Submitted by
Jacqueline Horn
Mailbox #535
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When patients facing chronic or terminal illnesses reach a state in which they cannot
longer voice their end-of-life care decisions, it is common for relatives to end up having to face
the difficult duty of making decisions concerning the quality of life or possible death the patient
will experience. A legal form of representation for incapacitated patients has been created to
avoid this kind of situations and to ensure that patients’ decisions are explicitly followed. This
legal document by which incapacitated patients are allowed to dictate the direction of their care is
known as an advance directive. The main purpose of advance directives is to prevent patients’
decisions from being erroneously taken by people who do not know their expectations for end-of-
life care. They “express the desires of competent adults regarding terminal care, life-sustaining
measures, and other issues pertaining to their dying and death” (Eliopoulus, 2005, p111). In most
cases it provides patients with reassurance that their end-of-life wishes are taken into
consideration. This paper will explore the significance of the different types of advance directives
There are three different types of advance directives: living wills, medical directives and
Durable Power of Attorney for Health Care (DPAHC). Living wills can be described as
documents that “become effective when an individual is terminally ill and usually express the
individual’s desire to die without the institution of prolonging medical interventions” (Perrin,
1997, p20). Living wills give patients the option to refuse medical care if they become unable to
express their wishes (Inman, 2002). One advantage living wills provide is the option of refusing
treatment (Perrin, 1997). The disadvantages of this type of advance directive are that living wills
do not stipulate which treatment to follow, and it does not specify which circumstances should
described (as cited in Inman, 2005) medical directives ask patients questions regarding the
medical care desired in specific situations to avoid the vagueness of living wills. The advantages
patients obtain from medical directives are that they can be specific about which treatments they
decide to receive; medical directives reassure patients that they will receive whatever treatment is
appropriate depending on which circumstances they are facing (Perrin, 1997, p21). Although
medical directives give the patient an opportunity of choosing which treatments to opt for, they
bring various disadvantages that may make patients doubt about its benefits. Pellegrino
mentioned (as cited in Perrin, 1997), medical directives may not be appropriate for patients that
worry about changing their minds if new treatments become available. Since circumstances may
differ from the ones specifically described in the medical directive, it can be difficult to decide how
A durable power of attorney is another kind of advance directive. As Perrin (1997) stated,
a durable power of attorney allows patients to appoint a designated individual to make decisions
for them if they become unable of voicing their desires for end-of-life care. The main advantage
agent who they trust can make decisions for them under different circumstances (Perrin, 1997).
According to Famble, McDonald, and Lichstein (as cited in Inman, 2002), although most elderly
people prefer to name a member of their family as the surrogate decision-maker, this can bring
discussing possible therapeutic options may result in the decision-maker opting for treatments that
the patient would not have approved. It is important to consider that in some instances decision-
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For this paper, I interviewed Scott Cashew, an 82 years old white man who has a durable
power of attorney. He said he decided to get an advance directive after being hospitalized as a
result of a stroke. He mentioned he was influenced by his daughter in making this decision. He
stated “my daughter is the most important person in my life, I don’t want to cause her much
trouble, so I told her I would trust her judgement if anything happens to me.” Scott mentioned he
told his daughter he did not want to be kept alive if there were no possibilities on him regaining
his independence. He openly made his point clear by stating, “why would I want to be kept alive
and dead at the same time? If I can’t live my life the way I’ve always lived it, then I don’t wanna
live.” He expressed his disagreement with prolonging someone’s life by means of life support. As
a Christian, he strongly felt it is not up to men to decide whether someone must remain alive or
not.
Scott completed his durable power of attorney directive while at Kaiser. One of the
nurses approached him with brochures for him to look at. He said he did not even look at them.
It was his daughter who asked the nurse for further details about the process of obtaining an
advanced directive. Scott also mentioned that his physician never took time to explain him he had
different options for end-of-life care decisions. Although he stated he would have preferred the
doctor approaching him to discuss this delicate matter, he was more than happy that the nurse
Scott’s decision on obtaining an advanced directive was strongly influenced by his desire
to not be kept alive if there was no hope for him to recover. His disagreement towards expanding
someone’s life coincides with Gamble, McDonald, and Lichstein research (as cited in Inman,
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2002, p42), as they explained that the majority of older adults that have advanced directives prefer
to limit the medical care they receive if they become terminally ill. Scott is part of this majority of
elders who believe quality of life should be placed before unnecessary life support in terminally ill
patients. He believes the utilization of mechanical devices to prolong the life of individuals in
chronic conditions is an inhumane way to feed hopeless illusions that only harm the patients’
One of the points that appeared to be surprising to Scott was the fact that his physician
never mentioned the possibility of him obtaining an advanced directive. According to Cotton (as
cited in Perrin, 1997, p 22), some physicians prefer not to discuss end-of-life care because of the
effects it could have on the patient (depression, stress, hopelessness). It is unfortunate that some
physicians do not even attempt to approach patients to discuss this matter. Scott mentioned he is
appreciative of nurses who take the time to explain to patients about their different options.
The influence of Scott’s daughter was essential for him to make the decision of obtaining
an advance directive. According to High (as cited in Perrin, 1997, p 23), elderly people tend to
choose family members to make end-of-life care decisions for them. Scott believes his daughter
would be his best option as a designated proxy because of the closeness he has with her. He said
he feels more comfortable knowing that a family member can make decisions for him. The
influence she had on him stemmed from the respect and love he has for her.
In this assignment, I learned that the role of nurses in providing education about advance
directives is essential to ensure our patients’ wishes regarding end-of-life care are heard. As
future nurses we have the important responsibility of advocating for the wellness of our patients.
Advanced directives are a delicate matter that need to be addressed to the patients. As nurses we
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have to ensure patients receive the best treatment possible which includes not only giving drugs or
taking vital signs but mainly providing them with education necessary to have their voices heard
The impact I can have as a future nurse, regarding advanced directives, is that of
educating patients and physicians. Nurses have more power than they think on influencing the
improvement of patient care. Although some people still think nurses work strictly under
physicians’ supervision, it is our duty to break that chain of thought that has undermined nurses’
role over so many years. Physicians and nurses should work together towards optimizing
patients’ care. As nurses, we have the responsibility of educating patients regarding delicate
matters such as this one. The decisions concerning the quality of life or possible death a patient
will experience should be based on the end-of-life care decisions the patient makes on his advance
References
Publishers.
Perrin, K. (1997). Giving voice to the wishes of elders. Journal of Gerontological Nursing,
23(3): 18-27.