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内镜臀中肌修复伴同期关节镜盂唇治疗的中期疗效:一项倾向评分匹配对照研究。

Mid-Term Outcomes of Endoscopic Gluteus Medius Repair With Concomitant Arthroscopic Labral Treatment: A Propensity-Matched Controlled Study.

机构信息

American Hip Institute Research Foundation, Des Plaines; AMITA Health St. Alexius Medical Center, Hoffman Estates, IIlinois, U.S.A.

American Hip Institute Research Foundation, Des Plaines.

出版信息

Arthroscopy. 2020 Nov;36(11):2856-2865. doi: 10.1016/j.arthro.2020.07.020. Epub 2020 Jul 27.

Abstract

PURPOSE

To report mid-term outcomes of patients who underwent endoscopic gluteus medius (GM) repair with arthroscopic labral treatment and to compare them with a control cohort of patients who underwent arthroscopic labral treatment without an endoscopic GM repair.

METHODS

Data were prospectively collected and retrospectively reviewed for all patients who underwent primary hip arthroscopy between February 2008 and August 2013. Patients were included if they underwent arthroscopic labral treatment, endoscopic GM repair, and had preoperative with minimum 5-year follow-up for the following patient-reported outcomes: modified Harris Hip Score (mHHS), Nonarthritic Hip Score (NAHS), and Hip Outcome Score-Sports Specific Subscale (HOS-SSS). Propensity score matching was used to create a control cohort of patients who underwent primary arthroscopic labral treatment without GM repair.

RESULTS

There were a total of 46 patients with GM repair eligible for the current study, of whom 43 (93.5%) had 5-year follow-up. The average follow-up time was 73.4 months. At minimum 5-year follow-up, all PROs significantly improved (P < .001). Among the entire GM repair cohort, rates for achieving the patient acceptable symptomatic state (PASS) for mHHS, HOS-SSS, and international Hip Outcome Tool (iHOT-12) were 74.4%, 51.9%, and 71.8%, respectively. Rates for reaching a minimal clinically important difference for mHHS, NAHS, and HOS-SSS were 79.5%, 89.7%, and 73.1%, respectively. When the GM repair cohort was matched, there were 37 cases in the GM repair cohort and 78 in the control cohort. The GM repair cohort outcomes compared satisfactorily to the control cohort for mHHS (82.3 vs 82.6), NAHS (81.9 vs 82.3), and HOS-SSS (66.3 vs 67.5). Rates of achieving minimal clinically important difference and PASS for mHHS, NAHS, HOS-SSS, and iHOT-12 were also favorable.

CONCLUSIONS

Endoscopic GM repair with arthroscopic labral treatment results in safe, durable, and significant improvement in PROs at a minimum 5-year follow-up. The outcomes compared favorably with a control cohort without GM tears.

LEVEL OF EVIDENCE

III, retrospective comparative study.

摘要

目的

报告接受关节镜下臀中肌(GM)修复联合关节盂唇治疗的患者的中期结果,并与未行 GM 镜下修复的单纯关节盂唇治疗的对照组患者进行比较。

方法

对 2008 年 2 月至 2013 年 8 月期间接受初次髋关节镜检查的所有患者进行前瞻性数据收集和回顾性研究。如果患者接受关节镜下盂唇治疗、GM 镜下修复,且有术前及至少 5 年随访的以下患者报告结局:改良 Harris 髋关节评分(mHHS)、非关节炎髋关节评分(NAHS)和髋关节结局评分-运动特异性量表(HOS-SSS),则将其纳入研究。采用倾向评分匹配的方法创建单纯行初次关节镜下盂唇治疗而未行 GM 修复的对照组患者。

结果

共有 46 例 GM 修复患者符合本研究标准,其中 43 例(93.5%)患者有 5 年随访。平均随访时间为 73.4 个月。在至少 5 年的随访中,所有 PRO 均显著改善(P<.001)。在整个 GM 修复组中,mHHS、HOS-SSS 和国际髋关节结果工具(iHOT-12)达到患者可接受的症状状态(PASS)的比例分别为 74.4%、51.9%和 71.8%。mHHS、NAHS 和 HOS-SSS 达到最小临床重要差异的比例分别为 79.5%、89.7%和 73.1%。当对 GM 修复组进行匹配时,GM 修复组有 37 例,对照组有 78 例。与对照组相比,GM 修复组在 mHHS(82.3 vs 82.6)、NAHS(81.9 vs 82.3)和 HOS-SSS(66.3 vs 67.5)方面的结果令人满意。mHHS、NAHS、HOS-SSS 和 iHOT-12 的最小临床重要差异和 PASS 率也很理想。

结论

关节镜下 GM 修复联合盂唇治疗在至少 5 年的随访中可获得安全、持久且显著的 PRO 改善。与未修复 GM 撕裂的对照组相比,该结果具有可比性。

证据等级

III,回顾性比较研究。

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