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Palliative Medicine
1 –13
© The Author(s) 2015
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DOI: 10.1177/0269216315616524
pmj.sagepub.com
What is already known about the topic?
The European Association for Palliative Care (EAPC) published a position paper on euthanasia and assisted suicide in 2003,
with concepts and definitions.
Changed legislation in some countries and an ongoing public discussion in many European countries indicate a broad range
of ethical norms and values underlying these discussions.
Euthanasia and physician-assisted
suicide: A white paper from the
European Association for Palliative Care
Lukas Radbruch1,2, Carlo Leget3, Patrick Bahr1, Christof Müller-Busch4,5,
John Ellershaw6, Franco de Conno7 and Paul Vanden Berghe8;
on behalf of the board members of the EAPC
Abstract
Background: In recognition of the ongoing discussion on euthanasia and physician-assisted suicide, the Board of Directors of the
European Association for Palliative Care commissioned this white paper from the palliative care perspective.
Aim: This white paper aims to provide an ethical framework for palliative care professionals on euthanasia and physician-assisted
suicide. It also aims to provide an overview on the available evidence as well as a discourse of ethical principles related to these issues.
Design: Starting from a 2003 European Association for Palliative Care position paper, 21 statements were drafted and submitted to
a five-round Delphi process
Participants: A panel with 17 experts commented on the paper in round 1. Board members of national palliative care or hospice
associations that are collective members of European Association for Palliative Care were invited to an online survey in rounds 2 and
3. The expert panel and the European Association for Palliative Care board members participated in rounds 4 and 5. This final version
was adopted as an official position paper of the European Association for Palliative Care in April 2015.
Results: Main topics of the white paper are concepts and definitions of palliative care, its values and philosophy, euthanasia and
physician-assisted suicide, key issues on the patient and the organizational level. The consensus process confirmed the 2003 European
Association for Palliative Care white paper and its position on the relationship between palliative care and euthanasia and physician-
assisted suicide.
Conclusion: The European Association for Palliative Care feels that it is important to contribute to informed public debates on these
issues. Complete consensus seems to be unachievable due to incompatible normative frameworks that clash.
Keywords
Euthanasia, physician-assisted suicide, palliative sedation, consensus process, online survey
1 Department of Palliative Medicine, University Hospital Bonn, Bonn,
Germany
2 Centre of Palliative Care, Malteser Hospital Seliger Gerhard Bonn/
Rhein-Sieg, Bonn, Germany
3 University of Humanistic Studies, Utrecht, The Netherlands
4Gemeinschaftskrankenhaus Havelhöhe, Berlin, Germany
5Witten/Herdecke University, Witten, Germany
616524PMJ0010.1177/0269216315616524Palliative MedicineRadbruch et al.
review-article2015
Review Article
6
Marie Curie Palliative Care Institute Liverpool (MCPCIL), University of
Liverpool, Liverpool, UK
7
European Association for Palliative Care, Milan, Italy
8Federation Palliative Care Flanders, Vilvoorde, Belgium
Corresponding author:
Lukas Radbruch, Department of Palliative Medicine, University Hospital
Bonn, Sigmund Freud Str. 25, 53127 Bonn, Germany.
Email: Lukas.radbruch@malteser.org
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2 Palliative Medicine
What this paper adds?
This paper provides an overview where there is consensus among European palliative care professionals and points out
controversies where there is no consensus.
The paper provides a clear stance by experts and representatives of national organizations on palliative care and an official
position of the Board of Directors of the EAPC with 21 statements on euthanasia, assisted suicide and palliative care.
Implications for practice, theory or policy
Individual requests for euthanasia and physician-assisted suicide (PAS) are complex in origin and may include personal, psy-
chological, spiritual, social, cultural, economic and demographic factors. Such requests require respect and careful attention,
together with open and sensitive communication in the clinical setting.
The EAPC position paper states that the provision of euthanasia and PAS should not be included into the practice of pallia-
tive care.
Individuals requesting euthanasia or PAS should have access to palliative care expertise. This should be achieved by the
establishment of palliative care within mainstream healthcare systems of all European countries supported by appropriate
finance, education and research.
Within Europe, several approaches to euthanasia and PAS are emerging, and open and respectful debate surrounding this is
to be encouraged.
Background
In 1991, a debate at the European Parliament on euthanasia
stimulated discussion at all levels in Europe. Subsequently,
the European Association for Palliative Care (EAPC) pro-
duced a first statement, Regarding Euthanasia,1 in order to
clarify the position the organization should adopt towards
euthanasia. In 2003, the EAPC task force on ethics pub-
lished a more detailed and updated statement.2 The editors
published a series of 53 comments from different experts
from the fields of medicine, philosophy, theology and eth-
ics describing a broad range of different attitudes towards
euthanasia and the EAPC position statement.
Subsequently, there have been major developments and
achievements in the field of palliative care, as well as much
discussion, some of it controversial, on euthanasia and phy-
sician-assisted suicide (PAS). There has also been new leg-
islation in some countries. Euthanasia has been legalized in
the Netherlands (2001), Belgium (2002) and Luxembourg
(2009), and legislation allowing PAS exists in Switzerland
as well as outside of Europe in three federal states in the
United States: Oregon, Vermont and Washington.
