Morris Daniel Leslie James, Minhas Avneet, Walstow Katherine, Pitt Lisa, Morgan Marie, Cresswell Tim, Espag Marius P, Clark David I, Tambe Amol A
Royal Derby Hospital, University Hospitals of Derby & Burton NHS Foundation Trust, Derby, UK.
Shoulder Elbow. 2024 Dec 10:17585732241301356. doi: 10.1177/17585732241301356.
Scoping review has identified a lack of evidence guiding long-term follow-up of elbow arthroplasty. We report the effectiveness of primary linked total elbow arthroplasty surveillance in identifying failing implants requiring revision.
A prospective database recording consecutive primary linked total elbow arthroplasty and subsequent surveillance in an elbow unit was analysed. Arthroplasties performed between 01.10.2013 and 31.07.2022 were included, with a minimum 1-year follow-up. Surveillance involves specialist physiotherapist review 1, 2, 3, 5, 8 and 10 years postoperatively. Patient-initiated review could occur between time points. Outcome measures include a number of surveillance reviews offered and attended; and the proportion that identified a failing implant requiring revision.
Ninety-seven primary linked total elbow arthroplasties with minimum 1-year follow-up were performed (76 Discovery, 14 Nexel, 7 Coonrad/Morrey). Sixteen patients died prior to 31.07.2023, and three implants required revision <1 year postoperatively. 290 of 328 offered surveillance appointments were attended (88.4%). Five implants required revision ≥1 year post-operatively, with revision requirements identified by surveillance in all cases. Three failures occurred at 5 years postoperatively, and two failures occurred at 8 years postoperatively. Overall, 1.7% attended surveillance appointments identified a failing implant requiring revision.
This is the first series reporting the effectiveness of primary linked total elbow arthroplasty surveillance in identifying implants requiring revision.
范围综述发现缺乏指导肘关节置换长期随访的证据。我们报告了初次关联全肘关节置换术监测在识别需要翻修的失败植入物方面的有效性。
分析了一个前瞻性数据库,该数据库记录了一个肘关节单元连续进行的初次关联全肘关节置换术及随后的监测情况。纳入了2013年10月1日至2022年7月31日期间进行的置换术,随访时间至少为1年。监测包括术后1年、2年、3年、5年、8年和10年由专科物理治疗师进行复查。在各时间点之间可能会有患者主动要求复查。结果指标包括提供并参加的监测复查次数;以及识别出需要翻修的失败植入物的比例。
共进行了97例初次关联全肘关节置换术,随访时间至少为1年(76例Discovery,14例Nexel,7例Coonrad/Morrey)。16例患者在2023年7月31日前死亡,3例植入物在术后不到1年需要翻修。328次提供的监测预约中有290次被参加(88.4%)。5例植入物在术后≥1年需要翻修,所有病例均通过监测发现了翻修需求。3例失败发生在术后5年,2例失败发生在术后8年。总体而言,1.7%参加监测预约的患者被识别出有需要翻修的失败植入物。
这是首个报告初次关联全肘关节置换术监测在识别需要翻修的植入物方面有效性的系列研究。