Department of Outpatient Rehabilitation, Swedish Medical Center, Seattle, Washington, USA.
Center for the Intrepid, Brooke Army Medical Center, Fort Sam Houston, Texas, USA.
Am J Sports Med. 2018 May;46(6):1306-1314. doi: 10.1177/0363546517751912. Epub 2018 Feb 14.
Arthroscopic hip surgery has risen 18-fold in the past decade; however, there is a dearth of clinical trials comparing surgery with nonoperative management.
To determine the comparative effectiveness of surgery and physical therapy for femoroacetabular impingement syndrome.
Randomized controlled trial; Level of evidence, 1.
Patients were recruited from a large military hospital after referral to the orthopaedic surgery clinic and were eligible for surgery. Of 104 eligible patients, 80 elected to participate, and the majority were active-duty service members (91.3%). No patients withdrew because of adverse events. The authors randomly selected patients to undergo either arthroscopic hip surgery (surgery group) or physical therapy (rehabilitation group). Patients in the rehabilitation group began a 12-session supervised clinic program within 3 weeks, and patients in the surgery group were scheduled for the next available surgery at a mean of 4 months after enrollment. Patient-reported outcomes of pain, disability, and perception of improvement over a 2-year period were collected. The primary outcome was the Hip Outcome Score (HOS; range, 0-100 [lower scores indicating greater disability]; 2 subscales: activities of daily living and sport). Secondary measures included the International Hip Outcome Tool (iHOT-33), Global Rating of Change (GRC), and return to work at 2 years. The primary analysis was on patients within their original randomization group.
Statistically significant improvements were seen in both groups on the HOS and iHOT-33, but the mean difference was not significant between the groups at 2 years (HOS activities of daily living, 3.8 [95% CI, -6.0 to 13.6]; HOS sport, 1.8 [95% CI, -11.2 to 14.7]; iHOT-33, 6.3 [95% CI, -6.1 to 18.7]). The median GRC across all patients was that they "felt about the same" (GRC = 0). Two patients assigned to the surgery group did not undergo surgery, and 28 patients in the rehabilitation group ended up undergoing surgery. A sensitivity analysis of "actual surgery" to "no surgery" did not change the outcome. Twenty (33.3%) patients who underwent surgery and 4 (33.3%) who did not undergo surgery were medically separated from military service at 2 years.
There was no significant difference between the groups at 2 years. Most patients perceived little to no change in status at 2 years, and one-third of military patients were not medically fit for duty at 2 years. Limitations include a single hospital, a single surgeon, and a high rate of crossover. Registration: NCT01993615 ( ClinicalTrials.gov identifier).
在过去十年中,关节镜髋关节手术增加了 18 倍;然而,比较手术与非手术治疗的临床试验却很少。
确定手术与物理治疗在股骨髋臼撞击综合征中的比较效果。
随机对照试验;证据水平,1 级。
患者在被转诊至矫形外科诊所后,从一家大型军队医院招募,并符合手术条件。在 104 名符合条件的患者中,有 80 名患者选择参加,其中大多数是现役军人(91.3%)。没有患者因不良事件而退出。作者随机选择接受关节镜髋关节手术(手术组)或物理治疗(康复组)的患者。康复组的患者在 3 周内开始进行 12 次监督诊所治疗计划,而手术组的患者在入组后平均 4 个月时安排下一次可进行的手术。在 2 年内收集患者的疼痛、残疾和改善感知的报告结果。主要结局是髋关节评分(HOS;范围,0-100[分数越低表示残疾程度越高];2 个子量表:日常生活活动和运动)。次要指标包括国际髋关节结局工具(iHOT-33)、总体改善评分(GRC)和 2 年时的恢复工作情况。主要分析是基于患者最初的随机分组。
两组患者在 HOS 和 iHOT-33 上均有显著改善,但 2 年时组间差异无统计学意义(HOS 日常生活活动,3.8[95%CI,-6.0 至 13.6];HOS 运动,1.8[95%CI,-11.2 至 14.7];iHOT-33,6.3[95%CI,-6.1 至 18.7])。所有患者的 GRC 中位数均为“感觉差不多”(GRC=0)。2 名被分配至手术组的患者未接受手术,而康复组的 28 名患者最终接受了手术。对“实际手术”与“无手术”的敏感性分析并未改变结果。20 名(33.3%)接受手术的患者和 4 名(33.3%)未接受手术的患者在 2 年内因健康原因从军队退役。
两组在 2 年时无显著差异。大多数患者在 2 年内感觉状态几乎没有变化,三分之一的现役军人在 2 年内不适合服兵役。局限性包括单家医院、单名外科医生和高交叉率。注册:NCT01993615(ClinicalTrials.gov 标识符)。