Ethics in Biomedical and Health Informatics: Users, Standards, and Outcomes

Author:

Goodman Kenneth W.,Miller Randolph A.

Publisher

Springer International Publishing

Reference69 articles.

1. Alpert, S. A. (1998). Health care information: Access, confidentiality, and good practice. In K. W. Goodman (Ed.), Ethics, computing, and medicine: Informatics and the transformation of health care (pp. 75–101). Cambridge: Cambridge University Press.

2. Anderson, J. G., & Aydin, C. E. (1994). Overview: Theoretical perspectives and methodologies for the evaluation of health care information systems. In J. G. Anderson, C. E. Aydin, & S. J. Jay (Eds.), Evaluating health care information systems: Methods and applications (pp. 346–354). Thousand Oaks: Sage.

3. Anderson, J. G., & Aydin, C. E. (1998). Evaluating medical information systems: Social contexts and ethical challenges. In K. W. Goodman (Ed.), Ethics, computing, and medicine: Informatics and the transformation of health care (pp. 57–74). Cambridge: Cambridge University Press.

4. 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, 95–101.

5. Benitez, K., & Malin, B. (2010). Evaluating re-identification risks with respect to the HIPAA privacy rule. Journal of the American Medical Informatics Association, 17, 169–177.

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