Shuang Ya-Juan, Mao Yi, Yu Kang-Kang, Li Chun-Bao, Zhang Ming-Bo
Department of Ultrasound, the First Medical Center of Chinese PLA General Hospital, Beijing, China.
Senior Department of Orthopedics, the Fourth Medical Center of PLA General Hospital, Beijing, China.
Orthop J Sports Med. 2024 Feb 9;12(2):23259671231224497. doi: 10.1177/23259671231224497. eCollection 2024 Feb.
An accurate and objective criterion is needed to determine candidates who are suitable for hip arthroscopy in patients with femoroacetabular impingement (FAI).
To determine whether improvement in pain after ultrasound (US)-guided intra-articular hip injection during standardized examinations can be used to predict the outcomes of hip arthroscopy in patients with FAI.
Cohort study; Level of evidence, 3.
We enrolled 119 patients with FAI who underwent US-guided intra-articular hip injection of local anesthesia during standardized examinations, carried out from May 2018 to February 2020 (within 2 weeks before hip arthroscopy). All patients had undergone a minimum of 6 months of nonoperative treatment without remission and had 2-year follow-up data. Pain visual analog scale (VAS) scores (0-10) were recorded for 7 different physical examination tests, and a total score (0 [best] to 70 [worst]) was obtained. In addition, International Hip Outcome Tool-12 (iHOT-12) and modified Harris Hip Score (mHHS) scores were recorded before hip arthroscopy and at final follow-up. According to whether patients achieved the substantial clinical benefit (SCB) on the iHOT-12, they were divided into SCB and non-SCB groups, and the improvement in VAS pain scores from preinjection to postinjection (ΔVAS pain) was compared between the 2 groups. Logistic regression analysis was used to predict the achievement of SCB, and the area under the receiver operating characteristic curve (AUC) was used to estimate the accuracy of the prediction.
There was a significant pre- to postoperative increase in iHOT-12 (31.6 points; < .001) and mHHS (20.0 points; < .001) scores, and 84 (70.6%) patients achieved the SCB. The ΔVAS pain score was significantly greater in the SCB versus the non-SCB group (16.0 vs 7.0 points; respectively; < .001). Logistic regression analysis demonstrated an optimal cutoff value of 8.5 points for ΔVAS pain (AUC, 0.772; 95% CI, 0.687-0.858). For patients with more severe symptoms (total preinjection VAS pain score of >10 out of 70), the accuracy of the prediction for ΔVAS pain had a better evaluation value (AUC, 0.834; 95% CI, 0.676-0.992).
Improvement in pain after US-guided intra-articular hip injection predicted the outcomes of hip arthroscopy in patients with FAI in this study, especially for patients with more severe pain.
需要一种准确、客观的标准来确定适合进行髋关节镜检查的股骨髋臼撞击症(FAI)患者。
确定在标准化检查期间超声(US)引导下髋关节腔内注射后疼痛的改善情况是否可用于预测FAI患者髋关节镜检查的结果。
队列研究;证据等级,3级。
我们纳入了119例FAI患者,这些患者在2018年5月至2020年2月期间(髋关节镜检查前2周内)接受了标准化检查时US引导下髋关节腔内局部麻醉注射。所有患者均接受了至少6个月的非手术治疗但未缓解,且有2年的随访数据。记录了7种不同体格检查测试的疼痛视觉模拟量表(VAS)评分(0 - 10分),并获得总分(0[最佳]至70[最差])。此外,在髋关节镜检查前和最终随访时记录国际髋关节结果工具-12(iHOT-12)和改良Harris髋关节评分(mHHS)。根据患者在iHOT-12上是否实现显著临床获益(SCB),将他们分为SCB组和非SCB组,并比较两组从注射前到注射后VAS疼痛评分的改善情况(ΔVAS疼痛)。采用逻辑回归分析预测SCB的实现情况,并使用受试者操作特征曲线下面积(AUC)估计预测的准确性。
iHOT-12评分(31.6分;P <.001)和mHHS评分(20.0分;P <.001)术后较术前有显著增加,84例(70.6%)患者实现了SCB。SCB组的ΔVAS疼痛评分显著高于非SCB组(分别为16.0分和7.0分;P <.001)。逻辑回归分析显示,ΔVAS疼痛的最佳截断值为8.5分(AUC,0.772;95%可信区间,0.687 - 0.858)。对于症状更严重的患者(注射前VAS疼痛总分>70分中的10分),ΔVAS疼痛预测的准确性具有更好的评估价值(AUC,0.834;95%可信区间,0.676 - 0.992)。
在本研究中,US引导下髋关节腔内注射后疼痛的改善情况可预测FAI患者髋关节镜检查的结果,尤其是对于疼痛更严重的患者。