PATIENT PARTICIPATION IN GENERAL PRACTICE
Transcript of PATIENT PARTICIPATION IN GENERAL PRACTICE
239
psychiatry in a coherent whole. As such it deservesattention and respect. Most of all it requires testingfurther. RACHMAN and PHILLIPS22 have boldlypredicted that "the medical students of the future canbe expected to spend less time studying HENRY GRAYon anatomy and more time reading JEFFREY GRAY onfear." "
PATIENT PARTICIPATION IN GENERAL PRACTICE
ALTHOUGH general practitioners have a reputation forstubborn conservatism, and resisting new ideas as threats totheir independence, there is evidence of a change in theiroutlook. New ideas are appearing more rapidly than everbefore in general practice. One of the most recent and mostradical is the patient participation group-an idea that hasblossomed into a national association and has received the
blessing of the Royal College of General Practitioners, whichhas published a series of essays on the subject.’ The essence ofthe idea is that a group of patients, representative of thepractice as a whole, holds regular meetings with the staff inorder to break down the barriers between doctor and patientor, to quote one of the authors, to "improve the closeness offitat the socio-medical interface". To many practitioners, fewinnovations can ever have seemed so threatening. At worst itsummons up the picture of the practice being taken over by anunholy mixture of the most frequent practice attenders, theunhappily married escaping from home, and a task force fromthe Militant Tendency. Fortunately, it seems it is seldom likethat, but awareness of the fear has led many of thecontributors to write in the firmly reassuring tones ofa parentcoaxing a nervous child into the sea for the first time: bebrave, try it and see, you won’t drown.In fact, there may be a greater danger of patient-
participation groups degenerating into mutual-esteem
meetings, in which practice representation is merelysymbolic; for one of the problems is how a group of twenty tothirty in a practice of ten or twelve thousand patients,whether elected or selected, can genuinely represent those inthe practice who are least articulate and possibly most inneed. This is a familiar problem of democracy, but it has aspecial significance when the purpose of the groups is-tocommunicate in both directions. Patients are able to
influence practice organisation and voice their complaints,but the groups are also seen as a means towards health
education, a stimulus to voluntary care in the community,and a powerful pressure group when the practice petitionsauthority.No-one could quarrel with any attempt to improve
communication between doctor and patient; but some seedeeper philosophical and political purposes in patient-participation groups. At one practice (where a notice in thewaiting area invites patients to inspect their own notes) thereare "weekly workers’ meetings [and] policy is decided at themonthly management collective which is open to all patients,participating as equals with the staff. One author sees thegroup not only as a means of improved communications butalso as having "a role of even deeper significance: it will
actually blur the margins between consumers andproviders".Fine as that sounds, it could be argued that relationships areimproved by clarifying rather than blurring the margins.
22 Rachman S, Phillips C Psychology and medicine. London: Temple Smith, 1975: 158.1 Peter Pritchard, ed. Patient participation in general practice. London- Royal College of
General Practitioners (occasional paper no. 17), 1981. £2.50
Patient participation has aroused the enthusiasm of thosewho have instituted such groups; and some of the enthusiasmis about changed attitudes not easily susceptible to
measurement. But there is an obvious need for evaluation.One wants to know, for instance, whether these groups haveled to real improvements in practice administration andorganisation; more important, it should be possible to
measure whether they have led to tangible benefits in healtheducation and preventive medicine-whether, for examplethey reduce the number of consultations for minor self-limiting conditions but increase the number of requests forcervical smears, screening for hypertension, and routineimmunisation in those socioeconomic groups in which such
requests are traditionally lowest. This would be a stern test,but if patient-participation groups passed it with flyingcolours they would rid themselves of any suspicion of beingno more than a gimmick or passing fashion; instead theymight become an established part of primary care.
AIDS TO VISION
IN Britain nearly three-quarters of the visually disabledpeople are over the age of 65 years, and most of them havemissed out on the technological advances of recent years.’ iAlmost all physiological and psychological research intovision is done on young people, often with normal sight, andmany of the low-vision aids are of little use to the elderly, forwhom poor vision is often not the only handicap. A newW.H.O. booklet, from the Regional Office for Europe,ldiscusses strategies for the visual rehabilitation of poorlysighted people. Inevitably, in seeking to make research anddevelopment recommendations suitable to the manydifferent patterns of health care in Europe, it suffers from toomany generalisations-to say nothing of that stiff and
forbidding prose that often characterises W.H.O.
publications. But it touches interestingly on techniques forenhancing visual stimuli, and on the use of other senses in theretraining of the visual process. It also makes a welcome pleafor more perceptive and sensitive measurement of visualacuity and ability than the customary Snellen and readingcards which depend on static high-contrast black-and-whitealphanumerics. Such conditions rarely exist in everyday life,especially for the ageing eye, and it is time that acuity underconditions of varying contrast was used more often in
assessment, and in the prescription of low-vision aids. Moreresearch is also needed into the phase relationships among thespatial-frequency components of visual targets and how theseare related to different optical and cerebral conditions. In fact,there is a wealth of new knowledge of the physiology andpsychology of vision3 but very little of it has yet been appliedto diseased eyes; the booklet cites some new work from West
Germany on the use of visual information from apparentlytotally "blind" fields after cerebrovascular accidents.As regards changes in services, the main recommendation
is that each visually disabled person should have early accessto a multidisciplinary centre where accurate ophthalmo-logical, optical and psychological assessment may be madeand visual retraining and rehabilitation organised. In thisrespect, as so often before, Scandinavia (especially Norway)seems to have taken a lead. In Britain no-one has even
1. Cullinan TR. Epidemiology of visual disability. Health Service Research Unit reportno 28. University of Kent at Canterbury, 1977.
2. Regional Office For Europe. The use of residual vision by visually disabled persons.Report of a W.H.O meeting. Copenhagen: W.H.O , 1981.
3. The psychology of vision. London: The Royal Society, 1980.