EMRs Improve Reporting of Hospitals' Adverse Events to Regulators

A new study found physicians' use of electronic medical records in hospitals led to a substantial increase in reporting of adverse events to the FDA, according to a report by the Wall Street Journal.

Previous studies have shown just a small fraction of physicians voluntarily submit reports on adverse events to the FDA. The EMR's automated system made sure the adverse event was reported, a study in Pharmacoepidemiology and Drug Safety found.

For example, when a physician recorded discontinuing a medication because a patient experienced an adverse event, the electronic patient record system generated an alert, asked the physician whether the side effect was serious and submitted a report to regulators.

About one in five of the automated reports involved serious side effects, such as hospitalizations, researchers at Massachusetts General and Brigham & Women's hospitals in Boston said.

Read the Wall Street Journal report on EMRs.

Read more coverage on EMRs and adverse events:

- Improving Medication Reconciliation With EMRs: Insight from John Klimek of NCPDP


- How Hospitals Can Benefit From EHR Implementation: Q&A With Alan Portela, President of CliniComp

- 5 Ways Hospitals Will Change Over the Next 10 Years



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