Abstract
Background:
An ageing prison population with complex health needs combined with punitive sentencing practices means palliative care for incarcerated individuals is increasingly important. However, there is limited evidence regarding the models of care delivery in high-income countries, and their associated challenges and benefits.
Aim:
To develop a typology of models of palliative care provision for incarcerated individuals, synthesise evidence of their outcomes and describe facilitators of and challenges in delivering different models of palliative and end-of-life care in prisons.
Design:
Scoping review following Arksey and O’Malley, with narrative synthesis. The protocol was registered prospectively (reviewregistry1260).
Data sources:
MEDLINE, EMBASE, CINAHL, PsycINFO, the Social Sciences Citation Index and grey literature were searched on 15th March 2023. The Mixed Methods Appraisal Tool (MMAT) was used for quality appraisal.
Results:
A total of 16,865 records were screened; 22 peer-reviewed articles and 18 grey literature sources met the inclusion criteria. Three models were identified: Embedded Hospice, Outsourcing Care and Community Collaboration. The Embedded Hospice model shows potential benefits for patients and prisons. Outsourcing Care may miss opportunities for comprehensive care. Collaborative Care relies on proactive prison-community relationships that could be formalised for improvement. Psychosocial and bereavement needs of those dying in prison and their caregivers lack sufficient documentation.
Conclusion:
Further research is needed to evaluate prison hospice costs and examine how prison hospices impact compassionate release usage. Beyond the USA, policies might formalise care pathways and recognise best practices. Further investigation to address psychosocial needs of people in prison with life-limiting illnesses and post-death bereavement support is required.
The ageing prison population is growing worldwide.
Access to quality palliative care for people in prison is a pressing requirement.
There are significant variations in how palliative care is delivered for people in prison across high-income countries.
We identified a typology of three models of care delivery for people in prison in high-income countries: (1) Embedded hospice model, typified by an interdisciplinary team and volunteer caregivers providing care on-site; (2) Outsourcing Care model, in which end-of-life care is provided outside the prison; (3) Collaborative community model, which involves prisons engagement with other healthcare facilities or practitioners.
Embedded hospice models in the USA are prevalent and demonstrate promising evidence for enhancing the care experience for recipients and peer caregivers. Chaplains, social workers and peer caregivers provide psychosocial support, yet documented assessment and strategies for managing the distinctive needs of this group and their families are lacking, despite their acknowledged complexity.
Local policies should formalise pathways between community palliative care providers and prisons, emphasise flexible visiting and consider expanding the definition of ‘family’ to include fellow individuals in prison.
Prioritising consultations with stakeholders at the national governmental level on sentencing practices for older people in prison is essential.
Frameworks such as the UK’s Dying Well in Custody Charter can support national quality standards but require robust implementation and monitoring.
Introduction
Prison populations in many high-income countries are growing, due to population ageing and increasingly punitive sentencing policies.1,2 Dedicated palliative care provision in prisons has become a pressing requirement; however, marked variability in models of care between high-income countries hinders meaningful comparison and the identification and implementation of best practice. 1
People in prison deserve equivalent access to healthcare as the general population, and barriers to care delivery can be considered a human rights issue.2,3 Initial studies on palliative care in prisons worldwide highlight gaps in current provision and a lack of research evidence to inform practice.3 –7 Services have developed at vastly different rates, both between high-income countries and within.1,8 Inequitable provisions for people in prison with life-limiting illnesses, who are often older, with multimorbidity and frailty, coupled with stringent early-release policies, continue to prevail. 1 Countries differ significantly in compassionate early-release policies. Common elements considered for granting early release include offence type, reoffending risk and suitability for transfer to a non-prison setting. In France, a person is temporarily moved to hospital but will return if they recover, whereas in the U.S.A., compassionate release allows those in prison to seek early release for severe health issues including age-related conditions, with medical parole employed as the primary mechanism across states. 1 Advocacy for compassionate release is in tension with a prevailing punitive approach that limits access to end-of-life care. This, combined with a lack of comprehensive reporting and appeals processes, has hindered evidence-based reforms.9,10
This study aimed to identify and categorise the different palliative and end-of-life care delivery mechanisms for people in prison across high-income countries, using a scoping methodology. We synthesised evidence from academic and grey literature, comprehensively delineating prison palliative care models in high-income countries to identify and share innovative practices and determine knowledge gaps.
The review builds on and extends previous research that defined prison hospice characteristics within the USA and examined the challenges of implementing community hospice standards within prisons, from a range of stakeholder perspectives,9,10 but did not delineate different models of care. This paper contributes to existing literature by offering a typology derived from international studies, broadening the predominantly USA-focussed evidence base.
