The Bulletin of Medical Ethics current issue


Issue Number 192 (October 2003)


You can browse the topics covered in the current issue by clicking on the headings below. The editorial is reproduced in full each month online.

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- Editorial
- In Parliament
- News
- Official statements
- Review
- Book reviews


OTHER ISSUES


191 (September 2003)
190 (August 2003)
189 (June/July 2003)
188 (May 2003)
187 (April 2003)











 

Editorial TOP OF PAGE

 

Your editor is sometimes wheeled out by the media as a critic of government policy on MMR, but that does not alter his strong support for protecting children against measles. The latter is what the UK government is failing to do, as immunisation rates against measles, mumps and rubella (MMR) fall to 80% or less, making a measles epidemic more possible. The problem is that officials prefer compulsion - unacknowledged, of course - to reason, as they try to maintain herd immunity.

The evidence for a link between MMR and childhood autism is very weak, but is not dispelled by small-scale retrospective epidemiology undertaken by fervent supporters of MMR. Prospective studies are needed for a true assessment of MMR risks. Most parents know that the risks are low, but may also understand that benefit to their child is unlikely: an unimmunised child has an annual risk of a damaging measles episode of less than 1 in 100,000. So some wish to give their children single vaccines, without the risk of MMR, thereby protecting them and maintaining herd immunity.

Government officials think differently. Single vaccines are dangerous, they say, because acquisition of immunity is delayed. This is false. Were this government not trying to make single vaccines unavailable, immunity against measles could be acquired just as fast as with MMR: the same measles strain is used in each. Immunity to rubella in infancy is less important: the disease is only a danger to pregnant women; and no one seriously thought it worth immunising against mumps until manufacturers provided it in a combined vaccine. Tellingly, when the government ran a mass vaccination against measles in 1994, they used a specially made combination of measles and rubella, rather than the readily available MMR.

Official attempts to compel the use of MMR are not working, even though some GPs are helping by giving MMR without parental consent as children are brought for Hib injections in another catch-up campaign. The need for a second Hib injection is incidentally another example of the failure to study new vaccines adequately before use.

What the government must now do is to reinstate legal aid for parents who say their children were damaged by MMR. If there is no evidence that MMR caused the damage, what better way to make that clear to all parents than to have the pros and cons aired in a public trial. To prevent the trial by withdrawing legal aid just adds fuel to the suspicion that there is evidence for the parents' claim which the government fears to have publicised.

 

In Parliament TOP OF PAGE

 

Health and Social Care (Community Health and Standards) Bill

 

News TOP OF PAGE

 

Euthanasia and assisted dying

 

 

French mother helps son to die

   

 

Assisted dying elsewhere in Europe


   

 

Official statements TOP OF PAGE


Prisoners - medical care, and in research

 

 


The exercise of medical activities in respect of detained persons: Medico-ethical guidelines of the Swiss Academy of Medical Sciences

OHRP guidance on the involvement of prisoners in research   An abridged version of the latest guidance from the US Office for Human Research Protections (OHRP), at the Department of Health and Human Services (HHS), on research with prisoners.

 

Review TOP OF PAGE
International Declaration on Human Genetic Data   In 1997, UNESCO adopted the Universal Declaration on the Human Genome and Human Rights. Since then its International Bioethics Committee has continued to work on genetic issues, resulting in the adoption of this declaration by the UNESCO General Conference at its meeting in Paris earlier this month. Although UNESCO is concerned at the rapid development of uses of genetic data, it chose to agree a declaration, which is not legally binding, instead of a convention, to allow future modifications that may be necessary as the field continues to evolve.

Genetic testing in the workplace   The European Group on Ethics in Science and New Technologies has given this opinion on ethical aspects of genetic testing in the workplace.

Mental Incapacity Bill (draft)  

The Law Commission began work to revise the law relating to mental incapacity a decade ago, and the resulting documents have been consid-ered in Bulletins from No. 106 onwards. A draft Bill has now been written and is being considered by a Parliamentary committee: it has nothing to say on medical research. Both that committee and the Dept. of Constitutional Affairs apparently find medical research too difficult to deal with. The sections included here deal with definitions, best interests, and advance and excluded decisions

 

Book reviews TOP OF PAGE

 

There are no books reviewed in this Bulletin.


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