This document outlines the process for establishing a palliative care program. It begins with initial discussions to start the program and identify needs, including patients, funding, resources, and personnel. Meetings are then held with various stakeholders to plan awareness activities, select service areas, and train volunteers. Data is gathered from observation visits to other programs. Finally, the process concludes with analyzing the data, implementing the program, and opening a new home care unit for palliative care patients.
Outlines the Irish Hospice Foundations Nurses for Night Care Programme and how the service supports people dying at home with illnesses other than cancer
The document outlines the dementia and palliative care programmes of the Irish Health Foundation (IHF) from 2013 to 2016. The programmes aimed to:
1) Prioritize palliative care for people with dementia in all care settings and support more people to die at home.
2) Improve end of life care in residential care settings for older people, with a focus on those with dementia.
3) Increase public awareness of death and dying, and encourage more people including those with dementia to engage in early advance planning.
This document discusses supporting people with dementia to die at home in Ireland. It identifies key factors that enable home death, including availability of family/friend care, decision making between the person and family, and access to GP and homecare supports. While home death remains rare for those with dementia, the document recommends increased palliative care, support for home care, and nationally recognized tools to plan for end of life care needs.
The document discusses dementia care in communities. It notes that communities will need to support more older adults as populations age. Positive attitudes, improved elderly care systems, pension and medical insurance, and cultivating independence are important. Maximizing community support for people living with dementia involves raising awareness, providing education and activities, and family support. Creating dementia-friendly communities integrates these principles and builds understanding of dementia through initiatives like Dementia Friends. Future directions include timely diagnosis, partnerships to promote care, and establishing dementia-friendly communities.
Age Alliances Wales_LTC Consensus Meeting 10-Nov-2015angewatkins
PRIME Centre Wales
Long Term Conditions Consensus Meeting
Tuesday 10th November 2015, St Mary's Priory, Abergavenny, NP7 5ND
http://www.primecentre.wales/ltc-consensus-meeting.php
This document outlines the process for establishing a palliative care program. It begins with initial discussions to start the program and identify needs, including patients, funding, resources, and personnel. Meetings are then held with various stakeholders to plan awareness activities, select service areas, and train volunteers. Data is gathered from observation visits to other programs. Finally, the process concludes with analyzing the data, implementing the program, and opening a new home care unit for palliative care patients.
Outlines the Irish Hospice Foundations Nurses for Night Care Programme and how the service supports people dying at home with illnesses other than cancer
The document outlines the dementia and palliative care programmes of the Irish Health Foundation (IHF) from 2013 to 2016. The programmes aimed to:
1) Prioritize palliative care for people with dementia in all care settings and support more people to die at home.
2) Improve end of life care in residential care settings for older people, with a focus on those with dementia.
3) Increase public awareness of death and dying, and encourage more people including those with dementia to engage in early advance planning.
This document discusses supporting people with dementia to die at home in Ireland. It identifies key factors that enable home death, including availability of family/friend care, decision making between the person and family, and access to GP and homecare supports. While home death remains rare for those with dementia, the document recommends increased palliative care, support for home care, and nationally recognized tools to plan for end of life care needs.
The document discusses dementia care in communities. It notes that communities will need to support more older adults as populations age. Positive attitudes, improved elderly care systems, pension and medical insurance, and cultivating independence are important. Maximizing community support for people living with dementia involves raising awareness, providing education and activities, and family support. Creating dementia-friendly communities integrates these principles and builds understanding of dementia through initiatives like Dementia Friends. Future directions include timely diagnosis, partnerships to promote care, and establishing dementia-friendly communities.
Age Alliances Wales_LTC Consensus Meeting 10-Nov-2015angewatkins
PRIME Centre Wales
Long Term Conditions Consensus Meeting
Tuesday 10th November 2015, St Mary's Priory, Abergavenny, NP7 5ND
http://www.primecentre.wales/ltc-consensus-meeting.php
Dementia board 21 june 12 pathfinder presentationJim Moore
The document summarizes a presentation by the Derby Local Involvement Network (LINk) about a Dementia Pathfinder project. The project aims to test how local Healthwatch organizations can influence commissioning across dementia patient care pathways and present compelling findings to decision makers. It discusses the framework used, research findings on information provision, formal and informal care for dementia patients, funding challenges, and lessons learned from developing partnerships and communication frameworks. It notes the pathfinder report will be presented on June 15th and findings will be shared with local Healthwatch organizations.
This document discusses global efforts to address dementia and presents strategies for improving dementia care. It notes that most of the burden of dementia is in low and middle income countries and outlines a public health approach. This includes integrating dementia care into primary care, task-shifting to train non-specialists, and addressing barriers to access. It also reviews evidence for approaches like the WHO ICOPE model and discusses challenges in high-income countries like increasing diagnostic rates and controlling costs while maintaining quality. Overall it advocates for implementing evidence-based packages of dementia care globally using scalable, affordable, home-based models.
Presentation of findings of an audit carried out on the nurses for night care service over a 6 month period that identifies the components of care that support people with dementia to die at home in Ireland
The document provides an overview of the Irish Hospice Foundation's Changing Minds project which aims to improve end-of-life care for people with dementia through three key outcomes: prioritizing palliative care, improving end-of-life care in residential settings, and increasing public awareness and advance care planning. The project involves developing resources for staff, families, and people with dementia, providing education and training, and supporting service development initiatives including grants and improving support for home deaths. The goal is to enhance care quality and dignity at the end of life for people with dementia.
Global research into Alzheimer's and dementia is needed to address the growing global crisis of these diseases. Alzheimer's Research UK works to increase awareness of dementia as brain diseases, fund scientific research around the world, and translate scientific findings into new treatments through partnerships like the Dementia Consortium and Drug Discovery Alliance. The UK government has also made a Challenge on Dementia 2020 to accelerate progress toward prevention, diagnosis, research and care.
