Harston Andrew, Lazarides Alexander L, Adams Samuel B, DeOrio James K, Easley Mark E, Nunley James A
1 Duke University Orthopaedic Department, Durham, NC, USA.
Foot Ankle Int. 2017 Dec;38(12):1295-1300. doi: 10.1177/1071100717731853. Epub 2017 Sep 26.
We present our results with an INBONE I (Wright Medical, Memphis, TN) prosthesis that have a minimum of 4 to 10 years of follow-up and include a preoperative deformity analysis on outcomes.
A consecutive series of 149 patients, from 2007 to 2011, at a single institution were enrolled. Pain and patient-reported function were assessed preoperatively and at yearly follow-ups. We analyzed the data for complications, reoperations, and failures (defined as undergoing revision for exchange or removal of one or both metallic components for any reason). Patients were also grouped according to coronal plane tibiotalar alignment; either ≥10 degrees or <10 degrees, and these outcomes were compared. Our follow-up ranged from 48 to 113 months (average 5.9 years).
There was significant improvement ( P < .05) in the visual analog scale for pain, American Orthopaedic Foot & Ankle Society hindfoot scale, Short Musculoskeletal Function Assessment, and Short Form 36-Item Health Survey scores at most recent follow-up. There were 14 implant failures with overall survivorship of 90.6% (135/149). Reasons for failure included cysts/loosening (7), talar subsidence (4), fractured component (1), impingement pain (1), and infection (1). Seventy-two patients (48.3%) with preoperative coronal plane deformity of ≥10 degrees varus or valgus were compared to 78 patients (51.7%) with <10 degrees deformity. There was no difference in patient outcome scores or revision rates between these patient groups. There was a statistically significant difference ( P = .039) in reoperation rates among patients with ≥10 degrees deformity (22.2%) compared to those without such a deformity (37.7%) Conclusion: Patients who underwent INBONE I fixed-bearing total ankle arthroplasty demonstrated significant improvement in outcomes at a mean of 5.9 years. Catastrophic talar component collapse did occur (2.7% of cases), but relatively rarely. The patients with preoperative coronal plane tibiotalar deformity had similar pain relief, function, and need for revision of implant components. Despite the presumed shortcomings of the INBONE I's design, this implant showed promising results, with or without deformity, at midterm follow-up with survivorship of 90.6%.
Level III, comparative study.
我们展示了使用INBONE I(Wright Medical,孟菲斯,田纳西州)假体的结果,该假体至少随访了4至10年,并对结果进行了术前畸形分析。
纳入了2007年至2011年在单一机构的连续149例患者。术前及每年随访时评估疼痛和患者报告的功能。我们分析了并发症、再次手术和失败(定义为因任何原因对一个或两个金属部件进行翻修置换或取出)的数据。患者还根据冠状面胫距关节对线情况分组,即≥10度或<10度,并比较这些结果。我们的随访时间为48至113个月(平均5.9年)。
在最近一次随访时,疼痛视觉模拟量表、美国矫形足踝协会后足量表、简短肌肉骨骼功能评估和简短36项健康调查评分均有显著改善(P <.05)。有14例植入失败,总体生存率为90.6%(135/149)。失败原因包括囊肿/松动(7例)、距骨下沉(4例)、部件骨折(1例)、撞击痛(1例)和感染(1例)。将72例(48.3%)术前冠状面畸形≥10度内翻或外翻的患者与78例(51.7%)畸形<10度的患者进行比较。这些患者组之间的患者结果评分或翻修率没有差异。与无此类畸形的患者(37.7%)相比,畸形≥10度的患者再次手术率有统计学显著差异(P = 0.039)。结论:接受INBONE I固定承重全踝关节置换术的患者在平均5.9年时结果有显著改善。确实发生了距骨部件灾难性塌陷(2.7%的病例),但相对较少。术前冠状面胫距关节畸形的患者在疼痛缓解、功能和植入部件翻修需求方面相似。尽管INBONE I设计存在公认的缺点,但该植入物在中期随访时显示出有前景的结果,无论有无畸形,生存率为90.6%。
III级,比较研究。