The document provides guidance for delivering high quality end of life care to prisoners, outlining 6 steps from initiating discussions as end of life approaches to care after death. It discusses the need to identify prisoners approaching end of life and have open conversations about their wishes, while also addressing the complex considerations around safety, security, and communication within the prison system. The goal is to ensure prisoners receive compassionate and dignified care at the end of life regardless of their setting.
Getting it right: end of life care in advanced kidney disease
Published by NHS Kidney Care
This document brings together the experiences and learning from three project groups that have been working over the last two years to implement the framework for end of life care in advanced kidney disease. It also addresses the data items that are associated with managing end of life care.
The purpose of this briefing is to help you to identify the immediate priority actions to commission effective end of life care.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
Dr. Michael Power, National Clinical Lead, Critical Care Programme, CSP HSeIMSTA
This document discusses critical care delivery in Ireland including:
1. It outlines the current "hub-and-spoke" critical care model in Ireland and references standards for critical care services.
2. It notes recommendations from HIQA and others calling for improved critical care networks and transfer protocols.
3. International examples of critical care systems aimed at improving outcomes for conditions like cardiac arrest and trauma are referenced.
NHS Improving Quality undertook a scoping exercise of rehabilitation services, which included:
Identification of the different practice models illustrated through case studies looking at integrated models of adult rehabilitation service provision
A high level baseline mapping exercise of the current availability of adult rehabilitation services across England.
NHS Improving Quality also assisted in capturing the views from key stakeholders by supporting and facilitating a series of stakeholder engagement events hosted by NHS England.These events aimed to develop and agree principles and expectations to underpin high quality rehabilitation services.
The document outlines plans to redesign cancer services across Mid Nottinghamshire. It proposes new models of care from diagnosis through to follow-up and aftercare, with a focus on earlier diagnosis, reviewing common cancer pathways, improving care for those living with and beyond cancer, and emergency care including late presentations. Key priorities include developing new earlier diagnosis pathways with an increased primary care role, reviewing pathways according to evidence-based guidelines, and implementing holistic needs assessments and care planning. The changes aim to improve cancer outcomes, patient experience, and make more efficient use of resources.
This document provides an in-depth overview of capital punishment in India and around the world, including:
- A brief history of capital punishment practices from ancient times to the present.
- An overview of the major religions' stances on capital punishment.
- Details on the implementation and controversies around capital punishment in countries like the US, China, India and others.
- International frameworks and treaties related to abolition of the death penalty.
The document discusses arguments for and against the death penalty in the United States. It notes that the US is one of few countries that still uses capital punishment and executes more people than nations like China, Iran, and Saudi Arabia. Arguments against the death penalty include that it is applied arbitrarily and in a racially discriminatory manner, amounts to cruel and unusual punishment, and violates international human rights laws. The document also discusses the high financial costs of the death penalty compared to life imprisonment without parole.
Human rights violation_in_custodial_tortureAvinash Rajput
This document provides an overview of custodial torture in India. It defines torture, describes common torture methods and types (police vs. judicial custody), presents statistics on custodial deaths from 2000-2011, outlines relevant international and domestic legal frameworks, and provides three case examples each of torture in police and judicial custody.
Getting it right: end of life care in advanced kidney disease
Published by NHS Kidney Care
This document brings together the experiences and learning from three project groups that have been working over the last two years to implement the framework for end of life care in advanced kidney disease. It also addresses the data items that are associated with managing end of life care.
The purpose of this briefing is to help you to identify the immediate priority actions to commission effective end of life care.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
Dr. Michael Power, National Clinical Lead, Critical Care Programme, CSP HSeIMSTA
This document discusses critical care delivery in Ireland including:
1. It outlines the current "hub-and-spoke" critical care model in Ireland and references standards for critical care services.
2. It notes recommendations from HIQA and others calling for improved critical care networks and transfer protocols.
3. International examples of critical care systems aimed at improving outcomes for conditions like cardiac arrest and trauma are referenced.
NHS Improving Quality undertook a scoping exercise of rehabilitation services, which included:
Identification of the different practice models illustrated through case studies looking at integrated models of adult rehabilitation service provision
A high level baseline mapping exercise of the current availability of adult rehabilitation services across England.
NHS Improving Quality also assisted in capturing the views from key stakeholders by supporting and facilitating a series of stakeholder engagement events hosted by NHS England.These events aimed to develop and agree principles and expectations to underpin high quality rehabilitation services.
The document outlines plans to redesign cancer services across Mid Nottinghamshire. It proposes new models of care from diagnosis through to follow-up and aftercare, with a focus on earlier diagnosis, reviewing common cancer pathways, improving care for those living with and beyond cancer, and emergency care including late presentations. Key priorities include developing new earlier diagnosis pathways with an increased primary care role, reviewing pathways according to evidence-based guidelines, and implementing holistic needs assessments and care planning. The changes aim to improve cancer outcomes, patient experience, and make more efficient use of resources.
This document provides an in-depth overview of capital punishment in India and around the world, including:
- A brief history of capital punishment practices from ancient times to the present.
- An overview of the major religions' stances on capital punishment.
- Details on the implementation and controversies around capital punishment in countries like the US, China, India and others.
- International frameworks and treaties related to abolition of the death penalty.
The document discusses arguments for and against the death penalty in the United States. It notes that the US is one of few countries that still uses capital punishment and executes more people than nations like China, Iran, and Saudi Arabia. Arguments against the death penalty include that it is applied arbitrarily and in a racially discriminatory manner, amounts to cruel and unusual punishment, and violates international human rights laws. The document also discusses the high financial costs of the death penalty compared to life imprisonment without parole.
Human rights violation_in_custodial_tortureAvinash Rajput
This document provides an overview of custodial torture in India. It defines torture, describes common torture methods and types (police vs. judicial custody), presents statistics on custodial deaths from 2000-2011, outlines relevant international and domestic legal frameworks, and provides three case examples each of torture in police and judicial custody.
When a person dies: guidance for professionals on developing bereavement services
The National End of Life Care Programme has supported the Bereavement Services Association and Primary Care Commissioning in the production of 'When a person dies: guidance for professionals on developing bereavement services.'
The manner in which professionals and volunteers respond to those who are bereaved can have a long term impact on how they grieve, their health and their memories of the individual who has died.
The publication covers the principles of bereavement services, along with bereavement care in the days preceding death, at the time of death and in the days following death. It also includes guidance on workforce and education and the commissioning and quality outcomes of bereavement care.
NHS Trusts, community providers and commissioners will wish to consider the guidance when developing policies and services relating to bereavement.
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
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
This 'how to' guide builds upon the overarching framework set out in The route to success in end of life care - achieving quality in acute hospitals, published in 2010. The route to success highlighted best practice models developed by acute hospital Trusts, providing a comprehensive framework to enable hospitals to deliver high quality care to people at the end of life.
This 'how to' guide aims to help clinicians, managers and directors implement The route to success more effectively, drawing on valuable learning from the NHS Institute for Innovation and Improvement's Productive Ward: Releasing time to care™ series.
This guide contains individual sections that can be worked on in any given order, dependent upon the individual hospital and its current end of life care provisions. These can be downloaded below:
Introduction
Section 1: prepare
Section 2: assess and diagnose
Section 3: plan
Section 4: treat
Section 5: evaluate
Section 6: sustain
Section 7: further resources
Cover
It places emphasis on existing 'enabling' tools and models, which support and follow a person-centred pathway. These are Advance Care Planning, Electronic Palliative Care Co-ordination Systems (EPaCCS), AMBER Care Bundle, Rapid Discharge Home to Die Pathway, and the Liverpool Care Pathway.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
Five priorities for care of the dying personMarie Curie
Dr Bill Noble, Medical Director of Marie Curie Cancer Care, speaks at the end of life sesion with Dr Adam Firth (RCGP Clinical Support Fellow for End of Life Care).
This session was chaired by Dr Peter Nightingale, Marie Curie and RCGP End of life lead at the RCGP Annual Conference, ACC Liverpool, 2-4 October, 2014.
For more information visit: mariecurie.org.uk/rcgp
06 July 2011 - National End of Life Care Programme
The guide highlights the key nursing contributions within the six steps of the end of life care pathway.
It focuses predominantly on how nurses can and do contribute to planned (and unplanned) end of life care for adults in England.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
The document provides guidance for hostel staff on delivering high quality end of life care to homeless individuals. It outlines 6 steps in an end of life care pathway, from initiating discussions as end approaches to care after death. The guidance emphasizes identifying triggers for discussions, developing care plans, coordinating services, and treating individuals with dignity and respect regardless of setting.
End of Life Care in Advanced Kidney Disease:
A Framework for Implementation
Published by NHS Kidney Care,
This document is an important step in
ensuring that people with advanced kidney
disease receive the very best care in the last
years, months and days of their lives. This
framework complements and extends work
already underway at a national level. It builds
on the vision of High Quality for All1 which
requires all strategic health authorities to
produce end of life clinical pathways. This
informed the End of Life Care Strategy2,
which aims to ensure that all adults receive
high quality care at the end of life, regardless
of their age, condition, diagnosis and place
of care.
This document discusses end of life care and provides definitions and guiding principles. It notes that end of life care aims to help those with advanced illnesses live as well as possible until death, through management of pain and other symptoms as well as psychological, social, spiritual and practical support for both patients and families. The document also outlines key policies and guidance related to end of life care in the UK, and discusses considerations around strategic planning, community engagement, and positioning an organization to provide high quality end of life care services.
1. The document discusses end-of-life care for people with learning disabilities and outlines several key publications and policies that have aimed to improve access to quality end-of-life care, including the 2008 End of Life Care Strategy.
2. It notes that people with learning disabilities face health inequities and often have multiple health issues but experience barriers to healthcare and end-of-life care.
3. The document describes a consultation process to map current end-of-life care resources and practices for people with learning disabilities and identify ways to better support staff and allow equitable access to care through established guidelines and frameworks.
This paper presents analysis of a Kent ‘whole population’ dataset, linking wholepopulation demographics with activity and cost data for the population from acute, community, mental health and social care providers. The data helps commissioners to understand the impact of different selections methods for people with ‘very complex’ health and social care needs, particularly in relation to the development of a LTC year of care currency.
This document should be seen alongside the ‘Recovery, Rehabilitation and Reablement – step-by-step guide’ which describes how providers can carry out the audit in their own organisation. Other documents and learning materials This document is part of a suite of learning materials being produced by the LTC Year of Care Commissioning Programme to support the spread and adoption of capitated budgets for people with complex care needs.
