Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-vfjqv Total loading time: 0 Render date: 2024-04-26T01:02:28.631Z Has data issue: false hasContentIssue false

References

Published online by Cambridge University Press:  18 December 2015

Kenneth W. Goodman
Affiliation:
University of Miami
Get access

Summary

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Chapter
Information
Ethics, Medicine, and Information Technology
Intelligent Machines and the Transformation of Health Care
, pp. 160 - 181
Publisher: Cambridge University Press
Print publication year: 2016

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abaidoo, B., Larweh, B.T. 2014. Consumer health informatics: The application of ICT in improving patient-provider partnership for a better health care. Online Journal of Public Health Informatics 16;6(2):e188. doi: 10.5210/ojphi.v6i2.4903.Google ScholarPubMed
Abelson, R., Creswell, J. 2015. Data breach at anthem may lead to others. The New York Times, February 6, available at www.nytimes.com/2015/02/07/business/data-breach-at-anthem-may-lead-to-others.html?_r=0.Google Scholar
AHIMA. 2009. Auditing copy and paste. Journal of AHIMA 80(1):26–9.Google Scholar
Al-Awqati, Q. 2006. How to write a case report: lessons from 1600 B.C. Kidney International 69(12):2113–4.CrossRefGoogle ScholarPubMed
Allen, A. 1988. Uneasy Access: Privacy for Women in a Free Society. Totowa, NJ: Rowman & Littlefield.Google Scholar
Alpert, S. 1993. Smart cards, smarter policy: medical records, privacy, and health care reform. Hastings Center Report 23(6):1323.CrossRefGoogle ScholarPubMed
Alpert, S. 1995. Privacy and intelligent highways: finding the right of way. Santa Clara Computer & High Technology Law Journal 11(1):97118.Google Scholar
Alpert, S. 1998. Health care information: access, confidentiality, and good practice. In Goodman, K.W., ed., Ethics, Computing and Medicine: Informatics and the Transformation of Health Care. Cambridge: Cambridge University Press, 75101.Google Scholar
Amber, K.T., Dhiman, G., Goodman, K.W. 2014. Conflict of interest in online point-of-care clinical support websites. Journal of Medical Ethics 40(8):578–80.CrossRefGoogle ScholarPubMed
American Medical Association. 1910 [copyright and publication date uncertain]. Nostrums and Quackery: articles on the nostrum evil and quackery reprinted from The Journal of the American Medical Association. Chicago: American Medical Association, available at https://archive.org/details/nostrumsquackery00amerrich.Google Scholar
American Medical Association. 2014. Improving Care: Priorities to Improve Electronic Health Record Usability. Chicago: American Medical Association, available at https://download.ama-assn.org/resources/doc/ps2/x-pub/ehr-priorities.pdf.Google Scholar
Anderson, M., Anderson, S.L., eds. 2011. Machine Ethics. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Anderson, J.G., Aydin, C.E. 1994. Overview: theoretical perspectives and methodologies for the evaluation of health care information systems. In Anderson, J.G., Aydin, C.E., Jay, S.J., eds., Evaluating Health Care Information Systems: Methods and Applications. Thousand Oaks, CA: Sage, 346–54.Google Scholar
Anderson, J.G., Aydin, C.E. 1998. Evaluating medical information systems: social contexts and ethical challenges. In Goodman, K.W., ed., Ethics, Computing, and Medicine: Informatics and the Transformation of Health Care. Cambridge: Cambridge University Press, 5774.Google Scholar
Anderson, J.G., Goodman, K.W. 2002. Ethics and Informatics: A Case-Study Approach to a Health System in Transition. New York: Springer.Google Scholar
Angst, C.M. 2009. Protect my privacy or support the common-good? Ethical questions about electronic health information exchanges. Journal of Business Ethics 90:169–78.CrossRefGoogle Scholar
Asimov, I. 1950. I, Robot. Greenwich, CT.: Fawcett Crest.Google Scholar
Atherton, H., Sawmynaden, P., Sheikh, A., Majeed, A., Car, J. 2012. Email for clinical communication between patients/caregivers and healthcare professionals. Cochrane Database of Systematic Reviews, November 14, 2011:CD007978, available at http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD007978.pub2/abstract.CrossRefGoogle Scholar
Atreya, R.V., Smith, J.C., McCoy, A.B., Malin, B., Miller, R.A. 2013. Reducing patient re-identification risk for laboratory results within research datasets. Journal of the American Medical Informatics Association 20(1):95101.CrossRefGoogle ScholarPubMed
Augestad, K.M., Berntsen, G., Lassen, K., Bellika, J.G., Wootton, R., Lindsetmo, R.O., Study Group of Research Quality in Medical Informatics and Decision Support (SQUID). 2012. Standards for reporting randomized controlled trials in medical informatics: a systematic review of CONSORT adherence in RCTs on clinical decision support. Journal of the American Medical Informatics Association 19(1):1321.CrossRefGoogle ScholarPubMed
Baily, M.A. 2008. Harming through protection? New England Journal of Medicine 358(8):768–9.CrossRefGoogle ScholarPubMed
Baker, L., Wagner, T.H., Singer, S., Bundorf, M.K. 2003. Use of the Internet and e-mail for health care information: results from a national survey. Journal of the American Medical Association 289(18):2400–6.Google ScholarPubMed
Baldwin, T.T., Magjuka, R.J., Loher, B.T. 1991. The perils of participation: effects of choice of training on trainee motivation and learning. Personnel Psychology 44(1):5165.CrossRefGoogle Scholar
Baptista, P.V. 2014. Nanodiagnostics: leaving the research lab to enter the clinics? Diagnosis 1(1):305–9.CrossRefGoogle ScholarPubMed
Barocas, S., Nissenbaum, H. 2014. Big Data’s end run around anonymity and consent. In Lane, J., Stodden, V., Bender, S., Nissenbaum, H., eds., Privacy, Big Data, and the Public Good. New York: Cambridge University Press, 4475.CrossRefGoogle Scholar
Baron, J. 1998. Judgment Misguided: Intuition and Error in Public Decision Making. New York: Oxford University Press.CrossRefGoogle Scholar
Bastani, A., Shaqiri, B., Palomba, K., Bananno, D., Anderson, W. 2014. An ED scribe program is able to improve throughput time and patient satisfaction. American Journal of Emergency Medicine 32(5):399402.CrossRefGoogle Scholar
Bates, D.W., Bitton, A. 2010. The future of health information technology in the patient-centered medical home. Health Affairs 29(4):614–21.CrossRefGoogle ScholarPubMed
Bayer, R., Fairchild, A. 2002. The limits of privacy: surveillance and the control of disease. Health Care Analysis 10:1935.CrossRefGoogle ScholarPubMed
Bayer, R., Santelli, J., Klitzman, R. 2015. New challenges for electronic health records: confidentiality and access to sensitive health information about parents and adolescents. Journal of the American Medical Association 313(1):2930.CrossRefGoogle ScholarPubMed
Beauchamp, T.L., Childress, J.F. 2012. Principles of Biomedical Ethics. 7th edn. Oxford: Oxford University Press.Google Scholar
Beck, F., Richard, J.-B., Nguyen-Thanh, V., Montagni, I., Parizot, I., Renahy, E. 2014. Use of the Internet as a health information resource among French young adults: results from a nationally representative survey. Journal of Medical Internet Research 16(5):e128.CrossRefGoogle ScholarPubMed
Bellow, S. 1977. To Jerusalem and Back: A Personal Account. New York: Avon.Google Scholar
Benitez, K., Malin, B. 2010. Evaluating re-identification risks with respect to the HIPAA privacy rule. Journal of the American Medical Informatics Association 17:169–77.CrossRefGoogle Scholar
Beratarrechea, A., Lee, A.G., Willner, J.M., Jahangir, E., Ciapponi, A., Rubinstein, A. 2014. The impact of mobile health interventions on chronic disease outcomes in developing countries: a systematic review. Telemedicine Journal and E-Health 20(1):7582.CrossRefGoogle ScholarPubMed
Bernat, J.L. 2013. Ethical and quality pitfalls in electronic health records. Neurology 80(11):1057–61.CrossRefGoogle ScholarPubMed
Berner, E.S. 2002. Ethical and legal issues in the use of clinical decision support systems. Journal of Healthcare Information Management 16(4):34–7.Google ScholarPubMed
Berner, E.S., ed. 2007. Clinical Decision Support Systems: Theory and Practice. 2nd edn. New York: Springer.CrossRefGoogle Scholar
Berner, E.S. 2014.What can be done to increase the use of diagnostic decision support systems? Diagnosis 1(1):119–23.CrossRefGoogle ScholarPubMed
Berner, E.S., Maisiak, R.S., Cobbs, C.G., Taunton, O.D. 1999. Effects of a decision support system on physicians’ diagnostic performance. Journal of the American Medical Informatics Association 6:420–7.CrossRefGoogle ScholarPubMed
Berner, E.S., Webster, G.D., Shugerman, A.A., Jackson, J.R., Algina, J., Baker, A.L. 1994. Performance of four computer-based diagnostic systems. New England Journal of Medicine 330:1792–6.CrossRefGoogle ScholarPubMed
Bhatia, H.L., Patel, N.R., Choma, N.N., Grande, J., Giuse, D.A., Lehmann, C.U. 2015. Code status and resuscitation options in the electronic health record. Resuscitation 87:1420CrossRefGoogle ScholarPubMed
Bhatt, A. 2010. Evolution of Clinical Research: A history before and beyond James Lind. Perspectives in Clinical Research 1(1):610.CrossRefGoogle ScholarPubMed
Bilimoria, N.M. 2009. HIPAA Privacy/Security Rules: where we’ve been and where we are going. Updates from the HITECH Act to dramatically impact HIPAA privacy/security. Journal of Medical Practice Management 25(3):149–52.Google ScholarPubMed
BMJ. 1998. The hippocratic oath (editorial). BMJ 317:1110.Google Scholar
BMJ. 2001. Medical oaths and declarations (editorial). BMJ 323:1440.CrossRefGoogle Scholar
BMJ. 2009. Surgical training using simulation (editorial). BMJ 338:b1001.CrossRefGoogle Scholar
Boguski, M.S., Mandl, K.D., Sukhatme, V.P. 2009. Repurposing with a difference. Science 324(5933):1394–5.CrossRefGoogle ScholarPubMed
Bok, S. 1983. Secrets: On the Ethics of Concealment and Revelation. New York: Vintage Books/Random House.Google Scholar
Borenstein, J., Pearson, Y. 2012. Robot caregivers: Ethical issues across the human lifespan. In Abney, K., Bekey, G.A., eds., Robot Ethics: The Ethical and Social Implications of Robots. Cambridge, MA: MIT Press, 251–65.Google Scholar
Boudreaux, E.D., Waring, M.E., Hayes, R.B., Sadasivam, R.S., Mullen, S., Pagoto, S. 2014. Evaluating and selecting mobile health apps: strategies for healthcare providers and healthcare organizations. Translational Behavioral Medicine 4(4):363–71.CrossRefGoogle ScholarPubMed
Bower, J.L., Christensen, C.M. 1995. Disruptive technologies: catching the wave. Harvard Business Review 73(1):4353.Google Scholar
Boyd, J.E., Adler, E.P., Otilingam, P.G., Peters, T. 2014. Internalized Stigma of Mental Illness (ISMI) scale: a multinational review. Comprehensive Psychiatry 55(1):221–31.CrossRefGoogle Scholar
Brady, K., Shariff, A. 2013. Virtual medical scribes: making electronic medical records work for you. Journal of Medical Practice Management 29(2):133–6.Google ScholarPubMed
Bredillet, C.N. 2003. Genesis and role of standards: theoretical foundations and socio-economical model for the construction and use of standards. International Journal of Project Management 21(6):463–70.CrossRefGoogle Scholar
Brennan, P.F., Downs, S., Casper, G. 2010. Project Health Design: rethinking the power and potential of personal health records. Journal of Biomedical Informatics 43(5 Suppl):S3-5.CrossRefGoogle ScholarPubMed
Brody, B.A. 1989. The ethics of using ICU scoring systems in individual patient management. Problems in Critical Care 3:662–70.Google Scholar
Brooks, F.P. 1995. The Mythical Man-Month: Essays on Software Engineering Anniversary Edition. Boston: Addison-Wesley.Google Scholar
Brown, J., Ryan, C., Harris, A. 2014. How doctors view and use social media: a national survey. Journal of Medical Internet Research 16(12):e267.CrossRefGoogle ScholarPubMed
Brownstein, J.S., Freifeld, C.C., Madoff, L.C. 2009. Digital disease detection – harnessing the Web for public health surveillance. New England Journal of Medicine 360(21):2153–7.CrossRefGoogle ScholarPubMed
Bryant, A.D., Fletcher, G.S., Payne, T.H. 2014. Drug interaction alert override rates in the Meaningful Use era: no evidence of progress. Applied Clinical Informatics 5(3):802–13.CrossRefGoogle ScholarPubMed
Bulaj, Z.J., Phillips, J.D., Ajioka, R.S., Franklin, M.R., Griffen, L.M., Guinee, D.J., Edwards, C.Q., Kushner, J.P. 2000. Hemochromatosis genes and other factors contributing to the pathogenesis of porphyria cutanea tarda. Blood 95:1565–71.CrossRefGoogle Scholar
