...
首页> 外文期刊>BMC Musculoskeletal Disorders >Augmentation of tibial plateau fractures with an injectable bone substitute: CERAMENT?. Three year follow-up from a prospective study
【24h】

Augmentation of tibial plateau fractures with an injectable bone substitute: CERAMENT?. Three year follow-up from a prospective study

机译:用可注射的骨替代物CERAMENT?增强胫骨平台骨折。一项前瞻性研究的三年随访

获取原文

摘要

Background Reduction of tibial plateau fractures and maintain a level of well aligned congruent joint is key to a satisfactory clinical outcome and is important for the return to pre-trauma level of activity. Stable internal fixation support early mobility and weight bearing. The augmentation with bone graft substitute is often required to support the fixation to mantain reduction. For these reasons there has been development of novel bone graft substitutes for trauma applications and in particular synthetic materials based on calcium phosphates and/or apatite combined with calcium sulfates. Injectable bone substitutes can optimize the filling of irregular bone defects. The purpose of this study was to assess the potential of a novel injectable bone substitute CERAMENT?|BONE VOID FILLER in supporting the initial reduction and preserving alignment of the joint surface until fracture healing. Methods From June 2010 through May 2011 adult patients presenting with acute, closed and unstable tibial plateau fractures which required both grafting and internal fixation, were included in a prospective study with percutaneous or open reduction and internal fixation (ORIF) augmented with an injectable ceramic biphasic bone substitute CERAMENT?|BONE VOID FILLER (BONESUPPORT?, Lund, Sweden) to fill residual voids. Clinical follow up was performed at 1, 3, 9 and 12?months and any subsequent year; including radiographic analysis and Rasmussen system for knee functional grading. Results Twenty four patients, balanced male-to-female, with a mean age of 47?years, were included and followed with an average of 44?months (range 41–52 months). Both Schatzker and Müller classifications were used and was type II or 41-B3 in 7 patients, type III or 41-B2 in 12 patients, type IV or 41-C1 in 2 patients and type VI or 41-C3 in 3 patients, respectively. The joint alignement was satisfactory and manteined within a range of 2?mm, with an average of 1.18?mm. The mean Rasmussen knee function score was 26.5, with 14 patients having an excellent result and the remaining 10 with a good result. Conclusion It can be concluded that radiological and clinical outcome was satisfactory and obtained in all cases without complications. This injectable novel biphasic hydroxyapatite and calcium sulfate ceramic material is a valuable armamentarium in the treatment of trauma where bone graft is required.
机译:背景技术减少胫骨平台骨折并保持水平一致的全关节水平是取得令人满意的临床结果的关键,对于恢复创伤前的活动水平至关重要。稳定的内部固定可支持早期活动和承重。通常需要使用植骨替代物进行增强以支持固定,以实现复位。由于这些原因,已经开发了用于创伤应用的新型骨移植替代物,特别是基于磷酸钙和/或磷灰石与硫酸钙结合的合成材料。可注射的骨替代物可以优化不规则骨缺损的填充。这项研究的目的是评估新型可注射骨替代物CERAMENT?| BONE VOID FILLER在支持初期复位和保持关节表面对齐直至骨折愈合之前的潜力。方法从2010年6月至2011年5月,将有急性,闭合和不稳定的胫骨平台骨折且需要同时植骨和内固定的成年患者纳入一项前瞻性研究,该研究采用经皮或切开复位内固定(ORIF)并加注双相陶瓷骨替代物CERAMENT?| BONE VOID FILLER(BONESUPPORT ?,瑞典隆德)以填充残留的空隙。在1、3、9和12个月以及随后的任何一年进行临床随访。包括射线照相分析和Rasmussen系统,以进行膝盖功能分级。结果纳入二十四例平均年龄为47岁的男女平衡的患者,其后平均44个月(41-52个月)。使用Schatzker和Müller两种分类,分别为7例患者为II型或41-B3、12例患者为III型或41-B2、2例患者为IV型或41-C1以及3例患者为VI型或41-C3。 。关节排列令人满意,并在2?mm的范围内进行修饰,平均为1.18?mm。拉斯穆森(Rasmussen)膝关节功能平均评分为26.5,其中14例取得优异结果,其余10例取得良好结果。结论可以得出结论,在所有无并发症的病例中,放射学和临床结果令人满意。这种可注射的新型双相羟基磷灰石和硫酸钙陶瓷材料是在需要骨移植的创伤治疗中的宝贵武器装备。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号