BPS DCP SIGOPAC Good Practice Guidance in Demonstrating Quality and Outcomes ...Alex King
This report outlines a rigorous, multidimensional framework for evaluating quality and outcomes in psycho-oncology services, which can be flexibly adapted to local needs and priorities.
It aims to challenge psycho-oncology services to develop and standardise procedures that address the clinical and operational aspects of quality, while maintaining a firm focus on the experiential.
The proposed framework focuses on six key domains of service quality:
- Is this service safe?
- Is this service equitable, while also focused on those most in need?
- Is this service timely and responsive?
- Is this service respectful, collaborative and patient-centred?
- Is this service offering effective interventions?
- Is this service contributing to efficient multidisciplinary care?
To address these domains, psycho-oncology services need to draw on multiple, convergent sources of data, including key performance indicators, activity levels, patient self-report measures, feedback from professional colleagues, etc.
This document provides information about a webinar on the Information Standards for End of Life Care (ISB150) that supports implementation of Electronic Palliative Care Coordination systems (EPaCCS). The webinar will introduce the standard and its core data requirements, how it supports care coordination and choice at end of life. Speakers include representatives from NHS Improving Quality, the Health and Social Care Information Centre, and a nurse leading the Long Term Conditions Programme.
Discussion paper
06 October 2010 - National End of Life Care Programme / Department of Health
This discussion paper focuses on the current context of practices and policies that impact on end of life, including those that need to be explored with people who have a personal health budget.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
Cure care and research in English dementia policyshibley
I set out to make current dementia policy in England open to the public. This is the final talk to be given by me, Dr Shibley Rahman, at BPP Law School this evening, on cure, care and research.
The route to success in end of life care - achieving quality in acute hospitals
20 June 2010 - National End of Life Care Programme
This guide aims to provide practical support for NHS managers and clinicians responsible for delivering end of life care.
It can help trusts re-shape how their staff work with each other, their patients, their community and their social care partners to improve care quality and meet the Quality, Innovation, Productivity and Prevention (QIPP) agenda.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
London Mental Health Crisis Commissioning GuideDavid Covington
The document provides acknowledgements and thanks to various individuals and organizations who contributed to developing standards for commissioning mental health crisis services in London. It recognizes the work of Dr. Seema Sukhwal for a literature review, Vanessa Brunning for organizing a service user consultation, and Stefanie Radford as the lead project manager. Special thanks are given to Rethink Mental Illness, Mind, and NSUN from the third sector for their input. The standards aim to improve access to crisis care, emergency response, treatment quality, and recovery support across London.
Jacquie White, Deputy Director of NHS England Long Term Conditions, Older People & End of Life Care and Dr Eileen Pepler, Academic, Researcher and Consultant in the Canadian Healthcare will discuss how NHS England work in chronic disease is being translated into a Canadian context.
Exploring the potential for using predictive modelling in identifying end of life care needs - 15 February 2013 - National End of Life Care Programme / Whole Systems Partnership
This report, produced in partnership with Whole Systems Partnership, is based on a project which reviewed the literature on predictive modelling, canvassed views and engaged with interested parties to formulate an initial response to the opportunities presented by predictive modelling approaches in identifying people likely to be nearing the end of life.
Predictive modelling involves the interrogation of datasets to inform professional judgement about potential needs. It is hoped that the findings of this report will be used to enable commissioners and providers of services to better understand and meet people's end of life care preferences and wishes, supporting more people to live and die well in their preferred place.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
This Guide for Executives is aimed at senior healthcare leaders. It provides 31 practical tips for leaders
who want to contribute positively to the culture for innovation in their organisations and systems.
A more in-depth practitioners guide, Creating the Culture for Innovation, provides much more
detailed advice and guidance, a host of additional examples, and information about an online staff
survey that can be used to assess, benchmark and understand the culture for innovation.
The Sustainability Model is a diagnostic tool that will identify strengths and
weaknesses in your implementation plan and predict the likelihood of sustainability
for your improvement initiative.
The Sustainability Guide provides practical advice on how you might increase the
likelihood of sustainability for your improvement initiative.
More Related Content
Similar to The route to success in end of life care - achieving quality in prisons and for prisoners
When a person dies: guidance for professionals on developing bereavement services
The National End of Life Care Programme has supported the Bereavement Services Association and Primary Care Commissioning in the production of 'When a person dies: guidance for professionals on developing bereavement services.'
The manner in which professionals and volunteers respond to those who are bereaved can have a long term impact on how they grieve, their health and their memories of the individual who has died.
The publication covers the principles of bereavement services, along with bereavement care in the days preceding death, at the time of death and in the days following death. It also includes guidance on workforce and education and the commissioning and quality outcomes of bereavement care.
NHS Trusts, community providers and commissioners will wish to consider the guidance when developing policies and services relating to bereavement.
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
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
This 'how to' guide builds upon the overarching framework set out in The route to success in end of life care - achieving quality in acute hospitals, published in 2010. The route to success highlighted best practice models developed by acute hospital Trusts, providing a comprehensive framework to enable hospitals to deliver high quality care to people at the end of life.
This 'how to' guide aims to help clinicians, managers and directors implement The route to success more effectively, drawing on valuable learning from the NHS Institute for Innovation and Improvement's Productive Ward: Releasing time to care™ series.
This guide contains individual sections that can be worked on in any given order, dependent upon the individual hospital and its current end of life care provisions. These can be downloaded below:
Introduction
Section 1: prepare
Section 2: assess and diagnose
Section 3: plan
Section 4: treat
Section 5: evaluate
Section 6: sustain
Section 7: further resources
Cover
It places emphasis on existing 'enabling' tools and models, which support and follow a person-centred pathway. These are Advance Care Planning, Electronic Palliative Care Co-ordination Systems (EPaCCS), AMBER Care Bundle, Rapid Discharge Home to Die Pathway, and the Liverpool Care Pathway.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
Five priorities for care of the dying personMarie Curie
Dr Bill Noble, Medical Director of Marie Curie Cancer Care, speaks at the end of life sesion with Dr Adam Firth (RCGP Clinical Support Fellow for End of Life Care).
This session was chaired by Dr Peter Nightingale, Marie Curie and RCGP End of life lead at the RCGP Annual Conference, ACC Liverpool, 2-4 October, 2014.
For more information visit: mariecurie.org.uk/rcgp
06 July 2011 - National End of Life Care Programme
The guide highlights the key nursing contributions within the six steps of the end of life care pathway.
It focuses predominantly on how nurses can and do contribute to planned (and unplanned) end of life care for adults in England.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
The document provides guidance for hostel staff on delivering high quality end of life care to homeless individuals. It outlines 6 steps in an end of life care pathway, from initiating discussions as end approaches to care after death. The guidance emphasizes identifying triggers for discussions, developing care plans, coordinating services, and treating individuals with dignity and respect regardless of setting.
End of Life Care in Advanced Kidney Disease:
A Framework for Implementation
Published by NHS Kidney Care,
This document is an important step in
ensuring that people with advanced kidney
disease receive the very best care in the last
years, months and days of their lives. This
framework complements and extends work
already underway at a national level. It builds
on the vision of High Quality for All1 which
requires all strategic health authorities to
produce end of life clinical pathways. This
informed the End of Life Care Strategy2,
which aims to ensure that all adults receive
high quality care at the end of life, regardless
of their age, condition, diagnosis and place
of care.
This document discusses end of life care and provides definitions and guiding principles. It notes that end of life care aims to help those with advanced illnesses live as well as possible until death, through management of pain and other symptoms as well as psychological, social, spiritual and practical support for both patients and families. The document also outlines key policies and guidance related to end of life care in the UK, and discusses considerations around strategic planning, community engagement, and positioning an organization to provide high quality end of life care services.
1. The document discusses end-of-life care for people with learning disabilities and outlines several key publications and policies that have aimed to improve access to quality end-of-life care, including the 2008 End of Life Care Strategy.
2. It notes that people with learning disabilities face health inequities and often have multiple health issues but experience barriers to healthcare and end-of-life care.
3. The document describes a consultation process to map current end-of-life care resources and practices for people with learning disabilities and identify ways to better support staff and allow equitable access to care through established guidelines and frameworks.
This paper presents analysis of a Kent ‘whole population’ dataset, linking wholepopulation demographics with activity and cost data for the population from acute, community, mental health and social care providers. The data helps commissioners to understand the impact of different selections methods for people with ‘very complex’ health and social care needs, particularly in relation to the development of a LTC year of care currency.
This document should be seen alongside the ‘Recovery, Rehabilitation and Reablement – step-by-step guide’ which describes how providers can carry out the audit in their own organisation. Other documents and learning materials This document is part of a suite of learning materials being produced by the LTC Year of Care Commissioning Programme to support the spread and adoption of capitated budgets for people with complex care needs.
BPS DCP SIGOPAC Good Practice Guidance in Demonstrating Quality and Outcomes ...Alex King
This report outlines a rigorous, multidimensional framework for evaluating quality and outcomes in psycho-oncology services, which can be flexibly adapted to local needs and priorities.
It aims to challenge psycho-oncology services to develop and standardise procedures that address the clinical and operational aspects of quality, while maintaining a firm focus on the experiential.
The proposed framework focuses on six key domains of service quality:
- Is this service safe?
- Is this service equitable, while also focused on those most in need?
- Is this service timely and responsive?
- Is this service respectful, collaborative and patient-centred?
- Is this service offering effective interventions?
- Is this service contributing to efficient multidisciplinary care?
To address these domains, psycho-oncology services need to draw on multiple, convergent sources of data, including key performance indicators, activity levels, patient self-report measures, feedback from professional colleagues, etc.
This document provides information about a webinar on the Information Standards for End of Life Care (ISB150) that supports implementation of Electronic Palliative Care Coordination systems (EPaCCS). The webinar will introduce the standard and its core data requirements, how it supports care coordination and choice at end of life. Speakers include representatives from NHS Improving Quality, the Health and Social Care Information Centre, and a nurse leading the Long Term Conditions Programme.
Discussion paper
06 October 2010 - National End of Life Care Programme / Department of Health
This discussion paper focuses on the current context of practices and policies that impact on end of life, including those that need to be explored with people who have a personal health budget.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
Cure care and research in English dementia policyshibley
I set out to make current dementia policy in England open to the public. This is the final talk to be given by me, Dr Shibley Rahman, at BPP Law School this evening, on cure, care and research.
