Abstract
Background:
Physicians play a key role in end-of-life decision-making. As research suggests a connection between physicians’ personal end-of-life preferences and their clinical practice, it is important to understand what physicians want for themselves at the end of life and what has shaped their preferences.
Objective:
To explore what physicians have considered for their end-of-life preferences, including life-sustaining and life-shortening practices, and their perceptions of the socio-cultural factors that influence their preferences.
Design:
Qualitative study using in-depth interviews.
Methods:
Forty-five interviews were conducted from January to November 2022 using a semi-structured interview guide. Participants included three types of physicians: general practitioners, palliative care physicians, and other medical specialists in Belgium (Flanders), Italy, and the United States (Wisconsin). Data collection and analysis were informed using the reflexive thematic analysis approach. Audio recordings were transcribed verbatim and NVivo 14 was used for coding and analysis. Consolidated criteria for reporting qualitative research (COREQ) were followed.
Results:
We found physicians, particularly those in palliative care, have reflected on their end-of-life preferences and have ideas about what constitutes a good death and what they hope to avoid. Most physicians prefer to avoid aggressive and life-prolonging treatment, physical and mental suffering, and being a burden. They prioritize being in a peaceful environment and communication with loved ones. Various factors influence preferences including cultural, social, and religious beliefs, and legislative environment, but most significant are the deaths of loved ones and clinical practice. Death and dying become normalized the more they are reflected upon and discussed, and this process can also provide personal growth which helps physicians provide better care to patients and families.
Conclusion:
Physicians have reflected on their end-of-life preferences and prefer a peaceful end of life without aggressive and life-prolonging treatment. Physicians’ views on end-of-life practices are influenced by evolving cultural and societal norms and legal and ethical factors.
Introduction
Physicians play a central role in conversations about end of life and decision-making for patients nearing death. These conversations often involve highly impactful decisions to limit treatment and focus on comfort or even to hasten death. 1 Research indicates a stark contrast between the care physicians provide to patients and the care they would choose for themselves at the end of life, due in part to their individual approaches to practice. 2 This discrepancy is significant, as it underscores differences in attitudes as well as the personal and professional dilemmas faced by physicians managing complex end-of-life issues. 3 Like many patients, physicians wish to forego high-intensity end-of-life treatments for themselves; this is especially true for physicians who have had high exposure to very sick patients.2,4 Moreover, most physicians would refuse life-sustaining treatments in a scenario with a poor prognosis. 5
Various factors influence physicians’ end-of-life preferences, including their personal and professional backgrounds, and ethical perspectives.5,6 The factors found to have the most significant impact on physicians’ preferences include religious background, personal values, age, health status, physician specialty, experience, country of origin, and place of training.7 –9 For example, physicians generally prefer less aggressive end-of-life treatment, particularly older physicians who are white and practicing in Western countries; younger physicians who have worked in a clinical environment are more comfortable withdrawing life support; and physicians with more strongly held religious beliefs are more likely to object to the withdrawal of life support and assisted dying practices.7 –9 The legislative environment’s influence on attitudes and end-of-life preferences is a another important consideration as assisted dying becomes available in more jurisdictions around the world. Research indicates that use and acceptance of assisted dying practices increase over time due to evolving cultural attitudes that prioritize autonomy and greater acceptance and familiarity among medical professionals and the public. 10 The influence of these complex and often intermingled factors may help explain how some physicians come to prefer one treatment decision for themselves and another for their patients and shed light on the tension that exists for some physicians in reconciling personal convictions and professional responsibility. 3
Palliative care integration is another factor that can significantly influence physicians’ attitudes toward end-of-life care, with levels of integration varying across jurisdictions based on each country’s healthcare policies and cultural contexts. In Belgium, palliative care began in the 1980s and has since become an integral part of its healthcare system, establishing comprehensive services, including home care, hospital-based units, and palliative day care centers, supported by regional federations and multidisciplinary teams. 11 Italy has also made significant strides in integrating palliative care, particularly for cancer patients, with services provided in various settings including hospitals, hospices, and at home. 12 Palliative care in the United States has had substantial growth over recent decades, becoming more embedded within the healthcare system and services are widely available across hospitals, outpatient clinics, and home-based settings. 13
Understanding the perspectives of physicians, who are at the frontline of end-of-life decision-making, is crucial for several reasons. First, physicians’ attitudes and experiences impact their approach to end-of-life care and influence their decisions to recommend some treatments over others. 6 Second, exploring the connection between physicians’ end-of-life preferences and their clinical practice can enhance the knowledge base by offering deeper insight into the complex factors shaping physicians’ attitudes toward end-of-life decisions. Finally, physicians encounter challenges aligning their personal beliefs with their professional practice so a more thorough understanding of why they think and feel as they do is critical. 3
Existing studies on physicians’ end-of-life preferences are limited in both geographical scope and the range of end-of-life decisions examined. International comparative research can provide valuable insights into how cultural, social, and system-level differences influence physicians’ personal end-of-life preferences. By exploring diverse perspectives, we can uncover commonalities and unique challenges, which lead to more informed, globally relevant evidence to help align clinical care with patient values. To the authors’ knowledge, no international comparative studies have been conducted.
