Incorporating PROMIS Symptom Measures into Primary Care Practice-a Randomized Clinical Trial
dc.contributor.author | Kroenke, Kurt | |
dc.contributor.author | Talib, Tasneem L. | |
dc.contributor.author | Stump, Timothy E. | |
dc.contributor.author | Kean, Jacob | |
dc.contributor.author | Haggstrom, David A. | |
dc.contributor.author | DeChant, Paige | |
dc.contributor.author | Lake, Kittie R. | |
dc.contributor.author | Stout, Madison | |
dc.contributor.author | Monahan, Patrick O. | |
dc.contributor.department | Biostatistics, School of Public Health | en_US |
dc.date.accessioned | 2019-10-04T17:29:07Z | |
dc.date.available | 2019-10-04T17:29:07Z | |
dc.date.issued | 2018-08 | |
dc.description.abstract | BACKGROUND: 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.citation | Kroenke, 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/s11606-018-4391-0 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/21048 | |
dc.language.iso | en_US | en_US |
dc.publisher | Springer Nature | en_US |
dc.relation.isversionof | 10.1007/s11606-018-4391-0 | en_US |
dc.relation.journal | Journal of General Internal Medicine | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | PMC | en_US |
dc.subject | Patient-reported outcomes | en_US |
dc.subject | Symptoms | en_US |
dc.subject | Primary care | en_US |
dc.subject | Feedback | en_US |
dc.subject | Clinial trial | en_US |
dc.title | Incorporating PROMIS Symptom Measures into Primary Care Practice-a Randomized Clinical Trial | en_US |
dc.type | Article | en_US |
ul.alternative.fulltext | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082211/ | en_US |
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