formation d’un consensus visant à traiter de ces contradictions. Autrement, l’utilisation standard des tests radiographiques confirmatifs, qui précèdent le prélèvement d’organes de donneurs répondant aux critères cliniques de mort cérébrale, devrait être considérée pour fournir la preuve concluante de la perte permanente et irréversible de la fonction cérébrale."


English version :

Brain death: resolving inconsistencies in the ethical declaration of death:

Christopher James Doig, MD MSc* and Ellen Burgess, MD
* From the Department of Critical Care Medicine and the Office of Medical Bioethics;
and the Division of Nephrology, Department of Medicine, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada.


"Purpose: The first criteria for the determination of brain death were developed in 1968 in part to address concerns that had arisen with the retrieval of organs for transplantation. Despite over 30 years of application, some professional and public doubt persists over the validity of the theoretical construct underlying this method of determining death. Our review will address historical perspectives on the development of brain death criteria, and inconsistencies in current clinical criteria.

Method: Narrative review from selected MEDLINE references and other published sources.

Principal findings: The primary construct of the determination of death is that either cardiopulmonary or neurological function irreversibly ceases. However, there is inconsistency in the neurological criteria for death between jurisdictions, between patient populations, and in the use of confirmatory tests. These inconsistencies may cause concern in the public or profession about the validity of the determination of death by neurological criteria.

Conclusions: Organ transplantation is premised on professional and public acceptance that the donor is dead. Given that the criteria for brain death or their application remain variable, we suggest that it is reasonable to consider a national consensus to address these inconsistencies. Alternatively, the standard use of confirmatory radiographic testing prior to the retrieval of organs from donors who meet clinical brain death criteria should be considered to provide conclusive evidence of permanent and irreversible loss of brain function."


AS A CONCLUSION :

"Increasing organ donation is an important and laudable objective. To do so at the expense of exploiting society’s most vulnerable cannot be supported despite the best of intentions. We share the opinion of Dossetor who states: "ethics dictates the following: organs should not be procured from bodies where there is life... no measures should be carried out on the dying person even with family consent, that are not directed at serving the best interests of the dying person... Our faith in the supposedly objective diagnosis of brain death leads us to remove organs from the dead body where the heart is still beating. We now need to take seriously the question of whether the criteria to establish brain death are as reliable as we claim them to be.

If they are not as satisfactory as we once thought, the whole matter should be brought into debate."


Revision received April 30, 2003. Accepted for publication March 17, 2003.

Christopher James Doig, MD MSc* and Ellen Burgess, MD
* From the Department of Critical Care Medicine and the Office of Medical Bioethics;
and the Division of Nephrology, Department of Medicine, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada.

Address correspondence to: Dr. Christopher James Doig, Rm EG23G, Foothills Medical Centre, 1403, 29th Street NW, Calgary Alberta T2N 2T9, Canada. E-mail: cdoig@ucalgary.ca

Qu'est ce qu'un donneur d'organes en état de mort cérébrale au Canada ?

"Le don d’organes et de tissus à l’unité des soins intensifs : des efforts concertés."



"En novembre 2002, un commentaire paru dans le Journal de l’Association médicale canadienne (1) a attiré notre attention sur les questions reliées au don d’organes et de tissus à l’unité des soins intensifs. Dans le résumé présenté par la Société canadienne de soins intensifs (SCSI), qui a conduit à une déclaration de principe sur le don d’organes et de tissus [disponible sur le site web de la SCSI (www.canadiancriticalcare.org)], la SCSI fait appel à la collaboration d’autres groupes dans un esprit de compréhension et de respect mutuels. C’est réconfortant de voir de tels liens se former. Une des initiatives a été de créer des liens plus étroits entre la SCSI et le Journal canadien d’anesthésie. Le résultat apparaît dans la publication, d’abord dans le présent numéro, d’une série d’articles écrits par les membres de la SCSI qui ont participé aux délibérations de notre groupe de travail sur le don d’organes et de tissus. L’article, intitulé Brain Death: resolving inconsistencies in the ethical declaration of death, correspond à l’examen personnel et professionnel de Doig et Burgess de l’évolution du concept de mort cérébrale depuis les premières discussions d’un comité de la Harvard Medical School, en 1968, jusqu’à aujourd’hui (2).