The Irish Hospice Foundation has developed a series of guidance documents on dementia palliative care to help healthcare professionals provide better end-of-life care for people with dementia. The documents address key issues like communication, advance care planning, managing loss and grief, hydration and nutrition, pain assessment, ethical decision making, and medication management. They were created based on a review of the literature and input from an expert advisory group. Each document provides background, considerations for good practice, guidance, and resources. The goal is to improve recognition and management of palliative care needs in people with dementia.
The document summarizes the objectives and key findings of the Dementia Palliare project, a European project aimed at improving care for people with advanced dementia. The project sought to 1) understand best practices for advanced dementia care and family support and 2) develop interprofessional education to equip the workforce. Literature reviews found advanced dementia is under-recognized and palliative care tends to focus on end of life rather than ongoing support. Case studies from 7 countries showed quality of care is influenced by continuity of care planning, dementia-friendly environments, skilled practitioners, comfort-focused care, social engagement, and family support. The project developed resources including a best practices statement, online community of practice, and education modules to strengthen advanced dementia care capabilities.
Adrian Edwards - PRIME Social Care Consensus Meeting 20151005angewatkins
This document summarizes the PRIME Centre Wales, which aims to improve health and well-being in Wales through high-quality research and influencing policy. The Center will take a multi-disciplinary approach and focus on research areas like long-term conditions, patient-centered care, infections, screening and prevention, and emergency care. It will work with patients and public groups, social care services, industry partners, and other research groups in Wales. The leadership team is led by Professor Adrian Edwards of Cardiff University and includes representatives from Bangor, Swansea, and the University of South Wales.
Dan Venables_LTC Consensus Meeting 10-Nov-2015angewatkins
PRIME Centre Wales
Long Term Conditions Consensus Meeting
Tuesday 10th November 2015, St Mary's Priory, Abergavenny, NP7 5ND
http://www.primecentre.wales/ltc-consensus-meeting.php
Marie Lynch gave a presentation on the Irish Hospice Foundation's Changing Minds projects which aim to improve end of life care for people with dementia. The projects have three main outcomes: prioritizing palliative care for dementia in all care settings, improving end of life care in residential care facilities, and increasing public awareness of advance care planning. To achieve these, the projects provide resources for staff, families, and people with dementia, education through seminars and training, service development grants, and strategic engagement with partners. The resources, education, and engagement help enhance communication about end of life wishes and provide a framework to support people with dementia living well and dying at home or in residential care.
Dementia: Quality of Care 2015 - Amy Dalrymple presentationAlexis May
The document discusses diagnosis and post-diagnostic support for dementia in Scotland. It notes that only 42% of people are diagnosed at the early, mild stage, and outlines Scotland's national strategy to promote earlier diagnosis and ensure all those diagnosed receive 12 months of coordinated, post-diagnostic support from a named link worker. This support is guided by a five pillar model and aims to provide holistic, person-centered care that upholds the personhood of those living with dementia and recognizes the unique experiences of caregivers.
Facilitating Discussions on Future and End of Life Care With People who have ...Irish Hospice Foundation
Workshop presentation on Irish Hospice Foundation Dementia guidance document 1 "Facilitating Discussions on Future and end of life care with a person with dementia"
Dementia: Quality of Care - Lorraine Burgess presentationAlexis May
This document discusses caring for people with both cancer and dementia. It notes that the prevalence of both diseases is rising as the population ages. People with both conditions present unique challenges for clinical care. The document also presents a case study of a woman named Mary admitted to the hospital with lymphoma and dementia, and how a person-centered approach to her care improved her quality of life and outcomes. It emphasizes the importance of communication, recognizing each patient's individual needs and personhood, and supporting patients and caregivers.
This document summarizes a report on addressing equality issues for groups with protected characteristics experiencing dementia in Scotland. It finds that diagnosis and care pathways must be modified to meet varied needs. Key recommendations include continuing efforts to raise culturally-sensitive awareness of dementia, ensuring clear support services, providing workforce training on individualized care, and further research on improving awareness and data collection for underserved groups.
The document discusses Alzheimer Scotland's Advanced Dementia Practice Model for understanding and transforming care for people with advanced dementia and at end of life. It aims to take a bio-psychosocial approach by bringing together the expertise of dementia care practitioners and palliative care specialists. The model facilitates a planned and coordinated approach using both the 8 Pillars Model of Community Support and an Advanced Dementia Specialist Team to provide high quality, person-centered care.
Ukrc may 2016 conversations about end of life[1]Susan Willis
This document discusses conversations about end of life and provides an example of an educational tool used to promote such conversations. It covers historical attitudes toward death, current drivers in the field, barriers to discussing end of life, and key themes in end of life conversations including preparing for death, cultural and spiritual issues, and bereavement. The educational program aimed to engage participants in conversations about death and dying through sharing perspectives and experiences. Participants found it an emotional but rewarding experience that improved their end of life care practices and communication skills.
This document outlines a project to enhance the contributions of allied health professionals (AHPs) in supporting people with dementia in Scotland from 2017-2020. It identifies 11 AHP roles and discusses 4 ambitions to improve access to AHP services, partnership/integration, a skilled AHP workforce, and innovation/research. Key activities include promoting a home-based memory rehabilitation program nationwide and establishing national communication networks between AHP dementia leads across 12 areas based on evidence from Dumfries & Galloway. Videos from the program show improved experiences for those with dementia and their caregivers. The document provides tips for improvement work, emphasizing listening to understand, the power of relationships, starting small, measurement, preparing to fail, and patience
This document summarizes a workshop on addressing the palliative and end-of-life care needs of people with dementia in hospitals. The workshop covered challenges in caring for people with dementia, communication strategies, recognizing dementia as a life-limiting illness, assessing pain and symptoms, the role of multidisciplinary teams, and available resources from the Irish Hospice Foundation. The presentation emphasized taking a person-centered approach, advance care planning, continuity of care, and the importance of staff training to meet the complex needs of people with dementia at the end of life.