The route to success in end of life care - achieving quality in acute hospitals
20 June 2010 - National End of Life Care Programme
This guide aims to provide practical support for NHS managers and clinicians responsible for delivering end of life care.
It can help trusts re-shape how their staff work with each other, their patients, their community and their social care partners to improve care quality and meet the Quality, Innovation, Productivity and Prevention (QIPP) agenda.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
London Mental Health Crisis Commissioning GuideDavid Covington
The document provides acknowledgements and thanks to various individuals and organizations who contributed to developing standards for commissioning mental health crisis services in London. It recognizes the work of Dr. Seema Sukhwal for a literature review, Vanessa Brunning for organizing a service user consultation, and Stefanie Radford as the lead project manager. Special thanks are given to Rethink Mental Illness, Mind, and NSUN from the third sector for their input. The standards aim to improve access to crisis care, emergency response, treatment quality, and recovery support across London.
Jacquie White, Deputy Director of NHS England Long Term Conditions, Older People & End of Life Care and Dr Eileen Pepler, Academic, Researcher and Consultant in the Canadian Healthcare will discuss how NHS England work in chronic disease is being translated into a Canadian context.
Exploring the potential for using predictive modelling in identifying end of life care needs - 15 February 2013 - National End of Life Care Programme / Whole Systems Partnership
This report, produced in partnership with Whole Systems Partnership, is based on a project which reviewed the literature on predictive modelling, canvassed views and engaged with interested parties to formulate an initial response to the opportunities presented by predictive modelling approaches in identifying people likely to be nearing the end of life.
Predictive modelling involves the interrogation of datasets to inform professional judgement about potential needs. It is hoped that the findings of this report will be used to enable commissioners and providers of services to better understand and meet people's end of life care preferences and wishes, supporting more people to live and die well in their preferred place.
Publication by the National End of Life Programme which became part of NHS Improving Quality in May 2013
Similar to The route to success in end of life care - achieving quality in prisons and for prisoners (20)
This Guide for Executives is aimed at senior healthcare leaders. It provides 31 practical tips for leaders
who want to contribute positively to the culture for innovation in their organisations and systems.
A more in-depth practitioners guide, Creating the Culture for Innovation, provides much more
detailed advice and guidance, a host of additional examples, and information about an online staff
survey that can be used to assess, benchmark and understand the culture for innovation.
The Sustainability Model is a diagnostic tool that will identify strengths and
weaknesses in your implementation plan and predict the likelihood of sustainability
for your improvement initiative.
The Sustainability Guide provides practical advice on how you might increase the
likelihood of sustainability for your improvement initiative.
The document provides information and guidance for patients on how to take an active role in their recovery process before and after a hospital operation or procedure. It emphasizes the importance of staying physically and mentally active before surgery, eating healthy foods, and making plans for support and transportation at home after being discharged from the hospital. Taking small, achievable steps each day toward recovery goals like walking, showering, and eating can help patients leave the hospital sooner and feel better faster.
This document discusses bringing social movement thinking to healthcare improvement by incorporating principles from successful social movements. It outlines five key principles for creating social movement dynamics within healthcare organizations: see change as a personal mission; frame issues to connect with core values; energize and mobilize individuals; organize for impact; and maintain forward momentum. The document argues that while traditional improvement approaches have had some success, social movement thinking can help deliver deeper, more sustainable changes to better serve patients. It provides several case studies of teams that have applied social movement ideas to spur healthcare improvements.
The 15 Steps Challenge provides a toolkit to help healthcare teams evaluate the quality of patient care from the patient's perspective. A 15 Steps Challenge team conducts ward walkarounds using the toolkit to assess four areas: Welcoming, Safe, Caring and Involving, and Well Organised and Calm. The team then provides feedback to the ward and trust sponsor to identify good practices and areas for improvement. Repeating the Challenge ensures continuous quality improvement by regularly incorporating the patient voice.
This document provides an overview of a toolkit aimed at helping NHS trusts reduce their Caesarean section rates. The toolkit was developed by the NHS Institute for Innovation and Improvement based on visits to maternity services with low C-section rates. It includes self-assessment tools covering key areas like first pregnancies, VBAC, and organizational characteristics. The goal is to help services evaluate their practices and develop action plans to promote normal birth and reduce C-section rates in a safe and sustainable way.
This document provides an introduction to thinking differently and why it is important, especially within the healthcare system. It discusses how thinking differently has led to innovations that have transformed various industries. Within healthcare, thinking differently created the NHS and has led to improvements like keyhole surgery. The document encourages readers to challenge traditional ways of doing things and consider new possibilities, like using interactive TV to book appointments. It argues that thinking differently is needed to achieve reforms and make significant gains in effectiveness and efficiency. Examples are given of projects that emerged from rethinking traditional models of service delivery.
If you are involved in treating patients, managing and/or improving health services or
managing or training those that do, you will understand the importance of providing the
best care possible for all our patients.
Great progress has been made in improving service standards and access and in reducing
waiting times, but there is still some way to go to ensure consistently high standards of
patient care across the NHS.
It is clear that we need to ensure we are getting it right first time, which means better care
and better value through the reduction of waste and errors and the prioritisation of effective
treatments. Quality, innovation, productivity and prevention (QIPP) is the mechanism through
which we can achieve this.
QIPP is about creating an environment in which change and improvement can flourish; it
is about leading differently and in a way that fosters a culture of innovation; and it is
about providing staff with the tools, techniques and support that will enable them to take
ownership of improving quality of care.
The Handbook of Quality and Service Improvement Tools from the NHS Institute brings
together a collection of proven tools, theories and techniques to help NHS staff design and
implement quality improvement projects that do not compromise on the quality and safety of
patient care but rather enhance the patient experience.
The ebd approach (experience based design) is a method of designing better experiences for patients, carers and staff. The approach captures the experiences of those involved in healthcare services. It involves looking at the care journey
and in addition the emotional journey people
experience when they come into contact with a particular pathway or part of the service. Staff work together with patients and carers to firstly understand these experiences and then to improve them.
This guide is an introduction to the ebd approach (experience based design).
This guide and toolkit has been produced as
a result of work that the NHS Institute for
Innovation and Improvement has undertaken in collaboration with NHS organisations and external agencies, using the experience of patients, carers and staff to design better
healthcare services.
- Slit lamp examination (including fundus)
- Perform biometry and focimetry
- Decide appropriateness for surgery
- Perform auto-refraction
- Discuss desired post-operative refractive status
with the patient (including current type of
spectacle correction) to enable the choice of lens
implant
- Perform ECG and blood tests
- Identify 2nd eye surgery where appropriate
Benefits
- reduces duplication of tasks
- reduces waiting time for patients
- frees up nursing time for other duties
- ensures all key tasks are completed in one visit
- improves patient experience
- reduces overall time in clinic
09
The Preferred Priorities for Care (PPC) is a tool that:
1. Facilitates discussions about end of life care wishes and preferences which can then be recorded.
2. Enables communication across care providers for care planning and decisions.
3. Acts as an advance statement if the person loses capacity, allowing their previously expressed wishes to inform best interest decisions about their care.
The PPC records an individual's end of life care preferences but these may change, so current views should take precedence. It is a voluntary and non-binding document but informs best interest decisions if capacity is lost.
The document discusses key principles for designing end-of-life care environments. It notes that the physical environment can directly impact patient experience and the memories of family and caregivers. Design should facilitate privacy, dignity, and respect. Key principles include being fit for purpose, providing comfort and connection to nature, use of natural light and materials, clarity of wayfinding, and enabling patient control and privacy. Improving environmental design can enhance patient and family experience through intuitive wayfinding, access to nature, consideration of heightened senses, provision of informal spaces, and co-located bereavement services. An environmental improvement project requires forming a multidisciplinary team to review needs, develop a plan and budget, and implement high quality design standards.
The Fast Track Tool is used to gain immediate access to funding for individuals who need urgent care packages due to rapidly deteriorating health conditions that may be terminal. It can be completed by nurses or doctors familiar with the patient's needs. The tool must be used when urgent continuing healthcare is required and replaces the regular assessment process. Patient consent is required unless they lack capacity, in which case clinicians make a best interests decision. Evidence of a completed Fast Track Tool is sufficient for eligibility and PCTs must accept and immediately action properly completed tools.
Support Sheet 13: Decisions made in a person's 'Best Interests'
This support sheet outlines the process for making decisions on behalf of someone who lacks capacity.
Support Sheet 12: Mental Capacity Act (2005)
This support sheet outlines the main provisions of the Mental Capacity Act the four tests essential for assessing capacity
Support Sheet 11: Quality Markers for Acute Hospitals
This support sheet outlines the quality markers by which acute hospitals can measure the standard of end of life care they provide.
Support Sheet 7: Models/Tools of Delivery
This support sheet outlines the key elements of
Advance Care Planning (ACP)
Gold Standards Framework (GSF)
Liverpool Care Pathway (LCP)
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
Study Resources:
1. Chapter 42, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
One health condition that is becoming more common day by day is diabetes.
According to research conducted by the National Family Health Survey of India, diabetic cases show a projection which might increase to 10.4% by 2030.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
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In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...
The route to success in end of life care - achieving quality in prisons and for prisoners
1. The route to success
in end of life care – achieving
quality in prisons and for
prisoners
2. A practical guide to implementing high quality
end of life care in prisons
3. Contents
3
Introduction
5
Aim of the guide
6
Background: end of life care within prisons
8
Key considerations
9
End of life care pathway
10 Step 1: Discussions as the end of life approaches
13 Step 2: Assessment, care planning and review
16 Step 3: Co-ordination of care
19 Step 4: Delivery of high quality care in prisons
22 Step 5: Care in the last days of life
25 Step 6: Care after death
28 Other circumstances to consider
31 Next steps
33 Appendix 1: Prison Service Instructions and Orders and
relevant reports and documents
37 Appendix 2: Quality markers for end of life care
38 Resources
38 References and weblinks
40 Websites for further information
41 Glossary of end of life care terminology
4. Introduction
As of March 2010, 85,184 people were being held in prisons in England and
Wales, with around a further 9,400 held in Scottish and Northern Irish prisons.
This figure does not include those in immigration detention and removal
centres. (Data from the Ministry of Justice, the Scottish Government and the
Northern Ireland Prison Service)
Photo courtesy of iD.8 Photography (Quote courtesy of Payne et al, 2009)
3
5. Introduction
It is generally acknowledged that many
prisoners have complex needs, mental health
problems and/or learning disabilities. Often,
this will also be compounded by complicated
family relationships, poor education and, for
some, revolving admissions to the criminal
justice system.