Previous reviews were either limited to the USA and the UK,11 –14 or excluded grey literature.3,5 Independent, third sector and charity organisations work extensively in the prison sector, so the inclusion of grey literature is essential to reflect current practice. The European Association of Palliative Care Task Force recently conducted a comprehensive mapping survey of palliative care within prison settings. 1 This survey highlighted the importance of comparative analyses of care delivery approaches such as that reported here.
Methods
We followed the five stages of Arksey and O’Malley’s scoping review methodology: specify the research question, identify relevant literature, select studies, map the data and synthesise the results. 15 This approach is appropriate when evidence is emerging and disparate, 15 and when attempting a thorough overview of the literature. 16
Narrative synthesis was used to address step five in of Arksey and O’Malley’s methodology, the collation and summary of the data. Narrative synthesis was selected owing to the heterogeneity of included studies and grey literature. We followed Popay et al’s. 17 approach, involving three iterative stages (developing a preliminary synthesis, exploring relationships within and between studies, assessing the robustness of the synthesis).
The review protocol was devised and reported according to the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews (PRISMA- SCR), 18 prospectively registered in the Research Registry (Unique ID number: reviewregistry1260) and published open access. 19
Eligibility criteria
The Setting, Perspective, Intervention, Comparison, Evaluation (SPICE) framework was used to frame the research question due to its applicability in broader evaluations, that encompass setting and stakeholder perspectives. 17
Inclusion and exclusion criteria are summarised in Table 1.
Inclusion and exclusion criteria for study selection.
Search strategy
In collaboration with a subject information specialist, the following databases were identified and searched: MEDLINE, EMBASE, CINAHL, PsycINFO and the Social Sciences Citation Index. The Medline search strategy (Table 2) was adapted for other databases (see Supplemental Material Files). All databases were searched on 15th March 2023 from 1st January 2000 to date, with results limited to the year 2000 onwards to ensure relevance to the current regulatory and policy context.
Sources of grey literature.
The search results were collated and de-duplicated (EG) in Covidence. 20
Grey literature
The inclusion of grey literature is recognised as a key component of a comprehensive review process,21 –27 but scoping reviews often lack detailed search strategies for grey literature, hindering replicability. 21
In this study, grey literature was collected by searching relevant websites and databases, including ProQuest and Google. Table 2 includes all websites/databases searched. Subject-matter experts were consulted to help design the search strategy and identify any key material (see Acknowledgements).
Grey literature searches utilised combinations of the most common academic database keywords.
As of November 2020, 77 countries were classified as high-income by the World Bank. 19 Following preliminary searches that suggested potential research activity, grey literature published in English was sought from the USA, Germany, UK, France, Canada, Australia, Netherlands, Sweden, Switzerland, Norway, Ireland, New Zealand and Iceland. A country qualifier was used in Google searches where feasible (e.g. ‘site:.au’ when searching for papers published in Australia). Not all countries have a qualifier; in this instance the advanced search in Google was used and the region-limiter function applied. Due to limitations in funding and time, the search was limited to the first four pages of Google results.
Selection process
Titles and abstracts of identified records were screened by the primary researcher, with a second researcher independently screening a random 25% of the results. Any discrepancies were discussed within the research team. Study authors were contacted for additional information or to obtain full datasets where needed.
Data extraction
Full-text articles were imported into Covidence for data extraction using a piloted template. The pre-piloted data extraction template (see Supplemental Material File) captured study design, country, information on care delivery (including providers, care settings, consideration of social/psychological/spiritual needs, admission criteria, training provided to staff and volunteers, multidisciplinary collaboration, older prisoner provision, interventions, prison policies, family rights, bereavement support and funding implications) and key outcomes.
A second reviewer reviewed extracted data from all papers with any discrepancies resolved by discussion.
Quality appraisal
The Mixed Methods Appraisal Tool (MMAT) was used to assess included studies. 28 The MMAT incorporates descriptive criteria for evaluating mixed-methods studies and has been widely tested for content validity. The 2018 MMAT version does not have a scoring function but proposes researchers present a robust rationale for the ratings of each criterion.
Records were assessed independently by two reviewers using the MMAT and a rating of ‘high’, ‘moderate’ or ‘low’ quality was agreed between them. For mixed-method studies, each component was assessed separately, and the lowest quality score was used. Publications assessed as high quality were considered more credible and relevant than those assessed as low or medium quality, but given the diffuse nature of evidence identified, low-quality evidence was also included.