The complexity of debate is also highlighted by an
ongoing discussion on treatment withdrawal or withhold-
ing of treatment (non-treatment decisions (NTD)) in some
European countries such as France, where an expert com-
mission recently reported to the government that although
NTD have been legal since 2005, physicians do not use the
full range of options, whereby needs and priorities of
patients related to end-of-life care are often ignored.3
The EAPC feels that it is important to contribute to
informed public debates on these issues. This is no straight-
forward task, as euthanasia and PAS are two of the most
frequently debated and most sensitive ethical issues in the
field of health care today. Complete consensus on these
topics seems to be unachievable due to incompatible nor-
mative frameworks that clash. This paper builds on current
debates and develops a viewpoint from the palliative care
perspective, which is sensitive to the manifold cultural and
legal differences across European countries.
Historical trends and current
situation
Around the world some important changes relating to
euthanasia and PAS have been taking place. In 1996, for
the first time in history, a democratic government enacted
a law that made both euthanasia and PAS legal acts, under
certain conditions as described in the Rights of the
Terminally Ill Amendment Act 1996, Northern Territory,
Australia.4 The law was, however, made ineffective by
the Euthanasia Laws Bill of the Parliament of Australia in
1997.5
In the same year, PAS (but not euthanasia) was legal-
ized through the Oregon Death with Dignity Act.6 This has
been followed by similar legislation in Washington (2008),
Vermont (2013) and California (2015) and is currently
being debated in New Jersey. In Montana, a court ruling
finding no constitutional objection to assisted suicide has
opened the way for similar practices in 2009, and a similar
court ruling in New Mexico in 2014 is currently under
appeal. In contrast to the legal requirements in European
countries, in Oregon, Washington and Vermont, patients
must have a terminal physical illness in order to qualify for
PAS. Data on frequencies of euthanasia and PAS are pre-
sented in Table 1.
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Radbruch et al. 3
Switzerland has a long tradition of assisted suicide, not
only for Swiss citizens but also for foreigners. Swiss law,
which dates back to 1942, is not specifically related to med-
ical illness. Right-to-die organizations are involved in the
majority of cases. The lethal drugs are prescribed by physi-
cians, but these do so at the request of the organizations. In
contrast to the regulations in the Netherlands, Belgium or
Luxemburg, the process is not one of PAS, as a doctor–
patient relationship is not required.10 The physician is gen-
erally not present when the patient commits suicide.17
The Netherlands, following a long public discussion
and a policy of tolerance, introduced the Termination of
Life on Request and Assisted Suicide (Review Procedures)
Act in 2001,18 suspending prosecution of euthanasia and
PAS if certain criteria are fulfilled: the patient’s suffering
is unbearable with no prospect of improvement; the patient
is fully aware of his condition and prognosis, and the
request is voluntary and persisting over time; a second
independent physician has confirmed the conditions; and
the procedure is performed in a medically appropriate way.
A combination of first barbiturate (to induce coma) and
then a muscle relaxant (causing respiratory arrest) is used
most often for euthanasia. After the death of the patient,
the doctor must report the procedure to the Regional
Euthanasia Review Committees (RERCs) which assess
whether or not the criteria have been met.
Euthanasia can be performed in adults and in adoles-
cents older than 16 years. Children between 12 and 16 years
require parental consent if they want to receive euthanasia.
The legislation also recognized the validity of a written
advance directive specifying conditions where the patient
might want to receive euthanasia.
Belgium also introduced legislation of euthanasia with
similar regulations to those in the Netherlands in 2002.19
Physicians will not be prosecuted if they provide euthana-
sia for competent patients of legal age, who have expressed
a repeated and consistent request made under no external
pressure who are subject to persistent and intolerable
Table 1. Prevalence of euthanasia and physician-assisted suicide in countries with legislation allowing these practices.
Country Year Deaths Percentage of all deaths
United States
Oregon71998 16 (24 people with prescriptions)
2014 105 (155 people with prescriptions) 0.31
Washington82009 36 (63 people with prescriptions)
2013 119 (173 people with prescriptions) 0.23
Vermont n.a.
Montana n.a.
California n.a.
New Mexico n.a.
New Jersey n.a.
Switzerland 20099Approx. 300 0.48
201010 353 (slow increase in the last decade)90.56
The Netherlands 200111 All 2.6
Without explicit request of the patient 0.7
200511 All 1.7
Without explicit request from the patient 0.4
201011 All 2.8
Without explicit request from the patient 0.2
201412 4188
201512 4829 3.4
4501 euthanasia 3.2
286 physician-assisted suicide 0.2
42 both <0.1
Belgium 200313 235
201113 1133
201214 1432
201314 1807 1.7
1454 in Flanders
353 in Wallonia
201315 Physician survey in Flanders 4.6
Luxemburg 2011–201216 14 0.18
n. a.: not available.
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4 Palliative Medicine
physical and/or mental suffering due to an irreversible
medical condition (accident or disease) with no prospect
of improvement, and if the physician follows the proce-
dures detailed in the law. Requests expressed in a written
advance directive are acceptable in the case of patients in
an irreversible state of unconsciousness.
According to the legislation, a patient requesting eutha-
nasia has to be of age >18 years or an emancipated minor
(being married or in exceptional cases with a judge’s ver-
dict). Euthanasia was performed only very rarely in young
people. In a recent parliamentary debate, the relevance of
age was regarded as less important than the capacity for
discernment of involved issues and implications, and in
consequence a new bill was approved in February 2014,
which rests on the same fundamental principles as the
2002 legislation, but which incorporates no reference to
any age limit, contrasting sharply with the Dutch legisla-
tion. However, although the Belgian legislation extends its
application to children, it restricts its scope by excluding
psychiatric disorders. More importantly, the new bill also
specifically addresses the issue of discernment, which has
to be assessed by a multidisciplinary team including a clin-
ical psychologist or psychiatrist. Parents or guardians must
agree with the request.20
New ethical questions have emerged, for example,
when patients in Belgium wish to be organ donors. For
several patients euthanasia has been performed immedi-
ately before organs were removed for transplantation,
although care was taken that the transplantation team acted
independently.21 The establishment of a virtual ‘life’s end
clinic’ in the Netherlands, for people whose euthanasia
request was not met by their own physician, providing
euthanasia for 134 cases in 2013 and 232 cases in 2014,22
has raised concerns as this mobile team exclusively ser-
vices euthanasia requests.
