Department of Orthopaedics, Our Lady of Lourdes Hospital, Drogheda, Ireland.
Injury. 2012 Jun;43(6):838-42. doi: 10.1016/j.injury.2011.10.002. Epub 2011 Oct 27.
Ankle syndesmotic injuries are complex and require anatomic reduction and fixation. Tightrope fixation is a relatively new technique and we present the largest series of syndesmosis fixation using Arthrex Tightrope™ (Naples, FL, USA).
Forty-nine patients with ankle diastasis, treated with Arthrex tightrope™, were reviewed retrospectively, using American Orthopaedic Foot and Ankle Society (AOFAS) and Foot and Ankle Disability Index (FADI) scores and radiographic parameters for syndesmosis integrity. The operative technique was slightly modified by the senior author in 31 cases to avoid soft-tissue complications requiring removal of the implant. The aim of this study was to assess the rate of hardware removal after tightrope fixation and the effect of the author's modification to avoid soft-tissue complications.
The mean age of patients was 37.7 years. Eighteen were performed with standard technique whilst 31 with the modified technique. The mean radiological follow-up was 6 months. Final data were collected using a confidential questionnaire and FADI score at an average of 24 (12-38) months postoperatively. The average time to full weight bearing was 7.7 weeks and to return to normal activities was 11.2 weeks. Postoperative radiographic measurements demonstrated satisfactory reduction of syndesmosis. The Mean AOFAS score was 85.57 (95% confidence interval (CI) 77.96-93.18) and the mean FADI score was 81.20 (95% CI 73.86-88.53). There were three cases of hardware removal in the standard technique group as compared to none in the group with the modified technique.
Arthrex Tightrope™ provides an effective method of syndesmosis stabilisation, which obviates the need for routine removal of implant and facilitates dynamic stabilisation. The results of this study are satisfactory and comparable to previously reported studies. We emphasise that surgeons must be aware of the potential risk of soft-tissue complications and recommend our modified technique. Further long-term prospective studies should be carried out to resolve this issue.
踝关节联合损伤较为复杂,需要解剖复位和固定。Tightrope 固定是一种相对较新的技术,我们报告了使用 Arthrex Tightrope™(美国佛罗里达州那不勒斯)固定联合最多的系列病例。
回顾性分析了 49 例踝关节分离患者,采用美国矫形足踝协会(AOFAS)评分和足踝残疾指数(FADI)评分及踝关节联合完整性的影像学参数评估,均采用 Arthrex Tightrope™进行治疗。为避免软组织并发症需要取出植入物,高级作者对 31 例手术技术进行了轻微修改。本研究的目的是评估 Tightrope 固定后取除内固定物的比率以及作者修改手术技术避免软组织并发症的效果。
患者的平均年龄为 37.7 岁。18 例采用标准技术,31 例采用改良技术。平均放射学随访时间为 6 个月。最终数据通过术后平均 24(12-38)个月的机密问卷调查和 FADI 评分收集。平均完全负重时间为 7.7 周,恢复正常活动时间为 11.2 周。术后放射影像学测量显示联合复位满意。平均 AOFAS 评分为 85.57(95%置信区间(CI)77.96-93.18),平均 FADI 评分为 81.20(95%CI 73.86-88.53)。标准技术组有 3 例取出内固定物,改良技术组无内固定物取出。
Arthrex Tightrope™为联合固定提供了一种有效的方法,避免了常规取出植入物的需要,并有利于动态稳定。本研究结果令人满意,与以往报道的研究结果相当。我们强调,外科医生必须意识到潜在的软组织并发症风险,并推荐使用我们的改良技术。应进一步开展长期前瞻性研究以解决这一问题。