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Essay on medical confidentiality
Confidentiality ethical dilemmas health care
Ethical dilemmas confidentiality in health care
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Often times when a patient has a health problem or concern, the health care professional will inform them of the potential diagnosis, circumstances, and treatments. However, this can become a predicament when that patient is terminally ill, for example, with cancer, and the health care professionals face the dilemma of telling the patient of their outcome. There is no easy way to go about this. Still, health professionals have the responsibility of telling patients if they are terminally ill –should they choose to know – because otherwise it can weaken the trust between the patient and their health care providers, take away from patient autonomy, and prevent proper closure for the patient that he or she may want.
A patient should be told
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All capable patients have the right “to make informed decisions about their own medical care” (Lowry). Withholding this information from a patient can limit informed consent, a fundamental ethical principle of health care (Lowry). Informed consent from a patient is necessary before a health care provider can provide treatment, and when a health care provider goes ahead and makes decisions for a patient because they want to prevent the patient from finding out they are terminally ill, this becomes an ethical and legal issue. As a result, patient autonomy is diminished here. Moreover, this may keep the patient questioning about what is going to happen to them and what options they have for their treatment. With a terminal diagnosis, there may still be treatments or medications that could be taken to lessen the severity of their condition for a less painful or more comfortable death. As the saying goes, "you don’t know what you don’t know.” Since the patient may not be fully aware of their diagnosis in the case that their health care provider does not disclose this information to them, the patient would not even know there might be other options. If the patient consents to knowing the state of their condition, he or she should know about these options to give them a role in making decisions about their care and …show more content…
In a case seen in December 2013, 24-year-old Vickie Harvey “had fought leukaemia twice - but went rapidly downhill after being told 'in graphic detail ' how she was going to die” (Hodgekiss). Her parents started a campaign for patients to have a choice on whether they want to know if they are terminally ill because they stated her daughter gave up all hope for life after she found out about her diagnosis (Hodgekiss). Her doctor believed that if Harvey had not known, she would not have been able to prepare herself and take appropriate measures to understand her prognosis (Hodgekiss). Reading the circumstances surrounding this case, it is important to give the patient a choice on if they would like to know the state of their condition, and how much they would like to know. They do not have to know all the details if they choose not to. At least this way the patient knows they have the choice to know and they do not continue to feel like information is being hidden from them. They should also have an equal choice to not know if they desire. This follows all ethical and legal aspects of patient autonomy while still considering their cultural background and family’s
On the morning of May 17th, 2005, Nola Walker was involved in a two-car collision. Police and Ambulance were dispatched and arrive on scene at the intersection of Kenny and Fernley Street. Ambulance conducted various assessments on Ms. Walker which revealed no major injuries and normal vital signs. Mrs walker denied further medical investigation and denied hospital treatment. Later on, Queensland police conducted a roadside breath test that returned a positive reading, police then escorted Ms. Walker to the cairns police station. Ms. Walker was found to be unconscious, without a pulse and not breathing. An ambulance was called but attempts to revive her failed (Coroner’s Inquest, Walker 2007). The standard of Legal and ethical obligation appeared by paramedics required for this situation are flawed and require further examination to conclude whether commitments of autonomy, beneficence, non-maleficence and justice were accomplished.
One of the most complex, ever-changing careers is the medical field. Physicians are not only faced with medical challenges, but also with ethical ones. In “Respect for Patients, Physicians, and the Truth”, by Susan Cullen and Margaret Klein, they discuss to great extent the complicated dilemmas physicians encounter during their practice. In their publication, Cullen and Klein discuss the pros and cons of disclosing the medical diagnosis (identifying the nature or cause of the disease), and the prognosis (the end result after treating the condition). But this subject is not easily regulated nor are there guidelines to follow. One example that clearly illustrates the ambiguity of the subject is when a patient is diagnosed with a serious, life-threatening
Thanks in part to the scientific and technological advances of todays’ society, enhanced medicinal treatment options are helping people battle illnesses and diseases and live longer than ever before. Despite these advances, however, many people with life threatening illnesses have needs and concerns that are unidentified and therefore unmet at the end of life, notes Arnold, Artin, Griffith, Person and Graham (2006, p. 62). They further noted that when these needs and concerns remain unmet, due in part to the failure of providers to correctly evaluate these needs, as well as the patients’ reluctance to discuss them (p. 63, as originally noted by Heaven & Maguire, 1997), a patient’s quality of life may be adversely affected. According to Bosma et al. (2010, p. 84), “Many generalist social work skills regarding counseling, family systems, community resources, and psychosocial assessments are relevant to working with patients and families with terminal illness”, thereby placing social workers in the distinctive position of being able to support and assist clients with end of life decisions and care planning needs. In fact, they further noted that at some point, “most social work practitioners will encounter adults, children, and families who are facing progressive life limiting illness, dying, death, or bereavement” (p. 79).
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.