In 2009, Luxemburg also introduced euthanasia and
PAS.23 Similar to the criteria in the Netherlands and
Belgium, patients must be suffering unbearably, with no
prospect of improvement, but the illness does not have to
be terminal.10
Across Europe as a whole, however, there is little evi-
dence in the last 10 years of concerted attempts to bring
about the legalization of euthanasia through parliamentary
processes. Indeed, in many European countries, the legali-
zation of euthanasia is opposed by a wide range of profes-
sional associations representing doctors, nurses and others,
groups representing disabled or older people and also by
palliative care organizations.
Assisted suicide is not prosecuted under the criminal
law of many European states. In Switzerland, assisted sui-
cide is a crime if and only if the motive is selfish according
to Article 115 of the Swiss penal code. The German legis-
lation is even more permissive, and assistance or encour-
agement is not punishable according to Article 216 of the
penal code. However, prosecution is possible for other
reasons such as neglected duty to rescue or homicide by
omission.
In the United Kingdom, assisted suicide is a criminal
offence in England and Wales according to the Suicide
Act 1961 and in Northern Ireland through sections 12
and 13 of the Criminal Justice Act (Northern Ireland)
1966. It does not apply to Scotland. Several attempts
have been made in recent years to introduce bills that
would legalize assisted suicide in England and Wales,
but all have been rejected by Parliament. In 2010, the
Director of Public Prosecutions has published a policy
for prosecutors describing public interest factors tending
in favour or tending against prosecution.24 The policy
indicates that prosecution is less likely if the victim had
reached a voluntary, clear, settled and informed decision
to commit suicide and the suspect had been wholly moti-
vated by compassion. An assisted dying bill has been
introduced to the House of Lords by Lord Falconer of
Thoroton in June 2015, but has been turned down as in
previous years.
Outside of Europe, most recently the Supreme Court of
Canada has extended the constitutional right to autonomy
by ruling that the criminal code has no force to prohibit
PAS for a competent adult person who clearly consents to it
and has a grievous and irremediable medical condition
(including illness, disease or disability) that causes endur-
ing suffering that is intolerable to the individual.25 However,
this is not yet put into laws or rules.
Aims
This paper aims to provide an ethical framework for pallia-
tive care professionals on euthanasia and PAS. It also aims
to provide an overview on recent research as well as a dis-
cussion of ethical principles related to these issues. The
paper takes into consideration the broad range of cultural
settings and attitudes in different European countries. It
provides clear recommendations where there is consensus
and points out controversies where there is no consensus.
It seeks to stimulate a broad discussion within the health-
care system about the role of medical professionals, goals
of care, epistemology of a medical indication and ethical
implications which strengthen the benefit of palliative and
end-of-life care for society and political decision-making.
The white paper does not discuss advance care planning
(ACP), attitudes towards euthanasia or PAS nor societal
changes in these attitudes.
Methods
A Delphi procedure was used to produce consented state-
ments on euthanasia and PAS from the palliative care per-
spective. This section outlines the process followed. More
information can be accessed in the online Supplementary
Material.
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Radbruch et al. 5
The work group met on four occasions: in Frankfurt,
Germany (August 2012), in Munich, Germany (April
2013), at the 13th EAPC Congress, Prague, Czech Republic
(June 2013) and in Bonn, Germany (September 2014).
The EAPC position paper on euthanasia and PAS from
20032 was used to produce a white paper draft with 21 state-
ments as the starting point for the consensus procedure. The
draft has been used in a consensus procedure using a five-
round Delphi process. The first round included feedback
from a number of palliative care or medical ethics experts.
The second, third, fourth and fifth rounds of the survey were
performed with an online survey tool (SurveyMonkey©).
The respondents were able to choose between different lev-
els of agreement for each statement presented on a five-step
Likert scale. The second and third rounds of the Delphi pro-
cess involved the board members of the national palliative
care and hospice associations that are collective members of
the EAPC. The fourth round included the expert panel from
the first round and round five the board members of EAPC.
After each of the five Delphi rounds, those statements
that did not reach consensus were revised in accordance
with the comments of the participants. Although some
statements did not reach the high level of agreement
required for consensus in the third round, no statement had
to be deleted from the draft as the lowest rate of agreement
still was 68% (agreement/complete agreement). For each
of these statements (2, 6, 11,14, 15 and 16), the lack of full
consensus was documented in the text. The final version of
the paper has been adopted as an official position paper of
the EAPC in April 2015.
Concepts and definitions
This section presents, in turn, definitions of palliative care,
euthanasia, PAS, withholding or withdrawing futile treat-
ment and palliative sedation:
1. Following the definition of the World Health
Organization (WHO), palliative care is an approach
that improves the quality of life of patients and
their families facing the problems associated with
life-threatening illness, through the prevention and
relief of suffering by means of early identification
and impeccable assessment and treatment of pain
and other problems, physical, psychosocial and
spiritual.26
According to the WHO definition, palliative care affirms
life and regards dying as a normal process, and it intends to
neither hasten nor postpone death. Palliative care offers a
support system to help patients live as actively as possible
until death.
