Select Committee on Science and Technology Minutes of Evidence


Examination of Witnesses (Questions 760-776)

DR GILL HART, MR RICHARD GUTOWSKI, MS HELEN YOUNG AND MR ANDREW DILLON

15 MARCH 2007

  Q760  Lord Colwyn: Are the Royal Colleges involved?

  Mr Dillon: Yes. The way we develop clinical guidelines is to do it in conjunction with the Colleges. The guidelines are developed through a series of national collaborating centres and these centres are collectives of the medical Royal Colleges and the other main, national, professional bodies.

  Q761  Lord Colwyn: Do you have any view on how these guidelines will fit into the current system of allergy service provision in view of the financial constraints of most PCTs?

  Mr Dillon: They fit into the existing services in that they would represent standard good practice, so the existing services would do what the NHS does generally when NICE produces a clinical guideline. That is to base line current service provision against recommendations and develop in effect a project plan to migrate towards broad accordance with those recommendations. They also have the effect of stimulating the creation of services where those services do not exist. There have been examples from other NICE clinical practice recommendations where that is happening. Clearly the NHS is expected to do an enormous amount for all of us and we all expect it to do all of that straight away. The reality is that local NHS organisations start from different positions for individual services. Some are well advanced in one service and less well advanced in another. The time it takes to get from where somebody might be at the point at which we publish a recommendation on a particular aspect of clinical practice to being able to say, "We are consistent with NICE recommendations" will vary. That variation is in part also a result of the ability of NHS organisations to allocate resources to implement what we have recommended.

  Q762  Lord Colwyn: I suppose we might be concerned that there is such a shortage of allergy consultants throughout the country that services might vary from region to region.

  Mr Dillon: They do. It is not just because of the distribution and number of allergy consultants. Most allergies can be very competently managed in primary care by generalists and that is where the majority of service delivery will be. NICE guidance though would recognise both where it is appropriate for generalist practitioners, both medical and nursing, and indeed whether other health professionals can make a contribution to treating and where it is necessary to refer on to more specialist care. One of the benefits of having that guidance is that it gives the service as a whole, as well as local NHS organisations, the ability to work out what they actually need in order to deliver a good quality service.

  Q763  Chairman: We have heard of GPs drowning under guidelines.

  Mr Dillon: They are but the only ones they really need are ours, so they need not drown.

  Q764  Lord Soulsby of Swaffham Prior: Can we turn to immunotherapy? We have heard from other witnesses that immunotherapy is not very popular, if that is the proper word, in this country compared with countries in the European Union. One wonders why this is so. Is it because the MHRA regulation for immunotherapy licences are particularly stringent compared with those in other countries? There has been a visit to Germany, for example, where the Committee found that immunotherapy was quite frequently used.

  Mr Gutowski: I can answer it very briefly in the sense that the Committee on Safety of Medicines within the UK restricted the use of desensitising vaccines in, I am told, about 1986 and 1994. They advised of inadequate evidence of benefit to support the use of these vaccines. They revisited that in 1994. They recommended that these treatments should be restricted to those patients who have not responded to anti-allergy drugs. I can give the Committee a more detailed explanation of the thinking behind the CSM's decision in this respect but I do not have any more detail of that in front of me.

  Q765  Lord Soulsby of Swaffham Prior: One wonders, for example, whether NICE have carried out an appraisal of allergen injection immunotherapy. Mr Dillon, have you any information?

  Mr Dillon: No.

  Q766  Lord Soulsby of Swaffham Prior: In view of the more general use of it in other countries in Europe, is it not worth looking at in greater detail than hitherto? Obviously its use has been rather negated by what you say.

  Mr Dillon: Anything that the NHS can and does offer, regardless of at whatever level and whatever variation, is worthy of some consideration but with limited capacity NICE has to prioritise what it looks at at any one point in time. That said, the process that we operate to generate topics allows anybody to suggest either a specific drug or another intervention or a whole disease area as being suitable for consideration. The new arrangements that we have put in place since the autumn of last year provide a much more transparent, objective approach to assessing the suitability of topics suggested and a much more objective approach to prioritising them. We could do it but in the end we have to make sure that we spread our available capacity across the whole range of diseases and conditions that people would expect.

  Q767  Chairman: The Cochrane review came out with quite positive results. How much of the Cochrane review is informing your process, particularly your guideline development?

  Mr Dillon: Looking at what Cochrane has produced is one of the first steps that the guideline development group take in assembling the evidence. Cochrane is a very important source of our studies and their database would be searched as a matter of routine by the guideline development group.

  Q768  Lord Colwyn: Have any of you a kind word about Vega testing or kinesiological testing or homeopathic treatment?

  Ms Young: I cannot offer an opinion from NHS Direct's perspective on that. I would not feel comfortable doing so.

  Mr Dillon: I do not have any unkind words but I do not have a view.

