The concept of advance care planning outlined. The Assisted Decision Making (Capacity) Act 2015. Using Think Ahead as a tool to engage with advance care planning and with advance healthcare directives
Advance Care Planning & Advance Healthcare Directives with People with DementiaIrish Hospice Foundation
1. The document provides guidance on advance care planning and advance healthcare directives for people with dementia, their families, and healthcare professionals.
2. It outlines four key considerations for good practice: understanding dementia, recognizing patient rights, understanding advance care planning, and being familiar with the Assisted Decision Making Act regarding capacity and advance directives.
3. The guidance stresses the presumption of capacity, engaging the patient, and considering previously expressed preferences when making decisions for those lacking capacity. It also describes what can be included in an advance healthcare directive.
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.
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.
The concept of advance care planning outlined. The Assisted Decision Making (Capacity) Act 2015. Using Think Ahead as a tool to engage with advance care planning and with advance healthcare directives
Advance Care Planning & Advance Healthcare Directives with People with DementiaIrish Hospice Foundation
1. The document provides guidance on advance care planning and advance healthcare directives for people with dementia, their families, and healthcare professionals.
2. It outlines four key considerations for good practice: understanding dementia, recognizing patient rights, understanding advance care planning, and being familiar with the Assisted Decision Making Act regarding capacity and advance directives.
3. The guidance stresses the presumption of capacity, engaging the patient, and considering previously expressed preferences when making decisions for those lacking capacity. It also describes what can be included in an advance healthcare directive.
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.
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.
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.
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.
Perspectives from northern ireland – development of bereavement care standard...Irish Hospice Foundation
This document discusses the development of bereavement care standards and the bereavement coordinator role in Northern Ireland. It summarizes the key events and initiatives that have improved bereavement care, including audits that identified areas for improvement, the creation of bereavement care standards and networks, and the role of bereavement coordinators in implementing strategies. It highlights ongoing work to further develop bereavement care and support through training, resources, and continued collaboration between organizations.
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"
Effective Integration of Palliative Care in Respiratory Setting - Using Actio...Irish Hospice Foundation
Overview of Action Research Project carried out to integrate palliative care into the care of those with respiratory illness. Presented at International Congress on Palliative Care, Montreal, September 2014
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.
This document discusses best interest decisions for adults who lack capacity under the Mental Capacity Act (MCA). It notes that for day-to-day decisions, the main carer such as a parent can make decisions, but for serious medical treatment the lead doctor is the decision maker. It emphasizes that best interest decisions should be made collaboratively, consulting others to understand the person's wishes. For disputes, the Court of Protection can appoint a Deputy decision maker.
Outlines the Irish Hospice Foundations Nurses for Night Care Programme and how the service supports people dying at home with illnesses other than cancer
Denise Heals presents on her role developing end of life care practices for people with learning disabilities. She outlines approaches used like working with managers and staff in one-off sessions or over 12 months using person-centered thinking tools. Examples of developments include end of life care plans, memorials for residents, and cultural changes at hospices like link nurses and accessible resources. The impact has been greater understanding of end of life care, more open discussions, and improved policies.
Facilitating discussions on future and end of life care with people who have ...Irish Hospice Foundation
This document provides guidance for facilitating discussions about future and end-of-life care with people who have dementia. It discusses the growing dementia population and policy context. It outlines the background and development process for the guidance document. Key considerations for effective communication are presented, along with 8 tips for communication. The AFIRM model of active listening is described. A case study example illustrates how AFIRM can be applied. Finally, a list of additional guidance documents in development is presented.
The document discusses supporting people with dementia at end of life. It outlines the Irish Hospice Foundation's (IHF) vision of ensuring dignity and comfort for all facing end of life. The IHF runs several programs, including on palliative care and bereavement. Data shows more people with dementia die in care homes than at home. The IHF nurses service data found most referrals were older adults and from certain areas. Literature suggests place of death is influenced by illness factors and care circumstances. The document outlines IHF education initiatives to improve end of life care and communication for people with dementia, their families, and staff. It stresses the importance of person-centered communication and considering the emotional needs of those with dementia.