The demand for prison spaces could increase
to nearly 95,000 by 2017 (Prison population
projections 2011-2017 England and Wales,
Ministry of Justice, 2011). As a result, and
due also to changes in sentencing practices,
it is expected that the number of older
prisoners will grow. A 2008 report by HM
chief inspector of prisons recommended a
national strategy for older prisoners which
would provide guidance on age-related issues,
including end of life care services (Older
prisoners in England and Wales: a follow-up to
the 2004 thematic review, HM Inspectorate of
Prisons).
The Prisons and Probation Ombudsman for
England and Wales Annual Report 20082009 similarly noted that “As the average
age of the prison population increases ... , it
seems reasonable to assume that the trend
in natural cause deaths will be upwards.” In
2008-2009 there were 181 deaths in custody,
with 159 of these occurring in prison. Of the
deaths in prison, 96 (60%) were from natural
causes. The most common natural causes of
death were heart attacks and cancer, and
the average age of the deceased was 52 for
men and 44 for women (ibid). A proportion
of these deaths would have been anticipated
and it is reasonable to assume that some of
those in prison could have benefited from
improvements in planning for their end of life
care An evaluation of current end of life care
provision in prisons in Lancashire and Cumbria,
Payne et al, International Observatory on End
of Life Care, Division of Health Research,
Lancaster University, 2009
Therefore it is with this in mind that Carrie
Cannings, Equality Group NOMS notes:
“No-one wants to have to deal with an
Photo courtesy of iD.8 Photography
end of life situation in prison, but with our
aging population, it is likely that most prison
staff will be faced with the need to manage
or be involved in one at some point. It is
important to remember that no-one should
be worried that they have to deal with the
situation on their own. The key to successfully
managing end of life in prison is working
together as a team: officers, governors,
healthcare staff and external and third sector
organisations. Each part contributes on those
areas that fall within their expertise, and
supports the other team members during what
is a difficult time for all. And remember we
have resources such as Employee Support that
can provide a professional service to staff who
may be finding the experience difficult.”
4
6. Background
Aim of the guide
The aim of this publication is to provide
a practical guide to support both prison
and health and social care professionals in
delivering high quality end of life care to
prisoners. The guide aims to complement
Department of Health (DH) and HM Prison
Service guidance and seeks to showcase good
practice examples from across the health and
prison communities in their work to support
prisoners at their end of life.
People approaching the end of their life need
high quality, accessible care if they are to make
genuine choices about how they are cared for
and where they wish to die. Competent and
compassionate care is also critical to allowing
prisoners who become unwell a dignified
death and to offering families support in
bereavement. This care should be of the same
high quality regardless of diagnosis and of
whether the care is carried out at home, in
hospital, in the community or in any other
setting, including prison.
The guide follows the six steps of the end of
life care pathway, beginning with initiating
discussions as end of life approaches and
concluding with care after death.
Each section outlines the relevant steps of
the pathway, questions to ask about the
individual’s care and the practitioner’s and
prison officer’s role in that care. Additional
guidance can be found within the Department
of Health’s End of life care strategy: quality
markers and measures for end of life care
(2009). See appendix 2 for a full list of quality
markers.
5
We also include case studies highlighting best
practice. Forthcoming NICE standards currently
being devised will also be relevant to the
delivery of end of life care in all settings.
It is hoped that the guide will help
practitioners and staff working within prison
health services to make connections across
service boundaries to:
• Identify prisoners approaching the end of
life phase
• Review care planning
• Help to review practice
• Support communication, team working and
learning
• Improve and measure quality.
Core principles for delivery of end
of life care
• Treat individuals with dignity and respect
• Identify and respect people’s preferences
• Provide information and support to families
and carers
• Recognise and respect an individual’s
spiritual and religious needs
• Provide effective pain and symptom
management
• Provide care after death
• Ensure care is patient-centred and
integrated
• Provide a safe comfortable environment for
care.
8. Background: end of life care within prisons
Meanwhile, in 2008, the Department of
Health’s End of life care strategy set out a
blueprint for change and improvement in end
of life care in England over the next 10 years.
Its aim, it said, was “to bring about a step
change in access to high quality care for all
people approaching the end of life. This should
be irrespective of age, gender, ethnicity,
religious belief, disability, sexual orientation,
diagnosis or socioeconomic status. High quality
care should be available wherever the person
may be: at home, in a care home, in hospital,
in a hospice or elsewhere. Implementation of
this strategy should enhance choice, quality,
equality and value for money.”
In the preceding year, the DH issued guidance
on care for older prisoners which also
references the importance of end of life care
(A pathway to care for older offenders: a
toolkit for good practice, 2007). This stressed
the importance of having robust palliative
care policies in place in all prisons. These
publications reflect the fact that end of life
care is increasingly being seen as a priority for
both the Department of Health and HM Prison
Service. It was also identified in the Prisons
and Probation Ombudsman Annual Report
2008-2009 (see also Review of older prisoners’
provisions, P Rich, North East Offender Health
Commissioning Unit, 2009).
However, as this resource guide seeks to show,
there is still much that could be achieved to
share current good practice and ensure all
prisoners receive good end of life care.
“Each prison addresses bereavement issues
differently according to: the type of sentence
committed; date of bereavement; manner
of death; relationship of the prisoner to the
deceased; level of security risk … category of
prison … and particular culture of the prison
in relation to death.” (“This is not just about
death – it’s about how we deal with the rest of
our lives”: coping with bereavement in prison,
M Wilson, Prison Service Journal, Jul 2010)
7
The future of the NHS
The government has set out its intentions for
the future of commissioning in the NHS in the
white paper Equity and excellence: liberating
the NHS (DH, 2010) and the supporting
consultation document Liberating the NHS:
commissioning for patients (DH, 2010).
These state that the NHS Commissioning
Board will assume future responsibility for
the commissioning of prison health services
in England, working closely with clinical
commissioning consortia. This guidance should
be read in the context of these forthcoming
changes.
9. Key considerations
Each prison environment should consider
whether the following processes or policies
have been addressed to support good end of
life care:
• Are prisoners and their environment safe?
This overrides all other principles of care.
Staff must be accountable for the safe
custody of the prisoner and that of the
whole prison environment
• What are the particular security
requirements within that prison for
individuals, visitors, and medical staff
coming in with prescribed medication and
for assessment and review purposes?
• What access is there to required end of
life care/symptom control medications?
Also, what is the policy on using morphine/
syringe drivers in custody?
• Have assessments included the prisoner/
patient’s physical condition as well as
likelihood of violence?
• What are the policies relating to dignity and
privacy for the individual/the environment
management strategy/the use of the open
door policy?
• Does a prison officer always have to be
present during visits/medical treatment and
death?
• What is the agreed communication
process?
• What is the process for considering whether
release is appropriate on compassionate
grounds as per PSO 6300: Release on
temporary licence (HM Prison Service,
2005)?
• What is in place to provide for the needs of
the family/carers? Also, how will these be
identified and recorded?
• Are there measures to aid communication
with those for whom English is not their
first language, those who have speech
and language difficulties and those whose
understanding may be compromised due
to cognitive impairment or a learning
difficulty?
• Is there access to appropriate training,
education and support for prison staff?
Photo courtesy of iD.8 Photography
8
10. End of life care pathway
Step 1
Step 1
Discussions
Discussions
as the end
as the end
of life
of life
approaches
approaches
• Open, honest
communication
• Identifying
triggers for
discussion.
Step 2
Step 2
Assessment,
Assessment,
care planning
care planning
and review
and review
Step 3
Step 3
Step 5
Step 5
Step 6
Step 6
Care in the
Care in the
last days
last days
of life
of life
Care after
Care after
death
death
Step 4
Step 4
Co-ordination
Co-ordination
of care
of care
Delivery of
Delivery of
high quality
high quality
services in
services in
different
different
settings
settings
• High quality
• Strategic co• Agreed care
care provisions
ordination
plan and
in all settings
regular review • Co-ordination
• Acute
of individual
of needs and
hospitals,
patient care
preferences
community,
• Rapid
• Assessing
care homes,
response
needs of
extra care
services.
carers.
housing
hospices,
community
hospitals,
prisons, secure
hospitals and
hostels
• Ambulance
services.
• Identification
of the dying
phase
• Review of
needs and
preferences
for place of
death
• Support for
both patient
and carer
• Recognition
of wishes
regarding
resuscitation
and organ
donation.
Social care
Social
Social care care
Spiritual care services
Spiritual care services
Support for carers and families
Support for carers and families
Information for patients and carers
Information for patients and carers
9
• Recognition that
end of life care
does not stop
at the point of
death
• Timely
verification and
certification of
death or referral
to coroner
• Care and support
of carer and
family, including
emotional
and practical
bereavement
support.
11. Step 1
Discussions as the end of life approaches
“I think the prison service may have felt a bit frightened by what they had to
deal with, especially the officers, not knowing what was going to happen with
a terminally ill patient.” Palliative care nurse*
Enabling people to die in comfort and with
dignity is a core function of the NHS. One of
the key challenges is knowing how and when
to begin a discussion with a prisoner – and
relatives – about what they would wish for as
they near the end of life. Agreement needs to
be reached on when discussions should occur,
who should initiate them and what skills and
competences staff require to take on this role.
Photo courtesy of iD.8 Photography *Quote courtesy of Payne et al, 2009
10
12. Discussions as the end of life approaches
Questions
• Have you identified a key worker or a way
in which the discussions should start?
• How can you identify those in your care
who are approaching the end of life?
• Have you noted triggers which indicate it is
an appropriate time for a discussion? Have
you considered who might support such a
discussion?
• What would help those discussions if
the prisoner has learning disabilities,
sensory needs or if English is not their first
language?
• Is the environment safe and comfortable
and does it offer privacy?
Your role
• Recognise when symptoms have increased
or condition has deteriorated
• Ask yourself the question, “Would I be
surprised if this person were to die in the
next 6-12 months?”
• Take account of recent changes in
circumstances such as the death of a
spouse or a change in family circumstances
outside the prison environment
• Make sure those who need to be are on an
end of life supportive care register
• Select an appropriate time to begin the
discussion process
• Have open and honest discussions about
prognosis and possible realistic future care
options
• Provide any relevant information required,
whether that is about the individual’s
condition, financial situation if appropriate,
or anything else.