Narrative synthesis and typology development
The stages of narrative synthesis, as outlined by Popay, were adapted for this review. 17 Through data extraction, appraisal and consensus with a second reviewer, studies with similar components, such as location of care, were grouped to develop a preliminary synthesis and derive the typology, with distinguishing properties as qualifiers for taxonomic differences. 29 We analysed evidence iteratively to identify the typology, describe the models and highlight their outcomes, facilitators and challenges. Thematic analysis was used to formulate a preliminary synthesis, map key concepts and explore relationships between studies. 17 A summary table with paper characteristics and summarised data is provided in Supplemental Materials. Grey literature provided useful context; in addition, findings relevant to the typology were integrated within the narrative.
Results
After deduplicating records, searching across databases, manual searches and contacting authors, a total of 16,865 records were identified; 16,615 were excluded at title and abstract screening (Figure 1). Two hundred and fifty full-text articles were screened; 22 reports in peer-reviewed journals and 18 grey literature publications met the eligibility criteria and were included in the synthesis. This included one additional paper 30 and Supplemental Material Data from another study 1 obtained from study authors.

PRISMA flow diagram.
Characteristics of included evidence
Fifteen qualitative, six mixed-methods and one quantitative study were included in the synthesis. Studies were conducted between 2000 and 2022. Thirteen studies were from the USA,11,12,30 –40 five from the UK,8,41 –43 including Scotland, 44 with individual studies from Canada, 45 France 46 and Australia, 47 as well as a survey study from eight countries. 1 Included studies and their key findings are presented in Table 3.
Summary of included studies.
EOL: end of life; MDT: multi-disciplinary team; PC: palliative care; HMPS: His Majesty’s Prison Service
Quality of studies
The methodological quality of the studies was mixed (see Supplemental Materials of the 22 studies, 15 met all appraisal criteria). Due to inadequate reporting, five were considered at medium risk of bias and two at high risk.
Grey literature
Typology of models of palliative care delivery
This scoping review identified three models of palliative care for people in prison in high-income countries: ‘Embedded Hospice’, ‘Outsourcing Care’ and the ‘Community Collaboration’ model.
Embedded hospice model
This model is typified by an interdisciplinary team (IDT) and volunteer caregivers providing care on-site.11,12,30 –32,35 –39 Thirteen out of 14 included studies reporting this model were from the USA. Studies were mostly high quality, although two were deemed medium quality and two were low. A survey identified 113 functioning prison hospices in the USA, 12 but the implementation of these programmes varied.12,33 Two papers (from one study) describe a regional healthcare resource, serving all people in prison within that American state.30,31 One Canadian study showcased the ‘Pal Program’, providing companionship for people in prison with serious illnesses. 45
All 13 USA studies reported inclusive IDTs with medical professionals and prison staff. 12 Data indicates that as early as 2011, 94% of surveyed hospices in the USA utilised unpaid peer caregivers. 11 Chaplains, social workers and inmate caregivers in the IDT primarily aided families by providing psychoeducation about dying and promoting familial reconciliation.33,38,35
Admission criteria for utilising the service varied between the 13 studies from the USA; from a prognosis of either 6 30 to 12 months11,40 to no requirement of time-to-death prognosis. 29 Three studies reported a requirement for a do-not-resuscitate (DNR) order, while others didn’t; the reason for this variation is unclear.26,34,35
Where compassionate release mechanisms were reported, pre-release planning involved the reinstatement of an individual’s benefits and organisation of their community care, 10 with most applications led by social workers. 32 Medical Assistance in Dying (MAiD) has been legally available in Canada since 2016. 45 Incarcerated patients encounter difficulties in equitable access to MAiD services. The cited Canadian study reveals challenges in accessing early release for people in prison, highlighting concerns that those with terminal illness may choose MAiD over preferred community-based palliative care due to such obstacles. These difficulties can contribute to heightened suicidal ideation, amplified by uncertainties about supportive medical staff and fears of repercussions for inquiring about MAiD. 45
The grey literature illustrated the rise of the Embedded Hospice model in the USA. The Humane Prison Hospice Project report cited low recidivism rates for inmate volunteers 48 and evidence of the transformative potential of inmate caregiving. The report includes accounts of hardened gang members demonstrating empathy towards the terminally ill, 49 and murderers with 50-year sentences finding redemption through caring.50,51