The document discusses setting up a multidisciplinary team (MDT) and resource pack to support palliative care for people with learning disabilities in West Hertfordshire. It notes challenges in establishing the MDT like differing computer systems. The MDT aims to ensure good communication and care coordination. The resource pack contains sections on demographics, daily living, common symptoms, end of life planning, family support, useful contacts and tools. It is meant to help document changes and enable easier access to palliative care. The MDT has seen increasing referrals over time and helped more service users receive end of life care in their preferred place. The document advocates for more education and expanding the approach to other areas.
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.
The document discusses using the Gold Standards Framework (GSF) to provide end-of-life care for clients with dementia. The GSF is a systematic approach that supports people living with a terminal illness and helps plan care based on individual needs, symptoms, and preferences. It has 20 standards covering areas like advance care planning, symptom management, documentation, and support for family members. The document provides examples of how the GSF was implemented in practice for a client named Patsy and her family through advance care planning, coordinated care in final days, and leadership to sustain quality end-of-life care.
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.
Person Centered Care through Integrating a Palliative Approach: Lessons from ...BCCPA
Aging adults are entering residential care facilities with more advanced disease than in the past and their length of stay is shorter. Most health care providers in these facilities do not receive targeted education and training in palliative care, nor are they confident to have crucial conversations about goals of care and end of life challenges with residents and their families. Due to limited capacity to manage predictable symptoms related to end of life and insufficient planning, many residents are transferred to hospital in crisis and die in the Emergency Department or acute care wards.
This presentation will showcase some of the initiatives by identifying common themes, unique features of each and strategies for success. Opportunity will be given for delegates to ask questions and brainstorm how lessons learned from these initiatives could inform the care provided at their own facility.
Presented by:
- Jane Webley, RN LLB Regional lead, End of Life, Vancouver Coastal Health (EPAIRS and the Daisy project)
- Dr Christine Jones, Island Health (SSC project: Improving end of life outcomes in residential care facilities: A palliative approach to care)
- Kathleen Yue, RN, BSN, MN, CHPCN (c) Education Coordinator, BC Center for Palliative Care
The document discusses supporting staff who work in stressful healthcare environments. It describes how the Point of Care Foundation works at various levels to help staff flourish, such as by raising awareness of effective support methods and providing training. Schwartz Rounds are discussed as one approach to addressing challenges staff face by allowing them to share difficult experiences in a supportive setting. Research shows links between staff wellbeing, engagement, and positive patient experiences. The framework proposes primary, secondary, and tertiary interventions for supporting staff wellbeing at the individual, team, and organizational levels to help prevent and address stress.
Evidence-Informed Guidelines for Recreation Therapy programs to Enhance the M...BCCPA
This presentation will provide an overview of the BCCPA Mitacs-SFU project to develop a best practices guide for recreational therapy (RT). OLTCA and ACCA are also partners in this project. Along with reviewing the results of a survey on recreational therapy in LTC that was undertaken in BC, Alberta and Ontario it will present the final RT best practices guide.
Presented by:
- Dr. Kim van Schooten, Centre for Hip Health and Mobility, University of British Columbia
- Dr. Yijian Yang, Centre for Hip Health and Mobility, University of British Columbia
- Brenda Kinch, President, BC Therapeutic Recreation Association
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.
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.
Perspectives from northern ireland – development of bereavement care standard...Irish Hospice Foundation
This document discusses the development of bereavement care standards and the bereavement coordinator role in Northern Ireland. It summarizes the key events and initiatives that have improved bereavement care, including audits that identified areas for improvement, the creation of bereavement care standards and networks, and the role of bereavement coordinators in implementing strategies. It highlights ongoing work to further develop bereavement care and support through training, resources, and continued collaboration between organizations.
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"
Effective Integration of Palliative Care in Respiratory Setting - Using Actio...Irish Hospice Foundation
Overview of Action Research Project carried out to integrate palliative care into the care of those with respiratory illness. Presented at International Congress on Palliative Care, Montreal, September 2014
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.
