Abstract
Background: Out-of-hours palliative care is a priority for patients, caregivers and policymakers. Approximately three quarters of the week occurs outside of typical working hours, and the need for support in care of serious and terminal illness during these times is commonplace. Evidence on relevant interventions is unclear.
Aim: To review systematically the evidence on the effect of out-of-hours specialist or generalist palliative care for adults on patient and caregiver outcomes, and costs and cost-effectiveness.
Methods: A systematic review of peer-reviewed and grey literature was conducted. We searched Embase, MEDLINE [Ovid], Cochrane Library, CINAHL, Allied and Complementary Medicine [Ovid], PsycINFO, Web of Science, Scopus, EconLit (Ovid), and grey literature published between 1 January 2000 and 12 th November 2019. Studies that comparatively evaluated the effect of out-of-hours specialist or generalist palliative care for adults on patient and caregiver outcomes, and on costs and cost-effectiveness were eligible, irrespective of design. Only English-language studies were eligible. Two reviewers independently examined the returned studies at each stage (title and abstract review, full-text review, and quality assessment).
Results: We identified one eligible peer-reviewed study, judged as insufficient quality. Other sources returned no eligible material. The systematic review therefore included no studies.
Conclusions: The importance of integrated, 24-hour care for people in line with a palliative care approach is not reflected in the literature, which lacks evidence on the effects of interventions provided outside typical working hours.
Registration: PROSPERO CRD42018111041.
Keywords: Palliative Care, Terminal Care, Health Care Quality, Health Care Access, Health Care Evaluation, After-Hours Care, Systematic Review
Introduction
Background
Demographic ageing brings a growing burden of complex and life-limiting disease, posing a major challenge for health systems worldwide 1, 2. The value of and need for an integrated palliative care approach to improve quality of life for people with life-limiting illness and their families is widely recognised 3– 6.
While preferences vary by conditions and personal circumstances, studies routinely find that a majority of people with terminal illness prefer to stay at home, provided that they can access appropriate services and supports 7– 12. Typical professional hours run from 9.00am to 5.00pm, Monday to Friday, or similar, meaning that three quarters of a patient’s week occurs ‘out of hours’. Meeting the policy goal of universal palliative care available according to need therefore requires comprehensive out-of-hours care provision. Poor patient outcomes have been linked to inadequate community supports and a lack of patient confidence in out-of-hours access 13, 14.
In the United Kingdom, guidelines from the National Institute for Clinical Excellence have recommended 24-hour specialist palliative care access for people with cancer since 2004 15. Nevertheless, priority-setting exercises with patients, carers, volunteers, and health and social care professionals have identified “the best ways of providing palliative care outside of working hours” as the top research priority in both the United Kingdom and Ireland 16, 17.
Policy context
Ireland was among the first countries in the world to adopt a national palliative care policy in 2001 18, 19. Policymakers have initiated an update of the policy, to start in 2020 20, which will be conducted within the Sláintecare agenda 21. Among multiple goals, Sláintecare aims to reorient the Irish health and social care system away from the acute setting to community-based services 22. In this context of system-level reform and palliative care policy review, the Irish Department of Health funded this study to establish best available international evidence on out-of-hours palliative care.
Palliative care is an interdisciplinary field that occurs across settings and cross-cuts many other medical specialisms. Out-of-hours services are therefore likely to be diverse, potentially including the further extension of existing services, e.g. a specialist inpatient team working evenings and/or weekends; development of new services, e.g. telehealth services offering symptom advice or counselling; or the upskilling of other branches of health care, e.g. palliative care education for emergency department triage nurses, general practitioners, or paramedics.
Development of out-of-hours services should be guided by high-quality evidence on best practice. This could include studies evaluating a range of important considerations such as patient and public preferences, population need, workforce planning, commissioning and approaches to implementation and integration of services. However, making policy recommendations requires evidence about their effectiveness or cost-effectiveness.
Rationale
Multiple systematic reviews have been reported in the field of palliative care. Some have examined effectiveness and/or cost-effectiveness across multiple settings and configurations 23– 33, while others have focused on specific models and settings, including hospital inpatient 34, 35 and outpatient 36, home care 37, and day care settings 38, as well as care provided by unpaid family carers 39. However, we were not aware of any review identifying and organising systematically the evidence on out-of-hours services.
