Browsing by keyword "Moral Obligations"
Now showing items 1-4 of 4
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Commentary: toward a unified theory of personal and professional ethicsIn response to Dr. Ezra Griffith's essay, we support the view that forensic practice cannot be cleanly divided from its ethics foundation in medical and general psychiatric practice. Personal and professional values cannot be separated in formulating a unified theory of ethics for professionalism in forensic practice. We support Dr. Griffith's narrative perspective and offer a delineation of how narratives may be considered in forensic work. We would like readers to focus on both the duties and the moral ideals that ultimately define professional ethics. By honoring personal and professional narratives together, forensic professionals can advocate and reshape a system that devalues non-dominant cultures. They can also recognize more easily the influences that affect their forensic work. This kind of forensic practice, informed by narrative ethics while respecting fundamental principles, can be an essential part of what we aspire to as forensic professionals. As we argued in an earlier work, a robust professionalism for forensic psychiatry cannot ignore our physician background or our diverse personal histories. Dr. Griffith's essay contributes forcefully to the development of such a view.
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Ethical and legal duties in conducting research on violence: lessons from the MacArthur Risk Assessment StudyThis article addresses the ethical and legal duties that must be confronted in any study of the risk of interpersonal violence in the community. Ongoing research--the MacArthur Risk Assessment Study--on the markers of violence among released mental patients is taken as illustrative. Methods by which the researchers are discharging their legal and ethical duties are described and justified. Strategies center around the duty to protect research subjects from their own violence, and the duties to protect research staff and third parties from subjects' violence. By airing these rarely discussed issues, the authors hope to initiate a professional dialogue on crucial ethical and legal aspects of the research process.
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Two models of implementing informed consentThe doctrine of informed consent has been controversial since its inception. In spite of the professed ideal of improving physician-patient communication, many commentators have argued that it interferes with the relationship. However, the problem may not be the doctrine itself but rather the manner in which it is usually implemented. This article describes two different ways in which informed consent can be implemented. The event model treats informed consent as a procedure to be performed once in each treatment course, which must cover all legal elements at that time. The process model, in contrast, tries to integrate informing the patient into the continuing dialogue between physician and patient that is a routine part of diagnosis and treatment. We suggest that the process model has many benefits.