This document discusses best interest decisions for adults who lack capacity under the Mental Capacity Act (MCA). It notes that for day-to-day decisions, the main carer such as a parent can make decisions, but for serious medical treatment the lead doctor is the decision maker. It emphasizes that best interest decisions should be made collaboratively, consulting others to understand the person's wishes. For disputes, the Court of Protection can appoint a Deputy decision maker.
Outlines the Irish Hospice Foundations Nurses for Night Care Programme and how the service supports people dying at home with illnesses other than cancer
Denise Heals presents on her role developing end of life care practices for people with learning disabilities. She outlines approaches used like working with managers and staff in one-off sessions or over 12 months using person-centered thinking tools. Examples of developments include end of life care plans, memorials for residents, and cultural changes at hospices like link nurses and accessible resources. The impact has been greater understanding of end of life care, more open discussions, and improved policies.
Facilitating discussions on future and end of life care with people who have ...Irish Hospice Foundation
This document provides guidance for facilitating discussions about future and end-of-life care with people who have dementia. It discusses the growing dementia population and policy context. It outlines the background and development process for the guidance document. Key considerations for effective communication are presented, along with 8 tips for communication. The AFIRM model of active listening is described. A case study example illustrates how AFIRM can be applied. Finally, a list of additional guidance documents in development is presented.
The document discusses supporting people with dementia at end of life. It outlines the Irish Hospice Foundation's (IHF) vision of ensuring dignity and comfort for all facing end of life. The IHF runs several programs, including on palliative care and bereavement. Data shows more people with dementia die in care homes than at home. The IHF nurses service data found most referrals were older adults and from certain areas. Literature suggests place of death is influenced by illness factors and care circumstances. The document outlines IHF education initiatives to improve end of life care and communication for people with dementia, their families, and staff. It stresses the importance of person-centered communication and considering the emotional needs of those with dementia.
The document discusses setting up a multidisciplinary team (MDT) and resource pack to support palliative care for people with learning disabilities in West Hertfordshire. It notes challenges in establishing the MDT like differing computer systems. The MDT aims to ensure good communication and care coordination. The resource pack contains sections on demographics, daily living, common symptoms, end of life planning, family support, useful contacts and tools. It is meant to help document changes and enable easier access to palliative care. The MDT has seen increasing referrals over time and helped more service users receive end of life care in their preferred place. The document advocates for more education and expanding the approach to other areas.
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.
The document discusses using the Gold Standards Framework (GSF) to provide end-of-life care for clients with dementia. The GSF is a systematic approach that supports people living with a terminal illness and helps plan care based on individual needs, symptoms, and preferences. It has 20 standards covering areas like advance care planning, symptom management, documentation, and support for family members. The document provides examples of how the GSF was implemented in practice for a client named Patsy and her family through advance care planning, coordinated care in final days, and leadership to sustain quality end-of-life care.
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.
Person Centered Care through Integrating a Palliative Approach: Lessons from ...BCCPA
Aging adults are entering residential care facilities with more advanced disease than in the past and their length of stay is shorter. Most health care providers in these facilities do not receive targeted education and training in palliative care, nor are they confident to have crucial conversations about goals of care and end of life challenges with residents and their families. Due to limited capacity to manage predictable symptoms related to end of life and insufficient planning, many residents are transferred to hospital in crisis and die in the Emergency Department or acute care wards.
This presentation will showcase some of the initiatives by identifying common themes, unique features of each and strategies for success. Opportunity will be given for delegates to ask questions and brainstorm how lessons learned from these initiatives could inform the care provided at their own facility.
