May 27, 2010
Source: Health Affairs Journal
Follow this link for abstract
Date of publication: May, 2010
Publication type: Journal
In a nutshell: Patients value the interpersonal aspects of their health care experiences. However, primary care practices may question the value of collecting and acting upon survey data that measure patients’ experiences of care.
Length of publication: 5 pages
Some important notes: Contact library for full text
Leave a Comment » | Consumer needs, Consumer representation, Empowerment, Organisational development, Patient communication, Patient empowerment, Patient Engagement, Patient experience, Uncategorized, Volume 2 Issue 3 | Permalink
Posted by lisanorton
May 27, 2010
Source: HSJ online
Follow this link for fulltext
Date of publication: May, 2010
Publication type: Journal
In a nutshell: The internet is an obvious choice for primary care trusts with lower budgets, aiming to engage with their local population through a popular and inexpensive medium. Research shows more could be done to turn internet use into better health outcomes.
Length of publication: one web page
Some important notes: contact library for full text
Leave a Comment » | Patient choice, Patient empowerment, Patient Engagement, Patient experience, Patient knowledge, Patient views, Uncategorized, Volume 2 Issue 3 | Permalink
Posted by lisanorton
May 27, 2010
Source: Emeraldinsight.com
Follow this link for abstract
Date of publication: April, 2010
Publication type: Journal Article
In a nutshell: Little is known about complaints made by psychiatric patients. The aim of this study is to analyse complaints made by, or behalf of, inpatients at a large independent psychiatric hospital.
Length of publication: 10 pages
Acknowledgement: NHS Evidence Innovation and Improvement Specialist Collection
Leave a Comment » | Patient communication, Patient empowerment, Patient Engagement, Patient experience, Patient participation, Uncategorized, Volume 2 Issue 3 | Permalink
Posted by lisanorton
May 27, 2010
Source: Emeraldinsight.com
Follow this link for fulltext
Publication type: Journal article
In a nutshell: This article uses four case studies to illustrate the contradictory logics shaping the personal empowerment process. Using these logics, an ICT user may play roles as patient, client, consumer, or citizen.
Length of publication: 15 pages
Acknowledgement: NHS Evidence Innovation and Improvement Specialist Collection
Leave a Comment » | Client participation, Consumer representation, Customer care, Empowerment, Patient communication, Patient empowerment, Patient Engagement, Patient knowledge, Patient rights, Patient satisfaction, Patient Service, Patient views, Uncategorized, Volume 2 Issue 3 | Permalink
Posted by lisanorton
March 24, 2010
Source: http://www.patient-experience.com/
Follow this link for introductory statement
Date of publication: February 2010
Publication type: Website
In a nutshell: A new website/forum has been launched. The Patient Experience describes itself as “a set of discussion forums where patients connect, express their views and share valuable experiences on the subjects of medicine and healthcare.”
Length of publication: Website
Leave a Comment » | Patient choice, Patient empowerment, Patient empowerment, Patient Engagement, Patient rights, Patient satisfaction, Press release, Volume 2 Issue 2 | Tagged: Discussion forum, Patient experience, Patient opinion | Permalink
Posted by Emily Hopkins
March 24, 2010
Source: BMA
Follow this link for fulltext
Date of publication: March 2010
Publication type: Press release
In a nutshell: In December, the Department of Health announced that the roll-out of the Summary Care Record would be accelerated, and the BMA has serious concerns that the process is being carried out too quickly. Patients can opt out of having a record created, and the BMA believes they are receiving insufficient information about the choices they can make.
Length of publication: 1 webpage
Leave a Comment » | Customer care, England, Patient advocacy, Patient empowerment, Patient Engagement, Patient rights, Patient satisfaction, Press release, Volume 2 Issue 2 | Tagged: Care records, Data protection, Patient databases, Patient records, Patient rights, SCR, Summary care records | Permalink
Posted by Emily Hopkins
September 4, 2009
Source: High Quality Care for All – Next Stage Review website
Follow this link for full text
Date of publication: August 2009
Publication type: News item
In a nutshell: The High Quality Care for all website reports on 3 new services, which it says will help improve patient experience. Baby Life Check, launched in August, NHS Teen Life Check, aimed at 12-15 year olds, launched in June, and NHS Mid-life LifeCheck, aimed at 45-60 year olds, will be launched by the end of the year. It says these sites are “empowering patients to make good healthcare choices – and keep themselves as healthy as possible.”
Length of publication: Webpage
Some important notes: The websites discussed in the article can be found here: Baby LifeCheck, NHS Teen LifeCheck
Leave a Comment » | News story, Patient advice and liasion services, Patient choice, Patient empowerment, Patient experience, Volume 1 Issue 6 | Tagged: Baby Life Check, Information, Patient choice, Patient empowerment, Patient information, Patient Information Services, Teen Life Check | Permalink
Posted by Emily Hopkins
April 3, 2009
Source: Healthcare Events
Follow this link for full text
Date of publication: 2009 [Date of conference- May 2009]
Publication type: Forthcoming conference
In a nutshell: “Chaired by Graham English Executive Director The NHS Centre for Involvement, this conference provides an important update on the recent changes in patient involvement and empowerment including delivering high quality care for all, involving patients in the delivery of quality indicators and quality accounts, involving the patients and the public in commissioning and working with patients to deliver improvement and redesign through lean thinking”
Length of publication: 1 webpage
Leave a Comment » | Patient empowerment, Press release, Volume 1 Issue 2 | Tagged: Conference, High Quality Care for All, Patient empowerment, Patient Involvement, Quality Indicators, Quality of care | Permalink
Posted by Emily Hopkins
March 12, 2009
Source: NHS Centre for Innovation and Improvement
For fulltext link here
Year of publication:2009
Publication type: Other
In a nutshell: Experienced based design (ebd) is an exciting new way of bringing patients and staff together to share the role of improving care and re-designing services. It is being developed by the NHS Institute for Innovation and Improvement as a way of helping frontline NHS teams make the improvements their patients really want.
Some important notes: This website gives you details of training session introducing you to the toolkit.
Leave a Comment » | News story, Patient empowerment, Volume 1 Issue 1 | Tagged: re-design, toolkit | Permalink
Posted by lucyanderson