Advice to the next national coordinator for health IT

Over the next few months, Jacob Reider will serve as the interim National Coordinator for Health Information Technology (ONC)  while the search continues for Farzad Mostashari’s permanent replacement.

What advice would I give to the next national coordinator?

David Blumenthal led the ONC during a period of remarkable regulatory change and expanding budgets. He was the right person for the “regulatory era.”

Farzad Mostashari led ONC during a period of implementation when resources peaked, grants were spent, and the industry ran marathons every day to keep up with the pace of change. He was the right person for the “implementation era.”

The next coordinator will preside over the “consolidate our gains” era. Grants largely run out in January 2014. Budgets are likely to shrink because of sequestration and the impact of fiscal pressures. Many regulatory deadlines converge in the next coordinator’s term.

The right person for this next phase must listen to stakeholder challenges, adjust timelines, polish existing regulations, ensure the combined burden of regulations from many agencies in HHS do not break the camel’s back, and keep Congress informed every step of the way. I did not include parting the Red Sea, so maybe there is a mere human who could do this.

What tools does the coordinator have in an era of shrinking budgets?

At present, meaningful use stage 2, ICD-10, the Affordable Care Act, HIPAA Omnibus Rule, and numerous CMS imperatives have overlapping timelines, making it nearly impossible for provider organizations to maintain operations while complying with all the new requirements.

Can resources be expanded?

Given that Medicare/Medicaid reimbursements are falling, private insurance payments are nearly flat, and costs continue to escalate, the pie of resources is a fixed size and very challenging for anyone to expand.

The new coordinator has only two levers — reduce scope or extend time. Changing the scope of initiatives already in progress may be very challenging (i.e. require acts of Congress), realignment of powerful stakeholders, or compromise of the important interoperability goals we’ve worked so hard to craft.

That leaves “time” as the one lever under the coordinator’s control. However, even revising schedules will be challenging because of competing stakeholder demands.

1. ICD-10. Although some large organizations have significant sunk costs and want the deadline to remain as October 1, 2014, smaller organizations will not be ready. Some payers (including government payers) may not be ready. It’s clear we need to extend the deadline at least 6 months. Maybe encourage voluntary ICD-10 transactions on October 1, 2014, but allow a 6 month grace period without regulatory enforcement for the industry to catchup with the software, training, and process change needed for ICD-10 success?

2. Meaningful use stage 2. Software products are still being certified, so many hospitals and professionals have not yet upgraded to meaningful use stage 2 certified applications, making a 2014 reporting period/attestation somewhat challenging. Meaningful use stage 2 reporting periods have already begun for hospitals, so no delay is possible, but the reporting period timeframe could be extended. Maybe provide an 18 month window for stage 2 attestation? I realize this could delay future stages of meaningful use, but the industry needs a breather to consolidate our gains.

3. ACA. The Affordable Care Act has motivated many organizations to focus on continuous wellness rather than episodic sickness. ACOs are building private data exchanges and outcomes registries. Progress is accelerating because every dollar spent on IT has the potential to reduce costs in risk-based contracts. ACA and private insurer equivalent programs (such as the Blue Cross Alternative Quality contract) include many quality measures. Unfortunately, these measures are not optimized for the EHR era and are retooled from a time when quality measurement was done by abstractors in health information management. Rather than escalate already burdensome quality reporting requirements, shouldn’t we step back and ask what measures are truly important and urgent in a fully electronic era? Reducing reporting burdens temporarily while s a consolidated set of new electronic measures is developed would be very helpful.

4. HIPAA Omnibus Rule. Audits require at least 10 operational hours for every auditor hour. While hospitals and practices are in the midst of enhancing policies, revising infrastructure, and learning about the operational implications of the Omnibus Rule, it would be prudent to slow the pace of audits, just temporarily. We all want to protect privacy and reduce risk but there is a fixed rate at which organizations can integrate change. We need to focus on the long term and build a robust multi-layered defense. At times in the past, we’ve moved faster with regulations/enforcement than standards and technology maturity could support.

5. Some have suggested that if industry does move fast enough, more regulations will cause stakeholders to move faster. I really believe that more regulations will be a case of haste makes waste. Let’s integrate existing regulations into the fabric of our operations, using the market forces created by the accountable care act to align incentives, and only consider new regulations when we have enough information about the impact of prior regulations. Although challenging, maybe the coordinator could even consider polishing existing regulations to reduce the artificially burdensome aspects which are not necessary to achieve policy objectives. I’d start with taking testimony about the certification scripts for view/download/transmit, transitions of care, quality measurement, automated numerator/denominator, and clinical decision support.

Jacob Reider will do a great job over the next few months and could become the permanent coordinator. I will do everything in my power as co-chair of the Standards Committee to support whatever scope and timing revisions the coordinator considers.

John Halamka is chief information officer, Beth Israel Deaconess Medical Center, and blogs at Life as a Healthcare CIO.

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  • ninguem

    How about spending some time trying to determine whether the tremendous expense does anything good at all?

    • Deceased MD

      It depends. For “market research” it has loads of “meaningful use”, data mining.

    • buzzkillerjsmith

      Best not to look to closely. Profits could plummet.

  • kjindal

    how about funneling lots of money to miscellaneous heavily-lobbying software vendors to design user-unfriendly EHRs that don’t talk to each other, with zero input from their purported users (ie. doctors)?

    oh wait, tried that.

  • Disqus_37216b4O

    “every dollar spent on IT has the potential to reduce costs in risk-based contracts.”

    Well that sounds like a great reason to throw billions of taxpayer dollars at it right there.

    /s

  • buzzkillerjsmith

    “Focus on continuous wellness rather than episodic sickness.”

    Ah, continuous wellness in this best of all possible worlds. And unending felicity for ever and ever, amen. And please give us no war, no pollution, no mean people, and no traffic, and no broccoli. And a bag of chips.

    I’m pumped. Aren’t you all pumped?