Presented by:
- Jane Webley, RN LLB Regional lead, End of Life, Vancouver Coastal Health (EPAIRS and the Daisy project)
- Dr Christine Jones, Island Health (SSC project: Improving end of life outcomes in residential care facilities: A palliative approach to care)
- Kathleen Yue, RN, BSN, MN, CHPCN (c) Education Coordinator, BC Center for Palliative Care
The document discusses supporting staff who work in stressful healthcare environments. It describes how the Point of Care Foundation works at various levels to help staff flourish, such as by raising awareness of effective support methods and providing training. Schwartz Rounds are discussed as one approach to addressing challenges staff face by allowing them to share difficult experiences in a supportive setting. Research shows links between staff wellbeing, engagement, and positive patient experiences. The framework proposes primary, secondary, and tertiary interventions for supporting staff wellbeing at the individual, team, and organizational levels to help prevent and address stress.
Evidence-Informed Guidelines for Recreation Therapy programs to Enhance the M...BCCPA
This presentation will provide an overview of the BCCPA Mitacs-SFU project to develop a best practices guide for recreational therapy (RT). OLTCA and ACCA are also partners in this project. Along with reviewing the results of a survey on recreational therapy in LTC that was undertaken in BC, Alberta and Ontario it will present the final RT best practices guide.
Presented by:
- Dr. Kim van Schooten, Centre for Hip Health and Mobility, University of British Columbia
- Dr. Yijian Yang, Centre for Hip Health and Mobility, University of British Columbia
- Brenda Kinch, President, BC Therapeutic Recreation Association
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.
- The document discusses a training course on the Mental Capacity Act 2005 and Deprivation of Liberty Safeguards.
- It provides an overview of the topics to be covered including the five key principles of the MCA, assessing capacity, best interests decisions, DoLS, and the role of IMCAs.
- The aims are to explore the MCA and its principles, enable staff to apply it properly, and understand the safeguards it introduces.
Presentation on Advance Healthcare Directives (From Acute Hospital Network, J...Irish Hospice Foundation
The document discusses proposed legislation in Ireland to establish a legal framework for advance healthcare directives (AHDs). Key points:
- AHDs would allow people to make healthcare decisions in advance if they lose capacity in the future, promoting autonomy and respecting personal values and choices.
- To be valid, an AHD must be in writing, made voluntarily by those with capacity, and witnessed. People can also appoint a healthcare representative.
- AHDs can refuse treatments but not basic care. Refusals must clearly specify treatments and circumstances. Life-sustaining refusals require additional verification.
- The legislation aims to comply with international standards while not affecting laws on euthanasia or
Presentation on Think Ahead (at Dublin Community Hospital Network, August 201...Irish Hospice Foundation
The document discusses Think Ahead, a form that allows people to record their healthcare preferences and wishes in the event they become unable to communicate themselves due to illness or incapacity. The form covers key personal information, care preferences, legal affairs, financial matters, end of life wishes, and information sharing preferences. It encourages people to think about and discuss their wishes with loved ones and healthcare providers. A pilot study found most patients found completing the form not upsetting and that it initiated important family discussions. The form aims to improve medical care and quality of life for patients, as well as the adjustment process for surviving family members.
CCher Nicholson Supported decision-making – the South Australian experience legislation
The document summarizes the Supported Decision Making (SDM) trial conducted in South Australia. The trial involved 26 participants who created agreements with supporters and monitors to make decisions with support instead of having a guardian appointed. Feedback found establishing supported decision making agreements improved participants' lives and decision making abilities. The trial demonstrated how supported decision making can uphold rights and provide choice rather than seeking incapacity. Some aspects that worked well included the recruitment process and providing information individually. Areas for improvement include expanding supporter training and continuing the project's work.
This document summarizes the Canadian Medical Association's (CMA) principles-based approach to assisted dying in Canada following a 2015 Supreme Court ruling. It outlines 10 principles, recommendations on patient qualifications and the physician's role. It also summarizes the CMA's consultation process with members, which found disagreement on appropriate eligibility criteria and how to balance access to assisted dying while protecting conscientious objection. The CMA is seeking feedback to help shape federal and provincial legislation.