Top tips
• Recognise that greater attention and
support may be required for those
prisoners who struggle to communicate
their needs due to dementia, learning
difficulties or other health problems
• Death and dying should not be hidden
from other prisoners, relatives and
carers. Building a trusting relationship
will help facilitate conversations that
may include end of life care
• As a caregiver and/or a prison officer
it is important to recognise how your
own attitude to death and dying may
influence the care you provide and your
ability to talk openly
• Consider how to integrate
conversations into existing activities
and/or assessments (eg, substance use)
or general key worker discussions
• Try to provide private spaces in which
to break bad news or initiate end of life
care discussions
• Ask your manager to find out what
training is available, or contact your
local palliative care team or hospice to
enquire about support and education.
Photo courtesy of iD.8 Photography
11
14. Step 2
Assessment, care planning and review
“Another thing that has been particularly challenging and difficult for me in
the prison is that it takes longer for them to get the medication in when there
is a change of prescription. So when I go in and advise that a drug needs to
be changed or increased on a Wednesday, that might not happen until the
Saturday. It takes them that long to get the drugs, whereas I am used in the
community to advising it and starting it the same day.” Macmillan nurse*
Early assessment of an individual’s needs is
vital to establish their preferences and choices
and identify any areas of unmet need. Too
often an individual’s needs and those of their
family and carers are not adequately assessed.
Holistic assessment needs to cover physical,
psychological, social, spiritual, cultural and,
where appropriate, environmental and
financial needs. This can be more complicated
for those within the prison system, especially if
they have learning difficulties or mental health
needs.
Photo courtesy of iD.8 Photography *Quote courtesy of Payne et al, 2009
13
15. Assessment, care planning and review
Questions
• Has a holistic needs assessment been
carried out?
• Can you initiate the advance care planning
process?
• Have the needs of the carer been
considered?
• How do prison regulations impact on the
outcome of the assessment?
Your role
• Undertake a holistic needs assessment
when the end of life phase has been
identified (see Holistic common assessment
of supportive and palliative care needs for
adults requiring end of life care, NEoLCP,
2010)
• Apply DisDAT (Disability Distress
Assessment Tool) process
• Listen to the individual and carer and
understand what is important to them and
record this
• Introduce advance care planning as a
continuous process as early on as possible
• Assess the individual’s ability to make
decisions. If in doubt, assume capacity in
the first instance and seek appropriate
methods in the case of prisoners who have
learning difficulties or for whom English
is not their first language. Make sure the
Mental Capacity Act (2005) process is used
where there are doubts about capacity
• Identify an individual’s wishes and
preferences about future care
• Record any advance decisions to refuse
treatment in appropriate documentation
• Review care plan and regularly reassess if a
long-term condition is deteriorating
• Communicate information appropriately
(with permission) to relevant people both
inside and outside of the prison
• Identify the main carer or professional
support worker - also taking into account
any close relationships that have formed
whilst in prison
• Respond appropriately to requests for a
carer’s assessment.
Top tips
• If a prisoner makes an advance decision
to refuse life-sustaining treatment
it must be in writing, signed by that
person (or representative) and witnessed
• Holding an open meeting with prisoners
and relatives/significant others can be
a way of raising awareness about the
possibility of expressing personal wishes
and preferences
• Assess the prison environment. If
someone is deteriorating, consider
how that environment may need to
be modified – for instance, in terms of
privacy, wash facilities and stairs
• Assessment may need to be undertaken
in stages to avoid tiring the patient
• Complete a key contact sheet pro forma
- that is, a form held with the prisoner’s
file providing easy access to relevant
information - and keep in a readily
accessible place
• Ensure you hold information about
community services that have been
involved with the prisoner and that they
are contacted where appropriate
Photo courtesy of iD.8 Photography
14
16. Assessment, care planning and review
Case study
Paul, a younger prisoner needing end
of life care
Paul (not his real name) was 39 years old
and was sentenced early in 2009. Shortly
afterwards he was diagnosed with lung
cancer and referred to an oncologist for
chemotherapy.
After undergoing chemotherapy he spent
time recovering at the inpatient unit at a
different prison but was keen to return
to the familiar surroundings of his own
prison. Despite treatment, the tumour
quickly doubled in size; Paul subsequently
had palliative radiotherapy but his
prognosis was poor (6-12 months).
Paul’s care was well managed by the
prison healthcare team but his care choices
were necessarily limited because he was
in prison. He named his home as his
preferred place and did not want to return
to the prison where he had two difficult
post-chemotherapy stays. However, his
application for compassionate release was
turned down and refused again at appeal
because he was expected to survive more
than three months.
The oncologist tailored Paul’s
chemotherapy doses to the prison
environment, he had a daily nurse review
and the same GP visited him every week to
monitor his medication. Other aspects of
his care included:
• Daily medication collected from the
healthcare unit and kept in a safe in his
cell
• The community Macmillan nurse visited
regularly. Paul could also phone her
directly with any medical concerns
15
Photo courtesy of iD.8 Photography
• Family liaison ensured he was supported
by his family, who had open visits and
were allowed to bring him extra food
and clothes
• The prison kitchens met his dietary
needs, providing soft foods as required
• The prison chaplain, his personal officer
and his peer group also continued to
provide emotional support.
Paul died at the end of November 2009.
Although his appeal for compassionate
release had been refused, his prison
governor granted him release on
temporary licence leave and he died at
home.
Case study from An evaluation of current
end of life care provision in prisons in
Lancashire and Cumbria, Payne et al,
International Observatory on End of
Life Care, Division of Health Research,
Lancaster University, 2009
17. Step 3
Co-ordination of care
“We have got a really good link, we have a really good service, the hospice
offers a lot of support – we have been really lucky, we have built up a good
network with them.” Member of prison healthcare staff*
Once a care plan has been agreed it is essential
that all the services the individual prisoner
needs are effectively co-ordinated. This should
cover primary, community and acute health
providers, the local hospice, prison transport
services and social care. A lack of co-ordination
can mean a prisoner’s needs and preferences
are not met. Prisoners should always give
permission for information to be shared with
other services.
Photo courtesy of iD.8 Photography *Quote courtesy of Payne et al, 2009
16
18. Co-ordination of care
Questions
• Is there a communication system in place to
keep all members of the multi-disciplinary
team fully informed and which includes all
services involved in and outside the prison?
This is particularly important if mental
health or learning disability teams have
been involved
• Has a professional key contact been
identified from the community services?
• Can the community services respond
rapidly and appropriately to changes in
circumstances?
• Is there a process to list key contacts for
emergencies or changes to circumstances?
Your role
• Identify individuals on an end of life
supportive care register (if applicable in your
area)
• Ensure communications systems are in place
with all relevant community services
• Appoint a key worker within the prison to
act as the link between services
• Provide, where possible, access to 24/7
advice, care and support
• Provide timely access to relevant equipment
• Inform out-of-hours services (in the prison)
of anticipated care needs
• Inform outside emergency services of
anticipated care needs
• Ensure you know who your key contacts are
across the provider services/voluntary/social
care sectors.
Top tips
• Find out which pharmacies your local
hospice uses. These are more likely to
offer out-of-hours delivery of drugs to
your institution
• Building strong relationships with other
services (for instance, GPs, palliative
care teams and social care) can help you
provide the prisoner with good end of
life care
• Remember: good communication
systems need to work in both directions
• Phone calls between a dying patient
and health professionals or relatives
can maintain contact and resolve some
issues without the need for a visit
• Consider identifying champions – from
prison or hospice – to lead the work
and build links between prisons and the
wider healthcare world.
Photo courtesy of iD.8 Photography
17
19. Co-ordination of care
Case study
HMP Durham prison cluster
The North Durham community palliative
care team has worked in partnership with
staff in HMP Durham prisons cluster over
the last six years to ensure dying prisoners’
wishes are respected wherever possible.
Collaborative working has resulted in:
• Identification of link nurses in each prison
• Access to palliative care education
• Three-monthly palliative care clinical
review meetings.
this year (2011). It has already started to
deliver palliative care distance learning
education and syringe pump training,
identified prison health and discipline
champions and developed a prisoner
working group.
Contact: Dr Lindsay Crack, consultant
in palliative medicine, lindsay.crack@
stcuthbertshospice.com Gill Scott,
Macmillan prison project lead, g.scott3@
nhs.net
The palliative care team works closely
with designated link nurses in the four
Durham prisons and liaises with the
prison authorities to facilitate improved
visitation rights and prompt applications
for compassionate release or discharge
on licence. Joint work is continuing to
develop a resuscitation policy for prisoners
approaching the end of life when death is
expected.
The team has been directly involved with
the clinical care of 24 prisoners. Over half
achieved their preferred place of care at the
end of life and the others have accepted
a compromise. The partnership approach
enabled one prisoner with an incurable
cancer to remain in his preferred place
of care on the wing with other inmates
for as long as possible before transferring
to the prison healthcare wing for closer
medical supervision and one-to-one nursing
support. Finally, at the very end of life, he
was transferred to a local hospice where he
died.
A service improvement pilot project funded
by Macmillan Cancer Support and aimed at
improving the standards in cancer, palliative
and end of life care in prison began earlier
Photo courtesy of iD.8 Photography
18
20. Step 4
Delivery of high quality care in prisons
“We have had a few people that have gone to [the hospice] for short stays.
We have got a policy in place where the governor has excused handcuffs
and officers have gone in civvy clothing so it doesn’t unsettle other patients.
We have had that happen on a few occasions. The symptoms have been
controlled and they come back to us.” Member of prison healthcare staff*
Prisoners, their families and carers may need
access to a complex combination of services
across many different settings. They should
be able to expect the same high level of care
regardless of where they are. Prisoners should
be treated with dignity and respect and given
as much choice as possible about the care they
receive as they approach the end of their lives.
This may mean they end their days in prison,
in familiar surroundings and with those they
know.
Photo courtesy of iD.8 Photography *Quote courtesy of Payne et al, 2009
19
21. Delivery of high quality care in prisons
Questions
• Has an operational policy for the
management of end of life care been
developed within the organisation?
• Can all staff access an appropriate on-going
training programme for end of life care?
• Does the environment offer privacy and
respect for the individual and their family?
• What systems are in place to monitor the
quality of end of life care?
Your role
• Establish or be aware of the operational
policy for implementing end of life care in
your setting
• Ensure all staff are aware of and understand
end of life care core principles and values
• Promote or participate in relevant end of
life care training, including communication
skills, assessment and care planning,
advance care planning, symptom
management and ensuring comfort and
well-being
• Ensure due consideration is given to the
environment in which end of life care and
support is delivered – for example, access to
a quiet room, to specialist equipment and
to facilities for relatives
• Identify key quality measures within
your organisation and the process for
collecting and sharing evidence of service
improvement/complaints
• Use prisoner/patient experience and carer
feedback to support continuous service
improvement.