In this study, we address the following research questions:
What are physicians’ considerations about their end-of-life preferences?
How do physicians perceive their end-of-life preferences are impacted by personal, professional, cultural, legislative, social, and religious influences?
Methods
Study design
Qualitative study using semi-structured in-depth interviews.
Context and setting
We selected physicians practicing in jurisdictions with diverse cultural environments and varied levels of experience with assisted dying legislation. We included physicians in Belgium (Flanders), Italy, and the United States (Wisconsin).
Participant recruitment
We used a purposive sample in each country. Due to their varied levels of experience treating adult patients at the end of life, we sought to include three types of physicians: general practitioners, palliative care physicians, and other medical specialists with a high likelihood of seeing patients facing end-of-life issues (i.e., cardiologists, emergency medicine, gastroenterologists, geriatricians, gynecologists, internal medicine, intensivists, nephrologists, neurologists, oncologists, pulmonologists). Our goal was a distribution of physician types that included a minimum of five general practitioners, five palliative care physicians, and five medical specialists in each jurisdiction, amounting to 15 in each jurisdiction and 45 total physicians. Physician participants were identified through the networks of our research partners in each country, as well as through medical associations and professional societies, and self-identification following participation in the PROPEL online survey. This qualitative exploration is part of a multi-method study called PROPEL: Physician Reported Preferences for End-of-Life Decisions. Following initial contact by email or telephone, physicians received an email invitation detailing the study, information on the research team, and eligibility for participation.
Inclusion and exclusion criteria
Currently practicing physicians in the following groups were eligible for participation: general practitioners, clinical specialists (cardiologists, emergency medicine, gastroenterologists, geriatricians, gynecologists, internal medicine, intensivists, nephrologists, neurologists, oncologists, pulmonologists), or palliative care physicians. Exclusion criteria were having less than 2 years of clinical experience and being unable to do the interview in English. We originally planned to include only physicians with 5 or more years of experience. However, since we encountered recruitment challenges, eligibility was expanded. Most of the recruited physicians had 10–40 years of experience.
Data collection
Data were collected between January and November 2022 using a semi-structured interview guide. The interview guide (Appendix A) was pilot-tested with three physicians and adjusted for clarity and appropriateness before use. Most interviews were conducted online using a video conferencing platform (Zoom or Teams) due to COVID-19 restrictions. However, five interviews were conducted in person, at the office or home of the participant, and one at a public library. The interviews varied in length from 30 to 80 min and no repeat interviews were conducted. Notes were made following each interview. All interviews were conducted by the lead author (S.M.), a female doctoral researcher with previous experience conducting qualitative research with physicians (credentials – MSc, MPH). S.M. had no prior relationship with the participants, apart from two Wisconsin physicians who had previously provided care for her mother. Due to the complex nature of the interview topic, participants were offered language support through the attendance of a second researcher who spoke their native language and could explain complex questions or responses. Some European physicians accepted this option (Italy 4, Belgium 1). A demographics form was completed at the start of each interview.
Data analysis
Interviews were audiotaped and transcribed verbatim. Data collection and analysis were informed using the reflexive thematic analysis approach. A reflexivity statement was developed by the lead researcher (Appendix B). Reflexive thematic analysis is an ideal approach for this study as its flexibility allows for a deep examination of the multifaceted nature of end-of-life preferences without the constraints of rigid frameworks, making it well-suited to capture the complexity of this topic. 14 It emphasizes personal meaning and perception and aligns with our focus on physicians’ subjective experiences and reflections. The iterative, reflexive nature of this method ensures that the researcher’s role in interpreting sensitive, personal data is acknowledged, providing room for richer, more nuanced insights. 14 It excels in exploring the intersection of broader social and cultural contexts with individual decision-making, making it ideal for understanding the varied influences on physicians’ preferences. Identifying patterns across the data helps uncover shared and divergent experiences, facilitating a comprehensive understanding of the study population. Additionally, it is an inductive, data-driven approach, which allows for open exploration, making it particularly useful for research without predefined categories, enabling the discovery of unexpected themes. 14
Interview transcripts were imported to Lumivero’s NVivo (version 12) for analysis. Our recruitment goal was met, and thematic saturation was achieved in each jurisdiction. Reaching saturation suggests that the themes generated from the interviews are comprehensive and robust enough to address the central research aims, allowing for a nuanced understanding of the phenomenon being studied without the need for further data collection. The lead author (S.M.) coded all transcripts, and another team member (F.D.) independently coded four transcripts for comparison. Transcripts were not shared with participants. Initial codes were discussed and refined (by S.M. and F.D.) and themes and sub-themes were developed. The themes were then refined and discussed further by the full research team and similar or overlapping themes were collapsed or removed. A thematic map was then developed and evaluated, and associated interview quotes were identified, discussed, and selected by the full research team. Participants did not provide feedback on the findings. Consolidated criteria for reporting qualitative research (COREQ) were followed (Supplemental Material).
