van Cappelle H G, Deutman R, van Horn J R
Martini Hospital, Groningen, The Netherlands.
J Bone Joint Surg Am. 2001 Jul;83(7):999-1004. doi: 10.2106/00004623-200107000-00004.
Instability of the prosthesis and silicone-induced synovitis have led most surgeons to abandon use of the Swanson trapezium implant for the treatment of primary osteoarthritis. However, the literature contains little information on the results of long-term follow-up. The present study was conducted to establish the long-term results and to highlight the problems associated with the implant.
Thirty-five patients (forty-five implants) of our initial forty-five patients (fifty-seven implants) were available for clinical review. The mean duration of follow-up was 13.8 years. The objective result was assessed with a 40-point clinical scoring system. The subjective result was measured with a visual analog scale. A clinical score of 30 to 40 points and a subjective score of 8, 9, or 10 points were considered a good-to-excellent result. Radiographs were evaluated to determine the position and deformation of the prosthesis and to check for osteolytic changes of the bone, indicating silicone-induced synovitis.
The overall clinical and subjective results were good for twenty-seven thumbs (60%). Eighteen thumbs (40%) had a dislocation, and nine of them had a revision. Three more revisions were carried out because of silicone-induced synovitis, persistent pain after reflex sympathetic dystrophy, and deep infection in one thumb each. Revision surgery consisted of resection of the implant, with or without tendon interposition, or implantation of a new prosthesis. Of the thirty-two prostheses (thirty that had not been revised and two that had been revised) for which follow-up radiographs were available, six (19%) showed wear and deformation and five (16%) also were associated with osteolytic changes.
The main problem associated with the prosthesis was dislocation. Surgical measures to improve stability did not prevent this complication. The results after revision because of dislocation were no better than those associated with unrevised dislocated implants. In addition to dislocation, radiographic signs of silicone-induced synovitis were frequently noted, although they did not necessarily lead to a poor result. We concluded that the results after long-term follow-up of the Swanson silicone trapezium implant for the treatment of primary osteoarthritis were poor and that our decision to stop using this implant in 1991 was correct.
假体不稳定和硅酮诱导的滑膜炎致使大多数外科医生不再使用斯旺森(Swanson)梯形植入物治疗原发性骨关节炎。然而,关于长期随访结果的文献资料很少。本研究旨在确定长期结果并突出与该植入物相关的问题。
我们最初的45例患者(57枚植入物)中有35例患者(45枚植入物)可供临床复查。平均随访时间为13.8年。客观结果采用40分临床评分系统进行评估。主观结果采用视觉模拟量表进行测量。临床评分为30至40分且主观评分为8、9或10分被视为优良结果。对X线片进行评估,以确定假体的位置和变形情况,并检查是否存在骨溶解改变,提示硅酮诱导的滑膜炎。
27例拇指(60%)的总体临床和主观结果良好。18例拇指(40%)发生脱位,其中9例进行了翻修手术。另外3例翻修手术分别是由于硅酮诱导的滑膜炎、反射性交感神经营养不良后持续疼痛以及1例拇指深部感染。翻修手术包括切除植入物(有或没有肌腱插入)或植入新的假体。在有随访X线片的32枚假体(30枚未翻修和2枚已翻修)中,6枚(19%)显示磨损和变形,5枚(16%)还伴有骨溶解改变。
与该假体相关的主要问题是脱位。改善稳定性的手术措施未能预防这一并发症。因脱位进行翻修后的结果并不比未翻修的脱位植入物更好。除脱位外,尽管硅酮诱导的滑膜炎的X线征象不一定导致不良结果,但也经常被发现。我们得出结论,斯旺森硅酮梯形植入物治疗原发性骨关节炎的长期随访结果不佳,我们在1991年停止使用该植入物的决定是正确的。