Shaping the future e-patient: The citizen-patient in public discourse on e-health
暂无分享,去创建一个
[1] Carl May,et al. Remote Doctors and Absent Patients: Acting at a Distance in Telemedicine? , 2003 .
[2] S. Timmermanns,et al. The Challenge of Evidence-Based Medicine and Standardization in Health Care , 2003 .
[3] A. Webster. Health, Technology and Society , 2007 .
[4] N. Stehr. Arbeit, Eigentum und Wissen : zur Theorie von Wissensgesellschaften , 1994 .
[5] U. Felt,et al. Coming to Terms with Biomedical Technologies in Different Technopolitical Cultures: A Comparative Analysis of Focus Groups on Organ Transplantation and Genetic Testing in Austria, France, and the Netherlands , 2010 .
[6] G. Bowker,et al. The multiple bodies of the medical record : Toward a sociology of an artifact , 1996 .
[7] John Law,et al. Notes on the theory of the actor-network: Ordering, strategy, and heterogeneity , 1992 .
[8] N. Oudshoorn. The Male Pill: A Biography of a Technology in the Making , 2003 .
[9] Sarah Nettleton,et al. The Emergence of E-Scaped Medicine? , 2004 .
[10] S. Jasanoff. States of Knowledge: The Co-production of Science and the Social Order , 2004 .
[11] A. Webster. Health, technology and society : a sociological critique , 2007 .
[12] Carl May,et al. Towards a wireless patient: chronic illness, scarce care and technological innovation in the United Kingdom. , 2005, Social science & medicine.
[13] D. Lupton. Consumerism, reflexivity and the medical encounter. , 1997, Social science & medicine.
[14] Lisa Cartwright,et al. Reach Out and Heal Someone: Telemedicine and the Globalization of Health Care , 2000 .
[15] A. Mol. The Body Multiple: Ontology in Medical Practice , 2003 .
[16] Peter Neil Temple Wells,et al. Digital healthcare: the impact of information and communication technologies on health and healthcare , 2006 .
[17] A. Strauss,et al. Basics of qualitative research: Grounded theory procedures and techniques. , 1993 .
[18] Ulrike Felt,et al. Refusing the information paradigm: informed consent, medical research, and patient participation , 2009, Health.
[19] Alex Broom,et al. Medical specialists’ accounts of the impact of the Internet on the doctor/patient relationship , 2005, Health.
[20] Sambit Mallick,et al. Designs on Nature: Science and Democracy in Europe and the United States , 2009 .
[21] Joseph A. Diaz,et al. Patients’ use of the internet for medical information , 2002, Journal of General Internal Medicine.
[22] M. Hardey. Doctor in the house: the Internet as a source of lay health knowledge and the challenge to expertise , 1999 .
[23] N. Oudshoorn,et al. Constructing the digital patient: Patient organizations and the development of health websites , 2006 .
[24] Julia Cartwright,et al. New Medical Technologies and Society - Reordering Life , 2005 .
[25] Lee Rainie,et al. The online health care revolution: how the web helps americans take better care of themselves , 2000 .
[26] Ulrike Felt,et al. The Bottom-up Meanings of the Concept of Public Participation in Science and Technology , 2008 .
[27] G. Eysenbach,et al. The Impact of CyberHealthcare on the Physician–Patient Relationship , 2003, Journal of Medical Systems.
[28] S. Wyatt,et al. 'Ignorance is bliss sometimes': constraints on the emergence of the 'informed patient' in the changing landscapes of health information. , 2003, Sociology of health & illness.
[29] A. Strauss,et al. Basics of qualitative research: Grounded theory procedures and techniques. , 1992 .
[30] M. Lo. The Gold Standard: The Challenge of Evidence‐Based Medicine and Standardization in Health Care. By Stefan Timmermans and Marc Berg. Philadelphia: Temple University Press, 2003. Pp. ix+269. $62.50 (cloth); $20.95 (paper). , 2004 .
[31] K N Lohr,et al. Health policy issues and applications for evidence-based medicine and clinical practice guidelines. , 1998, Health policy.
[32] Flis Henwood,et al. The digital divide, health information and everyday life , 2005, New Media Soc..