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Euthanasia legal and ethical issues
Euthanasia and ethics
Euthanasia and ethics
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The Living Will: Who has the Power in End-of-Life Cases? A living will is a type of advanced health care directive, which states an individual’s wishes for health care treatment when he/she is terminally ill. Living wills are often applied to end-of-life decision making when patients are no longer deemed competent to direct care for themselves. The form of living wills can vary widely. But, most address whether or not to use life-prolong medical treatment such as CPR, respirators, and artificial nutrition and hydration. These documents can also contain information about the importance of quality of life for patients and can name a healthcare proxy to make medical decisions in their place. Having a living will allows individuals to state their …show more content…
The family meeting started off rocky due to the son’s initial anger towards the hospital, due to a rule for visiting hours, which were different from the previous hospital. In the meeting, the son presented his mother’s living will, which was completed seven years prior. She created the living will after her experience as a hospice volunteer where she had participated in many cases of end-of-life care. Her notarized living will was fairly detailed, with information on the treatments that she was willing to receive as well as her beliefs on what she considered a good quality of life. The living will named her son, who at the time lived in another state across the country, as the primary proxy and her daughter-in-law, who was present when the living will was created/notarized, as a secondary proxy. When the living will was discussed in the family meeting, the son who presented it had very little information initially on what it contained. When the differences between the son’s suggested care plan and the information listed in the living will was pointed out by the attending, the son justified his version by the fact that she wrote the will seven years ago, and his mother’s views have shifted since …show more content…
This case comes down to: Does the written living will or the proxy named in the living will have the louder voice in end-of-life care discussions? In this case, the voice of the proxy won. In the best cases, such decisions should be made together at the time of the creation of the living will with both the patient and the proxy. If this occurred, the son would be more on the same page with the concerns for his mother’s end of life care. Another way of solving the issue of the possibility of the woman’s life changing over the past seven years, would be having a way for the woman to acknowledge that thoughts are still the same by updating/resigning the living will
Once I explained exactly what a living will is because some were unaware they were very comfortable with the idea of filling out a living will. The responses that I got all varied to different degrees. My brother stated that he did not yet have a living will but that they are very important to have and everyone should get one. He said that his wishes would be to pretty much “pull the plug in every circumstance”. He absolutely did not want to be put on life support, be artificially supplied with food, or get life sustaining drugs, machines, or other medical procedures. My mother had wishes the same as I would have which is to consider the circumstances and give me a month to evaluate if I have the possibility of making a full recovery. If there is no hope of having a full recovery then I want all life sustaining measures to be stopped because I don’t in any way want to be a burden on
When making decisions regarding treatment of another person, it is important to respect the expressed wishes of the individual. John says that his mother would want to live as long as she could, but questions arise related to her quality of life and perception of prolonged suffering by prolonging the dying process. The book states that quality of life changes throughout one’s life and experiences.
As we get older and delve into the real world, it is important to start thinking about end-of-life care and advance directives. Although it is something no one wants to imagine, there is an absolute necessity for living wills and a power of attorney. Learning about the Patient Self-Determination Act and the different legal basis in where you live is important because it will help people understand why advance care directives are so important. Although there are several barriers in implementing advance care directives, there are also several actions that healthcare professionals can take to overcome these obstacles. These are also important to know about, especially for someone going into the medical field.
The end of life is inevitable. For most it is for seen and understood what ones final wishes are. Living wills provide those issues in question with answers. What if an individual does not have a living will? Who would be in charge in making final decisions for someone who cannot physically make those decisions? The story of Terri Schiavo brings about many questions that represents moral, ethical, and legal issues.
One of the greatest dangers facing chronic and terminally ill patients is the grey area regarding PAS. In the Netherlands, there are strict criteria for the practice of PAS. Despite such stringencies, the Council on Ethical and Judicial Affairs (1992) found 28% of the PAS cases in the Netherlands did not meet the criteria. The evidence suggests some of the patient’s lives may have ended prematurely or involuntarily. This problem can be addressed via advance directives. These directives would be written by competent individuals explaining their decision to be aided in dying when they are no longer capable of making medical decisions. These interpretations are largely defined by ones morals, understanding of ethics, individual attitudes, religious and cultural values.
