Journal article
Patient-reported outcome measures in arthroplasty registries
- Alternative title:
- Report of the Patient-Reported Outcome Measures Working Group of the International Society of Arthroplasty RegistriesPart II. Recommendations for selection, administration, and analysis
- Abstract:
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The International Society of Arthroplasty Registries (ISAR) Patient-Reported Outcome Measures (PROMs) Working Group have evaluated and recommended best practices in the selection, administration, and interpretation of PROMs for hip and knee arthroplasty registries. The 2 generic PROMs in common use are the Short Form health surveys (SF-36 or SF-12) and EuroQol 5-dimension (EQ-5D). The Working Group recommends that registries should choose specific PROMs that have been appropriately developed with good measurement properties for arthroplasty patients. The Working Group recommend the use of a 1-item pain question (“During the past 4 weeks, how would you describe the pain you usually have in your [right/left] [hip/knee]?”; response: none, very mild, mild, moderate, or severe) and a single-item satisfaction outcome (“How satisfied are you with your [right/left] [hip/knee] replacement?”; response: very unsatisfied, dissatisfied, neutral, satisfied, or very satisfied). Survey logistics include patient instructions, paper- and electronic-based data collection, reminders for follow-up, centralized as opposed to hospital-based follow-up, sample size, patient- or joint-specific evaluation, collection intervals, frequency of response, missing values, and factors in establishing a PROMs registry program. The Working Group recommends including age, sex, diagnosis at joint, general health status preoperatively, and joint pain and function score in case-mix adjustment models. Interpretation and statistical analysis should consider the absolute level of pain, function, and general health status as well as improvement, missing data, approaches to analysis and case-mix adjustment, minimal clinically important difference, and minimal detectable change. The Working Group recommends data collection immediately before and 1 year after surgery, a threshold of 60% for acceptable frequency of response, documentation of non-responders, and documentation of incomplete or missing data.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 134.3KB, Terms of use)
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- Publisher copy:
- 10.1080/17453674.2016.1181816
Authors
- Publisher:
- Taylor and Francis
- Journal:
- Acta Orthopaedica More from this journal
- Volume:
- 87
- Issue:
- S1
- Pages:
- 9-23
- Publication date:
- 2016-05-26
- Acceptance date:
- 2015-09-17
- DOI:
- EISSN:
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1745-3682
- ISSN:
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1745-3674
- Pmid:
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27228230
- Language:
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English
- Keywords:
- Pubs id:
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pubs:625694
- UUID:
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uuid:f616d0b0-56e8-472a-ba4a-d5a263833ecb
- Local pid:
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pubs:625694
- Source identifiers:
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625694
- Deposit date:
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2017-03-25
Terms of use
- Copyright holder:
- Rolfson et al
- Copyright date:
- 2016
- Notes:
- © The Authors 2016. Published by Taylor & Francis on behalf of the Nordic Orthopedic Federation. This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License
- Licence:
- CC Attribution (CC BY)
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