This document summarizes a presentation about end of life care for people with dementia. It discusses what people with dementia say about end of life care, including challenges around communication and acknowledging loss. It also examines the palliative care needs of people with dementia, noting issues around symptoms, care transitions and multidisciplinary support. Further, it outlines how incorporating a palliative approach into routine dementia care can help with advance care planning, loss and grief, and staff education. Finally, it analyzes how supporting people with dementia to die at home requires individualized care, future planning, symptom management and access to family and community support services.
Dementia board 21 june 12 pathfinder presentationJim Moore
The document summarizes a presentation by the Derby Local Involvement Network (LINk) about a Dementia Pathfinder project. The project aims to test how local Healthwatch organizations can influence commissioning across dementia patient care pathways and present compelling findings to decision makers. It discusses the framework used, research findings on information provision, formal and informal care for dementia patients, funding challenges, and lessons learned from developing partnerships and communication frameworks. It notes the pathfinder report will be presented on June 15th and findings will be shared with local Healthwatch organizations.
This document discusses global efforts to address dementia and presents strategies for improving dementia care. It notes that most of the burden of dementia is in low and middle income countries and outlines a public health approach. This includes integrating dementia care into primary care, task-shifting to train non-specialists, and addressing barriers to access. It also reviews evidence for approaches like the WHO ICOPE model and discusses challenges in high-income countries like increasing diagnostic rates and controlling costs while maintaining quality. Overall it advocates for implementing evidence-based packages of dementia care globally using scalable, affordable, home-based models.
Presentation of findings of an audit carried out on the nurses for night care service over a 6 month period that identifies the components of care that support people with dementia to die at home in Ireland
The document provides an overview of the Irish Hospice Foundation's Changing Minds project which aims to improve end-of-life care for people with dementia through three key outcomes: prioritizing palliative care, improving end-of-life care in residential settings, and increasing public awareness and advance care planning. The project involves developing resources for staff, families, and people with dementia, providing education and training, and supporting service development initiatives including grants and improving support for home deaths. The goal is to enhance care quality and dignity at the end of life for people with dementia.
Global research into Alzheimer's and dementia is needed to address the growing global crisis of these diseases. Alzheimer's Research UK works to increase awareness of dementia as brain diseases, fund scientific research around the world, and translate scientific findings into new treatments through partnerships like the Dementia Consortium and Drug Discovery Alliance. The UK government has also made a Challenge on Dementia 2020 to accelerate progress toward prevention, diagnosis, research and care.
The Irish Hospice Foundation has developed a series of guidance documents on dementia palliative care to help healthcare professionals provide better end-of-life care for people with dementia. The documents address key issues like communication, advance care planning, managing loss and grief, hydration and nutrition, pain assessment, ethical decision making, and medication management. They were created based on a review of the literature and input from an expert advisory group. Each document provides background, considerations for good practice, guidance, and resources. The goal is to improve recognition and management of palliative care needs in people with dementia.
The document summarizes the objectives and key findings of the Dementia Palliare project, a European project aimed at improving care for people with advanced dementia. The project sought to 1) understand best practices for advanced dementia care and family support and 2) develop interprofessional education to equip the workforce. Literature reviews found advanced dementia is under-recognized and palliative care tends to focus on end of life rather than ongoing support. Case studies from 7 countries showed quality of care is influenced by continuity of care planning, dementia-friendly environments, skilled practitioners, comfort-focused care, social engagement, and family support. The project developed resources including a best practices statement, online community of practice, and education modules to strengthen advanced dementia care capabilities.
Adrian Edwards - PRIME Social Care Consensus Meeting 20151005angewatkins
This document summarizes the PRIME Centre Wales, which aims to improve health and well-being in Wales through high-quality research and influencing policy. The Center will take a multi-disciplinary approach and focus on research areas like long-term conditions, patient-centered care, infections, screening and prevention, and emergency care. It will work with patients and public groups, social care services, industry partners, and other research groups in Wales. The leadership team is led by Professor Adrian Edwards of Cardiff University and includes representatives from Bangor, Swansea, and the University of South Wales.
Dan Venables_LTC Consensus Meeting 10-Nov-2015angewatkins
PRIME Centre Wales
Long Term Conditions Consensus Meeting
Tuesday 10th November 2015, St Mary's Priory, Abergavenny, NP7 5ND
http://www.primecentre.wales/ltc-consensus-meeting.php
Marie Lynch gave a presentation on the Irish Hospice Foundation's Changing Minds projects which aim to improve end of life care for people with dementia. The projects have three main outcomes: prioritizing palliative care for dementia in all care settings, improving end of life care in residential care facilities, and increasing public awareness of advance care planning. To achieve these, the projects provide resources for staff, families, and people with dementia, education through seminars and training, service development grants, and strategic engagement with partners. The resources, education, and engagement help enhance communication about end of life wishes and provide a framework to support people with dementia living well and dying at home or in residential care.
Dementia: Quality of Care 2015 - Amy Dalrymple presentationAlexis May
The document discusses diagnosis and post-diagnostic support for dementia in Scotland. It notes that only 42% of people are diagnosed at the early, mild stage, and outlines Scotland's national strategy to promote earlier diagnosis and ensure all those diagnosed receive 12 months of coordinated, post-diagnostic support from a named link worker. This support is guided by a five pillar model and aims to provide holistic, person-centered care that upholds the personhood of those living with dementia and recognizes the unique experiences of caregivers.
