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Referrals might be made on the basis of women's anxiety
EDITOR Emery et al assume that the aim is to try to stop unnecessary referrals
to genetic clinics. Most referrals are made to local breast units, of
which there are more than 100 in the country doing family history
screening, whose staff are used to discussing the risks of and
necessity for screening. In our breast unit we send a questionnaire to
patients referred because of a family history risk, asking for details
of their relatives, and then only see the ones who meet guidelines for
screening. We send a detailed letter to the others explaining why their
risk is low; patients at very high risk are referred on to the genetics
service. This allows general practitioners to refer women to us on the basis of their anxiety and their own perceived risk rather than their
actual risk, and saves doctors from having to find a piece of paper
with rather complicated guidelines or a computer programme which they
have forgotten how to use. A study of this evaluation method (submitted
for publication) has shown that we end up seeing 50% of the patients
referred, the other 50% at low or no elevated risk being very
satisfied with the method.
I read with interest the paper by Emery et al on using different
methods of assessing genetic risk for breast and ovarian cancer and
also the previous paper by Emery with a different set of
coauthors.
1 2
In both these papers the authors assume that general practitioners have the time and will to take on new responsibilities and skills. Emery et al state that only three of the
36 general practitioners in the study were able to find the paper
management guidelines for referral.1 It is hard to imagine
that they are first going to find the computer software, remember how
to use it, and then remember how to interpret the results during a five
minute appointment. They cannot then just refer to a specialist or not;
they would have to give some form of counselling
another new skill to
learn and remember. There is evidence to suggest that general
practitioners are reluctant to take on these new roles.3
Breast Care Centre, Frenchay Hospital, Bristol BS16 1ND
mike.shere{at}north-bristol.swest.nhs.uk
| 1. |
Emery J, Walton R, Murphy M, Austoker A, Yudkin P, Chapman C, et al.
Computer support for interpreting family histories of breast and ovarian cancer in primary care: comparative study with simulated cases.
BMJ
2000;
321:
28-32 |
| 2. |
Emery J, Walton R, Coulson A, Glasspool D, Ziebland S, Fox J.
Computer support for recording and interpreting family histories of breast and ovarian cancer in primary care (RAGs): qualitative evaluation with simulated patients.
BMJ
1999;
319:
32-36 |
| 3. |
Kumar S, Gantley M.
Tensions between policy makers and general practitioners in implementing new genetics: grounded theory interview study.
BMJ
1999;
319:
1410-1413 |
Nurse led clinic may provide better service than computer program
EDITOR We have developed a family history clinic led by a nurse, to which
general practitioners can refer all patients concerned about their
cancer risk. The nurse underwent training in the regional cancer
genetics centre. Before their appointment, patients are given time to
look into their family history in more detail so that an accurate
pedigree can be drawn up and a risk group assigned. This clinic has the
advantage of providing reassurance and accurate advice within the
environment of a specialist local clinic in an unhurried atmosphere.
Patients at low risk often need as much explanation and advice as
those at higher risk. The selected subgroup of patients at high risk
can be referred to the regional cancer genetics centre, if they wish.
Patients at moderate risk can be advised of appropriate trials of
screening. Referrals can be made by any general practitioner who feels
he or she lacks the wherewithal to advise patients. In addition to
providing specialist advice at a local level this clinic has also
reduced the burden of referrals to the regional cancer genetics
centre. Overall we believe that this provides a better service than a
general practitioner armed with a computer program.
We welcome the development of tools to aid the assessment of
genetic risk in primary care, as reported by Emery et al in their
paper,1 but we do not believe that general practitioners are ideally placed to provide the counselling and reassurance required
for patients at perceived extra risk of developing breast cancer.
Neil Rothnie
Amanda Fowler
Southend Breast Unit, Southend Hospital, Southend SS0 0RY
1.
Emery J, Walton R, Murphy M, Austoker A, Yudkin P, Chapman C, et al.
Computer support for interpreting family histories of breast and ovarian cancer in primary care: comparative study with simulated cases.
BMJ
2000;
321:
28-32. (1 July.)
© BMJ 2000
Israeli students are refusing to perform intimate examinations on anaesthetised women without their informed consent.