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HHS panel pushes to turn behavioral‑health interoperability and AI into measurable outcomes

U.S. Department of Health and Human Services · April 27, 2026

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Summary

Federal and provider leaders at an HHS panel urged policymakers to pair investments in electronic health records and AI with measurable quality metrics, funding pathways and privacy safeguards—citing state variability, 42 CFR part 2 concerns and vendor claims about reduced clinician documentation time.

Jason Funderburk, deputy national coordinator and a practicing physician, opened a U.S. Department of Health and Human Services panel focused on how electronic health records (EHRs), health information exchanges and artificial intelligence can improve behavioral‑health care coordination.

The discussion centered on three aims: examples of EHR‑enabled coordination, how AI can improve clinical and patient outcomes, and the program and policy conditions needed to scale tools that expand access. "If we dig a little bit deeper, we get just past knowing somebody's a veteran to actually sharing records, diagnostic assessments, treatment plans," Quinn Bastian, national mental health director for informatics at the Department of Veterans Affairs, said. He argued interoperability must be tied to "digital quality measures" so communities can determine whether shared data changes outcomes.

Vendor, provider and state perspectives converged on practical barriers. Steve Herron of Oracle Health described AI workflows that transcribe sessions and summarize patient histories; he said some clinics reported faster documentation and capacity gains, noting one provider saw "57% less time to document the notes" and another saw "25% less time" spent in the EHR, which Herron presented as real‑world benefits of AI. He and other panelists stressed that AI’s value depends on having a complete, interoperable record.

Stephanie Brown, president and executive director of CRISP DC, described a "no wrong door" HIE approach that accepts behavioral‑health data from diverse vendors and offers a consent tool to capture 42 CFR part 2 permissions so sensitive substance‑use information can be segregated and released only when permitted. "We will take the data in any way you can give it to us," Brown said, explaining technical assistance and parsing workflows for mixed‑use facilities.

Speakers from the Indian Health Service, Centerstone and advocacy organizations emphasized cultural and geographic factors. Dr. Susie Postel, chief health informatics officer at Indian Health Service, highlighted telebehavioral health for patients on reservations who may be hours from care and urged culturally sensitive implementations. Ashley Newton of Centerstone emphasized care‑coordination services and workforce impacts: consistent metrics and data flows can reduce clinician burnout and improve follow‑through.

Policy levers were a recurring theme. Ms. Veronio of the National Association of State Mental Health Program Directors pointed to Centers for Medicare & Medicaid Services (CMS) guidance issued in June 2024 and the availability of enhanced federal match for state IT platforms as ways to organize state investments. Nathaniel Counts of the Kennedy Forum and other policy speakers urged integrating financing for interoperable data systems into value‑based payment models and using Medicaid 1115 waivers or Medicare demonstration models to scale promising approaches.

Panelists also raised risks. Tim Clement of Mental Health America described "diagnostic overshadowing," where mental‑health diagnoses in records can lead to lower rates of needed medical procedures, citing research and urging caution in how data flags are used. Multiple speakers emphasized cybersecurity, data quality standards (minimum data elements), and the need for provider education on HIPAA and 42 CFR part 2 differences.

The session closed with a call to convert interoperability investments into measurable improvements across care settings and patient outcomes. Funderburk reminded attendees of the next session and thanked the panelists for their insights.

The panel did not vote on any formal actions; participants identified policy options and implementation priorities for federal and state agencies to consider.