This document provides an overview of a training course on the Mental Capacity Act 2005. It discusses key topics that will be covered in the training including the five principles of the Act, assessing capacity, best interests decisions, deprivation of liberty safeguards, lasting powers of attorney, advanced decisions, the role of the Court of Protection and Public Guardian, and independent mental capacity advocates. The training aims to enable staff to apply the Mental Capacity Act in their work and understand the legal framework and safeguards in place for supporting those lacking capacity.
This guide is designed to help health and social care professionals understand and implement the law relating to advance decisions to refuse treatment (ADRT) contained in the Mental Capacity Act (2005).
This 2013 version replaces that published in September 2008 and covers:
How to make an advance decision to refuse treatment, who can make an advance decision, when a decision should be reviewed and how it can changed or withdrawn
What should be included
Rules applying to advance decisions to refuse life sustaining treatment and how they relate to other rules about decision-making
How to decide on the existence, validity and applicability of advance decisions and what healthcare professionals should do if an advance decision is not valid or applicable
The implications for healthcare professionals of advance care decisions, including situations where a healthcare professional has a conscientious objection to stopping or providing life-sustaining treatment
What happens if there is a disagreement about an advance decision.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
This document provides an overview of medical ethics, informed consent, and advance directives. It discusses key principles of medical ethics including autonomy, beneficence, non-maleficence, and justice. It defines informed consent and its legal and ethical basis, noting it is based on a patient's right to receive information and choose treatment. Exceptions to informed consent requirements are also outlined. Advance directives allow for healthcare decision making according to a patient's wishes if they become incapacitated. Case examples demonstrate how these principles apply to clinical scenarios.
Emergency medicine, psychiatry and the lawSCGH ED CME
The document discusses laws related to emergency psychiatry and involuntary treatment orders. It covers the criteria needed for a referral, including that a medical practitioner or authorized mental health practitioner must reasonably suspect the person needs involuntary treatment or their community treatment order needs changing. It explains the forms and process used for referrals, including providing rights to family members and allowing referrals to be extended or revoked.
This document discusses shared decision-making between patients and clinicians. It defines shared decision-making as a process where patients are active partners in choosing medical options. The document outlines how to encourage patient participation, assess a patient's desire and capacity for decision-making, discuss treatment preferences, develop treatment plans, address barriers to adherence, and support self-management. The goal is to empower patients and improve outcomes through open communication and providing resources.
Capacity, care planning and advance care planning in life limiting illness - executive summary
15 August 2008 - National End of Life Care Programme
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
This document provides an overview of Ireland's new Assisted Decision-Making (Capacity) Act and its implementation. It discusses:
- Guiding principles for decision-making assistance, including presumption of capacity.
- Three tiers of decision support available: decision-making assistance agreements, co-decision-making agreements, and decision-making representation orders.
- Two types of advance planning: enduring powers of attorney and advance healthcare directives.
- A new Decision Support Service to maintain registers of arrangements and oversee the system.
- Functional tests of capacity and options for applying to court if needed.
- Changes to the ward of court system and transitioning existing wards.
-
Health Care Consent, Aging and Dementia: Mapping Law and Practice in BCBCCPA
In October 2016, the Canadian Centre for Elder Law working with ASBC started a 16 month project on the law and practice around health care consent in BC with a focus on older adults and adults with dementia. This project will address issues around health care consent with a focus on older adults and adults with dementia. Along with addressing the legal framework surrounding health care consent it will highlighted related issues such as polypharmacy, etc.
Presented by:
- Krista James, National Director, Canadian Centre for Elder Law
- Alison Leaney, Provincial Coordinator, Vulnerable Adults Community Response, Public Guardian and Trustee
- Barbara Lindsay, Director, Advocacy and Education
Similar to Advance Care Planning and Advance Healthcare Directives (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 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.
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
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.
This document provides an agenda for the HFH Acute Hospital Network Meeting taking place on May 23rd, 2017 at the River Lee Hotel in Cork. The agenda includes presentations and discussions on palliative care programs and policies around Ireland, including updates from the Irish Hospice Foundation and the HSE/HFH Joint Oversight Group. There will also be panels on developing post-mortem policies, implementing DNACPR policies, and making acute hospitals more child-friendly. The meeting will conclude with an award ceremony to recognize 10th anniversary grants from the Irish Hospice Foundation.