Psychosocial support
Psychosocial support varied, with psychiatrists and psychologists included in only some IDTs. 33 One study found psychologists in only 7% of programmes surveyed in the USA. 34 Counselling by chaplains, social workers and peer caregivers was common, with volunteers also trained in psychosocial aspects of dying.35,36 Peer caregivers formed close bonds with patients, offering companionship and comfort.33,34 Chaplains were the main providers of spiritual care,29,35 –37 although peer caregivers, might read religious texts 11,38,45,39 and provide comfort through prayer. 34
Social care
Informal companionship (facilitated by peer caregivers) often went beyond assisting with daily activities to attending to an individual’s unique wants and needs.26,29,36,45 These relationships might offer protection, safeguarding people in prison from potential abuse. 37 Four studies did not report social care provision.33 –35
Rights of families
Visitation policies generally permitted non-incarcerated families and friends to visit, with some programmes facilitating videotaped messages. 12 Flexible visiting arrangements were emphasised,33,35 and the definition of family extended to include fellow inmates, reducing barriers associated with strict protocol adherence. 35
Bereavement support
Bereavement support involved regular meetings or ad hoc support. 29 Informal discussions with staff, memorial services and peer mentorship were observed.33,35 –37 Bereavement support could take the form of signposting to bereavement services, condolence cards, telephone calls or psychoeducation on the stages of dying and anticipatory grief. 35 Some programmes surveyed lacked opportunities to memorialise the deceased or access grief counselling. 12 The Canadian study highlighted challenging conditions faced by inmate volunteers, leading to emotional distress and potential Post Traumatic Stress Disorder following a death of a fellow inmate. 45
Funding implications
This model reports cost-effectiveness due to reduced hospital transport and DNR orders, reducing the cost of life-sustaining interventions.29,36 In the Canadian study, prison caregivers acknowledged low compensation in their work ($25 every 2 weeks on the PAL programme). 45 In contrast, a study in the USA found stable expenses despite high healthcare costs in the last 6–12 months. 33
Facilitators and challenges
This model appears to be supported by several key facilitators, principally the inmate caregivers’ person-centred practice.12,32,39 The importance of education and training, whether through formal programmes or informal mentoring, for both staff and volunteers, was underscored.33,34 The collaboration of an IDT was found to be crucial, 11 and the addition of a volunteer coordinator was positively noted. 35 Programmes administered by full-time prison staff assigned additional hospice duties were deemed effective. 34 Another important facilitator was the ability of families to feel included;8,35 –38,46 however some people in prison regarded fellow inmates as their family. 37
Prominent challenges in implementing this model included security considerations impacting opiate administration within prisons.11,12,45 Healthcare concerns were often overshadowed by security protocols, hindered by a lack of knowledge and training.29,35 Cultural differences between hospice and prison raised concerns about mistrust and potential exploitation.35 –37 Inadequate resources for a comfortable environment and limited public support were common.12,30,31,38 Prison staff were reported to question requests for specific food items 12 and be hesitant about relaxing visiting rules.29,35
The stability of the institution emerged as a potential challenge, with palliative care programmes identified as vulnerable during periods of infrastructural unrest. 33 Additionally, the insistence on having DNR orders in place could undermine trust, 29 or access to MAiD for Canada’s people in prison. 45
The Embedded Hospice model is associated with a pervasive theme of ‘humanizing the prisoner’. This applies to the peer caregiver volunteers as well as the dying individuals, fostering transformative experiences for all involved. The evidence from the Humane Prison Hospice Project report underscores the profound impact of inmate caregiving, showcasing instances of empathy from hardened gang members and stories of redemption among people in prison serving lengthy sentences. The person-centred care reported in this model facilitates a humanising experience for all involved.
The ‘outsourcing care’ approach
The three studies reported under this heading, all deemed high quality, represent an emerging approach, in which end-of-life care for people in prison is largely provided outside of the institution. Exceptions are found in the European Association for Palliative Care (EAPC) survey, 1 which reports some instances of palliative care suites in English and Welsh prisons, although they are in the minority.
