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End of Life Issues. Illness transition. For most patients with cancer, the initial aim and hope is for cure For those who develop recurrent malignant disease, there is the likelihood that the disease is incurable

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Illness transition
Illness transition

  • For most patients with cancer, the initial aim and hope is for cure

  • For those who develop recurrent malignant disease, there is the likelihood that the disease is incurable

  • The transition from curative intent to palliation is difficult for many, often resulting in despair, denial, depression, anxiety or resigned indifference

  • Patients and their carers require sensitive guidance through this transition


Goals of care
Goals of Care

Curative (“beating it”)

  • Cure or durable remission

  • Prognosis: years

    Palliative (“living with disease, anticipating death”)

  • Disease incurable and progressive

  • Prognosis: weeks, months (but can be years)

    Terminal (“dying very soon”)

  • Death imminent

  • Prognosis: hours or days

    Ashby M, Stoffell B.

    Therapeutic ratio and defined phases: proposal of ethical framework for palliative care.

    BMJ 1991; 302: 1322-1324


Key questions if ceasing active treatment is considered
Key questions if ceasing active treatment is considered

  • Are the clinical facts of the case well established? Is the diagnosis correct?

  • Has sufficient time elapsed to be reasonably confident that there is no reasonable prospect of substantial improvement or recovery?

  • Is there consensus among the clinicians about the diagnosis, prognosis and most appropriate course of medical action? Is a case conference necessary?


Key questions if ceasing active treatment is considered1
Key questions if ceasing active treatment is considered

  • Identify the key decision maker(s) in the family or friends

  • Have the family, carer(s) or legally appointed agent been advised of the above? Have they had a chance to express their opinions, and been involved in the decision making process?

  • Has the patient’s GP been involved?


Key questions if ceasing active treatment is considered2
Key questions if ceasing active treatment is considered

  • Has the decision to stop active treatment been documented? The plan for implementing it may involve a “time trial” of continued life-sustaining treatment. How will subsequent objections to the decision be dealt with?

  • Has a consultative palliative care team referral been considered?

    Ashby MA, Kellehear A, Stoffell BF.

    Resolving conflict in end of life care.

    Editorial MJA Vol 183 No 5: 5 Sept 2005 230-231


Progressive life limiting illness management approach
Progressive, life limiting illness management approach:

Patients, primary carers and families

  • are provided with information to allow them to make informed decisions

  • are encouraged to participate in the development of their care plan initially and on an ongoing basis

    Referral to palliative care specialist services when needs are, or will become complex

  • Complex pain or symptoms not responsive to established protocols

  • Complex psychological and/or social needs

  • Increased risk of complicated bereavement for the primary carer and family

    A Guide to Palliative Care

    Service Development:

    A Population based approach

    Palliative Care Australia Feb 2005


Negotiating ceasing active treatment
Negotiating Ceasing Active Treatment

  • The patient and caregivers deserve a frank assessment of the likelihood of response to treatment and its duration

  • Deal with the control issue - a feeling of loss of control may be a major component of patient’s distress

  • Both the patient and the doctor need to recognise that doctors do not stop treating patients when they stop active therapy. Rather, a different treatment program has been chosen

  • To continue toxic treatment solely to maintain hope of some response is inadequate medicine. To continue to allow patients and caregivers to put their hope in things that are highly likely to fail (eg, further chemotherapy) is at best ill advised and at worst avoiding the real issue.


Negotiating ceasing active treatment1
Negotiating Ceasing Active Treatment

  • There comes a time when a patient with incurable disease is best served by placing his or her hope in things that will not fail, be it a doctor’s ongoing care, the love of the family, religious beliefs, and so on.

  • Show the patient, and their family that you care

  • Don’t cut the patient loose at this time

  • Multidisciplinary team is needed to provide

    • Spiritual and psychosocial support

    • Symptom control

    • End of life care

    • Bereavement support

      Harnett PR, Moynihan TJ. But Doctor, What Have I Got to Lose…?

      JCO: Vol 19(13) July 1, 2001


Negotiating ceasing active treatment2
Negotiating Ceasing Active Treatment

  • Good communication with GP essential. GP may be asked for another opinion by patient and/or carers

  • Appropriate involvement of nursing resources, hospital and community. At this stage, good nursing care may become the most significant need for patients and carers


Preserving dignity
Preserving dignity

  • Patients are exposed to many events and situations during their illness which may enhance or impede their dignity

    • Healthcare processes

    • Illness related complications

    • Family systems

    • Welfare systems


Maintaining dignity
Maintaining dignity

  • Continuity of self - a sense that the essence of who one is, continues to remain intact, despite advancing illness

  • Role preservation - the ability to continue to function in usual roles

  • Legacy - the comfort in knowing that something lasting of oneself will transcend death

  • Maintaining pride - the ability to maintain a positive sense of self regard or respect

  • Maintaining hope - an ability to see life as enduring, or having sustained meaning or purpose

  • Autonomy/control

  • Acceptance - the internal process of resigning one’s self to changing life circumstances

    Chochinov H M, Dignity and the Eye of the Beholder

    JCO: Vol 22(7) April 2004


Challenging communication tasks 1
Challenging communication tasks - 1

  • Doc, how much time do I have left?

