1. Introduction
Cicely Saunder founded the St. Christopher’s Hospice in 1967, laying the foundations of the current palliative care movement and the need to implement end-of-life care. The initial use of the word “palliative” dates back to 1975 when the first palliative care service at the Royal Victoria Hospital in Montreal was created [
1]. The World Health Organization has defined palliative care as an approach to improve the quality of life of patients and families who are facing problems associated with life-threatening conditions. Its mission is to prevent and alleviate suffering through the early identification and treatment of pain and other problems, whether physical, psychosocial, or spiritual [
2,
3].
More than 56.8 million individuals are estimated to be in need of palliative care globally, including 31.1 million before and 25.7 million near the end of life. [
4]. It was used in 45.3% of all deaths in 2017 [
4]. Oncological disease accounts for about 28% of cases followed by human immunodeficiency virus (22%), cerebrovascular disease (14%), and dementia (12%) [
4]. Palliative patients from all over the world, aged over 20 years old, experienced 20 million days of suffering due to poor control of symptoms, namely, fatigue, pain, depression, anxiety, dyspnea, confusion, and delirium [
3]. These symptoms lead to admissions to the emergency department (ED) and hospital admissions, which, along with hospital death, negatively interfere with quality of life [
5].
Studies show that potentially avoidable admissions to the emergency department—defined as accesses to the emergency department that could have been managed in another type of health service or even avoided with preventive care—accounted for 19 to 58% of episodes [
6,
7,
8,
9]. These are associated with poor disease management, inadequate availability of services, and lack of patient literacy for decision-making [
10]. Decreased efficiency and increased healthcare costs are consequences of avoidable emergency department visits [
10]. Palliative care is cost effective and simple to apply at home; patients prefer it [
11,
12].
It is estimated that 400,000 health professionals are involved in the provision of palliative care, which represents only 0.9% of the total worldwide [
13]. The European Association of Palliative Care recommends two specialized palliative care services per 100,000 inhabitants; i.e., a hospital care team and a home care team [
13]. The growing need for palliative care implies that health systems know the reality, so that they are prepared to respond to it both in human and organizational terms [
13].
This study aimed to characterize the use of the emergency department by patients followed up in palliative care consultations between time of admission and time of death. Firstly, we wanted to characterize and identify differences between users and non-users of the emergency department. Secondly, we intended to characterize patients and the episodes in the emergency department and identify the factors associated with the use of the emergency department.
2. Materials and Methods
This retrospective study included patients who had their first consultation in palliative care at a public hospital in northern Portugal in 2019. We considered an average of 207 per year and the sample size was calculated taking into account a confidence level of 95% and a margin error of 5%, with random sampling, and obtained the necessary sample of 135 patients. [
14]. The study included deceased adults aged 18 years or more for whom there was complete information in their clinical files. Patients who were alive at the time of data collection, in May 2022, were excluded (
n = 10). A total of 135 patients were included in the study and accounted for 65.2% of the total patients admitted for palliative care consultation in 2019. This led to 255 admissions to the emergency department. The study was authorized by the Ethics and Data Protection Committee of the Hospital Center. The hospital center where the study took place has a palliative care team whose mission is to support patients and families in need of differentiated palliative care. It is a multidisciplinary team that includes doctors, nurses, a psychologist, and a social worker, working Monday to Friday, 8 a.m. to 5 p.m. Referral to the consultation can be carried out by doctors of any of the hospital services or by family doctors. The team has a telephone contact, available Monday to Friday, from 8 a.m. to 5 p.m., for patients and families as well as requests for advice from other health professionals. It is a consulting team without its own inpatient service and does not provide home care services. Home palliative care service is not available in this region.
