Kock H J, Stürmer K M, Letsch R
Abteilung für Unfallchirurgie, Universitätsklinikum Essen.
Unfallchirurg. 1991 Dec;94(12):594-602.
A total of 97 cruciate ligament prostheses were implanted in 70 patients following acute and chronic cruciate ligament rupture; the average life of these prostheses being 3 years (8-53 months), 5 (5.15%) were removed due to failure after a mean of 9 (3-15) months. In 67 cases of chronic cruciate instability, 60 anterior and 7 posterior Trevira cruciate ligament prostheses were implanted, and 25 acute anterior and five acute posterior cruciate ligament ruptures were also treated with Trevira ligaments augmentations. The follow-up rate of patients with Trevira cruciate ligament repair was 97%. Of the explanted polyethylene-terephthalate (PET) devices, 4 had intra-articular ruptures at the bone tunnel entry and 1 had become unstable with no dislocation of staples. Investigation by scanning electron and light microscopy showed no bony ingrowth of the Trevira ligaments. Instead there was fibrous tissue ingrowth in all parts of the prostheses (intra-articular, bone tunnels and anchoring regions). The extent of foreign-body reaction at the Trevira ligament boundary differed with the intensity of mechanical strain at the three parts of the implants (intra-articular, bone tunnel, periosteum). Inflammatory cells and foreign-body giant cells were abundant close to the site of ligament rupture at the intra-articular entries of the bone tunnels. These cells were scarce at the intra-articular parts of the ligament prostheses and at the periosteal anchor points. Evaluation of the reasons for prosthetic ligament failure shows that (1) nonideal placement of bone tunnels and (2) inadequate strain during rehabilitation resulted in instability and rupture after anterior cruciate replacement with Trevira ligaments.
在70例急慢性十字韧带断裂患者中总共植入了97个十字韧带假体;这些假体的平均使用年限为3年(8 - 53个月),其中5个(5.15%)在平均9个月(3 - 15个月)后因失效而被取出。在67例慢性十字韧带不稳病例中,植入了60个前交叉和7个后交叉的特丽纶十字韧带假体,另外25例急性前交叉和5例急性后交叉韧带断裂也采用特丽纶韧带增强术进行治疗。特丽纶十字韧带修复患者的随访率为97%。在取出的聚对苯二甲酸乙二酯(PET)装置中,4个在骨隧道入口处发生关节内破裂,1个变得不稳定但钉未脱位。扫描电子显微镜和光学显微镜检查显示特丽纶韧带无骨长入。相反,在假体的所有部位(关节内、骨隧道和锚固区域)均有纤维组织长入。特丽纶韧带边界处的异物反应程度因植入物三个部位(关节内、骨隧道、骨膜)机械应变强度的不同而有所差异。在骨隧道关节内入口处韧带断裂部位附近,炎性细胞和异物巨细胞丰富。在韧带假体的关节内部位和骨膜锚固点处,这些细胞较少。对假体韧带失效原因的评估表明:(1)骨隧道放置不理想;(2)康复期间应变不足,导致使用特丽纶韧带进行前交叉韧带置换后出现不稳定和破裂。