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Terrie Wetle 《Gerodontology》1987,6(2):73-78
Ethical issues involved in providing dental care to geriatric patients have generally been ignored in the practice and academic literatures. Elderly patients require special ethical consideration because of increased burden of illness, sensory deficits which may interfere with symptom interpretation and communication, fiscal constraints and ageism among both providers and patients. A taxonomy of ethical issues is provided including issues pertaining to the patient, the family, service providers, and the health care system. Suggestions are made for improving decision making in geriatric dental care. 相似文献
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《Bioethics》2004,18(4):379-381
Books reviewed:
Pharmacogenetics: Ethical Issues , Report by the Nuffield Council on Bioethics. London: Nuffield Council on Bioethics. 2003. xxiv + 103pp. £10 to all European countries (including postage); £15 to non-European countries (including postage); £0 to developing countries. Available free of charge at: http://www.nuffieldbioethics.org/filelibrary/pdf/pharmacogenetics_report 相似文献
Pharmacogenetics: Ethical Issues , Report by the Nuffield Council on Bioethics. London: Nuffield Council on Bioethics. 2003. xxiv + 103pp. £10 to all European countries (including postage); £15 to non-European countries (including postage); £0 to developing countries. Available free of charge at: http://www.nuffieldbioethics.org/filelibrary/pdf/pharmacogenetics_report 相似文献
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Hannes Knüppel Marcel Mertz Martina Schmidhuber Gerald Neitzke Daniel Strech 《PLoS medicine》2013,10(8)
Background
Clinical practice guidelines (CPGs) aim to improve professionalism in health care. However, current CPG development manuals fail to address how to include ethical issues in a systematic and transparent manner. The objective of this study was to assess the representation of ethical issues in general CPGs on dementia care.Methods and Findings
To identify national CPGs on dementia care, five databases of guidelines were searched and national psychiatric associations were contacted in August 2011 and in June 2013. A framework for the assessment of the identified CPGs'' ethical content was developed on the basis of a prior systematic review of ethical issues in dementia care. Thematic text analysis and a 4-point rating score were employed to assess how ethical issues were addressed in the identified CPGs. Twelve national CPGs were included. Thirty-one ethical issues in dementia care were identified by the prior systematic review. The proportion of these 31 ethical issues that were explicitly addressed by each CPG ranged from 22% to 77%, with a median of 49.5%. National guidelines differed substantially with respect to (a) which ethical issues were represented, (b) whether ethical recommendations were included, (c) whether justifications or citations were provided to support recommendations, and (d) to what extent the ethical issues were explained.Conclusions
Ethical issues were inconsistently addressed in national dementia guidelines, with some guidelines including most and some including few ethical issues. Guidelines should address ethical issues and how to deal with them to help the medical profession understand how to approach care of patients with dementia, and for patients, their relatives, and the general public, all of whom might seek information and advice in national guidelines. There is a need for further research to specify how detailed ethical issues and their respective recommendations can and should be addressed in dementia guidelines. Please see later in the article for the Editors'' Summary 相似文献12.
Catherine M. Hill 《American anthropologist》2002,104(4):1184-1194
Hunting and habitat destruction and alteration threaten the existence of many primate species. However, the conservation of these primates has significant costs, as well as benefits, for people living alongside them. Conservation policy now recognizes that people should not suffer impoverishment from wildlife preservation and that, instead, conservation programs should make a significant contribution to alleviating rural poverty. Ethical consideration requires that local communities have greater control over natural resources, and that conservation programs contribute to these people's livelihood security. Nevertheless, this conservation on the basis of potential economic value may not protect primates adequately and may render them still vulnerable to extinction, given their sensitivity to human activities. This presents an ethical dilemma: primates have intrinsic moral value so should be conserved for their own sake, yet conservation policies should not cause harm to local human populations. This article explores ethical issues that arise when primates and people live in close proximity. [Keywords: primate conservation, ethical issues, human–wildlife conflict] 相似文献
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Striefel S 《Applied psychophysiology and biofeedback》2001,26(1):39-59
