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Kompendium 2020 Forschung & Klinik

Das Kompendium 2020 der Universitätsklinik für Orthopädie und Unfallchirurgie von MedUni Wien und AKH Wien (o. Univ.-Prof. R. Windhager) stellt einen umfassenden Überblick über die medizinsichen Leistungen und auch die umfangreichen Forschungsfelder dar. Die Veröffentlichungen zeigen die klinische Relevanz und innovative Ansätze der einzelnen Forschungsrichtungen. Herausgeber: Universitätsklinik für Orthopädie und Unfallchirurgie MedUni Wien und AKH Wien Prof. Dr. R. Windhager ISBN 978-3-200-07715-7

Das Kompendium 2020 der Universitätsklinik für Orthopädie und Unfallchirurgie von MedUni Wien und AKH Wien (o. Univ.-Prof. R. Windhager) stellt einen umfassenden Überblick über die medizinsichen Leistungen und auch die umfangreichen Forschungsfelder dar. Die Veröffentlichungen zeigen die klinische Relevanz und innovative Ansätze der einzelnen Forschungsrichtungen.

Herausgeber: Universitätsklinik für Orthopädie und Unfallchirurgie
MedUni Wien und AKH Wien
Prof. Dr. R. Windhager

ISBN 978-3-200-07715-7

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TOP-Studien<br />

31<br />

Aseptic loosening is the most common<br />

cause for surgical revision after TJA with<br />

far-reaching implications.<br />

„Inflammation in RA patients, as<br />

evidenced by higher levels of disease<br />

activity, increases the risk for radiographic<br />

loosening after TJA. In OA<br />

patients, as a control disease without<br />

systemic inflammation, the risk is<br />

significantly lower.“<br />

Christoph Böhler<br />

tivity and the clinical diagnosis (OA/RA), evaluated the radiographs. Patients<br />

were seen after 6 weeks, 3 and 12 months, and then annually after the TJA.<br />

The Simplified Disease Activity Index (SDAI) was used to determine disease<br />

activity levels. At our rheumatology outpatient clinic, RA patients are followed<br />

every 3 months, and their clinical and laboratory variables are documented<br />

prospectively in an observational database. For statistical analysis we<br />

performed Cox regression to estimate RCL based on SDAI, adjusting for the<br />

anti-rheumatic therapy (conventional vs. biological disease modifying drugs,<br />

DMARDs). Furthermore, we compared the rates of aseptic loosening and RCL<br />

in RA and OA patients using the Chi-Square-Test, the Kaplan Meier method,<br />

and applied the Log-Rank test to statistically compare survival distributions.<br />

Results<br />

32 patients (65.3%) underwent TKA, and 17 (34.7%) THA. All TKA were<br />

cemented and all THA were fixated cementless. In total 18 (36.7%) showed<br />

signs of RCL. Time integrated SDAI was significantly higher in patients with<br />

RCL (median; 25th and 75th percentile: 10.8; 8.6 and 15.8) than in controls<br />

without RCL (7.0; 2.7 and 15.5) (Figure 1; p=0.043).<br />

When comparing RCL across patient groups in different RA disease activity states,<br />

we found that in the remission group no patient showed signs of RCL (0/10),<br />

whereas in the low and moderate/high disease activity groups 10/21 (47.6%)<br />

and 8/17 (47.1%) patients, respectively, showed signs of RCL (p=0.023). RA<br />

patients receiving biologicals had clearly lower rates of RCL (4/18; 22.2%) compared<br />

to RA patients under traditional DMARD therapy (14/28; 50%). In logistic<br />

regression analyses biologicals significantly reduced the risk of RCL with an<br />

odds ratio (OR) of 0.192 (95% CI 0.042-0.891; p=0.035). The RCL rate was 36.7%<br />

in the RA group and 13.6% in the OA group (p=0.002). This was mainly explained<br />

by a higher rate of RCL in the TKA group (RA: 34.4%; OA: 6.5%; p=0.001), while<br />

the rates in the THA group were only numerically higher in patients with RA<br />

compared to OA (41.2% vs. 30.8%, respectively; p=0.528).<br />

Discussion<br />

The current study for the first time links the risk of aseptic loosening in RA<br />

patients to the level of inflammation with higher disease activity being associated<br />

with more frequent occurrence of radiographic loosening. Biological

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