The notion of privacy in the healthcare domain is at least as old as the ancient Greeks. Several decades ago, as electronic medical record (EMR) systems began to take hold, the necessity of patient privacy was recognized as a core principle, or even a right, that must be upheld. This belief was re-enforced as computers and EMRs became more common in clinical environments. However, the arrival of ultra-cheap data collection and processing technologies is fundamentally changing the face of healthcare. The traditional boundaries of primary and tertiary care environments are breaking down and health information is increasingly collected through mobile devices, in personal domains (eg, in one’s home), and from sensors attached on or in the human body (eg, body area networks). At the same time, the detail and diversity of information collected in the context of healthcare and biomedical research is increasing at an unprecedented rate, with clinical and administrative health data being complemented with a range of *omics data, where genomics and proteomics12 are currently leading the charge, with other types of molecular data on the horizon.
Healthcare organizations (HCOs) are adopting and adapting information technologies to support an expanding array of activities designed to derive value from these growing data archives, in terms of enhanced health outcomes.
Malin BA, El Emam K, O’Keefe CM. Biomedical data privacy: problems, perspectives, and recent advances. J Am Med Inform Assoc [Internet]. 2012 Dec 6; Available from: http://jamia.bmj.com/content/early/2012/12/05/amiajnl-2012-001509