Campbell Andrew, Emara Ahmed K, Klika Alison, Piuzzi Nicolas S
Department of Orthopaedic Surgery, Cleveland Clinic, Cleveland, Ohio.
J Bone Joint Surg Am. 2021 Dec 15;103(24):2306-2317. doi: 10.2106/JBJS.20.01931.
Total hip arthroplasty (THA) is a reliable operation, but it is critical that orthopaedic surgeons characterize which surgical factors influence patient-reported outcomes. The purpose of this study was to determine whether implant selection at the time of THA affects the odds of having (1) inadequate improvement according to patient-reported pain, function, and activity; (2) failure to achieve a substantial clinical benefit (SCB) with respect to pain; or (3) failure to achieve a patient-acceptable symptomatic state (PASS) according to pain and function.
Prospective data were collected from 4,716 patients who underwent primary THA (from July 2015 to August 2018) in a single health-care system with standardized care pathways. Patients were categorized according to the type of femoral and acetabular components and bearing surface used. Outcomes included 1-year postoperative patient-reported outcome measures (PROMs) and improvement in the Hip disability and Osteoarthritis Outcome Score (HOOS) and the University of California at Los Angeles (UCLA) activity score. Inadequate improvement was defined as PROMs that changed by less than the minimal clinically important difference (MCID) for the HOOS pain and physical function short form (PS) and as failure to improve beyond a mostly homebound activity status for the UCLA activity score (a score of ≤3). The MCID and SCB thresholds were set at values reported in the literature.
One-year PROM data were available for 3,519 patients (74.6%). There were no differences in the proportion of patients who attained the MCID in terms of HOOS pain, HOOS PS, or UCLA activity scores at 1 year for all analyzed implant parameters. Multivariate regression demonstrated that implant selection was not a significant driver of inadequate improvement, according to HOOS pain and HOOS PS (p > 0.05). Larger (36-mm) femoral heads demonstrated lower odds of inadequate improvement versus 28-mm femoral heads according to UCLA activity scores (odds ratio [OR]: 0.64; 95% confidence interval, 0.47 to 0.86; p = 0.003). Implant-related criteria were not significant drivers of attaining a PASS or achieving an SCB with respect to HOOS pain.
For the most part, THA implant characteristics are not drivers of inadequate improvement with respect to pain and function. Surgeons should utilize implants with an acceptable track record that allow stable fixation and restoration of hip biomechanics.
Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.
全髋关节置换术(THA)是一种可靠的手术,但骨科医生明确哪些手术因素会影响患者报告的结局至关重要。本研究的目的是确定THA时的植入物选择是否会影响出现以下情况的几率:(1)根据患者报告的疼痛、功能和活动情况改善不足;(2)在疼痛方面未实现实质性临床获益(SCB);或(3)根据疼痛和功能未达到患者可接受的症状状态(PASS)。
前瞻性收集了在单一医疗系统中接受初次THA(2015年7月至2018年8月)且采用标准化护理路径的4716例患者的数据。根据所使用的股骨和髋臼组件类型以及承重表面对患者进行分类。结局包括术后1年患者报告的结局指标(PROMs)以及髋关节功能障碍和骨关节炎结局评分(HOOS)和加利福尼亚大学洛杉矶分校(UCLA)活动评分的改善情况。改善不足定义为HOOS疼痛和身体功能简表(PS)的PROMs变化小于最小临床重要差异(MCID),以及UCLA活动评分未改善至超过主要居家活动状态(评分≤3)。MCID和SCB阈值设定为文献中报道的值。
3519例患者(74.6%)有1年的PROM数据。对于所有分析植入物参数,在1年时达到HOOS疼痛、HOOS PS或UCLA活动评分MCID的患者比例无差异。多因素回归表明,根据HOOS疼痛和HOOS PS,植入物选择不是改善不足的显著驱动因素(p>0.05)。根据UCLA活动评分,较大(36毫米)股骨头与28毫米股骨头相比,改善不足的几率较低(优势比[OR]:0.64;95%置信区间,0.47至0.86;p=0.003)。植入物相关标准不是达到PASS或在HOOS疼痛方面实现SCB的显著驱动因素。
在很大程度上,THA植入物特性不是疼痛和功能改善不足的驱动因素。外科医生应使用具有可接受记录的植入物,这些植入物能实现稳定固定并恢复髋关节生物力学。
治疗性III级。有关证据水平的完整描述,请参阅作者指南。