The Hospice Friendly Hospitals Programme seeks to improve end of life care in hospitals. It supports individual hospitals and hospital groups. Updates include plans to celebrate the programme's 10th anniversary through advocacy and awareness events. The document discusses the programme's achievements, including linking over 120 hospitals. It outlines plans for 2017 like establishing an oversight group between the HSE and HFH. The programme aims to standardize end of life care and reduce variability across hospitals.
About this webinar: This talk will introduce what cancer rehabilitation is, where it fits into the cancer trajectory, and who can benefit from it. In addition, the current landscape of cancer rehabilitation in Canada will be discussed and the need for advocacy to increase access to this essential component of cancer care.
Michigan HealthTech Market Map 2024. Includes 7 categories: Policy Makers, Academic Innovation Centers, Digital Health Providers, Healthcare Providers, Payers / Insurance, Device Companies, Life Science Companies, Innovation Accelerators. Developed by the Michigan-Israel Business Accelerator
The facial nerve, also known as cranial nerve VII, is one of the 12 cranial nerves originating from the brain. It's a mixed nerve, meaning it contains both sensory and motor fibres, and it plays a crucial role in controlling various facial muscles, as well as conveying sensory information from the taste buds on the anterior two-thirds of the tongue.
Let's Talk About It: Breast Cancer (What is Mindset and Does it Really Matter?)bkling
Your mindset is the way you make sense of the world around you. This lens influences the way you think, the way you feel, and how you might behave in certain situations. Let's talk about mindset myths that can get us into trouble and ways to cultivate a mindset to support your cancer survivorship in authentic ways. Let’s Talk About It!
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - ...rightmanforbloodline
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
Can Allopathy and Homeopathy Be Used Together in India.pdfDharma Homoeopathy
This article explores the potential for combining allopathy and homeopathy in India, examining the benefits, challenges, and the emerging field of integrative medicine.
PET CT beginners Guide covers some of the underrepresented topics in PET CTMiadAlsulami
This lecture briefly covers some of the underrepresented topics in Molecular imaging with cases , such as:
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Hypertension and it's role of physiotherapy in it.Vishal kr Thakur
This particular slides consist of- what is hypertension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is summary of hypertension -
Hypertension, also known as high blood pressure, is a serious medical condition that occurs when blood pressure in the body's arteries is consistently too high. Blood pressure is the force of blood pushing against the walls of blood vessels as the heart pumps it. Hypertension can increase the risk of heart disease, brain disease, kidney disease, and premature death.
Hypertension and it's role of physiotherapy in it.
Advance Care Planning and Advance Healthcare Directives
1. ADVANCE CARE PLANNING AND
ADVANCE HEALTHCARE DIRECTIVES
Deirdre Shanagher, Marie Lynch, Dr John Weafer, Prof
Willie Molloy, Dr Sharon Beatty, Dr Geraldine McCarthy, Patricia
Rickard-Clarke, Emer Begley, Esther Beck, Sarah Murphy
Hospice Friendly Hospitals Network Meeting June 9th 2016
3. Today:
• Background & Context
• The legislation – useful facts
• Key considerations to inform good practice
• Functional approach to capacity
• Decision making supports
• Advance healthcare directives
• Guidance for healthcare staff
• Case study
7. The Assisted Decision Making (Capacity)
Act 2015:
• Replaces the Lunacy Regulation (Ireland) Act 1871
• Includes provision for Advance Healthcare Directives
which were previously legal under common law but had
no legislative underpinning.
