Summary
Objective: To summarize the state of the art during the year 2016 in the areas related to consumer
health informatics and education with a special emphasis in secondary use of patient
data.
Methods: We conducted a systematic review of articles published in 2016, using PubMed with
a predefined set of queries. We identified over 320 potential articles for review.
Papers were considered according to their relevance for the topic of the section.
Using consensus, we selected the 15 most representative papers, which were submitted
to external reviewers for full review and scoring. Based on the scoring and quality
criteria, five papers were finally selected as best papers
Results: The five best papers can be grouped in two major areas: 1) methods and tools to identify
and collect formal requirements for secondary use of data, and 2) innovative topics
highlighting the interest of carrying on “secondary” studies on patient data, more
specifically on the data self-expressed by patients through social media tools. Regarding
the formal requirements about informed consent, the selected papers report a comparison
of legal aspects in European countries to find a common and unified grammar around
the concept of “data donation”. Regarding innovative approaches to value patient data,
the selected papers report machine learning algorithms to extract knowledge from patient
experience and satisfaction with health care delivery, drug and medication use, treatment
compliance and barriers during cancer disease, or acceptation of public health actions
such as vaccination.
Conclusions: Secondary use of patient data (apart from personal health care record data) can be
expressed according to many ways. Requirements to allow this secondary use have to
be harmonized between countries, and social media platforms can be efficiently used
to explore and create knowledge on patient experience with health problems or activities.
Machine learning algorithms can explore those massive amounts of data to support health
care professionals, and institutions provide more accurate knowledge about use and
usage, behaviour, sentiment, or satisfaction about health care delivery.
Keywords
Consumer health informatics - personal health information - social media - secondary
data use - internet