首页> 外文期刊>Journal of Clinical Pathology >Proposal for a histopathological consensus classification of the periprosthetic interface membrane.
【24h】

Proposal for a histopathological consensus classification of the periprosthetic interface membrane.

机译:假体周围界面膜的组织病理学共识分类的建议。

获取原文
获取原文并翻译 | 示例
       

摘要

AIMS: The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery. METHODS: Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria. RESULTS: Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%). CONCLUSION: The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.
机译:目的:引入明确定义的组织病理学标准,以对假体周围膜进行标准化评估,这可能在全关节置换术翻修术中出现。方法:根据组织形态学标准,定义了四种类型的假体周围膜:磨损颗粒诱导型(检测异物颗粒;巨噬细胞和多核巨细胞至少占该区域的20%; I型);以及传染性类型(肉芽组织,具有嗜中性粒细胞,浆细胞,很少有磨损颗粒; II型);组合类型(I型和II型方面同时发生; III型);和不确定类型(I型和II型标准均未满足; IV型)。根据定义的标准分析了370例患者的假体周围膜(217名女性,153名男性;平均年龄67.6岁,平均到翻修手术的时间为7.4年)。结果:组织病理学膜类型的频率为:I型54.3%,II型19.7%,III型5.4%,IV型15.4%,不可评估的5.1%。 I型初次关节置换和翻修手术之间的平均时间为10.1年,II型为3.2年,III型为4.5年,IV型为5.4年。组织病理学和微生物学诊断之间的相关性很高(89.7%),观察者间的可重复性足够(85%)。结论:提出的分类可以实现假体周围膜的标准化分型,并且可以作为进一步研究全关节置换松动的发病机理的工具。该研究强调了在骨科手术(IV型膜)中非感染性,非颗粒性引起的假体装置松动的重要性,这一现象在15.4%的患者中观察到。

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