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Patient rights consist of enforceable duties that healthcare professionals and healthcare business persons owe to patients to provide them with certain services or benefits. [ 1] When such services or benefits become rights instead of simply privileges, then a patient can expect to receive them and can expect the support of people who enforce ...
The Patients' Charter is an official document by the government or an organization that enlists various Patients' Rights and Responsibility along with the Code of Practice, followed by a medical personnel. The Patient's Charter was first started out as a United Kingdom government official document, which sets out a number of Patient's rights ...
Patient education. A Radiographer explains an x-ray to a coal miner participating in screening. Patient education can include explaining the results of diagnostic tests. Patient education is a planned interactive learning process designed to support and enable expert patients [ 1] to manage their life with a disease and/or optimise their health ...
Patient advocacy is a process in health care concerned with advocacy for patients, survivors, and caregivers. The patient advocate[ 1] may be an individual or an organization, concerned with healthcare standards or with one specific group of disorders. The terms patient advocate and patient advocacy can refer both to individual advocates ...
Medical ethics is an applied branch of ethics which analyzes the practice of clinical medicine and related scientific research. [ 1] Medical ethics is based on a set of values that professionals can refer to in the case of any confusion or conflict. These values include the respect for autonomy, non-maleficence, beneficence, and justice. [ 2]
The doctor–patient relationship is a central part of health care and the practice of medicine. A doctor–patient relationship is formed when a doctor attends to a patient's medical needs and is usually through consent. [ 1] This relationship is built on trust, respect, communication, and a common understanding of both the doctor and patients ...
Informed consent is a principle in medical ethics, medical law, media studies, and other fields, that a person must have sufficient information and understanding before making decisions about accepting risk, such as their medical care. Pertinent information may include risks and benefits of treatments, alternative treatments, the patient's role ...
Canada has established a research chair that focusses on practical methods for promoting and implementing shared decision-making across the healthcare continuum. [65] Shared decision-making in medicine ( SDM) is a process in which both the patient and physician contribute to the medical decision-making process and agree on treatment decisions. [1]