Bundorf, M.K., Wagner, T.H., Singer, S.J., Baker, L.C. 2006. Who searches the internet for health information? Health Services Research 41(3 Pt. 1):819–36.CrossRefGoogle ScholarPubMed
Carrión Señor, I., Fernández-Alemán, J.L., Toval, A. 2012. Are personal health records safe? A review of free web-accessible personal health record privacy policies. Journal of Medical Internet Research 14(4):e114.CrossRefGoogle Scholar
CBC. 2011. Online health advice sought by more Canadians, available at www.cbc.ca/news/online-health-advice-sought-by-more-canadians-1.982301.Google Scholar
Chakma, J., Sun, G.H., Steinberg, J.D., Sammut, S.M., Jagsi, R. 2014. Asia’s ascent – global trends in biomedical R&D expenditures. New England Journal of Medicine 370(1):36.CrossRefGoogle ScholarPubMed
Chalmers, I., Clarke, M. 2004. Commentary: the 1944 patulin trial: the first properly controlled multicentre trial conducted under the aegis of the British Medical Research Council. International Journal of Epidemiology 33(2):253–60.CrossRefGoogle ScholarPubMed
Cho, I., Park, H., Choi, Y.J., Hwang, M.H., Bates, D.W. 2014. Understanding the nature of medication errors in an ICU with a computerized physician order entry system. PLoS One 9(12):e114243.CrossRefGoogle Scholar
Christensen, C.M. 1997 The Innovator’s Dilemma: When New Technologies Cause Great Firms to Fail. Boston: Harvard Business School Press.Google Scholar
Clark, P.A., Capuzzi, K., Harrison, J. 2010. Telemedicine: Medical, legal and ethical perspectives. Medical Science Monitor 16(12): RA26172.Google ScholarPubMed
Clendening, L. 1942. Source Book of Medical History. New York: Dover.Google Scholar
Cleveringa, F.G., Gorter, K.J., van den Donk, M., van Gijsel, J., Rutten, G.E. 2013. Computerized decision support systems in primary care for type 2 diabetes patients only improve patients’ outcomes when combined with feedback on performance and case management: a systematic review. Diabetes Technology & Therapeutics 15(2):180–92.CrossRefGoogle ScholarPubMed
Cline, R.J.W., Haynes, K.M. 2001. Consumer health information seeking on the Internet: the state of the art. Health Education Research 16(6):671–92.CrossRefGoogle ScholarPubMed
Cochrane, A.L. 1979. 1931–1971: a critical review, with particular reference to the medical profession. In Medicines for the year 2000. London: Office of Health Economics, 111.Google Scholar
Coeckelbergh, M. 2010. Health care, capabilities, and AI assistive technologies. Ethical Theory and Moral Practice 13(2):181–90.CrossRefGoogle Scholar
Cohen, D. 2013. Devices and desires: industry fights toughening of medical device regulation in Europe. BMJ 347:f6204.CrossRefGoogle ScholarPubMed
Cohn, J. 2013. The robot will see you now. The Atlantic, March, available at www.theatlantic.com/magazine/archive/2013/03/the-robot-will-see-you-now/309216/.Google Scholar
Collier, R. 2009. Legumes, lemons and streptomycin: a short history of the clinical trial. Canadian Medical Association Journal 180(1):23–4.CrossRefGoogle Scholar
Collins, G.S., Reitsma, J.B., Altman, D.G., Moons, K.G.M. 2015. Transparent Reporting of a multivariable prediction model for Individual Prognosis Or Diagnosis (TRIPOD): The TRIPOD Statement. Annals of Internal Medicine 162(1)5563.CrossRefGoogle ScholarPubMed
Collins, F.S., Tabak, L.A. 2014. Policy: NIH plans to enhance reproducibility. Nature 505:612–3.CrossRefGoogle ScholarPubMed
Collste, G., ed. 2000. Ethics in the Age of Information Technology. Studies in Applied Ethics 7. Linköping: Centre for Applied Ethics.Google Scholar
Cook, R.I. 2012. Dissenting statement: Health IT is a Class III medical device. In Institute of Medicine. Health IT and Patient Safety: Building Safer Systems for Better Care. Washington, DC: The National Academies Press, 193–7.Google Scholar
Cook, D.A., Hatala, R., Brydges, R., Zendejas, B., Szostek, J.H., Wang, A.T., Erwin, P.J., Hamstra, S.J. 2011. Technology-enhanced simulation for health professions education: a systematic review and meta-analysis. Journal of the American Medical Association 306(9):978–88.Google ScholarPubMed
Coorevits, P., Sundgren, M., Klein, G.O., Bahr, A., Claerhout, B., Daniel, C., Dugas, M., Dupont, D., Schmidt, A., Singleton, P., De Moor, G., Kalra, D. 2013. Electronic health records: new opportunities for clinical research. Journal of Internal Medicine 274(6):547–60.CrossRefGoogle ScholarPubMed
Cornet, G. 2013. Robot companions and ethics: a pragmatic approach of ethical design. Journal international de bioéthique 24(4):4958, 179–80.Google ScholarPubMed
Council of Europe. 1981. Convention for the Protection of Individuals with regard to Automatic Processing of Personal Data. Strasbourg: Council of Europe, available at http://conventions.coe.int/Treaty/en/Treaties/Html/108.htm.Google Scholar
Curtis, L.H., Brown, J., Platt, R. 2014. Four health data networks illustrate the potential for a shared national multipurpose big-data network. Health Affairs 33(7):1178–86CrossRefGoogle ScholarPubMed
Cushman, R., Froomkin, A.M., Cava, A., Abril, P., Goodman, K.W. 2010. Ethical, legal and social issues for personal health records and applications. Journal of Biomedical Informatics 43(5 Suppl):S515.CrossRefGoogle ScholarPubMed
Datteri, E. 2013. Predicting the long-term effects of human-robot interaction: a reflection on responsibility in medical robotics. Science & Engineering Ethics 19(1):139–60.CrossRefGoogle ScholarPubMed
Dautenhahn, K. 2007. Socially intelligent robots: dimensions of human-robot interaction. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 362(1480):679704.CrossRefGoogle ScholarPubMed
David, P.A., Steinmueller, W.E. 1994. Economics of compatibility standards and competition in telecommunication networks. Information Economics and Policy 6(3–4):217–41.CrossRefGoogle Scholar
DeAngelis, C.D. 2014. The electronic health record: boon or bust for good patient care? The Milbank Quarterly 92(3):442–45.Google ScholarPubMed
de Dombal, F.T. 1987. Ethical considerations concerning computers in medicine in the 1980s. Journal of Medical Ethics 13:179–84.CrossRefGoogle Scholar
de Lusignan, S., Mold, F., Sheikh, A., Majeed, A., Wyatt, J.C., Quinn, T., Cavill, M., Gronlund, T.A., Franco, C., Chauhan, U., Blakey, H., Kataria, N., Barker, F., Ellis, B., Koczan, P., Arvanitis, T.N., McCarthy, M., Jones, S., Rafi, I. 2014. Patients’ online access to their electronic health records and linked online services: a systematic interpretative review. BMJ Open 4(9):e006021.CrossRefGoogle ScholarPubMed
De Ville, K.A. 1999. Managed care and the ethics of regulation. Journal of Medicine and Philosophy 24(5):492517.CrossRefGoogle ScholarPubMed
Devine, E.B., Lee, C.J., Overby, C.L., Abernethy, N., McCune, J., Smith, J.W., Tarczy-Hornoch, P. 2014. Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach. International Journal of Medical Informatics 83(7):473–83.CrossRefGoogle Scholar
Dhiman, G.J., Amber, K.T., Goodman, K.W. 2015. Comparative outcome studies of clinical decision support software: limitations to the practice of evidence-based system acquisition. Journal of the American Medical Informatics Association, February 8. pii:ocu033.Google Scholar
Diero, L., Rotich, J.K., Bii, J., Mamlin, B.W., Einterz, R.M., Kalamai, I.Z., Tierney, W.M. 2006. A computer-based medical record system and personal digital assistants to assess and follow patients with respiratory tract infections visiting a rural Kenyan health centre. BMC Biomedical Informatics and Decision Making 6:21.CrossRefGoogle ScholarPubMed
Dolinski, K., Chatr-aryamontri, S., Tyers, M. 2013. Systematic curation of protein and genetic interaction data for computable biology. BMC Biology 11:43.CrossRefGoogle ScholarPubMed
Donaldson, L. 2003. Expert patients usher in a new era of opportunity for the NHS. BMJ 326(7402):1279–80.CrossRefGoogle Scholar
Downar, J. 2009. Even without our biases, the outlook for prognostication is grim. Critical Care 13(4):168.CrossRefGoogle ScholarPubMed
Duda, R.O., Shortliffe, E.H. 1983. Expert systems research. Science 220:261–8.CrossRefGoogle ScholarPubMed
Duggan, M., Smith, A. 2013. Social Media Update 2013, available at www.pewinternet.org/files/2013/12/PIP_Social-Networking-2013.pdf.Google Scholar
Dziuda, D.M. 2010. Data Mining for Genomics and Proteomics: Analyses of Gene and Protein Expression Data. Hoboken, NJ: John Wiley & Sons.CrossRefGoogle Scholar
Eastwood, G.L. 2009. When relatives and friends ask physicians for medical advice: ethical, legal, and practical considerations. Journal of General Internal Medicine 24:1333–5.CrossRefGoogle ScholarPubMed
Eder, J., Gottweis, H., Zatloukal, K. 2012. IT solutions for privacy protection in biobanking. Public Health Genomics 15(5):254–62.CrossRefGoogle ScholarPubMed
Edworthy, J. 2013. Medical audible alarms: a review. Journal of the American Medical Informatics Association 20(3):584–9.CrossRefGoogle ScholarPubMed
Ellickson, P.L., Hawes-Dawson, J. 1989. An Assessment of Active Versus Passive Consent for Obtaining Parental Consent. Santa Monica, CA: RAND.Google ScholarPubMed
Elliott, J.E. 1978. Marx’s “Grundrisse”: vision of capitalism’s creative destruction. Journal of Post Keynesian Economics 1(2):148169.CrossRefGoogle Scholar
Ells, C., Thombs, B.D. 2014. The ethics of how to manage incidental findings. Canadian Medical Association Journal 186(9):655–6.CrossRefGoogle ScholarPubMed
Embi, P.J., Leonard, A.C. 2012. Evaluating alert fatigue over time to EHR-based clinical trial alerts: findings from a randomized controlled study. Journal of the American Medical Informatics Association 19:e145e148.CrossRefGoogle ScholarPubMed
Encinosa, W.E., Bae, J. 2015. Meaningful Use IT reduces hospital-caused adverse drug events even at challenged hospitals. Healthcare 3(1):1217.CrossRefGoogle ScholarPubMed
Engelhardt, H.T. 1985. Typologies of disease: Nosologies revisited. In Schaffner, K.F., ed., Logic of Discovery and Diagnosis in Medicine. Berkeley: University of California Press, 5671.CrossRefGoogle Scholar
Epstein, R.A. 1992. The path to “The T. J. Hooper”: The theory and history of custom in the law of tort. The Journal of Legal Studies 21(1):138.CrossRefGoogle Scholar
Esposito, K., Goodman, K.W. 2009. Genethics 2.0: Phenotypes, genotypes, and the challenge of databases generated by personal genome testing. The American Journal of Bioethics 9(6):1921.CrossRefGoogle ScholarPubMed
European Science Foundation. 2011. The European Code of Conduct for Research Integrity. Strasbourg: European Science Foundation, available at www.esf.org/fileadmin/Public_documents/Publications/Code_Conduct_ResearchIntegrity.pdf.Google Scholar
Evetts, J. 2013. Professionalism: Value and ideology. Current Sociology 61(5–6):778–96.CrossRefGoogle Scholar
Faden, R.R., Kass, N.E., Goodman, S.N., Pronovost, P., Tunis, S., Beauchamp, T.L. 2013. An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics. Hastings Center Report 43(S1):S16S27.CrossRefGoogle Scholar
Farmer, A.D., Bruckner Holt, C.E., Cook, M.J., Hearing, S.D. 2009. Social networking sites: a novel portal for communication. Postgraduate Medical Journal 85(1007):455–9.CrossRefGoogle Scholar
Farnan, J.M., Snyder Sulmasy, L., Worster, B.K., Chaudhry, H.J., Rhyne, J.A., Arora, V.M., for the American College of Physicians Ethics, Professionalism and Human Rights Committee. 2013. Online Medical Professionalism: Patient and public relationships: Policy statement from the American College of Physicians and the Federation of State Medical Boards. Annals of Internal Medicine 158(8):620–7.CrossRefGoogle ScholarPubMed
Farr, W. 1837. The Provincial medical and surgical association. British Annals of Medicine, Pharmacy, Vital Statistics and General Science 1:692–5.Google Scholar
Farra, R., Sheppard, N.F., McCabe, L., Neer, R.M., Anderson, J.M., Santini, J.T., Cima, M.J., Langer, R. 2012. First-in-human testing of a wirelessly controlled drug delivery microchip. Science Translational Medicine 4(122):122ra21.CrossRefGoogle ScholarPubMed
Federal Aviation Administration. 2011. Federal Aviation Administration Task Force on Air Carrier Safety and Pilot Training: Report from the Air Carrier Safety and Pilot Training Aviation Rulemaking Committee. Washington, DC: Federal Aviation Administration.Google Scholar
