Elevated Blood Tantalum Concentrations in Patients Following Reconstruction of Severe Acetabular Defects in Total Hip Arthroplasty Using Modular Tantalum Augments in Combination With Uncemented Tantalum Cups

IF 3.4 2区 医学 Q1 ORTHOPEDICS Journal of Arthroplasty Pub Date : 2025-02-01 DOI:10.1016/j.arth.2024.05.068
David Spranz MD, Lisa-Marie Müller MD, Raphael Trefzer MD, Pit Hetto MD, Moritz Innmann MD, Tobias Renkawitz MD, Tilman Walker MD, Tobias Reiner MD
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引用次数: 0

Abstract

Background

The reconstruction of acetabular defects in total hip arthroplasty (THA) can be challenging. An option to treat uncontained acetabular defects is to use modular tantalum augments in combination with cementless press-fit cups. However, modularity is associated with an increased risk of debonding and mechanical failure. In addition, metal wear particles can be released due to micromotions at the implant interface. Clinical data on the long-term results of this treatment strategy is limited. The purposes of this study were: (1) to evaluate the clinical and radiological outcome of complex THA using modular trabecular metal augments and uncemented revision cups; (2) to investigate the blood tantalum concentrations in these patients at mid-term (mean 4.5 year) follow-up; and (3) to report complications and mechanisms of failure related to this procedure.

Methods

In this single-center study, we retrospectively reviewed data from a consecutive cohort of 27 patients who underwent complex acetabular defect reconstruction using a modular tantalum acetabular augment in combination with an uncemented tantalum cup. We evaluated the implant survival, and the radiological and clinical outcomes after a mean follow-up of 4.5 years (standard deviation 2.1; range 2.5 to 10.6 years) using patient-reported outcome scores. Blood samples were analyzed regarding tantalum concentration and compared with a control group.

Results

The cumulative survival rate at 4.5 years with the end point “revision of the acetabular component for aseptic loosening” was 94.4% (95% confidence interval [CI] 71.6 to 99.2) and 82.9% (95% CI 60.5 to 93.3) for the end point “revision for any reason.” The patient-reported outcome scores improved significantly up to the latest follow-up, and radiographic data showed no signs of loosening or implant migration. Median blood tantalum concentrations were significantly higher in the study group (0.15 μg/L) compared to the control group (0.002 μg/L) (P < .001).

Conclusions

This study demonstrated acceptable clinical and radiological results of cementless revision THA using modular trabecular metal implants for the reconstruction of large acetabular defects. Tantalum concentrations were significantly higher in patients who had tantalum implants compared to the control group; however, the systemic and local effects of an increased tantalum exposure are not yet fully understood and have to be further investigated.
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在全髋关节置换术中使用模块化钽假体和非骨水泥钽髋臼杯重建严重髋臼缺损的患者血液中钽浓度升高。
简介:在全髋关节置换术(THA)中重建髋臼缺损是一项挑战。治疗非封闭性髋臼缺损的一种方法是使用模块化钽增量体结合无骨水泥压入式髋臼杯。然而,模块化会增加脱粘和机械故障的风险。此外,金属磨损颗粒会因种植体界面的微运动而释放出来。有关这种治疗策略长期效果的临床数据非常有限。本研究的目的是(1)评估使用模块化小梁金属增量体和非骨水泥翻修杯的复杂 THA 的临床和放射学结果;(2)调查这些患者在中期(平均 4.5 年)随访时血液中的钽浓度;(3)报告与该手术相关的并发症和失败机制:在这项单中心研究中,我们回顾性地审查了27名患者的数据,这些患者连续接受了复杂髋臼缺损重建手术,使用了模块化钽髋臼增量器和非骨水泥钽髋臼杯。我们使用患者报告结果评分(PROMs)评估了平均随访 4.5 年(标清 2.1;范围 2.5 至 10.6 年)后的植入物存活率以及放射学和临床结果。对血液样本中的钽浓度进行了分析,并与对照组进行了比较:以 "髋臼组件因无菌性松动而翻修 "为终点,4.5年的累积存活率为94.4%(95%置信区间(CI)71.6至99.2);以 "因任何原因而翻修 "为终点,4.5年的累积存活率为82.9%(95%置信区间(CI)60.5至93.3)。在最近一次随访中,PROM明显改善,放射学数据显示没有松动或植入物移位的迹象。与对照组(0.002 μg/L)相比,研究组的血钽浓度中位数(0.15 μg/L)明显更高(P < 0.001):这项研究表明,使用模块化小梁金属植入物重建大面积髋臼缺损的无骨水泥翻修THA的临床和放射学结果均可接受。与对照组相比,植入钽植入物的患者体内的钽浓度明显较高,但钽暴露增加对全身和局部的影响尚未完全明了,还有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Arthroplasty
Journal of Arthroplasty 医学-整形外科
CiteScore
7.00
自引率
20.00%
发文量
734
审稿时长
48 days
期刊介绍: The Journal of Arthroplasty brings together the clinical and scientific foundations for joint replacement. This peer-reviewed journal publishes original research and manuscripts of the highest quality from all areas relating to joint replacement or the treatment of its complications, including those dealing with clinical series and experience, prosthetic design, biomechanics, biomaterials, metallurgy, biologic response to arthroplasty materials in vivo and in vitro.
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