Ankle Fusion Rates using Composite Peptide-enriched Bone Graft

Luke S. McKinnon, Michael J. Symes, Andrew Wines, R. Mittal
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Abstract

Joint fusion is a widely accepted treatment option for debilitating arthritis and deformity in the foot and ankle. Autologous bone grafting has long been accepted as the gold standard form of bone grafting; however, it can still be associated with non-union. This study aims to investigate joint fusion rates using Composite Peptide Enhanced Bone Graft (CPEBG) as an adjunct during ankle fusion surgery. Data was collected retrospectively for patients over the age of 18 years, undergoing ankle fusion between June 2016 and August 2020 with autologous bone graft and CPEBG. All patients had their primary or secondary procedure performed by a single surgeon with follow-up at 6 and 12 months post-operatively. Data included baseline demographic data and procedural characteristics. The primary endpoint was to assess joint union at 6 and 12 months, respectively. Secondary objectives included post-operative pain, mobility and the use of walking aids. Radiographic union rates for the primary group were 40/48 (83%) and 43/48 (90%) at 6 and 12 months and 2/3 (67%) and 3/3 (100%) at 6 and 12 months for the secondary group, respectively. The overall non-union rate for primary ankle fusions was 8%, while no non-unions were observed in the secondary group. CPEBG in foot and ankle fusion procedures yields similar union rates compared to other graft options. Further well-designed randomised control trials are warranted to confirm these findings.
使用复合肽骨移植的踝关节融合率
关节融合术是治疗足踝关节炎和畸形的一种广为接受的方法。长期以来,自体骨移植一直被认为是骨移植的金标准,但仍有可能出现不愈合的情况。本研究旨在调查在踝关节融合手术中使用复合肽增强型骨移植(CPEBG)作为辅助手段的关节融合率。 研究回顾性收集了2016年6月至2020年8月期间接受自体骨移植和CPEBG踝关节融合术的18岁以上患者的数据。所有患者的主要或次要手术均由一名外科医生完成,并在术后 6 个月和 12 个月进行随访。数据包括基线人口统计学数据和手术特征。主要终点分别是评估6个月和12个月时的关节结合情况。次要目标包括术后疼痛、活动能力和行走辅助工具的使用情况。 在6个月和12个月时,初级组的X光片结合率分别为40/48(83%)和43/48(90%);在6个月和12个月时,次级组的X光片结合率分别为2/3(67%)和3/3(100%)。初次踝关节融合术的总体非愈合率为 8%,而二次组未观察到非愈合。 与其他移植物相比,CPEBG 在足踝融合术中的结合率相近。为了证实这些研究结果,有必要进一步开展设计良好的随机对照试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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