The right-to-die is defined as expressing or advocating for the right to refuse extraordinary measures intended to prolong someone’s life when they are terminally ill or comatose. Generally people who use right-to-die laws do not do it because of the pain or financial reasons, but because they are worried about becoming a burden, or losing their autonomy. If a person exercises their right-to-die they already have their wills or property sorted out, but if that is not the case there are many places to help people sort out their wishes as well as property. “Medical professionals often encourage people to make a living will or advanced directives which is a document that lets individuals state their wishes for end of life care, in the case they become unable to communicate their decisions.”(Mayo Clinic, 2015). Living wills are more prominent now than they were before; with all the medical advances now people can live for years, even though they might not have wanted to, because the doctor was unaware of the patient 's wishes. In the past, when life threatening symptoms from accidents or
“Clearly the preservation of life is an important goal of the human community in general and of the profession of medicine in particular. Intuitively we know life is valuable and sacred; for were it not, then nothing else would be” (Shannon, 2011, 633). Living wills give patients control over their own bodies even when they are in a state of unconscious vegetate. It gives them the comfort of knowing that their wishes will be granted when they are not in a coherent state. The patient’s family does not have the right to override their living will. That should be a good reason to create a living will, reducing the weight on the patient’s family, because in the end, only the patient’s living will, will prevail.
While navigating the abundant and sometimes confusing legal language of advance directives can be time consuming, it would benefit every person to consider their end of life wishes and have some form of written statement available for their doctor and family to understand those wishes. Doing this in advance can prevent emotional anguish, suffering and expensive litigation. In the end, clearly and when possible, written, documentation of a medical directive, a living will, or a chosen health care power of attorney will lessen the burden for the medical professionals and family of a dying or incapacitated person.
It also illustrated that the end of life decision is highly impacted by personal characteristics such as age, ethnicity, gender, economic status, and disability. Therefore, the end of life decision making in the cases presented will be different depending upon the patient values and preferences. The ethical principle of autonomy will always take preference and the patient will be the one who will make decision on continuing with their treatment or choose end of life care such as palliative or hospice care. However, autonomy may be lost when a person has diminished decision-making ability. Fry et al. (2011) mentioned
living will is a document prepared and sighed in advance of illness, in which a
In an effort to provide the standard of care for such a patient the treating physicians placed Ms. Quinlan on mechanical ventilation preserving her basic life function. Ms. Quinlan’s condition persisted in a vegetative state for an extended period of time creating the ethical dilemma of quality of life, the right to choose, the right to privacy, and the end of life decision. The Quilan family believed they had their daughter’s best interests and her own personal wishes with regard to end of life treatment. The case became complicated with regard to Karen’s long-term care from the perspective of the attending physicians, the medical community, the legal community local/state/federal case law and the catholic hospital tenants. The attending physicians believed their obligation was to preserve life but feared legal action both criminal and malpractice if they instituted end of life procedures. There was prior case law to provide guidance for legal resolution of this case. The catholic hospital in New Jersey, St. Clare’s, and Vatican stated this was going down a slippery slope to legalization of euthanasia. The case continued for 11 years and 2 months with gaining national attention. The resolution was obtained following Karen’s father being granted guardianship and ultimately made decisions on Karen’s behalf regarding future medical
On April 15, 1975, the Quinlan family received a tragic phone call at approximately 2am; their daughter, Karen Ann, was in a coma. Earlier that evening, Quinlan was at a party and consumed drugs and alcohol. She became unconscious and eventually fell into an irreversible coma. She was conditioned to be in a persistent vegetative state. Since she was unable to recover from her coma, Quinlan’s parents requested her life support to be withheld. The removal of life support was more complicated than what the Quinlan family imagined it to be. They had to take the case to court to have the request approved. The first round in Superior court, the Quinlans lost. Eventually, the family took the case to the New Jersey Supreme Court. The court ruled that Quinlan’s father is appointed as her guardian and can make any decision regarding her care. It took the family over a year to have the approval to remove their daughter from life support; it took five days for Karen Ann Quinlan to be weaned off her respirator. Miraculously, she was able to breathe on her own for the next nine years until she died of pneumonia. This case led to the creation of the “living will” and required medical institutions to allow patients to live their last stage in life with dignity and respect (Karen Ann Quinlan Hospice
In BJ Millers TedTalk, “What Really Matters at the End of Life?” BJ Miller discusses on how we think on death and honor life. He speaks to the audience about how for the most people the scariest thing about death is not death itself, it is actually dying or suffering. The targeted audience is everyone in the world, because eventually everyone is going to die and everyone thinks about death. BJ 3 has big points in the article saying, Distinction between necessary and unnecessary suffering. Also by having a little ritual that helps with this shift in perspective. Another point is to lift and set our sights on well-being. We need to lift our sights, to set our sights on well-being, so that life and health and healthcare can become about making life more wonderful, rather than just less horrible.
We often ask, “What is the right thing to do?” when it comes to decision-making whether deciding for another or for one’s self. When making the decision for another we must apply our own moral and spiritual beliefs and life experiences to arrive at a decision we feel to be correct. Further more, we must try to understand his or her beliefs and consider of what the dying person may have wanted as a wish or will. The decision-making involving life and death is probably the most difficult task for any of us. Often physician required participating in decision-making regarding his/her patient. [1] In terminally ill patients case, the role of physicians is to facilitate an open discussion about the patient’s treatment plan, preferred medical care
terminally ill person at their will or if the patient is incapable of making the