Feyerabend, P. 1975/1984. Against Method. London: Verso.Google Scholar
Flores, K.E., Quinlan, M.B. 2014. Ethnomedicine of menstruation in rural Dominica, West Indies. Journal of Ethnopharmacology 153(3):624–34.CrossRefGoogle ScholarPubMed
Floridi, L. 2013. The Ethics of Information. Oxford: Oxford University Press.CrossRefGoogle Scholar
Fortney, J.C., Burgess, J.F., Bosworth, H.B., Booth, B.M., Kaboli, P.J. 2011. A Re-conceptualization of access for 21st century healthcare. Journal of General Internal Medicine 26(Suppl 2):639–47.CrossRefGoogle ScholarPubMed
Foster, I. 2011. Building a secure learning health system. In Institute of Medicine, Digital Infrastructure for the Learning Health System: The Foundation for Continuous Improvement in Health and Health Care: Workshop Series Summary. Washington, DC: The National Academies Press, 161–4.Google Scholar
Fox, S. 2013. What ails America? Dr. Google can tell you. Pew Research Center, December 17, available at www.pewresearch.org/fact-tank/2013/12/17/what-ails-america-dr-google-can-tell-you/.Google Scholar
Fox, S., Duggan, M. 2013. Health Online 2013. Pew Research Center, Pew Internet & American Life Project, available at www.pewinternet.org/files/old-media/Files/Reports/PIP_HealthOnline.pdf.Google Scholar
French, R. 2003. Medicine before Science: The Business of Medicine from the Middle Ages to the Enlightenment. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Freshwater, D., Fisher, P., Walsh, E. 2013. Revisiting the Panopticon: professional regulation, surveillance and sousveillance. Nursing Inquiry, available at http://onlinelibrary.wiley.com/doi/10.1111/nin.12038/pdf.CrossRefGoogle Scholar
Fried, C. 1968. Privacy (a moral analysis). Yale Law Journal 77:475–93.Google Scholar
Friedberg, M.W., Chen, P.G., Van Busum, K.E., Aunon, F., Pham, C., Caloyeras, J., Mattke, S., Pitchforth, E., Quigley, D.D., Brook, R.H., Crosson, F.J., Tutty, M. 2013. Factors Affecting Physician Professional Satisfaction and Their Implications for Patient Care, Health Systems, and Health Policy. Rand Corporation Report RR-439-AMA, Santa Monica, CA: Rand Corporation., available at www.rand.org/pubs/research_reports/RR439.html.CrossRefGoogle Scholar
Friedman, C.P. 2009. A “Fundamental Theorem” of biomedical informatics. Journal of the American Medical Informatics Association 16(2):169–70.CrossRefGoogle Scholar
Friend, S.H., Schadt, E.E. 2014. Translational genomics. Clues from the resilient. Science 344(6187):970–2.CrossRefGoogle ScholarPubMed
Fukuyama, F. 2006. America at the Crossroads: Democracy, Power, and the Neoconservative Legacy. New Haven: Yale University Press.Google Scholar
Funnell, M.M. 2000. Helping patients take charge of their chronic illnesses. Family Practice Management 7(3):4751.Google ScholarPubMed
Galbraith, G.L. 2014. Practical and ethical considerations for using social media in community consultation and public disclosure activities. Academic Emergency Medicine 21(10):1151–7.CrossRefGoogle ScholarPubMed
Garg, A.X., Adhikari, N.J., McDonald, H., Rosas-Arellano, M.P., Devereaux, P.J., Beyene, J., Sam, J., Haynes, R.B. 2005. Effects of computerized clinical decision support systems on practitioner performance and patient outcomes: a systematic review. Journal of the American Medical Association 293(10):1223–38.Google ScholarPubMed
Gauchat, G. 2012. Politicization of science in the public sphere: A study of public trust in the United States, 1974 to 2010. American Sociological Review 77(2):167–87.CrossRefGoogle Scholar
Gavison, R. 1984. Privacy and the limits of the law. In Schoeman, F.D., ed., Philosophical Dimensions of Privacy: An Anthology. Cambridge: Cambridge University Press, 346402.CrossRefGoogle Scholar
Gellert, G.A., Ramirea, R., Webster, S.L. 2014. The rise of the medical scribe industry: implications for the advancement of electronic health records. Journal of the American Medical Association, December 15. doi:10.1001/jama.2014.17128. [Epub ahead of print].CrossRefGoogle Scholar
Gert, B., Berger, E.M., Cahill, G.F., Clouser, K.D., Culver, C.M., Moeschler, J.B., Singer, G.H.S. 1996. Morality and the New Genetics. Portola Valley, CA: Jones and Bartlett.Google Scholar
Gillum, R.F. 2013. From papyrus to the electronic tablet: A brief history of the clinical medical record with lessons for the digital age. The American Journal of Medicine 126:853–7.CrossRefGoogle Scholar
Gibbs, S. 2014. Elon Musk: artificial intelligence is our biggest existential threat. The Guardian, October 27, available at www.theguardian.com/technology/2014/oct/27/elon-musk-artificial-intelligence-ai-biggest-existential-threat.Google Scholar
Glanzberg, M. 2014. Truth. In Zalta, E.N., ed., The Stanford Encyclopedia of Philosophy (Fall 2014 edn.), available at plato.stanford.edu/archives/fall2014/entries/truth.Google Scholar
Glasser, D.J., Goodman, K.W., Einspruch, N.G. 2007. Chips, tags and scanners: Ethical challenges for radio frequency identification. Ethics and Information Technology 9:101–9.CrossRefGoogle Scholar
Goldman, A.H. 1987. Ethical issues in proprietary restrictions on research results. Science, Technology and Human Values 1:2230.CrossRefGoogle Scholar
Goldspiel, B.R., Flegel, W.A., DiPatrizio, G., Sissung, T., Adams, S.D., Penzak, S.R., Biesecker, L.G., Fleisher, T.A., Patel, J.J., Herion, D., Figg, W.D., Lertora, J.J., McKeeby, J.W. 2014. Integrating pharmacogenetic information and clinical decision support into the electronic health record. Journal of the American Medical Informatics Association 21(3):522–8.CrossRefGoogle ScholarPubMed
Goldstein, M.M. 2010. Health information technology and the idea of informed consent. Journal of Law, Medicine & Ethics 38(1):2735.CrossRefGoogle ScholarPubMed
Goodman, K.W. 1993. Intellectual property and control. Academic Medicine 68(9):S88S91.CrossRefGoogle ScholarPubMed
Goodman, K.W. 1996a. Critical care computing: outcomes, confidentiality, and appropriate use. Critical Care Clinics 12:109–22.CrossRefGoogle ScholarPubMed
Goodman, K.W. 1996b. Codes of ethics in occupational and environmental health. Journal of Occupational and Environmental Medicine 38:882–3.CrossRefGoogle ScholarPubMed
Goodman, K.W. 1996c. Ethics, genomics and information retrieval. Computers in Biology and Medicine 26:223–9.CrossRefGoogle ScholarPubMed
Goodman, K.W., ed. 1998a. Ethics, Computing and Medicine: Informatics and the Transformation of Health Care, Cambridge: Cambridge University Press.Google Scholar
Goodman, K.W. 1998b. Bioethics and health informatics: an introduction. In Goodman, K.W., ed., Ethics, Computing and Medicine: Informatics and the Transformation of Health Care. Cambridge: Cambridge University Press, 131.Google Scholar
Goodman, K.W. 1998c. Outcomes, futility, and health policy research. In Goodman, K.W., ed., Ethics, Computing and Medicine: Informatics and the Transformation of Health Care. Cambridge: Cambridge University Press, 116–38.Google Scholar
Goodman, K.W. 1999. Health informatics and the hospital ethics committee. MD Computing 16(2):1720.Google ScholarPubMed
Goodman, K.W. 2003. Ethics and Evidence-Based Medicine: Fallibility and Responsibility in Clinical Science. Cambridge: Cambridge University Press.Google Scholar
Goodman, K.W. 2010. Ethics, information technology and public health: New challenges for the clinician-patient relationship. Journal of Law, Medicine and Ethics 38(1):5863.CrossRefGoogle Scholar
Goodman, K.W. 2011. Health information technology and globalization. In Chadwick, R., ten Have, H., Meslin, E.M., eds., Health Care Ethics: Core and Emerging Issues. Los Angeles: Sage, 117–25.Google Scholar
Goodman, K.W. 2014. Health analytics and big data. Lahey Health Journal of Medical Ethics Spring:910.Google Scholar
Goodman, K.W., Cava, A. 2008. Bioethics, business ethics, and science: Bioinformatics and the future of healthcare. Cambridge Quarterly of Healthcare Ethics 17(4):361–72.CrossRefGoogle ScholarPubMed
Goodman, K.W., Adams, S., Berner, E.S., Embi, P.J., Hsiung, R., Hurdle, J., Jones, D.A., Lehmann, C.U., Maulden, S., Petersen, C., Terrazas, E., Winkelstein, P. 2013. AMIA’s Code of Professional and Ethical Conduct. Journal of the American Medical Informatics Association 20:141–3.CrossRefGoogle ScholarPubMed
Goodman, K.W., Berner, E.S., Dente, M.A., Kaplan, B., Koppel, R., Rucker, D., Sands, D.Z., Winkelstein, P. 2011. Challenges in ethics, safety, best practices, and oversight regarding HIT vendors, their customers, and patients: a report of an AMIA special task force. Journal of the American Medical Informatics Association 18(1):7781.CrossRefGoogle ScholarPubMed
Goodman, K.W., Meslin, E.M. 2014. Ethics, information technology and public health: Duties and challenges in computational epidemiology. In Magnuson, J.A., Fu, P.C., eds., Public Health Informatics and Information Systems. 2nd edn. London: Springer, 191209.CrossRefGoogle Scholar
Goodman, K.W., Cushman, R., Miller, R.A. 2014. Ethics in biomedical informatics: users, standards, and outcomes. In Shortliffe, E.H., Cimino, J.J., eds., Biomedical Informatics: Computer Applications in Health Care and Biomedicine. 4th edn. New York: Springer, 329–54.Google Scholar
Goodman, K.W., Prineas, R.J. 2009. Ethics curricula in epidemiology. In Coughlin, S.S., Beauchamp, T.L., Weed, D.L., eds., Ethics and Epidemiology. 2nd edn. Oxford: Oxford University Press, 283303.CrossRefGoogle Scholar
Gostin, L.O., Hodge, J.G. Jr., Valdiserri, R.O. 2001. Informational privacy and the public’s health: the Model State Public Health Privacy Act. American Journal of Public Health 91(9):1388–92.CrossRefGoogle ScholarPubMed
Gostin, L.O., Turek-Brezina, J., Powers, M., Kozloff, R., Faden, R., Steinauer, D. 1993. Privacy and security of personal information in a new health care system. Journal of the American Medical Association 270:2487–93.Google Scholar
Gotterbarn, D. 2001. Informatics and professional responsibility. Science and Engineering Ethics 7(2):221–30.CrossRefGoogle ScholarPubMed
Gotz, D., Wang, F., Perer, A. 2014. A methodology for interactive mining and visual analysis of clinical event patterns using electronic health record data. Journal of Biomedical Informatics 48:148–59.CrossRefGoogle ScholarPubMed
Graber, M.L., Wachter, R.M., Cassel, C.K. 2012. Bringing diagnosis into the quality and safety equations. Journal of the American Medical Association 308(12):1211–12.Google ScholarPubMed
Grajales, F.J., Sheps, S., Ho, K., Novak-Lauscher, H., Eysenbach, G. 2014. Social media: a review and tutorial of applications in medicine and health care. Journal of Medical Internet Research 16(2):e13.CrossRefGoogle ScholarPubMed
Grande, D., Mitra, N., Shah, A., Wan, F., Asch, D.A. 2013. Public preferences about secondary uses of electronic health information. JAMA Internal Medicine 173(19):1798–806.CrossRefGoogle ScholarPubMed
Grande, D., Mitra, N., Shah, A., Wan, F., Asch, D.A. 2014. The importance of purpose: moving beyond consent in the societal use of personal health information. Annals of Internal Medicine 161(12):855–62.CrossRefGoogle ScholarPubMed
Green, M.J., Botkin, J.R. 2003. “Genetic exceptionalism” in medicine: clarifying the differences between genetic and nongenetic tests. Annals of Internal Medicine 138(7):571–5.CrossRefGoogle Scholar
Greene, R., Mo, K.S., eds. 2006. The Undead and Philosophy: Chicken Soup for the Soulless. Chicago: Open Court.Google Scholar
Greene, C.S., Tan, J., Ung, M., Moore, J.H., Cheng, C. 2014. Big data bioinformatics. Journal of Cell Physiology 229(12):1896–900.CrossRefGoogle ScholarPubMed
Greenhalgh, T.Keen, J. 2013. England’s national programme for IT. BMJ 346:f4130.CrossRefGoogle Scholar
Greenwald, J.L, Halasyamani, L., Greene, J., LaCivita, C., Stucky, E., Benjamin, B., Reid, W., Griffin, F.A., Vaida, A.J., Williams, M.V. 2010. Making inpatient medication reconciliation patient centered, clinically relevant and implementable: A consensus statement on key principles and necessary first steps. Journal of Hospital Medicine 5(8):477–85.CrossRefGoogle ScholarPubMed
Greenwood, M. 1948. Medical statistics from Graunt to Farr. Cambridge: Cambridge University Press.Google Scholar
Gymrek, M., McGuire, A.L., Golan, D., Halperin, E., Erlich, Y. 2013. Identifying personal genomes by surname inference. Science 339(6117):321–4.CrossRefGoogle ScholarPubMed
Hardwig, J. 1991. The role of trust in knowledge. The Journal of Philosophy 84(12):693707.CrossRefGoogle Scholar
