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Incorporating patient-reported outcome measures into the electronic health record for research

Application using the Patient Health Questionnaire (PHQ-9)

Bibliographic Data

ID15298396
AuthorsSandra D Griffith (Cleveland Clinic, corresponding author), Nicolas R Thompson (0000-0002-8973-5219, Cleveland Clinic), Jaivir Rathore (University of Illinois Chicago), Jaivir S Rathore, Lara Jehi (0000-0002-8041-6377, Cleveland Clinic), Lara E Jehi, George Tesar (0000-0001-5189-0478, Cleveland Clinic), George E Tesar, Irene Katzan (0000-0002-9006-7780, Cleveland Clinic), Irene L Katzan
Year2014
Volume24
Issue2
Pages295-303
Publication date2014-08-06
Open AccessYes
TypeARTICLE
VenueQuality of Life Research (JOURNAL)
Journal identifiersISSN: 0962-9343 • E-ISSN: 1573-2649
PublisherSpringer Science+Business Media (PUBLISHER • DE)
DOI10.1007/s11136-014-0764-y
PMID25099197
OpenAlexW2102408124
LanguageEN
References cited24

Depressive symptoms · Electronic health record · Family medicine · Health care · Health services research · Patient Health Questionnaire · Patient-reported outcome · Political science · Psychiatry · Public health · Quality of life (healthcare · Quality of Life Research · Chronic Disease Management Strategies · Electronic Health Records Systems · Medical Coding and Health Information · Medicine · Nursing · Psychology

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  • The PHQ-9

    Kurt Kroenke, Robert L Spitzer et al.•Journal of General Internal…•2001

  • Logistics of collecting patient-reported outcomes (PROs) in clinical practice

    Open Access•Matthias Rose, Andrea Bezjak•Quality of Life Research•2009

  • PatientViewpoint

    Open Access•Claire Snyder, Claire F Snyder et al.•Quality of Life Research•2009

Highly citedNo

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