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Implementation of data access and use procedures in clinical data warehouses. A systematic review of literature and publicly available policies.

Elena PavlenkoDaniel StrechHolger Langhof
Published in: BMC medical informatics and decision making (2020)
The description of data access and use governance in the scientific literature is characterized by a high level of heterogeneity and ambiguity. In practice, this might limit the effective data sharing needed to fulfil the high expectations of data-intensive approaches in medical research and health care. The lack of publicly available information on access policies conflicts with ethical requirements linked to principles of transparency and accountability. CDW should publicly disclose by whom and under which conditions data can be accessed, and provide designated governance structures and policies to increase transparency on data access. The results of this review may contribute to the development of practice-oriented minimal standards for the governance of data access, which could also result in a stronger harmonization, efficiency, and effectiveness of CDW.
Keyphrases
  • healthcare
  • electronic health record
  • big data
  • public health
  • primary care
  • randomized controlled trial
  • mass spectrometry
  • artificial intelligence