Joshua Seidman PhD
Joshua Seidman PhD's Latest Blog Posts
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Joint Hearing to Conceptualize Clinical Quality for Meaningful Use Stage 3
Recognizing the importance of evolving quality concepts within the Electronic Health Record (EHR) Incentive Programs, two ONC federal advisory committee workgroups jointly held a full day hearing on June 7, 2012 to identify ways in which Meaningful Use Stage 3 may advance the consistent delivery of high quality care in diverse care settings. Experts from health care delivery organizations, quality improvement organizations, industry, and academia shared insights regarding how clinical decision support, quality measurement, and the use of clinical data can improve care. Participants encouraged an increased focus on the dynamic ability to ask questions and get answers about patient populations, the use of clinical decision support as an “in-the-moment quality improvement” mechanism, and a transition from retrospective reporting to prospective identification of care improvement opportunities.
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Federal Advisory Committees Seeking Input on Incorporation of Patient-Generated Data for Stage 3 Meaningful Use
ONC’s federal advisory committees (FACAs) held a full-day hearing on June 8 (written testimony can be found here) to explore how patient-generated health data (PGHD) might be incorporated into Meaningful Use (MU) of EHRs for Stage 3 of the EHR Incentive Programs. Some examples of PGHD are data from a patient’s personal health record, data from a blood glucose monitor, or information about a patient’s functional status. Three FACA workgroups hosted the hearing: The Health IT Policy Committee’s MU and Quality Measurement Workgroups, and the Health IT Standards Committee’s Consumer Engagement Power Team.
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Public Input Shaped the Guiding Principles for Stage 2 Meaningful Use NPRM
The Department of Health and Human Services (HHS) recently released two notices of proposed rulemaking (NPRMs) related to Stage 2 of the Medicare and Medicaid EHR Incentive Programs that detail proposed Meaningful Use requirements for providers and the Standards & Certification Criteria (S&CC) that delineate proposed requirements for certified EHR products. The vast majority of the proposed criteria derive from the two federal advisory committees that have been lauded as a model for public, open, and transparent policy making processes.