Malahias Michael-Alexander, Chytas Dimitrios, Kostretzis Lazaros, Trellopoulos Angelos, Brilakis Emmanouil, Antonogiannakis Emmanouil
3rd Orthopaedic Department, Hygeia Hospital, Athens, Greece.
2nd Orthopaedic Department, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Shoulder Elbow. 2021 Feb;13(1):29-37. doi: 10.1177/1758573220914277. Epub 2020 Sep 25.
A number of papers have been published reporting on the clinical performance of modern trabecular metal-backed glenoid components in total shoulder arthroplasty. However, no systematic review of the literature has been published to date.
The US National Library of Medicine (PubMed/MEDLINE), and the Cochrane Database of Systematic Reviews and EMBASE were queried for publications from January 1980 to October 2019 utilizing keywords pertinent to total shoulder arthroplasty, trabecular metal, and clinical outcomes.
Overall, seven articles were included for analysis (322 operated shoulders, mean follow-up range: 2-4 years). The survival rate of modern trabecular metal-backed glenoid components was 96% (309 out of 322 cases) at 43 months mean follow-up, while the rate of aseptic loosening was 0.3% (1 out of 322 cases). There were 35 cases (10.9%) with glenoid component radiolucency (one of them required revision), and 37 cases (11.5%) of metal debris formation, with four of them undergoing revision.
There was low quality evidence to show that the use of modern trabecular metal-backed glenoid components in total shoulder arthroplasty may be safe and effective at short-term follow-up. However, this analysis showed alarmingly high rates of both radiolucency of the glenoid component and metal debris formation which raise concern for potential failure of this glenoid component in the long term. Therefore, we feel that modern trabecular metal-backed glenoid components should be still used with caution as part of a structured surveillance or research program until we know if there is a detriment to the prosthesis in the medium to long term. Systematic review, IV.
已有多篇论文发表,报道了现代小梁金属背衬的关节盂组件在全肩关节置换术中的临床性能。然而,迄今为止尚未发表对该文献的系统评价。
利用与全肩关节置换术、小梁金属和临床结果相关的关键词,检索美国国立医学图书馆(PubMed/MEDLINE)、Cochrane系统评价数据库和EMBASE中1980年1月至2019年10月期间的出版物。
总体而言,纳入7篇文章进行分析(共322例手术肩关节,平均随访时间范围:2 - 4年)。在平均43个月的随访中,现代小梁金属背衬的关节盂组件的生存率为96%(322例中的309例),而无菌性松动率为0.3%(322例中的1例)。有35例(10.9%)出现关节盂组件透光线(其中1例需要翻修),37例(11.5%)出现金属碎屑形成,其中4例接受了翻修。
低质量证据表明,在全肩关节置换术中使用现代小梁金属背衬的关节盂组件在短期随访中可能是安全有效的。然而,该分析显示关节盂组件透光线和金属碎屑形成的发生率高得惊人,这引发了对该关节盂组件长期潜在失败的担忧。因此,我们认为在我们了解中长期对假体是否有损害之前,现代小梁金属背衬的关节盂组件仍应谨慎使用,作为结构化监测或研究项目的一部分。系统评价,IV级。