髋臼中央减压治疗髋臼中央狭窄患者的中期预后:与匹配对照组的比较

Benjamin D Kuhns,Ady H Kahana-Rojkind,Tyler R McCarroll,Yasemin E Kingham,Benjamin G Domb
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引用次数: 0

摘要

背景:髋臼中央狭窄(CAS)被定义为髋臼窝内的一种骨疣,与股骨头软骨损伤的发生率较高有关,如果不及时治疗,则髋关节镜手术后的短期预后较差。髋臼中央减压术(CAD)是一种关节镜技术,切除骨赘并使髋臼窝表面重新出现,以改善股骨头的接触力学。目的:本研究的主要目的是提供股骨髋臼撞击(FAI)合并CAD的CAS患者接受髋关节镜手术的5年髋关节保存率和患者报告的结果。次要目的是比较CAD治疗的CAS患者与倾向评分匹配的无CAS患者对照组的结果。研究设计:队列研究;证据水平,3。方法回顾了在FAI的原发性髋关节镜手术中因CAS接受CAD治疗的患者的前瞻性收集的手术登记资料。该研究的主要结果是术后5年内转为关节置换术。次要结局包括关节镜翻修手术和患者报告的结局评分。进行多因素回归分析以评估进展到关节置换术的危险因素。根据术前年龄、性别、体重指数和Tönnis分级组成倾向评分匹配的对照组,对接受髋关节镜手术治疗无CAS的FAI患者进行对照,以评估两组结果的差异。结果189例符合条件的患者中有155例(82.0%)进行了至少5年的随访。在该队列中,平均年龄为45.9±10.8岁,女性患者90例(58.1%)。在5年时间点,无关节置换术生存率为80.6%(125/155)。对于不需要关节置换术的患者,术后显著的改善是持久的(P < 0.001),满意度高。在多变量分析中,严重的髋臼软骨缺损最能预测关节置换术的转变。无CAS的FAI患者的对照组显示出较低的软骨损伤率和较高的无关节置换术生存率(P < 0.01)。对于不需要关节置换术的患者,术后结果评分、达到临床相关结果阈值的比率和手术满意度在CAD组和对照组之间具有可比性。结论在FAI的初次髋关节镜手术中接受CAD的CAS患者在至少5年的随访中获得了持久的术后改善和较高的手术满意度。正如预期的那样,与对照组相比,CAD组术中软骨损伤率明显更高,无关节置换术生存率更低。尽管如此,81%不需要关节置换术的冠心病患者与对照组相比有显著改善。我们的结论是,在适当的期望下,FAI和CAS患者可以通过先进的关节镜技术成功治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Midterm Outcomes in Patients After Central Acetabular Decompression for Central Acetabular Stenosis: A Comparison With a Matched Control Group.
BACKGROUND Central acetabular stenosis (CAS), defined as an osteophyte within the acetabular fossa, is associated with higher rates of femoral head chondral damage and, when left untreated, inferior short-term outcomes after hip arthroscopic surgery. Central acetabular decompression (CAD) is an arthroscopic technique to resect the osteophyte and resurface the acetabular fossa to improve contact mechanics of the femoral head. PURPOSE The primary aim was to provide the 5-year hip preservation rate and patient-reported outcomes in patients undergoing hip arthroscopic surgery for femoroacetabular impingement (FAI) concomitantly with CAD for CAS. A secondary aim was to compare outcomes in patients treated with CAD for CAS to a propensity score-matched control group of patients without CAS. STUDY DESIGN Cohort study; Level of evidence, 3. METHODS A surgical registry with prospectively collected data was reviewed for patients who underwent CAD for CAS identified during primary hip arthroscopic surgery for FAI. The primary outcome for the study was conversion to arthroplasty within 5 years postoperatively. Secondary outcomes included revision arthroscopic surgery and patient-reported outcome scores. Multivariate regression analysis was performed to evaluate the risk factors for progression to arthroplasty. A propensity score-matched control group based on preoperative age, sex, body mass index, and Tönnis grade was formed of patients undergoing hip arthroscopic surgery for FAI without CAS to evaluate the differences in outcomes between the 2 groups. RESULTS There were 155 of 189 eligible patients (82.0%) who had a minimum 5-year follow-up. Within this cohort, the mean age was 45.9 ± 10.8 years, with 90 female patients (58.1%). At the 5-year time point, the arthroplasty-free survivorship rate was 80.6% (125/155). For patients not requiring arthroplasty, significant postoperative improvements were durable (P < .001), with high satisfaction. On multivariate analysis, severe acetabular chondral defects were most predictive of conversion to arthroplasty. The control group of patients with FAI without CAS demonstrated lower rates of chondral damage and higher rates of arthroplasty-free survivorship (P < .01). For patients not requiring arthroplasty, postoperative outcome scores, rates of achieving clinically relevant outcome thresholds, and satisfaction with surgery were comparable between the CAD and control groups. CONCLUSION Patients with CAS undergoing CAD during primary hip arthroscopic surgery for FAI had durable postoperative improvements and high satisfaction with surgery at a minimum 5-year follow-up. As expected, intraoperative chondral damage rates were significantly greater, and arthroplasty-free survivorship rates were lower, in the CAD group compared with the control group. Nonetheless, 81% of patients undergoing CAD who did not require arthroplasty had significant improvements that were comparable with the control group. We conclude that, with appropriate expectations, patients with FAI and CAS may be treated successfully with advanced arthroscopic techniques.
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