Top tips
• Don’t forget the role that other
prisoners may be able to play in
the planning and delivery of care,
particularly those who have developed a
close relationship with the person who
is dying
• Staff training needs should include not
only the physical aspects of care but
also psychological and spiritual care
• Help prisoners to maintain the
maximum level of independence, choice
and control for as long as possible
• You could discuss with community
matrons and community urgent care
providers when it would be appropriate
to contact them. Ask for information
and contact numbers
• Consider keeping a small stock of
medications on the prison unit for
anticipatory prescribing purposes similar
to Just in Case boxes (Motor Neurone
Disease Association). Always bear in
mind prison policies about medication
storage
• Consider adapting end of life care tools
such as the Gold Standards Framework
(GSF) and Preferred Priorities for Care
(PPC) specifically for use in the prison
environment.
20
22. Delivery of high quality care in prisons
Case study
Marie Curie Cancer Care guidelines
Marie Curie Cancer Care and County
Durham PCT have worked closely with staff
from the Durham prisons cluster to develop
local guidelines which enable high category
prisoners to be transferred to the Marie
Curie Hospice in Newcastle for end of life
care in accordance with their wishes.
The guidelines include the security
arrangements for transfer from the prison
to the hospice, care and support for the
prisoner in the hospice and arrangements
following death.
Roles and responsibilities are clearly defined
to enable staff to provide the best quality
of care at the end of life while maintaining
appropriate security in the hospice
environment. Prisoners are considered to
be patients first and prisoners second with
an absolute right to the same standard of
care as any other patient.
Photo courtesy of iD.8 Photography
The prison service retains responsibility for
maintaining security during transfer and
throughout a prisoner’s stay at the hospice.
High category prisoners (A and B) are
accompanied at all times by at least two
prison officers.
uniforms while at the hospice and this was
accepted. The prison service agreed to
inform key hospice staff about any specific
additional risk posed by the prisoner and
to conduct a pre-and post-transfer risk
assessment at the hospice.
The guidelines were drawn up by a
working group that included key staff
from the hospice, the prison healthcare
service, the community palliative care team
and the PCT, and involved considerable
negotiation.
Through liaison with the coroner and
prison governors it has also been agreed
that hospice doctors can certify deaths
and nursing staff can undertake care after
death. It is hoped the guidelines will be
adopted elsewhere, enabling more dying
prisoners to choose their preferred place of
care.
The hospice insisted, for example, that
no-one in their care should be handcuffed
and that prison officers should not wear
21
Contact: information@eolc.nhs.uk
23. Step 5
Care in the last days of life
“Normally when we start with an opiate we would go with 12-hourly dosings
but in order to do that we had to get special permission for him to take the
drug onto the wing and initially that caused a lot of angst. [So we had to think]
around how we can do that differently, like looking at drugs that last for 24
hours rather than the 12.” Macmillan nurse*
The point comes when an individual enters
the dying phase. For some this may seem to
happen suddenly and without warning but for
many others it can be a gradual process. It is
vital that those caring for them recognise they
are dying and take the appropriate action.
How someone dies remains a lasting memory
for their relatives and carers as well as the
health, social care and prison staff involved.
Photo courtesy of iD.8 Photography *Quote courtesy of Payne et al, 2009
22
24. Care in the last days of life
Questions
• Are the relevant prison staff and
professionals aware of the changes which
happen during the dying process?
• Are systems in place for involving families
and relatives in discussions as death
approaches?
• Is there a clear communication plan to keep
relevant others informed as the prisoner
becomes less well?
• Do the family have and know visiting rights
and processes during this phase?
• Have any specific wishes or preferences
been identified?
• Has the Liverpool Care Pathway (LCP) or
equivalent pathway been implemented
within your organisation?
• Do you have an open door policy for those
at the end of life whereby cell doors are left
open whenever possible and relatives have
increased access?
Your role
Top tips
• Consider adapting the LCP to
incorporate security issues. Starting on
the LCP can help to trigger a review of
the prisoner’s security status in relation
to medication management and open
door policies
• Where possible, plan to have someone
- a member of staff or a volunteer available to sit with the dying prisoner.
This will provide them with comfort and
reassurance
• Consider ways to support the relatives
who the prisoner wishes to have
present by providing, where possible,
transport, assistance via the Assisted
Prisons Visitors Unit (subject to eligibility
criteria), and emotional support
• Support people with the same respect
you would want for yourself or a
member of your own family.
• Be aware that using an end of life care
pathway does not hasten or postpone
death and that on occasions an individual’s
condition may improve and the pathway
can then be discontinued
• Have open discussions with relatives and
carers to ensure they know what to expect
during the last days of life and can visit
where appropriate
• Ensure, where possible, that an individual’s
wishes about their preferred place of care
and any other stated preferences are met
• Follow a validated integrated care pathway
for the last days of life such as the LCP
• Ensure anticipatory prescribing systems are
in place in advance of need.
Photo courtesy of iD.8 Photography
23
25. Care in the last days of life
Case study
HMP Whatton, Nottinghamshire
Terminally ill inmates at Whatton prison in
Nottinghamshire now have the option of
spending their last days in prison because
of a joint initiative between prison staff
and Nottinghamshire Community Health.
HMP Whatton accommodates 840
category C male offenders. It has an
ageing population with 60% over the age
of 40 and a high rate of cancer.
Significant improvements have now been
made to the accommodation for dying
patients and their visitors. A grant from
Offender Health through the King’s Fund
Enhancing the Healing Environment
programme has financed a purpose-built
end of life care suite attached to the health
centre together with facilities for visiting
families.
Contact: information@eolc.nhs.uk
Those with a terminal diagnosis are now
cared for according to the GSF and will be
placed on the LCP in their final days. They
are able to make advance care plans and
say if they do not want to be resuscitated.
They can also receive visits from their
family in privacy.
Senior practice nurse and palliative care
lead Karen Shaw says the healthcare team
had to overcome concerns from the prison
authorities about introducing palliative
care in a prison environment. Perhaps
most difficult was getting agreement to
house syringe drivers in the prison because
of fears they could be misused. “If we
hadn’t been able to provide that then sadly
the prisoners would have had to leave the
prison to die. But in the end we resolved
this.”
Several patients have died peacefully,
surrounded by their family and with their
pain well controlled, since the new policy
was introduced. This was made possible
by allocating a room on the residential
wing where families can visit terminally ill
patients who are too ill to attend the visits
hall.
Photo courtesy of iD.8 Photography
24
26. Step 6
Care after death
“The general view was that you don’t want to have a death in custody, even
an expected death, as that means post mortems and police involvement. It
was very alien to them and it took a lot of educating of staff to overcome.”
Senior practice nurse, Nottinghamshire
Good end of life care doesn’t stop at the point
of death. When someone dies all staff need to
follow good practice for the care and viewing
of the body as well as being responsive to
family wishes. The support and care provided
Photo courtesy of iD.8 Photography
25
to carers and relatives will help them cope
with their loss and is essential to achieving a
‘good death’. This is also important for staff,
many of whom will have become involved
with the prisoner.
28. Care after death
Case study
HMP Pentonville
Planning and forethought were the keys to
ensuring that the care provided to a dying
prisoner at HMP Pentonville, together with
support to his family afterwards, was as
compassionate and dignified as possible.
The prisoner had decided he wanted to
die in prison partly because the nature of
his crime meant moving to a hospice was
not an option. Together with clinical nurse
specialist colleagues, Carol Bullock, who
is rehabilitation assistant with Islington’s
palliative care team, was called in to
support him in his last weeks.
She pays tribute to the hard work and
flexibility of prison staff. “You might say
that I planted the seeds and watered
them but they were the ones who did the
work.”
She also believes that what happened at
Pentonville is transferable elsewhere. “If
it can work there it can be blueprinted
anywhere at all.”
Contact: information@eolc.nhs.uk
Following discussions with prison staff,
Carol and her colleagues ensured the
prisoner’s family were able to make visits,
even at night, and were there with him
when he eventually died.
They also ensured the normal procedures
for a death in custody – including sealing
the cell and declaring it a crime scene
– were set aside to allow the family to
remain alone with the body before it was
then taken to the local hospital mortuary.
Carol discussed in advance what was likely
to happen with the prison wing manager,
who then informed both CID and the
coroner. As a result the prison was given
permission to circumvent the normal
guidelines.
Photo courtesy of iD.8 Photography
“All the work was done beforehand”,
explains Carol. “It meant a priest gave the
prisoner a small blessing at the end of his
life and the family were able to sit with the
body after he had died. The family were
so grateful for the way everything was
handled.”
27
31. Other circumstances to consider
Case study
Visiting a dying relative
The following case study illustrates
what can happen when insufficient
thought and flexibility is involved in
planning an end of life care event.
There is usually only one chance to get
this right – how can we contribute?
More thought needs to be given to the
treatment of prisoners who have a relative
dying in the community, says Heather Joy,
modern matron for adults services and
modernisation with Hull City Health Care
Partnership.
Until recently, Heather was a member of
the palliative care team working with a
prison in the north. She relates the story of
a man, in prison for a very short sentence,
whose son was in a serious accident and
taken to intensive care.
This helped to resolve some of his
immediate distress. “In the end he almost
came to accept it but it was an awful
time for him and many of the staff”, says
Heather.
She feels the prison system needs to be
more flexible when dealing with end of life
care issues like this. “There definitely can’t
be a one-size-fits-all approach, it needs to
be far more holistic”, she says.
“I know prison orders and instructions
guide security staff. But unless there is
far closer working between health care
departments and the prison I don’t think
this is going to move on.”
Contact: information@eolc.nhs.uk
The prison authorities allowed the father
to visit his son in hospital – although he
remained in handcuffs – but 48 hours later
the hospital called to say that tests showed
the son was brain dead.
However, prison rules only allowed
prisoners a single visit on compassionate
grounds so the father was not allowed to
be with his son when the ventilator was
turned off.
The prisoner was extremely angry and
upset and had to be placed on suicide
watch for the following two days. He was
also given full access to his personal officer
and at a later stage was able to talk to a
prison listener about his experiences.
Photo courtesy of iD.8 Photography
30
32. Next steps
In the current economic climate and with
changes planned to how health care will be
commissioned in the future, this is a highly
appropriate time to consider how good
quality end of life care is commissioned and
delivered within the prison environment.