    • Acknowledge uncertainty

    • Foretell a general, realistic time frame - days, days to weeks, weeks to months

    • Provide realistic hope

    • Recommend “doing the things that should be done”

    • Provide realistic assurance that you’ll be available to help the patient through the dying process

    • Refer for emotional and spiritual support in “dying well”

    • Ask patients what they want to accomplish

    • Encourage additional questions

      Loprinzi C et al Doc, How Much Time Do I Have?

      JCO Volume 18(3), February 2000


Challenging communication tasks 2
Challenging communication tasks - 2

  • Goal setting framework

    • Create the right setting

    • Ask what the patient/family know

    • Explore what they are expecting or hoping for

    • Suggest realistic goals

    • Respond empathically to the emotions that will arise

    • Make a plan and follow through

    • Review and revise goals periodically

      Von Roenn JH, von Gunten CF Setting Goals to Maintain Hope

      JCO Volume 12(3), 1 February 2003


Addressing spiritual care calling for help
Addressing Spiritual Care: Calling for Help

  • A physician or health care professional who shows interest in spiritual care expresses concern for the “whole person” who has cancer.

  • The simple screening question, “What role does faith play in your life?”could be all that is needed to assess the dimension of faith in a patient, and to point the way for future support.

    Steer CJ & Lee C. Addressing Spiritual Care: Calling for Help

    JCO Volume 22(23), December 1, 2004


Addressing spiritual care calling for help1
Addressing Spiritual Care: Calling for Help

  • Spirituality relates to an individual’s capacity to seek meaning and purpose in life.

  • Cancer commonly affects the spiritual dimension of patients with cancer

  • Religious beliefs and practices play a significant part in the way that some patients cope with their disease and how they make sense of what is happening to them.

  • For many patients, religious faith plays a major role in their lives

  • Faith provides patients with emotional support, social support and a root to meaning, all of which help them cope with the diagnosis and treatment of cancer

    Steer CJ & Lee C. Addressing Spiritual Care: Calling for Help

    JCO Volume 22(23), December 1, 2004


Palliative care
Palliative Care

  • Palliative care is an approach that improves the quality of life of patients and their families facing the problem 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.

    WHO Nov 2003


Palliative care1
Palliative Care

  • Provides relief from pain and other distressing symptoms;

  • Affirms life and regards dying as a normal process;

  • Intends neither to hasten or postpone death;

  • Integrates the psychological and spiritual aspects of patient care;

  • Offers a support system to help patients live as actively as possible until death;

  • Offers a support system to help the family cope during the patients illness and in their own bereavement;


Palliative care2
Palliative Care

  • Uses a team approach to address the needs of patients and their families, including bereavement counselling, if indicated;

  • Will enhance quality of life, and may also positively influence the course of illness;

  • Is applicable early in the course of illness, in conjunction with other therapies that are intended to prolong life, such as chemotherapy or radiation therapy, and includes those investigations needed to better understand and manage distressing clinical complications.


Palliative care when
PALLIATIVE CARE - WHEN?

  • In incurable progressive disease, there is a gradual transfer of focus from active treatment to a focus on quality of life and symptom control, the dying process and subsequent bereavement

ACTIVETREATMENT

BEREAVE-MENT

DEATH

DIAGNOSIS

PALLIATIVE

CARE


Palliative care3
Palliative Care

  • Pain Management

  • Common Symptom Management

  • Communication

  • Family Support

  • Ethics and medical decision-making at end of life

  • Grief and Bereavement

  • Multidisciplinary Team Work

  • Emotional Care of Self


Palliative care4
Palliative Care

  • Relief of suffering

  • Quality of Life

  • Comfort

  • Holistic care

  • Dying with dignity


Multidiciplinary team

Nursing

Medical

Pharmacy

Physiotherapy

Occupational therapy

Diversional therapy

Social work

Psycho-oncology

Psychiatrists

Clinical psychology

Bereavement counselors

Pastoral care

Volunteers

Multidiciplinary team


Palliative care community
PALLIATIVE CARE - COMMUNITY

  • GP “case manager”