Results
We collected data from interviews with 45 physicians, 15 in each country. Participants included 23 female and 22 male physicians (Table 1). Most were white/European (43) and identified as either Christian (23), non-religious (16) or other religion (6) and fell within the age groups <40 years (18), 40–59 years (22), and >60 years (5). We nearly achieved our target balance of selected specialties with 15 general practitioners, 14 palliative care physicians, and 16 other medical specialists participating.
Characteristics of participating physicians, per jurisdiction.
Missing values: end-of-life patients:
What do physicians consider for their own end of life
The sample reported a wide range of personal preferences related to various end-of-life decisions, shared information about the influences on their preferences, detailed elements they consider important for having a good death, and undesirable scenarios they hope to avoid.
We developed three main themes related to physicians’ consideration for their own end-of-life preferences: (1) Notions of a good death – physicians have developed ideas about what a good death would look like for themselves; (2) Preferences can evolve – physicians recognize their preferences could change over time; and (3) Reflection and discussion bring comfort – death and dying become normalized through reflection and discussion (Figure 1).

Thematic map of physicians’ consideration for their own EOL preferences.
We found that most physicians have considered their personal end-of-life preferences, and for many, their ideas have clarified over time. Many physicians shared that they think regularly or often about their own mortality and have given some consideration to end-of-life issues. Palliative care physicians reported having reflected a lot on their own end-of-life preferences, which was not the case for general practitioners or other medical specialists.
Many physicians stated they have formed strong ideas about what constitutes a good death after witnessing experiences with family members or patients they considered peaceful and positive, and, conversely, situations they would prefer to avoid.
Physicians often cited the elements of a good death as being at home or in hospice, anticipating death, loved ones nearby, enough time for goodbyes, not suffering, pain and symptoms controlled, spiritual and practical affairs in order, a clear mind, and autonomy and dignity preserved.
Physicians largely preferred a death at home or in a peaceful environment. However, a small number said they have become accustomed to medical environments, and they would be fine with dying in a hospital. Many physicians specified that they would prefer to know that death was coming so they could prepare by putting their practical affairs in order and say goodbye to loved ones.
“Ideally, I am a much older man. I have a terminal illness that I see coming, so that way I have time to prepare and do the things that need to be done, say the things that need to be said. Family and people I care about around me, not in the hospital, in my own bed. Fairly free of symptoms, though I think a certain amount of suffering is just inevitable in end of life.” (Palliative care physician/internal medicine, Wisconsin)
Physicians also shared that they would prefer to avoid suffering and uncontrolled pain, and some specified they would like palliative care support and a competent medical team. If suffering could not be controlled, many physicians said they would want palliative sedation, and some would request assisted dying.
“I think (palliative sedation) it’s in line with the good death . . . I have seen what it can do and how people can say goodbye with more time and I think it’s a good alternative. It’s a good way of dying if you choose for it. If I would choose for it, I would. I think everything will be okay.” (Medical specialist, Belgium)
Other physicians shared that dignity and autonomy and having the ability to maintain cognitive clarity at the end of life are primary issues of concern to them.
“It’s all about what we call dignity. And it’s a very broad term, but I think (to) be aware of the situation is very important. Being able to say goodbye to your relatives, to your loved ones, to be as comfortable as possible and to be without fear and without worries. Because it’s not because I work in palliative care that I’m not afraid of dying. And I hope that I will be surrounded by people who can give me comfort and who can, because I think I will be very frightened.” (Palliative care physician, Belgium)
For some physicians, preserving a level of independence and not being a burden on their families at the end of life is a significant concern. Several palliative care physicians stated that part of a good death is that it is not medicalized.
Physicians shared that they have noticed patients and/or family members change their minds and want very different things at the end of life than they might have considered earlier. Personal preferences and what one considers acceptable can evolve as an illness progresses and physicians acknowledge this could also be the case for themselves.
“My intention . . . is to revisit that document every ten years to make sure it’s still applicable because, gosh darn it, so many patients I’ve run into change their mind. Over time you can get acclimated to new baselines you never thought that you could.” (Palliative care physician, Wisconsin) “How you change in the course of dementia, how you as a person change. And even if you think this will be burdened to me, once you are in that state, that burden often is not that clear anymore just the same as you would think. I don’t want to have chemo in my life because see how sick people are. But once you suffer from a cancer, you are willing to get chemo, so things change.” (General practitioner, Belgium)
Physicians expressed a level of acceptance about the fact that they may change their minds in time. In fact, some physicians cite this as the reason they have not yet done an advance directive, which was the case for many participants.