Harris, B.L. 1990. Becoming deprofessionalized: One aspect of the staff nurse’s perspective on computer-mediated nursing care plans. Advances in Nursing Science 13(2):6374.CrossRefGoogle ScholarPubMed
Hartmann, F. 1988. Paracelsus: Life and Prophecies. Blauvelt, NY: Steinerbooks, Garber Communications.Google Scholar
Hartzband, P., Groopman, J. 2008. Off the record – avoiding the pitfalls of going electronic. New England Journal of Medicine 358:1656–8.CrossRefGoogle ScholarPubMed
Hayek, F.A. 2007. The Road to Serfdom: Text and Documents, The Definitive Edition. Caldwell, B., ed. Chicago: University of Chicago Press.CrossRefGoogle Scholar
Häyry, M., Chadwick, R., Árnason, V., Árnason, G. 2007. The Ethics and Governance of Human Genetic Databases. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Hébert, P.C., Levin, A.V., Robertson, G. 2001. Bioethics for clinicians: 23. Disclosure of medical error. Canadian Medical Association Journal 164(4):509–13.Google ScholarPubMed
Hettrick, S. 2014. It’s impossible to conduct research without software, say 7 out of 10 UK researchers. Software Sustainability Institute, available at www.software.ac.uk/blog/2014-12-04-its-impossible-conduct-research-without-software-say-7-out-10-uk-researchers.Google Scholar
Hew, F.C. 2014. Artificial moral agents are infeasible with foresee technologies. Ethics and Information Technology 1:197206.CrossRefGoogle Scholar
Heyman, J. 2010. Health IT and solo practice: A love-hate relationship. Journal of Law, Medicine & Ethics 38(1):1416.CrossRefGoogle ScholarPubMed
Hilkevitch, J. 2012. Technology may be eroding pilot skills. Chicago Tribune, March 19, 2012, available at http://articles.chicagotribune.com/2012-03-19/classified/ct-met-getting-around-0319-20120319_1_colgan-air-flight-pilot-error-airline-jobs.Google Scholar
Hill, R.G., Sears, L.M., Melanson, S.W. 2013. 4000 clicks: a productivity analysis of electronic medical records in a community hospital ED. American Journal of Emergency Medicine 31(11):1591–4.CrossRefGoogle Scholar
Hill, E.M., Turner, E.L., Martin, R.M., Donovan, J.L. 2013. “Let’s get the best quality research we can”: public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study. BMC Medical Research Methodology 13:72, available at www.biomedcentral.com/1471–2288/13/72.CrossRefGoogle ScholarPubMed
Hiller, K.M., Stoneking, L., Min, A., Rhodes, S.M. 2013. Syndromic surveillance for influenza in the emergency department – a systematic review. PLoS One 8(9):e73832.CrossRefGoogle ScholarPubMed
Hippocrates, . 1983. Hippocratic Writings. Lloyd, G.E.R., ed., Chadwisk, J., Mann, W.N., trans. London: Penguin.Google Scholar
Hirsch, M.D. 2015. Docs to ONC: Change the EHR certification process. FierceEMR, January 22, available at www.fierceemr.com/story/docs-onc-change-ehr-certification-process/2015-01-22.Google Scholar
Hirschtick, R.E. 2006. A piece of my mind. Copy-and-paste. Journal of the American Medical Association 24;295(20):2335–6.Google Scholar
Hochachka, W.M., Fink, D., Hutchinson, R.A., Sheldon, D., Wong, W.K., Kelling, S. 2012. Data-intensive science applied to broad-scale citizen science. Trends in Ecology & Evolution 27(2):130–7.CrossRefGoogle ScholarPubMed
Hodge, J.G., Gostin, L.O. 2004. Public Health Practice vs. Research –A Report for Public Health Practitioners Including Cases and Guidance for Making Distinctions. Atlanta, GA: Council of State and Territorial Epidemiologists.Google Scholar
Hoffman, S., Podgurski, A. 2012. Drug-drug interaction alerts: emphasizing the evidence. St. Louis University Journal of Health Law & Policy 5:298309.Google Scholar
Holzemer, W.L., Uys, L.R., Chirwa, M.L., Greeff, M., Makoae, L.N., Kohi, T.W., Dlamini, P.S., Stewart, A.L., Mullan, J., Phetlhu, R.D., Wantland, D., Durrheim, K. 2007. Validation of the HIV/AIDS Stigma Instrument – PLWA (HASI-P). AIDS Care 19(8):1002–12.CrossRefGoogle Scholar
Hood, L., Lovejoy, J.C., Price, N.D. 2015. Integrating big data and actionable health coaching to optimize wellness. BMC Medicine 13(1):4.CrossRefGoogle ScholarPubMed
Horsky, J., Schiff, G.D., Johnston, D., Mercincavage, L., Bell, D., Middleton, B. 2012. Interface design principles for usable decision support: a targeted review of best practices for clinical prescribing interventions. Journal of Biomedical Informatics 45(6):1202–16.CrossRefGoogle ScholarPubMed
Hosking, G. 2014. Trust: A History. Oxford: Oxford University Press.CrossRefGoogle Scholar
Househ, M., Borycki, E., Kushniruk, A. 2014. Empowering patients through social media: the benefits and challenges. Health Informatics Journal 20(1):50–8.CrossRefGoogle ScholarPubMed
Howard, A.W. 2002. Automobile restraints for children: a review for clinicians. Canadian Medical Association Journal 167(7):769–73.Google ScholarPubMed
Howe, D., Costanzo, M., Fey, P., Gojobori, T., Hannick, L., Hide, W., Hill, D.P., Kania, R., Schaeffer, M., St Pierre, S., Twigger, S., White, O., Rhee, S.Y. 2008. Big data: The future of biocuration. Nature 455:4750.CrossRefGoogle ScholarPubMed
Hripcsak, G., Bloomrosen, M., FlatelyBrennan, P., Chute, C.G., Cimino, J., Detmer, D.E., Edmunds, M., Embi, P.J., Goldstein, M.M., Hammond, W.E., Keenan, G.M., Labkoff, S., Murphy, S., Safran, C., Speedie, S., Strasberg, H., Temple, F., Wilcox, A.B. 2014. Health data use, stewardship, and governance: ongoing gaps and challenges: a report from AMIA’s 2012 Health Policy Meeting. Journal of the American Medical Informatics Association 21:204–11.CrossRefGoogle ScholarPubMed
Hustinx, P. 2010. Privacy by design: delivering the promises. Identity in the Information Society 3(2):253–55.CrossRefGoogle Scholar
Illman, J. 2000. WHO’s plan to police health websites rejected. BMJ 321:1308.CrossRefGoogle Scholar
Institute of Medicine. 2001. Preserving Public Trust: Accreditation and Human Research Participant Protection Programs. Washington, DC: National Academies Press.Google Scholar
Institute of Medicine. 2011. Digital Infrastructure for the Learning Health System: The Foundation for Continuous Improvement in Health and Health Care: Workshop Series Summary. Washington, DC: The National Academies Press.Google Scholar
Institute of Medicine. 2012. Health IT and Patient Safety: Building Safer Systems for Better Care. Washington, DC: The National Academies Press.Google Scholar
Ioannidis, J.P. 2005. Why most published research findings are false. PLoS Medicine 2(8):e124.CrossRefGoogle ScholarPubMed
Ioannidis, J.P. 2014. How to make more published research true. PLoS Medicine 11(10):e1001747.CrossRefGoogle ScholarPubMed
Isidore of Seville. 2013. Isidore of Seville’s Etymologies: the complete translation of Isidori Hispalensis Episcopi Etymologiarum sive Originum Libri. Throop, P., trans. Charlotte, VT: MedievalMS.Google Scholar
Jackson, G.L., Powers, B.J., Chatterjee, R., Bettger, J.P., Kemper, A.R., Hasselblad, V., Dolor, R.J., Irvine, R.J., Heidenfelder, B.L., Kendrick, A.S., Gray, R., Williams, J.W. 2013. Improving patient care. The patient centered medical home. A Systematic Review. Annals of Internal Medicine 158(3):169–78.CrossRefGoogle ScholarPubMed
Jain, S.H. 2009. Practicing medicine in the age of Facebook. New England Journal of Medicine 361(7):649–51.CrossRefGoogle ScholarPubMed
JASON. 2014. A Robust Health Data Infrastructure. Prepared for the US Agency for Healthcare Research and Quality, AHRQ Publication No. 14-0041-EF. McLean, VA: MITRE Corporation, available at http://healthit.gov/sites/default/files/ptp13-700hhs_white.pdf.Google Scholar
Jecker, N.S., Schneiderman, L.J. 1993. Medical futility: the duty not to treat. Cambridge Quarterly of Health Care Ethics 2:151–9.CrossRefGoogle Scholar
Jennings, B. 2006. The politics of end-of-life decision-making: computerised decision-support tools, physicians’ jurisdiction and morality. Sociology of Health & Illness 28(3):350–75.CrossRefGoogle ScholarPubMed
Jha, A.K., Classen, D.C. 2011.Getting moving on patient safety – harnessing electronic data for safer care. New England Journal of Medicine 365(19):1756–8.CrossRefGoogle ScholarPubMed
Joe, J., Demiris, G. 2013. Older adults and mobile phones for health: a review. Journal of Biomedical Informatics 46(5):947–54.CrossRefGoogle ScholarPubMed
Johnson, D.G. 2006. Computer systems: moral entities but not moral agents. Ethics and Information Technology 8:195204.CrossRefGoogle Scholar
Johnson, D.G. 2009. Computer Ethics. 4th edn. Upper Saddle River, NJ: Pearson Education.Google Scholar
Johnson, E.J., Goldstein, D. 2003. Do defaults save lives? Science 302(5649):1338–9.CrossRefGoogle ScholarPubMed
Johnson, K.B. 2010. Project Health Design: advancing the vision of consumer-clinician-computer collaborations. Journal of Biomedical Informatics 43(5 Suppl):S12.CrossRefGoogle Scholar
Jonas, H. 1984. The Imperative of Responsibility. In search of an Ethics for the Technological Age. Chicago: The University of Chicago Press.Google Scholar
Jonsen, A.R. 1998. The Birth of Bioethics. Oxford: Oxford University Press.CrossRefGoogle Scholar
Kaplan, B., Shaw, N.T. 2004. Future directions in evaluation research: people, organizational, and social issues. Methods of Information in Medicine 43(3):215–31.Google ScholarPubMed
Kass, N.E., Faden, R. R., Goodman, S. N., Pronovost, P., Tunis, S., Beauchamp, T. L. 2013. The research-treatment distinction: A problematic approach for determining which activities should have ethical oversight. Hastings Center Report 43(S1):S4S15.CrossRefGoogle Scholar
Katz, R.V., Green, B.L., Kressin, N.R., Kegeles, S.S., Wang, M.Q., James, S.A., Russell, S.L., Claudio, C., McCallum, J.M. 2008. The legacy of the Tuskegee Syphilis Study: assessing its impact on willingness to participate in biomedical studies. Journal of Health Care for the Poor and Underserved (4):1168–80.Google ScholarPubMed
Kawamoto, K., Houlihan, C.A., Balas, E.A., Lobach, D.F. 2005. Improving clinical practice using clinical decision support systems: a systematic review of trials to identify features critical to success. BMJ 330(7494):765.CrossRefGoogle ScholarPubMed
Kaye, J. 2012. The tension between data sharing and the protection of privacy in genomics research. Annual Review of Genomics and Human Genetics 13:415–31.CrossRefGoogle ScholarPubMed
Kho, A.N., Rasmussen, L.V., Connolly, J.J., Peissig, P.L., Starren, J., Hakonarson, H., Hayes, M.G. 2013. Practical challenges in integrating genomic data into the electronic health record. Genetics in Medicine 15(10):772–8.CrossRefGoogle ScholarPubMed
Khum, H.D., Ahalt, S. 2013. Privacy-by-design: Understanding data access models for secondary data. AMIA Joint Summits on Translational Science Proceedings, March 18:126–30, available at www.ncbi.nlm.nih.gov/pmc/articles/PMC3845756/.Google Scholar
Kim, S., Kim, W., Park, R.W. 2011. A comparison of intensive care unit mortality prediction models through the use of data mining techniques. Healthcare Informatics Research 17(4):232–43.CrossRefGoogle ScholarPubMed
King, A.C., Bickmore, T.W., Campero, M.I., Pruitt, L.A., Yin, J.L. 2013. Employing virtual advisors in preventive care for underserved communities: results from the COMPASS study. Journal of Health Communication 18(12):1449–64.CrossRefGoogle ScholarPubMed
Kluge, E.-H. 2001. The Ethics of Electronic Patient Records. New York: Peter Lang.Google Scholar
Knaus, W.A. 1993. Ethical implications of risk stratification in the acute care setting. Cambridge Quarterly of Healthcare Ethics 2:193–6.CrossRefGoogle ScholarPubMed
Knaus, W.A. 2002. APACHE 1978–2001: the development of a quality assurance system based on prognosis: milestones and personal reflections. Archives of Surgery 137(1):37–41.CrossRefGoogle ScholarPubMed
Knaus, W.A., Draper, E.A., Wagner, D.P., Zimmerman, J.E. 1985. APACHE II: a severity of disease classification system. Critical Care Medicine 13:818–29.CrossRefGoogle ScholarPubMed
Knaus, W.A., Draper, E.A., Wagner, D.P., Zimmerman, J.E. 1986. An evaluation of outcome from intensive care in major medical centers. Annals of Internal Medicine 104:410–18.CrossRefGoogle ScholarPubMed
Knaus, W.A., Wagner, D.P., Lynn, J. 1991. Short-term mortality predictions for critically ill hospitalized adults: science and ethics. Science 254:389–94.CrossRefGoogle ScholarPubMed
Knaus, W.A., Zimmerman, J.E., Wagner, D.P., Draper, E.A., Lawrence, D.E. 1981. APACHE – acute physiology and chronic health evaluation: a physiologically based classification system. Critical Care Medicine (9):591–7.CrossRefGoogle ScholarPubMed
