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October 27, 2015, The Baltimore Sun Opinion page highlighted a controversial, but thought provoking question: “Why are we using so many health care resources on dying patients?” (Mazzeffi, 2015, p. 1). I was immediately enticed and proceeded to read the piece by Michael Mazzeffi, professor of anesthesiology at the University of Maryland School of Medicine, who knew EXACTLY how to catch readers attention. However, the question posed above cannot be answered in an educated manner without a theoretical backing. Although Michael Mazzeffi does not blatantly refer to social justice theory, his words say it all.
The Beginning: Implementation of the Affordable Care Act As an ICU physician for many years, Michael Mazzeffi has had ample opportunities
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18). Certainly Michael Mazzeffi cannot decide this all on his own. All of the above policy critiques can be analyzed through a Rawlsian lens of distributive justice, which refers to the perceived fairness of one’s outcomes. Traditionally, distributive justice has been utilized in many field to assess how resources are being distributed to individuals. Although Rawls never explicitly mentioned health care in his Theory of Social Justice, it can be interpreted that health care is, indeed, a primary social good to which all, regardless of socioeconomic status, have an unqualified right. Nonetheless, in order to assure this opportunity is open to all and not completely burdensome, a principle designed to equalize the financial costs to illness needs to be created—as Mazzeffi suggests. This principle would recognize that the financial burdens of medical misfortunes should be shared equally by healthy and sick alike (Almgren, 2013). Mirroring what Mazzeffi mentioned about a 30-day patient review pilot program, a more direct example of a real application of distributive justice is seen within this same process of establishing guidelines for patient utilization review. Not surprisingly, many large hospital networks have not quite mastered the art of utilization reviews for many reasons not mentioned here. In spite of all that though, where is the patient voice in this conversation? In considering how to limit the use of end of life health care costs, ethical conduct which respects one’s self-determination to accept or decline treatments for themselves, can lead to a reduction in costs too. Referring back to Mazzeffi once again, assisting individuals to deal with their death fears by offering palliative care options presents a wider range of potentially cost-saving choices (which also value higher quality of life)
In Samuelson and Antony’s book Power and Resistance, renowned sociologist Professor Pat Armstrong tackles the topic of health care reform from a critical feminist perspective. Her analytic critique of the historic tenets of Health Care policy in Canada, effectively points out a systemic disadvantage for the women of our society. Which, in the spirit of transparency, completely blind sighted me as a first time reader because, well, this is Canada. Canada, the internationally renowned first world nation with a reputation for progressive social reform. The same Canada that Americans make fun of for being ‘too soft’. As far as the world is concerned we’re the shining nation-state example of how to do health care right. Needless to say, Professor
Terminally ill patients deserve the right to have a dignified death. These patients should not be forced to suffer and be in agony their lasting days. The terminally ill should have this choice, because it is the only way to end their excruciating pain. These patients don’t have
The Dying of the Light is an article by Dr. Craig Bowron that captures the controversy surrounding the role of medication in prolonging life. The author describes that many medical advancements have become a burden to particularly elderly patients who in most instances are ready to embrace the reality of death. Dr. Bowron believes that dying in these modern times has become a tiring and unnatural process. “Everyone wants to grow old and die in his or her sleep, but the truth is most of us will die in pieces,” Bowron notes (Bowron). The article does not advocate for euthanasia or the management of health care costs due to terminal or chronic illness. Bowron faults humanity for not embracing life and death with dignity as it was in the past. He blames the emergence of modern medical advances and democracy as the sole reason why everyone is pursuing immortality or prolonging of life rather than embracing the natural course of things. The article is very articulate and comes out rather persuasive to its target audience that happens to be health-conscious. Craig Bowron uses effective rhetorical strategies such as logos, ethos, and pathos to pass on his message. The article’s credibility is impeccable due to the author’s authority in health matters as he is a hospital-based internist. A better placed individual to dissect this issue by analyzing his experiences in the healthcare profession. The article incorporates a passionate delivery that appeals to the readers’ hopes, opinions, and imagination.
Primarily, it is important to clarify Daniels’ views on the allocation of health care. As said in Lewis Vaughn’s Bioethics
Braddok III Clarence H. MD MPH .” Physician aid-in-dying: Ethical topics in medicine” n.d University of Washington school of medicinestate death with dignity act” N.p n.d University of Washington department of bioethics and humanities 2009 web 24 March 2012
Tom Harpur, in his 1990 article in the Toronto Star - "Human dignity must figure in decisions to prolong life" - presents numerous arguments in support of his thesis that the use of advanced medical technology to prolong life is often immoral and unethical, and does not take into consideration the wishes of the patient or their human dignity. However, it must be noted that the opening one-third of the article is devoted to a particular "human interest" story which the author uses to illustrate his broader argument, as well as to arouse pity among readers to support his view that human life should not always be prolonged by medical technology. This opening section suggests that a critical analysis of Harpur 's arguments may find widespread use of logical fallacies in support of the article 's thesis. In this essay I will argue that, given how greatly
There is great debate in this country and worldwide over whether or not terminally ill patients who are experiencing great suffering should have the right to choose death. A deep divide amongst the American public exists on the issue. It is extremely important to reach an ethical decision on whether or not terminally ill patients have this right to choose death, since many may be needlessly suffering, if an ethical solution exists.