“I think it is much more important at regular times to speak with my family (about) how I’m looking and maybe like I look now to health and to diseases and end of life circumstances. This is a dynamic process. Probably I will change my mind in the next years. That is possible and acceptable.” (Palliative care physician, Belgium)
Other physicians say their preferences have changed due to exposure to specific clinical situations or they have become more nuanced. For example, some physicians described having an opposition to assisted dying as an option for themselves early in their careers but becoming more open to assisted dying practices after seeing various difficult end-of-life scenarios. Others say their preferences developed early, such as avoiding aggressive life-prolonging measures, and have only deepened over time. Other physicians believe their core preferences have stayed constant over time and their wishes have altered little.
“At least six months of my residency was spent pretty heavily pondering what a good death can look like and what good deaths look like. And then, you know, probably at least monthly something crops up where it makes me reflect on my own mortality. Either at work or at home or in the universe. I don’t think I spend more than 30 seconds thinking about it, because I feel like, my opinions aren’t changing, my views aren’t changing.” (General practitioner, Wisconsin)
Some physicians reported feeling uncomfortable and uncertain during end-of-life conversations early in their careers but after more personal reflection on their own feelings and preferences and more clinical experience they came to feel more at ease initiating and navigating difficult end-of-life conversations with patients and families.
“Thinking about my own end of life preferences has made me, continues to make me more open with discussing different scenarios with my patients. So I think that has helped me, just, I think the more I’m introspective about things the better I’m able to talk about those scenarios with my patients. Not necessarily influence the way I talk about it, but just, you know, makes me more open to those conversations with people.” (Medical specialist, Wisconsin)
Physicians’ perceptions of how their own end-of-life preferences have been impacted by personal, professional, cultural, legislative, social, and religious influences
When we explored how physicians have reflected on their own end of life and perceive their preferences have been impacted by socio-cultural influences, physicians shared that their personal reflection on end of life is often triggered by a specific catalyst. These motivators include personal interest/curiosity, treating patients of a similar age, patient situations, history of illness in family, getting older, personal/family end-of-life experiences.
From the interview data, we identified four main themes and two sub-themes, including: (1) Death of loved ones – physicians have been significantly impacted by the death of loved ones; (2) Clinical practice experiences (sub-theme: Undesirable situations) – physicians have been influenced by their clinical practice, particularly negative experiences; (3) Assisted dying laws – physicians have been influenced by the existence/absence of assisted dying laws; and (4) Socio-cultural context (sub-theme: Religious beliefs/faith) – physicians have been influenced by a variety of factors including culture, ethnicity, education, social norms, personal/family values, and particularly, religion.
Many physicians shared experiences of having acted as a caregiver for a loved one or seeing the impactful death of parents, grandparents, family members, or other loved ones. Often the illness trajectory and/or cause of death was mentioned as shaping the experience as positive or negative and influencing their attitudes toward preferring or rejecting certain end-of-life decisions.
Many physicians discussed being strongly influenced by seeing loved ones die after a prolonged illness with dementia or cancer, which sometimes involved choices or treatments they would not prefer for themselves.
“That (mother’s illness) was probably the primary one. I saw her suffer through cancer for almost 18, 19 months and chemo, radiation, everything, and I, I think if I had a terminal diagnosis like that, I probably wouldn’t do anything.” (General practitioner, Wisconsin) “I think going through it personally was also helpful with my father’s experience, and he actually made choices I would not make for myself. And we respected and supported them . . . personal experience really made me much more comfortable and realizing how important it was to have these conversations.” (Palliative care physician, Wisconsin)
Other physicians discussed the sudden death of family members, especially young family members, as a particularly challenging experience and a significant influence on their lives and personal preferences.
“I would say my child’s death in some ways made it more personally difficult for me, but yet also a little bit more of a calling to try to make it be a better experience for, for patients and families.” (General practitioner, Wisconsin)
Seeing difficult end-of-life patient situations and helping patients make end-of-life decisions profoundly impacts what physicians prefer for themselves. Many physicians described challenging end-of-life scenarios that involved prolonged illnesses with high levels of physical or psychological suffering or situations with cognitive impairment and dependency as being influential. Many also described seeing patients receive aggressive or futile treatments that they would strongly prefer to avoid at the end of life. Some physicians described being impacted by treating patients of similar age to themselves. Other physicians described peaceful deaths, or sudden deaths, or assisted deaths they thought might be preferred, or not preferred, for themselves.
