Department of Orthopaedics and Rheumatology, University Hospital Marburg, Baldingerstrasse, 35043, Marburg, Germany.
Int Orthop. 2013 Feb;37(2):327-35. doi: 10.1007/s00264-012-1652-0. Epub 2012 Sep 14.
Based on the revival of artificial ligaments containing polyethylene terephthalate, this study aimed to evaluate objective intra-articular findings within scheduled second-look arthroscopy, patient-reported clinical outcome and stability after isolated augmented ACL reconstruction with polyethylene terephthalate (Trevira®) augmented patella-bone-tendon-bone graft.
In a retrospective analysis of our institutional database, we found 126 patients with polyethylene terephthalate (Trevira®) augmented ACL reconstruction. All these patients underwent standardised second-look arthroscopic evaluation when removal of the augmentation became necessary. These second-look arthroscopic analyses focused on graft integration and remodelling in line with the polyethylene terephthalate augmentation. Arthroscopic re-examination comprised a graft evaluation including a structural and functional classification according to the Marburger Arthroscopy Score (MAS). Additional clinical evaluation was performed via the IKDC score and the scores of Tegner and Lysholm. Instrumental anterior laxity testing was carried out with a KT-1000™ arthrometer. Furthermore, a correlation analysis between the clinical parameters, the instrumental stability assessment and the corresponding arthroscopic graft condition was performed.
The arthroscopic evaluation showed rupture of 87 (69 %) of 126 augmentation devices. In 27 (31 %) of these 87 cases, synovial reactions were found particularly in the anterior compartment. An intact synthetic augmentation with signs of graft integration with intact synovial coating was only found in 30 %. Evaluation according to the MAS showed good to excellent structural and functional characteristics in 88 % of patients. Presence of a type III graft (MAS) was found in an additional 11 %. A rudimentary (type IV) graft was only detected once. Eighty-five percent of patients were graded A or B according to IKDC score. The Lysholm score was 92.4 ± 4.8. Correlation analysis demonstrated a significant relationship between clinical outcome according to the IKDC score (p<0.05), instrumental stability performance according to the KT-1000™ assessment (p<0.05) and the corresponding arthroscopic graft evaluation according to the MAS.
Graft integration and remodelling has complex and multi-factorial origins, particularly with artificial augmentation. Correlation analysis showed a significant relation between clinical condition, instrumental stability performance and arthroscopic graft constitution. The release of polyethylene terephthalate fibres caused inflammation of synovial tissue of the knee. Characteristic sub-clinical graft changes of structural, morphological and functional qualities of the inserted graft appear on second-look arthroscopy despite good clinical results.
基于含聚对苯二甲酸乙二醇酯的人工韧带的复兴,本研究旨在评估计划中的二次关节镜检查中的关节内客观发现、患者报告的临床结果以及聚对苯二甲酸乙二醇酯(特威纶®)增强髌腱骨-骨-肌腱移植物重建后单独增强 ACL 的稳定性。
在对我们机构数据库的回顾性分析中,我们发现了 126 例接受聚对苯二甲酸乙二醇酯(特威纶®)增强 ACL 重建的患者。当需要去除增强物时,所有这些患者都接受了标准的二次关节镜评估。这些二次关节镜分析侧重于与聚对苯二甲酸乙二醇酯增强物一致的移植物整合和重塑。关节镜再检查包括根据 Marburger 关节镜评分(MAS)进行的结构和功能分类的移植物评估。通过 IKDC 评分和 Tegner 和 Lysholm 评分进行额外的临床评估。使用 KT-1000™关节测量仪进行仪器性前向松弛测试。此外,还对临床参数、仪器稳定性评估和相应的关节镜移植物状况之间进行了相关性分析。
关节镜评估显示 126 个增强装置中有 87 个(69%)出现破裂。在这些 87 例中有 27 例(31%)发现了滑膜反应,特别是在前间室。只有 30%的情况下发现完整的合成增强物,伴有完整的滑膜覆盖和移植物整合的迹象。根据 MAS 评估,88%的患者表现出良好至优秀的结构和功能特征。另外 11%的患者存在 III 型移植物(MAS)。仅检测到一次原始(IV 型)移植物。根据 IKDC 评分,85%的患者为 A 或 B 级。Lysholm 评分为 92.4±4.8。相关性分析表明,根据 IKDC 评分的临床结果(p<0.05)、根据 KT-1000™评估的仪器稳定性表现(p<0.05)和根据 MAS 的相应关节镜移植物评估之间存在显著关系。
移植物整合和重塑具有复杂的多因素起源,特别是在人工增强物的情况下。相关性分析显示,临床状况、仪器稳定性表现和关节镜下移植物构成之间存在显著关系。聚对苯二甲酸乙二醇酯纤维的释放引起了膝关节滑膜组织的炎症。尽管临床结果良好,但在二次关节镜检查中仍会出现插入移植物的结构、形态和功能特性的特征性亚临床移植物变化。