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Sidelines 17 (2)


Julie Glanville, Su Golder, Kate Light, Lindsey Myers and Kath Wright

Centre for Reviews and Dissemination

University of York

Web: http://www.york.ac.uk/inst/crd

 

Jones R B, Pearson J, Cawsey A J, Bental D, Barrett A, White J, White C A, Gilmour W H. Effect of different forms of information produced for cancer patients on their use of the information, social support and anxiety: randomised trial. BMJ. 2006;332:942-6.

 

This trial explored whether patients have different information preferences and coping styles, and whether these factors may influence the way cancer information should be offered. Four hundred patients, mostly suffering from breast or prostate cancer, were randomised to eight groups who received different combinations of information and advice. The information offered was presented as booklets. Four groups received personalised information and the other four received general information. Four groups selected the information they wanted to see and the other four received booklets produced automatically. Half the groups received anxiety management advice and half did not.

 

Three hundred and twenty-five patients were followed-up. They were more likely to view the booklets produced automatically as useful and less likely to see them as too limited. However, the larger size of the automatic booklets was more likely to produce feelings of overload, than those booklets created by the patients themselves. The personalised booklets were more likely to tell patients something new. However, when asked to rate their current understanding of their cancer there was no difference by any of the intervention factors. Patients with personalised information were more likely to show their booklets to another person and more likely to think it helped in discussing their cancer. Compared to the authors’ previous study they found no improvement in patient anxiety from the interventions and patients’ information preferences did not seem to have a strong effect on the impact of the different information formats.

 

The authors suggest that patients do like personalised information and are more likely to show it to others. However, they suggest further research should be conducted to learn how far information sharing affects patients’ social support and anxiety levels.

 

 

Fung V, Ortiz E, Huang J, Foreman B, Miller R, Selby JV, Hsu J. Early experiences with e-health services (1999-2002). Medical Care. 2006;44(5):491-6.

 

While the NHS Choose and Book service is not yet fully operational, some healthcare providers in the USA are already providing electronic health services such as appointment booking, prescription ordering, and medical and prescription drug advice. This study found that the overall level of use of e-health services is still limited although the use of appointment booking and prescription ordering services is increasing at a greater rate than the advice services. To improve quality and efficiency of services the authors suggest that healthcare providers need to target services at specific groups of patients.

 

 

Khatri N. Building IT capability in health-care organizations. Health Services Management Research. 2006;19:73-9.

 

This article provides a US perspective on how health care organisations should develop their IT capabilities to achieve integrated systems and improved business performance. The author uses the “theory of the firm” to argue that the possession of resources, such as IT capability, can give a company competitive advantage over rivals. The IT strategy adopted by healthcare organisations should include the appointment of IT professionals at a senior level within the organisation to emphasize the importance of IT to the organisation, the development of internal skills as opposed to reliance upon external expertise and the integration of IT with the organisation’s main activities.

 

 

Skinner, B. Web alert: opening up access to journal articles online. Quality in Primary Care. 2006;4:55-8.

 

Many obstacles exist when trying to access the full text of journal articles online, not least dramatic increases in subscription rates that may result in the cancelling of titles by library services. This article suggests a solution to this problem, open access publishing, which provides free access to journal articles.

 

In open access publishing neither the publisher nor the author have rights over the creation and distribution of copies of an article. This is because the author pays the publisher to peer-review the article, pays for typesetting and proofreading, and contributes to the maintenance of the publisher’s website. Therefore, as long as the author is credited, open access journals can be read, downloaded, copied and distributed without constraint.

 

The author describes in detail four open access resources:

 

 

Publishers have made a number of arguments against open access publishing, including the affordability of publishing for authors, but this pro-open access publishing paper outlines the main benefits.

 

 

Purham, K. The nation’s data? The UK census – guaranteed confidentiality but only limited information. Evidence & Policy. 2006;2:227-48.

 

This article explores some of the failings of census data in the UK. It covers aspects such as response rates, the relevance of the questions and access to the data.

