Sidelines 14 (3)
Compiled by Steven Duffy, Julie Glanville, Su Golder,
Kate Light, Lisa Mather and Vickie Orton of the Centre for Reviews
and Dissemination, University of York (http://www.york.ac.uk/inst/crd)
Sidelines articles for this issue focus on health
professionals’ and patients’ use of the Internet, developments in
publishing practice and recent research on the impact of health
services research and public health networks.
Dash P, Gowman N, Traynor M. Increasing the
impact of health services research BMJ 2003;237:1339–1341
This describes a report from the Health
Foundation and Nuffield Trust reviewing health services research in
the United Kingdom. The report suggests managers and policy makers
are not able to base decisions about reforming health services on
the best available evidence. Only 2-3% of the health services
research budget is spent on health research. It is unclear how much
of the information generated is used in practical health care
decisions. The article highlights three questions:
-
is research pursuing the right agenda?
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is research examining the right questions in
the right way?
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are the results of research being
communicated to and applied by the people who need them?
Generally the authors found that researchers and managers were
frustrated about the applicability of some health services
research. The recommendations of the report include:
-
establishing a more client centred approach to commissioning
research;
-
enabling users, funders and researchers to assess the value of
different approaches to generating research needed by health
service decision makers;
-
increasing opportunities for cross-sectorial collaboration at
every stage of the research process;
-
looking outside the health and public sectors for sources of
relevant research & information;
-
increasing the development of skills required to analyse, access
and utilise research;
-
presenting research & analysis in user friendly formats;
- developing, at a local level, new roles to
support the implementation of the conclusions of research.
Fahey DK, Carson ER, Cramp DG, Muir Gray JA
2003. User requirements and understanding of public health networks
in England. Journal of Epidemiology and Community Health 57:938-944.
This paper reports on a cross sectional survey
of 60 public health professionals working in England. In-person
interviews, using a mixture of open and closed questions, were
conducted to determine the professionals’ understanding of the term
“public health network” and to explore the functions that they would
like these networks to perform.
The paper introduces public health networks and
then describes in detail the methodology undertaken, from selecting
respondents, to question design and data analysis. A good response
rate of 75 percent was achieved although the sample was biased to
particular regions in England and particular types of organisations.
58 of the 60 respondents had an understanding of the term “public
health networks” and although only 22 of the 60 respondents were
asked if they were in favour of such networks, 82 percent of those
who replied were in favour. The functions that the respondents
would most like to see provided by the public health network were:
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identification of expertise and maximisation
of scarce resources
-
education,
training and CPD
-
information/knowledge management.
The majority of the respondents (93%) were also
in favour of a web site for local and national networks but not
individual sites (23%).
The authors concluded that public health
professionals have a similar, but broader, understanding of “public
health networks” than the government and that the public health
network is more likely to be successful if its priorities are
maximising scarce resources, identification of expertise,
CPD/education and knowledge management. They also suggested that web
sites should be created to provide information on current projects
of the network with a facility to search for people, expertise and
reports.
Jorgensen P.C., and Gotzche P. 2004. Presentation on websites of
possible benefits and harms from screening for breast cancer: cross
sectional study. BMJ 328:148-51.
A recent study showed
that 61% of women make their own decisions regarding mammography, so
the quality of information available to them is of the utmost
importance. The authors of this article assessed 27 websites to see
if the information they provided matched current findings relating
to screening for breast cancer.
The websites were
divided into three categories; those that were provided by
government organisations, those that were provided by advocacy
groups (for example, cancer charities) and those that were provided
by consumer groups. All sites were assessed to see if a balanced
account of benefits and harms were provided and whether the source
of funding appeared to have an impact on the advice given.
The government and
advocacy groups all recommended screening (at least implicitly),
whilst the consumer groups questioned its value.
All of the advocacy
sites accepted industry sponsorship, whilst only one out of the
three consumer sites accepted funding, and all three of the consumer
sites pointed out the risks of accepting industry sponsorship.
Most sites omitted
information on possible harms and emphasised the potential benefits
of screening.
The main potential
harm of breast screening is that of the false positive result. The
level of over diagnosis appears to be about 30%. All of the consumer
sites mentioned the dangers of over diagnosis and over treatment,
but only four of the remaining twenty-four sites did so. Five of the
government or advocacy websites claimed that screening led to fewer
mastectomies, whilst research suggests that the opposite is true.
