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Quantitative Evaluation of the Pivot Shift - Relationship to Clinical Pivot Shift Grade

机译:轴心位移的定量评估-与临床轴心位移等级的关系

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Objectives: The rotational laxity, or the pivot shift test, is a key to understanding the anterior cruciate ligament (ACL) function after the ACL injury and reconstruction. Various measurement methods have been developed to quantify the pivot shift test, but the clinical implications of the measurement results have not been established mainly because of a wide variability of the pivot shift test between examiners. The purpose of this study was to determine the relationship between quantitative measurement and clinical grade of the pivot shift test at four international centers. Methods: Seventy-three unilateral ACL injured patients at four different sites were included in this study. While performing the standardized pivot shift test under anesthesia, two quantitative technologies were utilized; an accelerometer and image analysis system using iPad. Accelerometer wireless sensor (KiRA, Orthokey, Italy) was attached on the lateral side of the tibial tubercle using a strap (Figure1A). The tibial acceleration was recorded through a Bluetooth connection to the tablet PC. Image analysis of lateral compartment translation was simultaneously performed using software implemented on iPad (Apple Inc, USA) which tracked the movement of three markers on the lateral side of the knee joint (two on the lateral tibial plateau and one on the lateral femoral epicondyle) to measure the anterior-posterior shift between the lateral tibia and femur (Figure 1B). Tibial acceleration and the lateral compartment translation were compared to the clinical pivot shift grade (grade 0, 1, 2 and 3). Spearman correlations were use to determine the relationship between the quantitative measurements and clinical pivot shift grade. Considering limited number of individuals with a grade 0 and 3 pivot shift test, we used independent t-tests to compare the quantitative measurements between those with a grade 0 or 1 (low grade) pivot shift versus grade 2 or 3 (high grade) pivot shift. The alpha level was set at p<0.05. Results: There were weak correlations between the quantitative measurements and clinical pivot shift grade (acceleration: 0.32, translation: 0.31, p<0.01). High grade pivot shifts had larger acceleration (4.1±1.8 m/sec2) than low grade (3.1±1.8 m/sec2, p<0.05). The difference in tibial translation between high and low grade pivot shifts approached significance (2.4±1.5 vs. 1.7±1.4 mm, p=0.054). Conclusion: This study confirms that clinical grading of the pivot shift is subjective and inconsistent. The tools to perform non-invasive, quantitative pivot shift measurements (tibial translation and acceleration) are simple to learn as shown across 4 centers in this study. However, there were only weak correlations between clinical grading and quantitative measurements. From the data of this study, it is suggested to use a simple positiveegative grading and add a quantitative value to it. Future research is needed to determine the correlation of quantitative pivot shift measurements and additional soft tissue injury in patients with ACL injury.
机译:目的:旋转松弛或枢轴位移测试是了解ACL损伤和重建后前交叉韧带(ACL)功能的关键。已经开发出各种测量方法来量化枢轴位移测试,但是主要由于检查者之间枢轴位移测试的广泛差异,尚未建立测量结果的临床意义。这项研究的目的是确定四个国际中心的定量测量和枢轴位移测试的临床等级之间的关系。方法:本研究包括在四个不同地点的73例单侧ACL受伤患者。在麻醉下进行标准化的枢轴位移测试时,使用了两种定量技术:使用iPad的加速度计和图像分析系统。使用皮带将加速计无线传感器(意大利Orthokey的KiRA)连接在胫骨结节的外侧(图1A)。通过与平板电脑的蓝牙连接记录胫骨加速度。使用在iPad(苹果公司,美国)上实现的软件同时进行外侧腔室平移的图像分析,该软件跟踪了膝关节外侧的三个标记的运动(两个位于胫骨平台上,一个位于股骨上con上)以测量胫骨外侧和股骨之间的前后位移(图1B)。将胫骨加速度和外侧腔室平移与临床枢轴移位等级(等级0、1、2和3)进行比较。使用Spearman相关性来确定定量测量结果与临床关键点移位等级之间的关系。考虑到0级和3级枢轴移位测试的个体数量有限,我们使用独立的t检验比较0级或1级(低级)枢轴移位与2级或3级(高级)枢轴的个体之间的定量测量转移。 α水平设定为p <0.05。结果:定量测量结果与临床枢纽位移等级之间的相关性较弱(加速度:0.32,翻译:0.31,p <0.01)。高等级枢轴换档的加速度(4.1±1.8 m / sec2)比低等级(3.1±1.8 m / sec2,p <0.05)大。上下枢转移位之间的胫骨平移差异接近显着性(2.4±1.5 vs. 1.7±1.4 mm,p = 0.054)。结论:这项研究证实枢轴移位的临床分级是主观且不一致的。如本研究中的四个中心所示,执行非侵入性,定量枢轴位移测量(胫骨平移和加速度)的工具很容易学习。但是,临床分级与定量测量之间只有很小的相关性。根据这项研究的数据,建议使用简单的正/负分级,并为其添加定量值。需要进行进一步的研究来确定ACL损伤患者中定量枢轴位移测量值与其他软组织损伤之间的相关性。

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