Comprehensive, uniform adoption of PRO |
Funding agency, FDA, payor, accreditor requirement for PRO data collection for specified conditions
Reimbursement and billing for PRO data collection
Research to establish process-outcome linkage for specified conditions
Bundle PROs with clinical measures for specified conditions
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Selection of PRO |
Consensus on recommended PROs for specified conditions and situations
Research on psychometric properties, natural history, heterogeneity
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Proprietary measures |
Studies to compare proprietary to public domain measures
Begin with PROs currently in use, in public domain, or copy-left
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Clinical interpretation |
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Literature synthesis/meta analysis |
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Confidentiality |
Establish standard procedures to evaluate PROs
Research on stakeholder preferences
Obtain input from patients and clinicians
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Coordination among organizations |
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Data linkage |
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Missing data |
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