Les raisons étaient nombreuses de créer un groupe de travail de la SCSI sur le don d’organes et de tissus, notre propre perception n’étant pas la moindre qu’en qualité de réanimateurs, nous ne sommes pas assez impliqués dans l’amélioration ou l’optimalisation du taux de donateurs d’organes et de tissus. Nous demeurons les médecins les plus susceptibles de participer aux soins prodigués aux donneurs d’organes potentiels à l’unité des soins intensifs (USI). De plus, les médecins de l’USI risquent d’être les plus concernés par toute stratégie introduite par les agences chargées d’améliorer le taux de donateurs d’organes et de tissus au Canada.

Parmi les stratégies possibles, il y a des changements à la législation pour permettre de fournir des renseignements, autrement restés confidentiels, sur des donneurs d’organes potentiels à des tiers. Il y a aussi de la possibilité d’un don d’organes de patients déclarés morts selon des critères cardiovasculaires, plutôt que l’habituel critère de mort cérébrale. Ces patients seraient des donneurs à coeur non battant (3). Cette façon de procéder est souvent utilisée aux Pays-Bas et dans quelques centres américains. Pour traiter de ces questions, et d’autres, nous avons réuni cinq personnes, non-médecins, et huit spécialistes de l’USI pour former un groupe de travail. Les non-médecins étaient : bioéthiciens (Kerry Bowman PhD, University of Toronto, Alister Browne PhD, Langara College, British Columbia), experts en droit de la santé (Jocelyn Downie SJD, Dalhousie University) et deux membres du public représentant la famille d’un donneur (Diane Craig, Ontario) et la famille d’un receveur d’organes (Lois Scott, New Brunswick). Les huit médecins de l’USI (Peter Dodek, Vancouver ; Paul Boiteau, Chip Doig, Calgary ; Catherine Farrell, Montréal ; Giuseppe Pagliarello, Ottawa ; Graeme Rocker, Halifax (président), Sam Shemie, Toronto et Gordon Wood, Victoria) représentaient six provinces et des centres de soins tertiaires ayant des intérêts communautaires tant adultes que pédiatriques.

Une fois composée l’ébauche de la déclaration de principe, de nombreuses versions ont traduit la ré- flexion en cours et la construction du consensus. La version finale du résumé a été distribuée en août 2002. Dans cette déclaration, nous souhaitions, par exemple, un moratoire sur les programmes de donneurs à cur non battant afin d’élargir la discussion et de débattre des questions éthiques soulevées par la situation. La SCSI s’est attirée quelques commentaires sur le conservatisme de sa position (ce qui ne nous a pas surpris), mais nous avons maintenu notre demande de nouvelle discussion. Pour cette raison, nous sommes heureux que le Journal canadien d’anesthésie ait accepté de publier prochainement un article sur les questions éthiques reliées à l’utilisation possible de donneurs à cur non battant. Dans les prochains numéros, le Journal va aussi publier des documents manuscrits sur l’élément culturel du diagnostic de mort cérébrale et sur la question controversée de la déclaration obligatoire de mort "imminente" qui permettrait de trouver des donneurs d’organes potentiels pour des organisations tierces. Aucun de ces articles ne prétend représenter la vision officielle de la SCSI sur le sujet en particulier, mais ils ont été présentés par leurs auteurs pour être publiés avec l’idée d’aborder certaines questions controversées auprès d’un auditoire plus large et de stimuler d’autres débats.

Une autre initiative de collaboration doit être soulignée. Répondant à la requête de la SCSI pour un dialogue et une collaboration sur les événements qui conduisent à la mort cérébrale, le Conseil canadien pour le don et la transplantation a parrainé en avril 2003 à Vancouver (4) un Forum canadien sur les lésions cérébrales graves menant à la détermination neurologique de la mort. Pendant le Forum, les spécialistes médicaux et non médicaux représentant la bioéthique, le droit de la santé, les soins intensifs, l’urgence, le milieu des sciences neurologiques, la transplantation, les soins palliatifs, les associations et collèges professionnels et le gouvernement fédéral, par Santé Canada et l’Institut canadien d’information sur la santé, ont évalué les politiques et les pratiques de traitement des patients gravement malades présentant des lésions cérébrales et/ou un mauvais pronostic neurologique. Un objectif était de formuler et d’utiliser une définition canadienne de la détermination neurologique de la mort, applicable de manière constante et fiable.