Across Europe, palliative care is an expanding and
acknowledged part of health care. At the same time, there
are continuing debates over what palliative care includes
and where it begins and ends (stage and type of disease,
prognosis and care setting).27,28 Palliative care is applica-
ble early in the course of illness, in conjunction with other
therapies that are intended to prolong life, such as chemo-
therapy or radiation therapy, and includes those investiga-
tions needed to better understand and manage distressing
clinical complications. Regional, national and cultural dif-
ferences exist in the approach to and organization of pal-
liative care.29 These different viewpoints are also reflected
in professional practice.30
2. Euthanasia is defined as follows: a physician (or
other person) intentionally killing a person by the
administration of drugs, at that person’s voluntary
and competent request.
When the expression ‘killing on request’ is used in connec-
tion with euthanasia, this is a technical description of the
act, based upon the procedure used usually: an injection of
a barbiturate to induce coma, followed by the injection of
a neuromuscular relaxant to stop respiration causing the
patient to die. Whether or not euthanasia may be justified
killing on request is another matter, addressed below. A
sharp distinction, therefore, exists here between what ‘is’
and what ‘ought’ to be.31
Medicalized killing of a person without the person’s
consent, whether non-voluntary (where the person is una-
ble to consent) or involuntary (against the person’s will), is
not euthanasia: it is murder. Hence, euthanasia can be vol-
untary only.32 Accordingly, the frequently used expression,
‘voluntary euthanasia’ should be abandoned since it by
logical implication, and incorrectly, suggests that there are
forms of euthanasia that are not voluntary. In the literature,
as well as in the public debate, a distinction is sometimes
drawn between so-called ‘active’ and ‘passive’ euthanasia.
It is our view that this distinction is inappropriate. In our
interpretation, as well as according to the Dutch under-
standing,33 euthanasia is active by definition, and so ‘pas-
sive’ euthanasia is a contradiction in terms (an oxymoron).
While this statement received high agreement in the
Delphi process, it did not reach consensus among the board
members of national palliative care associations in Europe
according to the strict definition used in this study.
Disagreement seemed to focus on the choice of the word
‘killing’; in addition, some comments maintained that it
should only be a physician who is entitled to perform
euthanasia, no other persons.
3. Assisted suicide is defined as follows: a person
intentionally helping another person to terminate
his or her life, at that person’s voluntary and com-
petent request.
In contrast with euthanasia, where the authority of action
lies with the other person administering the lethal drugs, for
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6 Palliative Medicine
assisted suicide the authority of action lies with the person
who wants to terminate his or her life. The decision-making
process remains with the person who wishes to end his or
her own life and is not different from euthanasia.
If a patient voluntarily stops eating and drinking, this
would not be considered assisted suicide as it would
require no assistance from another person.
4. PAS is defined as follows: a physician intentionally
helping a person to terminate his or her life by pro-
viding drugs for self-administration, at that per-
son’s voluntary and competent request.
Physicians may be urged to assist suicide as their medical
expertise is wanted for the prescription or advice in the use
of lethal drugs. However, there are also specific challenges
with PAS. Physicians usually have relief or cure as their
only goal, but if the ending of life becomes another option,
this might jeopardize the relationship between patient and
physician.
In contrast, the largest physician federation of the
Netherlands (KNMG) has produced a position paper on the
role of the physician in euthanasia and PAS, describing
clearly tasks and responsibilities in performing these acts.34
The medicalization of PAS has also been criticized as
part of a transformation of medicine from a caring profes-
sion into a business designed to serve demands for medical
services.35 Alternative concepts where euthanasia and PAS
are performed by non-physicians have been described.36
Differences between Switzerland as a non-medical legal
model and Oregon as a medical legal model concerning
the capacity of the person providing assistance in suicide
and the state of health of the person committing suicide
have also been described.37 In the Netherlands, the role of
the physician in the current forms of assisted dying has
been challenged in recent years by a public campaign
advocating for special, non-medically trained workers
educated as counsellors to help clarify the person’s wish to
die and administer a lethal drug that would be provided by
a physician. Also, the concept of auto-euthanasia has been
suggested, where patients would end their own lives with
the support of their children.38
Not only the ethical dimension but also specific legal
aspects may be relevant for PAS: For example, in Germany,
physicians (similar to parents, spouses or police officers)
are in a position as warrantor for the well-being of their
patients and are obliged to exert more than usual efforts to
prevent suicide and might be liable for homicide by omis-
sion if they assist the patient. In addition, PAS may be
penalized by civil law.
5. NTD are defined as follows: withholding or with-
drawing medical treatment from a person either
because of medical futility or at that person’s vol-
untary and competent request.
NTD are not euthanasia within the definitions used here
because NTD do not intend to hasten death, but rather
accept death as a natural phenomenon through omission of
ineffective, futile, very burdensome or unwanted life-pro-
longing procedures.39
NTD can be related to medical futility, for example,
deciding against antibiotic treatment in an imminently
dying patient with pneumonia and lung cancer. Another
example would be deciding against fourth-line chemother-
apy in a patient with rapidly progressive cancer and inad-
equate response to previous courses, if this chemotherapy
carries a high risk of side effects or increased treatment-
related mortality. NTD for futile medical interventions
should be discussed with the patient and relevant caregiv-
ers. Problems may arise with patients persisting in their
wish for futile treatments, either out of tenacity or out of
desperation.
