Incorporating PROMIS Symptom Measures into Primary Care Practice-a Randomized Clinical Trial

dc.contributor.authorKroenke, Kurt
dc.contributor.authorTalib, Tasneem L.
dc.contributor.authorStump, Timothy E.
dc.contributor.authorKean, Jacob
dc.contributor.authorHaggstrom, David A.
dc.contributor.authorDeChant, Paige
dc.contributor.authorLake, Kittie R.
dc.contributor.authorStout, Madison
dc.contributor.authorMonahan, Patrick O.
dc.contributor.departmentBiostatistics, School of Public Healthen_US
dc.date.accessioned2019-10-04T17:29:07Z
dc.date.available2019-10-04T17:29:07Z
dc.date.issued2018-08
dc.description.abstractBACKGROUND: Symptoms account for more than 400 million clinic visits annually in the USA. The SPADE symptoms (sleep, pain, anxiety, depression, and low energy/fatigue) are particularly prevalent and undertreated. OBJECTIVE: To assess the effectiveness of providing PROMIS (Patient-Reported Outcome Measure Information System) symptom scores to clinicians on symptom outcomes. DESIGN: Randomized clinical trial conducted from March 2015 through May 2016 in general internal medicine and family practice clinics in an academic healthcare system. PARTICIPANTS: Primary care patients who screened positive for at least one SPADE symptom. INTERVENTIONS: After completing the PROMIS symptom measures electronically immediately prior to their visit, the 300 study participants were randomized to a feedback group in which their clinician received a visual display of symptom scores or a control group in which scores were not provided to clinicians. MAIN MEASURES: The primary outcome was the 3-month change in composite SPADE score. Secondary outcomes were individual symptom scores, symptom documentation in the clinic note, symptom-specific clinician actions, and patient satisfaction. KEY RESULTS: Most patients (84%) had multiple clinically significant (T-score ≥ 55) SPADE symptoms. Both groups demonstrated moderate symptom improvement with a non-significant trend favoring the feedback compared to control group (between-group difference in composite T-score improvement, 1.1; P = 0.17). Symptoms present at baseline resolved at 3-month follow-up only one third of the time, and patients frequently still desired treatment. Except for pain, clinically significant symptoms were documented less than half the time. Neither symptom documentation, symptom-specific clinician actions, nor patient satisfaction differed between treatment arms. Predictors of greater symptom improvement included female sex, black race, fewer medical conditions, and receiving care in a family medicine clinic. CONCLUSIONS: Simple feedback of symptom scores to primary care clinicians in the absence of additional systems support or incentives is not superior to usual care in improving symptom outcomes.en_US
dc.identifier.citationKroenke, K., Talib, T. L., Stump, T. E., Kean, J., Haggstrom, D. A., DeChant, P., … Monahan, P. O. (2018). Incorporating PROMIS Symptom Measures into Primary Care Practice-a Randomized Clinical Trial. Journal of general internal medicine, 33(8), 1245–1252. doi:10.1007/s11606-018-4391-0en_US
dc.identifier.urihttps://hdl.handle.net/1805/21048
dc.language.isoen_USen_US
dc.publisherSpringer Natureen_US
dc.relation.isversionof10.1007/s11606-018-4391-0en_US
dc.relation.journalJournal of General Internal Medicineen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectPatient-reported outcomesen_US
dc.subjectSymptomsen_US
dc.subjectPrimary careen_US
dc.subjectFeedbacken_US
dc.subjectClinial trialen_US
dc.titleIncorporating PROMIS Symptom Measures into Primary Care Practice-a Randomized Clinical Trialen_US
dc.typeArticleen_US
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082211/en_US
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