Kobeissy, F.H., Gulbakan, B., Alawieh, A., Karam, P., Zhang, Z., Guingab-Cagmat, J.D., Mondello, S., Tan, W., Anagli, J., Wang, K. 2014. Post-genomics nanotechnology is gaining momentum: nanoproteomics and applications in life sciences. OMICS 18(2):111–31.CrossRefGoogle Scholar
Kohane, I.S. 2013. Secondary use of health information: are we asking the right question? JAMA Internal Medicine 173(19):1806–7.CrossRefGoogle ScholarPubMed
Kohn, L.T., Corrigan, J.M., Donaldson, M.S., eds. 1999. To Err Is Human: Building a Safer Health System. Washington, DC: National Academy Press.Google Scholar
Koppel, R., Kreda, D. 2009. Health care information technology vendors’ “hold harmless” clause: implications for patients and clinicians. Journal of the American Medical Association 301(12):1276–78.Google ScholarPubMed
Koppel, R., Metlay, J.P., Cohen, A., Abaluck, B., Localio, A.R., Kimmel, S.E., Strom, B.L. 2005. Role of computerized physician order entry systems in facilitating medication errors. Journal of the American Medical Association 293(10):1197–203.Google ScholarPubMed
Kraemer Diaz, A.E., Spears Johnson, C.R., Arcury, T.A. 2015. Perceptions that influence the maintenance of scientific integrity in community-based participatory research. Health, Education & Behavior, January 14. pii: 1090198114560016.Google Scholar
Kramer, A.A., Higgins, T.L., Zimmerman, J.E. 2013. The association between ICU readmission rate and patient outcomes. Critical Care Medicine 41(1):2433.CrossRefGoogle ScholarPubMed
Kramer, A.D.I., Guillory, J.E., Hancock, J.T. 2014. Experimental evidence of massive-scale emotional contagion through social networks. Proceedings of the National Academy of Sciences 111:8788–90.CrossRefGoogle ScholarPubMed
Kuhn, T., Basch, P., Barr, M., Yackel, T., for the Medical Informatics Committee of the American College of Physicians. 2015. Clinical documentation in the 21st century: Executive summary of a policy position paper from the American College of Physicians. Annals of Internal Medicine 162(2):301–3.CrossRefGoogle ScholarPubMed
Kullo, I.J., Haddad, R., Prows, C.A., Holm, I., Sanderson, S.C., Garrison, N.A., Sharp, R.R., Smith, M.E., Kuivaniemi, H., Bottinger, E.P., Connolly, J.J., Keating, B.J., McCarty, C.A., Williams, M.S., Jarvik, G.P. 2014. Return of results in the genomic medicine projects of the eMERGE network. Frontiers in Genetics 5:50.CrossRefGoogle ScholarPubMed
Kumar, A., Asaf, B.B. 2015. Robotic thoracic surgery: The state of the art. Journal of Minimal Access Surgery 11(1):60–7.CrossRefGoogle ScholarPubMed
Kush, R., Goldman, M. 2014. Fostering responsible data sharing through standards. New England Journal of Medicine 370:2163–5.CrossRefGoogle ScholarPubMed
Laennec, R.T.H. 1821. A Treatise on the Diseases of the Chest, in Which They Are Described According to Their Anatomical Characters, and Their Diagnosis Established on a New Principle by Means of Acoustick Instruments. Forbes, J., trans. London: T. and G. Underwood. [Full text available via The Gerstein Science Information Centre at the University of Toronto at http://archive.org/stream/treatiseondiseas00laen/treatiseondiseas00laen_djvu.txt.]Google Scholar
Lainer, M., Mann, E., Sönnichsen, A. 2013. Information technology interventions to improve medication safety in primary care: a systematic review. International Journal for Quality in Heath Care 25(5):590–8.Google ScholarPubMed
Lane, W.A. 1936. What the mouth reveals. New Health 11:34–5.Google Scholar
Lane, J., Schur, C. 2010. Balancing access to health data and privacy: a review of the issues and approaches for the future. Health Services Research 45(5 Pt 2):1456–67.CrossRefGoogle ScholarPubMed
Laranjo, L., Arguel, A., Neves, A.L., Gallagher, A.M., Kaplan, R., Mortimer, N., Mendes, G.A., Lau, A.Y. 2014. The influence of social networking sites on health behavior change: a systematic review and meta-analysis. Journal of the American Medical Informatics Association, July 8. pii: amiajnl-2014-002841.Google Scholar
Lau, A. 2009. What are repeatability and reproducibility? Part 1: A DO2 viewpoint for laboratories. ASTM Standardization News March/April, available at www.astm.org/SNEWS/MA_2009/datapoints_ma09.html.Google Scholar
Lau, K.H. 2014. Computer-based teaching module design: principles derived from learning theories. Medical Education 48(3):247-54.CrossRefGoogle ScholarPubMed
Law Commission. 1996. Privity of contract: Contracts for the benefit of third parties LC242, available at http://lawcommission.justice.gov.uk/docs/lc242_privity_of_contract_for_the_benefit_of_third_parties.pdf.Google Scholar
Law, L.M., Wason, J.M. 2014. Design of telehealth trials – Introducing adaptive approaches. International Journal of Medical Informatics 83(12):870–80.CrossRefGoogle ScholarPubMed
Lee, L.M. 2014. Health information in the background: justifying public health surveillance without patient consent. In Pimple, K.D., ed., Emerging Pervasive Information and Communication Technologies (PICT): Ethical Challenges, Opportunities and Safeguards. Dordrecht: Springer, 3953.CrossRefGoogle Scholar
Lee, L.M., Gostin, L.O. 2009. Ethical collection, storage, and use of public health data: A proposal for a national privacy protection. Journal of the American Medical Association 302(1):82–4.Google Scholar
Lee, L.M., Hellig, C.M., White, A. 2012. Ethical justification for conducting public health surveillance without patient consent. American Journal of Public Health 102(1):3844.CrossRefGoogle ScholarPubMed
Leviss, J., ed. 2013. HIT or Miss: Lessons Learned from Health Information Technology Implementations. 2nd edn. Chicago: AHIMA.Google Scholar
Lewandowsky, S., Gignac, G.E., Oberauer, K. 2013. The role of conspiracist ideation and worldviews in predicting rejection of science. PLoS One 8(10):e75637.CrossRefGoogle ScholarPubMed
Lim, J.L., Yih, Y., Gichunge, C., Tierney, W.M., Le, T.H., Zhang, J., Lawley, M.A, Petersen, T.J., Mamlin, J.J. 2009. The AMPATH Nutritional Information System: designing a food distribution electronic record system in rural Kenya. Journal of the American Medical Informatics Association 16(6):882–8.CrossRefGoogle ScholarPubMed
Lin, P., Abney, K., Bekey, G.A., eds. 2012. Robot Ethics: The Ethical and Social Implications of Robots. Cambridge, MA: MIT Press.Google Scholar
Lorsch, J.R., Collins, F.S., Lippincott-Schwartz, J. 2014. Fixing problems with cell lines. Science 346(6216):1452–3CrossRefGoogle ScholarPubMed
Louis, P.C.A. 1834. Essay on Clinical Instruction. Martin, P., trans. London: S. Highley. (Cited in Huth, E.J. and Murray, T.J., eds., Medicine in Quotations: Views of Health and Disease Through the Ages. Philadelphia: American College of Physicians.)Google Scholar
Louis, P.C.A. 1835/1960. Research on the effect of blood-letting in several inflammatory maladies. Translation of an article by Pierre-Charles-Alexander Louis (Arch. gen. Méd. 321–336, 1835), with introduction. Gaines, W.J., Langford, H.G., trans. Archives of Internal Medicine 106(4):571–9. doi:10.1001/archinte.1960.03820040109009.Google Scholar
Louis, P.C.A. 1836. Researches on the Effects of Bloodletting in Some Inflammatory Diseases, and on the Influence of Tartarized Antimony and Vesication in Pneumonitis. Putnam, C.G., trans. Boston: Hilliard, Gray & Co. Full text available via The Gerstein Science Information Centre at the University of Toronto at https://archive.org/details/researchesoneffe00louiuoft.Google Scholar
Lown, B.A., Rodriguez, D. 2012. Lost in translation? How electronic health records structure communication, relationships, and meaning. Academic Medicine 87(4):392–4.CrossRefGoogle ScholarPubMed
Lowy, J. 2011. Automation in the air dulls pilot skill. The Associated Press, available at http://news.yahoo.com/ap-impact-automation-air-dulls-pilot-skill-070507795.html.Google Scholar
Lowry, S.Z., Ramaiah, M., Patterson, E.S., Latkany, P., Brick, D., Gibbons, M.C. 2015. Integrating Electronic Health Records into Clinical Workflow: An Application of Human Factors Modeling Methods to Obstetrics and Gynecology and Ophthalmology. Washington, DC: National Institute of Standards and Technology (NISTIR 8042), available at http://nvlpubs.nist.gov/nistpubs/ir/2015/NIST.IR.8042.pdf.Google Scholar
Luce, J.M., Wachter, R.M. 1994. The ethical appropriateness of using prognostic scoring systems in clinical management. Critical Care Clinics 10:229–41.CrossRefGoogle ScholarPubMed
Mack, E.H., Wheeler, D.S., Embi, P.J. 2009. Clinical decision support systems in the pediatric intensive care unit. Pediatric Critical Care Medicine 10(1):23–8.CrossRefGoogle ScholarPubMed
Mackey, T.K., Liang, B.A., Attaran, A., Kohler, J.C. 2013. Ensuring the future of health information online. Lancet 382(9902):1404.CrossRefGoogle ScholarPubMed
Mackey, T.K., Liang, B.A., Kohler, J.C., Attaran, A. 2014. Health domains for sale: the need for global health Internet governance. Journal of Medical Internet Research 16(3):e62.CrossRefGoogle ScholarPubMed
Magnello, E. 2011. Vital Statistics: The measurement of public health. In Flood, R., Rice, A., Wilson, R., eds., Mathematics in Victorian Britain. Oxford: Oxford University Press, 261–82.Google Scholar
Magrabi, F., Baker, M., Sinha, I., Ong, M.S., Harrison, S., Kidd, M.R., Runciman, W.B., Coiera, E. 2015. Clinical safety of England’s national programme for IT: A retrospective analysis of all reported safety events 2005 to 2011. International Journal of Medical Informatics 84(3):198206.CrossRefGoogle ScholarPubMed
Malin, B. 2011. HIPAA and a learning healthcare system. In Institute of Medicine, Digital Infrastructure for the Learning Health System: The Foundation for Continuous Improvement in Health and Health Care: Workshop Series Summary. Washington, DC: The National Academies Press, 157–61.Google Scholar
Malin, B., Loukides, G., Benitez, K., Clayton, E.W. 2011. Identifiability in biobanks: models, measures, and mitigation strategies. Human Genetics 130:383–92.CrossRefGoogle ScholarPubMed
Malin, B., Sweeney, L. 2004. How (not) to protect genomic data privacy in a distributed network: using trail re-identification to evaluate and design anonymity protection systems Journal of Biomedical Informatics 37:179–92.CrossRefGoogle Scholar
Maloni, J.M, Brown, M.E. 2006. Corporate social responsibility in the supply chain: An application in the food industry. Journal of Business Ethics, 68:3552.CrossRefGoogle Scholar
Mamykina, L., Vawdrey, D.K., Stetson, P.D., Zheng, K., Hripcsak, G. 2012. Clinical documentation: composition or synthesis? Journal of the American Medical Informatics Association 19:1025–31.CrossRefGoogle ScholarPubMed
Mandl, K.D., Kohane, I.S. 2008. Tectonic shifts in the health information economy. New England Journal of Medicine 358:1732–7.CrossRefGoogle ScholarPubMed
Manhal-Baugus, M. 2001. E-therapy: practical, ethical, and legal issues. CyberPsychology & Behavior 4(5):551–63.CrossRefGoogle ScholarPubMed
Markle Foundation. 2006. Connecting Americans to Their Health Care: A Common Framework for Networked Personal Health Information. New York: Markle Foundation, available at www.markle.org.Google Scholar
Markle Foundation. 2008. Americans Overwhelmingly Believe Electronic Personal Health Records Could Improve Their Health (based on a survey by Prof. A.F. Westin). New York: Markle Foundation, available at www.markle.org.Google Scholar
Marquard, J.L., Brennan, P.F. 2009. Crying wolf: Consumers may be more willing to share medication information than policymakers think. Journal of Health Information Management 23(2):2632.Google ScholarPubMed
McCorduck, P. 2004. Machines Who Think: A Personal Inquiry into the History and Prospects of Artificial Intelligence. 2nd edn. London: CRC Press.CrossRefGoogle Scholar
McCoy, A.B., Melton, G.B., Wright, A., Sittig, D.F. 2013. Clinical decision support for colon and rectal surgery: an overview. Clinics in Colon and Rectal Surgery 26(1):2330.Google ScholarPubMed
McCoy, A.B., Waitman, L.R., Lewis, J.B., Wright, J.A., Choma, D.P., Miller, R.A., Peterson, J.F. 2012. A framework for evaluating the appropriateness of clinical decision support alerts and responses. Journal of the American Medical Informatics Association 19(3):346–52.CrossRefGoogle ScholarPubMed