Different from medical futility, NTD may also be
related to a patient’s decision to withhold or withdraw
medical therapies. This may lead to moral challenges
with the healthcare team, for example, when a patient
with renal failure decides to discontinue haemodialysis
treatment or if a patient with motor neuron disease
(MND) and complete respiratory failure requests with-
drawal of mechanical ventilation. However, these NTD
do not end life (as euthanasia does), but rather allow
imminent death from the underlying condition, which is
prevented by life-prolonging measures. Patient’s requests
for NTD require open and sensitive communication, in
order to ensure that the patient and his caregivers are
adequately informed and understand the implications and
consequences of the NTD.
6. Palliative sedation is defined as the monitored use
of medications intended to induce a state of
decreased or absent awareness (unconsciousness)
in order to relieve the burden of otherwise intracta-
ble suffering in a manner that is ethically acceptable
to the patient, family and healthcare providers.40
Palliative sedation is an accepted, ethical practice when
used in the appropriate situations.40 The EAPC white paper
on sedation considers sedation to be an important and nec-
essary therapy in the care of selected palliative care
patients with otherwise refractory distress. However, this
approach requires attention to proportionality and good
clinical practice and attention to potential risks and prob-
lematic practices that can lead to harmful and unethical
practices.
Potential ethical conflicts or problems should be duly
considered, and the indication, planning and administra-
tion of sedation should be based on consensus in the team
and between team, patient and at least in most cases also
caregivers. Detailed guidance is provided in the EAPC
framework for palliative sedation.40
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Radbruch et al. 7
The definition of palliative sedation has been the focus
of much debate, considering aspects of medical indication,
decision-making, ethical norms, goals, forms and philo-
sophical questions. This debate is also related to different
cultural and organizational settings. There is, for example,
an ongoing debate on whether the ethical precondition in
the last part of the EAPC definition40 is appropriate or
should be deleted.
While this statement received high agreement in the
Delphi process, it did not reach consensus among the board
members of national palliative care associations in Europe
according to the strict definition used in this study. The
ethical precondition caused much discussion, among the
participants in the consensus panel as well as among the
authors of this paper.
Palliative care values and philosophy
7. In palliative care, the intrinsic value of each person
as an autonomous and unique social individual is
acknowledged and respected. Ideally, the patient
preserves his or her self-determination regarding
the power of decision on place of care, treatment
options and access to specialist palliative care.28
A discourse analysis of the definition of palliative care
found that the main goals were relief and prevention of
suffering and improvement of quality of life.41 This was
based on common core values such as respect for auton-
omy. Power of decision-making on place of care, treatment
options and access to specialist palliative care receives
special emphasis, and patient’s empowerment is assigned
an important role. The human being is the focus of care.
Palliative care should be provided in a respectful, open and
sensitive way – sensitive to personal, cultural and religious
values, beliefs and practices as well as the law of each
country. Palliative care is foremost patient-centred and
contingent upon individual and familial needs. A saluto-
genic orientation with emphasis on the resources and com-
petencies of clients, and not simply on their difficulties,
might be preferable.
Key issues on the patient level
8. Individual requests for euthanasia and PAS are
complex in origin and may include personal, psy-
chological, spiritual, social, cultural, economic and
demographic factors.
The use of euthanasia or PAS has an inherent danger of
misinterpreting the patient’s preferences by failing to
acknowledge this divergence of underlying meanings and
ambivalence or changing priorities of the patients. In a
large survey of terminally ill patients, 10.6% reported seri-
ously considering euthanasia or PAS for themselves, but
the follow-up interview showed that 50.7% of these
patients had changed their mind after 6 months, while a
nearly equal number had started to consider it.42 Ultimately,
in this survey, only 5.6% of the deceased patients had dis-
cussed asking the physician for euthanasia or PAS.
In-depth evaluation found many meanings and uses of
the expression of desire for hastened death, ranging from a
manifestation of the will to live and a gesture of altruism to
a despairing cry depicting the misery of the current situa-
tion and to a manifestation of the last control the dying can
exert.43 The expression seems to be an important tool of
communication for the patients.
In a similar study, being a burden to others was a most
important motivation for the desire for hastened death.44,45
Suffering was described as a reason as well, although most
often it was anticipated suffering rather than suffering
right now: patients were very afraid of disease-related
deterioration in the future.
In clinical practice, patients often show major ambiva-
lence, with the wish for hastened death, on one hand, and
the will to live, on the other, often in parallel or with short-
term fluctuations. This coexistence of opposing wishes has
been explained as part of authentic, multi-layered experi-
ences and moral understandings at the end of life.46
9. Requests for euthanasia and PAS require respect
and careful attention, together with open and sensi-
tive communication in the clinical setting.
Palliative care staff should acknowledge and listen care-
fully to these requests and be able to enter an open dia-
logue about this request with patients, caregivers and
staff members. A request for euthanasia should lead to an
exploration with the patient and the family of the burden-
some experiences that are underlying the question. In
Germany, patients explained that the intention to address
their wish for hastened death to palliative care staff was
associated with the need for information and reassurance
and the perception of staff competence in symptom
control.44
10. Individuals requesting euthanasia or PAS should
have access to palliative care expertise.
Requests for euthanasia and PAS may be altered by the
provision of comprehensive palliative care. Suffering from
physical symptoms can be alleviated, and psychosocial
and spiritual care can improve well-being of patient and
caregivers. Information about the available palliative care
options may provide reassurance and diminish anxieties
about the subsequent disease trajectory.44
11. Palliative sedation may offer an option for many
conditions in which patients may request euthana-
sia or PAS.
