首页> 外文期刊>International Orthopaedics >One and two-year clinical outcomes for a polyethylene glenoid with a fluted peg: one thousand two hundred seventy individual patients from eleven centers
【24h】

One and two-year clinical outcomes for a polyethylene glenoid with a fluted peg: one thousand two hundred seventy individual patients from eleven centers

机译:具有吹笛性吊裙的聚乙烯关节盂的一两年和两年临床结果:来自11个中心的一千二百七十个患者

获取原文
获取原文并翻译 | 示例
       

摘要

PurposeClinical shoulder science lacks a benchmark against which the early clinical value of new glenoid components can be compared; such a benchmark may be derived from a multicenter study of patients receiving an established, internationally used design of glenoid component.MethodsWe obtained data from 11 centers on 1270 patients having total shoulder arthroplasty using an all-polyethylene component with a fluted central peg. We analyzed individual patient outcomes at 1 and 2years after surgery. We compared the improvement for each patient to the minimal clinically important difference (MCID) and calculated each patient's improvement as a percent of maximal possible improvement (MPI).ResultsThe preoperative scores improved from SST 32, ASES 37 +/- 15, Constant score 36 +/- 16, and Penn score 30 +/- 19 to SST 10 +/- 2, ASES 90 +/- 12, Constant 76 +/- 13, and Penn 80 +/- 24 (p<0.001 for each). A high percentage of patients improved by more than the MCID (SST 96%, ASES 98%, Constant 94%, Penn 93%) and obtained improvement of at least 30% of the MPI (SST 95%, ASES 98%, Constant 91%, Penn 87%). The clinical outcomes realized with this glenoid design were not worse for the 41% of shoulders with preoperative type B glenoids or for the 30% of shoulders with more than 15 degrees of glenoid retroversion.ConclusionsIndividual patients from 11 international practices having total shoulder arthroplasty using a basic glenoid component design obtained highly significant clinical outcomes, providing a benchmark against which the early outcomes of new designs can be compared to determine whether they provide increased clinical value.
机译:用品肩部肩部缺乏基准,可以比较新的关节盂部件的早期临床价值;这种基准可能来自于接受所建立的,国际上使用的胶质素组件的患者的多中心研究。近期使用肩部关节置换术的11个中心获得的数据来自11个患者,该患者使用具有凹槽中央栓的全聚乙烯组分。我们在手术后分析了1和2年的个体患者结果。将每位患者的改善与最小的临床重要差异(MCID)进行比较,并计算每个患者的改善,因为最大可能改善的百分比(MPI)。术前分数从SST 32改善,ASES 37 +/-15,恒定得分36 +/- 16和Penn得分30 +/- 19至SST 10 +/- 2,ASES 90 +/- 12,常数76 +/-13和Penn 80 +/- 24(每个P <0.001)。高百分比的患者通过比mcid(SST 96%,SST 96%,98%,恒定的94%,PENN 93%)提高,并获得了至少30%的MPI(SST 95%,ASES 98%,恒定91的改善%,Penn 87%)。使用术前型B个关节盂的41%的肩膀或肩部肩部的肩部的临床结果并没有更差,或者肩部超过15度的关节盂升压。合并来自11个国际练习的单独患者,使用A总肩部表现出来基本关节盂部件设计获得了高度显着的临床结果,提供了一种基准,可以进行新设计的早期结果,以确定它们是否提供增加的临床价值。

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