Select Committee on European Union Minutes of Evidence


Examination of Witnesses (Questions 411 - 419)

THURSDAY 20 MARCH 2008

Dr John Jenkins and Ms Jane O'Brien

  Q411  Chairman: Welcome to you. Would you like to make a short introductory statement before we begin?

  Dr Jenkins: Thank you, my Lord Chairman, and thank you to the Committee for affording us the opportunity to join you in your deliberations today. My name is Dr John Jenkins. I am Chairman of the Standards and Ethics Committee at the General Medical Council and in my day job I am a consultant paediatrician—as you probably gathered, in Northern Ireland. Really all I wanted to say by way of opening comment was to refer you to annex C of the yellow papers in which we have set out the role of the GMC. It is particularly important that in relation to specialist areas such as the one you are considering we need to point out the very broad remit of the GMC in relation to what we describe as our four interlocking functions: keeping an up-to-date register of qualified doctors; fostering good medical practice—which is the bit in which we are particularly involved; equally, promoting high standards of medical education right across the spectrum of medical education; and, finally—possibly the one which gets most publicity but which in our view is perhaps not the most important aspect—dealing firmly and fairly with doctors whose fitness to practice is in question. It is in the context of our remit as a whole within the overall functioning of the General Medical Council that we wish to give evidence today.

  Q412  Chairman: Having set out that context, I am not going to read out the whole question I have but simply say: in that context, what is the GMC's position in relation to fostering good practice in relation to organ donation and transplantation?

  Dr Jenkins: We go back to the Medical Act and from that we derive our authority to issue guidance to the medical profession on issues relating to standards and ethics. It is in that broader context that we would wish to give guidance to the profession which would be relevant to those working in this specialist area. Our general guidance is set out in our booklet Good Medical Practice which we reissued in 2006. We can certainly make copies available and it is also available on the website. That sets out the ethical framework for all doctors practising right across the very broad spectrum of medical practice and, while it will not relate to specific specialist areas, such as the one we are discussing today, it does deal with topics like the requirement for doctors to listen to patients and respect their views, for doctors to respect patients' dignity, to provide treatment within a context of consent or other valid authority, to act within the law, for doctors to keep up-to-date, to work within their competence and, indeed, to work effectively with other healthcare professionals in teams. All of those are relevant to the issue of transplantation although they do not deal with it specifically, but it is that ethical context which the GMC sets and within which each specialist area of medical practice has to interpret that guidance and then to act ethically.

  Q413  Chairman: What thinking has there been in the GMC about the balance between working with families and the careful work that has to be done at the point of asking for organs, and the worry about the queue, if you like—the people who are waiting for organs -and how you balance those two issues?

  Dr Jenkins: We have recently been considering the issue of consent particularly. We are just finalising our guidance on consent at the moment, so that type of issue has been one that we have considered, although not in the specific but in the more general sense. The concept which we have been trying to develop in recent years at the GMC is one of partnership. Doctors and patients and, indeed, the public need to develop partnerships to which they each bring different strengths, different knowledge, different concerns relating to any individual question, and a question relating to the availability of organs for transplant is one where we would see this having to develop. In effect, if a doctor has been working with a family in an intensive care setting or whatever setting and has developed a relationship with them, so that there is a common understanding of how the family are addressing the particular issue, it is much easier then for a decision to be made which is relevant to that particular setting and which is agreeable within that particular family setting. In developing our consent guidance, we have not specifically addressed the issue that is before us today. In particular, we have not specifically addressed the issue of presumed consent because, at the moment, that is not something which is within the legislative framework and so is not something which our remit would give us the authority to advise doctors. But we have looked at it in the broader context of how families, doctors and, indeed, patients can work together to reach agreed decisions.

  Chairman: Clearly there are other issues when people do not have a relationship because they have been knocked down in the road. That is one of the partnerships we know there is a problem about, and Lady Perry is going to follow this up.

  Q414  Baroness Perry of Southwark: We have been told there is a conflict between the Human Tissue Act and the Coroners Act and that this leads to a lack of clarity about the way in which potential organ donors should receive medical treatment. That seems to be particularly the case with non-heart-beating donors. How should this be determined so as to reconcile the conflict between the donors' best interests and retrieving organs of good quality? Does the GMC recognise this problem? How would you like to see clarification?

