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Abstract
Objectives To map the patient journey for individuals known to palliative care presenting to the emergency department (ED).
Methods A linked dataset from the CUREd database and palliative care services in a region in the North of England was used. The study describes day and time of presentations, events occurring in the ED, mode of leaving the department and length of hospital admissions for presentations occurring within 90 days of a contact with palliative care. Findings were compared with the wider population in the CUREd database.
Results A significant proportion of individuals known to palliative care (29.4%) presented to the ED. Presentations typically occurred in working hours. Most presented by ambulance (84.4%) and were admitted to hospital (75.1%); these observations persisted across age groups. Most presentations involved investigations (88.5%) and/or treatment (84.1%).
Conclusions Palliative patients exhibit significant use of the ED; some have the potential to benefit from attendances, but there is a minority for whom ED is unlikely to have improved their care. Advance care planning and communication between services are important for empowering those who stand to benefit from ED, while ensuring appropriate care is planned for those who prefer to avoid presenting.
- Hospital care
- Hospice care
- Transitional care
- Clinical assessment
- Clinical decisions
- Home care
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Key messages
What was already known?
Palliative patients wish to avoid hospital presentations.
Most people attend emergency department in their final year of life.
What are the new findings?
Most presentations by palliative patients attend in working hours, by ambulance and result in admission.
The majority involve investigations and treatment.
What is their significance?
Clinical
Advance care planning and communication are priorities.
Research
Understanding patient/carer experiences is vital.
Background
Emergency department (ED) use in the final year of life represents a significant challenge. A 2018 report by Marie Curie demonstrated that, in England, cancer patients in the final year of life experience an average of 3.49 emergency admissions, compared with 3.01 for non-cancer patients.1 While many admissions will play an important role in prolonging life and improving symptoms, most people wish to spend their final days at home,2 illustrating a discrepancy between expressed preference and reality. National guidance provides recommendations to support palliative patients attending ED, but there remains scope to reduce avoidable attendance.3
Palliative care services are well placed to support advance care planning, including establishing ceilings of treatment.4 The complex nature of palliative care means that such services frequently collate information from multiple services, providing constant support in a changing situation.5
Reducing inappropriate use of the ED, while still enabling appropriate use by those who need it, requires an understanding of population demographics and patterns of use. This study used linked data on care transitions provided to a palliative population across emergency services, emergency inpatient services and palliative community services in a single city over a 2-year period.
Aims
The aim of this study was to describe ED use by palliative patients in a 2-year period in a city in the North of England.
Methods
The study used the CUREd database, which is a research dataset of episodes linking the urgent and emergency care system. It contains over 23 million patient episodes of care between 2011 and 2017. CUREd is a unique resource, which enables the investigation of patient journeys across time, services and providers.6
The study dataset comprised CUREd data relating to ED attendances and hospital admissions, which was linked with data on community palliative care contacts, covering the period April 2014–March 2017. A de-identified dataset was used for analysis. The study cohort was all adults known to the palliative care service from January 2015 to December 2016, defined as having received at least 1 contact with palliative care within the preceding 90 days.
Analyses used Stata V.15.7 Pre-hoc outcomes were defined from existing literature and refined with a Patient and Public Involvement (PPI) group and included demographics, mode of presentation/discharge, events in ED and length of hospital stay.
Results
The complete dataset included 2983 cases known to the palliative care service. Of the cases, 1480 (49.6%) were male (mean age: 73.8 years) and 1503 (50.4%) female (mean age: 73.6 years).
Presentations, arrival and discharge
ED presentations were included if they occurred within 90 days of a palliative care contact, and 1395 presentations were recorded. Most occurred within normal working hours and early evening but appear shifted later in the day when compared with the wider population (online supplemental graphs 1 and 2).
Supplemental material
Supplemental material
Most (2105, 70.6%) individuals in the cohort had no ED presentations. The attendances occurred in 878 individuals (29.4%), with 584 (19.6%) having a single attendance and 294 (9.9%) presenting on two or more occasions. The majority (748, 53.6%) of ED presentations occurred within 7 days of a palliative contact.
Table 1 outlines the modes of arrival and discharge from the department, presented according to age. Most presentations (1183, 84.8%) occurred via ambulance, with 212 (15.2%) via self-presentation. In contrast, these figures for the wider population are 32.1% and 67.9%, respectively. The majority of patients were admitted (1048, 75.1%) or discharged (318, 22.8%); a small number transferred to a different area or died in the department (29, 2.1%). This contrasts with the overall population, where 23.7% are admitted.
