Under the "Patients Bill of Rights from the Association of American Physicians and Surgeon's (AAPS) a health care provider needs to understand that the AAPS merges with Affordable Care Act (ACA) to provide protection and offers rights regarding interactions with insurance companies, medical facility, or physicians (Woodard, 2017). It is the health care providers responsibility to make sure they know the current patient bill of rights law. For example, they need to know that the patient has the right to a second opinion. A patient has the right to refuse treatment (Woodard, 2017). As long as the patient is deemed competent when making the decision to refuse treatment. There is 21 patient bill of rights, and it would be the health care …show more content…
Third, the patient has the right to be informed about any illness/diagnosis. Therefore, it is the health care professionals responsibility to educate and inform the patient fully of the diagnosis and treatment choices. The fourth right is that the patient has the right to know the individuals that are treating them. Therefore it is the responsibility of the health care provider to provide their name to the patient. The fifth right the patient has the right to consent or refuse treatment. Therefore, it is the healthcare obligation to respect the choice that the patient makes. If the patient does consent treatment, then a consent form must be signed before treatment can take place. The six right the patient has the right to information pertaining to decision making. The seventh right is the patient has the right to know crises procedures. The eight right to any information about special treatment preventions and restrictions of rights. The ninth right patient has is that they can choose their own case manager, therapist or other service providers. The ten right is that the health care facility will protect the patient's privacy (Woodard, 2017). This means that the health care provider needs to make sure to protect the
In Nursing, there will always be instances where the patient's nurse needs to advocate for their patient. There are numerous reasons why a nurse would advocate for their patient ranging from getting the doctor to change the patient’s orders, helping the patient’s treatment team understand what it is the patient is requiring for the day, to expressing the patient’s last wishes before death. In every situation, the nurse should do what is in the patient’s best interest. Tomajan (2012), “Advocacy skills are the ability to successfully support a cause or interest on one’s own behalf or that of another. Advocacy requires a set of skills that include problem solving, communication, influence, and collaboration”(p. 2). With those skills, the
As well as having informed consent about a certain procedure or whether or not they want to provide their medical information for research. The other part of this provision is to make sure your patient is being provided with safe practice. In the past I have questioned care that was given to my patient that did not follow our hospitals policy. In this instance it was how fast I was ordered to infuse blood on a patient with a history of CHF. In this case the doctor was unaware of the change of patient status or policy and applauded me for speaking up. This is not always the case. In other instances you may need to report patient care providers to the appropriate personal to advocate for your patient and as of yet I have not experienced this first hand but know of occurrences elsewhere. It could be as small as a medication that is ordered in the wrong dose or route. We are the voice of the patient and are here to help promote their safety. This provision is in place to protect the patient and public from possible harm.
Patient’s fifth right is for respect and care without discrimination from all members in the healthcare field. The right to confidentiality and privacy of their health information is sixth on the bill of rights and addresses their right to read, copy and request corrections to their medical record, to talk privately their medical providers and be assured their healthcare information is secure. The seventh right is for patients to have a “fair, fast, and objective review of any health care complaints” (Consumer Bill of Rights and Responsibilities, 1998). And finally our eighth right as patients are our responsibilities we have as the consumer of healthcare services. Patients need to comply with the orders of the medical provider so they can get and stay well. As a patient you must treat other patients and healthcare workers with respect, pay your medical bills in a timely manner, and abide by your selected healthcare plans coverage. As patients become more involved in the total healthcare process they increase the success of their treatment while assisting in lowering associated costs without a reduction in the quality of the healthcare they receive.
Discuss what is required to disclose patient information to family members, friends, and when ordered by courts or government
Sule stated that, “The Patient Bill of Right adopted by American Hospitals Association states that ‘a patient possesses the right to be informed of the medical consequences of his or her actions and decisions and refuse treatment to the extent permitted by the law’. However, this is true only if the patient is in position to understand the consequences of his treatment. Incompetent, senile patients neither have the correct judgment regarding which treatment is appropriate for them, nor are they in a state of understanding the implications of their treatment. In such case, their willingness to grant or deny consent cannot dictate the course of treatment.” Problem with the Act is being able to find that the patient component enough to make such a call. Another issue that Sule stated was on confidentiality and autonomy. According to Sule, “This is another ethical issue erupting from the conflict of patient's rights and professional ethics in nursing job and profession. The Patient Bill of Right makes it mandatory for the medical practitioners to reveal the form and extent of the ailment along with the course of treatment to be undertaken by the practitioners. However, this law of autonomy clashes with the nursing ethic that the professional should maintain high degree of confidentiality regarding the patient's health and treatment.” This can cause conflicting issues in the NP’s
It is important that the patient is aware not only of their rights, but of their individual responsibilities.