“I just vividly remember this, an intensive care unit where every single person was a young man with Aids and pneumocystis pneumonia on a ventilator. None of them would survive, and it just would be one after another die, die, die, die. And, you know, finally . . . a lot of hospitals either said to people, you know, we’re not going to put you on a ventilator with this condition because you’re not going to survive it. So you’re better off just having palliative care or, you know, I think there was a certain amount of assisted, you know, assisted dying going on. You know, maybe sort of under the table, so to speak. But, you know, that was just horrible to see, you know, people just, you know, sort of be kind of bright and perky, get intubated, they’re awake at the time, and then that’s it, you know, then that’s the last moment that they’re awake or interacting with anybody. And I just thought, this is just really awful. So that, that I think really influenced me.” (Palliative care physician, Wisconsin)
Some physicians explained that their clinical experience working in an intensive care unit influenced them to prefer another type of environment at the end of life and others shared that exposure to palliative care teams or receiving palliative care training was influential and exemplified the kind of care they would prefer to receive at the end of life.
“My time in critical care is probably the biggest (influence). Well, and, if I could choose a second, I would say my interaction with the palliative and hospice care services, to know that that existed and to kind of get what they do and to think, wow, this feels so comfortable. And, and actually, it’s a strangely joyful place to spend time. And so my time in critical care showed me a lot of what I don’t want. And my time with in working with the palliative and hospice care folks was shorter, but probably equally meaningful.” (General practitioner, Wisconsin)
The undesirable situations detailed by physicians in the interviews included: sudden deaths, being in the hospital or intensive care unit at the end of life, having uncontrolled symptoms or severe pain, being on a ventilator long term without the ability to communicate, receiving futile or aggressive treatment, experiencing physical and/or psychological suffering, being alone, being dependent on others for care, being confused or cognitively impaired, and being a burden on their families.
“I hope I will not die alone. That’s what we see in some care units or that there we see patients that have not a lot of family, and where only the doctors and palliative care personnel is there for the patient, so I think that’s very important to me. Another thing is, is that the things you hear a lot like suffocation or a lot of pain that are the two main reasons that I hear a lot and that are also praying for myself that I hope to avoid. And I think we can avoid at the end of life.” (General practitioner, Belgium)
Most physicians expressed the desire to avoid life-prolonging treatment at the end of life including cardiopulmonary resuscitation, artificial nutrition and hydration, and mechanical ventilation. The concepts of being dependent and physical and mental suffering also came across as a main concern for physicians considering possible end-of-life scenarios.
“I guess (I hope to avoid) a lot of pain at the end where there’s trouble with pain relief. Also, like the physical indignities of the end stage where you are incontinent and you need to depend on other people. I think also like more the emotional burden, if you would be, if I would be very young to die and I would know it in advance. And you see the suffering of your family. I have four children myself so I think that would be horrible to know that I would have to leave my children. So I think it’s both the physical suffering as the, as the mental suffering.” (General practitioner, Belgium)
Some physicians feel assisted dying laws are a positive and important end-of-life option for themselves and patients and are grateful to live in a jurisdiction that allows these options or express a wish to have an assisted dying option available to them. Other physicians are opposed to assisted dying for themselves, or for everyone, and expressed concern and conflict about the notion of having to practice medicine in an environment that allows assisted dying should it become legal where they practice. These beliefs seem to be often aligned with the legal situation in the jurisdiction of the physician.
“I think this (assisted dying law) will influence us as physicians and just in our own personal view, if you can talk about something freely, I think it will alter your way of thinking also. Yeah, but in this way, I’m happy that we can. We don’t have to have any fear about this topic.” (Medical specialist, Belgium) “This can influence you because if nobody among you, nobody in the hospital, nobody among patients, nobody among your friends even have to speak about assisted suicide or something like that, you never start to think about it and you just think implicitly that this is not a solution to consider.” (Medical specialist, Italy) “I think not only Wisconsin, but, you know, the United States in general. So absolutely, it affects, it limited my scope of thought process because when I was filling out the survey, I thought, oh, wow, I really haven’t even thought about this. And it’s because, it’s not, it’s not an option for me or my patients or my family.” (Medical specialist, Wisconsin) (The “survey” refers to the related PROPEL quantitative survey study)
Some physicians acknowledged feeling undecided or conflicted about assisted dying practices or believe their preferences have not been impacted one way or another by the presence or absence of an assisted dying law. We also found that palliative care physicians strongly preferred palliative sedation to assisted dying at the end of life. Many general practitioners and other medical specialists said they would consider assisted dying if it were a legal option and all physicians said they would consider palliative sedation an option to relieve suffering at the end of life.