We therefore conducted a systematic review of peer-reviewed studies and grey literature that specifically addressed this research question:
What is the effect of out-of-hours specialist and generalist palliative care services on patient and family/caregiver outcomes, and on costs and cost-effectiveness?
Studies that comparatively evaluated the effect of out-of-hours specialist or generalist palliative care for adults on patient and caregiver outcomes, and on effectiveness and cost-effectiveness were eligible, irrespective of design.
Methods
Protocol and registration
We registered the review protocol on PROSPERO CRD42018111041 40.
Eligibility criteria
Studies reporting on the following PICOS (Participants, Interventions, Comparators, Outcomes, and Study design) were eligible for this review.
Types of participants. Studies were eligible if they examined adults (18 years and over) in their last year of life and/or had a terminal illness and/or had other serious/complex medical needs, and/or were a carer for someone who met these criteria.
We placed no restrictions on diagnosis/need, or on patient/carer perspective. Studies of children (under 18 years of age) and studies pooling children and adults without reporting the results separately were ineligible.
Types of interventions/exposure/comparators. Out of hours was defined as outside of typical working hours (i.e. 9.00am–5.00pm, Monday to Friday) and therefore including overnight, weekends, and public holidays. In the event of any ambiguities with respect to intervention timing in otherwise eligible studies, we decided prior to beginning our review to resolve these through discussion and consensus among the core researchers of the review team, and, where appropriate, through contact with the author of the study in question.
The best-established models of care internationally are inpatient hospices, inpatient and outpatient hospitals, home care, and day care. We did not define the term ‘palliative care’ before starting our review, seeking studies of out-of-hours care for people with life-limiting illnesses, resolving ambiguities through discussion and consensus among the review team, and, where appropriate, contacting the corresponding author. We did not restrict eligibility by either setting or generalist/specialist configuration of staff.
Eligible interventions therefore included both new models of care provided outside of typical working hours, and already established models of care where the effect of out-of-hours provision specifically was evaluated and reported on.
We required that studies were comparative in nature. Eligible comparators therefore included usual care and/or alternative models of out-of-hours palliative care.
Types of outcomes. Our primary outcomes of interest were the effectiveness (patient/carer outcomes) and cost-effectiveness (economic outcomes) of interventions.
We took a broad approach to all outcomes. Patient and/or carer outcomes could be quantitative or qualitative, and included quality of life and experience, as well as survival. Effectiveness outcomes had to be reported by the patients, carers, or a credible proxy. Perceptions of patient and/or carer outcomes from healthcare staff or administrators were not deemed eligible. Eligible economic outcomes included any resource utilisation typically considered to fall within the societal viewpoint (e.g. cost to payers, service users, and families, as well as unpaid care). We did not require resources to represent the literal cost of provision, but also classed non-cost measures of resource utilisation as eligible – e.g. insurance programme charges and frequency use data combined with validated unit costs. Any study reporting within cost-consequence frameworks, such as cost-effectiveness analysis and cost-utility analysis, was also eligible.
Ineligible outcomes were those that related to other parties, e.g. the experience or capacity of clinical staff or the perceptions of healthcare workers of the effectiveness and cost-effectiveness of services.
Types of studies/reports. Study designs vary considerably in research on serious illness in the context of profound ethical and practical considerations 41. As such, we did not restrict our search to any one design. We planned to include the following types of studies: prospective/retrospective cohort studies, before-and-after studies, randomised controlled trials, economic evaluations, qualitative/descriptive studies, and pilot studies.
We excluded studies that did not comparatively measure the effect of interventions on our outcomes of interest, since comparative evaluation was considered intrinsic to our research question.
Time period. Studies were only eligible if they finished data collection no earlier than 1 January 1996 and were published no earlier than 1 January 2000.
We based this decision both on the rapidly changing palliative care landscape in the period 1998–2018, and on our own national context: Ireland’s current official policy was written in 2001 (and therefore had the chance to incorporate relevant research prior to that point).
Cultural and linguistic range. Given the skills of the research team, only English-language materials were eligible for inclusion.
All returned studies in a language other than English were recorded and are reported separately in our results.
