Musculoskeletal Research Unit, Department of Academic Orthopaedics, University of Bristol, Southmead Hospital, Westbury-on-Trym, UK.
Acta Orthop. 2013 Aug;84(4):371-6. doi: 10.3109/17453674.2013.824801.
Loss of bone stock remains a challenge in revision hip surgery. Grafting with allograft is well established, but there are problems with availability, cost, infection, antigenicity, reproducibility, and stability of the created construct. BoneSave is a biphasic porous ceramic consisting of sintered 80% tricalcium phosphate and 20% hydroxyapatite. In vitro and in vivo studies, including its use mixed with allograft, have shown good results in impaction grafting. This is the first reported series of its use alone in impaction grafting of the acetabulum.
We conducted a retrospective review of a cohort of 43 consecutive patients undergoing impaction grafting of contained acetabular defects by multiple surgeons at a single centre. All patients received uncemented acetabular components. They were followed up radiographically, together with self-reported satisfaction scale (SAPS), Oxford hip score (OHS), and Short-Form 12 (SF12) health survey. Kaplan-Meier survivorship analysis was performed with revision of the acetabular component, revision of any part of the construct, and reoperation as endpoints.
The fate of all cases was known. Mean follow-up was 4 years. 5 patients died during follow-up, with their constructs in situ. The survivorship of the acetabular component was 98% (95% CI: 85-100) at 7 years. 1 acetabular component was revised for infection and there was 1 radiographic acetabular failure. The median OHS was 36 (6-48), the median SF12 PCS was 36 (14-57), the median SAPS was 75 (0-100), and the median SF12 MCS was 50 (23-64). The graft material had incorporated in all 3 zones of the acetabulum in 33 out of 37 cases with complete radiographic follow-up.
Medium-term results show that BoneSave alone is a reliable material for impaction grafting of contained defects in the acetabulum at revision surgery.
在翻修髋关节手术中,骨质缺损仍然是一个挑战。同种异体骨移植已得到广泛应用,但存在可用性、成本、感染、抗原性、可重复性和构建体稳定性等问题。BoneSave 是一种由 80%烧结磷酸三钙和 20%羟基磷灰石组成的双相多孔陶瓷。体外和体内研究,包括与同种异体骨混合使用,在压配移植中均显示出良好的效果。这是首次报道单独使用 BoneSave 进行髋臼压配移植的系列研究。
我们对 43 例连续患者进行了回顾性研究,这些患者由一名中心的多位外科医生进行了髋臼缺损的压配移植。所有患者均接受非骨水泥髋臼组件。通过放射学检查、自我报告满意度量表(SAPS)、牛津髋关节评分(OHS)和 12 项简短健康调查问卷(SF12)健康调查对其进行随访。以髋臼组件翻修、任何部分结构翻修和再次手术为终点,进行 Kaplan-Meier 生存分析。
所有病例的结局均已知。平均随访时间为 4 年。5 例患者在随访期间死亡,其植入物仍在位。髋臼组件的 7 年生存率为 98%(95%CI:85-100)。1 例髋臼组件因感染而翻修,1 例出现髋臼放射学失败。中位 OHS 为 36(6-48),中位 SF12 PCS 为 36(14-57),中位 SAPS 为 75(0-100),中位 SF12 MCS 为 50(23-64)。在 37 例具有完整放射学随访的病例中,有 33 例髋臼的 3 个区域均有移植物材料融合。
中期结果表明,单独使用 BoneSave 是一种可靠的翻修手术中用于髋臼内包含性缺损的压配移植材料。