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8 Palliative Medicine
Sedation is potentially indicated for patients with intol-
erable distress due to physical symptoms, when there is a
lack of other methods for palliation within an acceptable
time frame and without unacceptable adverse effects
(refractoriness). The specific intolerable symptoms should
be identified. The most common symptoms include agi-
tated delirium, dyspnoea, pain and convulsions. Emergency
situations may include massive haemorrhage, asphyxia-
tion, severe terminal dyspnoea or overwhelming pain cri-
sis. Continuous deep sedation should only be considered if
the patient is in the terminal phase as defined in the
Australian Palliative Care Phase definition (Death is likely
within days).47 Palliative sedation may in this stage also be
considered for severe non-physical problems such as
refractory depression, anxiety, demoralization or existen-
tial distress, although there is less consensus on the appro-
priateness of sedation for these indications.
In contrast to this, in France, a bill has been passed by
the National Assembly on palliative sedation, which
includes a right for patients with a life-limiting disease to
receive palliative sedation until the time of death.
Physicians would be compelled to provide palliative seda-
tion if the patient requests it. The bill has been turned down
by the senate in June 2015, but the bill is still in the legisla-
tive system.
There was low agreement in the Delphi process on this
statement and it did not reach consensus among the board
members of national palliative care associations in Europe.
Some comments expressed concern that palliative sedation
might be regarded as an alternative to euthanasia, which is
not in line with the intention of this white paper.
12. Palliative sedation in those imminently dying must
be distinguished from euthanasia. In palliative
sedation, the intention is to relieve intolerable suf-
fering, the procedure is to use a sedating drug for
symptom control and the successful outcome is the
alleviation of distress. In euthanasia, the intention
is to end the life of the patient, the procedure is to
administer a lethal drug and the successful out-
come is immediate death.
Palliative sedation should never have the intention to
shorten life.2,48 In a survey on the practice of palliative
sedation, 17% of the responding physicians stated that has-
tening death was the explicit intention,49 but this indicates
a misuse of the procedure. In very fragile patients, a non-
intended life-shortening side effect may not be excluded,
although two systematic reviews clarified that palliative
sedation does not shorten survival in terminally ill cancer
patients.50,51
It is important that the responsible physician reviews
and documents his or her own intention in initiating pallia-
tive sedation in order to avoid misuse or malpractice. It is
recommended that the decision to use palliative sedation
should be a team decision or at least should be scrutinized
with inter- or supervision.
13. Palliative care is provided up until the end of life
and is by definition never futile.
Palliative care is never discontinued as it is provided up
until the very moment of death (and even beyond with
bereavement support for the family). So, whereas life-
prolonging measures may be found to be futile, palliative
care never is.39 The patient may reject palliative care inter-
ventions, but this does not mean that the palliative care
approach is futile. Quite the contrary, palliative care is
effective in relieving distressing pain and symptoms, and
the care for patients – physical, psychosocial and spiritual
– continues until death.
Some have argued that the concept of palliative futility
supports the need for euthanasia.52 This term, however, is
a misnomer and a contradiction in terms, based on a false
understanding of what palliative care is.
14. The provision of euthanasia and PAS should not be
included into the practice of palliative care.
We hold that there are philosophical as well as medical
reasons against the use of euthanasia. From the philosophi-
cal point of view, euthanasia makes the human life a means
for ending suffering, as human life has to be forfeited in
the act of euthanasia to end suffering. From the medical
point of view, euthanasia is a medical act (injection of
lethal drugs), but not a medical treatment or therapy in any
sense of these words, as the primary task of the physician
is to alleviate and cure, but not to end life.39
However, Bernheim et al. discussed the interaction of
palliative care and legalization of euthanasia, claiming that
the case of Belgium suggests that there is a synergistic
effect between the two. They described a model called
integral palliative care, in which euthanasia is considered
as another option at the end of a palliative care pathway.52
In another more recent article, protagonists of the
Federation of Palliative Care Flanders explained how after
being confronted with the introduction of the legal possi-
bility of euthanasia different kinds of experiences led to
the growing involvement of palliative care professionals
and teams in what they call ‘the accompaniment of eutha-
nasia’. Referring to continuity of care, they chose not to
abandon patients asking for euthanasia by referring them
to external practitioners, outside the familiar care environ-
ment, but to continue to provide them with all the neces-
sary support. In this way, they wanted to express that
euthanasia and palliative care remain two distinct matters,
but that they can ‘occasionally be considered together
when caring for one and the same patient’.53
Palliative care clinicians in other countries are con-
cerned about these proposals, as their clinical experience
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Radbruch et al. 9
in palliative care has taught them to be sensitive in the
acknowledgement but also very careful with the interpre-
tation of the request for euthanasia from palliative care
patients.
The definition of palliative care does not seem to be
compatible with euthanasia. The WHO clearly stated in
2002 that palliative care neither hastens nor postpones
death,26 and this has been taken up in other definitions of
palliative care.41
However, even if palliative care is delivered with the
utmost quality, this will not prevent individual patients
from asking for hastened death, including requests for
euthanasia or PAS.54–56 It is the responsibility of palliative
care professionals to hear and explore the implicit or
explicit requests for euthanasia and address the suffering
underlying these requests.
There was moderate agreement on this statement in the
Delphi process, and it did not reach consensus among the
board members of national palliative care associations in
Europe. A number of respondents (mostly from Benelux
countries) disagreed strongly. The dissent thus reflects the
actual situation in Europe. However, this statement was
maintained as a normative statement, although it is under-
stood that the moral understanding of hastening death may
be different in different cultures or subcultures.