Database search: information sources and search terms
Two information specialists (CH and DM) searched the following electronic databases:
Embase
MEDLINE (Ovid)
Cochrane Library
CINAHL
Allied and Complementary Medicine (Ovid)
PsycINFO
Web of Science
Scopus
EconLit
Searches were conducted on November 12 th, 2019.
Information specialists (CH and DM) and subject experts (BMJ, PM, RMcQ, MR) devised searches for keywords in the titles, abstracts, subject headings, and controlled vocabulary of the databases ( Table 1). We searched only for articles published from 1 January 2000 onwards, in line with our eligibility criteria.
Table 1. Database search terms (example using Embase).
| # | Search terms |
|---|---|
| 1 | ‘palliative therapy’/exp OR ‘terminal care’/exp OR ‘terminally ill patient’/exp OR ‘hospice’/exp |
| 2 | Palliat*:ti,ab |
| 3 | ((terminal* OR hospice* OR ‘end-of-life’ OR ‘end-stage’ OR ‘last year of life’ OR LYOL OR ‘life’s end’)
NEAR/5 (care OR caring)):ab,ti |
| 4 | ((advanced OR terminal*) NEAR/5 (ill* OR disease*)):ti,ab |
| 5 | (‘end stage’ OR ‘end of life’ OR ‘last year of life’ OR LYOL or ‘life’s end’):ti,ab |
| 6 | #1 OR #2 OR #3 OR #4 OR #5 |
| 7 | ‘OOH care’/exp |
| 8 | (‘after-hour*’ OR ‘OOH’ OR ‘outside normal hours’ OR ‘out of office hours’ OR ‘outside office hours’ OR
‘after office hours’ OR ‘outside normal working hours’ OR weekend* OR holiday* OR ‘off-hour*’):ti,ab |
| 9 | #7 OR #8 |
| 10 | #6 AND #9 |
Grey literature search: information sources and search terms
Two information specialists (CH and DM) searched the following grey literature sources:
Google Scholar
OpenGrey
ClinicalTrials.gov
World Health Organization International Clinical Trials Registry Platform (WHO ICTRP)
ProQuest Dissertations & Theses (United Kingdom [UK] and Ireland)
RIAN.ie
Lenus
EThOS
Searches were conducted on November 12 th, 2019. Keywords from the database search were applied ( Table 2).
Table 2. Grey literature search terms (example using OpenGrey).
| # | Search terms |
|---|---|
| 1 | (palliative OR “terminal care” OR “terminally ill” OR hospice* OR “end-of-life” OR “end-stage”
OR “last year of life” OR LYOL OR “life’s end”) AND (“after-hours” OR “OOH” OR “outside normal hours” OR “out of office hours” OR “outside office hours” OR weekend* OR holiday* OR “off-hour*”) |
| 2 | Palliative hours |
| 3 | #1 OR #2 |
Other sources
We decided at the outset that all studies found to be eligible and passing quality assessment would be reviewed for references to other potentially relevant studies.
We also checked other systematic reviews for citations of relevant studies: We checked all studies included in all systematic reviews returned by our database search, and all studies included in 17 other reviews that we knew at the outset and covered all major palliative care settings 23– 39.
Study selection
Screening of titles and abstracts. Two information specialists (CH and DM) executed the searches and made the retrieved citations available in EndNote. Two team members (BMJ and PM) uploaded these citations to the online reviewer tool Covidence and reviewed titles and abstracts independently using the eligibility criteria described. Conflicts between the two reviewers were resolved using discussion and consensus.
Screening of full-text reports. Two team members (BMJ and PM) independently reviewed all studies that were advanced to full-text screening on Covidence using the eligibility criteria described above. Conflicts between the two reviewers were resolved using discussion and consensus.
Assessment of methodological quality/bias. Following agreement on eligibility, each study was assessed for methodological quality using one of a number of standardised instruments developed by the Critical Appraisal Skills Programme ( CASP), which also provides recommendations for exclusion of studies. Since multiple study designs were eligible, we decided prior to data collection to use the specific CASP tool most appropriate to each study (e.g. the CASP Case Control Study Checklist, the CASP Economic Evaluation Checklist, the CASP Qualitative Checklist, and so forth).
Two team members (BMJ and PM) quality-assessed all eligible studies independently. Conflicts between the two reviewers were resolved using discussion and consensus.
