Inter- and intra-tester reliability of selected clinical tests in examining patients with early phase lumbar spine and sacroiliac joint pain and dysfunction
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引用次数: 10
Abstract
Abstract Of all patients with low back pain (LBP), 85% are diagnosed as “non-specific lumbar pain”. It has been postulated that the only reliable test is a straight leg raise test for detecting sciatic pain, and for other diagnostic subgroups, tests are of varying value. Only a few standardized tests exist to test function, inspection, mobility, pain, muscle flexibility or stability for patients with early phase lumbar spine and sacroiliac joint pain and dysfunction in the non-laboratory setting. The aim of this study was therefore to examine the inter- and intra-tester reliability of selected standardized clinical tests. Fifteen eligible, consecutive and voluntary LBP patients (aged 18–56 years), whose pain had lasted less than 3 months were recruited by an invitation letter. Patients were examined by two physiotherapists specialized in orthopaedic manual therapy. These PTs examined the same patients at a 1-week interval, changing the examination order at the second session. The assessment consisted of seven categories: history, observation of posture, function of low back and lower extremities, stability tests, pain provocation and mobility tests, neurological and neurodynamic tests, and tests of muscle tightness. In analysing these seven test categories, the mean inter-tester kappa was 0.5 (95% CI –0.05 to 1.20) and intra-tester kappa 0.6 (95% CI –0.40 to 1.28). Overall inter- and intra-tester reliability was at an acceptable level, except for the inspection test category, where agreement was poor. However, the reliability of individual tests ranged from poor to very good. In conclusion, when assessing LBP patients in the early phase (<12-week duration), reliability of one or more tests were acceptable on a group level with inter- and intra-tester reliability in every test category. However, our results need confirmation in a larger sample, especially when this great number of examination findings is tested, to reduce the likelihood of spurious findings.
在所有腰痛(LBP)患者中,85%被诊断为“非特异性腰痛”。据推测,唯一可靠的测试是检测坐骨神经痛的直腿抬高测试,而对于其他诊断亚组,测试的价值各不相同。对于早期腰椎和骶髂关节疼痛和功能障碍患者,在非实验室环境中,只有少数标准化的测试可以测试功能、检查、活动、疼痛、肌肉柔韧性或稳定性。因此,本研究的目的是检验选定的标准化临床试验的测试者之间和测试者内部的信度。通过邀请函招募15例符合条件的、连续的、自愿的LBP患者(年龄18-56岁),其疼痛持续时间小于3个月。患者由两名专门从事骨科手工治疗的物理治疗师进行检查。这些PTs每隔一周对同一患者进行检查,在第二次检查时改变检查顺序。评估包括七个类别:病史、姿势观察、腰背和下肢功能、稳定性测试、疼痛诱发和活动测试、神经学和神经动力学测试以及肌肉紧度测试。在分析这七个测试类别时,测试者之间的平均kappa为0.5 (95% CI -0.05至1.20),测试者内部的平均kappa为0.6 (95% CI -0.40至1.28)。总的来说,测试者之间和内部的可靠性是在一个可接受的水平,除了检查测试类别,其中的一致性很差。然而,个别测试的可靠性从差到非常好。总之,在评估早期LBP患者(持续时间<12周)时,一个或多个测试的可靠性在组水平上是可接受的,每个测试类别的测试者之间和内部的可靠性都是可接受的。然而,我们的结果需要在更大的样本中得到证实,特别是在测试如此大量的检查结果时,以减少虚假结果的可能性。