The NHS Commissioning Board and clinical
commissioning consortia will need to know and
understand what good end of life care should
look like in a prison environment. There is good
practice out there and now is the time to share
this to ensure each prison and their healthcare
commissioner develops a model that works
well for them in their locality.
It will also be vital to offer staff support at a
time when they should be facing anxieties of
their own.
The tensions between the need to provide care
and the need to maintain security will always
be there in a prison environment. But staff
must never lose sight of the prisoner’s needs
and individuality. Preserving a prisoner’s dignity
and choice is never more important than at the
end of life.
This applies to a range of issues. When
managing visits to a terminally ill prisoner,
for example, staff need to ask themselves:
• How can I facilitate visits from family, friends
and fellow prisoners in the most humane
way?
• Does the cell door need to be locked at all
times?
avoid unnecessary and reduce often upsetting
bureaucracy.
In no circumstances should the guidance be
applied in a mechanistic way but rather in
a manner that demonstrates that death is
normal and shows the human face of death,
even in prison. This will include dealing with
the deceased, family, prison staff, health and
social care staff and other prisoners. It will also
cover the necessary legal processes that must
be followed. The care planning must ensure
that care, support and any further emotional
and practical bereavement support continue as
required.
Other issues that staff will need to address
in the immediate aftermath of a death are:
• Contacting next of kin
• Coroner’s inquest and certification
• Dealing with the prisoner’s property and
valuables
• Providing bereavement support.
Above all, prison and healthcare staff need
to remember that the overall aim of end of
life care is, in the words of the End of life
care strategy (DH, 2008), to “enhance choice,
quality, equality and value for money”. This
care should be made available “wherever the
person may be”, as appropriate to the need to
balance security considerations.
Similar considerations apply to the death
of a prisoner in custody. PSO 2710: Follow
up to deaths in custody (HM Prison Service,
2007) sets out specific requirements relating
to a death in custody which all staff have to
follow, often in conjunction with particular
local policies. In some circumstances it may be
appropriate to treat the death of someone with
a terminal illness as an expected death and so
31
Photo courtesy of iD.8 Photography
34. Appendix 1
Review of relevant documents
Reports and policy documents
Policy context and background
End of life care in prisons has been affected in
recent years by specific policy initiatives. These
include the responsibility for prison healthcare
being transferred (from 2004) to the NHS, and,
in 2008, the publication of the Department of
Health’s national end of life care strategy.
The End of life care strategy (DH, 2008) sets
out a ten year plan for implementing end
of life care (EoLC) in all settings. Its contents
explicitly extend to prisons and secure hospitals
and, in a section dedicated to care in these
environments, it states “To support improved
end of life care for prisoners, the Department
of Health and the Prison Service are working
together to ensure that the principles, as set
out in this strategy, are applied to prisoners.”
See:
• Review of older prisoners’ provisions,
P Rich, North East Offender Health
Commissioning Unit, 2009
• An evaluation of current end of life care
provision in prisons in Lancashire and
Cumbria, Payne et al, International
Observatory on End of Life Care, Division
of Health Research, Lancaster University,
2009
• Care or custody? An evaluation of palliative
care in prisons in North West England,
Turner et al, Palliative Medicine, Jan 2011
33
Chronological review of policy
development
March 2001: National service framework
for older people (DH)
A ten year programme of action and reform
to address the needs of older people, with
standards applied whether an older person
is being cared for at home, in a residential
setting, or in a hospital.
The NSF standards identified specific actions in
relation to the eight standards focusing on:
• rooting out age discrimination
• providing person centred care
• promoting older people’s health and
independence.
April 2001 PSI 21/2001: National service
framework for older people (HMPS)
PSI 21/2001 drew the NSF for older people to
the attention of governing governors within
HM Prison Service. The PSI required a copy
of the NSF to be retained within the health
care centre and that the PSI be brought to
the attention of the establishment’s senior
probation officer, senior officers responsible
for the supervision of resettlement services,
and personal officers involved in sentence
planning.
The PSI identified the specific reference
to older people in prison in the NSF and
emphasised the need for:
• An integrated system of care
• Single needs based assessment
• Resettlement planning to involve partner
organisations including social care and
health
• Liaison with social services: district of
residence issues
• Development of partnerships with local
health and social services to ensure older
prisoners with health and social care needs
get full access to services.
35. Appendix 1
2004: “No problems – old and quiet”:
older prisoners in England and Wales (HM
Inspectorate of Prisons)
In 2004, HM chief inspector of prisons
published a thematic review of the treatment
and conditions of the growing number of
older prisoners in England and Wales.
This report highlighted the lack of progress in
the development of partnerships between the
NHS and the prison service to meet the health
and social care needs of older prisoners.
The report also noted that while the Disability
Discrimination Act 1995 had applied to prisons
since October 2004 and required them to take
all reasonable steps to ensure that prisoners
with disabilities can access services, few
prisons were reaching the standards required
by the legislation and guidance. HM Prison
Service subsequently issued orders setting out
the steps prisons should take, including PSO
2855: Prisoners with disabilities, HMPS, 2008
and PSI 32/2011: Ensuring equality, HMPS
2011.
April 2005: Disability Discrimination Act
2005 (DDA)
The 2005 DDA Extended the requirements
of the Disability Discrimination Act 1995
placing a duty upon public bodies, including
prisons, to review the impact of all policies, to
promote equality of opportunity, to eliminate
harassment and to promote positive attitudes
to people with disabilities.
Jan 2006: Our health our care our say: a
new direction for community services (DH,
2006)
Health and social care services are moving
towards personalisation in response to this
white paper.
April 2008: PSO 2855: Prisoners with
disabilities
PSO 2855 detailed the overarching policy for
the handling of disabled offenders in custody.
The PSO also includes recommendations
to encourage the development of good
practice towards prisoners with disabilities,
and guidance on areas that establishments
may wish to consider when drawing up
their establishment action plan. (See also PSI
32/2011: Ensuring equality)
2008: Doing time: the experiences and
needs of older people in prison (Prison
Reform Trust)
This report was launched at Wandsworth
prison and called for strengthened joined-up
working between the prison and probation
services and the Department of Health.
June 2008: Older prisoners in England and
Wales: a follow-up to the 2004 thematic
review, (HM Inspectorate of Prisons)
This was a follow-up report to the
Inspectorate’s 2004 thematic review of older
prisoners in England and Wales (“No problems
– old and quiet”: older prisoners in England
and Wales). The 2004 report noted that
the National Offender Management Service
(NOMS) still had no national strategy for older
prisoners, and their needs were too often not
met.
It highlighted the lack of mandatory national
and local standards, and the gap between
the provision for older prisoners and the
government’s national strategy for an ageing
population.
The 2008 follow up report on older prisoners
recommends a national strategy, supported by
national and local standards, which “would
provide central guidance to prisons on ...
age-related issues [including] ... end of life
services.”
December 2008: Secretary of state report
on disability equality: health and care
services (DH)
This report by the secretary of state for health
identified that the medical and clinical care
of older prisoners is age dependent mainly in
relation to the management of their chronic
conditions such as type 2 diabetes, some
34
36. Appendix 1
cancers, and cardiovascular disease. Older
prisoners are also likely to have greater health
and social care needs due to the faster onset
of age-related disabilities from living in a
custodial setting. The continuity of their care
is an essential element of its overall quality;
this is challenged as people move into and
between prisons, are managed across NHS
and social care sectors, and are released to the
community, and also in relation to ensuring
care delivery at different times of the day.
April 2009: The Bradley report: Lord
Bradley’s review of people with mental
health problems or learning disabilities in
the criminal justice system (DH)
This was the report of the independent review
into the diversion of offenders with mental
health problems or learning disabilities away
from prison as appropriate. A national delivery
plan building on The Bradley report was
published later in the same year (Improving
health, supporting justice: the national
delivery plan of the health and criminal justice
programme board, DH, 2009). The coalition
government has subsequently accepted the
direction set out in The Bradley report and are
taking its recommendations forward via the
cross-government Health and Criminal Justice
Programme.
Prison Service Orders (PSOs) and Prison
Service Instructions (PSIs)
PSOs and PSIs (Prison Service Instructions) are
documents which outline the rules, regulations
and guidelines by which prisons are run.
Prison Service Orders (PSOs)
These were issued until 31 July 2009. They
were mandatory instructions with no expiry
date and remained in force until cancelled.
Existing PSOs will remain in force until
replaced.
Prison Service Instructions (PSIs)
From 1 August 2009, all prison service
operating instructions are published as PSIs.
They have a fixed expiry date. Prior to 1
35
August 2009, PSIs were issued to convey
short-term instructions or amendments to
PSOs and had a maximum validity of 12
months.
The following PSOs are concerned with end of
life care in prisons. These and all other PSOs
which are currently in force are available at
http://www.justice.gov.uk/guidance/prisonprobation-and-rehabilitation/psipso/psos.htm
PSO 3100: Clinical governance – quality in
prison healthcare (HMPS, 2003)
Although it makes no reference to end
of life or palliative care, this PSO sets out
requirements for governors to ensure that
arrangements are being made for clinical
governance in prison health care. Governors
are not responsible for setting up the detailed
arrangements for clinical governance – this
falls to the clinical governance lead and health
care team – but are accountable for ensuring
that the agenda is taken forward. This PSO
was published before the transfer of prison
healthcare responsibilities to the NHS, and
prior to the publication of the End of life care
strategy (DH, 2008).
PSO 3050: Continuity of healthcare for
prisoners (HMPS, 2006)
This PSO contains guidance to improve the
continuity of healthcare received by prisoners.
It includes guidance on reception, transfer and
discharge of prisoners, with particular focus on
those with ongoing health needs. It also sets
out clinical management of outpatient escorts
and NHS inpatient episodes.
PSO 2710: Follow up to deaths in custody
(HMPS, 2007)
This PSO contains instructions on action
to be taken following a death in custody.
It covers the immediate actions required;
notifications; family, staff and prisoner needs;
legal issues and investigations. All deaths in
prisons are subject to a police investigation;
an investigation by the prisons and probation
ombudsman; and a coroner’s inquest before a
jury.
37. Appendix 1
PSO 6000: Parole release and recall (HMPS,
2005)
Sets out procedures for permanent early
release on licence of all prisoners on
compassionate grounds. Before supporting an
application for early release the governor must
consider whether the prisoner’s needs can
be met by temporary release, for example on
compassionate licence. (See PSO 6300 below.)