Data were collected to characterize the patients and their use of health services: gender, age, marital status, residence (domicile, nursing home, continuing care unit, host family), time between admission to palliative care consultation and death, number of consultations between admission to palliative care consultation and death, number of hospitalizations between admission to palliative care consultation and death, time in the emergency department, place of death, death in the last admission to the emergency department or subsequent hospitalization, and hospitalization proposed in palliative care consultation. It also included data to characterize the episodes of admission to the emergency department: main complaint, number of complaints, time of admission, origin, request for the PC team’s opinion, length, and diagnosis. Statistical analysis was performed using SPSS, version 26.0. For description of the variables, the absolute (n) and relative (%) frequencies were used for categorical variables and medians (Mdn) and percentiles (P25 and P75) for the continuous variables, given their asymmetric distribution. The univariate associations of the categorical variables were evaluated using the chi-squared test or Fisher’s test in case the former’s assumptions were not met. Univariate associations of the continuous variables were evaluated using the Mann–Whitney test or the Kruskal–Wallis test for two (or more than two) groups. Multivariable associations were evaluated by constructing logistic models in case the dependent variables are binary. The work used a respective calculation of the adjusted odds ratio (aOR) and by constructing Poisson models in cases where the dependent variables are counts with a right-skewed distribution, with calculation of the adjusted relative risk (aRR). The inclusion of independent variables in these models was based on the criterion p < 0.10 in univariate analyses, to adjust variables that are more comprehensive. This, in turn, increases the models’ explanatory power. In multivariable models, the decision of statistical significance was guided by the criterion p < 0.05, with the confidence intervals, for this purpose, set at 95%.
4. Discussion
This study allowed us to investigate the characteristics of patients who attended a consultation to identify their profile regarding the use of health services as well as to globally analyze the episodes of admission to the emergency department.
Most patients included in this study were elderly, reflecting the important role of palliative care in the geriatric population. Worldwide, 40% of palliative care needs to address patients over 70 years of age [
4]. The predictions show that the need for palliative care will increase by about 183% by 2060 [
15].
The follow-up time was short and reflects late referral of patients to palliative care. Late referral collides with the approach that palliative care should be provided as early as possible in the course of the disease. Late referral is associated with poor symptomatic control, increased suffering, failure to discuss advanced care plans, caregiver burnout, and hospital deaths [
16]. Earlier transition to palliative care is associated with better symptoms control, reduced distress, and more respect for patients’ preferences [
17]. Early initiation of palliative care is also associated with reduced late-life acute hospital use [
18].
This study enrolled all patients regardless of pathology, although oncological disease was the most frequent. Worldwide, oncological disease has the highest representation in need of intervention by palliative care, but more than 70% of needs concern other health conditions, including human immunodeficiency virus, cerebrovascular disease, and dementia. These data show the importance of including these populations in studies [
13].
Most patients who use the emergency department lived at home, and most patients resorted to the emergency department despite follow-up in consultation. A greater number and time of follow-up in consultation was associated with more episodes and time spent in the emergency department. However, only a few users were advised by the palliative care team to use this service. Patients feel safer in the hospital than at home. They resorted to the emergency department due to difficulties in managing the clinical situation at home despite having caregivers [
12,
19]. Patients and families seek the hospital due to anxiety during episodes of worsening symptoms, lack of prior guidance by health teams, search for security and familiarity, and difficulty in accessing primary care in situations that they consider to be urgent, including outside regular office hours [
20]. The existence of a home team or telephone network of health professionals with training in palliative care that is permanent and available to respond to crisis situations potentially prevents patients from going to the emergency department [
20].
Among the patients who resorted to the emergency department, most died during the last admission or subsequent hospitalization. There were patients who were admitted in cardiorespiratory arrest and who died during their stay in the emergency department. Dying in hospital was associated with going to the emergency department. Patients who died during the last episode of the emergency department or subsequent hospitalization spent more time and were admitted more often into the emergency department. Patients with a higher number of emergency department admissions, hospitalizations, and hospital deaths possibly had a worse quality of life in the last months of life [
21]. Care and death at home are patients’ preference [
5,
21]. Home care promotes greater comfort, fewer hospital infections, and cost savings [
22]. Late referral of patients and, consequently, the presence of more severe diseases, might explain the difficulty in symptoms control, emergency department use, and hospital deaths [
16,
17].
