Schulthess Clinic, Zurich, Switzerland, and ETH Zurich, Schwerzenbach, Switzerland.
University of Alcalá, Madrid, Spain.
Arthritis Care Res (Hoboken). 2021 Aug;73(8):1140-1145. doi: 10.1002/acr.24234. Epub 2021 Jul 5.
To appraise the highest available evidence provided by randomized controlled trials (RCTs) on the effectiveness of hip arthroscopy versus physical therapy in patients with femoroacetabular impingement syndrome (FAIS).
Four databases (Medline, Embase, Web of Science, and Scopus) were systematically searched until October 1, 2019. Eligible studies were RCTs in which patients with FAIS underwent hip arthroscopy or physical therapy. The study outcome was the International Hip Outcome Tool, 33 Items (iHOT-33) score, a measure of hip pain, function, and quality of life, assessed at baseline and at the follow-up closer to 12 months after randomization. The pooled mean difference in iHOT-33 scores within and between the treatment arms was computed using a random effects model. The minimum clinically important difference in the iHOT-33 scores was set at 10 points.
Three RCTs evaluating iHOT-33 scores between 6 and 8 months after the interventions were included. Significant increases in iHOT-33 scores were observed from baseline to follow-up for both hip arthroscopy (22.3 points [95% confidence interval (95% CI) 17.3-27.4]) and physical therapy (13.0 points [95% CI 9.5-16.4]). Hip arthroscopy demonstrated significantly higher iHOT-33 scores at follow-up compared with physical therapy (10.9 points [95% CI 4.7-17.0]).
Both hip arthroscopy and physical therapy resulted in statistically and clinically significant short-term improvements in hip pain, function, and quality of life in patients with FAIS. Hip arthroscopy was statistically superior to physical therapy in improving the outcome at follow-up even if improvement may not be detected by patients.
评价针对股骨髋臼撞击综合征(FAIS)患者,髋关节镜与物理治疗相比的有效性的最高级别循证医学证据(随机对照试验[RCT])。
系统检索了 4 个数据库(Medline、Embase、Web of Science 和 Scopus),检索时间截至 2019 年 10 月 1 日。纳入研究为 FAIS 患者接受髋关节镜或物理治疗的 RCT。研究结局为髋关节结局工具,33 项(iHOT-33)评分,用于评估髋关节疼痛、功能和生活质量,在基线和随机分组后 12 个月左右的随访时进行评估。采用随机效应模型计算治疗组内和组间 iHOT-33 评分的平均差值。iHOT-33 评分的最小临床重要差异设定为 10 分。
纳入了 3 项 RCT,评估了干预后 6 至 8 个月的 iHOT-33 评分。髋关节镜(22.3 分[95%置信区间(95%CI)为 17.3-27.4])和物理治疗(13.0 分[95%CI 为 9.5-16.4])均从基线到随访显著增加 iHOT-33 评分。与物理治疗相比,髋关节镜在随访时的 iHOT-33 评分显著更高(10.9 分[95%CI 为 4.7-17.0])。
髋关节镜和物理治疗均在短期内显著改善了 FAIS 患者的髋关节疼痛、功能和生活质量。尽管髋关节镜治疗的改善可能无法被患者察觉,但在随访时,其改善结局优于物理治疗。