The EAPC survey included Australia, Belgium, Czech Republic, England and Wales, France, Portugal, Scotland and Slovakia; other studies in this category were conducted in France 46 and Australia1,47
Most countries offered primary healthcare within their prisons; however, in Portugal, 14 prisons out of 55 reported no prison healthcare units. 1 In Australia, Belgium, the Czech Republic, France, Portugal and Slovakia, people in prison are typically transferred to different prisons or hospitals to receive care.1,46,47 Inmate volunteers are not commonplace, and IDTs consist of physicians, nurses and social workers.1,46,47
In France, prisoner preference for receiving care within a hospital may be one factor driving this model. 46 Conversely, Australia faces challenges in providing diverse services across vast geographical areas, meaning people in prison may be transferred to a centrally located maximum security prison for hospital visits, regardless of their security status. 47 However, evidence suggests that in England and Scotland, prisons are beginning to collaborate with local services to support patients who are not transferred. Currently, England and Wales have some dedicated palliative care units in a few prisons. 1
Studies show how compassionate release policies affect service delivery. Chassagne’s 2017 study suggested that healthcare professionals favoured compassionate release as a suitable approach to palliative care, with dying individuals granted full ‘patient’ status. 46 In Australia, jurisdictions decide to release cases individually, 47 while Belgium involves a criminal court judge and written prisoner requests. 1 England, Scotland and Wales share early release criteria for low re-offence risk, whereas Portugal, Slovakia and the Czech Republic lack specific early release policies. 1
Psychosocial support
Psychosocial support was not referenced in studies describing this model, despite people in prison feeling isolated and unsupported. 46 The absence of comfort care like special food, therapies, music and cultural or religious practices, was noted due to prison protocols. 1
Social care
Some aspects of social care, such as meals or personal care, could not be provided outside the prison but also could not always be provided by the prison nursing staff.1,46,47 Consequently, the responsibility fell to fellow inmates, but care could be obstructed due to a lack of equipment (e.g. wheelchairs or specialist bedding) and an absence of specific policies relevant to people in prison’s palliative care needs. 1 A lack of specialist equipment, mistrust between people in prison and healthcare staff, insufficient communication and inadequate social care compromised the quality of care.46,47 The European Association for Palliative Care survey report highlighted ‘life support workers’ employed in French prisons to assist older people in prison, and some separate units for older people in prison in England and Wales. 1
Rights of families
Limited family involvement, infrequent communication from physicians and restricted visits from families could hinder adequate preparation for death. 46 Furthermore, secure ward settings were reportedly considered unsuitable for children to visit.46,47
Bereavement support
Bereavement support was not reported in these studies.
Funding implications
The funding implications of this model were largely not discussed. The European mapping study report noted only that funding for prison palliative care falls under each state’s responsibility. 1
Facilitators and challenges
Facilitators of delivering good end of life care via this model included prisons addressing the needs of their older and end-of-life population, 1 and staff managing to influence routine practice. 46 Prisons showed some flexibility regarding release policies to meet individual needs: people in prison in France have the option of requesting parole or electronic surveillance during treatment, 46 and in England and Wales governors can grant temporary release on compassionate grounds, to be recalled if circumstances change. 1
Several challenges were identified. Healthcare professionals can lack clarity on how to advocate for people in prison and support decision-making. 1 A lack of guidance for healthcare staff regarding pain medication in the secure setting, limited access to patients’ rooms or delays in authorisations led to poor continuity and quality of care.46,47 Prison healthcare staff showed reluctance in seeking help or actively collaborating with the hospital palliative care team.46,47 This lack of communication and collaboration may be attributable to organisational constraints,46,47 resulting in limitations in comfort care provisions and family visitations.1,46 In cases of transfers to different security-level prisons, some people in prison chose to forgo healthcare to stay in their preferred residence, resulting in treatment delays. 47 Due to the fragmented nature of care reported within this model, there were concerns about timely diagnosis. 1 A lack of initiatives was notable in Australia, Belgium, the Czech Republic, Portugal and Slovakia, 1 with no evidence of specialist palliative care for older people in prison.
The overarching theme of ‘missed opportunities’ was identified in this emerging model. Psychosocial support is often unaddressed despite people in prison feeling isolated, and key aspects of comfort care such as, special food, therapies and attention to cultural practices, are unreported. Additionally, challenges to social care provision, compounded by environmental challenges and a lack of policies to ensure the palliative care needs of people in prison are met highlight the need for research documenting best practice. The absence of reported bereavement support further underscores the model’s potential to omit adequately addressing holistic end-of-life needs.
The collaborative community model
Five studies, all from Scotland and England, reported the collaborative community model, which involves prisons’ engagement with other healthcare facilities or practitioners to assist patients. Specifically, prison teams actively pursued multidisciplinary collaboration with local palliative care specialists. 44 Staff from community palliative services, alongside prison healthcare personnel, offered care to people in prison through in-reach services.8,42 Some prisons had their own end-of-life care programmes, with a growing number of inmates trained as ‘buddies’ to support fellow people in prison. 8
Central to this model is the idea that individuals in prison with serious illnesses should ideally receive care within or close to their ‘home’ institution, ensuring comfort and familiarity for the person in prison coping with serious illness. Three of the studies reporting this model were assessed as medium quality8,44,41 and two as high.43,52
Research documenting this model showed compassionate release was perceived as a complex procedure by community hospices. 44 This might be attributed to stringent criteria, such as a requirement of less than 3 months to live, being met. 41 It is suggested that shifting policies in the UK to prioritise palliative care facilities within prisons, rather than reforming compassionate release, presents new challenges for prison staff, 43 a consideration for those adopting this model.
