Clinical freedom is the right of medical practitioners to decide and do whatever in their opinion was best for their patients. It had been common practice that medical practitioners subject patients to treatment procedures without any evidence of their efficacy, which not only will increase expenditures, but also may put patients to potential harm. Hampton considered clinical freedom as a myth and ‘a cloak of ignorance’, and believed that medical practitioners should base their clinical practice on evidence from randomized controlled trials to guide medical decision making and set aside dogma and biases (1). Using an example from the issue of active management of myocardial infarction, the author highlighted the importance of managing resources effectively on clinical and economic considerations, and suggested that interventions should not only be assessed for their efficacy in increasing likelihood of their desired effect, but also assessed with comparative trials against other alternative treatments. (1). In his conclusion, author felt that the end of clinical freedom is not to be regretted, for its end would allow treatment to be applied only after a properly conducted clinical trial and approved on a large scale after considering available resources and the efficacy of treatment.
This paper raises interesting questions in economics and resource management healthcare
Furthermore, the procedures would also have to be compared with other alternatives in terms of cost.
Katz states, “the conviction that physicians should decide what is best for their patients, and, therefore, that the authority and power to do so should remain bested in them, continued to have deep hold on the practices of the medical profession “(214).
Although there are several debates against this view point, it is not up to anyone else to make decisions of the ill and infirm. As such it should be recognized that “patients have a right to make
The law also allows a physician to deny performing the treatment for personal beliefs. Yet, if the harm is done and the patient is incurable, the doctor can save tremendous pain and suffering of patients. With the multitude of obstacle courses the protocol have set in place, have been thought out and designed to protect the rights of not only the patient but
In the realm of medical ethics, there are many topics that are debated and discussed, but there is not necessarily one clear, correct answer. One of these topics is paternalism. Many questions are bandied back and forth: is it beneficial, should it be disallowed entirely, are there instances when paternalism is good and beneficial, and the list goes on. For each of these questions there have been authors who have provided their comments. One such author is Alan Goldman. He draws a very firm line on paternalism, simply put: medical paternalism is deleterious to a patient because it intrudes on their primary rights of liberty and autonomy. This paper is going to expound upon Goldman’s viewpoint in detail, going through
must be on the patient rather than on an assumption about the nature of the patient’s problem and on arbitrary decisions about actions to be undertaken (Alligood, 2010).
The term “medical ethics” is defined by The American Medical Association as “(1) moral principles or practices and (2) matters of social policy involving issues of morality in the practice of medicine.” The nine principles of medical ethics as outlined by the AMA tell how a physician should conduct themselves in the profession, the third and fourth of which states “(3) A physician shall respect the law and also recognize a responsibility to seek changes in those requirements which are contrary to the best interests of the patient. (4) A physician shall respect the rights of patients, colleagues, and other health professionals, and shall safeguard patient confidences and privacy within the constraints of the
I could not phantom what my family’s life would be like if my mother had agreed to those risky experimental procedures. I’m so thankful she said no each time because if she’d given in, I don’t know if my father would be here today. This experience has lead me to realize some critical disparities within health care. Healthcare should be provided to everyone. The potential cost of health care can deter persons in need of treatment. Whether a general checkup or an emergency room visit, the expenses that arise from either of these visits can result in a financial burden for patients -- especially the ones who do not have much money to begin with. From how I see it, healthcare is a privilege. Money directly affects health care and treatments. This is turn can question informed consent for proposed medical treatments. One major health care disparity is the proper implementation of informed consent from health care professional to patient. This is an issue because money's influence on health care can deter from what should be in the best interest of the
To support my stand, I will use the Principlism approach articulated by Beauchamp and Childress (B&C) in their textbook principles of biomedical ethics (Beauchamp & Childress, 2013). B & C thoroughly develop and advocate for four principles that lie at the core of moral reasoning in health care: respect for autonomy, nonmaleficence, beneficence, and justice. The reason behind selecting this approach is because these Principles derived from the “common morality” and thus, they are universally binding in all healthcare settings everywhere. The principles are binding regardless of the ethical theory one adhere to or believe in, because everybody recognizes the importance and the strength of the common morality. Consequently, the Principlism approach provides a means for proceeding with ethical analysis even when persons disagree in theoretical matters.
In our culture, respect for individual autonomy is valued to the highest degree. We want to do what we want to do, what we think will give us fulfillment and meaning in life. In other words, we value our liberty and the last thing we want is somebody or some circumstance infringing on it.
Two completely different viewpoints of randomized clinical trials are given, article one is against the idea and article two is for it. Article one argues that when a patient sees a physician; the physician has the duty to provide the best treatment for that
A slave society, what could be called the “original sin”. The injustice that had to of been paid to form this new democracy, but even with the new freedom the black society would find this was just the beginning to there quest for their democratic equality. Proving that blacks struggling in a white society could suffer in many more ways than when on a plantation; with not just the physical abuse but mental. What hit them and their youth the most was financials, neglect, and the unrelenting irony of the place they considered home.
In the video “Sick around the world” we see how different countries accommodate their population’s health care needs, through their customized systems. Great Britain’s National Health Service (NHS) developed a very considerate system that offers no copay, or any fees in general. The NHS pays for everything, which is a great feature and is beneficial to the people. A major disadvantage of the NHS is the wait time for elective care. Although the wait time has improved from 16 to 18 months in the past, to currently 6 months, the wait time is still a bad component of Britain’s NHS. As for the second richest country in the world, Japan’s health care system appears to be affordable, due to the fixed prices for every aspect of health care and a one payment system. The downfall is that fifty percent of hospitals are in fiscal deficit, which may add to this wealthy country’s huge economic burden. Similarly, Germany keeps its citizen’s best interest in mind, due to the fact that 90% of
The Joint Commission and Centers for Medicare and Medicaid Service (CMS) have acknowledged, “Physical restraints are considered an infringement of patient rights and a patient safety concern” (Mion, Sandhu, Khan, Ludwick, Claridge, Pile, & ... Winchell, 2010, p. 1279). These organizations have amended and aligned their regulation requirements on the use of restraints which is mainly focused on limiting its use and putting emphasis on staff education and training (Cosper, Morelock & Provine, 2015). The nursing discipline guided by these regulations should aim to improve standards of care and patient outcomes through best nursing practice. “Best practice supports individualized care that permits nursing the person safely and without physical or chemical restraint” (Cotter & Evans, 2010, p.197). The goal of this review is seek evidence to substantiate the implications of such guidelines.
Between a patient’s rights to privacy and autonomy, the safeguards listed in the Bill of Rights, and the duties of a healthcare professional to protect his or her patient’s safety, what takes precedence? Such is the ethical dilemma faced by the nursing staff of Mr. Green, a patient with end-stage aggressive prostate cancer who is planning to choose suicide over suffering. Discussion, the Ethical Dilemma
I chose to look at the above scenario using the Autonomy ethical principle. Autonomy principle says, “you should have the ability to act independently and make decisions for yourself” (Warnock, 2017). Using this approach If a patient has an advanced directive you would follow it because it is the patient’s chose written down in advanced. However, using this principle may violate some social laws or morals. Because, brain dead is the same thing as being dead, the person should be removed from life support (Baillie, McGeehan, Garrett, & Garrett. 2012, p. 260).