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The Ethics of Placebos
Placebos, whether we know it or not, are being used and prescribed to us throughout our lives. However, there are some questions that are tied to the use and suggestion to use placebos. The major question is, is it ethical to be prescribed a placebo while still maintaining our autonomy as a patient? This topic has been a subject of debate for over a century, however, little scientific data has been found to prefer the use of placebos over nonuse. The author will attempt to come to a conclusion of this debate, one that respects and acknowledges the ethics of the health care field and the patient. Before doing so, the author will provide information on what a placebo is, scientific comparisons to real drugs, pay consideration
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to the patient’s autonomy, consider the health care provider’s role, and argue both for and against the use of placebos. What is a Placebo? “A placebo is a substance provided to a patient that the physician believes has no specific pharmacological effect upon the condition being treated” (Barnhill 2012, p.
30). These inactive substances are administered by a health care professional as if it were any other active medication. The purpose of a placebo fluctuates depending on the situation given. However, for the most part, placebos are given in order to achieve a desired treatment in which a pharmacological agent could have reached the same outcome. This is done, usually, without the patient knowing that the ‘medication’ has no actual pharmacological properties. Asai and Kadooka (2012), further break down the definition of a placebo into two categories. There is a pure placebo and an impure placebo. A pure placebo is made of substances with no known clinical use. An impure placebo is composed of substances that are not made to treat that patient’s condition, but another condition. Barnhill (2012), adds one more type of placebo to the list. Joining sugar pills and active drugs that are effective for a different disease, are active drugs that are administered at too low of a dose to be effective. All of these can be considered placebos and are occasionally given without the patient’s …show more content…
knowledge. Placebo Results in Comparison to Real Drugs Being given a medication that has no actual purpose would make anybody question its widespread use.
However, as research goes on, there seems to be instances of placebos resulting in desired outcomes. “About one-third of patients have experiences some degree of improvement in conditions such as pain, angina pectoris, cough, anxiety, depression, hypertension, headeache, seasickness, and the common cold with placebos” (Asai & Kadooka 2012, p. 188). Rawlins (2015), discusses another instance in which patients who knew they were taking placebos had relief of irritable bowel syndrome symptoms. Not only are these placebos reaching a desired result, they are doing so without the risks of medication side effects and interactions. Cohen and Shapiro (2013) even consider placebo use as the gold standard of treatment. “The placebo effect, is this defines as an improvement in a patient’s condition resulting from the symbolic aspects of the encounter with a healer o a healing setting, rather than the pharmacologic or physiologic actions of the intervention” (Asai & Kadooka 2012, p.
187). Right to Autonomy If there is one thing that a health care professional must honor and respect in a patient, it is their right to autonomy. Patients have the right to steer their treatment in whichever direction they desire, as long as they are provided with the necessary information to do so. Being prescribed a placebo is thought to take away from that right. Patient’s rely on their health care providers to do what they think is best for them and this establishes a trust. When a physician prescribes a placebo, it is thought to break that trust between them. For example, if a patient develops a trusting relationship with their provider and they discover that they have been given a placebo as treatment, they may feel angry or betrayed. The trust that they had with their physician (and possibly all physicians) is gone and instead they may develop worse or even new symptoms due to stress. However, many do not see it this way. “…most considered placebo use acceptable under certain conditions, such as prior positive results, informing patients of placebo use, or if research evidence indicated that the placebo was effective” (Asai & Kadooka 2012, p. 187). While placebo use seems controversial in that it deceives the patient, it is the bigger picture that matters most. Cohen and Shapiro (2013), give an example to better help relate placebos to an everyday topic. They compare the lie associated with giving a placebo to that which you would lie to a spouse about throwing them a surprise party. “The moral affirmation is in the spouse’s loving gratitude when the lie unravels” (Cohen & Shapiro 2013, p. 701). Beneficence versus autonomy is discussed by Asai and Kadooka (2012). The lie that comes along with giving a placebo may be overlooked when the intent was to help the patient’s condition improve.
In Marcia Angell’s article, “The Ethics of Clinical Research in the Third World,” she strongly argues the use of clinical placebo-controlled trials done in developing countries are unethical if an effective treatment already exists. Angell believes studies that compare potential new treatment with a placebo controlled group is ineffective and unnecessary. All research studies should offer the best standard of care and give participants the most beneficial outcome and treatment possible. The main priority of a study is not the goals of the research itself, but the well-being of the participants. Angell uses many sources to defend her argument, such as WHO.
I begin in section 2 by discussing Grünbaum's detailed analysis of what a placebo is. I then use his idea of a generic intentional Placebo and discuss one of many similar experiments concerning the phenomenon of clinical depression, experiments that use the monoamine hypothesis and the notion of a generic intentional placebo. This experiment is described in section 3. In section 4 I analyze the results of this study and in section 5 I offer concluding remarks.
Ernst, E., & Resch, K. L. (1995). Concept of true and perceived placebo effects. British Medical
The first article is entitled “of mice but not men: problems of randomized clinical trials,” is written by Samuel Hellman and Deborah S. Hellman discusses the issues of randomized medical testing and experiments on patients. The article describes the role of the personal physician and how the physician can take an ethical or unethical path of treating his/her patients. The relationship between the patient and physician is greatly emphasized because according to the article trust is very valuable in medicine especially when a patient’s life is at risk. A Kantian and a Utilitarian view of randomized clinical trials are debated but the authors clearly steers towards a Kantian point of view.