PSO 6300: Release on temporary licence
(HMPS, 2005)
PSIs issued from 2010 onwards are available
at http://www.justice.gov.uk/guidance/prisonprobation-and-rehabilitation/psipso/psis.htm.
The following PSI is also relevant to end of life
care:
PSI 31/2008: Allocation of prisoners with
disabilities (HMPS, 2008)
This PSI introduces a number of additional
measures to ensure that prisoners with
disabilities are allocated to appropriate
accommodation as soon as possible after
reception and on recategorisation.
This is not an exhaustive list of all PSOs and
PSIs. A full list can be found at http://www.
justice.gov.uk/guidance/prison-probation-andrehabilitation/psipso/index.htm.
A search for further relevant policy and
guidance documents brought little that relates
directly to end of life care in prisons.
36
38. Appendix 2
Quality markers for end of life care
(End of life care strategy: quality markers and
measures for end of life care, Department of
Health, 2009)
1. Have an action plan for the delivery of high
quality end of life care, which encompasses
patients with all diagnoses, and is reviewed
for impact and progress.
2. Institute effective mechanisms to identify
those who are approaching the end of life.
3. Ensure that people approaching the end of
life are offered a care plan.
4. Ensure that individuals’ preferences and
choices, when they wish to express them,
are documented and communicated to
appropriate professionals.
5. Ensure that the needs of carers are
appropriately assessed and recorded
through a carer’s assessment.
6. Have mechanisms in place to ensure that
care for individuals is coordinated across
organisational boundaries 24/7.
7. Have essential services available and
accessible 24/7 to all those approaching
the end of life who need them.
8. Be aware of end of life care training
opportunities and enable relevant
workers to access or attend appropriate
programmes dependent on their needs.
9. Adopt a standardised approach (Liverpool
Care Pathway or equivalent) to care for
people in the last days of life.
10. Monitor the quality and outputs of end of
life care and submit relevant information
for local and national audits.
37
39. Resources
Resources
References and weblinks
Suicide and self-harm in prison service establishments in England and Wales, HM Inspectorate of
Prisons, 1990
Older prisoners in England and Wales: a follow-up to the 2004 thematic review, HM Inspectorate
of Prisons, 2008
Annual Report 2008-2009, Prisons and Probation Ombudsman for England and Wales, 2009
Review of older prisoners’ provisions, P Rich, North East Offender Health Commissioning Unit,
2009
An evaluation of current end of life care provision in prisons in Lancashire and Cumbria,
Payne et al, International Observatory on End of Life Care, Division of Health Research,
Lancaster University, 2009
Care or custody? An evaluation of palliative care in prisons in North West England, Turner et al,
Palliative Medicine, Jan 2011
Care and the prison officer: beyond ‘turnkeys’ and ‘care bears’, S Tait, Prison Service Journal,
Nov 2008
“This is not just about death – it’s about how we deal with the rest of our lives”: coping with
bereavement in prison, M Wilson, Prison Service Journal, Jul 2010
Common core competences and principles for health and social care workers working with
adults at the end of life, NEoLCP/Skills for Health/Skills for Care/Department of Health, 2009
Carers at the heart of 21st century families and communities: a caring system on your side, a life
of your own, DH, 2008
Preferred Priorities for Care (PPC), National End of Life Care Programme (NEoLCP), 2007
Capacity, care planning and advance care planning in life limiting illness: a guide for health and
social care staff, NEoLCP, May 2011
Advance decisions to refuse treatment: a guide for health and social care professionals, NEoLCP/
National Council for Palliative Care, 2008
Mental Capacity Act (2005) code of practice, Department for Constitutional Affairs, 2007
38
40. Resources
Planning for your future care: a guide, NEoLCP/National Council for Palliative Care/University
of Nottingham, 2009
Making a will (Directgov guidance on wills including links to Citizens Advice Bureau guide to
making a will and Age UK fact sheet)
End of life care strategy: quality markers and measures for end of life care, DH, 2009
Out-of-hours toolkit, Macmillan Learn Zone (online learning resources for professionals)
Gold Standards Framework (GSF)
The Liverpool Care Pathway for the Dying Patient (LCP)
What to do after a death (Directgov guidance)
National end of life care strategy: promoting high quality care for all adults at the end of
life, DH, 2008
No one knows: offenders with learning difficulties and learning disabilities:the prevalence
and associated needs of offenders with learning difficulties and learning disabilities,
N Loucks, Prison Reform Trust, 2007
People with learning disabilities as offenders or alleged offenders in the UK criminal justice
system, G Murphy/I Clare, Journal of the Royal Society of Medicine, Apr 1998
39
41. Resources
Websites for further information
National End of Life Care Programme
http://www.endoflifecareforadults.nhs.uk
National Council for Palliative Care
www.ncpc.org.uk
Marie Curie Cancer Care
www.mariecurie.org.uk
Help the Hospices
www.helpthehospices.org.uk
The King’s Fund
www.kingsfund.org.uk
Gold Standards Framework
http://www.goldstandardsframework.nhs.uk
Liverpool Care Pathway for the Dying Patient (LCP)
http://www.liv.ac.uk/mcpcil/liverpool-care-pathway
Ministry of Justice prison and probation statistics and
data for England and Wales
http://www.justice.gov.uk/publications/statistics-anddata/prisons-and-probation/index.htm
The Scottish Government prison population statistics
http://scotland.gov.uk/Topics/Statistics/Browse/CrimeJustice/TrendPris
The Northern Ireland Prison Service population statistics
http://www.niprisonservice.gov.uk/module.cfm/opt/8/
area/Population%20Report/page/population/
40
42. Resources
Glossary of end of life care
terminology
Advance care plan: This is the document
which arises as a result of the advance care
planning (ACP) process, which is described
as ”a process of discussion between an
individual and their care provider irrespective
of discipline. The difference between ACP
and more general planning is that the
process of ACP is to make clear a person’s
wishes and will usually take place in the
context of an anticipated deterioration of the
individual’s condition” (Advance care planning
(Support sheet 3), NEoLCP, 2010). This
document should be regularly reviewed and
communicated to key persons involved in the
individual’s end of life care.
Advance decision to refuse treatment
(ADRT): Individuals cannot demand that they
receive specific treatments but have the right
to refuse them. An advance decision to refuse
treatment (previously known as a living will
or advance directive) is a decision you can
make to refuse a specific medical treatment
in whatever circumstances you specify. This
can include the choice to refuse treatment
even if doing so might put your life at risk.
The advance decision to refuse treatment
will not be used if you are able to make your
own choices at the time that the treatment
is needed and offered. The Mental Capacity
Act (2005) lays out the ways in which these
decisions must be communicated.
Do not attempt resuscitation (DNAR): A do
not resuscitate document, often called a living
will, is a binding legal document that states
that resuscitation should not be carried out in
any of the following circumstances:
• Where it would be considered medically
‘futile’. Eg, where someone has
experienced a cardiac arrest and is likely to
have another one irrespective of treatment.
In this situation the person need not have a
document but medical staff may have made
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that decision in advance and documented
this within the patient’s notes
• Where the person has an advance directive
which states that they do not wish to be
resuscitated in the particular situation
which they are currently experiencing. Eg,
they have advanced cancer or advanced
dementia and a life-threatening infection
• Where someone entitled to make decisions
on behalf of the patient by holding a health
focused power of attorney for them decides
that the patient would not wish to be
resuscitated in the current situation.
Gold Standards Framework (GSF): The Gold
Standards Framework is a systematic evidencebased approach to optimising the care for
patients nearing the end of life delivered
by general health and social care staff. It is
concerned with helping people to live well
until the end of life and includes care in the
final years of life for people with any end
stage illness in any setting.
GSF improves the quality, co-ordination and
organisation of care in primary care, care
homes and acute hospitals. This enables more
patients to receive the type of care they want,
in their preferred place, with greater cost
efficiency through reduced hospitalisation.
Independent mental capacity advocate
(IMCA): The Mental Capacity Act (2005)
places a responsibility on local authorities
to ensure that people who are assessed as
lacking the mental capacity have access to an
independent advocate when they are having
decisions made about them relating to:
• Serious medical treatment (SMT)
• Changes of NHS accommodation for 28
days or more
• Change of local authority accommodation
for more than 8 weeks.
People can also access IMCA support in
accommodation reviews and safeguarding
adults situations or when they have no family
or friends to represent them.
43. Resources
IMCAs meet with the person and try to assist
them in communicating and being as involved
as possible in the decision making process. The
IMCAs represent the wishes and feelings of
the person and will consult with other people.
IMCAs check that those working with the
person adhere to the main principles of the
Mental Capacity Act and act as a safeguard for
the person’s rights.
IMCAs provide the decision maker with
a written pre-decision report, making
recommendations, and will visit the person
again after the decision has been made and
provide a written post-decision report. IMCAs
will challenge decisions if necessary.
The Liverpool Care Pathway (LCP): The
LCP is an integrated care pathway that is used
at the bedside to drive up sustained quality
of life for the dying patient in the last hours
and days of life. It is a means to transfer the
best quality for care of the dying from the
hospice movement into other clinical areas, so
that wherever the person is dying there can
be an equitable model of care. The LCP has
been implemented into hospitals, care homes,
individuals’ own homes/ communities, and
hospices. It is recommended as a best practice
model, most recently by the Department of
Health in the UK.
Preferred Priorities for Care (PPC): This
patient held document was designed to
facilitate patient choice in relation to end of
life issues. Through good communication
and by documenting their choices, both
patient and carers become empowered
through the sharing of this information with
all professionals involved in their care. The
PPC document provides the opportunity to
discuss difficult issues that may not otherwise
be addressed (to the detriment of patient
care). The explicit recording of patients/carers
wishes can form the basis of care planning in
multi-disciplinary teams and other services,
minimising inappropriate admissions and
interventions.
The PPC also records services available, services
being accessed and reasons for changes in
the care trajectory. PPC is a process which
facilitates service review, further empowering
professionals to negotiate service requirements
on behalf of patients and becoming an
integral part of service commissioning and
design.
Person centred planning: Person centred
planning is a process of life planning for
individuals based on the principles of inclusion
and the social model of disability. In person
centred planning the process, as well as the
product, is owned and controlled by the
person (and sometimes their closest family
and friends). As there are no prescribed
forms, tick boxes or checklists, the resulting
plan of support is totally individual. It creates
a comprehensive portrait of who the person
is and what they want to do with their life
and brings together all of the people who
are important to the person including family,
friends, neighbours, support workers and
other professionals involved in their lives.
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