[Between Huxley and Orwell: Big Data and Health].

Autor: Álvarez Díaz JA; Universidad Autónoma Metropolitana Unidad Xochimilco, México, bioetica_reproductiva@hotmail.com., Duro EA; Facultad de Ciencias de la Salud, Universidad de Morón, Argentina, eaduro@hotmail.com., Gubert IC; Comité de Ética en Investigación, Universidad Federal de Paraná, Brasil, gubertida@gmail.com., de Martínez CAC; Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Chile, carmen_aliciademartinez@yahoo.co.uk., Sotomayor MA; Comité de Ética, Universidad de Santiago de Chile, Chile, masotomay@gmail.com., López L; Facultad de Ciencias Médicas, Universidad de San Carlos de Guatemala, Guatemala, ensayos.clinicos@gmail.com., Duro A; Instituto Tecnológico y de Estudios Superiores de Monterrey, Argentina, alejandroduro@yahoo.com.ar., Moya RN; Facultad de Medicina, Universidad de Chile, Facultad de Salud y Odontología, Universidad Diego Portales, Chile, rninomoya@hotmail.com., Sorokin P; Facultad de Medicina, Universidad de Buenos Aires, Argentina, patriciasorokin@gmail.com.
Jazyk: Spanish; Castilian
Zdroj: Revista latina de sociologia [Rev Lat Sociol] 2018; Vol. 8 (2), pp. 23-33. Date of Electronic Publication: 2018 Oct 23.
DOI: 10.17979/relaso.2018.8.2.2951
Abstrakt: When in 1966 the United Nations stated in its International Covenant on Civil and Political Rights, the ideal of a free human being with respect to his privacy through the prohibition of arbitrary interference in his private life, it was not possible to imagine the impact of global unlimited connectivity, autonomy of new information technologies, the development of huge interconnected databases, the independent and unrestricted circulation of data, which have led to ethical and legal questions arising from this to treat personal and health data.
Databáze: MEDLINE