Physicians shared personal stories and traditions related to death and dying within their families, often of their parents or grandparents, as well as impactful exposures to films, books, media stories, etc. For example, the books
“I traveled a lot for purpose of studying and working, and that really helped me a lot in seeing different perspectives in different relationships with doctors and their patients. The cultural situation and also practical aspects of care and, and I’m sure that they helped me a lot in feeling more comfortable, because I think if I just lived in Italy, probably I would be more narrow minded because I would have I would not have seen so many things. That really impacted the way that I opened the discussion about end of life.” (Palliative care physician, Italy) “Reading about people dying, even in a fictional setting, or probably more so in a fictional setting, has influenced me. I mean, there’s some of the most beautiful and accurate passages about death in literature.” (General practitioner, Wisconsin)
Some physicians described having a strong connection with God and/or their faith and a comforting belief that their lives and end of life are in the hands of a higher power. Some cite their religious beliefs as the basis for their opposition to assisted dying practices and belief that the end of life should not be hastened. Other physicians describe being influenced by treating patients with strong religious beliefs, who received what the physician considered overtreatment due to religious objection to ending treatment. This seems to be a key issue as several physicians expressed concern and objection to receiving aggressive or futile treatment at the end of life and this was influential on their personal preferences.
Our study found that physicians with more strongly held religious beliefs were more opposed to assisted dying practices. This was prominent with physicians from Italy but also with the more religious physicians in Belgium and Wisconsin.
“I think that religion influences me only to artificial death . . . I’m against to artificial death. I think because of religion, cultural aspects, really in myself and I think that this aspect could influence.” (General practitioner, Italy) “And the way you are raised as a child, for example, I’ve been raised in a rather, a very Catholic family, actually. So my, mother and father, they went to mass every Sunday. We prayed. I had to go there, too. I don’t do it anymore now. So I’ve lost that kind of necessity but I still consider myself a Catholic, so I didn’t. I still consider myself as being a Christian, a Christian man. But it all shapes you to what you want also. You . . . have to think about it because it influences, of course, your way of working with people. Which might, which might be a danger because you might want to fill in for the patient like the way you want it to be.” (General practitioner, Belgium)
Other non-religious physicians shared that they held spiritual or other personal beliefs that influenced their preferences. Some non-religious physicians noted that it is hypocritical to argue that medicine should not interfere at the end of life since medicine has developed in significant ways and often intervenes and impacts the beginning of life.
“I’m not religious. So for me deciding or taking end-of-life decisions, for me, there is no religious component in, or like, life is sacred. I think that medicine had already developed. I always think it’s a bit hypocritical to say that we can’t decide for God, because we do it already. If you see what we do with little children when they’re born, when they’re 23, 24 weeks, we already play for God. So when we can play for God in the beginning of the life, I don’t see why we shouldn’t, can’t do that at the end of life. Yeah. That’s really, so I totally, I respect the religious people but I totally disagree with that because we do it already.” (General practitioner, Belgium)
Discussion
This study found many physicians, particularly those in palliative care, have reflected on what they would want for themselves at the end of life and have developed ideas about what they consider a good death and what they hope to avoid. Physicians have notions about what they would prefer but acknowledge their preferences could evolve and become more nuanced. Most physicians prefer to avoid aggressive and life-prolonging treatment, physical and mental suffering, and being a burden. They prioritize being in a peaceful environment and retaining the ability to communicate with loved ones. Physicians’ preferences are shaped by various factors, including cultural, social, and religious beliefs, and legislative environment. However, their experiences with the deaths of loved ones and their clinical practice play a particularly significant role. Physicians emphasized that death and dying become more comfortable and normalized the more they are reflected upon and discussed and feel this process can also provide personal growth and help them provide better care to patients and families.
It is not unexpected that physicians with extensive experience caring for end-of-life patients have reflected deeply on the type of care they would desire for themselves at the end of life. However, it is notable that physicians across all specialty groups and countries have developed ideas about what they would prefer for themselves and what constitutes a good death, and many have well-formed opinions about the scenarios they hope to avoid. Physicians’ ideas are mainly based on the suffering they have witnessed during the death of a loved one, caring for end-of-life patients with extremely challenging clinical situations or seeing patient choices they would not prefer for themselves. This aligns with research indicating that the emotional challenges of caring for dying patients can influence physicians’ thought processes and decision-making.15,16 Although some physicians highlighted experiences of observing peaceful and meaningful deaths, the most powerful influence seems to be the end-of-life experiences they found most challenging and hope to avoid. While we have tried to include a diverse group of physicians, it is possible that physicians with less exposure to end-of-life patients would have less developed ideas about their own end-of-life preferences.
Personal and professional experiences have considerable effect on physicians’ end-of-life preferences. For some physicians, personal experiences including acting as a caregiver, making end-of-life decisions for family members, or witnessing the death of loved ones, has had a profound impact on their lives and preferences. Seeing a loved one suffer from a prolonged illness and receive intensive treatment has led some physicians to prefer some end-of-life decisions over others, or generally less aggressive treatments for themselves. This finding is in line with research indicating that physicians generally prefer less intensive and life-prolonging treatment, particularly those with high exposure to very sick patients.2,4 Professional experiences like caring for patients with challenging end-of-life scenarios or working in intensive care units have also significantly impacted and clarified their personal preferences. This is likely due to observing intensely challenging circumstances firsthand, seeing diverse outcomes, and developing expertise over time through active involvement in patient care. This exposure has led many physicians to prefer a peaceful, non-medical environment at the end of life. These experiences also raise ethical considerations, as physicians must navigate intense emotional responses in high-stress medical situations involving patients or loved ones, which have the potential to cause moral distress.