  Q769  Chairman: Can I go to over the counter medication, second generation antihistamines and potent nasal corticosteroids? These are now available from pharmacies in the high street. I wonder whether you feel—I guess it would be particularly Ms Young—that the level of regulation is right or whether there is an over-availability or an under-availability?

  Ms Young: in relation to whether the regulation is right, it is probably not directly my sphere but what I could perhaps offer is that it is our experience that, from a user perspective, the patients' perspective, both the availability of these products and their usage is significantly both valued and used. Although NHS Direct do not prescribe over the telephone and we do not directly advise patients to go and take a particular drug, we do advise on groups of drugs that might be helpful in managing their symptom or their condition. It has been fedback to us and it is our nurses' view that the availability of the products plus importantly the pharmacists' advice on the usage of those products is very much valued by patients. Whilst I would not personally have a comment on regulation, I would say that the availability and usage of such products has certainly increased, as you would expect. It is a favourable option for many members of the public and unblocks other parts of the NHS for other care.

  Mr Gutowski: The move of products from prescription only to pharmacy status was following careful consideration by the Agency as part of the general policy of making more treatments available to the general public, rather than by a general practitioner. It was based on a number of considerations: a favourable safety profiling in respect of diagnosis and misdiagnosis of these products. The lack of abuse potential is another consideration in making that determination and then there is the convenience of the availability of products from a pharmacy or general sale. When the consultation was made with regard to moving these products to pharmacy status, there was no objection raised with the Agency with regard to the new availability of these products.

  Q770  Chairman: Does this mean pharmacists are now managing allergy?

  Mr Gutowski: I do not know. I cannot answer that question.

  Ms Young: It would be a personal view that they are a very important part of allergy management as are general practitioners but, because of the increase in the usage of products over the country and the quality of advice that needs to go with that, it is certainly worth consulting with that group because they play a particularly important role in self-care management.

  Q771  Chairman: You mentioned just now that you would advise a caller to look at a particular group of drugs perhaps in terms of managing their condition. Do you advise them to seek advice from a pharmacist or do you advise them to go to their GP before purchasing drugs from that group?

  Ms Young: It depends on the nature of the call. In urgent symptoms that we believe need to be seen by a GP, we would automatically screen and send to the general practitioner. Roughly speaking, about one per cent go to 999. 50 per cent of the calls that we take in relation to allergy will end up either directly going to a GP practice or some form of out of hours care. The rest of it will be self-care. We will say that a particular group of drugs might be helpful in alleviating symptoms. We will then advise them to go to the pharmacy, speak to the pharmacist and be advised on what is the best product. The difficulty for NHS Direct is that we are not always face to face so our advice to go to a pharmacy is often based on whether we have a view on what group of drugs will work but we would obviously want another clinician to have a face to face opportunity where that patient is exhibiting a rash et cetera.

  Q772  Chairman: Do you think the pharmacists have clinical training appropriate to the diagnosis of these sorts of conditions?

  Ms Young: I cannot specifically comment on pharmacist training. I only know about our collaboration with them in relation to sending patients or callers to them.

  Q773  Viscount Simon: Novel therapies for allergic diseases are currently being developed such as anti-IgE therapies and sublingual desensitisation vaccines. Are these being appraised by NICE or MHRA and who can administer them?

  Mr Dillon: We are looking at one of these therapies called omalizumab and it is for treating severe, persistent, allergic asthma. The plan at the moment, subject to appeal, would be to publish recommendations about the use of it in August this year.

  Q774  Chairman: Do you have any view on the role of pharmacists in the diagnosis of allergy?

  Mr Dillon: Not from the NICE perspective but there will be a general view inside the Institute that pharmacists have an important role to play in delivering services and that role over the years has increased and is likely to increase further. The judgment is all about risk set against convenience for patients or individuals accessing a pharmacy as opposed to going to a GP.

  Q775  Chairman: Dr Hart, from the people who are sending in to you, do you have a feel for how many have sought advice from health care professionals, other than going through their GP, and have found that advice helpful or unhelpful?

  Dr Hart: I do not have exact numbers or details. People who come to us have suffered for a long time and they tend to come to us as for other therapies as more of a last resort because they do not feel their needs have been met.

  Q776  Chairman: I wonder whether you anticipate that NICE might be evaluating some of the oral hay fever vaccines such as Grazax, whether that is on your "to do" list or whether it has not yet featured.

  Mr Dillon: It is not on our "to do" list. It has been something that we have looked at and tested against the selection criteria for topics for the Institute. At the time we did that, it was looked at by what was then the joint NICE Department of Health Committee in September last year. The view was that it was not suitable for appraisal by the Institute.

  Chairman: If none of you has any particular comment to make where you disagree with something said by somebody else on the panel, could I thank you for having come this morning. If there are additional pieces of information you would like to send to us, please do. We will look at them as part of your evidence today.


15 MARCH 2007



 
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