  Ms O'Brien: I am Jane O'Brien. I am Assistant Director in the Standards and Fitness to Practise Directorate. We do know about this issue. I think it arises where there has been a sudden or violent death which needs to be reported to a coroner. At that point, the coroner is responsible for what happens to the body and, clearly, in some cases, where a serious crime is suspected, a murder or whatever, there would be a post-mortem, which may have police evidential value, where it may never be sensible or appropriate to try to use the organs for donation purposes. There are a number of cases where it is not nearly so clear cut and there is no particular reason why the donation should not go ahead. As we understand it, the main problem is the variation across the country in the view that coroners take. There is nothing in the law which precludes them from immediately releasing the body for donation, but it is, if you like, a question of personal caution in the way they would interpret their responsibilities. Some unified government advice would be probably the solution to try to get consistency and not to have very cautious coroners preventing donations which other coroners would be perfectly happy to go ahead with. There is a slightly separate problem, I might say, which has been raised with us which is with the Mental Capacity Act, which occurs where a person who is not brain-stem dead but who has had major neurological trauma will be assessed to see whether they should receive treatment, whether they are going to get any benefit from continuing treatment, usually in an intensive care unit. Clearly a decision has to be made in these difficult cases as to whether there is any benefit to patients in providing that treatment. That decision has to be made completely in that patient's interests. If there is no overall benefit to the patient, no prospect of recovery and their treatment is simply prolonging the process of dying, then the normal procedure would be to stop the treatment and the patient would die fairly quickly after that. The difficulty there is that if you want to have a hope of using this difficult infrastructure to use the organs from that person, then you need some time, usually a matter of hours, to organise the transplant teams to undertake the necessary tests, to get things in place, and so, in the past, normally that treatment would continue during those two/four/six hours. It is very unclear that that is lawful under the Mental Capacity Act. You have to take a decision in the patient's best interests and best interests is defined. The criteria you use are defined in the Act and elaborated in the Code of Practice which supports the Act. However, while this Code goes quite a long way in encouraging a kind of substituted judgment test of saying, "What is it that the patient would have wanted in these circumstances? We will do that as being in their best interests?" it does not quite go all the way in doing that. It pulls back at the end, particularly in the Code of Practice, where it says, "You can do things which benefit others but they must be in the patient's best interests". At this point, you have decided absolutely that it is not in the patient's interests to continue with treatment. Nonetheless you are going to do so, so you are saying this is really in the interests of the recipient. Can you make that square with the Act? I think it is possible. There are ways of reading it in which it is perfectly reasonable to do so, to say, "Because it is clearly what the patient wanted" or "Because they have lived a life in which their values have been x and y which would lead us to believe that," but it is not clear.

  Q415  Baroness Perry of Southwark: Has there ever been a test case?

  Ms O'Brien: No. I think that does lead doctors to interpret it differently and some to be very cautious about doing something which they see to be unlawful. Again, we would see clarification through the Code of Practice as being really helpful in this area, to remove that question of doubt one way or the other. It may be that government would wish to say, "No, best interests cannot simply serve somebody else's interests at that point in life." Fine, but at least it would resolve the conflict.

  Q416  Lord Lea of Crondall: Are you a doctor?

  Ms O'Brien: No.

  Q417  Lord Lea of Crondall: You sound to know a lot about it.

  Ms O'Brien: That is a very good act!

  Q418  Chairman: The job of this Committee is really to look at the European Union dimension. Lord Wade is going to do that but presumably that very good exposition will have been made to the taskforce whose job it is to clarify some of those issues.

  Ms O'Brien: That is right, yes.

  Lord Wade of Chorlton: Perhaps I could ask another question first. You seem to be an expert on these sort of things. What is the legal status of a body?

  Q419  Lord Trefgarne: I asked this question last week and got no answer.

  Ms O'Brien: The body is in the possession of somebody—usually the hospital, the Trust -once the patient has died and it will then be released to the family. That will not be the case where there is a need to report the death to the coroner, where the coroner has responsibility for the body until cremation or burial.


 
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