  • Generalist Community Nurse - GCN

  • Clinical Nurse Specialist - CNS

  • Clinical Nurse Consultant - CNC

  • Palliative Care Medical Officer

  • Community Palliative Care Specialist


Advanced care directives aims
Advanced care directives - aims

  • Identifying what is important as a patient approaches death, especially the place of life sustaining treatment

  • Achieve a sense of control

  • Engage others in decision making, family friends

  • Provide flexibility in decision making

  • Advance care directions are optional

Using Advance Care Directives

NSW Dept of Health 2004

http://www.health.nsw.gov.au/policies/gl/2005/GL2005_056.html


Advanced care directives barriers
Advanced care directives - barriers

  • Time constraints

  • Discomfort in talking about death: patient, family, health professionals

  • Patient perceptions about who should or does control medical decision making

  • Fears about being able to change one’s mind

  • Lack of knowledge about availability of advance care directives, or

  • Health professionals may not appreciate the legal standing of advance directives

Using Advance Care Directives

NSW Dept of Health 2004

http://www.health.nsw.gov.au/policies/gl/2005/GL2005_056.html


End of life care dying
End of Life Care - Dying

  • Recognise it

  • Acknowledge it

  • Respect it

  • Treat symptoms

  • Support carers


Terminal care phase
TERMINAL CARE PHASE

  • The typical features of a person in this phase include the following:

    • Profoundly weak.

    • Essentially bed bound.

    • Drowsy for extended periods.

    • Disoriented for time and has a severely limited attention span.

    • Increasingly disinterested in food and drink.

    • Finding it difficult to swallow medication.


2 ROADS TO DEATH

THE DIFFICULT ROAD

Confused

Tremulous

Restless

Hallucinations

Normal

Mumbling Delirium

Sleepy

Myoclonic Jerks

Lethargic

Seizures

Obtunded

THE USUAL ROAD

Semicomatose

Comatose

Dead


Handy hints
HANDY HINTS

  • Determine early where the patient would like to be cared for: home, hospital, hospice

  • Identify barriers that may prevent this from occurring

  • Encourage flexibility. Circumstances may change during the final stage

  • Use only medications essential for symptom control. Stop other medications and continue to offer opioids.

  • Remember accumulating serum concentrations of active drug and metabolites may lead to toxicity and terminal delirium.

  • Recognise the signs of the dying process.


Grief and bereavement
Grief and Bereavement

  • Bereavement support is integral to palliative care

  • Grief after loss is a normal process, but may be complicated and compromise the health of an individual

  • Routine bereavement care helps to identify people at risk

  • Burden of grief can last for years

  • Need to pay attention to cultural differences

  • Excellent resources are available for grief management

    Maddocks, I.Grief and Bereavement.

    Medical Journal of Australia

    15 Sept 2004, Vol 179, No 6 Supplement


Bereavement tasks
Bereavement tasks

  • Accept the reality of the loss

  • Experience the pain of grief

  • Adjust to an environment from which the deceased is missing

  • Reinvest energy in other possibilities

    Worden, J. Grief Counselling and Grief Therapy.

    London: Tavistock, 1991


Bereavement resources
Bereavement Resources

  • Palliative care bereavement services

  • GP’s

  • Community nursing and mental health teams

  • Psycho-oncology services

  • Social work

  • Private bereavement services

  • Pastoral care


  • Facing the consequences of a progressive, life limiting illness can exhaust the physical and emotional resources of patients, primary carers and their families, and indeed can also deplete those of the health care professionals who care for them

    A Guide to Palliative Care

    Service Development:

    A Population based approach

    Palliative Care Australia Feb 2005


Impacts on carers
Impacts on carers illness can exhaust the physical and emotional resources of patients, primary carers and their families, and indeed can also deplete those of the health care professionals who care for them

  • Stress

  • Disruptions and emotional strains

  • Health problems

  • Mental health issues

  • Reduced life opportunities

  • Financial strains

    Caring for a Dying Person in Australia

    Palliative Care Australia May 2004


Positive aspects of caring
Positive aspects of caring illness can exhaust the physical and emotional resources of patients, primary carers and their families, and indeed can also deplete those of the health care professionals who care for them

  • Carers

    • expressed strong positive emotions about their care giving experiences

    • found significant meaning in their roles

    • felt self satisfaction knowing that they are doing a good job

      Grbich, C. Parker, D. & Maddocks, I. (2001)

      The Emotions and Coping Strategies of Caregivers of

      Family members with a Terminal Cancer.

      Journal of Palliative Care, 17(1), 30-36


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