In the grey literature, a 2019 report by the Australian Department of Health highlighted barriers to palliative care in prison, recommending more formalised collaboration between prisons and community care providers. 53 At the 2022 Conference on Correctional Health Care in Australia, the Network Palliative Care Model was introduced to provide tailored care to incarcerated patients and enhance clinician skills. 54 In Scotland, a community collaboration model was reported between a local hospice and HMP Edinburgh. 55 A UK study outlined three approaches to palliative care delivery: individual prison, cluster and regional, emphasising the need for an integrated model of care in UK prisons. 56 Evidence from England illustrated notable examples of the model, including a Norwich prison with a 15-bed unit for older adults which provides care within the prison environment with support from hospice nurses and medical staff. 57 Dartmoor Prison collaborates with the local hospice’s outpatient specialist palliative care nurses, providing personalised end-of-life care through nurse-led clinics and advice on in-cell adjustments. 58
Psychosocial support
There was considerable variation in prison staff’s self-reported ability to meet people in prison’ psychosocial and spiritual support needs. 42 High levels of anxiety and vulnerability were reported among older people in prison, intimidated by younger inmates due to physical and mental frailty. 42 People in prison feared receiving inadequate care, due to the perceived rigidity and unkindness of the system. 43 One study showed that some Scottish hospices provided support to their local prison’s psychiatrist. 44 There was some evidence that prison ‘buddies’ provided pastoral support, and in certain prisons, individuals were granted increased visitation privileges. 8
Social care
Even though some prisons have converted cells to accommodate beds, hoists and specialised equipment, 41 the use of ‘buddies’ to deliver personal care amongst an older population of predominantly sex offenders is considered unsafe and inappropriate. 41
Rights of families
Certain inmates cultivate their closest bonds with fellow people in prison. 41,42 However, less than one-fifth of British prisons surveyed permitted visits from children towards the end of life. 41 A noteworthy facilitator for this model was when hospices actively sought out family members to facilitate visits. 44
Bereavement support
Weaknesses in bereavement care were highlighted, linked to insufficient staff training. 42 Family liaison officers described the ‘grim’ task of attending funerals, with little support for staff in this aspect of their work. 41 A discernible contrast was noted in the training levels between hospice and prison staff. 41 Chaplaincy was reported to provide care for both the dying person and their relatives, 42 and to grieving people in prison after the death of an inmate through communal prayer. 41 Spiritual care was offered via chaplains and prison psychiatry.41,42,44 Additionally, peer groups and staff offered emotional support outside of formal structures.41,42
Funding implications
The funding implications of this model were not discussed in these studies.
Facilitators and challenges
Some prisons had begun to develop palliative care suites, enabling some care to be delivered on-site. 41 A UK study reported that environmental adaptations, like creating an older prisoner's wing and implementing the use of ‘buddies’, had been well received. 8 Collaboration with nearby community palliative care services facilitated training and knowledge exchange. 44 Hospices actively seeking family members to facilitate visits also utilised this model. 44 Successful hospice care for prisoner patients or those released from prison requires staff to be ready, trained and aware of potential risks associated with the individuals’ criminal backgrounds. 44
Barriers to the success of this model can be both systemic and environmental.
