Department of Orthopaedics, Faculty of Medicine and Dentistry, University Hospital, Palacky University Olomouc, I.P. Pavlova Str. 6, CZ-775 20 Olomouc, Czech Republic.
Acta Biomater. 2013 Sep;9(9):8046-58. doi: 10.1016/j.actbio.2013.05.005. Epub 2013 May 10.
Aseptic loosening and other wear-related complications are some of the most frequent late reasons for revision of total knee arthroplasty (TKA). Periprosthetic osteolysis (PPOL) pre-dates aseptic loosening in many cases, indicating the clinical significance of this pathogenic mechanism. A variety of implant-, surgery- and host-related factors have been delineated to explain the development of PPOL. These factors influence the development of PPOL because of changes in mechanical stresses within the vicinity of the prosthetic device, excessive wear of the polyethylene liner, and joint fluid pressure and flow acting on the peri-implant bone. The process of aseptic loosening is initially governed by factors such as implant/limb alignment, device fixation quality and muscle coordination/strength. Later, large numbers of wear particles detached from TKA trigger and perpetuate particle disease, as highlighted by progressive growth of inflammatory/granulomatous tissue around the joint cavity. An increased accumulation of osteoclasts at the bone-implant interface, impairment of osteoblast function, mechanical stresses and increased production of joint fluid contribute to bone resorption and subsequent loosening of the implant. In addition, hypersensitivity and adverse reactions to metal debris may contribute to aseptic TKA failure, but should be determined more precisely. Patient activity level appears to be the most important factor when the long-term development of PPOL is considered. Surgical technique, implant design and material factors are the most important preventative factors, because they influence both the generation of wear debris and excessive mechanical stresses. New generations of bearing surfaces and designs for TKA should carefully address these important issues in extensive preclinical studies. Currently, there is little evidence that PPOL can be prevented by pharmacological intervention.
无菌性松动和其他与磨损相关的并发症是全膝关节置换术 (TKA) 后期翻修的最常见原因之一。在许多情况下,假体周围骨溶解 (PPOL) 先于无菌性松动,这表明了这种致病机制的临床意义。已经确定了多种与植入物、手术和宿主相关的因素,以解释 PPOL 的发展。这些因素通过改变假体附近的机械应力、聚乙烯衬垫的过度磨损以及作用于植入物周围骨骼的关节液压力和流动来影响 PPOL 的发展。无菌性松动的过程最初受植入物/肢体对线、器械固定质量和肌肉协调性/力量等因素的控制。后来,大量从 TKA 上脱落的磨损颗粒引发并延续了颗粒病,这突出表现为关节腔内周围炎症/肉芽肿组织的逐渐生长。破骨细胞在骨-植入物界面的大量堆积、成骨细胞功能受损、机械应力增加和关节液产生增加导致骨吸收和随后植入物松动。此外,对金属碎片的超敏反应和不良反应可能导致无菌性 TKA 失效,但应更准确地确定。当考虑 PPOL 的长期发展时,患者的活动水平似乎是最重要的因素。手术技术、植入物设计和材料因素是最重要的预防因素,因为它们会影响磨损颗粒的产生和过度的机械应力。新一代 TKA 的轴承表面和设计应在广泛的临床前研究中仔细解决这些重要问题。目前,几乎没有证据表明药物干预可以预防 PPOL。