Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper.
By C. Safran, Meryl Bloomrosen, W. E. Hammond, Steven E. Labkoff, Suzanne Markel-Fox, Paul C. Tang, D. E. Detmer, Ma, Doug Barton, W. Hammond and 9 more. JAMIA Journal of the American Medical Informatics Association, 2007
705 citations recorded by the source corpus.
Subfields: Economics and Econometrics, Health Information Management, Public Health, Environmental and Occupational Health
View Paper: https://www.semanticscholar.org/paper/9a07367969507b2209c94a4b23992a50d425dfab
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Citations in the corpus
- Methods and dimensions of electronic health record data quality assessment: enabling reuse for clinical research (2013, methodology): “As the adoption of electronic health records (EHRs) has made it easier to access and aggregate clinical data, there has been growing interest in conducting research with data collected during the course of clinical care.(1) 2 The Natonal Institutes of Health has called for increasing the reuse of el”
- Grand challenges in clinical decision support (2008, background): “For example, as these clinical data resources begin to cross institutional and organizational boundaries, much effort will be required to insure that patient-identifiable information will remain private and secure [20].”
- A method for evaluating marketer re-identification risk (2010, background): “INTRODUCTION As more ostensibly de-identified health data sets are disclosed for secondary purposes [1, 2], it is becoming important to measure the risk of patient re-identification (i.”
- Defining and measuring completeness of electronic health records for secondary use (2013, neutral): “With the growing availability of large electronic health record (EHR) databases, clinical researchers are increasingly interested in the secondary use of clinical data [1,2].”