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Part of the “Enhancing Prostate Cancer Care” MOOC 
Catherine Holborn 
Senior Lecturer in Radiotherapy & Oncology 
Sheffield Hallam University
Decision making 
Patients and carers need to have the opportunity to 
make decisions about their care through their care. 
It is vital that patients are only offered treatment that 
will have benefit 
It is therefore important that health care professionals 
are able to facilitate these decisions ensuring that they 
act in an ethical and legal way. 
This PowerPoint explores some of the issues involved
End of life care 
This refers to the last year of life 
Physicians often use what is referred to as the 'surprise 
question' 
That is it likely that the person will die in the next year 
Acknowledgement of this leads to planning for the care 
that may be required.
Advance Care Planning 
Patients should have the option of planning for future 
care, especially if they are entering end of life care. 
These conversations can be difficult for patients, family 
and staff, so staff need to have the necessary 
communication skills and support to facilitate these 
discussions
National End of Life Care Programme (2012) 
Care planning embraces the care of people with and 
without capacity to make their own decisions. It involves 
a process of assessment and person centred dialogue to 
establish the person’s needs, preferences and goals of 
care, and making decisions about how to meet these in 
the context of available resources. 
It can be oriented towards meeting immediate needs, as 
well as predicting future needs and making appropriate 
arrangements or contingency plans to address these.
It first has to be recognised and acknowledged when a 
patient is entering the last year of life, as the study 
below has found... 
'In order that appropriate care plans can be made and 
delivered for patients, there is a strong need for hospitals 
to adopt a more vigorous approach to identify patients 
who are entering the last year of their lives. 
 We contend that the culture and organisation of 
hospitals need to become more attuned to the high 
proportion of inpatients in imminent need of end-of-life 
care'. (Clark et al , 2014)
Discussions about dying 
As a society, we could all raise awareness of the fact that 
we are all dying 
Dying Matters is an organisation that works to encourage 
people to talk more openly about dying, death and 
bereavement. This can make it easier for the patient or 
professional to broach the subject of dying. Further 
details can be found at:- 
http://dyingmatters.org/
Decision making may also be aided by 
reference to the ethical principles 
(Beauchamp and Childress, 2013) 
A framework for moral judgement and decision making in 
the light of developments in health care 
RESPECT FOR AUTONOMY 
BENEFICENCE 
NON-MALEFICENCE 
JUSTICE
Respect for autonomy 
The moral obligation to respect the autonomy of others, 
in so far as the respect is compatible with equal respect 
for the autonomy of all those who may be affected. 
Finding out what the patient and family would prefer is 
crucial. Sometimes, their wishes may differ and it is the 
healthcare professional's role to enhance communication 
in this situation. A patient can only receive care that is 
considered of benefit to the patient by the professionals
Beneficence 
A moral obligation to act for the benefit of others, or in 
their best interests 
What is a benefit to the patient and family can 
sometimes be contentious. Some treatments that a 
patient may be going through willingly can be difficult 
for the family.
Non-maleficence 
The duty to do no harm 
Maleficent - bad consequences 
Florence Nightingale - the hospital shall do the sick no 
harm 
To ensure there is a net benefit over harm - whose? 
Risk/probability (research) 
Iatrogenesis 
This is where individualised care is important as what may 
be a benefit to one person can be a burden to another
Justice 
The moral obligation to act on the basis of fair 
adjudication between competing claims 
This involves ensuring that the treatment and care 
offered (or not offered) is equal to that offered to other 
patients locally and nationally. There may be difficulties 
here when a patient feels they are not being offered 
what may be available in another country
Decision making 
One way that patients can be empowered in their 
decision making is to have the opportunity to make 
advance decisions, known as Advance Care Planning 
(ACP) (2009) 
There are three different aspects of ACP (see next slides)
1. An advance statement: a statement of 
wishes and preferences 
These are not legally binding, but health care professionals 
will work towards ensuring these wishes are carried out. They 
may involve. 