Other sources. Two information specialists (CH and DM) compiled all returned grey literature in EndNote. For Google Scholar, the first 10 pages (100 items) were collated; for all other sources, all returned items were collated. One team member (RMcC or PM) reviewed each grey literature item for potential relevance to this review. Studies published in the peer-reviewed literature were discarded if they had already been returned by the database search. Where the reviewer was uncertain of relevance, s/he conferred with another team member (BMJ).
One team member (PM) performed the review of the reference lists of other systematic reviews.
Data collection process
Two team members (BMJ and PM) were to extract data independently. Conflicts between the two reviewers would be resolved using discussion and consensus.
Data items
We decided prior to data collection to extract the following data items from studies that were eligible and of sufficient quality: design (e.g. randomised controlled trial, prospective cohort study, case-control study, etc.); country of origin; care setting; model of care; level(s) of provider expertise/training; sample size; patient characteristics; carer characteristics; recruitment and sampling; ethical issues, including consent; research question; outcomes; approach to confounding; statistical methods; and findings.
Synthesis of results
We decided to perform meta-analyses of included studies where possible due to homogeneity of methods, participants, interventions, and reporting. Given the wide range of outcomes of interest, it was not possible to specify all outcome measures or synthesis methods prior to data collection.
Prior versions of this work
An earlier version of this systematic review, along with other components of the HRB/DOH-funded project, were previously published on the HRB website 42. The only substantive change to the review between versions is that we updated the search strategy from August 2018 to November 2019. No new studies of relevance were identified.
An oral presentation of this project was made at the SPHeRE Network 5th Annual Conference, Dublin, February 2019. A poster presentation was made at the 16 th World Congress, European Association for Palliative Care, Berlin, May 2019.
Results
Database search
Our search of nine databases is summarised in Figure 1.
Figure 1. PRISMA diagram: database search, grey literature review and study selection.
The search yielded 1,694 citations, of which 958 were duplicates. We reviewed the remaining 736 unique titles/abstracts, of which 696 did not meet the eligibility criteria. One paper was excluded at this stage due to not being in the English language; it was in Dutch 43.
We then reviewed the remaining 40 full texts, of which one met the eligibility criteria 44.
We reviewed this study using the cohort study checklist. Under this checklist, the first section is ‘Section A: Are the results of the study valid?’. Section A consists of two questions:
-
1.
Did the study address a clearly focused issue (e.g. population studied, risk factors, outcomes)?
-
2.
Was the cohort recruited in an acceptable way (e.g. representativeness, criteria, exhaustiveness)?
Two independent reviewers concluded that the answer to each question was ‘No’. Specifically, reviewers recorded concerns about how the comparison group were identified. The authors do not provide eligibility criteria (Question 1) or methods of recruitment/identification (Question 2). The study was therefore not advanced to full CASP assessment.
The database search therefore identified zero peer-reviewed studies evaluating the impact of out-of-hours palliative care for adults on patient/carer outcomes and/or economic outcomes.
Other sources
Our search of grey literature sources yielded 180 items, of which 108 were peer-reviewed articles already returned by the database search. The remaining 72 items were reviewed for duplicates, which were discarded (n=4). None of the remaining 68 items were found to contain evaluations relevant to this systematic review.
Our review of the citations found in other systematic reviews examined one published systematic review returned by our database search 45, and from 17 other reviews that we were already aware of 23– 39. No additional eligible papers were identified.
Discussion
Main results
We identified no study of sufficient quality that evaluated the effectiveness or cost-effectiveness of out-of-hours specialist or generalist palliative care for adults.
The reasons for this lack of evidence are important to understand if future research is to address an established priority for patients, carers, volunteers and professionals. Some reasons may be generic within palliative and end-of-life care. Primary research studies face practical and ethical challenges, resulting in a small evidence base in all settings relative to policy relevance 31, 33. The relative newness of palliative care as a specialism is also a potential factor. For example, medical research activity is highest in the United States, where palliative care is heavily hospital-based and hospital costs are a major public policy issue 46. Yet a systematic search of the literature to 2018 identified only one prospective economic study of this model of care 35. Since out-of-hours services are new even within this relatively young field, it is perhaps not surprising that research is underdeveloped.
