- BMJ Editorial: Caldicott 2 and Patient Data
- "Patient Safety, Law Policy and Practice" Published in Paperback
- UCL Joins the European Connected Health Alliance
- UCL CHIME is Early Contributor to New Health Informatics Online Resource
- Professor Dipak Kalra takes up Presidency of the EuroRec Institute
- 2012 European Summit on Trustworthy Reuse of Health Data – plenary sessions now available on YouTube
- "Patient Safety, Law Policy and Practice"
- Ethnicity and academic performance in medicine
- Uptake of flu vaccine among healthcare workers
- Open Source, Open Standards, and Health Care Information Systems
- howRU, a new short generic measure of health status
- Dr Don E. Detmer honoured by American Medical Informatics Association (AMIA)
- Public 'reassured' by swine flu media coverage
- Key NHS IT Programmes – UCL report
- UKHIT online - Computers and the Internet
- Group membership and staff turnover affect outcomes in group CBT for persistent pain
- Electronic patient records are not a panacea
- Using computerised CBT to prevent mental health problems: a systematic review and a case study of Xanthis
- New Students Begin UCL Postgraduate Programme in Health Informatics
- CHIME researcher contributes to new book
Key NHS IT Programmes – UCL report
28 June 2010
With a new Government reviewing Connecting for Health (CfH) and health
IT policy more generally, a major evaluation of the Summary Care Record
and HealthSpace, two key systems that CfH is charged to deliver, comes
at the right time.
But the conclusions do not offer any easy answers, as
the report's title, "The devil's in the detail" (full text available
here <https://www.ucl.ac.uk/news/scriefullreport.pdf>; executive summary
available here <https://www.ucl.ac.uk/news/scriesummary.pdf>), makes clear. The project, which has also produced this accompanying BMJ paper
<http://www.bmj.com/cgi/content/full/340/jun16_4/c3111>, was led by
Prof. Trish Greenhalgh, who recently moved from UCL to Queen Mary,
University of London. Co-authors include CHIME's Henry Potts and Emma
Byrne, plus former CHIME member, Katja Stramer.
The study found that progress in the programmes was delayed by several 'wicked' (pervasive and seemingly insoluble) problems, including the difficulty of defining a 'minimal dataset' of key medical data, ensuring that GP records were complete and accurate and the need for informed consent from 50 million people (many of whom appeared to throw away the information letter unread). Thus, benefits to date had been much more moderate than initial hope or rhetoric.
But more than that, the research found that, while many stakeholders shared a broad vision for a national electronic record system, making this vision a reality required collaboration across very different worlds: political, clinical, technical, commercial and personal.
CHIME researcher, Dr Henry Potts said that he hoped the lessons learned from the English experience would be taken on board in the US as they begin to look at electronic records and that the "baby wasn't thrown out with the bath water" in England. "There are benefits to be realised here and just because it’s more difficult than was expected doesn’t mean it isn’t worth doing."
Contact: Henry Potts
Links: UCL News story