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The importance of patients rights
Hippocratic oath epthics paper
Individual informed consent
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Conventional wisdom use to hold that the “doctor knows what is best for the patient”, leading to a paternalistic and unbalanced relationship between most physicians and patients. This idea of medical paternalism stems from the Hippocratic oath which states that “ [a physician] will apply dietetic measures for the benefit of the sick according to [his or her] ability and judgment”. The Hippocratic oath as historically said by all physicians and medical students is based on a foundation of beneficence yet the oath does not emphasize the personal autonomy of the patient. The oath focuses on the characteristics of a doctor and his or her duties, yet does not mention the role of doctors in respecting the patients wishes. This principle of paternalism …show more content…
There are two essential components that compose the legal right of patient autonomy. The first component involves the patient having the capacity and ability to make a willful decision. The second component involves the autonomous decision itself which relies on independent informed decision making process. The first components is well illustrated by Justice Benjamin Cardozo in the 1914 court case of Scloendorff v. Society of New York Hospital where he stated that “every human being of adult years and sound mind has a right to determine what shall be done with his own body...”. The second component is better illustrated through the process of informed consent as the person who is autonomous may find him or herself constrained from acting freely due to the fact that the physician or hospital didn’t ensure that the patient had adequate comprehension of the information provided. The autonomous decision involves the process, context and content involved in the decision between the health professional and the patient. Informed consent is a shared decision made in an …show more content…
courts repeatedly affirmed the right of autonomous individuals to refuse medical intervention even if refusal would lead to his or her own death. Many doctors, moral philosophers and patient family members disagreed with the notion of autonomy ultimately leading to death. This controversy is best exemplified by the 1986 court case of Elizabeth Bouvia v. Superior Court. Elizabeth Bouvia was a mentally competent quadriplegic who suffered from cerebral palsy causing her to be bedridden and dependent on others. Elizabeth was unable to support herself so she had to rely on public assistance for medical care. In 1983, Elizabeth Bouvia expressed a desire to end her life through self-starvation at a Los Angeles County hospital. The physicians monitoring Elizabeth at the hospital had determined that she was not eating enough and her weight loss was a life-threatening condition. The staff and physicians at High Desert Hospital in Los Angeles County, California, inserted a nasogastric feeding tube into Elizabeth against her wishes in order to ensure proper nutrition. The staff at the hospital justified their actions through the state’s interest in persevering life as her prognosis indicated that she could survive an additional 15 years with adequate nutrition. Elizabeth sued the hospital and it’s staff while seeking an injunction for the removal of the tube. The trail court denied her request and justified the action’s of the hospital staff in preserving
Autonomy is a concept found in moral, political, and bioethical reasoning. Inside these connections, it is the limit of a sound individual to make an educated, unpressured decision. Patient autonomy can conflict with clinician autonomy and, in such a clash of values, it is not obvious which should prevail. (Lantos, Matlock & Wendler, 2011). In order to gain informed consent, a patient
According to Terrence F. Ackerman, as of the 1980s the American Medical Association had to include the respect for a person’s autonomy as a principle of medical ethics (Ackerman 14, 1982). This includes having the physician provide all the medical information to the patient even if the information could cause negative implication onto the patient. The physician is also expected to withhold all information of the patient from 3rd parties (Ackerman 14, 1982). Although it is seen as standard in today’s world, in
Even though Barbara’s intentions in this paper are directly stated, her claims she gives does not back her argument at all. After reading her major claim, which states that we do not have the right to die (97), I feel the complete opposite of what she thinks and I believe a person should have the right to die if there is no chance of them getting better in the future. The author’s grounds explained all of the struggles of keeping a very sick man alive, which I believe gave me some very good evidence to write my counter argument.
Patient autonomy was the predominant concern during the time of publication of both Ezekiel and Linda Emanuel, and Edmund D. Pellegrino and David C. Thomasma's texts. During that time, the paternalistic model, in which a doctor uses their skills to understand the disease and choose a best course of action for the patient to take, had been replaced by the informative model, one which centered around patient autonomy. The latter model featured a relationship where the control over medical decisions was solely given to the patient and the doctor was reduced to a technical expert. Pellegrino and Thomasma and the Emanuel’s found that the shift from one extreme, the paternalistic model, to the other, the informative model, did not adequately move towards an ideal model. The problem with the informative model, according to the Emanuel’s, is that the autonomy described is simple, which means the model “presupposes that p...
Within public health, the issue of paternalism has become a controversial topic. Questions about the ethics of public health are being asked. The role of ethics in medical practice is now receiving close scrutiny, so it is timely that ethical concepts, such as autonomy and paternalism, be re-examined in their applied context (Med J Aust. 1994). Clinically, patients are treated on a one on one basis, but public health’s obligation is toward the protection and promotion of an entire population’s health. So, based on this difference, the gaping questions targeting public health now becomes, under what conditions is it right to intervene and override an individuals’ autonomy? And if so, is the paternalistic intervention justified? Part of the concern
Because the Missouri Supreme Court ruled against the removal of Nancy Cruzan’s artificial hydration and nutrition on the grounds that “clear and convincing” evidence of Nancy’s wishes was not provided, the Cruzan family appealed the decision to the United States Supreme Court arguing that Nancy was being deprived of her right to refuse medical treatment. The Supreme Court ruling affirmed that competent patients have the right to refuse unwanted medical treatment, but also noted that incompetent patients are not capable of exercising this right. Consequently, states may establish their own safe-guards to govern cases in which a substituted decision maker wishes to refuse treatment for an incompetent patient. This ruling therefore upheld the decision of Missouri’s Supreme Court.