Other reasons may be specific to out-of-hours services. From an overall service perspective, out-of-hours is one component of a model of care 47. Where out-of-hours care is one element of the model under evaluation, it may not be identified specifically in reporting under keywords, MeSH terms or abstracts. There is therefore a risk of under-identification in our methods. However, any study isolating the effect of out-of-hours within a wider evaluation of palliative care provision was eligible for our review, and any study evaluating that specific effect would likely report this in the abstract. Studies most likely to go unidentified by our review are those where a service is provided on a 24-hour basis, and the out-of-hours elements were not separated in analysis. In this case, the study would not have been eligible under our criteria in any case.
Finally, it is important to note that our findings do not mean that no literature on out-of-hours palliative care exists, simply that evaluations specifically were not identified. Our review identified, but did not include as eligible, topics including general practitioner perspectives on out-of-hours palliative care 48, 49; pilot programmes on, inter alia, prescribing and telehealth 50, 51; and an ongoing systematic review to identify quality improvement projects in out-of-hours palliative care 52. These studies and others advance understanding outside of our evaluative focus, as well as potentially improving future evaluative studies.
Strengths and limitations
Any systematic review is vulnerable to missing relevant material, either through mis-specification of search terms or errors in review. We minimised these risks by establishing clear PICOS and eligibility criteria prior to data collection, employing a combination of subject and information specialists in executing searches, using two reviewers independently throughout the process, and examining studies that were included in multiple other prior reviews of palliative care in different settings.
We excluded studies from prior to 2000, which in principle may have excluded relevant evidence. Time cut-offs are inherently arbitrary but in this context were deemed important, palliative care practice from over two decades ago being very different to today in all countries. Specifically, this project was commissioned by Irish policymakers ahead of a review of national policy 20; prior policy was published in 2001 meaning that all relevant evidence to that point ought to have been collated already and so we established 2000 as an obvious cut point. As noted in Figure 1, one study was excluded due to the time criterion 53. We excluded one study due to our English language criterion 43.
What this study adds
This study illustrates that while out-of-hours palliative care is a recognised priority for patients and policymakers, no evidence base exists on which services are beneficial for patients and worthy of health care funding.
The lack of evidence underscores the need for future studies to incorporate measurement of the effectiveness and/or cost-effectiveness of out-of-hours services. In principle there are two ways that such evaluations might be initiated. First, data are already collected by statutory bodies and other providers on existing out-of-hours services. Appropriate analyses of these data could produce the sort of evidence that this review hoped to identify, albeit statutory data tend to focus more on process than outcomes, which limits analytic scope 19.
Second, original research must be conducted to collect data and evaluate out-of-hours care across its multitude of settings and practitioners. Consistent with other areas of palliative and end-of-life care research, this agenda will have to be flexible and pragmatic in matching methodological approaches to specific problems 41.
Conclusion
We conducted a systematic review of peer-reviewed and grey literature in order to identify evidence on the impact of out-of-hours palliative care for adults on patient and carer outcomes, and on economic outcomes.
We searched nine databases using both information and subject specialists, and we searched grey literature, including doctoral theses and policy repositories. Our database search yielded only one relevant study, which two independent reviewers judged to be of insufficient quality to include in the review. Our search of other sources found no relevant material.
The evidence base on out-of-hours palliative care is very small relative to importance to patients and policymakers. These evidence gaps must be urgently addressed.
Data availability
Underlying data
All data underlying the results are available as part of the article and no additional source data are required.
Reporting guidelines
Open Science Framework: Appendix to: [Effectiveness and cost-effectiveness of out-of-hours palliative care: a systematic review]. https://doi.org/10.17605/OSF.IO/6EP9A 54.
Data are available under the terms of the Creative Commons Zero “No rights reserved” data waiver (CC0 1.0 Public domain dedication).
Disclaimer
This work does not represent the opinions of the DOH or the HRB, and any errors or omissions are the responsibility of the authors.
Acknowledgements
We thank Louise Farragher and Dr Jean Long of the HRB for their support and input throughout the systematic review process.
Funding Statement
This work was funded by the Health Research Board (HRB) for use by the Department of Health (DOH) in Ireland under the identifier [HRB/RESEARCH/2018/10].
