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Tag Archives: Access to Palliative Care
Healthcare Pathways For People Living With Dementia: World Alzheimer Report 2016 (Alzheimer’s Disease International)
Summary The World Alzheimer Report 2016, entitled “Improving healthcare for people living with dementia” reviews evidence on aspects of healthcare for people with dementia and suggests how improvements and efficiency savings can be made. The authors are against over-specialization of … Continue reading →
Posted in Acute Hospitals, Alzheimer’s Disease International (ADI), Charitable Bodies, Commissioning, Community Care, Diagnosis, End of Life Care, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Integrated Care, International, Management of Condition, Mental Health, Models of Dementia Care, Non-Pharmacological Treatments, Patient Care Pathway, Person-Centred Care, Quick Insights, Standards, Statistics, Systematic Reviews, UK, Universal Interest
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Tagged 10/66 Dementia Research Group, Access to Palliative Care, ADI’s World Alzheimer Reports, Advance Care Planning (ACP), Ageing Population, Ageing Society, Alzheimer’s Disease International (ADI), Alzheimer’s Disease International’s 10/66 Dementia Research Group, Benefits of Case Management, Better Policies for People with Dementia, Canada, Canadian Centre for Family Medicine Family Health Team (CCFM-FHT) Ontario Memory Clinic, Canadian Comfort Care Booklet, Canadian Comfort Care Principles, Canadian Mild Dementia Knowledge Transfer Toolkit, Care Coordination / Case Management Approaches For People With Dementia Living at Home, Care Coordination and Navigation, Case Management for Dementia, Challenges of Living with Dementia, China, Clinical Practice Guidelines and Care Pathways for People with Dementia Living in the Community (Queensland University of Technology), Community Care, Community Care Services, Community-Based Care, Community-Based Care for People With Dementia, Cost Implications of Dementia Healthcare Pathways, Counter-Factual Service Modelling, Dedicated Care Coordination, Dementia Care in Acute General Hospitals, Dementia Care Pathways, Dementia Healthcare Pathways, Dementia Post-Diagnostic Care and Support, Dementia Research Priorities For Healthcare Sector (WHO Research Prioritization Exercise), Dementia Risk Reduction, Dementia Risk Reduction and Prevention, Dementia: Prevalence and Detection, Early Detection of Alzheimer’s Disease, European Association for Palliative Care White Paper, Global Action Against Dementia, Global Burden of Dementia, Global Context, Global Costs of Dementia, Global Dementia Crisis, Global Dementia Crisis: Adaptations to Services, Global Dementia Crisis: Re-Balancing of Funding For Services, Global Dementia Crisis: Re-Balancing of Services, Global Health, Global Observatory for Ageing and Dementia Care, Global Observatory for Ageing and Dementia Care: King’s College London, Global Outlook, Health Service and Population Research Department: King’s College London, Improving Healthcare For People Living With Dementia: World Alzheimer Report 2016, Improving Outcomes for People Living With Dementia, Indonesia, Integrated and Community-Based Care, Integration of Primary Secondary and Community Care, King’s College London, Living with Dementia, London School of Economics and Political Science (LSE), LSE's Personal Social Services Research Unit (PSSRU), Managing Comorbidity and Complexity, Mexico, Palliative Care, Personal Social Services Research Unit (PSSRU), Personal Social Services Research Unit (PSSRU): London School of Economics and Political Science, Primary Care, Professor Martin Knapp: Director of the Personal Social Services Research Unit at the London School of Economics and Political Science (LSE), PSSRU at London School of Economics and Political Science, Queensland University of Technology Clinical Practice Guidelines and Care Pathways for People with Dementia Living in the Community, South Africa, South Korea, Switzerland, Systematic Reviews and Meta-Analyses, Task-Sharing, Task-Shifting, Typical Duration of Care Inputs Across the Care Pathway, Typical Intensity / Frequency of Care Inputs Across the Care Pathway, World Alzheimer Report 2016, World Health Organization Mental Health Gap Action Programme (mhGAP) Evidence Based Guidelines
