September 3, 2015
Source: NHS Improving Quality
Follow this link for the full-text report
Date of publication: August 2015
Publication type: Case study
In a nutshell: In September 2012, Marie Curie employed a keyworker at its Cardiff and the Vale hospice to work with people in local Black, Asian and Minority Ethnic communities to improve awareness of palliative care and to increase access.
Length of publication: 3 pages
Leave a Comment » | Contents, Hospice Care, Innovations, Marie Curie, Pain Management, Palliative Care, Patient Centred Care, Publication type, Report, Terminal Care, Terminal Illness, United Kingdom, Volume 7 Issue 8-9, Wales | Tagged: Access to Health Services, Access to Support, Black and minority ethnic, End of Life Care, Marie Curie, Palliative Care, Service Provision, Wales | Permalink
Posted by hmedley99
July 9, 2015
Source: International Journal of Palliative Nursing 2015 v.21(5) p236-44
Follow this link for the article abstract
Date of publication: May 2015
Publication type: Article
In a nutshell: The Department of Health in the UK suggests that hostel staff are the most appropriate key workers for their dying homeless residents and that hospital based palliative care maybe the best way forward. However, little is known about the views of hostel staff with regard to this. The article findings clearly lend support to the suggestion that hostel workers probably are indeed the most appropriate people to support a dying homeless person. However, enhanced collaborative working, access to accurate and up-to-date medical information and clearer lines of communication between health professionals and hostel workers could result in better outcomes for this population in terms of having a voice that is heard, being offered choices regarding care options, and being treated with the same dignity and respect that the rest of the population has come to expect at the end of life
Length of publication: 9 pages
Some important notes: This article is available in full text to all NHS Staff using Athens, for more information about accessing full text follow this link to find your local NHS Library
Leave a Comment » | Article, Contents, Health services research, Palliative Care, Patient Centred Care, Professionalism, Publication type, Staff Training, Terminal Care, Terminal Illness, United Kingdom, Volume 7 Issue 7 | Tagged: End of Life Care, Homelessness, Hostel Staff, Service Provision | Permalink
Posted by hmedley99
May 6, 2015
Source: Marie Curie 2015
Follow this link for the webpage
Date of publication: April 2015
Publication type: News
In a nutshell: Significant investment in the Marie Curie Rapid Response Service in Northern Ireland has led to more people being able to access the service and helped reduce hospital admissions.
Length of publication: 1 page
Leave a Comment » | Commissioning, Contents, Marie Curie, News Story, Northern Ireland, Patient Centred Care, Publication type, Terminal Illness, United Kingdom, Volume 7 Issue 5, Website | Tagged: Northern Ireland, Rapid Response Service, Reduced Hospital Admissions, Service Provision | Permalink
Posted by hmedley99
April 10, 2015
Source: House of Commons Health Committee
Follow this link for the full report
Date of publication: March 2015
Publication type: Parliamentary report
In a nutshell: This report looks at the state of End of Life Care since the Independent Review of the Liverpool Care Pathway. This report makes a number of recommendations for improvement.
Length of publication: 54p.
Leave a Comment » | Contents, Death, Dementia, Health services research, Hospice Care, Pain Management, Palliative Care, Patient Centred Care, Patient Choice, Professionalism, Publication type, Report, Research, Staff Training, Terminal Care, Terminal Care Hospitals, Terminal Illness, United Kingdom, Volume 7 Issue 4 | Tagged: Access, Advance Care Planning, Bereavement Support, Commissioning, Dementia, End of Life Care, Equality, Leadership, Outcome Measures, Quality of Care, Research, Service Improvement, Service Provision, Social Care, Staff Education, Staff Training, Staffing | Permalink
Posted by hmedley99
April 10, 2015
Source: Personal Social Services Research Unit
Follow this link for the full report
Date of publication: April 2015
Publication type: Report
In a nutshell: Personal Social Services Research Unit London School of Economics and Political Science (LSE) was commissioned by Marie Curie to explore the evidence on equity in palliative care and to consider the economic implications of extending palliative care to those currently under-served.
Length of publication: 148p.
