Deadlines can never bring forth innovation. When everything is under the MU pressure, the need to meet Federal Mandates overshadows everything else. This results in loopholes, and in many cases, leads to bad engineering. [twitter.com/healthitplus]
Many a times, EMRs are produced to meet the MU requirements but doesn’t meet the needs of the consumers. As a result, MU is failing to create the environment it is attempting to create through the stringent regulations and deadlines.
Yes, Meaningful Use has supported innovation in ways such as:
- The Blue Button Plus supports a new, higher level of patient access to their data,and is built from components and requirements already present in Stage 2.
- The Query Health initiative has done innovative work that supports not only its stated focus (health research) but also automation of quality measurement using HL7′s HQMF.
But eventually the Meaningful Use will stress on EMR developers to come up to the MU standards but not innovation. So, maybe we will see a gradual rise in applications that provide a different set of functionalities to EMRs.
Readers, what innovations would you like to see?
- It’s Time for Consumers to Get Serious about Their EMRs (healthitplus.wordpress.com)