 

The author begins by reflecting on the surprisingly low response rate (especially among particular groups) despite the compulsory nature of the census in the UK. They then discuss the lack of relevance of certain questions to current policy decisions. For example, they cite the absence of explicit questions on housing condition, income and disability. The currency of the census data is also seen as a problem. This is not only a result of the frequency of the census (every ten years) but also of the slow release of data. The use of anonymisation techniques (in order to retain confidentiality of the data) leads to limited detail and even to inaccuracies in the published (as opposed to the collected) data.

 

Although this article mostly discusses the limitations of the census the author does recognise the improvements in data access as availability is increased though publication on the internet and in CD format and summary reports. A range of methods to improve data capture will be tested in 2007 for possible implementation in the 2011 census. The author discusses how other government surveys could be used to improve population data. Although there has been a growth in the collection of population data in the private sector which, in theory, could be used instead of census data, the quality of private sector information is often poorer than census information.

 

The author concludes that despite its limitations the census is one of the most robust data sources available and is a key resource for policy makers. However, there is a need to make the data more relevant and usable.

 

This is a long, detailed and interesting article on a vital statistical resource.

 

 

Hare C, Davies C, Sheperd M. Safer medicine administration through the use of e-learning. Nursing Times. 2006;102(16):25-2.

 

Patient safety is of paramount importance and much has been published on this issue. This paper reports on one aspect of patient safety, the correct administration of medicines by nurses. The authors carried out a survey in an NHS Hospital Trust and uncovered significant shortcomings in the level of knowledge and awareness of nursing staff with regard to safe medication practice.

 

In response to the results of this survey the authors then went on to set up a formal education and assessment process for nurses at the trust via an e-learning package. The paper presents the results from 34 nurses who completed the package. Most of the nurses found the package easy to use and said they would use the system again. The authors conclude that the tool is a significant asset for improving ‘standards of care’.

 

Although interesting this article would have benefited from further evaluation of the e-learning package to demonstrate how its use could lead to improvements in practice and the standards of care.

 

 

Jacobson N, Goering P. Credibility and credibility work in knowledge transfer. Evidence & Policy. 2006;2(2):151-65.

 

This article examines the different factors that affect the success of knowledge transfer (the communication of information and its subsequent implementation).

 

The authors start with a brief review of the literature on credibility theory, ranging from Aristotle to the present day. This section provides a succinct background of the theory of credibility and is followed by qualitative case studies that illustrate the importance of credibility and how it can be achieved.

 

All the studies were conducted at the Health Systems Research and Consulting Unit (HSRCU) in Toronto, Canada. In three separate projects, consultants were employed to give advice on various management issues. For example, one consultant was asked to suggest the best way to utilise psychiatric beds at an in-patient facility. Extensive interviews were conducted with the consultants and their clients, to capture their experiences of the knowledge transfer process and to try to establish the factors that influenced whether recommendations were implemented.

 

The authors conclude that credibility was “a key factor in successful knowledge transfer”. They suggest that credibility has four dimensions. Scientific credibility relates to the perceived accuracy of the data upon which the recommendations are based. Secondly, expertise refers to the knowledge, experience and skills held by the communicator. The third factor is the authority of the communicator. This includes not only their status within the organisation and their professional credentials, but the way they present themselves. Finally, a neutral stance (indicating a lack of bias) enhances credibility.

 

This article is based on case studies of management consultants and the authors warn that the results may not be generalisable, but the theories they suggest do seem likely to be applicable to information workers.

 

There are two messages in this article that seem particularly important. The first is the danger of the loss of credibility. A project or person can start out with a high level of credibility but, once lost, this can be very hard to regain. Therefore anyone involved in knowledge transfer needs to assess their level of credibility at each stage of the project. Secondly, in order to ensure the implementation of recommendations the information needs to be not just credible, but also accurate, practical and useful.

   

 

Back to Inform 17 (2)

 

This page was last updated on: 21 November 2006


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