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James Lind Alliance : ウィキペディア英語版 | James Lind Alliance
Image:JamesLind.jpg|James Lind 1716-1794
The James Lind Alliance is a non-profit making initiative which was established in 2004.〔(The Lancet, Volume 364, Issue 9449, Pages 1923 - 1924, 27 November 2004 )〕 It has been established to bring patients, carers and clinicians together, in Priority Setting Partnerships, to identify and prioritise the unanswered questions about treatments that they agree are most important. This information will help ensure that those who fund health research are aware of what matters to patients, carers and clinicians. Since 1 April 2013, the secretariat of the James Lind Alliance has been hosted by the National Institute for Health Research Evaluation, Trials and Studies Coordinating Centre (NETSCC). This work includes recruiting and training JLA Advisers, coordinating Priority Setting Partnerships, looking after central James Lind Alliance communications and liaising with other parts of the National Institute for Health Research (NIHR). == Background ==
Research on the effects of treatments often overlooks the shared interests of patients and clinicians. As a result, questions they both consider important are not addressed. The pharmaceutical and medical technology industries and academia play essential roles in developing new treatments, but their priorities are not necessarily the same as those of patients and clinicians. For this reason many areas of potentially valuable research are neglected. Bringing patients and clinicians together to prioritise questions in treatment uncertainty is thought to be rare.〔(British Medical Journal 2008;336:903-904 (26 April), ) 〕
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