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Quality of Death Index: UK End-Of-Life Care Second To None? (BBC News / EIU / NHS England / CQC / National Palliative and End of Life Care Partnership)
Summary A comparative study of palliative care across 80 countries by the Economist Intelligence Unit has declared that end-of-life care in the UK can be ranked the best in the world. The UK was ranked first due to comprehensive national … Continue reading →
Posted in BBC News, Charitable Bodies, Commissioning, CQC: Care Quality Commission, End of Life Care, For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), In the News, Integrated Care, International, Models of Dementia Care, National, NHS, NHS England, Non-Pharmacological Treatments, Patient Care Pathway, Person-Centred Care, Pharmacological Treatments, Quick Insights, Standards, UK, Universal Interest
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Tagged 2015 Quality of Death Index, Access to Palliative Care, Access to Palliative Care Services, Affordability of Care, African Palliative Care Association, Ambitions for Palliative and End of Life Care, Ambitions for Palliative and End of Life Care (2015), Americas, Andrea Sutcliffe: Chief Inspector of Adult Social Care, Argentina, Asia-Pacific, Association for Palliative Medicine, Association of Ambulance Chief Executives, Association of Directors of Adult Social Services, Association of Palliative Care Social Workers, Australia, Austria, Availability of Opioid Painkillers, Bangladesh, BBC Health News, Belgium, Benchmarking, Botswana, Brazil, Bulgaria, Bupa Care Services, Burden of Disease, Canada, Care Quality, Care Quality Commission, Care Quality Commission (CQC), Children’s Palliative Care, Chile, China, College of Health Care Chaplains, Colombia, Community Engagement, Costa Rica, CQC Hospice Inspections, Cross-Country Comparisons, Cuba, Czech Republic, Death Cafés, Death With Dignity Act (DWDA), Definitions of Palliative and End of Life Care, Demand for Palliative Care Indicators, Denmark, Department of Palliative Care at Fudan University Cancer Hospital, Dominican Republic, Dr Ros Taylor MBE: National Director for Hospice Care at Hospice UK, Dying Out of Hospital, Economist Intelligence Unit (EIU), Ecuador, Egypt, End of Life Care in Care Homes, Engagement and Patient Preferences., Ethiopia, Europe, European Association for Palliative Care (EAPC), Finland, France, General Medical Council, Germany, Ghana, Global Atlas of Palliative Care at the End of Life, Government-Led National Palliative Care Strategies, Greece, Guatemala, Health Education England, Hong Kong, Hospice Care, Hospice Care Research Center at Tianjin Medical University, Hospice Care Week (2015), Hospice Care Week: Connecting Care, Hospice Movement, Hospice Palliative Care Association of South Africa, Hospice UK, Hospices, Human Resources, Hungary, India, Indonesia, International Children’s Palliative Care Network, International Health Care Comparisons, International Observatory on End of Life Care at Lancaster University, International Perspectives, Iran, Iraq, Ireland, Israel, Italy, Japan, Jonathan Ellis: Director of Policy and Advocacy at Hospice UK, Jordan, Kazakhstan, Kensington Care Home, Kenya, Latin American Association for Palliative Care, Lien Foundation of Singapore, Lithuania, Macmillan Cancer Support, Malawi, Malaysia, Marie Curie, Mexico, Middle East and Africa, Mongolia, Mongolian Palliative Care Society (MPCS), Morocco, Motor Neurone Disease Association, Myanmar, National Bereavement Alliance, National Care Forum, National Council for Palliative Care, National Palliative and End of Life Care Partnership, National Palliative and End of