Patients are ultimately responsible for their own health and wellbeing and should be held responsible for the consequences of their decisions and actions. All people have the right to refuse treatment even where refusal may result in harm to themselves or in their own death and providers are legally bound to respect their decision. If patients cannot decide for themselves, but have previously decided to refuse treatment while still competent, their decision is legally binding. Where a patient's views are not known, the doctor has a responsibility to make a decision, but should consult other healthcare professionals and people close to the patient.
However, it has been reported that telling a patient the truth may significantly improve their wellbeing as they approach the end of their life. One study revealed that truth telling may reduce terminal cancer patients’ uncertainty and anxiety, as indicated by lower scores on a Hospital Anxiety and Depression scale, and higher scores on a Spiritual Well-being scale (Kao et al. 2013). Furthermore, while there is no explicit principle regarding lying within the Hippocratic Oath, honesty is a virtue that is closely associated with physicians and health care providers. In fact, honesty can be closely related to respect for persons, which implies that it is necessary for the maintenance of the physician-patient relationship. Honesty about all relevant aspects of a patient’s diagnosis, prognosis and treatment are necessary to build trust, and to obtain informed consent.
When it comes to a bad diagnosis it is often difficult for doctors to tell their patients this devastating news. The doctor will likely hold back from telling the patient the whole truth about their health because they believe the patient will become depressed. However, Schwartz argues that telling the patient the whole truth about their illness will cause depression and anxiety, but rather telling the patient the whole truth will empower and motivate the patient to make the most of their days. Many doctors will often also prescribe or offer treatment that will likely not help their health, but the doctors do so to make patients feel as though their may be a solution to the problem as they are unaware to the limited number of days they may have left. In comparison, people who are aware there is no cure to their diagnosis and many choose to live their last days not in the hospital or pain free from medications without a treatment holding them back. They can choose to live their last days with their family and will have more time and awareness to handle a will. Schwartz argues the importance of telling patients the truth about their diagnosis and communicating the person’s likely amount of time left as it will affect how the patient chooses to live their limited
In my own personal story, I truly appreciated the doctor telling me that it would be painful. Also, in I Am Not a Patella, I felt as though the doctor was not honest by not telling the patient anything about her condition. According to Arnold and Boggs, “honesty is a basic building block in establishing trust. Studies show that clients…prefer complete disclosure” (pg. 205). The client is in an extremely vulnerable position. It is extremely important that the nurse or other health care provider be sensitive to this and ensure that trust is maintained. (College of Nurses of Ontario, 2013). Those who are terminally ill, appreciate those professional who are willing to talk to them honestly about dying and end of life preparations (Terminally Ill Deserve Honesty,
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
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.
...d how these determinations effect a physician’s approach to various types of critically ill patients? These types of questions come in to play when one attempts to critically analyze the differences between the types of terminally ill patients and the subtle ethical/legal nuances between withholding and withdrawing treatment. According to a review by Larry Gostin and Robert Weir about Nancy Cruzan, “…courts examine the physician’s respect for the desires of the patient and the level of care administered. A rule forbidding physicians from discontinuing a treatment that could have been withheld initially will discourage doctors from attempting certain types of care and force them prematurely to allow a patient to die. Physicians must be free to exercise their best professional judgment, especially when facing the sensitive question of whether to administer treatment.”
Moving forward, people should be able to be put out of their misery of their terminal illness. This is something that without a doubt will tear a person to shreds. This type of news, “can trigger feelings of depression, in both patient and loved one. These feelings can be severe or mild and can often be just one of the stages that a person goes through when learning of catastrophic news” (Terminal Illness). Some terminal illnesses this time is also very stressful with decisions that one can make. Although depending on what the patient has, the illness can be brutal and
Some feel that a terminally ill patient should have a legal right to control the manner in which they die. Physicians and nurses have fought for the right to aid a patient in their death. Many families of the terminally ill have exhausted all of their funds caring for a dying patient and would prefer the option of assisted suicide to bankruptcy. While there are many strong opposing viewpoints, one of the strongest is that the terminally ill patient has the right to die in a humane, dignified manner. However, dignity in dying is not necessarily assured when a trusted doctor, whose professional ethics are to promote and maintain life, injects a terminally ill patient with a lethal dose of morphine.
Many healthcare providers suffer from the dilemma of which is the best option for the patient to know about their health. In the United States the law inform that the patient have the right to know how sick they are, what to expect from it, and what are the consequences. It is the patient’s right to decide if they want treatment or not depending on the severity of the disease. But, many of the health care professional confront the dilemma of know how the news is going to affect the patients in the positive and negative way and what is the family members opinion about informing the patients.
The delivery of healthcare mandates a lot of difficult decision making for healthcare providers as well as patients. For patients, much of the responsibility is left to them especially when serious health problems occur. This responsibility deals with what treatments could be accepted, what treatments could be continued, and what treatments could be stopped. Overall, it considers what route should be taken in regards to the health interests of the patient. However, there are circumstances in which patients cannot decide for themselves or communicate what they want in terms of their healthcare. This is where the ethical issue concerning who should be responsible for making these important healthcare decisions occur if a patient was to be in this sort of situation. Healthcare providers can play a role in the healthcare decision making as their duty is to act in the best interest of the patient.