The placebo effect has been one of the most interesting but irritating topics within biomedical science for over the past 60 years. Through this speech I wish to inform and educate while I discuss the placebo effect and cover what it is, how it works and why that is.
A divergent set of issues and opinions involving medical care for the very seriously ill patient have dogged the bioethics community for decades. While sophisticated medical technology has allowed people to live longer, it has also caused protracted death, most often to the severe detriment of individuals and their families. Ira Byock, director of palliative medicine at Dartmouth-Hitchcock Medical Center, believes too many Americans are “dying badly.” In discussing this issue, he stated, “Families cannot imagine there could be anything worse than their loved one dying, but in fact, there are things worse.” “It’s having someone you love…suffering, dying connected to machines” (CBS News, 2014). In the not distant past, the knowledge, skills, and technology were simply not available to cure, much less prolong the deaths of gravely ill people. In addition to the ethical and moral dilemmas this presents, the costs of intensive treatment often do not realize appreciable benefits. However, cost alone should not determine when care becomes “futile” as this veers medicine into an even more dangerous ethical quagmire. While preserving life with the best possible care is always good medicine, the suffering and protracted deaths caused from the continued use of futile measures benefits no one. For this reason, the determination of futility should be a joint decision between the physician, the patient, and his or her surrogate.
...rs; Roy just thought they were. The thing is, it helped Roy; the severity of his disorders lessened even though the medication was not affecting him. When you take something that you think should help, but it really doesn't, and its just your brain thinking you feel better because you should, then its a placebo.
Physician-assisted suicide refers to the physician acting indirectly in the death of the patient -- providing the means for death. The ethics of PAS is a continually debated topic. The range of arguments in support and opposition of PAS are vast. Justice, compassion, the moral irrelevance of the difference between killing and letting die, individual liberty are many arguments for PAS. The distinction between killing and letting die, sanctity of life, "do no harm" principle of medicine, and the potential for abuse are some of the arguments in favor of making PAS illegal. However, self-determination, and ultimately respect for autonomy are relied on heavily as principle arguments in the PAS issue.
An ethical dilemma that is currently happening in the medical field regards pain management. Doctors as well as other medical professionals are faced with this ethical decision on whether to prescribe strong pain medication to patients who claim to be experiencing pain, or to not in skepticism that the patient is lying to get opioids and other strong medications. “Opioids are drugs that act on the nervous system to relieve pain. Continued use in addition to abuse can lead to physical dependence and withdrawal symptoms,” (Drug Free World Online). Opioids are often prescribed to patients experiencing excruciating pain, but doctors are faced with prescribing these drugs as an ethical issue because only a patient can measure the
In this diverse society we are confronted everyday with so many ethical choices in provision of healthcare for individuals. It becomes very difficult to find a guideline that would include a border perspective which might include individual’s beliefs and preference across the world. Due to these controversies, the four principles in biomedical ethic which includes autonomy, beneficence, non-maleficence and justice help us understand and explain which medical practices are ethical and acceptable. These principles are not only used to protect the rights of a patient but also the physician from being violated.
Placebos are a form of treatment that is typically prescribed by medical professionals to benefit an individual’s psychological or physiological state. The placebo is a sugar-based pill that has no active ingredient, also known as a dummy pill. A Professor named Marcello Costa stated that “the substance may have a therapeutic effect on a person when in a doctor’s office or a professional in the medical field”. Placebos are also used as a control variable when testing new medicine in clinical trials. This is to help scientists evaluate whether the new drug produced is safe for a person to consume whilst ensuring it will work effectively and efficiently. A placebo is given to a person
Today, most people who travel to a doctor 's office don 't give any idea to the type of doctor that they 're starting to find out. The traditionally trained physicians in the globe. Are trained in one way, whereas holistic doctors, also known as natural medicine practitioners, are trained in a completely different way. Many of us believe our doctors implicitly, and then when we prescribe a pharmaceutical, we merely fill the prescription and get hold of it as we are ordered. In truth is you can 't assume that your doctor always gets it right. It is very common for doctors to misdiagnose patients and prescribe them medications that they don 't need. This essay will discuss why should use the Alternative medicine.
Introduction Clinical trials are a gateway to proven practical medical treatment, so it requires accuracy and validity of the outcomes. Placebo control trials are therefore employed in clinical trials as nearly half of academic physicians have answered in a questionnaire that they had used a placebo in their clinical trials (Sherman and Hickner, 2007). To have the higher scientific validity of results on the clinical trials requires that prospective, carefully selected subjects and endpoints, a control group, randomly allocated subjects into a treatment group and a control group, blinded both subject groups and investigators, sufficient sample size, and an approved independent ethics committee and monitoring by data safety and monitoring board to have stronger the scientific validity on the clinical trials (Brody, 1997). The use of placebos will enable more scientifically reliable outcomes. However, unnecessarily or ineffectiveness of placebo use is also claimed, therefore considering appropriate conditions and suitable cases would be needed for placebo use. .
The study of Shang et al compared placebo-controlled trails of homeopathy and allopathy (2). The study consisted of a literature search for placebo-controlled homeopathic trials in a wide variety of databases. The authors found 110 eligible placebo controlled trials of homeopathy that they could use in this study. Furthermore, the Cochrane Controlled Trials Register was used to identify placebo-controlled trials of conventional medicine. These conventional medicine trails were matched with the homeopathic trials for comparison. These pairs of trials were categorised by clinical topic.
Studies have shown that about 75% of alternative remedies are not backed up by any scientific research. Most remedies or therapies are backed up by biased research instead of actual studies.