In conclusion, the authors found that the websites of consumer
groups were more balanced and comprehensive than those of advocacy
groups or government sites. This article suggests that improvements
are required in the level of information given to women about breast
screening; the harms as well as the benefits must be presented.
Delamothe T., and Smith R. 2004. Open
access publishing takes off: the dream is now achievable.
BMJ;328:1-3.
This BMJ editorial discusses recent
advances in the drive towards open access publishing. The aim of
this method of publishing is to make the full text of original
research articles freely available via the World Wide Web.
Rather than the current 'reader pays' system of
journal subscription, medical publishers such as BioMed Central
and the Journal of Clinical Investigation operate an
'author pays' system where authors are charged for an accepted
article to cover the costs of processing the article and for its
electronic distribution.
The main motivation behind this change is the
cost of journal subscriptions, which are increasing far faster than
the underlying rate of inflation. As librarians are forced to cut
back on journal subscriptions to stay within budget, publishers
increase their prices even further to compensate for lost profits.
The result is that medical research, mainly funded by governments,
universities and charities, has been available only at higher and
higher costs to its users.
Open access publishing and an 'author pays'
system offers the research community a way out of this problem, as
publishing on the world wide web is virtually cost free. Any fixed
costs passed on to the research community are lower than the costs
of paying for journal subscriptions under the current system.
The BMJ supports this method of publishing, and
offers suggestions for a long-term sustainable model for open access
publishing.
Benigeri M., and Pluye P. 2003. Shortcomings
of health information on the Internet. Health Promotion
International;18(4):381-6.
Recent studies have
shown that the majority of Internet users use the World Wide Web to
seek health information. When used correctly, with good quality
resources, the Internet can be a valuable tool in the dissemination
of health and medical information from healthcare professionals to
the general public. However, the web has several shortcomings, such
as the quality of health information available on the Internet,
uneven access to the Internet across society, patient difficulties
in finding, using and understanding health information on the
Internet, and the potential for harm and the risk of
over-consumption.
This article
discusses each of these issues. The authors conclude that the
Internet can offer great promise for educated people, who know how
to find and critically assess useful information on the Internet
about self-care and disease prevention. However, for many others,
including the less educated, the elderly and those with multiple
health problems, the Internet will only offer benefits if health
information is designed according to users’ needs and capacities.
Internet access needs to be increased and supported, and health
information needs to be more accurate, relevant and easier to find.
Health care professionals must be integrated into the process of
diffusing medical information on the Internet, for example by
suggesting web sites to patients. Finally, the authors suggest that
the impact of medical information on the Internet should be measured
in order to determine the extent to which the promise held by this
new medium is fulfilled.
Smith J. J., Mallard-Smith R. J., Beattie V., and
Beattie D.K. 2003. Use of information technology in general
practice. Journal of the Royal Society of Medicine 96:395-397.
The use of information technology (IT) by an
increasingly computer-literate population is growing, and with it
are expectations for easily accessible, good quality health
information and advice on the Internet.
This paper presents the results of a
questionnaire survey to assess how the Internet and the NHSNet are
being used in general practice, and what other IT services are being
offered to patients, particularly via practice-based websites. The
questionnaire was sent to 141 randomly chosen general practices in
southern England (London, Buckinghamshire and Hertfordshire). 77
(55%) questionnaires were returned, with 60 practices reporting a
connection to the Internet and 71 to the NHSNet. This data
immediately displays a fundamental misunderstanding of what the
NHSNet provides, as connection to NHS Net automatically allows
access to the Internet. Furthermore, it was found that specific
facilities provided by NHSNet, such as access to patient results and
direct hospital outpatient bookings are being little used. Further
research would be useful to identify why NHSNet is being
underutilised, why there is obvious confusion about what it can
provide, and how these problems can be resolved.
Two further problems were revealed by the
questionnaire. The costs involved in setting up and maintaining a
practice website are usually under-estimated, and there is a problem
of data security on existing websites. None of the practices using
online forms for transmitting patient data had secure connections.
Although the study highlights some of the problems
that might explain the slow uptake of IT in general practice, the
authors do recognise that their findings have to be qualified by the
low response rate to the questionnaire.
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