Facilitating Discussions on Future and End of Life Care With People who have ...Irish Hospice Foundation
Workshop presentation on Irish Hospice Foundation Dementia guidance document 1 "Facilitating Discussions on Future and end of life care with a person with dementia"
Dementia: Quality of Care - Lorraine Burgess presentationAlexis May
This document discusses caring for people with both cancer and dementia. It notes that the prevalence of both diseases is rising as the population ages. People with both conditions present unique challenges for clinical care. The document also presents a case study of a woman named Mary admitted to the hospital with lymphoma and dementia, and how a person-centered approach to her care improved her quality of life and outcomes. It emphasizes the importance of communication, recognizing each patient's individual needs and personhood, and supporting patients and caregivers.
This document summarizes a report on addressing equality issues for groups with protected characteristics experiencing dementia in Scotland. It finds that diagnosis and care pathways must be modified to meet varied needs. Key recommendations include continuing efforts to raise culturally-sensitive awareness of dementia, ensuring clear support services, providing workforce training on individualized care, and further research on improving awareness and data collection for underserved groups.
The document discusses Alzheimer Scotland's Advanced Dementia Practice Model for understanding and transforming care for people with advanced dementia and at end of life. It aims to take a bio-psychosocial approach by bringing together the expertise of dementia care practitioners and palliative care specialists. The model facilitates a planned and coordinated approach using both the 8 Pillars Model of Community Support and an Advanced Dementia Specialist Team to provide high quality, person-centered care.
Ukrc may 2016 conversations about end of life[1]Susan Willis
This document discusses conversations about end of life and provides an example of an educational tool used to promote such conversations. It covers historical attitudes toward death, current drivers in the field, barriers to discussing end of life, and key themes in end of life conversations including preparing for death, cultural and spiritual issues, and bereavement. The educational program aimed to engage participants in conversations about death and dying through sharing perspectives and experiences. Participants found it an emotional but rewarding experience that improved their end of life care practices and communication skills.
This document outlines a project to enhance the contributions of allied health professionals (AHPs) in supporting people with dementia in Scotland from 2017-2020. It identifies 11 AHP roles and discusses 4 ambitions to improve access to AHP services, partnership/integration, a skilled AHP workforce, and innovation/research. Key activities include promoting a home-based memory rehabilitation program nationwide and establishing national communication networks between AHP dementia leads across 12 areas based on evidence from Dumfries & Galloway. Videos from the program show improved experiences for those with dementia and their caregivers. The document provides tips for improvement work, emphasizing listening to understand, the power of relationships, starting small, measurement, preparing to fail, and patience
This document summarizes a workshop on addressing the palliative and end-of-life care needs of people with dementia in hospitals. The workshop covered challenges in caring for people with dementia, communication strategies, recognizing dementia as a life-limiting illness, assessing pain and symptoms, the role of multidisciplinary teams, and available resources from the Irish Hospice Foundation. The presentation emphasized taking a person-centered approach, advance care planning, continuity of care, and the importance of staff training to meet the complex needs of people with dementia at the end of life.
This document summarizes a presentation about end of life care for people with dementia. It discusses what people with dementia say about end of life care, including challenges around communication and acknowledging loss. It also examines the palliative care needs of people with dementia, noting issues around symptoms, care transitions and multidisciplinary support. Further, it outlines how incorporating a palliative approach into routine dementia care can help with advance care planning, loss and grief, and staff education. Finally, it analyzes how supporting people with dementia to die at home requires individualized care, future planning, symptom management and access to family and community support services.
The document outlines the dementia and palliative care programmes of the Irish Health Foundation (IHF) from 2013 to 2016. The programmes aimed to:
1) Prioritize palliative care for people with dementia in all care settings and support more people to die at home.
2) Improve end of life care in residential care settings for older people, with a focus on those with dementia.
3) Increase public awareness of death and dying, and encourage more people including those with dementia to engage in early advance planning.
Nathan Goldstein-Palliative care making the case jewishhome
Palliative care aims to improve quality of life for patients with serious illnesses and their families. Nathan Goldstein argues that hospital-based palliative care is growing in the US for four key reasons: 1) It improves clinical quality by better managing pain and symptoms. 2) It better aligns with patient and family preferences for comfort and honest discussions. 3) It is well-suited to address the growing population of older adults with multiple chronic conditions. 4) It can reduce costs by facilitating decisions to leave the hospital or withhold treatments not achieving patient goals.
23 September 2010 - National End of Life Care Programme
This guide is principally for professionals working in health and social care and allied professions. Its main aim is to provide links to information sources, resources and good practice in end of life care (EoLC) for people with dementia, particularly for those who work with people with dementia who are not EoLC experts and EoLC experts who are not particularly knowledgeable about dementia.
While the document is not principally written for patients and carers, some of the information will be relevant to them.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
All the major religions and belief systems in the UK support the principles of organ donation and transplantation and accept that organ donation is an individual choice.
We understand that you may have questions about whether your faith or beliefs affect your ability to become an organ donor. We're here to help support your decision, and have provided a selection of resources to help make sure you get the information you need.
Find out more about different attitudes to organ donation by selecting a faith or belief system below, or alternatively please consult the adviser from your religion or belief group.
Dementia innovation maggie stobbart-rowlands presentation - open forum eventsAlexis May
This document discusses end of life care for people with dementia. It provides information on the Gold Standards Framework (GSF) training program for caring for people with dementia at the end of life. The GSF uses a holistic approach focusing on clinical knowledge, care coordination, and compassionate care. The training program aims to improve person-centered care, advance care planning, and reduce inappropriate hospital admissions at the end of life. Evaluation found the program increased staff knowledge and led to decreased hospitalization and crisis admissions for nursing home residents with dementia.
