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Study
Using FDA reports to inform a classification for health information technology safety problems.
December 31, 2014
Magrabi F, Ong M-S, Runciman WB, et al. J Am Med Inform Assoc. 2012;19(1):45-53.
This study reviewed nearly 900,000 reports from the FDA Manufacturer and User Facility Device Experience database (MAUDE) and identified 678 reports describing health information technology issues. Investigators uncovered problems with software functionality, system configuration, interface with devices, and network configuration as new categories to the existing classification system.
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