Life Care Partnership Ambition Five: All staff Prepared to Care, National Palliative and End of Life Care Partnership Ambition Four: Care is Coordinated, National Palliative and End of Life Care Partnership Ambition One: Each Person Seen as an Individual, National Palliative and End of Life Care Partnership Ambition Six: Each Community Prepared to Help, National Palliative and End of Life Care Partnership Ambition Three: Maximising Comfort and Wellbeing, National Palliative and End of Life Care Partnership Ambition Two: Each Person Gets Fair Access to Care, National Palliative Care Nurse Consultants Group, National Voices, Netherlands, New Zealand, NHS England, NHS Improving Quality, Nigeria, Norway, Palliative and End of Life Care, Palliative Care, Palliative Care and the Right to Die, Palliative Care Bill, Palliative Care Demand and Supply, Palliative Care in the UK, Panama, Patients Association, Peru, Philippines, Poland, Portugal, Preferred Place of Death, Public Awareness of Palliative Care, Public Funding for Palliative Care, Public Health England, Puerto Rico, Quality, Quality in the NHS, Quality of Care, Quality of Death Index (EIU), Quality of Death Index Methodology, Romania, Royal College of General Practitioners, Royal College of Nursing, Royal College of Physicians, Russia, Saudi Arabia, Singapore, Slovakia, Social Care Institute for Excellence, South Africa, South Korea, Spain, Specialised Palliative Care Workers, Sri Lanka, Sue Ryder, Sweden, Switzerland, Taiwan, Taiwan’s National Health Insurance (NHI) System, Tanzania, Thailand, Together for Short Lives, Turkey, Uganda, UK End-of-Life Care, Ukraine, Uruguay, US, Venezuela, Vietnam, World Health Assembly (WHA), World Health Organization’s Global Burden of Disease, World Hospice and Palliative Care Day (2015), Worldwide Hospice Palliative Care Alliance (WHPCA), Zambia, Zimbabwe
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OECD’s 2015 Dementia Report (OECD)
Summary The following report appeared before, and preparatory to, the WHO’s First Ministerial Conference on Global Action Against Dementia Conference, and provided an assessment of the Organisation for Economic Co-operation and Development (OECD)’s international position on dementia. The OECD recommended … Continue reading →
Posted in Acute Hospitals, Commissioning, Community Care, Diagnosis, End of Life Care, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Integrated Care, International, Management of Condition, Mental Health, Models of Dementia Care, Non-Pharmacological Treatments, Patient Care Pathway, Person-Centred Care, Quick Insights, Standards, Statistics, Universal Interest
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Tagged Access to Palliative Care, Addressing Dementia: The OECD Response (2015), Ageing Population, Big Data, Burden of Dementia, Collaboration, Collaborative Projects, Confidentiality, Cross-Sector Partnerships, Dementia Diagnosis, Dementia Discovery Fund, Dementia Research, Disease Modifying Treatment by 2025 (Aim), Disease-Modifying Therapies, Disease-Modifying Therapies for Dementia, End-of-Life Care at Home, End-of-Life Care Pathways, End-of-Life Dementia Care Barriers: Access to Palliative Care, End-of-Life Dementia Care Barriers: Discrimination, End-of-Life Dementia Care Barriers: Inappropriate Hospital Admissions, End-of-Life Nursing Services, Ethical Considerations, Ethical Dilemmas, Ethical Issues of Dementia Care, First Global Ministerial Conference on Global Action Against Dementia, First WHO Ministerial Conference on Global Action Against Dementia, G8 Dementia Summit: Global Action Against Dementia, Global Action Against Dementia (GAAD), Global Ministerial Conference on Global Action Against Dementia (WHO), Global Outlook, Leveraging Big Data, OECD Big Data and Sustainability Initiative for Large-Scale Research on Dementia, OECD Health Policy Studies, OECD’s 2015 Dementia Report, Open Data and Big Data, Organisation for Economic Co-operation and Development (OECD), Palliative Care, Patient Confidentiality, Place of Death, Preferred Place of Death, Quality of Care, Quality of Care and Support, Quality of Care for People With Dementia, Reducing Stigma, Research and Development, Research and Innovation, Research Commitment, Supportive and Palliative Care