McDaid, D., Park, A-L. 2011. Online Health: Untangling the Web. BUPA Health Pulse 2010. London School of Economics and British United Provident Association (BUPA), available at www.bupa.com.au/staticfiles/Bupa/HealthAndWellness/MediaFiles/PDF/LSE_Report_Online_Health.pdf.Google Scholar
McDonald, C.J. 1976. Protocol-based computer reminders, the quality of care and the non-perfectability of man. New England Journal of Medicine 295(24):1351–5.CrossRefGoogle ScholarPubMed
McEwen, J.E., Boyer, J.T., Sun, K.Y., Rothenberg, K.H., Lockhart, N.C., Guyer, M.S. 2014. The ethical, legal, and social implications program of the national human genome research institute: reflections on an ongoing experiment. Annual Review of Genomics and Human Genetics 15:481505.CrossRefGoogle Scholar
McGraw, D. 2011. Policies and practices to build public trust. In Institute of Medicine, Digital Infrastructure for the Learning Health System: The Foundation for Continuous Improvement in Health and Health Care: Workshop Series Summary. Washington, DC: The National Academies Press, 155–7.Google Scholar
Meeks, D.W., Smith, M.W., Taylor, L., Sittig, D.F., Scott, J.M., Singh, H. 2014. An analysis of electronic health record-related patient safety concerns. Journal of the American Medical Informatics Association 21(6):1053–59.CrossRefGoogle ScholarPubMed
Menon, S., Smith, M.W., Sittig, D.F., Petersen, N.J., Hysong, S.J., Espadas, D., Modi, V., Singh, H. 2014. How context affects electronic health record-based test result follow-up: a mixed-methods evaluation. BMJ Open 4(11):e005985.CrossRefGoogle ScholarPubMed
Meslin, E.M., Alpert, S.A., Carroll, A.E., Odell, J.D., Tierney, W.M., Schwartz, P.H. 2013. Giving patients granular control of personal health information: using an ethics ‘Points to Consider’ to inform informatics system designers. International Journal of Medical Informatics 82(12):1136–43.CrossRefGoogle ScholarPubMed
Meslin, E.M., Goodman, K.W. 2010. Bank on it: An ethics and policy agenda for biobanks and electronic health records. Science Progress, Center for American Progress, http://scienceprogress.org/2010/02/bank-on-it/#_edn25.Google Scholar
Meslin, E.M., Schwartz, P.H. 2014. How bioethics principles can aid design of electronic health records to accommodate patient granular control. Journal of General Internal Medicine 30(Suppl 1):S36.CrossRefGoogle Scholar
Meyers, D., Quinn, M., Clancy, C.M. 2010. Health Information Technology: Turning the Patient-Centered Medical Home from Concept to Reality. Rockville, MD: Agency for Healthcare Research and Quality, available at www.ahrq.gov/news/newsroom/commentaries/pcmh-concept-to-reality.html.Google Scholar
Middleton, B., Bloomrosen, M., Dente, M.A., Hashmat, B., Koppel, R., Overhage, J.M., Payne, T.H., Rosenbloom, S.T., Weaver, C., Zhang, J. 2013. Enhancing patient safety and quality of care by improving the usability of electronic health record systems: recommendations from AMIA. Journal of the American Medical Informatics Association 20:e2e8.CrossRefGoogle ScholarPubMed
Mill, J.S. 1956 (1859). On Liberty. Indianapolis: The Bobbs-Merrill Company.Google Scholar
Miller, R.A. 1990. Why the standard view is standard: people, not machines, understand patients’ problems. Journal of Medicine and Philosophy 15:581–91.CrossRefGoogle Scholar
Miller, R.A., Gardner, R.M. 1997a. Summary recommendations for the responsible monitoring and regulation of clinical software systems. Annals of Internal Medicine 127(9):842–5.CrossRefGoogle ScholarPubMed
Miller, R.A., Gardner, R.M. 1997b. Recommendations for responsible monitoring and regulation of clinical software systems. Journal of the American Medical Informatics Association 4:442–57.CrossRefGoogle ScholarPubMed
Miller, R.A., Schaffner, K.F., Meisel, A. 1985. Ethical and legal issues related to the use of computer programs in clinical medicine. Annals of Internal Medicine 102:529–36.CrossRefGoogle Scholar
Moor, J.H. 1979. Are there decisions computers should never make? Nature and System 1:217–29.Google Scholar
Moore, D.A., Tetlock, P.E., Tanlu, L., Bazerman, M.H. 2006. Conflict of interest and the case of auditor independence: Moral seduction and strategic issue cycling. Academy of Management Review 31(1):1029.CrossRefGoogle Scholar
Moreno, R., Afonso, S. 2006. Ethical, legal and organizational issues in the ICU: prediction of outcome. Current Opinions in Critical Care 12(6):619–23.CrossRefGoogle ScholarPubMed
Morens, D.M. 1999. Death of a president. New England Journal of Medicine 341:1845–50.CrossRefGoogle ScholarPubMed
Morris, G., Farnum, G., Afzal, S., Robinson, C., Greene, J., Coughlin, C. 2014. Patient Identification and Matching Final Report. Office of the National Coordinator for Health Information Technology, contract HHSP233201300029C, available at www.healthit.gov/sites/default/files/patient_identification_matching_final_report.pdf.Google Scholar
Mushiaki, S. 2013. Ethica ex machina: issues in roboethics. Journal international de bioéthique 24(4):1726, 176–7.Google ScholarPubMed
Nanji, K.C., Slight, S.P., Seger, D.L., Cho, I., Fiskio, J.M., Redden, L.M., Volk, L.A., Bates, D.W. 2014. Overrides of medication-related clinical decision support alerts in outpatients. Journal of the American Medical Informatics Association 21(3):487–91.CrossRefGoogle ScholarPubMed
National Bioethics Advisory Commission. 2001. Ethical and Policy Issues in International Research: Clinical Trials in Developing Countries. Vol. 1. Bethesda, MD: National Bioethics Advisory Commission.Google Scholar
National Research Council. 1997. For the Record: Protecting Electronic Health Information. Washington, DC: National Academy Press.Google Scholar
Nazi, K.M., Hogan, T.P., Wagner, T.H., McInnes, D.K., Smith, B.M., Haggstrom, D., Chumbler, N.R., Gifford, A.L., Charters, K.G., Saleem, J.J., Weingardt, K.R., Fischetti, L.F., Weaver, F.M. 2010. Embracing a health services research perspective on personal health records: Lessons learned from the VA My HealtheVet system. Journal of General Internal Medicine 25(Suppl 1):62–7.CrossRefGoogle ScholarPubMed
Newman-Toker, D.E., Pronovost, P.J. 2009. Diagnostic errors–the next frontier for patient safety. Journal of the American Medical Association 301:1060–2.Google ScholarPubMed
Nissenbaum, H. 1994. Computing and accountability. Communications of the Association for Computing Machinery 37(1):7280.CrossRefGoogle Scholar
Nissenbaum, H. 2000. Values in computer system design: Bias and autonomy. In Collste, G., ed., Ethics in the Age of Information Technology. Studies in Applied Ethics 7. Linköping: Centre for Applied Ethics, 5969.Google Scholar
Noorman, M. 2014. Computing and moral responsibility. In Zalta, E.N., ed., The Stanford Encyclopedia of Philosophy (Summer 2014 edn.), available at http://plato.stanford.edu/archives/sum2014/entries/computing-responsibility/.Google Scholar
Nuffield Council on Bioethics. 2015. The Collection, Linking and Use of Data in Biomedical Research and Health Care: Ethical Issues. London: Nuffield Council on Bioethics, available at http://nuffieldbioethics.org/wp-content/uploads/Biological_and_health_data_web.pdf.Google Scholar
Nutton, V. 1996. The rise of medicine. In Porter, R., ed., The Cambridge Illustrated History of Medicine. Cambridge: Cambridge University Press, 5281.Google Scholar
Office for National Statistics. 2013. Internet Access – Households and Individuals, 2013, available at www.ons.gov.uk/ons/dcp171778_322713.pdf.Google Scholar
Office of Technology Assessment (OTA). 1993a. Report Brief: Protecting Privacy in Computerized Medical Information. Washington, DC: US Government Printing Office.Google Scholar
Office of Technology Assessment (OTA). 1993b. Protecting Privacy in Computerized Medical Information. Washington, DC: US Government Printing Office (OTA-TCT-576).Google Scholar
Or, C.K., Tao, D. 2014. Does the use of consumer health information technology improve outcomes in the patient self-management of diabetes? A meta-analysis and narrative review of randomized controlled trials. International Journal of Medical Informatics 83(5):320–9.CrossRefGoogle ScholarPubMed
Orr, R.D., Pang, N., Pellegrino, E.D., Siegler, M. 1997. Use of the Hippocratic Oath: a review of twentieth century practice and a content analysis of oaths administered in medical schools in the US and Canada in 1993. Journal of Clinical Ethics 8(4):377–88.CrossRefGoogle Scholar
Overby, C.L., Tarczy-Hornoch, P., Kalet, I.J., Thummel, K.E., Smith, J.W., Del Fiol, G., Fenstermacher, D., Devine, E.B. 2012. Developing a Prototype system for integrating pharmacogenomics findings into clinical practice. Journal of Personalized Medicine 2, 241–56.CrossRefGoogle ScholarPubMed
Ozoliņa, Z., Mitcham, C., Stilgoe, J., Andanda, P., Kaiser, M., Nielsen, L., Stehr, N., Qiu, R.-Z. 2009. Global Governance of Science: Report of the Expert Group on Global Governance of Science to the Science, Economy and Society Directorate, Directorate-General for Research, European Commission, EUR23616 EN, available at http://ec.europa.eu/research/swafs/pdf/pub_archive/global-governance-020609_en.pdf.Google Scholar
Palmer, B. 2014. Jonas Salk: Good at virology, bad at economics. Slate, April 13, 2014, available at www.slate.com/articles/technology/history_of_innovation/2014/04/the_real_reasons_jonas_salk_didn_t_patent_the_polio_vaccine.html.Google Scholar
Palmer, V. 1983. Why privity entered tort – an historical reexamination of Winterbottom v. Wright. The American Journal of Legal History 27(1):8598.CrossRefGoogle Scholar
Palmer, V. 1992. The Paths to Privity: A History of Third Party Beneficiary Contracts at English Law. San Francisco: Austin & Winfield.Google Scholar
Patel, M.S., Asch, D.A., Volpp, K.G. 2015. Wearable devices as facilitators, not drivers, of health behavior change. Journal of the American Medical Association 323(5):459–60.Google Scholar
Patel, V., Barker, W., Siminerio, E. 2014. Individuals’ Access and Use of their Online Medical Record Nationwide. ONC Data Brief No. 2. Washington, DC: Office of the National Coordinator for Health Information Technology, available at www.healthit.gov/sites/default/files/consumeraccessdatabrief_9_10_14.pdf.Google Scholar
Pauker, S.G., Kassirer, J.P. 1981. Clinical decision analysis by personal computer. Archives of Internal Medicine 141(13):1831–7.CrossRefGoogle ScholarPubMed
Pearson, S.-A., Moxey, A., Robertson, J., Hains, I., Williamson, M., Reeve, J., Newby, D. 2009. Do computerised clinical decision support systems for prescribing change practice? A systematic review of the literature (1990–2007). BMC Health Services Research 9:154.CrossRefGoogle Scholar
Penson, R.T., Kyriakou, H., Zuckerman, D., Chabner, B.A., Lynch, T.J. 2006. Teams: communication in multidisciplinary care. Oncologist 11(5):520526.CrossRefGoogle ScholarPubMed
Perry, J.E., Cox, D., Cox, A.D. 2014. Trust and transparency: patient perceptions of physicians’ financial relationships with pharmaceutical companies. Journal of Law, Medicine, and Ethics 42(4):475–91.CrossRefGoogle ScholarPubMed
Petersen, C., DeMuro, P. 2015. Legal and regulatory considerations associated with use of patient-generated health data from social media and mobile health (mHealth) devices. Applied Clinical Informatics 6(1):1626.Google ScholarPubMed
Petersen, C., DeMuro, P., Goodman, K.W., Kaplan, B. 2013. Sorrell v. IMS Health: issues and opportunities for informaticians. Journal of the American Medical Informatics Association 20(1):35–7.CrossRefGoogle Scholar
Phansalkar, S., Zachariah, M., Seidling, H.M., Mendes, C., Volk, L., Bates, D.W. 2014. Evaluation of medication alerts in electronic health records for compliance with human factors principles. Journal of the American Medical Informatics Association 21(e2):e33240.CrossRefGoogle ScholarPubMed
Phelps, R.G., Taylor, J., Simpson, K., Samuel, J., Turner, A.N. 2014. Patients’ continuing use of an online health record: a quantitative evaluation of 14,000 patient years of access data. Journal of Medical Internet Research 16(10):e241.CrossRefGoogle Scholar
Picciano, K.S., Goodman, K.W. 2014. Clinical Decision Support Systems: A Survey of Some Legal and Ethical Implications. Working Papers in Bioethics. Miami: University of Miami Bioethics Program.Google Scholar
Pimple, K.D. 2014. Introduction: The Impact, Benefits, and Hazards of PICT. In Pimple, K.D., ed., Emerging Pervasive Information and Communication Technologies (PICT): Ethical Challenges, Opportunities and Safeguards. Dordrecht: Springer, 112.CrossRefGoogle Scholar