Mental illness and homelessness mar13.pptSuharnoUsman1
The document summarizes the relationship between homelessness, mental illness, and addiction. It discusses how deinstitutionalization of psychiatric facilities and a lack of affordable housing and income support have contributed to higher rates of homelessness among those with mental health and substance use issues. The document also reviews approaches to prevent homelessness following psychiatric treatment, including providing housing assistance and financial supports. Finally, it discusses the unique challenges of homeless youth and the importance of understanding their needs and goals through research.
Cheshire and Wirral Best Practice event - 8 NovemberInnovation Agency
The document outlines plans for developing integrated care communities across South Cheshire and Vale Royal. Key points include:
- The formation of 5 care community teams to provide coordinated, patient-centered care across the region.
- Initial priority projects include developing the care community teams, improving GP out-of-hours care, and musculoskeletal physiotherapy.
- Achievements so far include aligning staff to the 5 communities, implementing rapid response services, and beginning multidisciplinary team meetings.
- Future goals involve strengthening primary care partnerships, expanding social care support, and using data to better manage patient risk levels.
This document summarizes the key findings of a thesis presentation on healthcare challenges for older people at the end of life. The presentation found that older people living at home are more likely to be transferred in the last months of life compared to those in residential homes. Palliative care is increasing in long-term care settings but stagnating elsewhere. Communication between patients, doctors, and family is often insufficient, especially for those with dementia. Care in long-term care facilities is one of the most expensive types of end-of-life care. Recommendations include investing in home care, improving communication especially regarding dementia, and involving palliative care earlier.
PYA Principal Kent Bottles, MD, who is also Chief Medical Officer of PYA Analytics, presented before healthcare information technology (IT) professionals at the Summit of the Southeast—Driving the Future of Technology held at Nashville Music City Center, September 16-17, 2014. Dr. Bottles’ presentation covered population health.
This document discusses challenges faced by seniors in the Canadian healthcare system when being discharged from the hospital. It aims to raise awareness of issues like Alternate Level of Care (ALC) where patients no longer require acute care but face obstacles to leaving the hospital. It also discusses the "Home First" philosophy of supporting patients to transition home with high levels of home care rather than waiting in the hospital. Resources provided cover topics like hospital discharge planning, shaping attitudes towards seniors, and the role of communication in navigating patient choices and power dynamics during discharge.
This document discusses meningitis sequelae, follow-up care, and challenges in assessing outcomes in low-income countries. Key points include:
1) Meningitis can cause long-term neurodisability in 20% of survivors, including cognitive, sensory, and behavioral impairments. Follow-up care is limited in low-income settings.
2) Evaluating neurodevelopmental outcomes is challenging due to a lack of standardized assessment tools adapted for different cultures and limited rehabilitation services.
3) Joseph's story illustrates the lack of follow-up care available, leading to severe disabilities not addressed for years. Improving recognition, services, and community acceptance is needed.
Patricia Leahy Warren, Senior Lecturer School of Nursing and Midwifery, UCCInvestnet
The document summarizes the key challenges at the interface between primary and secondary healthcare in Ireland. It notes the changing demographic profiles of an aging population and increasing rates of chronic conditions. There are also challenges around communication and integration between primary care teams and specialist services due to incompatible IT systems and a lack of standardized documentation. The document calls for innovations to further develop integrated care centered around the needs of the individual and focused on preventative measures and community-based support over hospital-based care.
A care home 'is' someone's home, one day it could be yours too … best practice in end of life care in care homes. Presentation from Eleanor Sherwen, Elaine Owen and Caroline Flynn from England's National End of Life Care Programme as part of the Department of Health's QIPP end of life care workstream seminar series at Healthcare Innovation Expo 2011
Deirdre Shanagher and Sarah Cronin presented at an MS Ireland Information Day on challenges of end of life care for progressive neurological patients. They discussed the Irish Hospice Foundation's vision of ensuring all receive end of life support and care. Group work identified needs of neurological patients like long illnesses, recognizing end stages, and complex care. Issues in care discussions included sensitivity, access to palliative services, and timing conversations. Identifying and responding to care needs means providing information, support, and awareness to prompt conversations.
1) The document discusses challenges in end-of-life care including an aging population with complex medical needs, lack of advance care planning, and misalignment between patient values and treatment.
2) It presents the case of Jim, a 72-year-old man in the ICU following a serious car accident, and the difficulties determining his care preferences without an advance directive.
3) Key themes are the importance of communication about patient values and goals, aligning care with those preferences, and promoting advance care planning so treatment reflects what matters most to individuals.
The goal of this webinar was to educate healthcare professionals about the differences between palliative and curative care while exploring the history and philosophy of the hospice movement.
Similar to Supporting people with dementia to die at home in Ireland (20)
Reflections on the National Summary of Patient Activity Data for Adult Specia...Irish Hospice Foundation
The document summarizes key findings from a report analyzing patient activity data for specialist palliative care services in Ireland from 2012-2015. It finds that while access to palliative care has improved, more resources are still needed to meet increasing demand. Over half of new inpatient admissions came from home, showing the role of inpatient units in supporting patient preferences and hospitals. Significant improvements were seen in community palliative care access and wait times. However, disparities remain in access between cancer and non-cancer patients, and by region. Updated staffing guidelines are also needed to guide service provision and support changing places of care.
Explores palliative and end of life care. Outlines advance care planning and provides information about planning ahead to include using advance healthcare directives
Reflections on the National Summary of Patient Activity Data for Adult Specia...Irish Hospice Foundation
IHF reflections on MDS data in relation to specialist palliative care services. Reflections offered on SPC beds, access to SPC services. This presentation highlights inequities that exist.
This document discusses advance healthcare directives (AHDs) in Ireland. It notes that only 6% of people in Ireland have written an AHD. It defines AHDs as documents where a person can write down medical treatments they do not want if they lose decision-making capacity. For an AHD to be legally binding, the person must have had capacity when writing it and it must apply to their current medical situation. The document outlines the requirements for making a valid AHD in Ireland and implications for healthcare professionals, including that they have no liability for complying with a valid AHD or not complying if there are doubts about its validity.
