Contributions of human tissue analysis to understanding the mechanisms of loosening and osteolysis in total hip replacement

被引:100
作者
Gallo, Jiri [1 ]
Vaculova, Jana [2 ]
Goodman, Stuart B. [3 ]
Konttinen, Yrjoe T. [4 ,5 ,6 ]
Thyssen, Jacob P. [7 ]
机构
[1] Palacky Univ Olomouc, Univ Hosp, Fac Med & Dent, Dept Orthopaed, Olomouc, Czech Republic
[2] Univ Hosp Ostrava, Dept Pathol, Ostrava, Czech Republic
[3] Stanford Univ, Sch Med, Dept Orthopaed Surg, Stanford, CA 94305 USA
[4] Inst Clin Med, Dept Med, FIN-00029 Helsinki, Finland
[5] Invalid Fdn, ORTON Orthopaed Hosp, Helsinki, Finland
[6] COXA Hosp Joint Replacement, Tampere, Finland
[7] Univ Copenhagen, Gentofte Hosp, Dept Dermatol & Allergol, DK-1168 Copenhagen, Denmark
关键词
Aseptic loosening; Osteolysis; Total hip; Tissue analysis; Immunostaining; ON-METAL BEARINGS; INTRAOPERATIVE GRAM STAIN; BONE-IMPLANT INTERFACE; SYNOVIAL-LIKE MEMBRANE; KAPPA-B LIGAND; PERIPROSTHETIC OSTEOLYSIS; PROSTHESIS FAILURE; RECEPTOR ACTIVATOR; GROWTH-FACTOR; LONG-TERM;
D O I
10.1016/j.actbio.2014.02.003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Aseptic loosening and osteolysis are the most frequent late complications of total hip arthroplasty (THA) leading to revision of the prosthesis. This review aims to demonstrate how histopathological studies contribute to our understanding of the mechanisms of aseptic loosening/osteolysis development. Only studies analysing periprosthetic tissues retrieved from failed implants in humans were included. Data from 101 studies (5532 patients with failure of THA implants) published in English or German between 1974 and 2013 were included. "Control" samples were reported in 45 of the 101 studies. The most frequently examined tissues were the bone-implant interface membrane and pseudosynovial tissues. Histopathological studies contribute importantly to determination of key cell populations underlying the biological mechanisms of aseptic loosening and osteolysis. The studies demonstrated the key molecules of the host response at the protein level (chemokines, cytokines, nitric oxide metabolites, metalloproteinases). However, these studies also have important limitations. Tissues harvested at revision surgery reflect specifically end-stage failure and may not adequately reveal the evolution of pathophysiological events that lead to prosthetic loosening and osteolysis. One possible solution is to examine tissues harvested from stable total hip arthroplasties that have been revised at various time periods due to dislocation or periprosthetic fracture in multicenter studies. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2354 / 2366
页数:13
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