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
[version 1; peer review: 3 approved]
References
- 1. Lehnert T, Heider D, Leicht H, et al. : Review: health care utilization and costs of elderly persons with multiple chronic conditions. Med Care Res Rev. 2011;68(4):387–420. 10.1177/1077558711399580 [DOI] [PubMed] [Google Scholar]
- 2. GBD 2013 Mortality and Causes of Death Collaborators: Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2015;385(9963):117–171. 10.1016/S0140-6736(14)61682-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. World Health Organization: WHO Definition of Palliative Care.2017; Accessed August 15th, 2017. Reference Source [Google Scholar]
- 4. Ferrell BR, Temel JS, Temin S, et al. : Integration of Palliative Care Into Standard Oncology Care: American Society of Clinical Oncology Clinical Practice Guideline Update. J Clin Oncol. 2017;35(1):96–112. 10.1200/JCO.2016.70.1474 [DOI] [PubMed] [Google Scholar]
- 5. Economist Intelligence Unit: The Quality of Death Index: Ranking palliative care across the world.2015. Reference Source [Google Scholar]
- 6. Centeno C, Lynch T, Donea O, et al. : EAPC Atlas of Palliative Care in Europe. Milan, 2013. Reference Source [Google Scholar]
- 7. National Audit Office: End of life care. London, 2008. Reference Source [Google Scholar]
- 8. Woodman C, Baillie J, Sivell S: Relatives' preferred place of care at the end-of-life: implications for palliative care in the future. BMJ Support Palliat Care. 2015;5(1):116–117. 10.1136/bmjspcare-2014-000838.38 [DOI] [Google Scholar]
- 9. Weafer JA: Irish attitudes to death, dying and bereavement 2004-2014. Dublin: Irish Hospice Foundation;2014; 095665908X. Reference Source [Google Scholar]
- 10. Skorstengaard MH, Neergaard MA, Andreassen P, et al. : Preferred Place of Care and Death in Terminally Ill Patients with Lung and Heart Disease Compared to Cancer Patients. J Palliat Med. 2017;20(11):1217–1224. 10.1089/jpm.2017.0082 [DOI] [PubMed] [Google Scholar]
- 11. Loh AZ, Tan JS, Jinxuan T, et al. : Place of Care at End of Life: What Factors Are Associated With Patients' and Their Family Members' Preferences? Am J Hosp Palliat Care. 2016;33(7):669–677. 10.1177/1049909115583045 [DOI] [PubMed] [Google Scholar]
- 12. Hawley P: Barriers to Access to Palliative Care. Palliat Care. 2017;10:1178224216688887. 10.1177/1178224216688887 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Central Statistics Office (CSO): Vital statistics fourth quarter and yearly summary 2013.2013. Reference Source [Google Scholar]
- 14. Irish Hospice Foundation Initiative: A nationwide survey of public attitudes and experiences regarding death and dying.2004;30:2007 Reference Source [Google Scholar]
- 15. National Institute for Clinical Excellence: Improving Supportive and Palliative Care for Adults with Cancer. The Manual, London,2004. Reference Source [Google Scholar]
- 16. Marie Curie UK: Top 10 research priorities for palliative and end of life care.2016. Reference Source [Google Scholar]
- 17. McIlfatrick S: Palliative and End of Life Research Priority Setting Project for Northern Ireland and Republic of Ireland: Putting patients, carers and clinicians at the heart of palliative and end of life care research. Dublin: All-Ireland Institute for Hospice and Palliative Care;2015. Reference Source [Google Scholar]
- 18. National Advisory Committee on Palliative Care: The Report of the National Advisory Committee on Palliative Care. Dublin: Department of Health and Children;2001. Reference Source [Google Scholar]
- 19. May P, Hynes G, McCallion P, et al. : Policy analysis: palliative care in Ireland. Health Policy. 2014;115(1):68–74. 10.1016/j.healthpol.2013.07.016 [DOI] [PubMed] [Google Scholar]
- 20. Health Service Executive: Palliative Care Services: Three-year development framework. Dublin,2017. Reference Source [Google Scholar]
