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Influence of the loading frequency on the wear rate of a polyethylene-on-metal lumbar intervertebral disc replacement.

机译:装载频率对聚乙烯 - 金属腰椎间盘置换液磨损率的影响。

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摘要

Pre-clinical wear testing of intervertebral disc prostheses is commonly carried out according to ISO 18192-1. Ten million multiaxial loading cycles are applied at a frequency of 1 Hz. At this frequency, testing takes about 4 months. Testing at higher frequencies would therefore be desirable. ISO 18192-1 also offers testing at 2 Hz; however, it says the impact on the implant material behaviour as well as on the accuracy of the test machine shall be investigated by the user. Since such data are not available so far, the aim of this study was to carry out comparative wear tests at 1 and 2 Hz. Seven Prodisc-L lumbar disc prostheses were tested. After a pre-soak period, the implants were placed in specimen cups filled with calf serum, mounted to a Spine Wear Simulator and loaded according to ISO 18192-1. Testing was carried out at a temperature of 37 ± 2 °C. Four million loading cycles were applied at 1 Hz and eight million at 2 Hz in an alternating sequence. Each time after 12 days of testing the implants were removed to measure the weight and the height of the polyethylene cores. Then, the test serum was exchanged and the implants were remounted to the testing machine. The mean wear rate was 5.6 ± 2.3 mg per million cycles at 1 Hz and 7.7 ± 1.6 mg per million cycles at 2 Hz during the first six million loading cycles (p < 0.05) and 2.0 ± 0.6 and 4.1 ± 0.7 mg per million cycles during the second six million cycles (p < 0.05). Similarly, the mean heightloss was also smaller at 1 Hz than at 2 Hz (p < 0.05) with -0.02 ± 0.02 mm versus -0.04 ± 0.02 mm per million cycles during the first half of testing and -0.01 ± 0.01 versus -0.02 ± 0.01 mm per million cycles during the second half. The accuracy of the test machine was within the limits described by ISO 18192-1 at both frequencies. The results showed that the wear rate was higher at the beginning than at the end of testing. Also, the results indicated that testing at 2 Hz increases the wear rate compared with 1 Hz in case of a polyethylene-on-metal implant design. In the absence of retrieval studies it is difficult to decide which rate results in a more physiological wear pattern. However, a loading frequency of 1 Hz is probably closer to physiology than 2 Hz since the loading amplitudes prescribed by ISO 18192-1 are high. They rather represent movements like tying shoes or standing up from a chair than walking or sitting. The authors therefore suggest testing at 1 Hz.
机译:椎间盘前佩戴的临床前磨损试验通常根据ISO 18192-1进行。以1 Hz的频率施加千万多轴装载周期。在这种频率下,测试需要大约4个月。因此,需要在较高频率下进行测试。 ISO 18192-1还提供2 Hz的测试;然而,它表示对植入物质行为的影响以及对测试机的准确性应由用户调查。由于到目前为止,此类数据不可用,因此本研究的目的是在1和2 Hz进行比较磨损试验。测试七个Prodisc-L腰椎圆盘假体进行了测试。在浸泡的时间后,将植入物置于填充有小牛血清的标本杯中,安装在脊柱磨损模拟器上并根据ISO 18192-1装载。测试在37±2℃的温度下进行。在1 Hz和八百000以交替顺序施用400万装载循环。每次测试12天后,取出植入物以测量聚乙烯核心的重量和高度。然后,交换测试血清,将植入物重新安装到试验机上。平均磨损率为每百万次循环为5.6±2.3毫克,在前六百万个装载周期(P <0.05)和2.0±0.6和4.1±0.7毫克/百万循环期间,每百万次循环为每百万次循环,7.7±1.6毫克/百万次循环。在第二六百万次循环中(P <0.05)。类似地,平均高度滚下在1 Hz的比例下比2 Hz(P <0.05)较小,在测试的前半部分和-0.01±0.01与-0.01±0.01与-0.02±0.02±0.02±0.02 mm±0.04±0.02 mm。下半年期间0.01毫米百万循环。测试机器的准确性在两个频率下ISO 18192-1描述的限制范围内。结果表明,在测试结束时磨损率在开始时较高。此外,结果表明,在聚乙烯 - 金属植入物设计的情况下,2Hz的测试增加了与1 Hz的磨损率。在没有检索研究的情况下,难以确定哪种速率导致更具生理磨损模式。然而,由于ISO 18192-1规定的装载幅度高,因此1 Hz的装载频率可能比2 Hz更接近2 Hz。他们宁愿代表像捆绑鞋子或站在椅子上的动作,而不是走路或坐着。因此,作者建议在1 Hz测试。

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