Pourquoi une telle approche est-elle nécessaire ? L’article de Doig et Burgess (2) présente une preuve assez claire des incohérences qui président actuellement au diagnostic de mort cérébrale. Un exemple manifeste est la différence observée entre les États-Unis et le Royaume-Uni. Les Américains ont adopté le concept de coma dépassé. Au R-U, un diagnostic de mort cérébrale est principalement fondé sur l’irréversibilité de la fonction du tronc cérébrale. Un rapport sur les débats du Forum canadien sur les lésions cérébrales graves paraîtra sous peu. D’autres collaborations similaires sont visées pour accroître, au Canada, la prise de conscience sur d’autres questions touchant le don d’organes (par ex., le recours, ou non, à des donneurs à cur non battant) en intéressant de nombreuses disciplines à prendre part à la clarification des enjeux clés, légaux ou éthiques, médicaux ou techniques.

Modifier une politique ou un comportement professionnel comporte la mise en oeuvre réussie de nouvelles stratégies. La diffusion de nouveaux renseignements est alors indispensable. La collaboration avec des journaux médicaux d’un vaste lectorat peut être une partie clé du processus. La SCSI est fière de faire partie de cette collaboration. Nous remercions le Journal canadien d’anesthésie d’avoir permis à la SCSI de présenter son travail à une plus large public intéressé à la réanimation. Nous attendons avec impatience d’autres initiatives qui bénéficieront, en définitive, aux patients et aux familles dont nous prenons soin."


Organ and tissue donation in the intensive care unit: collaborative endeavours:

"In November 2002 a Canadian Medical Association Journal commentary (1) drew attention to several organ and tissue donation-related issues in the critical care unit. In this summary of the Canadian Critical Care Society (CCCS) process that led to a position paper on organ and tissue donation, [available from the CCCS web-site (www.canadiancriticalcare.org)], the CCCS called for collaboration with other groups in a "spirit of mutual understanding and respect." It is heartening to see such collaborations taking shape. One initiative has been the forging of stronger links between the CCCS and the Canadian Journal of Anesthesia. This has resulted in the publication, beginning with this edition, of a series of articles by CCCS members who participated in our organ and tissue donation working group deliberations. In this edition of the Canadian Journal of Anesthesia, an article entitled "Brain Death: resolving inconsistencies in the ethical declaration of death" reflects Doig’s and Burgess’ personal and professional assessment of the development of the concepts of brain death from the early deliberations of a 1968 committee at Harvard Medical School up to the present(2).

There were many reasons to create a working group of the CCCS to address organ and tissue donation, not the least of which was our own perception that as critical care physicians, we were not sufficiently involved in processes to improve or optimize organ and tissue donation rates. We remain the physicians most likely to be involved in the care of potential organ donors in the intensive care unit (ICU). In addition, ICU physicians are the clinicians most likely to be affected by any strategies introduced by agencies charged with seeking to improve Canada’s organ and tissue donation rates.

Some of these potential strategies include changes to legislation to allow information about potential organ donors to be forwarded to third parties that would otherwise have remained confidential. Other strategies under discussion include consideration of organ donation from patients declared dead by cardiovascular criteria (rather than by conventional brain death criteria). These patients would become non-heart beating donors (3). This approach is often used in the Netherlands and in some US centres. To address these and other issues, we brought together five non-physicians and eight ICU specialists to comprise our working group. The non-physicians were: bioethicists (Kerry Bowman PhD, University of Toronto, Alister Browne PhD, Langara College, British Columbia) a health law expert (Jocelyn Downie SJD, Dalhousie University) and two members of the public representing the family of an organ donor (Diane Craig, Ontario) and the family of an organ recipient (Lois Scott, New Brunswick). The eight ICU physicians (Peter Dodek, Vancouver; Paul Boiteau, Chip Doig, Calgary; Catherine Farrell, Montreal; Giuseppe Pagliarello, Ottawa; Graeme Rocker, Halifax (Chair), Sam Shemie, Toronto and Gordon Wood, Victoria represented six provinces with both tertiary centre, community, adult and pediatric interests.

