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髋关节撞击综合征髋关节检查试验的可靠性。

Reliability of hip examination tests for femoroacetabular impingement.

机构信息

Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts; Arthritis Research Centre of Canada, Vancouver, British Columbia, Canada.

出版信息

Arthritis Care Res (Hoboken). 2013 Oct;65(10):1690-6. doi: 10.1002/acr.22036.

Abstract

OBJECTIVE

To assess the interrater reliability of hip examination tests used to assess femoroacetabular impingement (FAI) among clinicians from different disciplines.

METHODS

Twelve subjects were examined by 9 clinicians using 12 hip tests drawn from a review of the literature and consultation with experts in hip pain and FAI. Examiners assessed both hips of each subject and were blinded to subject history. The order in which subjects were seen, the order of tests, and order of examination of the 2 hips within each subject were all randomized. Interrater reliability (IRR) for the 10 categorical tests was summarized using overall raw agreement (ORA), positive agreement (agreement on abnormal findings), and negative agreement (agreement on normal findings). An ORA of >0.75 was considered to indicate adequate reliability. For the 2 range of motion (ROM) outcomes, IRR was summarized using the median of the absolute difference (MAD) in measurements obtained by any 2 examiners on any patient. MAD reflects the "typical" difference (in degrees) between 2 raters.

RESULTS

Adequate reliability (ORA >0.75) was achieved for 6 of the 10 hip examination tests with categorical outcomes. Positive agreement ranged from 0.35 to 0.84, while negative agreement ranged from 0.62 to 0.99. For the ROM outcomes, examiners were, on average, within 5° of each other for flexion and 7° for internal rotation.

CONCLUSION

The results provide evidence that the most common hip examination tests would likely be sufficiently reliable to allow agreement between examiners when discriminating between painful FAI and normal hips in a clinical setting.

摘要

目的

评估不同学科临床医生用于评估股骨髋臼撞击症(FAI)的髋关节检查试验的组内可靠性。

方法

12 名受试者由 9 名临床医生使用 12 种髋关节试验进行检查,这些试验是从文献综述和髋关节疼痛及 FAI 专家咨询中得出的。检查者评估了每位受试者的双侧髋关节,对受试者的病史不知情。受试者的就诊顺序、检查的顺序以及每位受试者的双侧髋关节检查顺序均随机排列。使用总原始一致性(ORA)、阳性一致性(异常发现的一致性)和阴性一致性(正常发现的一致性)来总结 10 项分类测试的组内可靠性(IRR)。ORA >0.75 被认为具有足够的可靠性。对于 2 项关节活动度(ROM)结果,使用任何 2 名检查者在任何患者上获得的测量值的绝对差值(MAD)中位数来总结 IRR。MAD 反映了 2 名评分者之间的“典型”差异(以度为单位)。

结果

对于具有分类结果的 10 项髋关节检查测试中的 6 项,获得了足够的可靠性(ORA>0.75)。阳性一致性范围为 0.35 至 0.84,而阴性一致性范围为 0.62 至 0.99。对于 ROM 结果,检查者在屈曲时平均彼此相差 5°,在内旋时平均相差 7°。

结论

研究结果表明,在临床环境中,最常见的髋关节检查测试可能具有足够的可靠性,以允许检查者在区分疼痛性 FAI 和正常髋关节时达成一致。

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