Alan Goldman argues that medical paternalism is unjustified except in very rare cases. He states that disregarding patient autonomy, forcing patients to undergo procedures, and withholding important information regarding diagnoses and medical procedures is morally wrong. Goldman argues that it is more important to allow patients to have the ability to make autonomous decisions with their health and what treatment options if any they want to pursue. He argues that medical professionals must respect patient autonomy regardless of the results that may or may not be beneficial to a patient’s health. I will both offer an objection and support Goldman’s argument. I will
This provides people with control over their health care when they cannot speak for themselves. In other words, a health care directive is a legal document recognized by a legislative body to promote autonomy (The Health Care Directives Act, 1992). Autonomy is described as the quality to function independently (Mosby, 2013). Autonomy is the fundamental concept of health care directives, it allows people to openly express their personal values and beliefs, without judgement of health care decisions, “…autonomous decisions as those made intentionally and with substantial understanding and freedom from controlling influences” (Entwistle, Carter, Cribb, & McCaffery, 2010). When all information is provided, the individual can make an informed decision about their health care and have a right to no influencing factors. The health care directive document provide people the opportunity to consent to or refuse treatment and who will have the authority to make decisions on the individual’s behalf if unconscious, or mental incapacity arise (The Health Care Directives Act, 1992). In order to fully practice autonomy, especially in regards to health care directives, the appropriate mental development is key to comprehending
Informed consent is the basis for all legal and moral aspects of a patient’s autonomy. Implied consent is when you and your physician interact in which the consent is assumed, such as in a physical exam by your doctor. Written consent is a more extensive form in which it mostly applies when there is testing or experiments involved over a period of time. The long process is making sure the patient properly understands the risk and benefits that could possible happen during and after the treatment. As a physician, he must respect the patient’s autonomy. For a patient to be an autonomous agent, he must have legitimate moral values. The patient has all the rights to his medical health and conditions that arise. When considering informed consent, the patient must be aware and should be able to give a voluntary consent for the treatment and testing without being coerced, even if coercion is very little. Being coerced into giving consent is not voluntary because others people’s opinions account for part of his decision. Prisoners and the poor population are two areas where coercion is found the most when giving consent. Terminally ill patients also give consent in hope of recovering from their illness. Although the possibilities are slim of having a successful recovery, they proceed with the research with the expectation of having a positive outcome. As stated by Raab, “informed consent process flows naturally from the ‘partnership’ between physician and patient” (Raab). Despite the fact that informed consent is supposed to educate the patients, it is now more of an avoidance of liability for physicians (Raab). Although the physician provides adequate information to his patient, how can he ensure that his patient properly ...
In this paper I am going to justify that the interdisciplinary team should support Ms. R’s decision to live at home alone using the ethical principles of autonomy and beneficence.
Will, J. F. (2011). A brief historical and theoretical perspective on patient autonomy and medical decision making: Part ii: The autonomy model. American College of Chest Physicians 139(6), 1491-1497.
Autonomy is identified as another professional value and one that the nurse must possess. Autonomy is the right to self-determination. Nurse’s respect the patient’s right to make a decision regarding their healthcare. Practical application includes, educating patients and their families on their choices, honoring their right to make their own decision and stay in control of their health, developing care plans in collaboration with the patient (Taylor, C. Lillis, C. LeMone, P. Lynn, P,
This is a fascinating case because it presents the distinction between a patient’s right to refuse treatment and a physician’s assistance with suicide. Legally, Diane possessed the right to refuse treatment, but she would have faced a debilitating, painful death, so the issue of treatment would be a moot point. It would be moot in the sense that Diane seemed to refuse treatment because the odds were low, even if she survived she would spend significant periods of time in the hospital and in pain, and if she didn’t survive she would spend her last days in the hospital. If Diane were to merely refuse treatment and nothing else (as the law prescribes) than she would not have been able to avoid the death which she so dearly wanted to avoid.
The analysis of this case aims to identify the patients and paramedics human and legal rights as well as explore and identify the ethical conflicts of the the case by applying the framework based on Kerridge et al., (2013). The ethical dilemmas within this particular was the patient’s refusal of treatment, despite the fact that she may die without undergoing treatment. Also, the ethical dilemma of the paramedics, to treat or not to treat and risk facilitated suicide. A suicide in this situation implies a breach of duty. This could include overlooking the risk, and/or not effectively using resources that may have mitigated the risk.
As stated in Beauchamp’s article, the autonomy of individuals expressed through informed consent is a fundamental value within this approach. In the case of Mrs. Francois, the surgeon is put in a difficult situation whereby the patient is in a life-threatening position and refuses treatment. If the surgeon takes on a paternalistic approach to treating this patient who appears to be coherent, the surgeon will be disregarding their patients