Mode of presentation and leaving department by age
Events in department
Investigations were undertaken in 88.5% of cases, with blood tests being the most common (74.9% of cases), followed by X-rays (58% of cases). Others involved ECGs (41.9%), arterial blood gas (22.5%), microbiology tests (20.5%) and other imaging (12.6%).
Treatments were administered in 84.1% of presentations, with 51.5% being invasive (intravenous interventions, oxygen and invasive procedures). The full list of treatments in each category is outlined in online supplemental table 1.
Supplemental material
Overall, there were only 74 ED presentations (5.3%) involving neither investigation nor treatment. This is smaller than that of the general population, where over 20% have neither treatment nor investigation.8
Subsequent hospital stays
From the 1048 cases admitted to hospital, admission data were available for 1038 cases. These admissions resulted in a median length of stay of 6 days (mean: 10.6 days).
Discussion
The palliative population make significant use of the ED, with 29.4% presenting at least once within 3 months of a palliative care contact, over half of these within a week and mainly via emergency transport. A minority has no investigations or treatments in ED; arguably, their presentations could have been avoided.8 For those that are admitted, these patients have a median length of stay of 6 days; for many, this is a period where time at home would ordinarily be a high priority. Average length of stay figures are comparable with English data from Marie Curie exploring service use in the final year of life.1
While ED use in this population is high compared with the wider population, recent reports in the West Midlands show that the majority (around 80%) of individuals in their final 2 years of life present at least once to the ED.9 It should be noted, however, that this study cohort is likely to comprise a much shorter time period. Data limitations regarding date of discharge from palliative care and date of death mean that precise time known to palliative care is not recorded here; nevertheless, a 2016 UK study10 highlighted that median time between referral to palliative care and death was 34 days.
We have defined the study population pragmatically. Given national variation in palliative care caseload management and discharge processes, this generates a definition of being ‘known’ to a service that can be contextualised in other areas. Data limitations affected our ability to explore some findings, specifically NHS 111 telephone service, emergency ambulance service data and death registry data. Our study reflects a single area, which includes both an independent and an NHS palliative care in-patient unit; as service design for palliative care services varies, this will affect the transferability of the findings.
Models for responsive palliative care community services should recognise that most emergency presentations occur during the day. Community teams use varied models for delivery,11 with crisis support out of hours. Our data suggest that an ideal form of crisis response needs to able to respond at any time.
The high number of presentations in this population means that palliative services should pre-empt emergency admissions, through advance care planning and guidance for management of crises. Such advice is in keeping with national strategy, ambitions and guidelines.4 12
Rapid access to medical information is vital to ensure that decisions are made with the best available data and ensures that an ED presentation has the best opportunity to improve an individual’s care; the importance of such systems is recognised but not consistently implemented.13
Education for ambulance service and ED professionals, and ensuring links with local palliative care services, are recommended to improve the care of those patients who do present. This is in keeping with Royal College of Emergency Medicine’s guidance3 and patient/family observations in existing studies regarding the difficulty in navigating local services.14
For further research, our key recommendation is to work within legal and ethical frameworks to make continued use of linked data for developing interventions, service evaluation and research. Such approaches should be supplemented by research into the experience of the patient and their loved ones, to understand the human impact of emergency presentations in palliative patients.
Conclusion
This study has outlined modes of attendance and events during and following ED presentation in patients who are known to a palliative care service. While clinically relevant definitions of ‘palliative’ may vary, this is a population which can be readily identified and targeted with interventions to ensure appropriate use of EDs. The results outline a number of key findings, which will help to target use of such interventions and guide further research.
Ethics statements
Patient consent for publication
Ethics approval
The CUREd database has approval from the Leeds East National Health Service Research Ethics Committee (18/YH/0234) and the NHS Health Research Authority’s Confidentiality Advisory Group (18/CAG/0126) to receive, link and provide data for research purposes. This study was granted approval by the CUREd Data Release Committee for access to a de-personalised dataset.
Acknowledgments
The authors thank Dr James Davies, consultant in Palliative Medicine, for reviewing the manuscript and providing additional insights on the interface between emergency medicine and hospital palliative care.
Supplementary materials
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Footnotes
Contributors All authors revised and contributed to the manuscript and met to develop the project, discuss and support research progress. PT developed the question, analysed data and wrote the manuscript. TS linked data, generated a study database and provided governance support. RS analysed data, generated images and provided statistical guidance. SK provided clinical insight and support from clinical palliative care service. SM led the project, manages the CUREd database and provided clinical insight from emergency medicine.
Funding This study was funded by a grant from the Sheffield Healthcare Challenges Collaboration, a local partnership between Universities and healthcare organisations. (grant no. X/012793-13).
Competing interests None declared.
Provenance and peer review Not commissioned; internally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.