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Inequalities in Access to Palliative Care in the UK (BBC News / LSE / Marie Curie Cancer Care / International Journal of Palliative Nursing)
Summary Research by the London School of Economics on behalf of Marie Curie Cancer Care suggests that over 100,000 people a year who could benefit from palliative care fail to receive it. Patients sometimes lack suitable pain relief and respite, … Continue reading →
Posted in BBC News, Charitable Bodies, Commissioning, Community Care, End of Life Care, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), In the News, Integrated Care, Management of Condition, National, NHS, Non-Pharmacological Treatments, Northern Ireland, Pain, Patient Care Pathway, Person-Centred Care, Personalisation, Quick Insights, Scotland, Standards, Statistics, UK, Universal Interest, Wales
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Tagged Access to Palliative Care, Ageing Population, Awareness, Awareness Campaigns, Awareness Raising, Barriers: Access to Funding, Barriers: Access to Hospice Care, Barriers: Access to Palliative Care, Barriers: Discrimination, Barriers: Failure to Identify Dementia as a Cause of Death, Barriers: Inappropriate Hospital Admissions, BBC Health News, Black Asian and Minority Ethnic (BAME), Black Asian and Minority Ethnic Communities (UK), Dementia as Cause of Death, End of Life in Dementia-Satisfaction With Care Scale (EOLD-SWC), End-of-Life Care at Home, End-of-Life Care Pathways, End-of-Life Dementia Care Barriers: Access to Palliative Care, End-of-Life Dementia Care Barriers: Discrimination, End-of-Life Dementia Care Barriers: Inappropriate Hospital Admissions, End-of-Life Dementia Care Barriers: Inappropriate Interventions, End-of-Life Dementia Care Barriers: Lack of Recognition of Dementia as a Terminal Condition, End-of-Life Dementia Care Barriers: Lack of Support for Carers, End-of-Life Dementia Care Barriers: Poor Pain Management, End-of-Life Nursing Services, End-of-Life Transitions, EOLD-Comfort Assessment in Dying Scale (EOLD-CAD), Equality & Health Inequalities, Equity in the Provision of Palliative Care in the UK, Ethnic Inequalities, Health Inequalities, Inappropriate Hospital Admissions, Inappropriate Interventions, Inequalities of Health Care, Ireland, London School of Economics and Political Science (LSE), Marie Curie Cancer Care, Marie Curie Nursing Service (MCNS), Marie Curie Nursing Services, National Survey of Bereaved People in England (2013), National University of Ireland, Our Lady’s Hospice (Ireland), Pain Management, Palliative and End of Life Care for Black Asian and Minority Ethnic Groups in UK, Palliative Care, Palliative Care in Dementia (and Dementia Severity), Palliative Care in the UK, Personal Social Services Research Unit (PSSRU), Place of Death, Preferred Place of Death, PSSRU at London School of Economics and Political Science, PSSRU: Personal Social Services Research Unit (LSE), Recognition of Dementia as a Terminal Condition, Reducing Health Inequalities, School of Nursing and Midwifery: University of Ireland, School of Nursing Midwifery and Health Systems: University College Dublin, Specialist Palliative Care, Specialist Palliative Care Teams, Sue Ryder, Supportive and Palliative Care, UK Black Asian and Minority Ethnic Communities, University College Dublin, University of Ireland, VOICES Survey
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End-of-Life Care: Under-Recognition of People With Dementia? (BBC News / Marie Curie Cancer Care)
Summary A report by Marie Curie Cancer Care and the Alzheimer’s Society asserts that dementia sufferers may not always get the quality of care needed, possibly because their condition is not recognised sufficiently (at a societal level and in commissioning … Continue reading →
