Evaluation of total hip arthroplasty devices using a total joint replacement registry

被引:9
作者
Paxton, Elizabeth W. [1 ]
Ake, Christopher F. [1 ]
Inacio, Maria C. S. [1 ]
Khatod, Monti [2 ]
Marinac-Dabic, Danica [3 ]
Sedrakyan, Art [3 ,4 ]
机构
[1] Kaiser Permanente, Dept Surg Outcomes & Anal, San Diego, CA 92109 USA
[2] Kaiser Permanente, Dept Orthoped Surg, Baldwin Pk, CA USA
[3] US FDA, Ctr Devices & Radiol Hlth, Silver Spring, MD USA
[4] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
关键词
total joint replacement; arthroplasty; registry; selection model; bearing surfaces; UNITED-STATES; VALUES;
D O I
10.1002/pds.3228
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose The purpose of this paper is to describe the infrastructure of the total joint replacement registry of a large integrated healthcare system's and emphasize challenges associated with orthopedic device classification and evaluation. Methods Using a large integrated healthcare system innovative infrastructure including electronic health record data, administrative data sources, and registry data collection, we evaluated device choice and outcomes of total hip arthroplasty (THA). Devices were classified into type of bearing surface (alternative versus traditional). Multiple imputation was used to accommodate missing data, and a logistic regression model was applied to assess the impact of patient and surgeon factors on choice of bearing surface. A Cox regression model was used to evaluate risk of aseptic revision while controlling for surgeon, site, and patient characteristics. Adjusted cumulative probability-of-event curves were created, comparing survival of alternative against traditional bearings of devices, with aseptic revision as the outcome of interest. Results The study sample consisted of 25 377 primary THAs with an average follow-up of 2.7?years. Choice of bearing surface varied by surgeon and patient characteristics. After adjusting for patient, surgeon, and hospital covariates, results showed that the risk of aseptic revision associated with alternative bearings did not differ significantly from traditional bearing surfaces (hazard ratio?=?1.33; 95% confidence interval: 0.90, 1.98). Conclusions Clinically rich data from a registry with linkages to electronic health records and other administrative databases improve identification of exposures, outcomes, and patient subgroups in medical device evaluation. These various data sources facilitate refined adjustment for potential confounders such as hospital, surgeon, and patient factors and ensure comprehensive device performance evaluation within registries. Copyright (C) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:53 / 59
页数:7
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