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Public, Experts, and Acceptance of Advanced Medical Technologies: The Case of Organ Transplant and Gene Therapy in Japan

机译:公众,专家和先进医学技术的接受:日本的器官移植和基因治疗案例

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In 1997, after long social debates, the Japanese government enacted a law on organ transplantation from brain-dead bodies. Since 1993, on gene therapy, administrative agencies have issued a series of guidelines. This study seeks to elucidate when people became aware of the issues and when they formed their opinions on organ transplant and gene therapy. At the same time, it aims to examine at which point in time experts, those in university ethical committees and in academic societies, consider these technologies became accepted among the public. A self-administered questionnaire was sent by mail to a stratified random sampling of 3000 people nationwide in Japan. Another questionnaire was sent both to the member societies of the Japanese Association of Medical Sciences and to the ethical committees of all the medical schools in Japan. Results of the surveys indicated that many of the public remained undecided on the desirability of organ transplant or gene therapy at the time of enactment of official guidelines. A substantial part of them formed their opinions in subsequent periods, especially around the time of first implementation and thereafter. Experts of the academic societies and of the university ethical committees regarded the time of implementation as an important factor in the acceptance of the technologies in society. Since many people formed their opinion during the period of technological implementation, communications efforts to facilitate public understanding of science and technology, as well as to advance practical discussion on policy alternatives in this period can play a key role in determining the fate of technological innovation and ethical debates in medicine.
机译:在经过长时间的社会辩论之后,日本政府于1997年颁布了一项有关从脑死者尸体进行器官移植的法律。自1993年以来,关于基因疗法的问题,行政机构发布了一系列指导方针。本研究旨在阐明人们何时意识到这些问题以及何时对器官移植和基因治疗形成自己的见解。同时,它旨在研究专家,大学道德委员会和学术团体中的专家在何时认为这些技术已为公众所接受。自行寄出的问卷通过邮件发送到日本全国3000人的分层随机抽样中。另一份调查表发送给了日本医学学会的会员协会和日本所有医学院校的伦理委员会。调查结果表明,在制定官方指南时,许多公众仍不确定是否需要器官移植或基因治疗。他们中的很大一部分在随后的时期,尤其是在第一次实施之时及其之后,发表了自己的意见。学术协会和大学伦理委员会的专家认为,实施时间是社会上接受技术的重要因素。由于许多人在技术实施期间形成了自己的意见,因此在这一时期,人们为促进公众对科学和技术的理解以及进行有关政策选择的实际讨论而进行的交流努力,对于决定技术创新和创新的命运起着关键作用。医学中的伦理辩论。

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