• Codes of Practice/Guidelines for full implementation
required
• Minister for Justice will commence most of the Act
• Minister for Health will commence the AHD section
8. Key Changes:
Ward of Court system to be abolished - review of all wards
• New legal process to deal with decision-making for a
relevant person in respect of a relevant decision
• New - Court process
• New role and office: Director of The Decision Support
Service
• New - Panels to be established by the Director
• New - provisions for Enduring Powers of Attorneys
• New - advance healthcare directives
9. Review of wards of court:
• Within 3 years of relevant section coming into force all current
wards of court will be discharged
• Court may:
1. Declare that there is no issue with the wards decision making
capacity
OR
2. Make one or more than one of the following declarations:
• That the ward lacks decision making capacity, unless the assistance of
a suitable person as a co-decision-maker is made available to him or
her, to make one or more than one decision
• That the wards lacks decision making capacity, even if the assistance
of a suitable person as a co-decision-maker were made available to
him or her
10. Key considerations to inform good practice:
1. Develop understanding of dementia
2. Become familiar with aspects of the Assisted Decision Making
(Capacity) Act 2015, specifically in relation to:
• The Functional approach to capacity
• Advance Healthcare directives
11. Functional Approach to Capacity:
• Presumption of capacity
Responsibility of those questioning decision
making capacity to prove there is an issue…
• Time and issue specific
13. Advance Healthcare Directives:
• A document where a person can write down what they
would like to happen in relation to certain medical care
treatments
• Only comes into force when a person loses capacity,
becomes ill and the circumstances in their advance
healthcare directive arise. (A record of advance healthcare directives will
be held by the Director of Decision Support Services).
14. Issues that may be covered in an advance
healthcare directive:
• Treatments that a person would refuse in the future – this is legally
binding
• A request for a specific treatment. This is not legally binding but must be taken
into consideration during any decision-making process which relates to treatment for the
person in question if that specific treatment is relevant to the medical condition for which
the person may require treatment.
15. What makes an advance healthcare
directive legal?
1. At the time in question a person lack decision making
capacity to give consent to the treatment
2. The treatment to be refused is clearly identified in the
advance healthcare directive
3. The circumstances in which the refusal of treatment is
intended to apply are clearly identified in the advance
healthcare directive
4. The advance healthcare directive was made voluntarily.
5. The advance healthcare directive was not altered or
revoked.
6. The person did not do anything inconsistent with the terms
of the advance healthcare directive while they had decision
making capacity.
16. Guidance for healthcare professionals:
• Always presume decision making capacity
• Help the person to maximise their decision making
capacity
• Remember that the person with dementia can choose
not to take part in the advance care planning process
• Be aware of how to assess a persons decision making
capacity if required to do so
• Gain knowledge on what steps to take if decision
making capacity is an issue
• Check existing advance care plans with the person
regularly for validity and applicability
17. Maximising decision-making capacity:
• Discuss treatment options in a place and at a time when the
person is best able to understand and retain information.
• Ask the person if there is anything that would help them
remember information or make it easier to make a decision;
such as:
• Bringing another person to healthcare meetings or
• Having audio or pictorial information about their condition
• Writing things down
• Using simple language
• Finding out how the person usually communicates
• Giving the person space to think quietly
• Involving others where necessary such as speech and language
therapists or psychologists
18. 8 Tips for Effective Communication
1. Adopt a person centred approach to
communication
2. Connect with the person
3. Consider the communication environment
4. Be aware of your own communication style and
approach
5. Use active listening
6. Use simple language
7. Focus on one question at a time
8. Clarify Information and check understanding
See G. Doc 1
20. Assessing decision-making capacity:
• Consider what decision has to be made
• Do not discriminate
• Is there something currently happening that may
temporarily affect the person’s decision-making capacity
• Consider what supports have been provided
• Consider if decision-making capacity is absent even with
all practicable support
21. Assessing decision-making capacity:
• Can the person:
• Understand information relative to the decision
• Retain the information long enough to make a voluntary choice
• Use or weigh the information as part of the process of making the
decision
• Communicate their decision?
22. If decision-making capacity is an issue:
1. Support the person to be involved in the decision-
making process by engaging in capacity building and
maximising.
2. Consider the level of support that the person
requires to make the decision in question.
3. Seek evidence of previously expressed
preferences.
4. Consider which option, including not to treat, would
be least restrictive of the person’s future choices.
