If our EMR doesn’t have an order import interface capability and the lab receives a “plan item/request” and then manually enters the order, does this affect meaningful use?
Based on how this question is worded, we assume the EMR does not have the capability for a CPOE interface. Stage 1 meaningful use does not require CPOE of lab orders. However, page 44321 42 CFR Incentive Program final rule suggests that Stage 2 will propose CPOE as a requirement. We, therefore, highly recommend working with your current EMR vendor to determine their plans for certification, including CPOE and the expected requirements for exchanging information.