Key issues on the organizational level
15. It is recognized that within Europe several
approaches to euthanasia and PAS are emerging,
and open and respectful debate surrounding this is
to be encouraged.
This debate should contribute to an understanding of the
areas of consensus and dissent on euthanasia and PAS in
Europe and inform the social, existential, spiritual, ethical
and legal implications of the different approaches, both for
patients and for caregivers, for healthcare professionals
and for society.
While this statement received high agreement in the
Delphi process, it did not reach consensus among the board
members of national palliative care associations in Europe
according to the strict definition used in this study.
16. Studies of attitudes to euthanasia and PAS among
professionals, patients and the wider public as well
as studies of their experiences of these issues may
inform the wider debate.
Many published studies, however, suffer from methodo-
logical weaknesses, starting with deficient definition of the
concepts used, raising doubts about the evidence base.57 A
more coordinated approach to these studies is needed.
Palliative care might undertake research on issues
related to euthanasia and PAS, although this should be
embedded in the context of the palliative care field, for
example, on knowledge or attitudes related to euthanasia
or PAS. Care has to be taken that studies are of good qual-
ity and high generalizability.
While this statement received high agreement in the
Delphi process, it did not reach consensus among the board
members of national palliative care associations in Europe
according to the strict definition used in this study.
17. Fear of loss of autonomy at the end of life can be
addressed using advance directives and ACP, con-
tributing to improved communication and thereby
enhancing the autonomy of the patient.
Within the modern medical system, patients may fear that
life will be prolonged unnecessarily or end in unbearable
distress. As a result, euthanasia or PAS may appear as an
option. However, patient consent is an ethical prerequisite
of medical treatment, and the patient’s right to refuse any
treatment is increasingly acknowledged in most European
countries.
Advance directives (‘living wills’), power of attorney
for a surrogate decision-maker and other instruments of
ACP may strengthen the autonomy of the patient and may
alleviate anxiety. However, a legal framework for ACP is
not yet provided in all European countries.
18. If euthanasia or PAS is legalized in any society,
there should be special attention to avoid (1) the
underdevelopment or devaluation of palliative care
and (2) conflict between legal requirements and the
personal and professional values of physicians and
other healthcare professionals.
Empirical data on the effect of euthanasia and PAS on a
societal level may be hard to obtain for a number of rea-
sons: (1) only very few countries have legalized euthanasia
and PAS; (2) it takes a long time before legal changes have
effect on a societal level and legalizations are relatively
recent; (3) it is hard to gain evidence for the correlation
between legal changes and changes on a societal level,
legal changes being embedded in a broad socio-cultural
spectrum of causes; and (4) research may be consciously
or unconsciously biased by ethical presuppositions.
Nevertheless, from a palliative care perspective, a number
of worries can be formulated with regard to the legaliza-
tion of euthanasia and PAS, which may contribute to spe-
cial attention to avoiding undesired developments.
Only little information is available on how often pallia-
tive care is offered or provided for patients requesting
euthanasia or PAS. In Belgium as in the Netherlands,
involvement of palliative care experts is no prerequisite of
euthanasia or PAS, although the Belgian legislation states
that the patient must be informed about the possibilities of
palliative care. In Belgium, there is no clear information in
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10 Palliative Medicine
the reports of the Federal Committee,58 although all reports
conclude that physicians and palliative teams were often
voluntarily consulted outside the legally obligatory con-
sultations. The numbers of consultations with palliative
care teams are registered in most of the reports (710 cases
in 2013).14 In a recent nationwide survey, participating
physicians reported a much higher percentage, with
involvement of palliative care services in 73.7% of cases
in 2013.15 Reports of the Federal Committee regularly
express concerns of some committee members that pallia-
tive care consultations should not become a constraint on
patient autonomy.14
Throughout history it has been imperative that medi-
cine is concerned with healing and caring and not with
purposeful ending of life.36 Most physicians include this in
their personal and professional values, even in jurisdic-
tions where the public favours or the legislation allows
euthanasia or PAS. Establishing physicians as collabora-
tors in euthanasia and PAS thus may lead to role con-
flicts.53,59 However, the impact of characterizing euthanasia
as medical treatment on physicians’ professional identity
and on the institutions of medicine and law has not been
evaluated yet.
19. In the case of legalization of euthanasia or PAS,
special attention should also be paid to avoid (1)
the widening of the clinical criteria to include other
groups in society, (2) pressure on vulnerable per-
sons and (3) killing to become accepted within
society.
An evaluation of the rates of assisted dying in Oregon and
in the Netherlands showed no evidence of heightened risk
for vulnerable groups such as racial or ethnic minorities,
compared with background populations.60 However, the
first population-based study in Switzerland described that
assisted suicide was associated with female gender and
situations that may indicate greater vulnerability such as
living alone or being divorced, although it was also associ-
ated with higher education and higher socio-economic
position.61
In the context of euthanasia, the danger of sliding down
a ‘slippery slope’ has been discussed. This means that even
if legislation for euthanasia is formulated with clear indi-
cations, the regulations will be extended and finally be
overruled by ongoing practice.38,53 Bernheim and col-
leagues as well as other authors have stated that data from
the Netherlands and Belgium do not provide any evidence
of a slippery slope.52,62 However, drug-induced ending of
life without patient’s request – by definition not euthanasia
– and abuse of palliative sedation are two indicators for
such a ‘slippery slope’.
