| Автор | Shamoo, Adil E. |
| Автор | Irving, Dianne N. |
| Дата выпуска | 1993 |
| dc.description | Although medical research involving the use of persons with mental illness is critically important, in order for the research to be ethical and legal there are certain considerations and restrictions which should be immediately readdressed in order to insure that the welfare of these vulnerable research subjects is protected, and their best interests are assured. A brief historical examination of medical research codes, guidelines, recommendations and Federal Regulations reveals the various considerations and restrictions on informed consent and accountability applicable to the use of persons with mental illness in medical research. Several concerns are raised about how these considerations and restrictions have been interpreted, and specific recommendations are offered to improve them immediately by means of representation from consumers and/or their families, and organizations, e.g., NAMI members. |
| Формат | application.pdf |
| Издатель | Taylor & Francis Group |
| Копирайт | Copyright Taylor and Francis Group, LLC |
| Тема | mental illness |
| Тема | Federal Research Regulations |
| Тема | informed and proxy consent |
| Тема | accountability |
| Тема | NAMI |
| Название | Accountability in research using persons with mental illness |
| Тип | research-article |
| DOI | 10.1080/08989629308573826 |
| Electronic ISSN | 1545-5815 |
| Print ISSN | 0898-9621 |
| Журнал | Accountability in Research |
| Том | 3 |
| Первая страница | 1 |
| Последняя страница | 17 |
| Аффилиация | Shamoo, Adil E.; Center for Biomedical Ethics, and the Department of Biological Chemistry, School of Medicine, University of Maryland |
| Аффилиация | Irving, Dianne N.; Department of Philosophy, De Sales School of Theology |
| Выпуск | 1 |
| Библиографическая ссылка | Appelbaum, P., Lidz, C. and Meisel, A. 1987. Informed Consent—Legal Theory and Clinical Practise, Oxford: Oxford University Press. |
| Библиографическая ссылка | Barber, Bernard. 1973. Research on Human Subjects, New York: Russell Sage Foundation. |
| Библиографическая ссылка | Baudouin, J. 1990. Medicine and Law, 9: 1052–1061. |
| Библиографическая ссылка | Beecher, H.E. 1966. Ethics and clinical research. New England Journal of Medicine, 274: 1354–60. |
| Библиографическая ссылка | Capron, A.M. 1992. “Where is the sure interpreter?”. In Hasting Center Report Vol. 22, 26–27. |
| Библиографическая ссылка | Case Studies. 1992. “Substituting our judgment”. In Hastings Center Report 22 |
| Библиографическая ссылка | Dresser, R. 1984. “Bound to treatment: the Ulysses contract”. In Hastings Center Report Vol. 14, 313–16. |
| Библиографическая ссылка | Fletcher, J., Dommel, E and Cowell, D. 1985. A trial policy for the intramural programs of the National Institutes of Health: consent to research with impaired human subjects. IRB, 7(6): 1–6. |
| Библиографическая ссылка | Frankel. 1975. The development of policy guidelines covering human experimentation in the United States. Ethics in Science and Medicine, 2: 43–59. |
| Библиографическая ссылка | Ganzini, L., Lee, M.A., Heintz, R.T. and Bloom, J.D. 1993. Is the Patient Self‐Determination Act appropriate for elderly persons hospitalized for depression?. Journal of Clinical Ethics, 4(1): 46–50. |
| Библиографическая ссылка | Gillespie, R. 1989. Research on human beings: an historical overview. Bioethics News, 8(2): 4–15. |
| Библиографическая ссылка | Hoffmann, D. 1993. Associate Professor of Law, Baltimore, MD: University of Maryland. (personal communication, May 13, 1993) |
| Библиографическая ссылка | Irving, D. 1993. The impact of scientific misinformation on other fields: philosophy, theology, biomedical ethics, public policy. Accountability in Research, 2(4): 243–272. |
