A location-based (US) social media and community engagement initiative that aims to improve the patient experience through the collection and sharing of digital content. This cultural data – video, data visualisations, photographs and text – is collected in the waiting room by creating frameworks for sharing that range from anonymous expressions of feeling to deeper storytelling.
The primary aim of the resource is to uncover the needs of underserved patients at a moment when the role of the 'safety net' is being debated both in America and abroad.
Patient Voices digital stories use video, audio, still images and music to convey patients', carers', practitioners' and managers' own stories in a unique way. They are intended to touch the hearts of managers, clinicians and others striving to improve the quality of health and social care. Workshops are increasingly being used to engage with, and evidence outputs from, the Patient and Public Involvement (PPI) and patient engagement agendas, together with being used to provide qualitative evidence of the patient experience.
Project that describes the current status of continuity of healthcare for offenders and identifies areas of best practice; identifies some clear mechanisms for ensuring initial access and continuity of care throughout the health and criminal justice systems; and produces some conjectured hypotheses of the essential elements of effective models of healthcare service delivery for offenders.
This briefing updates a previous systematic review by Cameron and Lart that reported on the factors that promote and hinder joint working between health and social care services. Given their prominence in terms of policy debates about joint and integrated working, the briefing focuses on jointly-organised services for older people and people with mental health problems in the UK only. Briefing published by Social Care Institute for Excellence (SCIE) in May 2012. Review date is May 2015.
Document of the final output of an evaluation of the 16 DH Integrated Care Pilots (ICPs). It provides an account of the evaluation activities conducted, the data collected and the analyses completed.
Based on this it identifies key findings and conclusions about the processes and outcomes seen within the pilots during the evaluation. The evaluation was conducted by a team from RAND Europe and Ernst and Young LLP, with additional statistical analysis provided by the RAND Corporation and The Nuffield Trust.
Report that is primarily concerned with environmental sustainability in health and social care.
A review of how the health care needs of disabled children and young people are met by the commissioners and providers of health care in England.
Paper that surveys the current use of new health technologies and telecare in social care and explores ways to start building a technology-enabled vision for the future of care.
Review which aimed to look at how well the health care needs of people living in care homes were met, based on commissioning and provider behaviours.
The scope for the review set out to consider practice not just in individual care homes, but to focus attention on the rights of people in care homes to access NHS services that met their needs. This included GP services and pathways for continence care, NHS support for care homes to ensure quality of health care through direct provision of district nursing services, and training for care home staff.
People with long-term physical health conditions – the most frequent users of health care services – commonly experience mental health problems such as depression and anxiety, or dementia in the case of older people. As a result of these co-morbid problems, the prognosis for their long-term condition and the quality of life they experience can both deteriorate markedly. In addition, the costs of providing care to this group of people are increased as a result of less effective self-care and other complicating factors related to poor mental health.