The patient and family can decide where the person would 
like to die, who they would prefer to have with them, whether 
they would like some specific music played etc... 
They can also express wishes for what treatment they would 
like ( respecting their autonomy). However the healthcare 
team will also decide whether this is in the patient's best 
interests (beneficence) and whether the treatment would 
cause more harm than good ( non-maleficence).
Decision making may be difficult when 
patients/families disagree with the 
treatment offered... 
Lord Saachi's Bill (2014) currently in the House of Lords is 
intended to:- 
'encourage responsible innovation in medical treatment (and 
accordingly to deter reckless irresponsible innovation)'. 
If successful, how this may affect treatment decisions is 
currently unknown 
A decision whether to access ( if possible) innovative 
treatment may be challenging for all involved and weighed 
against the potential benefits of the treatment.
2. Advance Decision to Refuse Treatment 
(ADRT) 
A specific refusal of treatment(s) in a predefined 
potential future situation e.g. a patient may choose not 
to be resuscitated or to have a specific treatment. 
Their autonomy would be respected in these refusals 
even if the healthcare team believed that the treatment 
may be of benefit to the patient (beneficence).
3. Lasting Power of Attorney (LPA) 
The appointment of a personal welfare LPA - this would 
mean a designated person can make decisions for the 
patient if there is doubt about which treatment is the 
most appropriate to give in a specific situation. 
This is only used when a patient is no longer able to 
make their own decisions. 
This would assist in respecting the patient's autonomy 
when they are unable to express their wishes.
LPA cont. 
Patient chooses a person to take decisions on their 
behalf if they lose capacity 
Personal welfare rather than financial 
Register with Office of Public Guardian
Recognition that the person may be dying in 
the next hours or days can be complex 
This requires sensitive communication between the 
patient, carers and healthcare staff in its recognition 
and acknowledgement. 
Aspects of the advanced care plan may be 
implemented. 
The Leadership Alliance for the Care of Dying People 
(2014) puts the patient and families at the centre of 
decisions about treatment and care. The priorities for 
care are implemented.
Recognition of dying 
Common symptoms that may be experienced are: 
Physically wasted and profoundly weak ⇨ bedbound 
Drowsy for much of the day ⇨ coma 
Very limited attention span ⇨ disoriented 
Unable to take tablets or has difficulty swallowing them 
Little of no oral intake of food or fluid 
Palliative care specialists can give guidance here as to the 
most appropriate treatment to be given
As death approaches... 
Relatives/friends who are clearly informed that a 
patient is dying have the chance to stay with the 
person, say their good-byes, contact other and 
prepare for the death 
Grande and Ewing (2009) found that the level of 
support, particularly psychological may be more 
important for carer's bereavement than achievement 
of preferred place of death
Continued decision making 
When someone is dying it is necessary to assess whether 
current treatments are still appropriate. Individualised care is 
paramount, with no blanket policies 
For example, it may become inappropriate to continue 
encouraging fluids with a person who is becoming increasingly 
more drowsy with a chesty cough( and also dangerous if they 
can't swallow). Sips of water and keeping the mouth moist 
may become the most appropriate treatment
Spending time with dying patients 
(Becker, 2009) 
'There is always a sense of powerlessness when 
confronted with death. No one can change this. The 
real skill is learning to be comfortable with that 
powerlessness and using it to help patients and 
families.' 
Valuing being sensitive to what is intuitive and felt 
can be as important as what has been learned.
The four principles need to be applied against the 
background of respect for life and an acceptance of 
the ultimate inevitability of death... 
Three dicotomies need to be held in balance 
The potential benefits of treatment versus potential risks and 
burdens 
Striving to preserve life but, when the burdens of life-sustaining 
treatment outweigh the potential benefits, 
withdrawing or withholding such treatments and providing 
comfort in dying 
Individual needs versus the needs of society 
(Twycross & Wilcock, 2001)
Decision making is never easy. However, decisions can only be 
made based on the information at the time. Communication is 
an essential component throughout 
Not just to look forward to make predictions 
But also looking backward to try to interpret the past 
‘Life is lived forwards, but understood backwards’ 
Kierkegaard, Danish Philosopher
References 
 BEAUCHAMP, T.L., CHILDRESS, J.F. (2013) Principles of Biomedical Ethics, 7th Ed. University Press Oxford. 
