Electronic Health Records (EHRs) - Meaningful Use

Centers for Medicare & Medicaid Services Administrator Seema Verma yesterday challenged technology developers and insurers to make health information more interoperable and available to patients.
The Food and Drug Administration this week issued guidance intended to clarify the agency’s expectations when electronic health records are used as a source of data in clinical investigations.
A new study involving clinicians using electronic health records to perform certain common tasks found that the design, development and implementation of these systems should be improved to make them easier to use by clinicians and safer for patients.
Please see the AHA Special Bulletin for a summary of the rule, including key takeaways for hospital and health system leaders, as well as AHA’s reaction.
The Centers for Medicare & Medicaid Services today released a resource to help electronic health record vendors and others incorporate post-acute care assessment instrument data elements into electronic health record products to improve interoperability and facilitate care coordination.
We’re pleased to see CMS follow through on its commitment to reduce regulatory burden. This is crucially needed as we continue, and accelerate, the transition to value-based care.