La Vaque and Rossiter made a strong, supported argument that it is unethical to use a no treatment control group in a research study if a known, effective treatment is available. Their argument is based on the supposition that the Declaration of Helsinki is the ethical world standard for research with humans. Their argument appears to be straightforward, but is not simple to apply. The issues are very complex, include issues not discussed in their argument, and can lead to a different conclusion as pointed out in this paper. The World Medical Association developed the Declaration of Helsinki as one of their official policies. The Declaration of Helsinki, however, is not accepted as the world ethical standard, as demonstrated by its lack of adoption by many professional associations or even by the United States Federal Government. Perhaps it is not mentioned because its ethical provisions are aspirational rather than mandatory as implied by La Vaque and Rossiter. Researchers and clinicians should also be aware of other ethical issues not directly discussed in the La Vaque and Rossiter paper. The Belmont Report is the basis for the ethical protection of human research subjects for at least 17 federal agencies and does not mention the Declaration of Helsinki. The Belmont Report mentions several ethical principles that form the basis for informed consent, risk/benefit assessment, confidentiality of data, subject selection, Institutional Review Boards, and other protections needed when doing research with human subjects. At least 2 of these core principles have direct implications to the discussion related to the use of placebo controls. The ethical principle of fidelity is also important in guiding research activities with human subjects. Researchers should be familiar with the La Vaque and Rossiter argument, the Belmont Report, and the federal policies developed to implement the provisions of that report, for example, Regulation 45 CFR 46. 相似文献
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Nikolajs Zeps Marianna J Bledsoe 《The Clinical biochemist. Reviews / Australian Association of Clinical Biochemists》2015,36(1):21-27
Biobanks of human biospecimens involving tissue taken from surgery require close relationships with diagnostic pathology practices. As most of the tissue will be analysed using genetic or genomic technologies there is the possibility that new information is created that could be of relevance to the donors. Although attention has been recently focused on the responsibilities that may arise from researchers and biobanks in terms of giving back individual genetic research results (IGRRs) to research participants, little has been said in relation to the role of pathology services. In this Commentary, we summarise the issues with respect to pathology services and what guidelines and professional practice documents say about their responsibilities. We also provide points to consider in the development of an ethically defensible plan for giving back individual research results. 相似文献
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Craniofacial birth defects occur in 1 out of every 700 live births, but etiology is rarely known due to limited understanding of craniofacial development. To identify where signaling pathways and tissues act during patterning of the developing face, a ''face transplant'' technique has been developed in embryos of the frog Xenopus laevis. A region of presumptive facial tissue (the "Extreme Anterior Domain" (EAD)) is removed from a donor embryo at tailbud stage, and transplanted to a host embryo of the same stage, from which the equivalent region has been removed. This can be used to generate a chimeric face where the host or donor tissue has a loss or gain of function in a gene, and/or includes a lineage label. After healing, the outcome of development is monitored, and indicates roles of the signaling pathway within the donor or surrounding host tissues. Xenopus is a valuable model for face development, as the facial region is large and readily accessible for micromanipulation. Many embryos can be assayed, over a short time period since development occurs rapidly. Findings in the frog are relevant to human development, since craniofacial processes appear conserved between Xenopus and mammals. 相似文献
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This paper provides an empirical account of commercial genetic predisposition testing in mainland China, based on interviews
with company mangers, regulators and clients, and literature research during fieldwork in mainland China from July to September
2006. This research demonstrates that the commercialization of genetic testing and the lack of adequate regulation have created
an environment in which dubious advertising practices and misleading and unprofessional medical advice are commonplace. The
consequences of these ethically problematic activities for the users of predictive tests are, as yet, unknown. The paper concludes
with a bioethical and social science perspective on the social and ethical issues raised by the dissemination and utilization
of genetic testing in mainland China. 相似文献
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David B. Resnik 《Developing world bioethics》2014,14(1):37-46
Mosquito‐borne diseases take a tremendous toll on human populations, especially in developing nations. In the last decade, scientists have developed mosquitoes that have been genetically modified to prevent transmission of mosquito‐borne diseases, and field trials have been conducted. Some mosquitoes have been rendered infertile, some have been equipped with a vaccine they transmit to humans, and some have been designed to resist diseases. This article focuses on ethical issues raised by field trials of disease‐resistant, genetically modified mosquitoes. Some of these issues include: protecting the public and the environment from harm, balancing benefits and risks, collaborating with the local community, avoiding exploitation, and safeguarding the rights and welfare of research subjects. One of the most difficult problems involves protecting the welfare of community members who will be impacted by the release of mosquitoes but who are not enrolled in the study as research subjects. To address this concern, field trials should take place only when the targeted disease is a significant public health problem in an isolated area, the benefits of the trial for the community are likely to outweigh the risks, community leaders approve of the trial, and there are measures in place to protect the welfare of un‐enrolled community members, such as informing the community about the study and offering free treatment to people who contract mosquito‐borne diseases. Since the justification of any field trial depends on a careful examination of the scientific and ethical issues, proposed studies should be evaluated on a case‐by‐case basis. 相似文献