 BEARD Barbara ( 2011) Legal and ethical issues in palliative care in Moyra Baldwin and Jan Woodhouse (Eds.) Key 
concepts in palliative care. London, Sage 
 BECKER Bob (2009) Palliative care 3: Using palliative nursing skills in clinical practice Nursing Times 105(15): 18-21 
 CLARK, David et al (2014) Imminence of death among hospital inpatients: prevalent cohort study Palliative 
Medicine 28(4): 474-479 
 GENERAL MEDICAL COUNCIL (2010) Treatment and care towards the end of life: good practice in decision making. 
GMC, London. Last accessed 08.09.14 at 
 http://www.gmc-uk.org/guidance/ethical_guidance/end_of_life_care.asp 
 HUGHES Philippa (2010) What progress has been made towards implementing national guidance on end of life 
care? A national survey of UK general practices Palliative Medicine 24(1): 68-78 
 ROYAL COLLEGE OF PHYSICIANS ET AL ( 2009) Advance Care Planning - National Guidelines. London, Royal College 
of Physicians 
 SAACHI Lord (2014) Medical Innovations Bill Accessed on 08.09.14 at 
http://www.publications.parliament.uk/pa/bills/lbill/2014-2015/0004/15004.pdf 
 End of Life Care Strategy - First Annual Report (2009 )London, Department of Health 
http://www.dh.gov.uk/en/Publicationsandstatistics/Publications/DH_102433 
 TWYCROSS R, WILCOCK A (2001) Symptom Management in Advanced Cancer 5th Ed Oxford, Radcliffe Medical Press 
 TWYCROSS Robert, WILCOCK Andrew (2007) Palliative Care Formulary 3rd Ed. Oxfordshire, Palliativedrugs.com 
Ltd 
 TWYCROSS, Robert, WILCOCK Andrew, TOLLER Clare Stark (2009). Symptom Management in Advanced Cancer 4th 
Ed. Oxfordshire, Palliativedrugs.com Ltd

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Decision making in end of life care

  • 1. Part of the “Enhancing Prostate Cancer Care” MOOC Catherine Holborn Senior Lecturer in Radiotherapy & Oncology Sheffield Hallam University
  • 2. Decision making Patients and carers need to have the opportunity to make decisions about their care through their care. It is vital that patients are only offered treatment that will have benefit It is therefore important that health care professionals are able to facilitate these decisions ensuring that they act in an ethical and legal way. This PowerPoint explores some of the issues involved
  • 3. End of life care This refers to the last year of life Physicians often use what is referred to as the 'surprise question' That is it likely that the person will die in the next year Acknowledgement of this leads to planning for the care that may be required.
  • 4. Advance Care Planning Patients should have the option of planning for future care, especially if they are entering end of life care. These conversations can be difficult for patients, family and staff, so staff need to have the necessary communication skills and support to facilitate these discussions
  • 5. National End of Life Care Programme (2012) Care planning embraces the care of people with and without capacity to make their own decisions. It involves a process of assessment and person centred dialogue to establish the person’s needs, preferences and goals of care, and making decisions about how to meet these in the context of available resources. It can be oriented towards meeting immediate needs, as well as predicting future needs and making appropriate arrangements or contingency plans to address these.
