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A moral emergency and a medical problem: negotiating the control of venereal disease--the Saskatchewan Venereal Disease Protection Act, 1946. 道德紧急情况和医疗问题:协商控制性病————1946年《萨斯喀彻温省性病保护法》。
Pub Date : 2004-01-01
Lindsay M Ferguson

The author examines Saskatchewan legislation that regulated venereal disease. Although venereal disease legislation was introduced in Saskatchewan in 1919, the centrepiece of this article is The Venereal Disease Prevention Act, 1946. In an attempt to understand the nuances of and underlying rationale for these laws, the author situates the legislation within its social context. The author demonstrates that the trends and contradictions apparent in society's approach to the regulation of venereal disease were reflected in the legislation. The concept of a continuum is used to illustrate the coexistence of two approaches to the control of venereal disease. On one side of the continuum, venereal disease was a moral problem and a taboo subject. Force was the key to controlling venereal disease; involuntary examinations and intrusions into people's personal lives were the solution. On the other side of the continuum, venereal disease was a medical problem. If approached rationally and openly, control of venereal disease was possible; through education and social acceptance of venereal disease as just another illness, people would voluntarily come forward for treatment. The approaches represented at the extreme ends of the continuum did not exist in isolation; these views existed simultaneously, producing contradictory and colourful rhetoric.

作者审查了萨斯喀彻温省管制性病的立法。虽然性病立法于1919年在萨斯喀彻温省出台,但本文的核心是1946年的《性病防治法》。为了理解这些法律的细微差别和基本原理,作者将立法置于其社会背景中。作者认为,立法反映了社会对性病管制的倾向和矛盾。连续体的概念被用来说明控制性病的两种方法的共存。一方面,性病是一个道德问题和禁忌话题。武力是控制性病的关键;非自愿的检查和侵入人们的个人生活是解决办法。另一方面,性病是一个医学问题。如果理性、公开地对待,性病的控制是可能的;通过教育和社会接受性病作为另一种疾病,人们会自愿站出来接受治疗。在连续体的极端两端所代表的方法不是孤立存在的;这些观点同时存在,产生了相互矛盾和丰富多彩的修辞。
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引用次数: 0
Canada's Assisted Human Reproductive Act: is it scientific censorship, or a reasoned approach to the regulation of rapidly emerging reproductive technologies? 加拿大的《辅助人类生殖法》:是科学审查,还是对迅速兴起的生殖技术进行合理监管?
Pub Date : 2004-01-01
Colin Rasmussen

After more than a decade of study, discussion and debate, the Canadian House of Commons and Senate have approved the Assisted Human Reproduction Act. Building on the earlier Bill C-47, which died on the order paper in 1997, the Act bans human cloning for reproductive or therapeutic purposes, payment for surrogacy arrangements, and trading in human reproductive materials or their use without informed consent. In addition, the Act significantly restricts research using human reproductive materials. This article compares the Act to legislative regimes in other nations with advanced human reproductive science. It concludes that while the Act has many laudable goals, it is flawed in that it tries to cover too much legislative ground. As a result it unreasonable impairs the ability of Canadian scientists to compete in areas such as stem cell research, and area that is expected to yield significant new approaches to treating human disease.

经过十多年的研究、讨论和辩论,加拿大参众两院通过了《辅助人类生殖法》。该法案建立在早前的C-47法案的基础上,该法案禁止以生殖或治疗为目的克隆人类,禁止为代孕安排支付费用,禁止买卖人类生殖材料或未经知情同意使用这些材料。此外,该法案还对使用人类生殖材料的研究进行了严格限制。本文将该法与其他生殖科学发达国家的立法制度进行了比较。它的结论是,尽管该法案有许多值得称赞的目标,但它存在缺陷,因为它试图涵盖太多的立法领域。因此,它不合理地损害了加拿大科学家在干细胞研究等领域的竞争能力,这些领域有望产生治疗人类疾病的重要新方法。
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引用次数: 0
Sustainability and the balancing of the health care and innovation agendas: the commercialization of genetic research. 卫生保健和创新议程的可持续性和平衡:基因研究的商业化。
Pub Date : 2003-01-01
Timothy Caulfield
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引用次数: 0
Misusing informed consent: a critique of limitations on research subjects' access to genetic research results. 滥用知情同意:对研究对象获取基因研究结果的限制的批评。
Pub Date : 2000-01-01
T M Banks

Express denials of access to genetic research results are being drafted into consent instruments. Some commentators suggest that the principle of beneficence can justify such a denial of access. This paper provides an ethical and legal critique of the use of consent instruments to disclaim responsibility for on-going disclosure by genetic researchers. Currently, the law of torts provides only weak protection for on-going disclosure for research subjects. The most substantive rights are to be found in the law of fiduciary obligations. The author concludes that, notwithstanding arguments to the contrary, there should be a presumption of disclosure in genetic research, unless the research subject elects otherwise. The author outlines one possible exception to this general presumption.

明确拒绝获得基因研究结果的做法正在被起草成同意文书。一些评论家认为,慈善原则可以为这种拒绝进入辩护。这篇论文提供了一个伦理和法律上的批评,使用同意文书来否认责任的基因研究人员正在进行的披露。目前,侵权行为法对研究对象的持续披露保护不力。最实质性的权利体现在信义义务法中。作者的结论是,尽管有相反的论点,但在基因研究中应该有披露的假设,除非研究对象另有选择。作者概述了这种普遍假设的一个可能的例外。
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引用次数: 0
An examination of Saskatchewan law on the sterilization of persons with mental disabilities. 审查萨斯喀彻温省关于精神残疾者绝育的法律。
Pub Date : 1999-01-01
D Newman
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引用次数: 0
Pregnant embodiment and women's autonomy rights in law: an analysis of the language and politics of Winnipeg Child and Family Services v. D.F.G. 怀孕的体现与妇女的法律自治权:温尼伯儿童与家庭服务诉D.F.G.案的语言与政治分析
Pub Date : 1999-01-01
M Randall
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引用次数: 0
Dobson v. Dobson: tort liability for expectant mothers? 多布森诉多布森:孕妇的侵权责任?
Pub Date : 1998-01-01
T Foley
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引用次数: 0
Redefining the moment of death: implications on sustaining life. 重新定义死亡时刻:维持生命的意义。
Pub Date : 1983-01-01
M J Rotnem
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引用次数: 0
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Saskatchewan law review
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