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OJAI, Calif.–The goal was to make meaningful use ambitious, but achievable, said Farzad Mostashari, senior advisor for policy and programming at the Office of the National Coordinator for Health IT (ONC), who clarified several points and answered many questions about meaningful use at the AMDIS Physician-Computer Connection Symposium Thursday. “No one got everything they wanted, but I think we got it right,” Mostashari said. He highlighted changes in the final rule that were made based on input from clinicians:
The originator of the order, not a transcriber, should input the order: “The goal is to be able to have intelligence at the point of care,” he said. Non-physicians with legal authority, those with ordering privileges, can initiate an order into the system. These changes in the final rule will help make meaningful use easier to attain, Mostashari said. “It’s going to be hard, but it’s doable. I hope you’ll agree that for motivated providers, meaningful use is much more achievable than it was before.” Following are some of the questions from the audience: Q: There is some concern that the bar has been lowered. Are you concerned that reducing core measures and changing CPOE requirements might mislead facilities into thinking we don’t have to do very much differently than we’re doing today? A: I think we struck a balance, because it’s important that there be a sense of momentum around this, so we can bring pressure on the ecosystem as a whole. Achieving meaningful use is not crazy-hard, but there’s some basic stuff that’s not being done consistently that can help. Q: Do you have a goal for the number of doctors year to year who will become meaningful users? A: We’re going to have to wait and see. We don’t have a hard target, but by 2015 the vast majority will be meaningful users. Q: Regarding e-prescribing of controlled drugs: are you talking to the Drug Enforcement Administration (DEA)? A: We’ve been talking to the DEA. Part of what we pushed for was to get the rule out. People needed enough clarity to start trying it out. This is another example where the rule is out; we have clarity and now it’s up to people to see if it’s workable. Q: What about requirements for Phase 2 and beyond? A: Everything that was in the NPRM [notice of proposed rulemaking] for meaningful use, we want to be there in Stage 2. Part of [the final rule objective] is helping people to set the road map. Q: Will vendors need to upgrade systems for Stage 2? A: Yes. The certification process is not ideal, but we wanted to get something out there quickly. The limited approach will run out at the end of Stage 1. Q: If we’ve changed the goals for meaningful use, will we still have the data accessible to transform healthcare? A: Standards for information exchange are going to get a lot tougher in Stage 2: Stage 1 information exchange has been limited by the absence of infrastructure. Q: Is ONC working to figure out how much improvement we’re going to get in terms of cost and improved quality of care? A: ONC is doing some modeling around that. A lot of this is about how you implement. The big unknown is whether we are going to see a bigger bang for the buck, or … whether new entrants who are doing this to get meaningful use payments will get less than superior results than those who have been leading the charge in the past.
Last Updated ( Tuesday, July 20 2010 )
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