This document provides an overview and updates from a meeting of the HFH Acute Hospital Network. It discusses the HFH programme which supports end of life care in hospitals. It outlines the staff and structure of the HFH programme. It provides an update on activities including outreach, oversight with the HSE, and a feasibility study on enhancing bereavement care in Ireland. It discusses identifying priorities around developing standards, services mapping, and advocacy. The next steps include presenting findings at a bereavement care forum.
This document discusses plans to improve end of life care in Ireland. It notes that a business case for funding is being drafted for submission in 2019 and will be presented to Liam Woods on June 26th. It also mentions that there were over 800 deaths in emergency departments in 2016, and that collaboration between the Health Service Executive and Healthcare for the Future aims to enhance end of life care, learning from practices in England where most admissions in the last year of life are emergencies. An update will be provided to Liam Woods and plans include reducing variability and a business case for end of life care coordinators.
This document discusses end-of-life care (EOLC) in hospitals in Ireland. It outlines the aims of the Healthcare for the Future (HFH) Programme which are to develop standards for EOLC, increase capacity for these standards, and change the culture around dying, death and bereavement. It notes feedback from an outreach officer's visits to 12 hospitals which found varying levels of EOLC implementation and engagement. Examples of positive EOLC developments and ongoing challenges are provided. The document calls for establishing a collective vision and strategy to continue improving EOLC and measuring progress.
Final Journey’s is a staff development workshop for Acute Hospital Staff which raises awareness regarding quality of care at end of life.
Final Journeys was developed by the Irish Hospice Foundation as part of its Hospice Friendly Hospitals programme in 2010.
The workshop is now eight years old and is due for updating and review to ensure the content of the workshop is relevant and fresh.
Stephen Toft - Programme Officer Palliative Care, HSE Primary Care Division, specialist palliative care minimum data set acute hospital figures 2016 and 2017 per hospital.
This document discusses patient involvement in developing information leaflets. It defines patient involvement as enabling people to be actively involved in issues concerning them and decisions affecting their lives. Involving patients demonstrates their unique perspectives, values their expertise, and empowers them. It also ensures resources are relevant and improves relationships, efficiency, and public perception of services. Challenges include difficulties with the concept, perceived criticism, resources, and data protection. The document describes how one organization previously involved patients through workshops and reviews, and how it plans to continue through coalitions.
Karen Charnley: Patient engagement - encourage and provide service user, carer and community engagement within the context of AIIHPC's work and the work of the wider palliative care community on the island of Ireland. Will inform and influence palliative care education, research, policy and practice, in a collaborative and supportive manner.
Emer Carroll, National Health & Safety Manager, National Health and Safety Function, Workplace Health and Wellbeing Unit, presents on HSE Workplace Stress Management.
The document outlines grants provided by the Healthcare Foundation in Ireland (HFH) to various hospitals in Ireland to support end of life care initiatives. It describes several projects funded by HFH including education workshops, bereavement support groups, customized handover bags for families, awareness events, a calming lamp, and study days. It also lists additional end of life care projects, resources, and improvements implemented by hospitals, such as family viewing rooms, bereavement packs, end of life symbol drapes, and participation in national audits.
This document discusses the work of the HSE-HfH Joint Oversight Group. It provides updates on:
- The inaugural and subsequent meetings of the oversight group in 2017.
- Key themes discussed including patient experience, linkages with clinical programs, education/training, and reducing variability in end-of-life care.
- The working relationships between the oversight group and hospital groups/CEOs.
- Demographic trends showing Ireland's aging population and the importance of supporting end-of-life care through initiatives like the HfH program.
The Mater Misericordiae University Hospital and St. James’s Hospital and their academic partners UCD and TCD surveyed bereaved relatives about their experience of end-of-life care in hospital. Results reveal the high standard of care provided in both hospitals and further indicate where improvements could be made to enhance the care experience.
Dr. Hanna Linane - Disturbing and Distressing - The Tasks and Dilemmas Associ...Irish Hospice Foundation
Determines the frequency with which SHOs deal with tasks and dilemmas associated with end-of-life care and evaluates the impact of patient death on their psychological well-being.
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VEDANTA AIR AMBULANCE SERVICES IN REWA AT A COST-EFFECTIVE PRICE.pdfVedanta A
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The cyclothymia test is a pivotal tool in the diagnostic process. It helps clinicians assess the presence and severity of symptoms associated with cyclothymia.
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NURSING MANAGEMENT OF PATIENT WITH EMPHYSEMA .PPTblessyjannu21
Prepared by Prof. BLESSY THOMAS, VICE PRINCIPAL, FNCON, SPN.
Emphysema is a disease condition of respiratory system.
Emphysema is an abnormal permanent enlargement of the air spaces distal to terminal bronchioles, accompanied by destruction of their walls and without obvious fibrosis.
Emphysema of lung is defined as hyper inflation of the lung ais spaces due to obstruction of non respiratory bronchioles as due to loss of elasticity of alveoli.
It is a type of chronic obstructive
pulmonary disease.
It is a progressive disease of lungs.
The story of Dr. Ranjit Jagtap's daughters is more than a tale of inherited responsibility; it's a narrative of passion, innovation, and unwavering commitment to a cause greater than oneself. In Poulami and Aditi Jagtap, we see the beautiful continuum of a father's dream and the limitless potential of compassion-driven healthcare.
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The Ultimate Guide in Setting Up Market Research System in Health-TechGokul Rangarajan
How to effectively start market research in the health tech industry by defining objectives, crafting problem statements, selecting methods, identifying data collection sources, and setting clear timelines. This guide covers all the preliminary steps needed to lay a strong foundation for your research.
