Literature DB >> 34288899

Collection and Reporting of Patient-reported Outcome Measures in Arthroplasty Registries: Multinational Survey and Recommendations.

Eric R Bohm1, Sarah Kirby2, Elly Trepman1,3,4, Brian R Hallstrom5, Ola Rolfson6, J Mark Wilkinson7, Adrian Sayers8, Søren Overgaard9,10,11,12, Stephen Lyman13,14, Patricia D Franklin15, Jennifer Dunn16, Geke Denissen17, Annette W-Dahl18, Lina Holm Ingelsrud19, Ronald A Navarro20.   

Abstract

BACKGROUND: Patient-reported outcome measures (PROMs) are validated questionnaires that are completed by patients. Arthroplasty registries vary in PROM collection and use. Current information about registry collection and use of PROMs is important to help improve methods of PROM data analysis, reporting, comparison, and use toward improving clinical practice. QUESTIONS/PURPOSES: To characterize PROM collection and use by registries, we asked: (1) What is the current practice of PROM collection by arthroplasty registries that are current or former members of the International Society of Arthroplasty Registries, and are there sufficient similarities in PROM collection between registries to enable useful international comparisons that could inform the improvement of arthroplasty care? (2) How do registries differ in PROM administration and demographic, clinical, and comorbidity index variables collected for case-mix adjustment in data analysis and reporting? (3) What quality assurance methods are used for PROMs, and how are PROM results reported and used by registries? (4) What recommendations to arthroplasty registries may improve PROM reporting and facilitate international comparisons?
METHODS: An electronic survey was developed with questions about registry structure and collection, analysis, reporting, and use of PROM data and distributed to directors or senior administrators of 39 arthroplasty registries that were current or former members of the International Society of Arthroplasty Registries. In all, 64% (25 of 39) of registries responded and completed the survey. Missing responses from incomplete surveys were captured by contacting the registries, and up to three reminder emails were sent to nonresponding registries. Recommendations about PROM collection were drafted, revised, and approved by the International Society of Arthroplasty Registries PROMs Working Group members.
RESULTS: Of the 25 registries that completed the survey, 15 collected generic PROMs, most frequently the EuroQol-5 Dimension survey; 16 collected joint-specific PROMs, most frequently the Knee Injury and Osteoarthritis Outcome Score and Hip Disability and Osteoarthritis Outcome Score; and 11 registries collected a satisfaction item. Most registries administered PROM questionnaires within 3 months before and 1 year after surgery. All 16 registries that collected PROM data collected patient age, sex or gender, BMI, indication for the primary arthroplasty, reason for revision arthroplasty, and a comorbidity index, most often the American Society of Anesthesiologists classification. All 16 registries performed regular auditing and reporting of data quality, and most registries reported PROM results to hospitals and linked PROM data to other data sets such as hospital, medication, billing, and emergency care databases. Recommendations for transparent reporting of PROMs were grouped into four categories: demographic and clinical, survey administration, data analysis, and results.
CONCLUSION: Although registries differed in PROM collection and use, there were sufficient similarities that may enable useful data comparisons. The International Society of Arthroplasty Registries PROMs Working Group recommendations identify issues that may be important to most registries such as the need to make decisions about survey times and collection methods, as well as how to select generic and joint-specific surveys, handle missing data and attrition, report data, and ensure representativeness of the sample. CLINICAL RELEVANCE: By collecting PROMs, registries can provide patient-centered data to surgeons, hospitals, and national entities to improve arthroplasty care.
Copyright © 2021 by the Association of Bone and Joint Surgeons.

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Mesh:

Year:  2021        PMID: 34288899      PMCID: PMC8445553          DOI: 10.1097/CORR.0000000000001852

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.755


  10 in total

1.  Poor Knee-specific and Generic Patient-reported Outcome Measure Scores at 6 Months Are Associated With Early Revision Knee Arthroplasty: A Study From the Australian Orthopaedic Association National Joint Replacement Registry.

Authors:  Ilana N Ackerman; Ian A Harris; Kara Cashman; Neville Rowden; Michelle Lorimer; Stephen E Graves
Journal:  Clin Orthop Relat Res       Date:  2022-06-30       Impact factor: 4.755

2.  How do Patient-reported Outcome Scores in International Hip and Knee Arthroplasty Registries Compare?

Authors:  Lina Holm Ingelsrud; J Mark Wilkinson; Soren Overgaard; Ola Rolfson; Brian Hallstrom; Ronald A Navarro; Michael Terner; Sunita Karmakar-Hore; Greg Webster; Luke Slawomirski; Adrian Sayers; Candan Kendir; Katherine de Bienassis; Niek Klazinga; Annette W Dahl; Eric Bohm
Journal:  Clin Orthop Relat Res       Date:  2022-07-08       Impact factor: 4.755

3.  CORR Insights®: Can Bar Code Scanning Improve Data Capture in a National Register? Findings From the Irish National Orthopaedic Register.

Authors:  Kelly G Vince
Journal:  Clin Orthop Relat Res       Date:  2022-08-22       Impact factor: 4.755

4.  CORR Insights®: Poor Knee-specific and Generic Patient-reported Outcome Measure Scores at 6 Months Are Associated With Early Revision Knee Arthroplasty: A Study From the Australian Orthopaedic Association National Joint Replacement Registry.

Authors:  Thomas J Blumenfeld
Journal:  Clin Orthop Relat Res       Date:  2022-08-23       Impact factor: 4.755

5.  CORR Insights®: Collection and Reporting of Patient-reported Outcome Measures in Arthroplasty Registries: Multinational Survey and Recommendations.

Authors:  Thomas J Blumenfeld
Journal:  Clin Orthop Relat Res       Date:  2021-10-01       Impact factor: 4.755

6.  Editorial Comment: Selected Papers from the 9th International Congress of Arthroplasty Registries.

Authors:  Ola Rolfson
Journal:  Clin Orthop Relat Res       Date:  2021-10-01       Impact factor: 4.755

7.  Loss to patient-reported outcome measure follow-up after hip arthroplasty and knee arthroplasty : patient satisfaction, associations with non-response, and maximizing returns.

Authors:  Lauren A Ross; Sara C O'Rourke; Gemma Toland; Deborah J MacDonald; Nick D Clement; Chloe E H Scott
Journal:  Bone Jt Open       Date:  2022-04

8.  National Implementation of an Electronic Patient-Reported Outcome Measures Program for Joint Replacement Surgery: Pilot Study.

Authors:  Emma L Heath; Ilana Ackerman; Michelle Lorimer; Sophia Rainbird; Grace O'Donohue; Andrew Brock; Stephen Graves; Ian Harris
Journal:  JMIR Form Res       Date:  2022-04-08

9.  Patients' perspectives on the benefits of feedback on patient-reported outcome measures in a web-based personalized decision report for hip and knee osteoarthritis.

Authors:  Brocha Z Stern; Sarah Pila; Layla I Joseph; Nan E Rothrock; Patricia D Franklin
Journal:  BMC Musculoskelet Disord       Date:  2022-08-23       Impact factor: 2.562

10.  Editorial Comment: Selected Papers from the 10th International Congress of Arthroplasty Registries.

Authors:  Ola Rolfson
Journal:  Clin Orthop Relat Res       Date:  2022-08-23       Impact factor: 4.755

  10 in total

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