Pinker, S. 2008. The Stupidity of Dignity: Conservative bioethics’ latest, most dangerous ploy. The New Republic, May 28, available at http://pinker.wjh.harvard.edu/articles/media/The%20Stupidity%20of%20Dignity.htm.Google Scholar
Platt, J., Kardia, S. 2015. Public trust in health information sharing: implications for biobanking and electronic health record systems. Journal of Personalized Medicine 5(1):321.CrossRefGoogle ScholarPubMed
Popper, K.R. 1959/1980. The Logic of Scientific Discovery. London: Hutchinson.Google Scholar
Porter, R. 1992. The rise of medical journalism in Britain to 1800. In Bynum, W.F., Lock, S., and Porter, R., eds., Medical Journals and Medical Knowledge: Historical Essays. London and New York: Routledge, 628.Google Scholar
Postel, J. 1994. Domain Name System Structure and Delegation. University of Southern California Information Sciences Institute, available at http://tools.ietf.org/pdf/rfc1591.pdf.CrossRefGoogle Scholar
Presidential Commission for the Study of Bioethical Issues. 2011. Moral Science: Protecting Participants in Human Subjects Research. Washington, DC: Presidential Commission for the Study of Bioethical Issues.Google Scholar
Prinzel, L.J., Pope, A.T., Freeman, F.G., 2002. Physiological self-regulation and adaptive automation. International Journal of Aviation Psychology 12(2):179–96.Google Scholar
Rachels, J. 1975. Why is privacy important? Philosophy & Public Affairs 4(4):323–33.Google Scholar
Radley, D.C., Wasserman, M.R., Olsho, L.E., Shoemaker, S.J., Spranca, M.D., Bradshaw, B. 2013. Reduction in medication errors in hospitals due to adoption of computerized provider order entry systems. Journal of the American Medical Informatics Association 20(3):470–6.CrossRefGoogle ScholarPubMed
Reiser, S.J. 1991.The clinical record in medicine. Part 1: Learning from cases. Annals of Internal Medicine 114:902–7.Google Scholar
Reynolds, T., Kong, M.-L. 2011. Learning without patients: How far can medical simulation replace clinical experience? BMJ 342:83–4.Google Scholar
Rosenthal, T.C. 2008. The medical home: Growing evidence to support a new approach to primary care. Journal of the American Board of Family Medicine 21(5):427–40.CrossRefGoogle ScholarPubMed
Rotich, J.K., Hannan, T.J., Smith, F.E., Bii, J., Odero, W.W., Vu, N., Mamlin, B.W., Mamlin, J.J., Einterz, R.M., Tierney, W.M. 2003. Installing and implementing a computer-based patient record system in sub-Saharan Africa: the Mosoriot Medical Record System. Journal of the American Medical Informatics Association 10(4):295303.CrossRefGoogle ScholarPubMed
Ridgely, M.S., Greenberg, M.D. 2012. Too many alerts, too much liability: sorting through the malpratice implications of drug-drug interaction clinical decision support. St. Louis University Journal of Health Law & Policy 5:257–96.Google Scholar
Rogers, J.A. 2015. Electronics for the human body. Journal of the American Medical Association 313(6):561–2.Google ScholarPubMed
Ross, M.K., Wei, W., Ohno-Machado, L. 2014. “Big data” and the electronic health record. Yearbook of Medical Informatics 9(1):97104.Google ScholarPubMed
Rothstein, M.S. 2010. The Hippocratic bargain and health information technology. Journal of Law, Medicine & Ethics 38(1):713.CrossRefGoogle ScholarPubMed
Rubel, A. 2012. Justifying public health surveillance: basic interests, unreasonable exercise, and privacy. Kennedy Institute of Ethics Journal 22(1):133.CrossRefGoogle Scholar
Rubin, D.L., Lewis, S.E., Mungall, C.J., Misra, S., Westerfield, M., Ashburner, M., Sim, I., Chute, C.G., Solbrig, H., Storey, M.A., Smith, B., Day-Richter, J., Noy, N.F., Musen, M.A. 2006. National Center for Biomedical Ontology: advancing biomedicine through structured organization of scientific knowledge. OMICS 10(2):185–98.CrossRefGoogle ScholarPubMed
Russell, A.L. 2014. Open Standards and the Digital Age: History, Ideology, and Networks. New York: Cambridge University Press.CrossRefGoogle Scholar
Ryan, T., Chester, A., Reece, J., Xenos, S. 2014. The uses and abuses of Facebook: A review of Facebook addiction. Journal of Behavioral Addictions 3(3):133–48.CrossRefGoogle ScholarPubMed
Sackett, D.L., Straus, S.E., Richardson, W.S., Rosenberg, W., Haynes, R.B. 2000. Evidence-Based Medicine: How to Practice and Teach EBM. 2nd edn. Edinburgh: Churchill Livingstone.Google Scholar
Sadegh-Zadeh, K. 2012. Handbook of Analytic Philosophy of Medicine. Dordrecht: Springer.CrossRefGoogle Scholar
Sadler, N.L., Sadler, A.M. 2012. Can Social Media Increase Transplant Donation and Save Lives? Science and Society, Hastings Center Bioethics Forum, available at www.thehastingscenter.org/Bioethicsforum/Post.aspx?id=5950.Google Scholar
Safran, C., Bloomrosen, M., Hammond, W.E., Labkoff, S., Markel-Fox, S., Tang, P.C., Detmer, D.E. 2007. Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper. Journal of the American Medical Informatics Association 14(1):19.CrossRefGoogle Scholar
Salathé, M., Freifeld, C.C., Mekaru, S.R., Tomasulo, A.F., Brownstein, J.S. 2013. Influenza A (H7N9) and the importance of digital epidemiology. New England Journal of Medicine 369:401–4.CrossRefGoogle ScholarPubMed
Schneiderman, L.J., Jecker, N.S. 1995. Wrong Medicine: Doctors, Patients, and Futile Treatment. Baltimore: Johns Hopkins University Press.Google Scholar
Scullard, P., Peacock, C., Davies, P. 2010. Googling children’s health: reliability of medical advice on the internet. Archives of Disease in Childhood 95(8):580–2.CrossRefGoogle ScholarPubMed
Seck, M.D., Evans, D.D. 2004. Major U.S. Cities Using National Standard Fire Hydrants, One Century After the Great Baltimore Fire. Gaithersburg, MD: National Institute of Standards and Technology (NISTIR 7158), available at www.fire.nist.gov/bfrlpubs/fire04/PDF/f04095.pdf.Google Scholar
Shannon, G.W., Buker, C.M. 2010. Determining accessibility to dermatologists and teledermatology locations in Kentucky: demonstration of an innovative geographic information systems approach. Telemedicine Journal and e-Health 16(6):670–7.Google ScholarPubMed
Sharkey, N., Sharkey, A. 2012. The rights and wrongs of Robot Care. In Lin, P., Abney, K., Bekey, G.A., eds., Robot Ethics: The Ethical and Social Implications of Robots. Cambridge, MA: MIT Press, 267–82.Google Scholar
Shaw, G. 1909. The Doctor’s Dilemma: With Preface on Doctors. New York: Brentano’s.Google Scholar
Shaw, J. 2006. Intention in ethics. Canadian Journal of Philosophy 36(2):187223.CrossRefGoogle Scholar
Shortliffe, E.H. 1993. Doctors, patients, and computers: Will information technology dehumanize health-care delivery? Proceedings of the American Philosophical Society 137(3):390–8.Google ScholarPubMed
Shortliffe, E.H. 1994. Dehumanization of patient care: Are computers the problem or the solution? Journal of the American Medical Informatics Association 1:7678.CrossRefGoogle ScholarPubMed
Shortliffe, E.H. 2011. Demonstrating value to secure trust. In Institute of Medicine, Digital Infrastructure for the Learning Health System: The Foundation for Continuous Improvement in Health and Health Care: Workshop Series Summary. Washington, DC: The National Academies Press, 151–5.Google Scholar
Shortliffe, E.H., Blois, M.S. 2014. Biomedical informatics: the science and the pragmatics. In Shortliffe, E.H., Cimino, J.J., eds., Biomedical Informatics: Computer Applications in Health Care and Biomedicine. 4th edn. New York: Springer, 337.CrossRefGoogle Scholar
Shortliffe, E.H., Cimino, J.J., eds. 2014. Biomedical Informatics: Computer Applications in Health Care and Biomedicine. 4th edn. New York: Springer.CrossRefGoogle Scholar
Siegler, E.L. 2010. The evolving medical record. Annals of Internal Medicine 153:671–7.CrossRefGoogle ScholarPubMed
Siegler, E.L., Adelman, R. 2009. Copy and paste: A remediable hazard of electronic health records. American Journal of Medicine 122:495–6.CrossRefGoogle Scholar
Simon, H.A. 1971. Designing organizations for an information-rich world. In Greenberger, M., ed., Computers, Communication, and the Public Interest. Baltimore, MD: The Johns Hopkins Press, 3752.Google Scholar
Simon, H.A. 1985. Artificial-intelligence approaches to problem solving and clinical diagnosis. In Schaffner, K.F., ed., Logic of Discovery and Diagnosis in Medicine. Berkeley: University of California Press, 7293.CrossRefGoogle Scholar
Sims, R. R., Brinkmann, J. 2003. Enron ethics (or culture matters more than codes). Journal of Business Ethics 45(3),243–56.CrossRefGoogle Scholar
Singer, P. 1972. Famine, affluence, and morality. Philosophy and Public Affairs 1(1):229–43.Google Scholar
Slack, W.V. 1989. The computer and the doctor-patient relationship. M.D. Computing 6(6):320–1.Google ScholarPubMed
Smith, L. 2011. The Kahun Gynaecological Papyrus: ancient Egyptian medicine. Journal of Family Planning and Reproductive Health Care 37:54–5.CrossRefGoogle ScholarPubMed
Smith, L. 2013. The history of contraception. In Briggs, P., Kovacs, G., Guillebaud, J., eds., Contraception: A Casebook from Menarche to Menopause. Cambridge: Cambridge University Press, 18–25.Google Scholar
Snapper, J.W. 1998. Responsibility for computer-based decisions in health care. In Goodman, K.W., ed., Ethics, Computing, and Medicine: Informatics and the Transformation of Health Care. Cambridge: Cambridge University Press, 4356.Google Scholar
Snell, K., Starkbaum, J., Lauß, G., Vermeer, A., Helén, I. 2012. From protection of privacy to control of data streams: a focus group study on biobanks in the information society. Public Health Genomics 15(5):293302.CrossRefGoogle Scholar
Snyder, L., American College of Physicians Ethics, Professionalism, and Human Rights Committee. 2012. American college of physicians ethics manual: sixth edition. Annals of Internal Medicine 156(1 Pt. 2):73104.CrossRefGoogle ScholarPubMed
Sommers, B.D., Baicker, K., Epstein, A.M. 2012. Mortality and access to care among adults after state Medicaid expansions. New England Journal of Medicine 367:1025–34.CrossRefGoogle ScholarPubMed
Sorenson, C., Drummond, M. 2014. Improving medical device regulation: the United States and Europe in perspective. Milbank Quarterly 92(1):114–50.CrossRefGoogle Scholar
Spruill, J.A. 1941. Privity of contract as a requisite for recovery on warranty. North Carolina Law Review 19:551–67.Google Scholar
Stangl, A.L., Lloyd, J.K., Brady, L.M., Holland, C.E., Baral, S. 2013. A systematic review of interventions to reduce HIV-related stigma and discrimination from 2002 to 2013: how far have we come? Journal of the International AIDS Society 16(3 Suppl. 2):18734.CrossRefGoogle ScholarPubMed
Stanley, F.J., Meslin, E.M. 2007. Australia needs a better system for health care evaluation. Medical Journal of Australia 186:220–1.CrossRefGoogle Scholar
Stell, L.K. 2014. Volume-outcome disparities and informed consent: What should surgeons disclose? Journal of Surgical Oncology, July 8. doi:10.1002/jso.23718. [Epub ahead of print].CrossRefGoogle Scholar
Stevens, J.M. 1975. Gynaecology from ancient Egypt: The papyrus Kahun: A translation of the oldest treatise on gynaecology that has survived from the ancient world. Medical Journal of Australia 2(25–26):949–52.CrossRefGoogle ScholarPubMed
Stroup, D.F., Berkelman, R.L. 1988. History of statistical methods in public health. In Stroup, D.F., Teutsch, S.M., eds., Statistics in Public Health: Quantitative Approaches to Public Health Problems. Oxford: Oxford University Press, 118.Google Scholar
Sulmasy, D.P., Marx, E.S. 1997. A computerized system for entering orders to limit treatment: implementation and evaluation. Journal of Clinical Ethics 8(3):258–63.CrossRefGoogle ScholarPubMed
Swan, M. 2009. Emerging patient-driven health care models: an examination of health social networks, consumer personalized medicine and quantified self-tracking. International Journal of Environmental Research and Public Health 6(2):492525.CrossRefGoogle ScholarPubMed
Swan, M. 2012a. Health 2050: The realization of personalized medicine through crowdsourcing, the quantified self, and the participatory biocitizen. Journal of Personalized Medicine 2(3):93118.CrossRefGoogle ScholarPubMed
Swan, M. 2012b. Crowdsourced health research studies: an important emerging complement to clinical trials in the public health research ecosystem. Journal of Medical Internet Research 14(2):e46.CrossRefGoogle ScholarPubMed
