Division of Adult Reconstruction and Joint Replacement, Hospital for Special Surgery, New York, NY.
J Arthroplasty. 2022 Aug;37(8S):S954-S957. doi: 10.1016/j.arth.2022.01.044. Epub 2022 Jan 26.
Outcomes after aseptic revision total hip arthroplasty (THA) are variable, and it is unknown whether the indication for aseptic revision THA influences postoperative clinical improvement. The minimal clinically important difference (MCID) assesses if changes in patient-reported outcome measure result in meaningful clinical benefit to patients. The purpose of this study was to quantify the 1-year postoperative MCID for aseptic revision THA and to assess the percentage of patients achieving the MCID for each revision diagnosis.
A prospective, single-institution registry of revision total joint arthroplasties was used. Retrospective review of 413 first-time aseptic revision THAs was performed. Demographics, revision diagnosis, preoperative Hip Disability and Osteoarthritis Outcome Score, Joint Replacement (HOOS Jr.), and 1-year postoperative HOOS Jr. were recorded. The MCID for the HOOS Jr. at one year postoperatively was calculated for each revision diagnosis using a distribution-based method. The percentage of patients exceeding the MCID with each diagnosis was determined.
There were 9 aseptic revision diagnoses, all with n ≥ 5. The 3 most common revision diagnosis were aseptic loosening (n = 114), dislocation or instability (n = 103), and polyethylene wear or osteolysis (n = 73). The MCID for all the aseptic revision THAs was 10.9. Seven of the nine revision diagnoses achieved the MCID. The highest percentage of patients achieving the MCID was for aseptic loosening (84.2%) and implant fracture (81.3%), whereas lowest was for adverse local tissue reaction (35.3%) and implant recall (20.0%).
The one-year revision THA MCID is 10.9 for the HOOS Jr. There is variability in the percentage of patients achieving the MCID based on diagnosis. Our data can be used to counsel patients undergoing revision THA for noninfectious etiologies.
无菌性翻修全髋关节置换术(THA)后的结果各不相同,目前尚不清楚无菌性翻修 THA 的适应证是否会影响术后临床改善。最小临床重要差异(MCID)评估患者报告的结果是否发生变化,是否对患者有意义的临床获益。本研究的目的是量化无菌性翻修 THA 的 1 年术后 MCID,并评估每个翻修诊断达到 MCID 的患者比例。
使用前瞻性、单机构关节置换翻修登记处。对 413 例首次无菌性翻修 THA 进行回顾性研究。记录患者的人口统计学、翻修诊断、术前髋关节残疾和骨关节炎结果评分(HOOS Jr.)、关节置换(HOOS Jr.)和 1 年术后 HOOS Jr.。使用基于分布的方法计算每个翻修诊断的 1 年术后 HOOS Jr.的 MCID。确定每个诊断超过 MCID 的患者比例。
有 9 种无菌性翻修诊断,所有诊断 n ≥ 5。最常见的 3 种翻修诊断为无菌性松动(n = 114)、脱位或不稳定(n = 103)和聚乙烯磨损或骨溶解(n = 73)。所有无菌性翻修 THA 的 MCID 为 10.9。9 种翻修诊断中有 7 种达到了 MCID。达到 MCID 的患者比例最高的是无菌性松动(84.2%)和植入物骨折(81.3%),而最低的是局部组织不良反应(35.3%)和植入物召回(20.0%)。
HOOS Jr.的 1 年翻修 THA MCID 为 10.9。根据诊断,达到 MCID 的患者比例存在差异。我们的数据可以用于为接受非感染性病因翻修 THA 的患者提供咨询。