5. Consider the views of anyone indicated by the
person. These people may be those appointed by
the person to support them when making decisions.
6. A Consider involving advocacy support.
28. Acknowledgements
Thank you and
Questions
For more information:
Deirdre Shanagher
Deirdre.shanagher@hospicefoundation.ie
People with dementia and carers who have
contributed and advised IHF
IHF Changing Minds Team
Project and Expert Advisory and Governance
Groups
Atlantic Philanthropies
Editor's Notes
Constitution of Ireland
Universal Declaration on Bioethics & Human Rights (2005)
United Nations Convention on the Rights of Persons with Disabilities (2006)
Council of Europe Recommendations
Assisted Decision Making (Capacity) Act 2015
Re codes of practice:
Will & Preferences
Least restrictive
Proportionate
Limited in duration
Take into account beliefs and values
Progressive, staff need to respond appropriately when opportunities arise
The Universal Declaration on Bioethics and Human Rights (2005) addresses the right of a person to consent to and to refuse medical treatment. United Nations Convention on the Rights of Persons with Disabilities (2006) called on countries to facilitate people with disabilities to exercise their right to make choices and express preferences in relation to their care on a similar basis equal to those who do not have any disability . Council of Europe Recommendations: Self determination and to protect the rights of older people. Constitution of Ireland right of people to decide for themselves and bodily integrity when a person does not have the capacity to consent the intervention may only be carried out with the authorisation of his or her representative, an authority or a person or body provided by law, a person has the right to make decisions (even unwise decisions) on their own behalf and is assumed to have capacity to do this unless proven otherwise. The responsibility for proving otherwise rests with the person challenging capacity.
The Health Service Executive National Consent Policy clearly states that advance care planning is a process of discussion. A person can choose to or not to engage with this
A person can refuse treatment up to and including life-sustaining treatments but cannot refuse what is termed “basic care”. The legislation on advance healthcare directives defines basic care as including, (but is not limited to), warmth, shelter, oral nutrition, oral hydration and hygiene measures but does not include artificial nutrition or artificial hydration (which would be termed as medical treatment) (6). A person has the legal right to refuse life-sustaining treatment in an advance healthcare directive even if it means that their life is at risk. This promotes individual autonomy and respect for a person’s will and preferences. A healthcare professional will be obliged to follow a person’s valid advance healthcare directive even if he/she disagrees with such decision.
Minister for Health will be appointing a multi-disciplinary Working Group to make recommendations for a code of practice specifically for the guidance of designated healthcare representatives and healthcare professionals.. The Director of the Decision Support Service has the function of preparing and publishing the code of practice when finalised.
The difference between an ACP and AHD is the refusal and legal binding with refusing treatments.
Presuming covered under the functional approach to capacity
See guidance document 1
So we came up with these 8 tips for effective communication.
Adopt a person centred approach. So find out how best to support a person to understand information, use aids, talking mats, sign language, be creative & open, observe behaviours and build a collaborative picture
Connect with the person. Prioritise this and don’t get focused on exchanging information and facts. Use life story work as a means of developing relationships and focus on the feelings BEHIND words.
Consider the communication environment such as lighting, noise, seating and resources such as aids required (picture boards or talking mats)
Be aware of your own communication style. So approach to the front, make eye contact, get to the same level as the person, introduce yourself, call them by their name, explain what you’re there for, speak slowly and clearly using a calm tone of voice
Use active listening techniques such as conversational cues like “hmm” “I see” or “really”, don’t rush to fill silences and give the person extra time to process information,
Use simple language and the persons name, focus on one topic at a time, avoid jargon, use aids and different words
Focus on one question at a time so reframe open ended questions to closed questions focusing on 1 idea at a time
Clarify information and check understanding so ask questions and repeat back information
If there is nobody appointed by the person whose decision making capacity is at issue and/or an urgent decision is required, an application can be brought to the circuit court seeking the appointment of one or more persons to act as a decision making representative.
I’d like to acknowledge these people and will now take some questions if there are any.