- 21. Oireachtas Committee on the Future of Healthcare: Sláintecare Report.Dublin: Houses of the Oireachtas;2017. Reference Source [Google Scholar]
- 22. Burke S, Barry S, Siersbaek R, et al. : Sláintecare - A ten-year plan to achieve universal healthcare in Ireland. Health Policy. 2018;122(12):1278–1282. 10.1016/j.healthpol.2018.05.006 [DOI] [PubMed] [Google Scholar]
- 23. Hearn J, Higginson IJ: Do specialist palliative care teams improve outcomes for cancer patients? A systematic literature review. Palliat Med. 1998;12(5):317–332. 10.1191/026921698676226729 [DOI] [PubMed] [Google Scholar]
- 24. Higginson IJ, Finlay IG, Goodwin DM, et al. : Is there evidence that palliative care teams alter end-of-life experiences of patients and their caregivers? J Pain Symptom Manage. 2003;25(2):150–168. 10.1016/s0885-3924(02)00599-7 [DOI] [PubMed] [Google Scholar]
- 25. Thomas RE, Wilson D, Sheps S: A literature review of randomized controlled trials of the organization of care at the end of life. Can J Aging. 2006;25(3):271–293. 10.1353/cja.2007.0011 [DOI] [PubMed] [Google Scholar]
- 26. Zimmermann C, Riechelmann R, Krzyzanowska M, et al. : Effectiveness of specialized palliative care: a systematic review. JAMA. 2008;299(14):1698–1709. 10.1001/jama.299.14.1698 [DOI] [PubMed] [Google Scholar]
- 27. Higginson IJ, Evans CJ: What is the evidence that palliative care teams improve outcomes for cancer patients and their families? Cancer J. 2010;16(5):423–435. 10.1097/PPO.0b013e3181f684e5 [DOI] [PubMed] [Google Scholar]
- 28. El-Jawahri A, Greer JA, Temel JS: Does palliative care improve outcomes for patients with incurable illness? A review of the evidence. J Support Oncol. 2011;9(3):87–94. [DOI] [PubMed] [Google Scholar]
- 29. Harris I, Murray SA: Can palliative care reduce futile treatment? A systematic review. BMJ Support Palliat Care. 2013;3(4):389–398. 10.1136/bmjspcare-2012-000343 [DOI] [PubMed] [Google Scholar]
- 30. Luckett T, Phillips J, Agar M, et al. : Elements of effective palliative care models: a rapid review. BMC Health Serv Res. 2014;14: 136. 10.1186/1472-6963-14-136 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Smith S, Brick A, O'Hara S, et al. : Evidence on the cost and cost-effectiveness of palliative care: a literature review. Palliat Med. 2014;28(2):130–150. 10.1177/0269216313493466 [DOI] [PubMed] [Google Scholar]
- 32. Langton JM, Blanch B, Drew AK, et al. : Retrospective studies of end-of-life resource utilization and costs in cancer care using health administrative data: a systematic review. Palliat Med. 2014;28(10):1167–1196. 10.1177/0269216314533813 [DOI] [PubMed] [Google Scholar]
- 33. Kavalieratos D, Corbelli J, Zhang D, et al. : Association Between Palliative Care and Patient and Caregiver Outcomes: A Systematic Review and Meta-analysis. JAMA. 2016;316(20):2104–2114. 10.1001/jama.2016.16840 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34. Higginson IJ, Finlay I, Goodwin DM, et al. : Do hospital-based palliative teams improve care for patients or families at the end of life? J Pain Symptom Manage. 2002;23(2):96–106. 10.1016/s0885-3924(01)00406-7 [DOI] [PubMed] [Google Scholar]
- 35. May P, Normand C, Cassel JB, et al. : Economics of Palliative Care for Hospitalized Adults With Serious Illness: A Meta-analysis. JAMA Intern Med. 2018;178(6):820–829. 10.1001/jamainternmed.2018.0750 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Rabow M, Kvale E, Barbour L, et al. : Moving upstream: a review of the evidence of the impact of outpatient palliative care. J Palliat Med. 2013;16(12):1540–1549. 10.1089/jpm.2013.0153 [DOI] [PubMed] [Google Scholar]
