Competence refers to the practitioner's accurate self-representation of credentials as well as contributing to the profession by undergoing ongoing professional development throughout the career. Although competence is a distinct value from integrity, it is also related to integrity because all social workers should have the personal and professional integrity to practice only within their realm of professional training and competence, and also to upgrade their skills according to emerging research, theory, and policy. The NASW (n.d.) also points out in its Code of Ethics that competence is integral to the protection of clients from harm (p. 2). Informed consent, although a distinct ethical practice, is linked to professional competence in several ways. According to the NASW (n.d.), "social workers should provide services to clients only in the context of a professional relationship based, when appropriate, on valid informed consent," (1.03). Informed consent promotes respect for clients as well as client autonomy, and informed consent also protects clients from harm. Both informed consent and competence are covered under the rubric of social workers' ethical responsibilities to clients.
Informed consent and competence are both ethical responsibilities to clients because both provide clients with the knowledge and power they need to make educated decisions. Competence ensures that the client is receiving information from the best possible source, and informed consent ensures that the client has received all information accurately and is not being deceived in any way. When a social worker is working with "an emerging area of practice," for which "no generally recognized standards exist," the professional and ethical obligation to the client remains full disclosure as well as acquiring either research or supervision to protect the client from harm (NASW, n.d., 1.04). Both informed consent and competence protect clients by ensuring clients have access to any and all information relevant to their case and their needs, ensuring also that the social worker will have the ethical judgment to refer the client to additional services or information when necessary.
2. The Dutch euthanasia law is progressive and responsible. Although it is a controversial issue, I do believe that assisted suicides in cases like that of Mark Langedijk are morally and ethically permissible from several principles. For one, the Dutch system ensures that a physician presides over each case and did so in Langedijk's case. "His death was approved by a doctor from Support and Consultation on Euthanasia in the Netherlands, a medical body that oversees requests from those who wish to die with the help of the state," (Richardson, 2016, p. 1). The assurance of competence from an established medical board and competent physicians ensures that the process of euthanasia occurs with rigorous clinical oversight and good professional -- as well as ethical -- judgment. Informed consent is built into the system, as the patient must initiate the euthanasia...
C). AAPC Code of Ethics is shorter compared to ACA's, centering more on specific issues such as confidentiality and professional practices, among others. Identified as Principle IV in the AAPC code of ethics, Confidentiality is synonymously identified as 'respect for the integrity and protection of the welfare' of its clients, a claim that is similar to ACA's stance on confidentiality. ACA and AAPC discussed the issue of confidentiality similarly, although AAPC
Consent & Ethics Complications stemming from patient-counselor interactions remain a key source of ethical violations and complaints. Informed consent is a major issue with a direct bearing on the counselor-patient relationship. In clinical avenues, the origin of informed consent continues to have a direct outgrowth of advances in professional ethics, legal precedents, and continuous moral development. Through informed consent, patients have been able to take responsibility and explore options for
Confidentiality Breaches in Clinical Practice The confidentiality and privacy of patients are considered as one of the fundamental freedoms that they should enjoy and are safeguarded under Health Insurance Portability and Accountability Act of 1996 (HIPPA). It is also a precept of the American Medical Association’s Code of Ethics and the Hippocratic Oath. The breach of confidentiality is unethical and illegal. Medical professionals are under the obligation of protecting the patient’s confidentiality.
Anna's rationale for not obtaining informed consent? Not informing research subjects regarding one's purpose is unethical. In order to see just how unethical her decision is, Anna must understand ethical concerns linked to studies that utilize human participants. The basic principles of justice, independence, and goodness form the basis of the aforementioned ethical concerns and warrant attention (UNC Charlotte| Research& Economic Development Centre, n.d).). Ethics guidelines and codes explain the
statistics have on shaping healthcare policy and guiding evidence-based practice, it is critical that researchers understand how to present the results of their studies. It is also critical that healthcare workers develop strong skills in statistical literacy, so that the results of studies are not misconstrued. Not all research results are generalizable to a population outside of the sample. Even the most carefully constructed research designs need to be
Patient Rights and Informed Consent The relevant legal issues at stake in this case are those related to the question of whether Mr. Jones is indeed incompetent and if Mr. Jones is indeed incompetent then what is the authority that should be assigned to the surrogate daughter of the patient in this case. The hospital physician and staff must avoid legal liability and ensure that they are in adherence to
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