  • 6. It first has to be recognised and acknowledged when a patient is entering the last year of life, as the study below has found... 'In order that appropriate care plans can be made and delivered for patients, there is a strong need for hospitals to adopt a more vigorous approach to identify patients who are entering the last year of their lives.  We contend that the culture and organisation of hospitals need to become more attuned to the high proportion of inpatients in imminent need of end-of-life care'. (Clark et al , 2014)
  • 7. Discussions about dying As a society, we could all raise awareness of the fact that we are all dying Dying Matters is an organisation that works to encourage people to talk more openly about dying, death and bereavement. This can make it easier for the patient or professional to broach the subject of dying. Further details can be found at:- http://dyingmatters.org/
  • 8. Decision making may also be aided by reference to the ethical principles (Beauchamp and Childress, 2013) A framework for moral judgement and decision making in the light of developments in health care RESPECT FOR AUTONOMY BENEFICENCE NON-MALEFICENCE JUSTICE
  • 9. Respect for autonomy The moral obligation to respect the autonomy of others, in so far as the respect is compatible with equal respect for the autonomy of all those who may be affected. Finding out what the patient and family would prefer is crucial. Sometimes, their wishes may differ and it is the healthcare professional's role to enhance communication in this situation. A patient can only receive care that is considered of benefit to the patient by the professionals
  • 10. Beneficence A moral obligation to act for the benefit of others, or in their best interests What is a benefit to the patient and family can sometimes be contentious. Some treatments that a patient may be going through willingly can be difficult for the family.
  • 11. Non-maleficence The duty to do no harm Maleficent - bad consequences Florence Nightingale - the hospital shall do the sick no harm To ensure there is a net benefit over harm - whose? Risk/probability (research) Iatrogenesis This is where individualised care is important as what may be a benefit to one person can be a burden to another
  • 12. Justice The moral obligation to act on the basis of fair adjudication between competing claims This involves ensuring that the treatment and care offered (or not offered) is equal to that offered to other patients locally and nationally. There may be difficulties here when a patient feels they are not being offered what may be available in another country
  • 13. Decision making One way that patients can be empowered in their decision making is to have the opportunity to make advance decisions, known as Advance Care Planning (ACP) (2009) There are three different aspects of ACP (see next slides)
  • 14. 1. An advance statement: a statement of wishes and preferences These are not legally binding, but health care professionals will work towards ensuring these wishes are carried out. They may involve. The patient and family can decide where the person would like to die, who they would prefer to have with them, whether they would like some specific music played etc... They can also express wishes for what treatment they would like ( respecting their autonomy). However the healthcare team will also decide whether this is in the patient's best interests (beneficence) and whether the treatment would cause more harm than good ( non-maleficence).
  • 15. Decision making may be difficult when patients/families disagree with the treatment offered... Lord Saachi's Bill (2014) currently in the House of Lords is intended to:- 'encourage responsible innovation in medical treatment (and accordingly to deter reckless irresponsible innovation)'. If successful, how this may affect treatment decisions is currently unknown A decision whether to access ( if possible) innovative treatment may be challenging for all involved and weighed against the potential benefits of the treatment.
  • 16. 2. Advance Decision to Refuse Treatment (ADRT) A specific refusal of treatment(s) in a predefined potential future situation e.g. a patient may choose not to be resuscitated or to have a specific treatment. Their autonomy would be respected in these refusals even if the healthcare team believed that the treatment may be of benefit to the patient (beneficence).
  • 17. 3. Lasting Power of Attorney (LPA) The appointment of a personal welfare LPA - this would mean a designated person can make decisions for the patient if there is doubt about which treatment is the most appropriate to give in a specific situation. This is only used when a patient is no longer able to make their own decisions. This would assist in respecting the patient's autonomy when they are unable to express their wishes.
  • 18. LPA cont. Patient chooses a person to take decisions on their behalf if they lose capacity Personal welfare rather than financial Register with Office of Public Guardian
  • 19. Recognition that the person may be dying in the next hours or days can be complex This requires sensitive communication between the patient, carers and healthcare staff in its recognition and acknowledgement. Aspects of the advanced care plan may be implemented. The Leadership Alliance for the Care of Dying People (2014) puts the patient and families at the centre of decisions about treatment and care. The priorities for care are implemented.