- 37. Gomes B, Calanzani N, Curiale V, et al. : Effectiveness and cost-effectiveness of home palliative care services for adults with advanced illness and their caregivers. Cochrane Database Syst Rev. 2013; (6):CD007760. 10.1002/14651858.CD007760.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38. Davies E, Higginson IJ: Systematic review of specialist palliative day-care for adults with cancer. Support Care Cancer. 2005;13(8):607–627. 10.1007/s00520-004-0739-6 [DOI] [PubMed] [Google Scholar]
- 39. Gardiner C, Brereton L, Frey R, et al. : Exploring the financial impact of caring for family members receiving palliative and end-of-life care: a systematic review of the literature. Palliat Med. 2014;28(5):375–390. 10.1177/0269216313510588 [DOI] [PubMed] [Google Scholar]
- 40. May P, Johnston BM, McCauley R, et al. : Effectiveness and cost-effectiveness of out-of-hours generalist and specialist palliative care provision.2018; Accessed 2018-10-29. Reference Source [Google Scholar]
- 41. Higginson IJ, Evans CJ, Grande G, et al. : Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews. BMC Med. 2013;11: 111. 10.1186/1741-7015-11-111 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42. Johnston BM, May P, McCauley R, et al. : Out-of-hours specialist and generalist palliative care provision: An evidence review.Dublin: Health Research Board;2019. Reference Source [Google Scholar]
- 43. Giesen P, Veldhoven C, Vlaar N, et al. : Patiëntervaringen met palliatievezorghuisartsen tijdens weekenddiensten. Huisarts Wet. 2011;54(12):646–649. 10.1007/s12445-011-0319-1 [DOI] [Google Scholar]
- 44. Baird-Bower D, Roach J, Andrews M, et al. : Help is just a phone call away: after-hours support for palliative care patients wishing to die at home. Int J Palliat Nurs. 2016;22(6):286–291. 10.12968/ijpn.2016.22.6.286 [DOI] [PubMed] [Google Scholar]
- 45. Finucane AM, Carduff E, Lugton J, et al. : Palliative and end-of-life care research in Scotland 2006-2015: a systematic scoping review. BMC Palliat Care. 2018;17(1):19. 10.1186/s12904-017-0266-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46. Morrison RS: Models of palliative care delivery in the United States. Curr Opin Support Palliat Care. 2013;7(2):201–206. 10.1097/SPC.0b013e32836103e5 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47. Seow H, Bainbridge D: A Review of the Essential Components of Quality Palliative Care in the Home. J Palliat Med. 2017;21(S1):S37–S44. 10.1089/jpm.2017.0392 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48. Senior H, Grant M, Rhee JJ, et al. : General practice physicians' and nurses' self-reported multidisciplinary end-of-life care: a systematic review. BMJ Support Palliat Care. 2019: pii: bmjspcare-2019-001852. 10.1136/bmjspcare-2019-001852 [DOI] [PubMed] [Google Scholar]
- 49. Carey ML, Zucca AC, Freund MA, et al. : Systematic review of barriers and enablers to the delivery of palliative care by primary care practitioners. Palliat Med. 2019;33(9):1131–1145. 10.1177/0269216319865414 [DOI] [PubMed] [Google Scholar]
- 50. Akram G, Corcoran ED, MacRobbie A, et al. : Developing a Model for Pharmaceutical Palliative Care in Rural Areas-Experience from Scotland. Pharmacy (Basel). 2017;5(1): pii: E6. 10.3390/pharmacy5010006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51. Carlebach S, Shucksmith J: A review of an out-of-hours telephone support service for palliative care patients and their families. Int J Palliat Nurs. 2010;16(9):445–450. 10.12968/ijpn.2010.16.9.78647 [DOI] [PubMed] [Google Scholar]
- 52. Jones E, McDaid C, Parker A, et al. : Interventions for improving 'out of hours' palliative care: a systematic review.2017; Accessed 2018-07-27. Reference Source [Google Scholar]
- 53. Fontaine K, Rositani R: Cost, quality, and satisfaction with hospice after-hours care. Hosp J. 2000;15(1):1–13. 10.1080/0742-969x.2000.11882944 [DOI] [PubMed] [Google Scholar]
- 54. May P: Appendix to: [Effectiveness and cost-effectiveness of out-of-hours palliative care: a systematic review].2020. 10.17605/OSF.IO/6EP9A [DOI] [PMC free article] [PubMed] [Google Scholar]