Posted in Acute Hospitals, Alzheimer's Society, BBC News, Charitable Bodies, Commissioning, Community Care, End of Life Care, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), In the News, Integrated Care, Management of Condition, Models of Dementia Care, National, Patient Care Pathway, Person-Centred Care, Quick Insights, Standards, Statistics, UK, Universal Interest
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Tagged Access to Funding, Access to Palliative Care, Advance Care Planning, Ageing Population, Awareness, Awareness and Understanding, Awareness Campaigns, Awareness Raising, Barriers: Access to Funding, Barriers: Access to Hospice Care, Barriers: Access to Palliative Care, Barriers: Discrimination, Barriers: Failure to Adapt Practice to Reflect the Different Nature of Dementia, Barriers: Failure to Identify Dementia as a Cause of Death, Barriers: Inappropriate Hospital Admissions, Barriers: Inappropriate Interventions, Barriers: Inconsistency in Care Standards in Hospitals, Barriers: Ineffective Advance Care Planning, Barriers: Lack of Continuity of Care, Barriers: Lack of Recognition of Dementia as a Terminal Condition, Barriers: Lack of Support for Carers, Barriers: Lack of Timely and Appropriate Diagnosis, Barriers: Poor Pain Management, BBC Health News, Black Asian and Minority Ethnic (BAME), Black Asian and Minority Ethnic Communities (UK), Care Standards in Hospitals, Carer Support, Cause of Death, Continuing Care, Continuity of Care, Decision Support Tools, Dementia as Cause of Death, Dementia Awareness Training, Dementia Severity, Discrimination, Dying Matters, Dying Matters Coalition, End Stage Dementia, End-of-Life Care Pathways, End-of-Life Dementia Care Barriers: Access to Funding, End-of-Life Dementia Care Barriers: Access to Hospice Care, End-of-Life Dementia Care Barriers: Access to Palliative Care, End-of-Life Dementia Care Barriers: Discrimination, End-of-Life Dementia Care Barriers: Failure to Adapt Practice to Reflect the Different Nature of Dementia, End-of-Life Dementia Care Barriers: Failure to Identify Dementia as a Cause of Death, End-of-Life Dementia Care Barriers: Inappropriate Hospital Admissions, End-of-Life Dementia Care Barriers: Inappropriate Interventions, End-of-Life Dementia Care Barriers: Inconsistency in Care Standards in Hospitals, End-of-Life Dementia Care Barriers: Ineffective Advance Care Planning, End-of-Life Dementia Care Barriers: Lack of Continuity of Care, End-of-Life Dementia Care Barriers: Lack of Recognition of Dementia as a Terminal Condition, End-of-Life Dementia Care Barriers: Lack of Support for Carers, End-of-Life Dementia Care Barriers: Lack of Timely and Appropriate Diagnosis, End-of-Life Dementia Care Barriers: Poor Pain Management, End-of-Life Nursing Services, End-of-Life Transitions, European Association for Palliative Care’s White Paper, Funding of Continuing Care, Hospice Care, Inappropriate Hospital Admissions, Inappropriate Interventions, Kings College London, Local Dementia Prevalence, Marie Curie Cancer Care, Marie Curie’s and Alzheimer’s Society’s Dementia Report, My Life Until the End: Dying Well With Dementia (Alzheimer’s Society), National Audit of Dementia (Care in General Hospitals), National Care of the Dying Audit for Hospitals, National Council for Palliative Care (NCPC), National Dementia Prevalence, NHS Continuing Care, Pain Assessment in Advanced Dementia (PAINAD), Pain Management, PAINAD (Pain Assessment in Advanced Dementia) Tool, Palliative and End of Life Care for Black Asian and Minority Ethnic Groups in UK, Palliative Care, Palliative Care in Dementia (and Dementia Severity), Recognition of Dementia as a Terminal Condition, Recorded Dementia Prevalence, Stigma, Support for Carers, Terminal Illness, Terminal Trajectories Typical of Cancer and Dementia (adapted from (Sachs [et al] 2004), Timely Diagnosis, UK Black Asian and Minority Ethnic Communities
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