Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/118806
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dc.contributor.authorInacio, M.C.S.-
dc.contributor.authorPratt, N.L.-
dc.contributor.authorRoughead, E.E.-
dc.contributor.authorGraves, S.E.-
dc.date.issued2015-
dc.identifier.citationBMC Musculoskeletal Disorders, 2015; 16(1):385-1-385-9-
dc.identifier.issn1471-2474-
dc.identifier.issn1471-2474-
dc.identifier.urihttp://hdl.handle.net/2440/118806-
dc.description.abstractBackground: Joint arthroplasty patients have a high prevalence of co-morbidities and this impacts their surgical outcomes. There are different ways to ascertain co-morbidities and appropriate measurement is necessary. The purpose of this study was to: (1) describe the prevalence of co-morbidities in a cohort of total hip arthroplasty (THA) and knee arthroplasty (TKA) patients using two diagnoses-based measures (Charlson and Elixhauser) and one prescription-based measure (RxRisk-V); (2) compare the agreement of co-morbidities amongst the measures. Methods: A cross-sectional study of Australian veterans undergoing THAs (n = 11,848) and TKAs (n = 18,972) between 2001 and 2012 was conducted. Seventeen co-morbidities were identified using the Charlson, 30 using the Elixhauser, and 42 using the RxRisk-V measure. Agreement between co-morbidities was calculated using Kappa (κ) statistics. Results: Combining measures, 64 conditions were identified, of these 28 were only identified using the RxRisk-V, 11 using the Elixhauser, and 2 using the Charlson. The most prevalent conditions was pain treated with anti-inflammatories (58.7 % THAs, 55.9 % TKAs), pain treated with narcotics (55.0 % THAs, 50.9 % TKAs), hypertension (56.0 % THAs and TKAs), and anticoagulation disorders (53.0 % THAs, 48.6 % TKAs). Diabetes was the only condition with substantial agreement (all κ > 0.6) amongst all measures. When comparing the diagnoses based algorithms, agreement was high for overlapping conditions (all κ > 0.71). Conclusions: Different measures identified different co-morbidities, provided different estimates for the same co-morbidity, and had different levels of agreement for common co-morbidities. This highlights the importance of understanding co-morbidity measures and using them appropriately in studies and case-mix adjustments analyses.-
dc.description.statementofresponsibilityMaria C. S. Inacio, Nicole L. Pratt, Elizabeth E. Roughead and Stephen E. Graves-
dc.language.isoen-
dc.publisherBioMed Central-
dc.rights© 2015 Inacio et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.-
dc.source.urihttp://dx.doi.org/10.1186/s12891-015-0835-4-
dc.subjectCo-morbidities; total joint arthroplasty; pharmacy data; RxRisk-V; Charlson; Elixhauser-
dc.titleComparing co-morbidities in total joint arthroplasty patients using the RxRisk-V, Elixhauser, and Charlson Measures: a cross-sectional evaluation-
dc.typeJournal article-
dc.identifier.doi10.1186/s12891-015-0835-4-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1040938-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1035889-
pubs.publication-statusPublished-
dc.identifier.orcidPratt, N.L. [0000-0001-8730-8910]-
dc.identifier.orcidGraves, S.E. [0000-0002-1629-319X]-
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