Existing research on end-of-life preferences reveals significant differences between physicians, patients, and the general public.3,17,18 While physicians tend to prefer less aggressive interventions, patients and the public often opt for life-prolonging treatments despite expressing a desire for comfort-focused care.3,17 Studies have found that physicians are more aware of the burdens of life-sustaining treatments and are more likely to forgo interventions like mechanical ventilation and cardiopulmonary resuscitation (CPR), and receive fewer invasive treatments at the end of life.3,17,18 Physicians appear to prioritize the quality of life over longevity, while patients and the general public are inclined toward life-sustaining treatments, possibly due to fear, uncertainty, or lack of medical knowledge. 3 Despite cultural differences, physicians, patients, and the general public share common views on what constitutes a good death, often associating it with maintaining dignity, effective pain and symptom management, and being with loved ones at the end of life.19 –21 This suggests that some end-of-life priorities may be universally held.
We found striking variation in physicians’ end-of-life preferences connected to cultural influence, legislative environment, and physician specialty. Physicians’ attitudes about assisted dying seem to vary based on cultural and legal environment and personal beliefs. Physicians in jurisdictions where assisted dying is legal or where laws have been considered (Belgium and Wisconsin) more often view it as a positive and important end-of-life option, while others express discomfort, especially if their cultural or religious beliefs, or the legal framework of their country, opposes it (Italy). Religious beliefs can also contribute to the complex emotions’ physicians experience, influencing both their personal preferences and their moral interpretation of clinical and personal experiences. Palliative care physicians clearly prefer palliative sedation to assisted dying, which may be a result of their familiarity with the practice and belief that appropriate palliative care can manage suffering at the end of life. This supports previous research which finds variation in attitudes toward end-of-life practices based on medical specialty. 22 Many general practitioners and other medical specialists would consider both palliative sedation and assisted dying for intractable suffering at the end of life. Cultural norms, family traditions, and exposures to death through art and media have also clearly played a role in shaping physicians’ normative beliefs and preferences. These findings suggest that physicians’ beliefs, including religious and ethical convictions, significantly shape their views on assisted dying and other end-of-life practices, highlighting the complex interplay between individual values and professional practice.
Our findings provide insights into the factors shaping physicians’ end-of-life preferences and highlight how these preferences, which may differ from the treatments they provide to patients, are formed. It also raises important questions that warrant further research. For instance, how do physicians’ own preferences influence their clinical practice and recommendations to patients? Are physicians effectively separating their personal preferences and deferring to patients’ wishes? What supports do physicians have in balancing the tensions that exist between personal values and professional responsibility? How does the reluctance of some physicians to reflect on their own end of life or openly discuss such issues with patients, colleagues, or loved ones impact clinical practice? Should personal reflection and training in end-of-life conversations be obligatory in medical education or continuing professional development? Does exposure to assisted dying legislation increase acceptance over time, regardless of personal religious beliefs?
Strengths and limitations
A strength of our study is the cross-national qualitative design, including physicians across three countries representing varied legal and cultural environments and the participation of three groups of physicians – general practitioners, palliative care physicians, and other medical specialists. Our preferred balance of physician groups was successfully recruited and the total sample of 45 physicians was ideal to gather comprehensive insights given our research questions, the diversity within the sample, and our analytical approach. By focusing on how physicians have considered their end-of-life preferences and the factors that influence them, we provide a much-needed addition to the current literature on physicians’ end-of-life preferences. The study had certain limitations. Although the final sample included a variety of physician groups in three countries, it was ethnically homogenous, and there may be selection bias as the interview study could have attracted those with a particular interest in end-of-life issues, resulting in a sample that may have reflected more intensely on the topic.
Policy and practice implications
These study findings suggest several important implications for policy and practice. First, clear policies and ethical guidelines are needed to help physicians manage moral conflicts and maintain professional boundaries to ensure that clinical recommendations are based on patient preferences rather than personal beliefs or biases, particularly in end-of-life care. Second, ethical guidelines would help physicians navigate complex decisions, such as those involving physician-assisted suicide or euthanasia. Third, promoting palliative care training, which fosters a person-centered approach, could help reduce the influence of personal preferences on patient recommendations, making it crucial to integrate palliative care principles into general medical education. Fourth, addressing cultural and religious influences on physician decision-making through cultural competency training is also essential, especially in jurisdictions where strong religious traditions impact patient care.
