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Clinical Priorities Workgroup

This workgroup focuses on statewide quality standards, aggregation of key data elements, clinical decision support across care settings, and the intersection with medication management. It also addresses physician adoption and trust, patient education and decision support, patient identification and consent, and the readiness of personal health record (PHR) products. Additionally, it explores integrating public health data sources, promoting e-prescribing, and prioritizing clinical needs for financial incentive models.

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Clinical Priorities Workgroup

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  1. Clinical Priorities Workgroup May 12, 2008

  2. Quality reporting • Statewide quality standards • Locus of aggregation • Key data elements/specifications • CDS across care settings • Intersection with medication management • Physician adoption/trust

  3. New Yorkers and Clinician • PHR and medication management crossover • Emergency services and coordination (DNR) • Patient education and decision support • Patient identification and consent • Current PHR product readiness • Continuity of care record with the personal health record • Secure patient-clinician clinician-clinician interaction • Additional patient data sources

  4. Public Health • Integrating current public health data sources – coordinated input • High priority to deal with projects already out • Bi-directional data flow through the Universal Public Health Node • Access to public programs as an issue for public health • Coordination with other efforts – CDC and NHIN

  5. Medicaid Medication Mgmt • Reconciliation relies on cross-continuum data • Coordination with NHIN projects • Promote e-prescribing in context of advancement to a full EHR with CDS • Prioritization of clinical needs for financial incentive models

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