Once we had crafted our first draft of the position paper much iteration followed in course of reflection and building of consensus. The bound version of the executive summary was distributed in August 2002. In this position paper we called, for example, for a moratorium on non-heart beating donor programs in Canada to allow for wider discussion and debate of the ethical issues that arise in such a context. The CCCS has attracted some comments on its conservative stance on this issue (which we expected), but we stand by our call for wider discussion. For this reason we are delighted that the Canadian Journal of Anesthesia has agreed to publish an article in a later issue on ethical issues related to potential use of non-heart beating donors. In subsequent issues the Canadian Journal of Anesthesia will also publish manuscripts on cultural consideration in the diagnosis of brain death and on the contentious issue of mandatory reporting of "imminent" death to identify "potential" organ donors to third party organizations. None of these papers should be considered to represent the official view of the CCCS on the specific topic, but they have been offered for publication by their authors in the spirit of bringing some contentious issues to a wider audience to stimulate further discussion and debate.

Another collaborative initiative in organ and tissue donation should be highlighted. Responding to the CCCS request for discourse and collaboration around events leading to brain death, the Canadian Council for Donation and Transplantation sponsored a Canadian Forum on severe brain injury to neurological determination of death in Vancouver in April 2003 (4). During the Forum, medical and non-medical specialists representing bioethics, health law, critical care, the emergency department, neuroscience communities, transplantation, palliative care, professional associations and colleges as well as Federal representation through Health Canada and the Canadian Institute of Health Information evaluated policies and practices concerning the management of critically injured patients with brain injury and/or poor neurological outcome. One purpose was to create and implement a Canadian definition of a neurological determination of death that can be applied consistently and reliably.

Why is there a need for a such an approach? The article by Doig and Burgess (2) provides some stark evidence of the inconsistencies with which the current diagnosis of brain death is approached. One glaring example is the difference between the US and the UK. The US has adopted the concept of whole brain death. In the UK a diagnosis of brain death is based primarily on irreversible function of the brain stem. A report of the proceedings of the Canadian Forum on severe brain injury will be forthcoming shortly. Subsequent similar collaborations will be aimed at increasing awareness in Canada of other organ donation issues (e.g., use or non-use of non-heart beating donors) by involving the many disciplines that need to be part of processes aimed at clarifying key issues, whether legal or ethical, medical or procedural.

Change to policy or professional behaviour involves successful implementation of new strategies. Dissemination of new information is integral to this success. Collaboration with medical journals with wide readership can be a key part of that process. The CCCS is proud to be part of this process of collaboration. We are grateful to the Canadian Journal of Anesthesia for enabling the work of the CCCS to reach a wider audience with interests in critical care. We look forward to other initiatives that ultimately will be to the benefit of the patients and families we care for."


References:
1. Rocker GM. Organ and tissue donation in the intensive care unit. CMAJ 2002; 167: 1248–9
2. Doig CJ, Burgess E. Brain death: resolving inconsistencies in the ethical declaration of death. Can J Anesth 2003; 50: 725–31.
3. Campbell GM, Sutherland FR. Non-heart-beating organ donors as a source of kidneys for transplantation: a chart review. CMAJ 1999; 160: 1573–6.
4. Shemie SD, Doig C, Belitsky P. Advancing toward a modern death: the path from severe brain injury to neurological determination of death. CMAJ 2003; 168: 993–5.

Source:
Graeme Rocker, MHSc DM FRCP FRCPC
Department of Medicine (Respirology), Dalhousie University, Halifax, Nova Scotia, Canada.
Address correspondence to: Dr. Graeme Rocker, President, Canadian Critical Care Society, 4457 Halifax Infirmary, 1796 Summer Street, Halifax, Nova Scotia B3H 3A7, Canada. Phone: 902-473-6611; Fax: 902-473-6202; E-mail: gmrocker@dal.ca