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Patient rights and responsibilities thesis
The importance of patients rights
Causes and effects of discrimination in healthcare
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Recommended: Patient rights and responsibilities thesis
Within the Patient’s Bill of Rights, there are eight major rights. There are five of which I find most important for patients to receive the highest quality of care. These five include the following: access to emergency services, taking part in treatment decisions, respect and non-discrimination, confidentiality of health information, and choice of providers and plans. The most important area of the Patient Bills of Rights, in my opinion, is the access to emergency services. I work in an assisted living facility and often times, families will deny the service of sending their loved one to the hospital when an accident or fall occurs due to the financial burden. The down side of that decision is the family won’t have the reassurance that their loved one doesn’t have anything more severe going on due to the accident. I find it very important that access to emergency services be available at all times in order to provide high quality care without the financial burden. Secondly, all patients deserve to make executive decisions about their own treatments. I find this important because let’s say a patient is diagnosed with cancer late in life. Their options to treatment are given as chemotherapy, radiation therapy or surgery. It is unfair for a doctor to make the decision …show more content…
No one wants to go back to a doctor who treats them differently due to ethnicity, gender or race. Also, health care professionals who discriminate will lose patients left and right. Along the same lines, the patient is paying for the services and seeking help, they will stop seeking help if they keep running into doctors that discriminate against them. Therefore, the patients’ health could be in harm and they won’t know it. Thus, a mutual respectful relationship between doctor and patient is crucial to prevent a patient from being afraid to seek medical
Racial and ethnic inequalities in healthcare results in non-white patients receiving lower quality care that White patients. Additionally, people who speak limited English encounter more communication issues with doctors and nurses that people whose primary language is English. (AHRQ, 2011). Consequently, as people with chronic conditions utilize more healthcare services, they are more likely to complain of issues with the doctor-patient relationship. They feel as though they are not able to participate in their care, their doctors do not allow them to contribute to their medical decisions and they feel like doctors are not disclosing all information related to care. People who encounter this type of cultural ignorance become dissatisfied with their treatment and overall healthcare experience and are at high risk for negative
Cultural competency is a very significant necessity in health care today and the lack of it in leadership and in the health workforce, is quite pressing. The lack of cultural competency can bring about dire consequences such as racial and ethnic disparities in health care. It may not be the sole reason for these disparities, but it certainly places a significant role. A patient and health care provider relationship is very significant and can make or break the quality of care that is given. The lack of cultural competency leads to poor communication which then leads to those of diverse backgrounds to feel either unheard or just plain misunderstood. As an East African
In conclusion, It it is very necessary that our health care officials try harder to gain trust with minorities so that medicine can be focused more on equality. We all know that for decades our country was very diverse and everyone was treated differently. Although things have changed and it is sometimes important to preserve our past, past actions should not still be carried out. Even today, racism still occurs and it hard for minorities to feel safe when visiting hospitals and doctor’s offices. Minorities should be given equal medical opportunities, be given the honest truth on their diagnosis and treatments and most importantly be given some sort of health care so they can be treated.
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.
Advocating for diverse patients is important. In this paper I will be discuss a personal ethical dilemma in which I have encountered. I will give an objective interpretation of both my side as well as my patient’s side of the dilemma. Then I will describe the conflicting values and beliefs that I and the patient had. Then I will give the information I was lacking concerning the patient’s culture. Lastly, I will define culturally congruent care.
The medical Profession recognizes that patients have a number of basic rights. These include but are not limited to the following: the right to reasonable response to his or her requests and need and needs for treatment within the hospital's capacity. The right to considerate, respectful care focused on the patient's individual needs. The right of the patient to make health care decisions, including the right to refuse treatment. The right to formulate advance directives. The right to be provided with information regarding treatment that enables the patient to make treatment decisions that reflect his or her wishes. The right to be provided upon admission to a health care facility with information about the health care provider's policies regarding advance directives, patient rights, and patient complaints. The right to participate in ethical decision making that may arise in the course of treatment. The right to be notified of any medical research or educational projects that may affect the patient's care. The right to privacy and confid...
Today, many Americans face the struggle of the daily hustle and bustle, and at times can experience this pressure to rush even in their medical appointments. Conversely, the introduction of “patient-centered care” has been pushed immensely, to ensure that patients and families feel they get the medical attention they are seeking and paying for. Unlike years past, patient centered care places the focus on the patient, as opposed to the physician.1 The Institute of Medicine (IOM) separates patient centered care into eight dimensions, including respect, emotional support, coordination of care, involvement of the family, physical comfort, continuity and transition and access to care.2
Similarly, they are more likely to live in a medically underserved area that lacks an adequate supply of healthcare providers (Poghosyan & Carthon, 2017). There is also the effect of cultural and racial matter that can affect population health, like communication. Patient-centered care can be more challenging when medical providers and patient has cultural communication barriers. This can be a difference between the provider and the patient on ideas of treatment and expectations of treatment (Orom, 2016). This can interfere with patient improvement
The concept of a right to refuse treatment was built on basic rights to privacy, equal protection under the law, and due process. In other words, involuntarily hospitalized patients still have a right to decide what happens to their bodies. The right of a patient to refuse treatment is based upon five constitutional protections the 8th amendment’s protection against cruel and unusual punishment the 1st amendment’s protection of free speech (freedom of thought / ideas) the 1st amendment’s protection of freedom of religion the more broadly interpreted right to privacy the 14th amendment’s protection of liberty (the right to be free from unjustified intrusions on personal security).
...ns. Patients should not be so medically ill that they are unable to make this decision. Patients should be fully conscious and understand the implications of their decision. Everything should be documented possibly even videotaped that way the doctor doesn’t lose their job, receive a lawsuit or worst jail!
If a loved one, friend, or neighbor were to be diagnosed with cancer or any other disease and had a week or so to live, they should have the right to die on their own term. In most cases, people don’t have the right to control their death. In many states in the US, it is illegal to give terminally ill patients the right to die. Being terminally ill takes a toll on a person. It hurts them physically and mentally.
The “Patient Bill of Rights” was adopted in 1988 by the U.S. Advisory Commision on Consumer Protection and Quality in the Healthcare Industry to assure and protect patients’ rights. These rights provide the patient with
The health care spending in the United States is rapidly growing at an unsustainable rate. Unfortunately, there is a lack of preventive services compared to the tertiary care that constitute the bulk of our healthcare expenditure. As a future prominent leader in the field of public health and healthcare, I decided to pursue a career in this area as a result of the health inequities that exist across all minority groups—particularly minority older adults. The reasons for these disparities are complex, but I strongly believe that one of the main contributors to discrimination in patient care is the lack of cultural and linguistic competency; this deficiency greatly affects the health of many groups.
Improving care of patients living with long-term conditions like Diabetes and Arthritis should be an international priority. There is some confirmation that recommends multiplication of people suffering from one or more long term condition are struggling to manage their condition (Coleman & Newton, 2005). The Person living with long term condition and health problems will impact on their families and the society also it depends on their care needs, circumstances, their personal goals and capable to look after themselves and their lifestyle (Asbridge & Davies 2017). Current approaches stress enhancing understanding of contribution in care and supporting self-management, which involve “cooperatively helping people also, their carers to build
To promote patient health, it is necessary to form an active relationship with the patient by understanding their cultural differences and showing respect to their