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使用仪器化测试设备对膝关节进行前后抽屉试验测量。

Anteroposterior drawer measurements in the knee using an instrumented test device.

作者信息

Edixhoven P, Huiskes R, de Graaf R

机构信息

Department of Orthopaedics, Canisius Hospital, Nijmegen, The Netherlands.

出版信息

Clin Orthop Relat Res. 1989 Oct(247):232-42.

PMID:2791392
Abstract

A newly developed instrumented knee laxity tester was used to measure anteroposterior (AP) drawer parameters (Lachmann test) in populations of normal subjects and patients with anterior cruciate ligament (ACL) and posterior cruciate ligament (PCL) insufficiencies. The AP drawer tester features a differential electronic measuring procedure of displacements between patella and tuberosity over a continuous range between 180 and -180 N of AP forces. In the statistical evaluation, shift and compliance (or stiffness) parameters at various forces are considered. In a representative normal population, all relevant parameters were established, thus creating a normal data base for future reference. The average normal AP drawer shift between maximal anterior and posterior forces (180 N) was 6.4 +/- 1.7 mm. Right-left differences and male-female differences were found not to be statistically significant in any of the parameters. The validity of the instrumented drawer tester was confirmed relative to a group of patients with acute documented ligament insufficiencies. Measurements in two groups of patients with chronic postoperative knee instabilities revealed that although the diagnosis of instability could be confirmed, the results could hardly discriminate between ACL and PCL insufficiencies, probably due to unrecognized associated lesions at the time of operation and/or gradual postoperative developments of insufficiencies and deformities. An unexpected finding was that the mean laxities of the uninjured contralateral knees were significantly extended relative to the normal reference group, suggesting that these patients could have been classified as a high-risk group even before the time of injury.

摘要

一种新开发的带仪器的膝关节松弛度测试仪被用于测量正常受试者群体以及前交叉韧带(ACL)和后交叉韧带(PCL)功能不全患者的前后(AP)抽屉试验参数(拉赫曼试验)。该AP抽屉试验仪的特点是在180至 -180 N的AP力连续范围内,对髌骨和胫骨结节之间的位移采用差分电子测量程序。在统计评估中,会考虑不同力下的位移和顺应性(或刚度)参数。在一个具有代表性的正常人群中,确定了所有相关参数,从而创建了一个供未来参考的正常数据库。最大前后力(180 N)之间的平均正常AP抽屉位移为6.4 +/- 1.7 mm。在任何参数中,左右差异和男女差异均无统计学意义。相对于一组有明确记录的急性韧带功能不全患者,该带仪器的抽屉试验仪的有效性得到了证实。对两组慢性术后膝关节不稳定患者的测量结果显示,尽管可以确认不稳定的诊断,但结果几乎无法区分ACL和PCL功能不全,这可能是由于手术时未识别出相关病变和/或术后逐渐出现的功能不全和畸形。一个意外的发现是,未受伤对侧膝关节的平均松弛度相对于正常参考组有显著增加,这表明这些患者甚至在受伤前就可能被归类为高危人群。

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