Do people have the right to die? Is there, in fact, a right to die? Assisted suicide is a controversial topic in the public eye today. Individuals choose their side of the controversy based on a number of variables ranging from their religious views and moral standings to political factors. Several aspects of this issue have been examined in books, TV shows, movies, magazine articles, and other means of bringing the subject to the attention of the public. However, perhaps the best way to look at this issue in the hopes of understanding the motives behind those involved is from the perspective of those concerned: the terminally ill and the disabled.
Gabrielle Saveri. "An ethicist insists patients need help living, not dying." People May 1995. Vol. 43
The just delivery of health care falls into a pattern of rights. Medicaid and the US political view aside, the right to health care is a basic human right whose only requirement is that someone be a human being regardless of their gender, ethnicity, or socioeconomic class. That is, the right is a non-relational right that every human needs irrespective of differences in individual goals (Lomasky, 1981). As a positive right, it is the obligation of others to provide for one’s health needs, within limits. In satisfying the right to health care, society contributes toward the fulfillment of the right for the individual. In Medicaid for example, the right is supported through taxation, among other mechanisms and delivered by a
It is hard to imagine life without health insurance. If you have any type of medical problem that requires attention, and you have appropriate health care insurance, you can be cared for in the finest of private hospitals. You can get great treatment and your ailments, depending on the severity, can be treated as soon as possible. Doctors, physicians and surgeons are willing to put out a big effort if they know that they are dealing with patients who are insured and have the money to go under extensive medical treatment. But imagine life without such luxuries. For example, what happens if a relative requires much needed surgery, but does not have health insurance to cover the procedure? What happens if a lack of medical insurance prevents you or your family from seeing a doctor, which could result in health problems that had not been identified but could have been treated before they became life threatening? These scenarios may seem far-fetched, but these types of situations happen to people who lack health coverage everyday. There is a true story about a patient who was insured and diagnosed with treatable cervical cancer. Unfortunately, she lost her job and with it her insurance. She was then unable to see her private doctor, and was turned away from other hospitals because ?cancer treatment is not considered an emergency in a patient who can?t pay? (?Help for D.C.?s Uninsured?). The woman later died at her home without ever being treated. This example raises the question, since when are people with less money less deserving of health care or appropriate treatment?
In the past centuries, health care was the responsibility of individuals and their own families but today Medicine comes to be an institution only as societies are more productive and people take on specialized work. At the same time as people become dependent on governments and organizations to provide them their health care and insurance, here is the problem. Social conflict analysis points out the connection between health and social inequality. Following the ideas of Karl Marx, we can match health to the operation of capitalism. Most attention has gone to three main issues: access to medical care, the effects of the profit motive, and the politics of medicine.
Today, medical interventions have made it possible to save or prolong lives, but should the process of dying be left to nature? (Brogden, 2001). Phrases such as, “killing is always considered murder,” and “while life is present, so is hope” are not enough to contract with the present medical knowledge in the Canadian health care system, which is proficient of giving injured patients a chance to live, which in the past would not have been possible (Brogden, 2001). According to Brogden, a number of economic and ethical questions arise concerning the increasing elderly population. This is the reason why the Canadian society ought to endeavor to come to a decision on what is right and ethical when it comes to facing death. Uhlmann (1998) mentions that individuals’ attitudes towards euthanasia differ. From a utilitarianism point of view – holding that an action is judged as good or bad in relation to the consequence, outcome, or end result that is derived from it, and people choosing actions that will, in a given circumstance, increase the overall good (Lum, 2010) - euthanasia could become a means of health care cost containment, and also, with specific safeguards and in certain circumstances the taking of a human life is merciful and that all of us are entitled to end our lives when we see fit.
Resources have always been inadequate for food, economics and healthcare and all scarce resources are rationed in one way or another. Healthcare resources can be in the forms of medicine, machinery, expensive treatment and organ transplantation. For decades, allocation of healthcare resources in an equitable manner has always been the subject of debate, concern and analysis, yet the issue has persistently resisted resolution. Scarcity of resources for healthcare and issue of allocation is permanent and inescapable (Harris, “Deciding between Patients”). Scarcity can be defined in general, in emergency and in crises as well as shortage of certain kind of treatment, medicine or organs. As a result of scarcity of resources, and some people may be left untreated or die when certain patients are prioritized and intention of is that everyone will ultimately be treated (Harris, 2009: 335). Allocation of limited resources is an ethical issue since it is vital to address the question of justice and making fair decisions. Ethical judgments and concerns are part of daily choice in allocation of health resources and also to ensure these resources are allocated in a fair and just way. This paper will explore how QALYs, ageism and responsibility in particular influence the allocation of healthcare resources in general through the lens of justice, equity, social worth, fairness, and deservingness.
There is not the same focus on compassion and emotions that would be found with the ethics of care. The authors conclude that the ethics of justice contain three concepts; “principles, purpose, and results” (p.126). Rawls (2009) agrees and adds that the major components of justice theory are equity, objectivity, and neutrality. The idea that justice should be fair to all those involved, which creates a system where there should be consistent ethical decisions appears to be a guiding concept of justice. Rawls (2009) would contend that through the theory of justice that there is a social contract. The theory values people as free, rational, and autonomous. The focus on the ethics of justice is on rights, laws, fairness, and equity. The terms of the contract would agree in principle that each person would act according to their own personal