Most hospitalizations took place following admission to the emergency department. This result may reflect the fact that the in-hospital palliative care team does not have its own inpatient unit, which leads patients and families to resort to the emergency department. Thus, there is an association between going to the emergency department and having been hospitalized at least once. Patients who had more than one hospitalization presented a greater number of admissions and a greater total length of stay in the emergency department. Patients hospitalized one or more times are twice as likely to be readmitted to the emergency department [
23].
Regarding the analysis of episodes in the emergency department, the frequency of complaints matches other studies that also found pain (15–46%), respiratory disease (13–26%), and digestive symptoms (12–26%) as the main admission symptoms [
7,
9,
12]. A wide variety of final diagnoses was obtained, but it is not statistically feasible to look for associations with the remaining variables. [
7,
9,
12]. Gastrointestinal and genitourinary complaints were associated with a shorter length of stay in the emergency department. There was often a correlation with easily resolved clinical conditions that correspond to likely potentially avoidable episodes, such as constipation, retention, or urinary tract infection. All health professionals who have contact with palliative patients should be familiar with the management of this symptomatology to improve symptom control and them resorting to the emergency department [
7,
9,
12].
There were more admissions after working hours. The palliative care team is only available from 8 a.m. to 5 p.m., Monday to Friday. Thus, admissions after working hours might happen because the emergency department is the only health service available in this period to respond to existing needs. [
7,
9]. Emergency medical or first aid ambulance was the most common means of accessing the emergency department. Health professionals involved in emergency transport recognize the advantages of death at home, but they have difficulty in promoting this deferral. The use of this resource is associated with a lack of alternatives in after-work hours, lack of clinical information about patients, and the health system’s focus on providing life support care [
24].
End-of-life patients should not need to resort to an emergency department and should remain at home, or, when this is not appropriate, be directly referred to a palliative care unit. It is thus necessary to invest in training and in the organization of the network of professionals qualified to act, thereby increasing the period of availability of face-to-face, telephone, or home service. Consultancy to other professionals is also needed to support the management of crisis situations [
19,
25,
26]. In 2019, Portugal had a ratio of 0.9 palliative medicine services per 100,000 inhabitants, which is less than the recommendations [
13]. In the geographic area studied here, there is no palliative care team available to provide care at home. The existence of palliative care teams composed of specialists from different areas (specialized palliative care doctors, nurses, and family doctors) with permanent accessibility is associated with a lower frequency of admission to the emergency department. Palliative care at home significantly increases patient satisfaction, reduces the use of medical services—whether visiting the emergency department or being admitted to the hospital—and lowers end-of-life medical care costs. [
27].
This study has some limitations. A retrospective analysis was performed, and hence the collection of information was dependent on its availability in clinical records. The sample reflects the reality of one region, and patients that were alive at the time of data collection were excluded, given the small number of patients. These factors should be considered for the construction and improvement of future studies on the subject. Nevertheless, this study does address a topic that lacks information both at a national and international level. The conclusions drawn here will help improve health services.
5. Conclusions
The aim of this study was to describe the use of the emergency department by patients followed up in palliative care consultations until death. The results show that the responses of the health system do not suit the needs of patients and families given that the majority had to resort to the emergency department. Dying in hospital was associated with going to the emergency department, and patients who died in the hospital had more admissions and spent more time there.
Among the strategies to improve the provision of care, there is the establishment and creation of action guidelines for professionals. This can combine palliative medicine services and primary care so that crisis situations can be better managed in the community. An automatic consulting system can be created for specialized clinicians based on pre-defined clinical criteria [
19,
28,
29,
30,
31]. A fragmented health system cannot effectively deal with the increased demand for care due to aging populations, thus increasing long-term chronic diseases and multimorbidity. Palliative care must be integrated at all levels of health systems to ensure smooth transitions and continuity of care [
32]. Undergraduate and postgraduate training in palliative care is essential to create a network of health professionals that can adequately manage the needs of patients [
13]. It is necessary to invest in patient and caregiver education and establish an early care plan. There must also be organizational responses; e.g., telephone and digital assistance across more hours, for a timely response to a crisis situation. There is a need for regular contacts and communication as well as more home visits.
The use of an emergency department by palliative patients is a sign that there are gaps to be filled in the provision of care. Therefore, solutions must be implemented to respond to the growing needs in this area.