In the Netherlands, despite the new law of 2002, 0.4%
of all deaths are instances of medicalized killing without
an explicit request from the patient.63 Recent reports have
suggested that there is also an increased abuse of ‘terminal
sedation’ in that country. Physicians report having initiated
continuous deep sedation with the intention to overdose
patients to hasten death.49 ‘Slippery slope’ is also the pro-
vision of euthanasia and of PAS for depressed persons and
those in the early stages of dementia, when the patient is
still able to formulate an explicit request as proposed by
the organization Nederlandse Vereniging voor een
Vrijwillig Levenseinde (NVVE) in the Netherlands. The
latest report from the RERCs stated that in 2013 euthana-
sia had been performed for 97 patients with dementia and
42 patients with psychiatric diseases.12 Dutch legislation
also permits physicians to terminate the lives of newborn
infants if they are born with such serious disorders that
termination of life is regarded as the best option.64
In addition, specific cases in Belgium and the
Netherlands have shown an extension of indications. In the
Netherlands, dementia or depression is accepted as an
indication for euthanasia.65 In Belgium, since the introduc-
tion of the euthanasia law in 2002, 25 projects for enlarge-
ment of the law have been proposed.3 Just recently, the
Belgium parliament voted that children and adolescents
also are allowed to receive euthanasia or PAS.20
In Belgium, a tendency of family members to consider
the dying process as undignified, useless and meaningless,
even if it happens peacefully, comfortably and with profes-
sional support has been described.53
20. The EAPC encourages its members to engage in
direct and open dialogue with those who promote
the legalization of euthanasia and PAS.
Understanding and respect for alternative viewpoints
are not the same as the ethical acceptance of either eutha-
nasia or PAS. An open dialogue is required to clarify the
underlying values and priorities and map out the meta-
ethical incompatibilities and cultural differences that cause
misunderstanding and condemnation. The discussion
should focus on optimal holistic care for the patient and his
caregivers, from a palliative care perspective. Healthcare
ethics and the personal and professional values of health-
care professionals may also play an important role and
must be included in the discussion.
Even with critical reflection on the experiences in
Belgium, the Netherlands and Oregon, it has to be
acknowledged that there may be more transparency and
open discussion around end-of-life than in most other
countries, where similar procedures may happen in a more
covert way.66
21. EAPC does respect individual choices for euthana-
sia and PAS but stresses the importance of refocus-
ing attention onto the responsibility of all societies
to provide care for their older, dying and vulnera-
ble citizens. A major component in achieving this
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Radbruch et al. 11
is the establishment of palliative care within the
mainstream healthcare systems of all European
countries supported by appropriate finance, educa-
tion and research.
Realizing this goal is one of the most powerful alternatives
to calls for the legalization of euthanasia and PAS, the
EAPC advocates for access to adequate palliative care for
all who need it as a human right.67 Good provision of pal-
liative care is paramount in order to ensure that people
don’t ask for euthanasia through lack of optimal symptom
control or private or societal marginalization.
Conclusion
The EAPC position paper states that euthanasia is not a
part of palliative care. Certainly, even the best palliative
care model or service cannot prevent patients sometimes
asking for hastened death. However, there is a fundamen-
tal difference in the approach to these patients between
euthanasia and palliative care. Proponents of the legali-
zation of euthanasia take the request of the patient as the
point of reference of the patient’s autonomy and try to
comply with this personal preference. Palliative care
experts should also acknowledge the requests for eutha-
nasia in those patients who express them, but make this
the starting point of holistic care, beginning with compre-
hensive assessment and communication and trying to
understand the motivation and attitude behind the
patient’s wish.
In conclusion, patients requesting a lethal injection to
end their suffering by the induction of death are a great
challenge in palliative care. Those patients deserve not
only the best form of medical therapy for symptom control
but also special psychosocial and spiritual counselling,
based on individual respect and understanding in situa-
tions of misery and despair.2
Palliative care is based on the view that even in a
patient’s most miserable moments, sensitive communica-
tion, based on trust and partnership, can improve the situa-
tion and change views that his or her life is worth living.
Acknowledgements
The Ethics Task Force expresses thanks to Lars Johan
Materstvedt, David Clark, John Ellershaw, Reidun Fùrde, Anne-
Marie Boeck Gravgaard, H Christof Müller-Busch, Josep Porta i
Sales and Charles-Henri Rapin, who produced the EAPC posi-
tion paper on euthanasia and physician-assisted suicide in 2003
(Materstvedt et al., 2003), which formed the basis of this white
paper. The task force also thanks the experts who participated in
the first and fourth Delphi round and contributed significantly to
the content of the paper: Ira Byock, Ilora Finlay, Bert Broeckaert,
Luc Deliens, Judith Rietjens, Friedemann Nauck, Morana
Brkljacic, Georg Bosshard, Carl Johan Fürst, Jose Pereira,
Patrick Peretti-Watel, Reidun Førde, Josep Porta i Sales, Agnes
van der Heide, Marcel Louis Viallard, Dominique Jacquemin and
Anne-Marie Boeck Gravgaard. The task force thanks the EAPC
Board of Directors, Claudia Bausewein, Michaela Bercovitch,
Paul van den Berghe, Marilene Filbert, Carlo Leget, Irene
Murphy, Maria Nabal, David Oliber, Sheila Payne, Carlo
Peruselli, Per Sjögren, Tiina Saarto and Esther Schmidlin, who
contributed to the discussion in the fifth Delphi round and
adopted the paper as an EAPC white paper at the EAPC Board
meeting in Lyon in April 2015.
Declaration of conflicting interests
The author(s) declared no potential conflicts of interest with
respect to the research, authorship and/or publication of this
article.
Funding
The author(s) received no financial support for the research,
authorship and/or publication of this article.
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