| Библиографическая ссылка | Irving, D. 1993. Philosophical and scientific expertise: an evaluation of the arguments on ‘person‐hood’. Linacre Quarterly, 60(1): 18–46. |
| Библиографическая ссылка | Ivy, A.C. 1948. The history and ethics of the use of human subjects in medical experiments. Science, 108: 1–5. |
| Библиографическая ссылка | Jonas, H. 1984. The Imperative of Responsibility, Chicago: University of Chicago Press. |
| Библиографическая ссылка | Katz, J. 1992. “The consent principle of the Nuremberg Code: its significance then and now”. In The Nazi Doctors and the Nuremberg Code: Human Rights in Human Experimentation, Edited by: Annas, George J. and Grodin, Michael A. New York: Oxford University Press. |
| Библиографическая ссылка | Katz, J. 1972. Experimentation with Human Beings, 305–306. 312–313. New York: Russell Sage Foundation. |
| Библиографическая ссылка | King, N.P. 1992. “Transparency in neonatal intensive care”. In Hastings Center Report Vol. 22, 18–25. |
| Библиографическая ссылка | Levine, R.J. 1986. Ethics and Regulation of Clinical Research, New Haven: Yale University Press. |
| Библиографическая ссылка | Lifton, R.J. 1986. The Nazi Doctors, New York: Basic Books, Inc. |
| Библиографическая ссылка | Maloney, D. 1984. Protection of Human Research Subjects, New York: Plenum Press. |
| Библиографическая ссылка | Mitscherlich, A. and Mielke, E. 1962. The Death Doctors, London: Elek Books. |
| Библиографическая ссылка | Muller‐Hill, B. 1988. Murderous Science, Oxford: Oxford University Press. |
| Библиографическая ссылка | National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. 1978. The Belmont Report, Washington, D.C,: U.S. Department of Health, Education, and Welfare. |
| Библиографическая ссылка | Nelson, J.L. 1992. “Taking families seriously”. In Hastings Center Report Vol. 22, 6–12. |
| Библиографическая ссылка | President's Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research. 1983. Summing Up., Washington, D.C.: U.S. Government Printing Office. |
| Библиографическая ссылка | Proctor, R.N. 1988. Racial Hygiene, Massachusettes: Harvard University Press. |
| Библиографическая ссылка | Santurri, E.N. 1982. Substituted judgment and the terminally‐ill incompetent. Thought, 57: 227484–501. |
| Библиографическая ссылка | Shamoo, A.E. 1993. “Role of conflict of interests in public advisory councils. Chapt. 17”. In “Ethical Issues in Research,”, Edited by: Cheney, D. 159–174. Maryland: University Publishing Group, Inc. Frederick. 21701 |
| Библиографическая ссылка | Shamoo, A.E. 1992. Role of conflict of interest in scientific objectivity: a case of a Nobel Prize work. Accountability in Research, 2: 55–75. |
| Библиографическая ссылка | Shamoo, A.E. 1991. Policies and quality assurances in the pharmeceutical industry. Accountability in Research, 1: 273–284. |
| Библиографическая ссылка | Shamoo, A.E. and Annau, Z. 1989. “Data audit: historical perspectives”. In Principles of Research Data Audit, Edited by: Shamoo, A.E. 1–12. New York: Gordon and Breach, Science Publishers, Inc.. Chapter 1 |
| Библиографическая ссылка | Shamoo, A.E. and Irving, D.N. 1993. The PSDA and the depressed elderly: intermittent competency revisited. Journal of Clinical Ethics, 4(1): 74–80. |
| Библиографическая ссылка | Truog, R.D. 1992. “Triage in the ICU”. In Hastings Center Report Vol. 22, 13–17. |
| Библиографическая ссылка | United States Code of Federal Regulations: Protection of Human Subjects 45 CFR 46 (revised Jan. 12, 1981; revised Mar. 8, 1983; reprinted July, 1989), (a), p. 7. |
| Библиографическая ссылка | Veatch, R. 1987. The Patient as Partner: A Theory of Human Experimentation Ethics, Bloomington, IN: Indiana University Press. |
