Last week's
report on the nation's health spelt out clearly how
poorly Britain has done with many public health
measures. The report came as no surprise; it is well-known
that Britain has performed badly with, for example,
immunization, cervical screening, mammography,
preventing coronary-artery disease, and reducing
inequities in health. One key reason for the failure
is probably the absence of a national health policy
on health and of a national policy on health research
to underpin it. A recent World Health Organizations
conference in Tampere, Finland showed how Britain's
lack of nationally-agreed policies on health and
research is causing us to be left behind many other
countries in Europe.
In contrast
to Britain the European regional office of the World
Health Organization does have a clear policy, and in
1985 it published 38 targets for health in the year
2000 (2). Few countries, if any, will achieve all
these targets, but their existence gives countries
the chance to plan coherently. The European Office
soon recognized that countries would need to conduct
research to help get close to these targets: research
to provide new knowledge, to measure whether progress
is being made, and to work out the blocks to progress.
The conference in Tampere was held to publish two
documents on the sort of research that needs to be
done (3,4). Research policy for Health for All
is aimed at policy-makers and suggests how they might
re-orient research programmes (1); Priority Research
for Health for All makes specific suggestions to
researchers on the sort of work that might be done (4).
In a
nutshell the aim is to make the health-research
programmes more relevant to ordinary people and to
those such as doctors who use the results of research.
WHO does not want to knock down traditional medical
research but rather to build up public health
research, research into life-styles and health
promotion; collaborative research among medical
scientists, social scientists, and economists; and
health-services research. In most countries in
Europe, including Britain, medical research is
conducted primarily under the auspices of the
Ministry of Education rather than the Ministry of
Health, which is one of the factors reducing the
relevance of the research. The authors of the books,
which were widely circulated before being finalized,
are also concerned that the consumers of the results
of health research - patients, doctors, nurses and
other health workers - are often widely separated
from the researchers. This not only further reduces
the relevance of the research but also delays the
implementation of the results.
This
diagnosis of the ills of medical research is close to
that reached by the House of Lords Select Committee
on Science and Technology in its report on priorities
in medical research (5), and the clerk of the
committee, Douglas Slater, was in Tampere to talk
about the committee's findings. The committee did not
mention WHO's proposals in its report (although it
had seen them) but advocated a National Health
Service Research Authority to make sure that some of
the problems it identified were tackled. The
government has not yet responded to the report, but
the idea of the special health authority seems to be
a dead duck (6). Perhaps what is needed instead is a
national health-research policy.
As WHO
emphasizes, such a policy would have to be developed
by all those who would be concerned - researchers,
the bodies that fund research, health workers and
health authorities. Ideally, it would grow out of a
national health policy, which should itself be based
on the targets of health for all in the year 2000.
Britain has associated itself with these targets (7),
and [target] number 32 calls for the setting up of a
research policy WHO suggests that the policy should
establish goals; identify priorities, neglected
subjects of research, and manpower and training
needs; allocate resources according to priorities;
and encourage the uptake of research findings.
Experience from Japan suggests that the very process
of drawing up such a policy would stimulate research
(8, 9).
British
doctors reading this might think that it is all
"typical WHO gobbledegook and fantasy", but
the conference heard how Finland, The Netherlands,
Spain, Hungary, Ireland and Yugoslavia have already
been through many of these steps. The Dutch research
policy has just been published (p 816) in English (10),
and Dr. Kimmo Leppo from the National Board of Health
in Finland told the conference how Finland developed
a research policy in the 1970s that made many of the
shifts subsequently recommended by WHO. The
extraordinarily high standard of epidemiology and
public health research in Finland is one practical
result, as may be its infant mortality, which is the
lowest in the world. Britain has also set a high
standard in traditional epidemiology but has done
poorly at translating the results into practice.
There are
more obstacles to establishing such a policy in
Britain than the natural reluctance of the British to
think in abstractions. Firstly, the targets of the
'Health for All' programme are not well known and the
government is doing little to encourage their
dissemination. This is not surprising when the first
target is to reduce inequalities in health by a
quarter; in Britain we are going in the opposite
direction. Secondly, as several speakers at the
conference emphasized, shifts in the pattern of
health research are hard to achieve without extra
money. If funds are going to have to be taken away
from biomedical reserach to fund public health
research then the research establishment - the
Medical Research Council - is going to sabotage the
plans. Thirdly, governments everywhere - and
certainly the British government - are unenthusiastic
about health services research because it illustrates
their failures. They much prefer scientists to
mess around with rat mitochondria.
Finally, a
research policy might be especially difficult to
achieve in Britain because medical research is
effectively being "privatized": industry
and the charities are funding more reserach than the
government (12, 14). But, although this diversity may
make the task of developing a policy more difficult,
it also makes a policy more essential.
1. Smith A,
Jacobson B. eds. The nation's health: a strategy
for the 1990's. London: King Edward's Hospital
Fund.
2. World
Health Organization Regional Office for Europe. Targets
for health for all. Copenhagen: WHO, 1985.
3. World
Health Organization Regional Office for Europe.
Research policy for health for all. Copenhagen:
WHO, 1988.
4. World
Health Organization Regional Office for Europe. Priority
research for health for all. Copenhagen: WHO,
1988.
5. House of
Lords Select Committee on Science and Technology. Priorities
in medical research. London: HMSO, 1988.
6. Anonymous.
Intercalating medical research. Br Med J 1988;
195:1802
7. Delamothe
T. First United Kingdom healthy cities conference.
Liverpool. Br Med J 1988; 296:1117-20.
8. Irvine J,
Martin BR. Foresight in science: picking the
winners. London: Printer, 1984.
9. Smith R. Peering
into the bowels of MRC. Part 1- Setting
priorities. Br Med J 1988; 296:484-8.
10.
Department of Health Policy Development. Health
research policy in The Netherlands. Rijswijk, The
Netherlands; Ministry of Welfare, Health and Cultural
Affairs, 1988.
11. Townsend
P, Davidson N, Whitehead M. Inequalities in health.
Hardmondsworth; Penguin, 1988.
12. Wells N.
Crisis in research. London: Office of Health
Economics, 1986.
13. Smith R.
Is research to be privatized? Br Med J 1988;296:185-8.
14. Smith R.
The funding of medical research; going up or going
down? Br Med J 1988;296:267-70.
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