Typical prison cells are reported to be too small for hospital beds, and limited access to clean bedding, showers and clothing poses challenges in addressing social care needs for some people in prison. 41 Establishing collaborative relationships between prisons and community palliative care providers relies on ‘a complex process of relationship building, staff preparation, effective communication, and clear oversight’, where the balance between care and custody requires understanding both contexts and a willingness to adapt policies accordingly. 44 Prison staff shortages significantly impact the time nurses can allocate to people in prison, especially those who are older with multimorbidity.41,42 Limited access to specialised equipment, restricted availability of pain relief and the absence of a peaceful environment exacerbate the challenging conditions for delivering palliative care.41 –43 Moreover, in the UK only 53% of prisons have any palliative care policies, 17% lack policies and 30% are unaware of their policy status. 8
The grey literature search yielded an additional 18 publications for inclusion, from eight countries (USA, Switzerland, Scotland, Ireland, Canada, Australia, New Zealand and the UK). There were eight web articles,48 –51,59 –62 two poster presentations,55,56 one conference abstract, 54 two official reports,63,64 four policy documents58,65,66 and one charity publication. 57
Findings from the grey literature highlighted two key themes illustrating policy and practice debates. The first concerned compassionate release, that is the process by which inmates in criminal justice systems may be eligible for immediate early release on grounds of particularly extraordinary or compelling circumstances, including facing imminent death, 9 enabling access to palliative care services. There were reports of an increase in demand for compassionate release since the COVID-19 pandemic. 60 Challenges were documented because policies often rely on a prognosis of 12 months or less, which can rarely be declared with certainty. 59 For areas with a large older prison population like Massachusetts, where over 15% of inmates are over 55, this is a concern. 60 A 2018 Irish investigation report following the death of a terminally ill prisoner recommended Compassionate Temporary Release as the preferred policy for terminally ill people in prison in Ireland, to avoid undue suffering. 63
The second theme related to challenges in palliative care delivery. A Swiss report detailed insufficient staff training, an absence of relevant legislation, and conflicting priorities between punishment and rehabilitation. 61 These were echoed in Canada, where the Office of the Correctional Investigator found deficiencies in provision such as limited family support, insufficient training and obstacles to round-the-clock care. 65 In New Zealand, the case of Vicki Letele was widely reported: a 35-year-old mother diagnosed with terminal cancer during her sentence, and granted compassionate release following an appeal. The establishment of high-dependency units in prisons and compassionate release policies was anticipated to increase following the visibility of this story. 62
Hospice UK’s 2021 report highlighted inequalities for people in prison in the UK accessing palliative care, proposing recommendations like standardised bereavement support. 66 The Royal College of Nursing also called for improved end-of-life care across the prison estate. 64 A central theme within the collaborative community model was ‘building relationships’ through prisons’ proactive engagement with community healthcare. These collaborations involve multidisciplinary efforts with local palliative care specialists, and some prisons have developed their end-of-life care programmes, training inmates as ‘buddies’ to support peers.
Discussion
Embedded hospice models in the USA are prevalent and demonstrate promising evidence for enhancing the care experience for recipients and peer caregivers. Chaplains, social workers and peer caregivers provide psychosocial support, yet documented assessment and strategies for managing the distinctive needs of this group and their families are lacking, despite their acknowledged complexity.
Main findings
In this comprehensive scoping review, we identified a typology of three models of care delivery for people in prison in high-income countries: (1) Embedded hospice model, typified by an interdisciplinary team and volunteer caregivers providing care on-site; (2) Outsourcing Care model, in which end-of-life care is provided outside the prison; (3) Collaborative Community model, which involves prisons engagement with other healthcare facilities or practitioners. End-of-life care provision in prisons in high-income countries also varies in the application of policies regarding Early Release on Compassionate Grounds, the consideration of which should form part of palliative care for a dying prisoner.
The USA primarily utilises the Embedded Hospice model with inmate caregivers, and there is some evidence that this model results in high-quality care, cost reduction and potentially transformative experiences for peer caregivers. Although the Canadian study also reports this model, the extent to which this model has been adopted across the country is unclear.
The voluntary status of peer caregivers should be highlighted, as their choice to take on this role underscores the potentially transformative benefits and relies on the quality of the relationships between caregiver and patient. Considering potential exploitation concerns, research is needed to understand the value of fostering these meaningful connections and the contextual factors that allow them to flourish.
The fragmented Outsourcing Care model risks missing timely diagnosis, effective pain management and family communication for those in prison. Evidence regarding psychosocial needs and bereavement support were generally lacking and hospital clinicians’ lack of information regarding prison protocols had a negative impact on holistic care.
Good practice in the Community Collaboration model depends on motivated staff and grassroots initiatives, where prison or community palliative care providers actively seek working relationships. However, not all prisons have palliative care policies, which could compromise staff’s incentive to implement pre-emptive planning by establishing relationships with relevant community services.
There is limited evidence regarding the psychosocial needs of people in prison facing serious illness and their management, including who is best equipped to provide psychosocial services to the dying in a prison context. 3 Bereavement support was well documented in Embedded Hospice model studies, however, studies in the Collaborative Community model indicate insufficiencies in the support available. There is preliminary evidence of financial benefit within the Embedded Hospice model, but the cost-effectiveness of the other models has not been examined.
What this study adds?
Previous systematic reviews synthesised evidence regarding different aspects of death, dying and palliative care within prisons,3 –7,13,14 but either focussed solely on psychosocial care, 4 or did not identify and describe different models.5,7,11 –14 This review identifies and describes three broad typologies of palliative care delivery in prisons within high-income countries and their associated facilitators and challenges.
It reaffirms previous findings on inadequate specialised equipment, conflicting care and custody principles and the transformative impact of hospice care on volunteers.2,5,6 It further highlights the role of peer caregivers in delivering social care and reports available data on funding implications. Incorporating grey literature provides essential non-academic content that enriches our understanding of current policy and practice priorities.
