When the Centers for Medicare & Medicaid Services (CMS) issued a proposed rule for Stage 3 of the meaningful use program in March, and then again for program modifications from 2015-2017 in April, immediate industry feedback and commentary followed. Since then, over the early summer months, all was quiet on the meaningful use front. But now, as the calendar reads August, and final rules could be on the verge of being published, health IT stakeholders have once again geared up for one last push to get the feds to address their concerns with the program.
Indeed, starting in late July, the calls from Congress began for a Stage 3 delay when during a Senate Health, Education, Labor & Pensions (HELP) Committee hearing, Sen. Lamar Alexander (R-TN), chair of the committee, said that he has requested that the U.S. Department of Health and Human Services (HHS) push it back from its scheduled start in 2017. Then, in a July 31 letter to HHS, several healthcare stakeholder organizations wrote a letter to HHS urging the department to publish the final rule for the modifications to the meaningful use program from 2015-2017. Also thrown into the mix was the recent introduction of the Flexibility in Health IT Reporting and Advancing Interoperability Act of 2015 or “Flex-IT 2” (H.R. 3309) into Congress by Congresswoman Renee Ellmers (R-NC-02). The legislation offers improvements to the meaningful use program, including a delay in the release Stage 3 rules.
Put all together, it’s become clear that the industry wants some answers—and soon. As such, HCI recently spoke with Jason Fortin, senior advisor at the Naperville, Ill.-based Impact Advisors about what’s in store for meaningful use throughout the rest of 2015, if stakeholders will get what they want, and what providers are grappling most about. Below are excerpts of t hat interview.
The health IT industry has been pretty up in arms lately about MU. What impact do you see this having at the end of the day?
First off, I haven’t heard anything that you haven’t regarding when things might happen regarding the MU modifications rule. There is a formal process to it that involves CMS publishing the rule in the Federal Register. I don’t know when it could happen, but it should be soon. If history is any indication, it should be in the next few weeks. The sooner the better for providers, since you are talking about changes to this reporting year and next year too. Until we hear something definitive though, we just don’t know. CMS isn’t tipping their hand either, and that could be because they can’t talk about it at this point.
In regard to the modifications rule, what changes do you see from the feds’ proposal?
I think they will keep a lot of what they proposed. I will be shocked if they don’t align the reporting periods on the calendar and move to a 90-day reporting period. For hospitals, if there wasn’t a proposed rule, the reporting period ends at end of September. That’s not enough time.
It could get tricky if they decide to add back in some of the measures they proposed to drop. There are a few things they said they might not require anymore because they are redundant, but if they add those back in that could be tricky even if they are measures that hospitals or EPs have met before. Everything they proposed would make this year easier, but the tough thing is for 2016. Take e-prescribing in hospitals for instance. If you are a hospital waiting for Stage 3 in 2018 to do e-prescribing, and all of a sudden, that will be something that is required in 2016 based on how the changes for Stage 2 measures are restructured. So 2016 is a year where some of the heartburn could occur.
Back to patient engagement—what is the logic behind going from having 5 percent of patients view/download/transmit (VDT) their information down to one single patient, and finally back up to 25 percent in Stage 3?
The patient engagement measure is one change they have to make when you consider how hard that has been for providers. I wish I could tell you the logic behind that. Some of the logic for the 25 percent is that they would allow access through an ONC-certified API, but anything that requires certification is a big unknown. There isn’t a technology out there that could get us to 25 percent as is. There are pockets regionally that could do it, but at the level of 25 percent, it’s not really about technology anymore, but more about a fundamental shift in behavior about how patients look at their information.
Also, the transitions of care (TOC) measure went from 10 percent to 50 percent via CMS’ proposal, but the transitions could occur via any electronic means. What about Direct, where does it fit in? They left that open for comments so that will be interesting too. When this rule first came out, 10 percent didn’t seem nearly as bad and then people started implementing it and realized that it’s very hard.
Onto Stage 3, will the calls for a delay have any traction?
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