In 2003, a federal law that provided privacy and security protection was imposed upon all healthcare organizations including hospitals, physician practices, health insurance companies, Medicare, Medicaid, employers, and labs, as well as other providers. With passage of this law all patients now have a right to their PHI -Protected Health Information- under HIPAA which includes the right to receive a notice of privacy practices, to copy and view information in their medical record, request amendments, receive an accounting of disclosures, request communication about medical matters, restrict the use and disclosure of their medical record, and to file a complaint about violations of privacy (Modifications to the HIPAA, 2013).
The Health Insurance and Portability Act of 1996, known by the acronym HIPAA, is a civil rights law that was passed to give patients important rights and protections in regards to their protected health information (Herold, R., and Beaver, K, 2014). This federal law was imposed upon all healthcare organizations and affects hospitals, physician practices, health insurance companies, Medicare, Medicaid, employers, labs, as well as other providers. All patients should now have a right to their PHI -Protected Health Information- under HIPAA which include the right to receive a notice of privacy practices, to copy and view information in their medical record, request amendments to their medical record, receive an accounting of disclosures, request communication about medical matters, restrict the use and disclosure of their medical record, and to file a complaint for
The elements of the principles of confidentiality can be broken down into four separate categories: (1) Information provided by the patient is kept confidential unless consent from the patient has otherwise been given—unless it has direct legal implications or endangers the general public. (2) Informed Consent: is given freely, because the correct information has been supplied and the patient has sufficient information on the impacts involved. Information is otherwise given out on a need to know basis. (3) Duty of Care: Information is given out in order to protect the safety and health of others and the patient. Legal and general public health fall under this category. (4) Documenting Decisions: Consultations and actions that lead to
The Patient Protection and Affordable Care Act, which is also known to many as Obamacare, was signed into law on March 23, 2010 in order to reform the healthcare industry in the United States. The Patient Protection and Affordable Care Act is made up of the Affordable Health Care for America Act, the Patient Protection Act, the Health Care and Education Reconciliation Act of 2010 and the Student Aid and Fiscal Responsibility Act. It also includes amendments to many existing U.S. laws. The Affordable Care Act is very long to read, according to Obamacarefacts.com, “The Affordable care Act contains over a thousand pages of reforms to the insurance and health care industries.” However, most of the important reforms are included in the first
According to Healthy People 2012 there are more then 800,000 new cases of diabetes each year, with the numbers on the rise. With this in mind, Healthy People 2012 has identified diabetes as their number five focus area. In order to reach their goal of improving the quality of life for people with diabetes they have identified diabetes teaching as their number one objective. Furthermore, in order to reduce the number of complications of diabetes, Healthy People 2012 has identified foot ulcers as their ninth objective. Through patient education Healthy People 2012 hopes to reduce the number of foot ulcers in people with diabetes, as diabetes is the number one cause of nontraumatic amputations in the United States. In order to
Patient’s Bill of Rights essentially guarantees treatment to the recipient, as well as all full disclosure, and consent to care. This illustrates that the power and level of care is in the individuals hands. Furthermore, a new Bill of Right was enacted with the Affordable Care Act in 2010 much of what was outlined gave new patients protection against insurance company’s (“Rights” 1). This is important because it only strengthens the
The first principle is that with very few exceptions, health care information about a consumer should be disclosed for health purposes only. The information should be easy to use for those purposes, and very difficult to use otherwise. The second principle is that technical security safeguards be maintained for computerized data. Including audit trails that identify who accessed the data and the prosecution against anyone who used the records for illegal or improper purposes. The third principle is consumer access. The patient should have ability to access his or her records and know others that also have access to them. Patients should be aware of the laws, regulations, and policies that protect their information. The fourth policy is defined as accountability, which is of relation to security and consumer control. Fines and imprisonment are required to those who breach security of personal health information. The final policy is public responsibility. Legislation must be balanced between personal, private interests and national priorities of public health, research, and law enforcement. The excessive flow of information, without patient authorization, is essential to the immediate discovery and investigation in public health crisis. AHIMA's acknowledgement of these five principles are abroad outline of a sensible public policy that balances personal privacy
Today I had a great day at the clinic. For the morning section, I had Omar Lora as my patient. Last time when he came, I collected all my assessment data. Today I updated his medical history, dental history, vitals, and EIOE, then I completed filling out the gingival assessment, the treatment plan, and the SAOP. Finally, I was ready to have my assessment data checked. It went really well, and I learned ways to helped me be more efficient with my time management, for example, I did not know how to have my radiographs up in the other monitor while I was doing my assessments. It was a little time consuming having to open and minimized the window every time I needed to look at the radiographs. Also, I discovered that having a piece of paper out and taking
As health care consumers, everyone has certain rights; this is often referred to as a Patient’s Bill of Rights. While there is not a universal Patient’s Bill of Rights, it typically addresses an individual’s right to information concerning their condition and treatment options, and autonomy over their medical treatment decisions. This means that individuals have the right to choose what medical treatments they may or may not want to receive. You have the right to refuse treatment that has been recommended by your treating physician, as long as you understand the nature and consequences of the health care decision, even if it might prolong your life (Patients, 2016.)