The ethical controversies between patients and families and health care providers, regarding advanced directives dilemma of research and conflict with providers of care towards end of life choices, or accidental injuries leading to comatose state with patients who had never made or signed their advance directives, deciding on how they preferred to be cared for when those times came. This complex issue has in the past to present resulted in countless lawsuits, against healthcare providers by families who believed that no matter the state, meaning whether comatose, or in situations where a loved one had no choice in deciding for them, families have always assumed they automatically gain the power of attorney in any given circumstance of end of life. The account of most of these cases according to research from the articles I have read personally and the one used for this case study on advanced directives ethical dilemma, in healthcare relates the problem to inadequate family teaching by health care providers in educating loved ones, on the proper understanding of advance directives without compromising patients’ privacy as well as confidentiality, we, as healthcare providers are held accountable for. Historically, education about end-of-life issues and medical needs have been lacking.
There are different advanced directives that are either legal in manner or is recognized otherwise as a personal decision by the patient. A federal law, called the self-determination act, involves healthcare providers to a mandatory discussion on information regarding the different interventions in advanced directives. A patient 's "personal wish" is further evaluated legally so that the information is discussed...
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...th G-tube feeding, as well as other necessary medical equipment to sustain their lives. Since it is a paper on ethics, I believe that without any personal bias, my perspective in these patients, all I have seen is suffering, infections, frequent fliers in and out of hospitals until the day they die. No one deserves to end a life in agony. Even though they call that palliative care, we cannot fail to see the sufferings of these patients, to a point that we become insensitive in a sense that we forget that they might be or may happen in our loved ones. The question remains as what we could do? What will I do? Hence, what needs to be done more in these situations can be further studied by the federal government and public to educate families, provides literature and explain to families whether they would prefer that kind of misery as if it were them in that situation.
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