"Market Research it too text-booky, I am in the market for a decade, I am living research book" this is what the founder I met on the event claimed, few of my colleagues rolled their eyes. Its true that one cannot over look the real life experience, but one cannot out beat structured gold mine of market research.
Many 0 to 1 startup founders often overlook market research, but this critical step can make or break a venture, especially in health tech.
But Why do they skip it?
Limited resources—time, money, and manpower—are common culprits.
"In fact, a survey by CB Insights found that 42% of startups fail due to no market need, which is like building a spaceship to Mars only to realise you forgot the fuel."
Sudharsan Srinivasan
Operational Partner Pitchworks VC Studio
Overconfidence in their product’s success leads founders to assume it will naturally find its market, especially in health tech where patient needs, entire system issues and regulatory requirements are as complex as trying to perform brain surgery with a butter knife. Additionally, the pressure to launch quickly and the belief in their own intuition further contribute to this oversight. Yet, thorough market research in health tech could be the key to transforming a startup's vision into a life-saving reality, instead of a medical mishap waiting to happen.
Example of Market Research working
Innovaccer, founded by Abhinav Shashank in 2014, focuses on improving healthcare delivery through data-driven insights and interoperability solutions. Before launching their platform, Innovaccer conducted extensive market research to understand the challenges faced by healthcare organizations and the potential for innovation in healthcare IT.
Identifying Pain Points: Innovaccer surveyed healthcare providers to understand their difficulties with data integration, care coordination, and patient engagement. They found widespread frustration with siloed systems and inefficient workflows.
Competitive Analysis: Analyzed competitors offering similar solutions in healthcare analytics and interoperability. Identified gaps in comprehensive data aggregation, real-time analytics, and actionable insights.
Regulatory Compliance: Ensured their platform complied with HIPAA and other healthcare data privacy regulations. This compliance was crucial to gaining trust from healthcare providers wary of data security issues.
Customer Validation: Conducted pilot programs with several healthcare organizations to validate the platform's effectiveness in improving care outcomes and operational efficiency. Gathered feedback to refine features and user interface.
Basics of Electrocardiogram
CONTENTS
●Conduction System of the Heart
●What is ECG or EKG?
●ECG Leads
●Normal waves of ECG.
●Dimensions of ECG.
● Abnormalities of ECG
CONDUCTION SYSTEM OF THE HEART
ECG:
●ECG is a graphic record of the electrical activity of the heart.
●Electrical activity precedes the mechanical activity of the heart.
●Electrical activity has two phases:
Depolarization- contraction of muscle
Repolarization- relaxation of muscle
ECG Leads:
●6 Chest leads
●6 Limb leads
1. Bipolar Limb Leads:
Lead 1- Between right arm(-ve) and left arm(+ve)
Lead 2- Between right arm(-ve) and left leg(+ve)
Lead 3- Between left arm(-ve)
and left leg(+ve)
2. Augmented unipolar Limb Leads:
AvR- Right arm
AvL- Left arm
AvF- Left leg
3.Chest Leads:
V1 : Over 4th intercostal
space near right sternal margin
V2: Over 4th intercostal space near left sternal margin
V3:In between V2 and V4
V4:Over left 5th intercostal space on the mid
clavicular line
V5:Over left 5th intercostal space on the anterior
axillary line
V6:Over left 5th intercostal space on the mid
axillary line.
Normal ECG:
Waves of ECG:
P Wave
•P Wave is a positive wave and the first wave in ECG.
•It is also called as atrial complex.
Cause: Atrial depolarisation
Duration: 0.1 sec
QRS Complex:
•QRS’ complex is also called the initial ventricular complex.
•‘Q’ wave is a small negative wave. It is continued as the tall ‘R’ wave, which is a positive wave.
‘R’ wave is followed by a small negative wave, the ‘S’ wave.
Cause:Ventricular depolarization and atrial repolarization
Duration: 0.08- 0.10 sec
T Wave:
•‘T’ wave is the final ventricular complex and is a positive wave.
Cause:Ventricular repolarization Duration: 0.2 sec
Intervals and Segments of ECG:
P-R Interval:
•‘P-R’ interval is the interval
between the onset of ‘P’wave and onset of ‘Q’ wave.
•‘P-R’ interval cause atrial depolarization and conduction of impulses through AV node.
Duration:0.18 (0.12 to 0.2) sec
Q-T Interval:
•‘Q-T’ interval is the interval between the onset of ‘Q’
wave and the end of ‘T’ wave.
•‘Q-T’ interval indicates the ventricular depolarization
and ventricular repolarization,
i.e. it signifies the
electrical activity in ventricles.
Duration:0.4-0.42sec
S-T Segment:
•‘S-T’ segment is the time interval between the end of ‘S’ wave and the onset of ‘T’ wave.
Duration: 0.08 sec
R-R Interval:
•‘R-R’ interval is the time interval between two consecutive ‘R’ waves.
•It signifies the duration of one cardiac cycle.
Duration: 0.8 sec
Dimension of ECG:
How to find heart rhytm of the heart?
Regular rhytm:
Irregular rhytm:
More than or less than 4
How to find heart rate using ECG?
If heart Rhytm is Regular :
Heart rate =
300/No.of large b/w 2 QRS complex
= 300/4
=75 beats/mins
How to find heart rate using ECG?