Leave a Comment » | Contents, Death, Health services research, Hospice Care, Palliative Care, Patient Centred Care, Patient Choice, Publication type, Report, Research, Terminal Care, Terminal Illness, United Kingdom, Volume 7 Issue 4 | Tagged: End of Life Care, Equity, Palliative Care, Service Provision | Permalink
Posted by hmedley99
March 11, 2015
Source: National Council for Palliative Care; National Voices
Follow this link for the full document
Date of publication: March 2015
Publication type: Narrative document
In a nutshell: Every Moment Counts: a narrative for person centred coordinated care for people near the end of life sets out how good, coordinated – or integrated – care looks to people near the end of life and is written from their point of view.
Length of publication: 26 pages
Leave a Comment » | Contents, Hospice Care, Pain Management, Palliative Care, Patient Centred Care, Patient Choice, Reform, Terminal Care, Volume 7 Issue 3 | Tagged: Care Coordination, End of Life Care, Integrated Care, Patient Centred Care, Patient Choice, Service Provision | Permalink
Posted by hmedley99
December 11, 2014
Source: Marie Curie Cancer Care and Alzheimer’s Society
Follow this link for the report
Date of publication: December 2014
Publication type: Report
In a nutshell: A new report from Marie Curie and Alzheimer’s Society today reveals the barriers that prevent people with dementia from accessing high-quality care at the end of life in England
Living and Dying with Dementia – Barriers to Care addresses the often overlooked final stage of dementia – a progressive, terminal illness. It highlights that dementia is often not recognised as a terminal diagnosis, which can lead to poor access to care, inconsistent quality of care and inadequate pain management.
Length of publication: 24p.
Leave a Comment » | Contents, Dementia, England, Hospice Care, Marie Curie, Palliative Care, Patient Centred Care, Patient Choice, Publication type, Report, Terminal Care, United Kingdom, Volume 6 Issue 12 | Tagged: Alzheimer's Disease, Barriers to Care, Dementia, Marie Curie, Pain Management, Quality of Care, Service Provision | Permalink
Posted by hmedley99
October 20, 2014
Source: ehospice.com
Follow this link for the webpage
Date of publication: October 2014
Publication type: Web article
In a nutshell: Sue Ryder has launched a new campaign to draw attention to the national lack of comprehensive 24/7 expert support services for people who are dying and their loved ones that care for them. According to research by Sue Ryder, only 8% of clinical commissioning groups in England provide comprehensive 24/7 expert emotional support, practical advice and coordination for the dying, their carers and families. This lack of provision leaves people scared, alone and desperate for help – without anywhere immediate and appropriate to turn to outside of 9-5 working hours.
Length of publication: 1 page
Leave a Comment » | Commissioning, Contents, Palliative Care, Patient Centred Care, Patient Choice, Terminal Care, Volume 6 Issue 11 | Tagged: End of Life Care, Out-of-Hours, Palliative Care, Service Provision, Sue Ryder Care | Permalink
Posted by hmedley99
May 6, 2014
Source: Marie Curie Cancer Care
Follow this link for the full report
Date of publication: April 2014
Publication type: Report
In a nutshell: Each individual will have personal wishes about where they wish to be cared for and where they wish to die. They will also have many non-healthcare needs which impact on their well-being just as much as their healthcare does. In a new report, Listening to Dying People in Wales, Marie Curie Cancer Care looks at the methods currently in place for gathering experience feedback from terminally ill people and their families and carers. The report argues that if current services are to do the best for dying people in Wales they must find out about people’s experiences of the care they received at the end of their lives. Only then will those that plan and deliver services be able to make informed decisions based upon people’s needs.
Length of publication: 14 pages
Leave a Comment » | Change, Commissioning, Contents, Death, Pain Management, Palliative Care, Patient Centred Care, Patient Choice, Publication type, Reform, Terminal Care, Terminal Illness, Volume 6 Issue 4/5, Wales | Tagged: Carers, End of Life Care, Families, Feedback, Patient Choice, Patients, Service Provision, Wales | Permalink
Posted by hmedley99
May 6, 2014
Source: Marie Curie Cancer Care
Follow this link for the full report
Date of publication: April 2014
Publication type: Report
In a nutshell: This paper reports on the findings of a Real Time Reporting pilot project developed by the National End of Life Care Programme (now part of the NHS Improving Quality), Marie Curie Cancer Care and Help the Hospices working in partnership. The aim of the project was to find more effective ways to collect, analyse and present data on the experience of people receiving care in their last year of life, as a basis for service improvement.
