IOM Report addresses Patient Safety
To protect Americans from potential medical errors associated with the use of information technology in patient safety, a new report by
the Institute of Medicine calls for greater oversight by the public and
private sectors. The report examines a broad range of health
information technologies, including electronic health records, secure
patient portals, and health information exchanges, but not software for
medical devices.
The secretary of the U.S. Department of Health and Human Services
should publish a plan within 12 months to minimize patient safety risks
associated with health IT and report annually on the progress being
made, the report says. The plan should include a schedule for working
with the private sector to assess the impact of health IT on patient
safety. However, if the secretary determines that progress toward
improving patient safety is insufficient within a year, the U.S. Food and Drug
Administration should exercise its authority to regulate these
technologies. Concurrently, FDA should begin planning the framework
needed for potential regulation so that the agency is ready to act if
necessary.
To read the full article please visit Patient Safety & Quality Healthcare
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