Cancer Burden: Global Picture. Number of New Cancer Cases (In Millions)
Cancer Burden: Global Picture. Number of New Cancer Cases (In Millions)
Cancer Burden: Global Picture. Number of New Cancer Cases (In Millions)
Palliative care
- ‘to mitigate the sufferings of the
patient, not to effect a cure’-
Macpherson, 2002.
- Any form of medical care or
treatment that attempts to reduce DEATH AND DYING
the severity of symptoms of a • A person is regarded as dead when
disease rather than stopping or his or her physiological processes
delaying or truing to cure it. have stopped:
- It is aimed at relieving suffering and • WHEN THE HEART HAS STOPPED
improving the quality of life for BEATING
people who are seriously ill. • WHEN BREATHING HAS
STOPPED
TERMINOLOGIES • NO LONGER REGISTERS BRAIN
ACTIVITY
1. Autonomy – the state of being self- • Death has negative connotation for
governed (CPCA, 2001).Thinking and most people.
acting independently without outside • Fear of physical suffering
influence and direction. • Fear of isolation and loneliness
2. Bereavement – the state of having • Fear of nonbeing
suffered the death of someone significant • Fear of cowardice and humiliation
(CPCA,2001) • Fear of failing to achieve important
3. Caregiver goals:
- Anyone who provides care. • Fear of the impact of death on those
- Caregivers are willing to listen to ill who outlive you
persons and responds to their individual • Fear of the death of others:
experiences (Twycross R 2003).
- Formal caregivers are members of an GRIEF AND LOSS
organization and accountable to defined
norms of conduct and practice. • Loss is a universal experience that
- They may be professionals, support occurs throughout the lifespan.
workers, or volunteers. • Grief is a form of sorrow involving
- Informal caregivers are not members of feelings, thoughts and behaviors
an organization. They [usually] do not have caused by bereavement.
formal training and are not accountable to • Responses to loss are strongly
norms of conduct or practice. They may be influenced by one’s cultural
family members or friends (CPCA, 2001). background.
• The grief process involves a
4. Dignity – To treat individuals with sequence of affective, cognitive and
respect, esteem and regard psychological states as a person
responds to and finally accepts a • Physical wellbeing: Free of pain and
loss. discomfort, functional ability etc.,
LOSS = something of value is gone • Psychological well being: free from
GRIEF = total response to emotional anxiety/fears, ability to experience
happiness etc.,
experience related to loss
• Social well being: Purposeful life role,
BEREAVEMENT = subjective response to free from financial burden.
by loved ones • Spiritual well being: feelings of hope,
MOURNING = behavioral response meaning to life.
Holistic approach:
• Holistic means the patient is viewed as a
person with Physical, psychological,
social, spiritual and cultural gifts and
needs which are special to that person.
Each of these aspects must be taken COMPONENTS OF PALLIATIVE CARE
into account. (Anne Merriman, 2006)
• The team takes a holistic approach, • Symptom control
using the different talents in a team to • Effective communication
assist in various aspects of the illness. • Rehabilitation
• Reflects whole aspects care. It • Continuity of care
combines the humanistic approach with • Terminal care
a scientific approach. • Support in bereavement
• Education
• Research 3. 3. Emotional and spiritual support is
important for both the patient and family
GOALS OF PALLIATIVE CARE in dealing with the emotional demands
- Palliative care is still sometimes defined of critical illness.
as solely being for people with cancer,
but palliative care is more often now
defined as being for people facing a life- ATTRIBUTES
threatening illness.
- Palliative care is not usually defined as • Individualized patient care
being for people with chronic diseases • Support for the family
such as diabetes. • Interdisciplinary teamwork
• Trust
- Palliative care focuses on symptoms
• Safety
such as pain, shortness of breath,
• Effective Communication
fatigue, constipation, nausea, loss of
appetite, difficulty sleeping and
depression. It also helps you gain the
strength to carry on with daily life. It
improves your ability to tolerate medical
treatments. And it helps you have more
control over your care by improving
communication so that you can better
understand your choices for treatment.
A PALLIATIVE APPROACH
Aims:
• to improve the quality of life for
individuals with a life-limiting illness and
their families, by reducing their suffering
through early identification, assessment
and treatment of pain, physical, cultural,
psychological, social and spiritual needs
• Accessis Foundational
• Care is Patient-Focused
• People Have the Right To Choice
• Dying is Part of Life
• Quality of Life Guides Decisions
• Teamwork Is Essential
• Service is Coordinated
• Accountability is Demonstrated Through
Outcomes
• Confidentiality is Central
• Care Setting Is Important
• Caregiver Well-Being Is Fundamental
• On-going Education is Essential
• Research Leads to Advancement in
Care
• Resources Influence Program Quality
• Collaborative Leadership is
Advantageous