Group 9 - DYING AND BEREAVEMENT
Group 9 - DYING AND BEREAVEMENT
Group 9 - DYING AND BEREAVEMENT
ETHICAL ISSUE
● BIOETHICS
- Grew from two bases: respect for individual freedom and the impossibility of
establishing any single version of morality by rational argument or common sense. Both of these
factors are increasingly based on empirical evidence and cultural contexts (Priaulx, 2013;
Sherwin, 2011). In practice, bioethics emphasizes the importance of individual choice and the
minimization of harm over the maximization of good.
-In the arena of death and dying, the most important bioethical issue is euthanasia.
● EUTHANASIA
-Active euthanasia involves the deliberate ending of someone’s life, that may be
based on a clear statement of the person’s wishes or be a decision made by someone else who
has the legal authority to do so.
-Passive euthanasia, involves allowing a person to die by withholding available
treatment.
● PHYSICIAN-ASSISTED SUICIDE
-Process in which physicians provide dying patients with a fatal dose of medication
that the patient self-administers.
-Several countries—including Switzerland, Belgium, the Netherlands, and
Colombia—have legalized physician-assisted suicide. In Netherlands has five criteria
must be met before a terminally ill person can request physician-assisted suicide as an
option:
DEATH ANXIETY
-Death anxiety refers to people’s anxiety or even fear of death and dying. Death anxiety is tough
to pin down; indeed, it is the ethereal, unknown nature of death, rather than something about it
in particular, that makes us feel so uncomfortable.
“Is death the sort of thing that could happen to me right now?”
End-of-Life Issues
-When given the chance, many adults would like to discuss a variety of issues, collectively
called end-of-life issues: management of the final phase of life, after-death disposition of their
body, memorial services, and distribution of assets (Moeller et al., 2010).
-Making such choices known about how they do and do not want their lives to end constItutes a
final scenario.
HOSPICE OPTION
-An approach to care based on an ethic of controlling and relieving pain or other symptoms and
not on attempting to cure disease is called palliative care. Hospice is the leading provider of
such care,but palliative care is also adopted in other settings.
Hospice is the leading provider of such care,but palliative care is also adopted in other settings.
The differences are evident in the principles that underlie hospice care (Knee, 2010):
● Clients and their families are viewed as a unit, clients should be kept free of pain, emotional
and social impoverishment must be minimal;
● Clients must be free to begin or end relationships, an interdisciplinary team approach is used,
and staff members must seek to alleviate pain and fear.
● What options are available at this point in the progress of the person’s disease? Knowing
about all available treatment options is critical. Exploring treatment options also requires
healthcare professionals to be aware of the latest approaches and be willing to disclose them.
● What are the person’s expectations, fears, and hopes? Some older adults, like Jean,
remember or have heard stories about people who suffered greatly at the end of their
lives. This can produce anxiety about one’s own death. Similarly, fears of becoming
dependents play an important role in a person’s decision making. Discovering and discussing
these anxieties help clarify options.
● How well do people in the person’s social network communicate with each other? Talking
about death is taboo in many families. In others, intergenerational communication is
difficult or impossible. Even in families with good communication, the pending death
of a loved relative is difficult. As a result, the dying person may have difficulty express-
ing his or her wishes. The decision to explore the hospice option is best made when it
is discussed openly.
● Are family members available to participate actively in terminal care? Hospice relies
on family members to provide much of the care that is supplemented by professionals
and volunteers. Having a family member who is willing to accept this responsibility is essential
for the hospice option to work.
● Is a high-quality hospice care program available? Hospice programs are not uniformly
good. As with any healthcare provider, patients and family members must investigate
the quality of local hospice programs before making a choice.
1. In a living will, a person simply states his or her wishes about life support and other
treatments.
2. In a healthcare power of attorney, an individual appoints someone to act as his or her
agent for healthcare decisions
-A do not resuscitate (DNR) order means cardiopulmonary resuscitation (CPR) is not started
should one’s heart and breathing stop.
To aid healthcare providers in this process, the Patient Self-Determination Act, passed in 1990,
requires most healthcare facilities to provide information to patients in writing that they have the
right to:
● Acknowledge the reality of the loss. We must overcome the temptation to deny the
reality of our loss; we must fully and openly acknowledge it and realize it affects every
aspect of our life.
● Work through the emotional turmoil. We must find effective ways to confront and
express the complete range of emotions we feel after the loss and must not avoid or repress
them.
● Adjust to the environment where the deceased is absent. We must define new patterns of
living that adjust appropriately and meaningfully to the fact the deceased is not present.
● Loosen ties to the deceased. We must free ourselves from the bonds of the deceased in order
to reengage with our social network. This means finding effective ways to say
good-bye.
GROUP MEMBERS: G9
Nujapa, Fevelyn
Pamen, Winsome
Sorvida, Mark Andrey