If heart Rhytm is irregular:
Heart rate = 10×No.of QRS complex in 6 sec 5large box = 1sec
5×6=30
10×7 = 70 Beats/min
Abnormalities of ECG:
Cardiac Arrythmias:
1.Tachycardia
Heart Rate more than 100 beats/min
Supporting people with dementia to die at home in Ireland
1. Marie Lynch, Head of Healthcare
Programmes
Sarah Cronin, Dementia Development Officer
Deirdre Shanagher, Development Officer
Supporting people
with dementia to
die at home
2. “ While a good death at home may not
be feasible or desirable for everyone,
it could undoubtedly be a reality for
many more people if we nurture the
services to support it”
NHS 2012
3. Supporting people with dementia to die at
home
Dementia
Referrals
2015
14% (n=118)
Total No
Referrals
2015
86%
(n=742)
Dementia referrals versus total no of
referrals 2015
5. Presentation Today
Where do people with
Dementia die?
What are the factors that
support people with dementia
to die at home?
What would help to enable
more people with dementia
die at home?
6. Where do people with Dementia
die?
• Home deaths remain rare for people with dementia across Europe
with rates varying from 3.3% in Wales to 16.4% in Belgium (Houttekier et al
2010)
• Less than 5% of dementia patients died in home (Public Health England 2014)
• People with dementia are 4 times more likely to die in residential care
(Murtagh et al 2012)
• 2 in 5 people with dementia die in hospital (Sleeman et al 2014)
7. What are the factors that support people with
dementia to die at home?
Personal and Demographic Factors
• Carers
• Gender
• Age
• Marital Status
• Level of Education
• Presence of Advance Care Plan
• Socioeconomic Status
Disease-related factors
• Diagnosis
• Co-morbidities
• Symptom management
• Pain
Environmental factors
• Urban vs rural location
• Availability of local services and supports – GP, OOH,
SPCT
• Hospital and residential care beds
• Access to equipment
• Formal supports
References at end of presentation
8. What are the factors that support people
with dementia to die at home?
Audit on Dementia Referrals
Supplementary information gathered on 52 referrals of people with a
diagnosis of dementia who were referred to the NNC service:
• Demographics – gender, age, address, living situation, length of time living with
dementia, co-morbidities, presence of an ACP
• Length of time involved with SPCT
• Reason for referral
• Supports – informal and formal
• Care in the home provided by family versus homecare packages/ other formal
supports
What are the key components of care which enable a person
with dementia to die at home in Ireland?
9. What are the factors that
support people with dementia to
die at home?
12. What would help to enable more people with
dementia
die at home?
“ Where someone with dementia dies should
be led by their needs, what is known of their
wishes and the needs of the people caring for
them” (Kane, 2012)
13. What would help to enable more people with
dementia
die at home?
15. References
• Weafer, J (2014). Irish attitudes to death, dying and bereavement 2004-2014. Dublin: Irish Hospice
Foundation.
• Murtagh, F.E.M, Bausewein, C., Petkova, H, Sleeman, K.E., Dodd, R.H., Gysels, M., Johnston, B., Murray,
S., Banerjee, S., Shipman, C., Hansford, P, Wakefield, D., Gomes, B and Higginson, I.J. (2012).
Understanding place of death for patients with non malignant conditions: a systematic review. NHS:
National Institute for Health Research Service Delivery and Organisation Programme.
• Sleeman, K.E., Ho, Y.K, Verne, J, Gao, W. and Higginson, I.J. on behalf of the GUIDE_Care project (2014).
Reversal of English trend towards hospital death in dementia: a population-based study of place and
death and associated individual and regional factors, 2001-2010. BMC Neurology 14:59.
• Houttekier, D., Cohen, J., Bilsen, J., Addington-Hall, J., Bregie, D., Onwuteaka-Philipsen, Deliens, L.
(2010). Place of Death of Older Persons with Dementia. A Study in Five European Countries. Journal of
the American Geriatrics Society, 58(4):751-6
• NHS National End of Life Care Programme(2012). Critical success factors that enable individuals die in
their preferred place of death. A report based on contributions from End of Life Care commissioners and
providers of services within 7 PCT areas. UK: Department of Health.
• Kane, M (2012). My Life until the end: Dying well with Dementia. Alzheimers Society UK.
Editor's Notes
Nurses for nightcare is a service which is funded by the IHF and provided through the Irish Cancer Society. 548 people received the service last year with a total of 1734 nights delivered. This supports people with non malignant illnesses to die at home.
14% of total referrals
37% increase last year
In 2016, 28 referrals so far this year , representing a 180% increase on the same period
Population based study in the UK
In the US, home deaths are more common
Two in five people with dementia die in hospital,
Less than 5% of dementia patients died at home or in hospice.
Care home bed provision has been found to be the key to this trend reversal.
Home/hospice death was more likely in affluent areas, for women, and for those with cancer as underlying cause of death, and less likely in the unmarried.
Literature
Referrals are made through SPCT -
Most people required full nursing care with seizures, recurrent respiratory tract and urinary tract infections frequently reported. Difficulties with hydration and nutrition referenced ++
Use of profiling beds, pressure mattresses, hoists, wheelchairs in the home common.
Many family members living in close proximity to the person with dementia, allowing them to stay between their own home and the home of the person with dementia
Having a supportive GP was cited as extremely important in 40% of the sample.
DNACPR and not for transfer to hospital info shared with OOH providers in a number of cases
HCPs – PHN involved in 77% of cases – geriatrician, POLL, commmunity psy nurse
People really valued specialist input re dementia – available in 31% of sample
Respite
89% of the sample were availing of some formal (paid supports). Many families supplemented the homecare packages using private funding with a small number of families (7%) paying for live in 24 hour care.
Having a supportive GP was cited as extremely important in 40% of the sample.
DNACPR and not for transfer to hospital info shared with OOH providers in a number of cases
HCPs – PHN involved in 77% of cases – geriatrician, POLL, commmunity psy nurse
People really valued specialist input re dementia – available in 31% of sample
Respite
89% of the sample were availing of some formal (paid supports). Many families supplemented the homecare packages using private funding with a small number of families (7%) paying for live in 24 hour care.