Switch to: References

Add citations

You must login to add citations.
  1. Revisiting consent for health information databanks.Stephan Millett & Peter O’Leary - 2015 - Research Ethics 11 (3):151-163.
    This paper argues that specific individual informed consent and other forms of consent predicated on a right to autonomy may not in all circumstances be appropriate for the establishment and use of large data sets of health information. We suggest that there are inherent failings in such an approach, shortcomings that we analyse below. We argue that individuals share an obligation to contribute their data, as doing so is cost-free and benefits accrue to the population as a whole. Large health (...)
    Direct download  
     
    Export citation  
     
    Bookmark  
  • Editorial: The publication of unethical research.David Hunter - 2012 - Research Ethics 8 (2):67-70.
  • Big Data Analytics, Infectious Diseases and Associated Ethical Impacts.Chiara Garattini, Jade Raffle, Dewi N. Aisyah, Felicity Sartain & Zisis Kozlakidis - 2019 - Philosophy and Technology 32 (1):69-85.
    The exponential accumulation, processing and accrual of big data in healthcare are only possible through an equally rapidly evolving field of big data analytics. The latter offers the capacity to rationalize, understand and use big data to serve many different purposes, from improved services modelling to prediction of treatment outcomes, to greater patient and disease stratification. In the area of infectious diseases, the application of big data analytics has introduced a number of changes in the information accumulation models. These are (...)
    Direct download (2 more)  
     
    Export citation  
     
    Bookmark   6 citations