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dc.contributor.authorNadarajah, Vidushan
dc.contributor.authorSood, Anshum
dc.contributor.authorKator, Jamie L
dc.contributor.authorFoster, Michael J
dc.contributor.authorJauregui, Julio J
dc.contributor.authorGilotra, Mohit N
dc.contributor.authorHasan, S Ashfaq
dc.contributor.authorHenn, R Frank
dc.date.accessioned2022-09-27T18:32:01Z
dc.date.available2022-09-27T18:32:01Z
dc.date.issued2020-04-30
dc.identifier.citationNadarajah V, Sood A, Kator JL, Foster MJ, Jauregui JJ, Gilotra MN, Hasan SA, Henn RF 3rd. Evaluation of preoperative pain in patients undergoing shoulder surgery using the PROMIS pain interference computer-adaptive test. J Clin Orthop Trauma. 2020 Jul;11(Suppl 4):S539-S545. doi: 10.1016/j.jcot.2020.04.025. Epub 2020 Apr 30. PMID: 32774026; PMCID: PMC7394780.en_US
dc.identifier.issn0976-5662
dc.identifier.doi10.1016/j.jcot.2020.04.025
dc.identifier.pmid32774026
dc.identifier.urihttp://hdl.handle.net/20.500.12648/7578
dc.description.abstractObjective: The purpose of this study was to evaluate the Patient Reported Outcomes Measurement Information System (PROMIS) computerized adaptive testing Pain Interference (PROMIS PI) item bank in patients undergoing shoulder surgery. We hypothesized that PROMIS PI would exhibit a strong positive correlation with the numerical pain scale for the operative shoulder (shoulder NPS) with less floor and ceiling effects. Secondary study aims included assessing the relationships between patient characteristics and PROMIS PI. Design: Analytical cross-sectional study. Setting: Urban academic medical center. Patients: One-hundred and ninety-five patients undergoing shoulder surgery between June 2015 to June 2017. Main outcome measures: All patients completed a series of patient-reported outcomes measures, including PROMIS PI and NPS. Non-parametric tests were used for bivariate analysis. Multivariable regression models were used to determine independent associations. Results: There was a moderate correlation between the PROMIS PI and shoulder NPS scores (rs = 0.53; p < 0.001). PROMIS PI had no ceiling or floor effects while shoulder NPS had 26 patients (13.3%) at either the floor or the ceiling. PROMIS PI demonstrated a strong correlation with PROMIS Physical Function (rs = -0.65; p < 0.001), ASES total score (rs = -0.67; p < 0.001), and PROMIS Fatigue (rs = 0.64; p < 0.001). Conclusions: The strong association noted between PROMIS PI and psychosocial and behavioral factors, versus that of NPS, demonstrates that PROMIS Pain Interference may be a more appropriate choice as an outcome measure where the surgeon is concerned about a patient's improvement of functioning and decrease in the impact of pain in other aspects of wellbeing following shoulder surgery. Level of evidence: IV.en_US
dc.language.isoenen_US
dc.relation.urlhttps://www.sciencedirect.com/science/article/pii/S0976566220301399en_US
dc.rights© 2020 Delhi Orthopedic Association. All rights reserved.
dc.rightsAttribution-NonCommercial 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectCross-sectionalen_US
dc.subjectPROMISen_US
dc.subjectPain intensityen_US
dc.subjectPain interferenceen_US
dc.subjectPatient-reported outcomesen_US
dc.subjectShoulderen_US
dc.titleEvaluation of preoperative pain in patients undergoing shoulder surgery using the PROMIS pain interference computer-adaptive test.en_US
dc.typeArticle/Reviewen_US
dc.source.journaltitleJournal of clinical orthopaedics and traumaen_US
dc.source.volume11
dc.source.issueSuppl 4
dc.source.beginpageS539
dc.source.endpageS545
dc.source.countryIndia
dc.description.versionVoRen_US
refterms.dateFOA2022-09-27T18:32:01Z
dc.description.institutionSUNY Downstateen_US
dc.description.departmentOrthopaedic Surgery & Rehabilitation Medicineen_US
dc.description.degreelevelN/Aen_US
dc.identifier.journalJournal of clinical orthopaedics and trauma


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