  • 20. Recognition of dying Common symptoms that may be experienced are: Physically wasted and profoundly weak ⇨ bedbound Drowsy for much of the day ⇨ coma Very limited attention span ⇨ disoriented Unable to take tablets or has difficulty swallowing them Little of no oral intake of food or fluid Palliative care specialists can give guidance here as to the most appropriate treatment to be given
  • 21. As death approaches... Relatives/friends who are clearly informed that a patient is dying have the chance to stay with the person, say their good-byes, contact other and prepare for the death Grande and Ewing (2009) found that the level of support, particularly psychological may be more important for carer's bereavement than achievement of preferred place of death
  • 22. Continued decision making When someone is dying it is necessary to assess whether current treatments are still appropriate. Individualised care is paramount, with no blanket policies For example, it may become inappropriate to continue encouraging fluids with a person who is becoming increasingly more drowsy with a chesty cough( and also dangerous if they can't swallow). Sips of water and keeping the mouth moist may become the most appropriate treatment
  • 23. Spending time with dying patients (Becker, 2009) 'There is always a sense of powerlessness when confronted with death. No one can change this. The real skill is learning to be comfortable with that powerlessness and using it to help patients and families.' Valuing being sensitive to what is intuitive and felt can be as important as what has been learned.
  • 24. The four principles need to be applied against the background of respect for life and an acceptance of the ultimate inevitability of death... Three dicotomies need to be held in balance The potential benefits of treatment versus potential risks and burdens Striving to preserve life but, when the burdens of life-sustaining treatment outweigh the potential benefits, withdrawing or withholding such treatments and providing comfort in dying Individual needs versus the needs of society (Twycross & Wilcock, 2001)
  • 25. Decision making is never easy. However, decisions can only be made based on the information at the time. Communication is an essential component throughout Not just to look forward to make predictions But also looking backward to try to interpret the past ‘Life is lived forwards, but understood backwards’ Kierkegaard, Danish Philosopher
  • 26. References  BEAUCHAMP, T.L., CHILDRESS, J.F. (2013) Principles of Biomedical Ethics, 7th Ed. University Press Oxford.  BEARD Barbara ( 2011) Legal and ethical issues in palliative care in Moyra Baldwin and Jan Woodhouse (Eds.) Key concepts in palliative care. London, Sage  BECKER Bob (2009) Palliative care 3: Using palliative nursing skills in clinical practice Nursing Times 105(15): 18-21  CLARK, David et al (2014) Imminence of death among hospital inpatients: prevalent cohort study Palliative Medicine 28(4): 474-479  GENERAL MEDICAL COUNCIL (2010) Treatment and care towards the end of life: good practice in decision making. GMC, London. Last accessed 08.09.14 at  http://www.gmc-uk.org/guidance/ethical_guidance/end_of_life_care.asp  HUGHES Philippa (2010) What progress has been made towards implementing national guidance on end of life care? A national survey of UK general practices Palliative Medicine 24(1): 68-78  ROYAL COLLEGE OF PHYSICIANS ET AL ( 2009) Advance Care Planning - National Guidelines. London, Royal College of Physicians  SAACHI Lord (2014) Medical Innovations Bill Accessed on 08.09.14 at http://www.publications.parliament.uk/pa/bills/lbill/2014-2015/0004/15004.pdf  End of Life Care Strategy - First Annual Report (2009 )London, Department of Health http://www.dh.gov.uk/en/Publicationsandstatistics/Publications/DH_102433  TWYCROSS R, WILCOCK A (2001) Symptom Management in Advanced Cancer 5th Ed Oxford, Radcliffe Medical Press  TWYCROSS Robert, WILCOCK Andrew (2007) Palliative Care Formulary 3rd Ed. Oxfordshire, Palliativedrugs.com Ltd  TWYCROSS, Robert, WILCOCK Andrew, TOLLER Clare Stark (2009). Symptom Management in Advanced Cancer 4th Ed. Oxfordshire, Palliativedrugs.com Ltd