Conclusion
Many physicians have reflected on their end-of-life preferences, particularly those who work in palliative care. They generally favor less aggressive and life-prolonging treatment and prioritize communication with loved ones and minimizing pain and suffering. Their preferences are largely shaped by experiences, such as the death of a loved one and clinical practice, and are also influenced by social, cultural, and legal factors including religious beliefs and assistance dying legislation. We found variation in attitudes across physician groups and countries, which suggests that physicians’ views on end-of-life practices are evolving, particularly in response to changing cultural and societal norms, legal and ethical factors, and changes in medical practice. Some physicians feel engaging in end-of-life reflection and discussions can foster personal growth and help them provide better care. Further research is needed to gain deeper insight on physicians’ personal end-of-life preferences as well as their underlying socio-ethical-cultural basis.
Supplemental Material
sj-docx-1-pcr-10.1177_26323524251351349 – Supplemental material for What do physicians want at the end? An international qualitative study on physicians’ personal end-of-life preferences and what influences them
Supplemental material, sj-docx-1-pcr-10.1177_26323524251351349 for What do physicians want at the end? An international qualitative study on physicians’ personal end-of-life preferences and what influences them by Sarah Mroz, Frederick Daenen, Sigrid Dierickx, Freddy Mortier, Ludovica De Panfilis, Luca Ghirotto, Toby Campbell, Kenneth Chambaere and Luc Deliens in Palliative Care and Social Practice
Supplemental Material
sj-docx-2-pcr-10.1177_26323524251351349 – Supplemental material for What do physicians want at the end? An international qualitative study on physicians’ personal end-of-life preferences and what influences them
Supplemental material, sj-docx-2-pcr-10.1177_26323524251351349 for What do physicians want at the end? An international qualitative study on physicians’ personal end-of-life preferences and what influences them by Sarah Mroz, Frederick Daenen, Sigrid Dierickx, Freddy Mortier, Ludovica De Panfilis, Luca Ghirotto, Toby Campbell, Kenneth Chambaere and Luc Deliens in Palliative Care and Social Practice
Supplemental Material
sj-docx-3-pcr-10.1177_26323524251351349 – Supplemental material for What do physicians want at the end? An international qualitative study on physicians’ personal end-of-life preferences and what influences them
Supplemental material, sj-docx-3-pcr-10.1177_26323524251351349 for What do physicians want at the end? An international qualitative study on physicians’ personal end-of-life preferences and what influences them by Sarah Mroz, Frederick Daenen, Sigrid Dierickx, Freddy Mortier, Ludovica De Panfilis, Luca Ghirotto, Toby Campbell, Kenneth Chambaere and Luc Deliens in Palliative Care and Social Practice
Footnotes
Appendix A: Propel semi-structured interview guide
Appendix B: Researcher reflexivity statement
As the lead researcher conducting this study, I (Sarah Mroz) recognize that my personal, professional, and cultural background may shape my approach to both data collection and analysis. My prior experiences with healthcare and end-of-life care, particularly as a caregiver for my mother during her cancer treatment, along with my cultural and social beliefs about death, dying, and medical decision-making, have the potential to influence how I interpret the participants’ reflections. Specifically, my experience with physicians who appeared uncomfortable or reluctant to discuss end-of-life issues during my mother’s illness trajectory reinforced my belief that end-of-life communication should be better incorporated within clinical care. I try to approach qualitative research with an open mind and listen compassionately to anything participants wish to share. I am deeply grateful for the opportunity to do this work and I respect the trust others place in me when they share their personal feelings and stories.
Additionally, I acknowledge that my assumptions about how professional, legislative, and religious influences intersect with personal preferences may affect the themes I emphasize during analysis. I am aware of the need to continuously reflect on how my positionality might impact the research process and I aim to remain open to the diverse ways physicians may consider their end-of-life preferences and to the possibility that their beliefs and influences may diverge from my own. To mitigate the influence of my preconceptions, I will maintain an iterative process of reflection and seek feedback from colleagues to challenge and broaden my interpretations. I aim to ensure that the themes that are developed are grounded in the physicians’ voices and experiences rather than my assumptions.
Ethical considerations
The study protocol was approved by the medical ethics committee of the Brussels University Hospital, which acts as the central ethics committee (BUN: 1432021000562, September 29, 2021). Approvals were also obtained from the ethics committee in Italy (AUSL, Comitato Etico dell’Area Vasta Emilia Nord: 748EE93B, April 7, 2022). The other participating institution did not require formal ethics approval.
Consent to participate
Participants signed a written consent form at each interview.
Consent for publication
Participants signed a written consent form at each interview.
Author contributions
Funding
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by internal funding from the Vrije Universiteit Brussel and Ghent University.
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.
Data availability statement
The datasets are available upon request. Requests may be addressed to the first author. Every request will be evaluated on an individual basis and the ethics committee of the Vrije Universiteit Brussels will be contacted for approval before any sharing of participant-level data.
Supplemental material
Supplemental material for this article is available online.
References
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