Length of publication: 30 pages
Leave a Comment » | Change, Commissioning, Contents, Hospice Care, Innovations, Marie Curie, Palliative Care, Patient Centred Care, Patient Choice, Publication type, Report, Terminal Care, Volume 6 Issue 4/5 | Tagged: Data Analysis, Data Collection, End of Life Care, Feedback, Patient Experience, Real Time Reporting, Service Delivery, Service Improvement, Service Provision | Permalink
Posted by hmedley99
July 1, 2013
Source: Journal of Palliative Medicine
Follow this link for the abstract
Date of publication: Online ahead of print: 8 June 2013
Publication type: Article
In a nutshell: The purpose of this study was to determine whether high symptom burden decreases following Home-Based Primary and Palliative Care (HBPC) enrollment. The article concludes that in a chronically ill population of urban home-bound, patient symptoms can be successfully managed in the home. The authors recommend future work should continue to explore symptom assessment and management over time for the chronically ill home-bound.
Some important notes: Please contact your local NHS Library for the full text of the article. Follow this link to find your local NHS Library.
Leave a Comment » | Article, Contents, Health services research, Pain Management, Palliative Care, Patient Centred Care, Publication type, Terminal Care, Volume 5 Issue 7 | Tagged: Domiciliary Palliative Care, Home Care, Palliative Care, Service Provision, Symptom Management | Permalink
Posted by hmedley99
July 1, 2013
Source: Marie Curie
Follow this link for the full report
Date of publication: June 2013
Publication type: Report
In a nutshell: This Public Health England commissioned report highlights the growing need to make end of life care more accessible and appropriate for minority ethnic groups. It highlights that the end of life care needs of BAME communities are varied, growing, and despite examples of good practice, overall not adequately met. It recommends that service providers and commissioners recognise the growing need for improved end of life care for BAME communities and that they learn from examples of best practice, some of which are highlighted in the report.
Length of publication: 79p.
Leave a Comment » | Commissioning, Contents, Health services research, Palliative Care, Patient Centred Care, Publication type, Report, Terminal Care, United Kingdom, Volume 5 Issue 7 | Tagged: Aslan, Black and minority ethnic, Commissioning, Enf of Life Care, Palliative Care, Service Provision | Permalink
Posted by hmedley99
May 22, 2013
Source: Help the Hospices Commission
Follow this link for the report
Date of publication:April 2013
Publication type: Report
In a nutshell: This report considers how hospices need to develop over the next three to five years to be prepared for the challenges facing them in the future, challenges including building new partnerships and developing stronger business acumen to working more closely with care home and doing more to value carers.
Length of publication: 57p
Leave a Comment » | Change, Commissioning, Death, Hospice Care, Organisational change, Organisational development, Palliative Care, Patient Centred Care, Patient Choice, Publication type, Reform, Reorganisation, Report, Strategic change, Terminal Illness, United Kingdom, Volume 5 Number 6 | Tagged: Carers. Telehealth, Commissioning, Hospice, Hospice Care, Partnerships, Service Provision | Permalink
Posted by hmedley99
April 4, 2013
Source: Marie Curie
Follow this link for the report
Date of publication: February 2013
Publication type: Report
In a nutshell: Death and Dying brings together data previously published elsewhere, much of which is available via the Marie Curie End of Life Care Atlas. The Atlas has been developed to help Clinical Commissioning Groups (CCGs) and others identify gaps and differences of experiences across all end of life care services. It enables commissioners to see how their area compares, to address unmet needs and improve care for all.
Length of publication: 4 pages
Acknowledgement: We need to refocus end of life care as a health priority by Dr Phil McCarvill
Leave a Comment » | Commissioning, Death, Hospice Care, Marie Curie, Pain Management, Palliative Care, Patient Centred Care, Patient Choice, Publication type, Report, Terminal Care, Terminal Illness, United Kingdom, Volume 5 Issue 4 | Tagged: Commissioning, End of Life Care, Marie Curie, Patient Centred Care, Service Provision | Permalink
Posted by hmedley99