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生物样本库建设中保护与共享的伦理纠结 被引量:10

Ethics Struggle of Protection and Sharing in the Construction of Biobank
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摘要 当前我国样本库的发展尚处于起步阶段,存在诸多问题,如缺乏科学管理和共享机制、转化应用不够、持续发展乏力等。通过分析建设生物样本库的伦理挑战引出生物样本来源的权益保护诉求,如样本来源的知情同意、样本管理的隐私保护问题;要实现样本库建设的保护与共享之间的平衡,就要提高隐私保护意识、采取有效的隐私保护手段、充分考虑和预见技术高速发展后的伦理问题。最后指出在成果转化中要体现公益性原则、成果分配的公平性原则、权衡预判性原则。 At present,the development of biobank in China is still at the initial stage,and there are many problems,such as lack of scientific management and sharing mechanism,insufficient application of transformation and weak sustainable development.Through constructing the ethical challenge of biobank,the author draw out the rights protection claims of biological sample sources,such as the informed consent of samples source and the privacy protection of samples management.In order to achieve the balance between the protection and sharing of biobank construction,we should improve the awareness of privacy protection,take effective means of privacy protection and fully consider and foresee ethical issues after rapid development of technology.Finally,it is pointed out that the principle of public welfare,the principle of fairness in the distribution of results and the predictive principle should be reflected in the transformation of results.
作者 张秋菊 蒋辉 ZHANG Qiuju;JIANG Hui(Department of Military Ethics,School of Basic Medical Sciences,Air Force Military Medical University,Xi’an 710032,China;Department of Science and Education,ZhangzhouAffiliated Hospital of Fujian Medical University,Zhangzhou 363000,China)
出处 《中国医学伦理学》 2019年第3期335-339,共5页 Chinese Medical Ethics
关键词 知情同意 隐私保护 公益性 公平性 权衡预判 Informed Consent Privacy Protection Public Welfare Fairness Predictive Principle
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  • 1赵晓航,钱阳明.生物样本库——个体化医学的基础[J].转化医学杂志,2014,3(2):69-73. 被引量:23
  • 2戴二黑,李京湘,杜宗敏,吴清发,王效义,杨玲,刘海洪,庞昕,韩延平,翟俊辉,江凌晓,陈泽良,邱茂锋,王津,王宏霞,郭兆彪,汪建,杨瑞馥.逆转录套式PCR检测粪便样本中的SARS冠状病毒[J].微生物学免疫学进展,2004,32(4):22-25. 被引量:2
  • 3OECD. guidelines on the protection of privacy and transborder flows of personal data[M].{H}Paris:OECD,1980.
  • 4Tim Benson. Principles of Health Interoperability HL7 and SNOMED[M].{H}London:Springer,2012.9-14.
  • 5De Souza Y G, Greenspan J S. Biobanking past, present and future: responsibilities and benefits. AIDS, 2013, 27(3): 303-312.
  • 6Hirschberg I, Kahrass H, Strech D. International requirements for consent in biobank research: qualitative review of research guidelines. JMed Genet, 2014, 51(12): 773-781.
  • 7Masca N, Burton P R, Sheehan N A. Participant identification in genetic association studies: improved methods and practical implications. IntJEpidemiol, 2011, 40(6): 1629-1642.
  • 8Ramstein G P, Lipka A E, Lu F, et al. Genome-wide association study based on multiple imputation with low-depth sequencing data: application to biofuel traits in reed canarygrass. G3 (Bethesda). 2015, 5(5): 891-909.
  • 9Wright G E, Koornhof P G, Adeyemo A A, et al. Ethical and legal implications of whole genome and whole exome sequencing in African populations. BMC Med Ethics, 2013, 14: 21.
  • 10Foster M W, Sharp R R. Ethical issues in medical-sequencing research: implications of genotype-phenotype studies for individuals and populations. Hum Mol Genet, 2006, 15(Suppl 1): 45-49.

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