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dc.contributor.authorGlasgow, Russell E.
dc.contributor.authorKaplan, Robert M.
dc.contributor.authorOckene, Judith K.
dc.contributor.authorFisher, Edwin B.
dc.contributor.authorEmmons, Karen M.
dc.date2022-08-11T08:10:21.000
dc.date.accessioned2022-08-23T17:05:13Z
dc.date.available2022-08-23T17:05:13Z
dc.date.issued2012-03-01
dc.date.submitted2012-10-19
dc.identifier.citationHealth Aff (Millwood). 2012 Mar;31(3):497-504.<a href="http://dx.doi.org/10.1377/hlthaff.2010.1295" target="_blank"> Link to article on publisher's site</a>
dc.identifier.issn0278-2715 (Linking)
dc.identifier.doi10.1377/hlthaff.2010.1295
dc.identifier.pmid22392660
dc.identifier.urihttp://hdl.handle.net/20.500.14038/44810
dc.description.abstractRecent legislation and delivery system reform efforts are greatly expanding the use of electronic health records. For these efforts to reach their full potential, they must actively involve patients and include patient-reported information about such topics as health behavior, preferences, and psychosocial functioning. We offer a plan for including standardized, practical patient-reported measures as part of electronic health records, quality and performance indexes, the primary care medical home, and research collaborations. These measures must meet certain criteria, including being valid, reliable, sensitive to change, and available in multiple languages. Clinicians, patients, and policy makers also must be able to understand the measures and take action based on them. Including more patient-reported items in electronic health records would enhance health, patient-centered care, and the capacity to undertake population-based research.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=22392660&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1377/hlthaff.2010.1295
dc.subjectElectronic Health Records
dc.subject*Health Behavior
dc.subjectHumans
dc.subjectPatient Protection and Affordable Care Act
dc.subjectPatient-Centered Care
dc.subject*Quality of Life
dc.subjectReproducibility of Results
dc.subjectUnited States
dc.subjectBehavioral Disciplines and Activities
dc.subjectBehavior and Behavior Mechanisms
dc.subjectCommunity Health and Preventive Medicine
dc.subjectPreventive Medicine
dc.subjectPublic Health
dc.titlePatient-reported measures of psychosocial issues and health behavior should be added to electronic health records
dc.typeJournal Article
dc.source.journaltitleHealth affairs (Project Hope)
dc.source.volume31
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/prevbeh_pp/233
dc.identifier.contextkey3410685
html.description.abstract<p>Recent legislation and delivery system reform efforts are greatly expanding the use of electronic health records. For these efforts to reach their full potential, they must actively involve patients and include patient-reported information about such topics as health behavior, preferences, and psychosocial functioning. We offer a plan for including standardized, practical patient-reported measures as part of electronic health records, quality and performance indexes, the primary care medical home, and research collaborations. These measures must meet certain criteria, including being valid, reliable, sensitive to change, and available in multiple languages. Clinicians, patients, and policy makers also must be able to understand the measures and take action based on them. Including more patient-reported items in electronic health records would enhance health, patient-centered care, and the capacity to undertake population-based research.</p>
dc.identifier.submissionpathprevbeh_pp/233
dc.contributor.departmentDepartment of Medicine, Division of Preventive and Behavioral Medicine
dc.source.pages497-504


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