Future research should prioritise studying countries where evidence is lacking, to enable comparisons and ensure equal access to appropriate care for incarcerated individuals, as well as systematically describe and assess palliative care models in prisons to establish a robust evidence base for service design and policy making. Research should assess the financial impact of inmate caregiver programmes, compare community versus prison hospice and different compassionate release policies, identify the psychosocial and bereavement support needs of seriously ill people in prison and their close persons within and outside the prison, and explore the ethical implications of inmates as volunteers, and the use of MAiD for people in prison.
In countries not implementing the Embedded Hospice Model, collaboration between hospitals, community palliative care and prison healthcare services appears crucial for managing people in prison’s end-of-life care. Developing local policies and sharing good practice could promote sustainability while ensuring compliance with frameworks (e.g. UK’s Dying Well in Custody Charter) would guarantee consistent adherence to quality standards. 67 Strategic priorities include consulting on sentencing practices for older people in prison, optimising compassionate release policies and providing suitable provisions and trained staff for the ageing prison population.
Strengths and limitations
Study selection used clear criteria and a systematic data extraction process for replicability. Quality appraisal was systematic and robust. Only English-language studies published since 2000, including grey literature, were included for contemporary evidence.
The use of Google poses limitations due to variable search results influenced by factors like location and search history. Despite attempts to mitigate bias through measures including clearing history and using incognito mode, complete elimination of bias remains a challenge. Due to time and resource constraints, only one screener was utilised in searching the grey literature, focussing on the initial four pages of Google results. The narrative synthesis was limited by study scope and heterogeneity, addressing various palliative care models. Families’ views were underrepresented in the majority of included studies. The articles that conducted interviews with incarcerated individuals were undertaken in male prisons only and not female prisons.
Conclusion
In high-income countries, end-of-life care approaches in prisons vary significantly. The USA predominantly uses the Embedded Hospice model with inmate caregivers, which shows potential for quality care and cost reduction. Outsourcing end-of-life care can lead to fragmentation and missed opportunities for comprehensive care. The Community Collaboration model shows promise but relies on motivated staff and grassroots initiatives. Limited evidence exists regarding the psychosocial needs of seriously ill people in prison and the most suitable caregivers for addressing their potential complexities, and bereavement support is limited outside the Embedded Hospice model. Addressing these disparities is crucial for providing dignified and compassionate care to all incarcerated individuals nearing the end of life.
Supplemental Material
sj-pdf-1-pmj-10.1177_02692163241242647 – Supplemental material for How do people in prison access palliative care? A scoping review of models of palliative care delivery for people in prison in high-income countries
Supplemental material, sj-pdf-1-pmj-10.1177_02692163241242647 for How do people in prison access palliative care? A scoping review of models of palliative care delivery for people in prison in high-income countries by Emma Gilbert, Nick De Viggiani, Joana de Sousa Martins, Tanuka Palit, Jessica Sears, Daniel Knights, Audrey Roulston, Mary Turner and Lucy E Selman in Palliative Medicine
Footnotes
Acknowledgements
Thanks to Isla Kuhn, Head of Medical Library Services, University of Cambridge, and Barry R Ashpole, Communications Consultant & Educator, International Palliative Care Resource Centre, for help and advice in developing the grey literature search strategy and identifying key documents.
Author contributions
Emma Gilbert – conception and design of the review, analysis and interpretation of data, drafting the paper. Nick de Viggiani – design and interpretation of data. Joana de Sousa Martins – screening, quality appraisal, data extraction. Tanuka Palit – screening, quality appraisal, data extraction. Jess Sears – screening, quality appraisal, data extraction. Daniel Knights – screening, quality appraisal, data extraction. Audrey Roulston – screening, quality appraisal, data extraction. Mary Turner – design and interpretation of data. Lucy Selman – design of the review, interpretation of data, supervision. All authors reviewed and revised the paper critically for important intellectual content and approved the final version.
Declaration of conflicting interests
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: Emma Gilbert, NIHR Pre-doctoral Fellow (NIHR301173) and Lucy Selman, NIHR Career Development Fellow (CDF-2018-11-ST2-009), are funded by the NIHR for this research project. Daniel Knights is a Cambridge Clinical Research Fellow funded by Addenbrookes Charitable Trust, Grant No. 900318.
The views expressed in this publication are those of the authors and not necessarily those of the NIHR, NHS or the UK Department of Health and Social Care.
Data management and sharing
All data generated or analysed during this study are included in this published article [and its Supplemental Material Information Files].
Research ethics and patient consent
Not applicable.
Supplemental material
Supplemental material for this article is available online.
References
Supplementary Material
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