Sweeney, L. 1997. Weaving technology and policy together to maintain confidentiality. Journal of Law, Medicine and Ethics 25:98110.CrossRefGoogle ScholarPubMed
Szczepaniak, M.C., Goodman, K.W., Wagner, M.W., Hutman, J., Daswani, S. 2006. Advancing organizational integration: negotiation, data use agreements, law, and ethics. In Wagner, M.W., Moore, A.W., Aryel, R.M., eds. Handbook of Biosurveillance. Boston: Academic Press, 465–80.Google Scholar
Szolovits, P., Pauker, S.G. 1979. Computers and clinical decision making: whether, how much, and for whom? Proceedings of the IEEE 67:1224–6.CrossRefGoogle Scholar
Tamersoy, A., Loukides, G., Nergiz, M.E., Saygin, Y., Malin, B. 2012. Anonymization of longitudinal electronic medical records. IEEE Transactions on Information Technology in Biomedicine 16:413–23.CrossRefGoogle ScholarPubMed
Tait, I. 1981. History of our records. British Medical Journal 282:702–4.CrossRefGoogle ScholarPubMed
Tang, P.C., Ashe, J.S., Bates, D.W., Overhage, J.M., Sands, D.Z. 2006. Personal health records: definitions, benefits, and strategies for overcoming barriers to adoption. Journal of the American Medical Informatics Association 13(2):121–6.CrossRefGoogle ScholarPubMed
Tassey, G. 2000. Standardization in technology-based markets. Research Policy 29(4–5):587602.CrossRefGoogle Scholar
Tenke, P., Köves, B., Johansen, T.E. 2014. An update on prevention and treatment of catheter-associated urinary tract infections. Current Opinion in Infectious Diseases 27(1):102–7.CrossRefGoogle ScholarPubMed
Thielke, S., Hammond, K., Helbig, S. 2007. Copying and pasting of examinations within the electronic medical record. International Journal of Medical Informatics 76S:122–8.Google Scholar
Treloar, D., Hawayek, J., Montgomery, J.R., Russell, W., Medical Readiness Trainer Team. 2001. On-site and distance education of emergency medicine personnel with a human patient simulator. Military Medicine 166(11):1003–6.Google ScholarPubMed
Turkle, S. 2010. In good company? On the threshold of robotic companions. In Wilks, Y., ed., Close Engagements with Artificial Companions: Key Social, Psychological, Ethical and Design Issues. Amsterdam: John Benjamins, 310.CrossRefGoogle Scholar
Turvey, C., Klein, D., Fix, G., Hogan, T.P., Woods, S., Simon, S.R., Charlton, M., Vaughan-Sarrazin, M., Zulman, D.M., Dindo, L., Wakefield, B., Graham, G., Nazi, K. 2014. Blue Button use by patients to access and share health record information using the Department of Veterans Affairs’ online patient portal. Journal of the American Medical Informatics Association 21(4):657–63.CrossRefGoogle ScholarPubMed
University of Toronto Joint Centre for Bioethics. 2005. Stand On Guard for Thee: Ethical Considerations in Preparedness Planning for Pandemic Influenza. Pandemic Influenza Working Group, Toronto: University of Toronto Joint Centre for Bioethics, available at www.jcb.utoronto.ca/people/documents/upshur_stand_guard.pdf.Google Scholar
Upadhyay, D.K., Sittig, D.F., Singh, H. 2014. Ebola US Patient Zero: lessons on misdiagnosis and effective use of electronic health records. Diagnosis, October. Epub ahead of print, DOI:10.1515/dx-2014-0064.CrossRefGoogle Scholar
Urban, S. 2010. The electronic health record and the death of diagnosis. Texas Internist, Summer 2010, available at www.txacp.org/i4a/pages/index.cfm?pageID=876.Google Scholar
Urbanski, B.L., Lazenby, M. 2012. Distress among hospitalized pediatric cancer patients modified by pet-therapy intervention to improve quality of life. Journal of Pediatric Oncology Nursing 29(5):272–82.CrossRefGoogle ScholarPubMed
US Department of Health, Education and Welfare. 1973. Records, Computers and the Rights of Citizens. (Report of the Secretary’s Advisory Committee on Automated Personal Data Systems [OS]73–94.) Washington, DC: US Department of Health, Education and Welfare, available at www.justice.gov/opcl/docs/rec-com-rights.pdf and www.epic.org/privacy/hew1973report/.Google Scholar
van den Berge, K., Mamede, S. 2013. Cognitive diagnostic error in internal medicine. European Journal of Internal Medicine 24(6):525–9CrossRefGoogle ScholarPubMed
Vandenbroucke, J.P. 1998. Medical journals and the shaping of medical knowledge. The Lancet 352:2001–6.CrossRefGoogle ScholarPubMed
van der Sijs, H., Aarts, J., Vulto, A., Berg, M. 2006. Overriding of drug safety alerts in computerized physician order entry. Journal of the American Medical Informatics Association 13(2):138–47.CrossRefGoogle ScholarPubMed
Ventres, W.B., Frankel, R.M. 2010. Patient-centered care and electronic health records: it’s still about the relationship. Family Medicine 42(5):364–6.Google ScholarPubMed
Verma, I.M. 2014. Editorial expression of concern: Experimental evidence of massive-scale emotional contagion through social networks. Proceedings of the National Academy of Sciences 111(29):10779.Google ScholarPubMed
von Muhlen, M., Ohno-Machado, L. 2012. Reviewing social media use by clinicians. Journal of the American Medical Informatics Association 19(5):777–81.CrossRefGoogle ScholarPubMed
Wachter, R. 2010. Why diagnostic errors don′t get any respect – And what can be done about them. Health Affairs 29:1605–10.CrossRefGoogle Scholar
Walker, J., Leveille, S.G., Ngo, L., Vodicka, E., Darer, J.D., Dhanireddy, S., Elmore, J.G., Feldman, H.J., Lichtenfeld, M.J., Oster, N., Ralston, J.D., Ross, S.E., Delbanco, T. 2011. Inviting patients to read their doctors’ notes: patients and doctors look ahead: patient and physician surveys. Annals of Internal Medicine 155(12):811–9.CrossRefGoogle ScholarPubMed
Walsh, C., Siegler, E.L., Cheston, E., O’Donnell, H., Collins, S., Stein, D., Vawdrey, D.K., Stetson, P.D., Informatics Intervention Research Collaboration (I2RC). 2013. Provider-to-provider electronic communication in the era of meaningful use: a review of the evidence. Journal of Hospital Medicine 8(10):589–97.CrossRefGoogle ScholarPubMed
Wang, W,. Baggerly, K.A., Knudsen, S., Askaa, J., Mazin, W., Coombes, K.R. 2013. Independent validation of a model using cell line chemosensitivity to predict response to therapy. Journal of the National Cancer Institute 105(17):1284–91.CrossRefGoogle Scholar
Ward, J.J., Wattier, B.A. 2011. Technology for enhancing chest auscultation in clinical simulation. Respiratory Care 56(6):834–45.CrossRefGoogle ScholarPubMed
Warren, S.D., Brandeis, L.D. 1890. The right to privacy. Harvard Law Review 4(5):193221.CrossRefGoogle Scholar
Wears, R.L. 2008. The chart is dead—long live the chart. Annals of Emergency Medicine 52(4):390–1.CrossRefGoogle Scholar
Wears, R.L. 2015. Health information technology and victory. Annals of Emergency Medicine 65(2):143–5.CrossRefGoogle ScholarPubMed
Weinberg, F. 1993. The history of the stethoscope. Canadian Family Physician 39:2223–4.Google ScholarPubMed
Weis, J.M., Levy, P.C. 2014. Copy, paste, and cloned notes in electronic health records: prevalence, benefits, risks, and best practice recommendations. Chest 145(3):632–8.CrossRefGoogle ScholarPubMed
Were, M.C., Nyandiko, W.M., Huang, K.T., Slaven, J.E., Shen, C., Tierney, W.M., Vreeman, R.C. 2013. Computer-generated reminders and quality of pediatric HIV care in a resource-limited setting. Pediatrics 131(3):e78996.CrossRefGoogle Scholar
Were, M.C., Shen, C., Tierney, W.M., Mamlin, J.J., Biondich, P.G., Li, X., Kimaiyo, S., Mamlin, B.W. 2011. Evaluation of computer-generated reminders to improve CD4 laboratory monitoring in sub-Saharan Africa: a prospective comparative study. Journal of the American Medical Informatics Association 18(2):150–5.CrossRefGoogle ScholarPubMed
Whiting-O’Keefe, Q.E., Simborg, D.W., Epstein, W.V., Warger, A. 1985. A computerized summary medical record system can provide more information than the standard medical record. Journal of the American Medical Association 254(9):1185–92.Google Scholar
Wilbanks, J. 2014. Portable approaches to informed consent and open data. In Lane, J., Stodden, V., Bender, S., Nissenbaum, H., eds., Privacy, Big Data, and the Public Good. New York: Cambridge University Press, 235–52.Google Scholar
Wilks, Y. 2007. Is There Progress on Talking Sensibly to Machines? Science 318:927–8.CrossRefGoogle ScholarPubMed
Wilks, Y., Fass, D., Guo, C.M., McDonald, J., Plate, T., Slator, B. 1990. A tractable machine dictionary as a basis for computational semantics. Machine Translation 5:99154.CrossRefGoogle Scholar
Williams, H., Spencer, K., Sanders, C., Lund, D., Whitley, E.A., Kaye, J., Dixon, W.G. 2015. Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research. JMIR Medical Informatics 3(1):e3.CrossRefGoogle ScholarPubMed
Williams, R., Bunduchi, R., Gerst, M., Graham, I., Pollock, N., Procter, R.N., Voss, A. 2004. Understanding the evolution of standards : alignment and reconfiguration in standards development and implementation arenas. In Proceedings Society for Social Studies of Science (4S) & European Association for the Study of Science and Technology (EASST) conference, Paris, August 24–28, 2004, 116.Google Scholar
Wilson, G., Aruliah, D.A., Brown, C.T., Chue Hong, N.P., Davis, M., Guy, R.T., Haddock, S.H.D., Huff, K.D., Mitchell, I.M., Plumbley, M.D., Waugh, B., White, E.P., Wilson, P. 2014. Best practices for scientific computing. PLoS Biology 12(1):e1001745.CrossRefGoogle ScholarPubMed
Winkelstein, P. 2013. Medicine 2.0. ethical challenges of social media for the health profession. In George, C., Whitehouse, D., Duquenoy, P., eds. eHealth: Legal, Ethical and Governance Challenges. Heidelberg: Springer, 227–43.Google Scholar
Winner, L. 1980. Do artifacts have politics? Daedalus 109(1):121–36.Google Scholar
Wolf, S.M. 2013. Return of individual research results and incidental findings: facing the challenges of translational science. Annual Review of Genomics and Human Genetics 14:557–77.CrossRefGoogle ScholarPubMed
World Health Organization. 2010. International Statistical Classification of Diseases and Related Health Problems. 10th Revision, Vol. 2, Instruction Manual. Geneva: World Health Organization, available at www.who.int/classifications/icd/ICD10Volume2_en_2010.pdf?ua=1.Google Scholar
World Health Organization. 2011. Safety and security on the Internet: Challenges and advances in Member States. Global Observatory for eHealth series – Volume 4, available at www.who.int/goe/publications/goe_security_web.pdf.Google Scholar
World Health Organization. 2014. Governing principles for a .health top-level domain, May 15, 2014, available at www.who.int/ehealth/programmes/governance/en/index3.html.Google Scholar
Yakupcin, J.P. 2005. Child passenger safety in the school-age population. Pediatric Emergency Care 21(4):286–90.CrossRefGoogle ScholarPubMed
Yarborough, M. 2014. Taking steps to increase the trustworthiness of scientific research. The FASEB Journal 28:3841–6.CrossRefGoogle ScholarPubMed
Yarborough, M., Hunter, L. 2013. Teaching research ethics better: focus on excellent science, not bad scientists. Clinical and Translational Science 6(3):201–3.CrossRefGoogle Scholar
You, J. 2015. DARPA sets out to automate research. Science 347(6221):465.CrossRefGoogle ScholarPubMed
Youngner, S.J. 1988. Who defines futility? Journal of the American. Medical Association 260:2094–95.Google ScholarPubMed
Yu, A.C. 2006. Methods in biomedical ontology. Journal of Biomedical Informatics 39(3):252–66.CrossRefGoogle ScholarPubMed
Zittrain, J. 2014. No, Barack Obama isn’t handing control of the Internet over to China: The misguided freakout over ICANN. The New Republic, March 24, 2014, available at www.newrepublic.com/article/117093/us-withdraws-icann-why-its-no-big-deal.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

  • References
  • Kenneth W. Goodman, University of Miami
  • Book: Ethics, Medicine, and Information Technology
  • Online publication: 18 December 2015
  • Chapter DOI: https://doi.org/10.1017/CBO9781139600330.012
Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • References
  • Kenneth W. Goodman, University of Miami
  • Book: Ethics, Medicine, and Information Technology
  • Online publication: 18 December 2015
  • Chapter DOI: https://doi.org/10.1017/CBO9781139600330.012
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • References
  • Kenneth W. Goodman, University of Miami
  • Book: Ethics, Medicine, and Information Technology
  • Online publication: 18 December 2015
  • Chapter DOI: https://doi.org/10.1017/CBO9781139600330.012
Available formats
×