Contributions of human tissue analysis to understanding the mechanisms of loosening and osteolysis in total hip replacement
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
Grantová podpora
R01 AR055650
NIAMS NIH HHS - United States
R01 AR063717
NIAMS NIH HHS - United States
PubMed
24525037
PubMed Central
PMC4389682
DOI
10.1016/j.actbio.2014.02.003
PII: S1742-7061(14)00055-5
Knihovny.cz E-zdroje
- Klíčová slova
- Aseptic loosening, Immunostaining, Osteolysis, Tissue analysis, Total hip,
- MeSH
- lidé MeSH
- náhrada kyčelního kloubu * MeSH
- osteolýza * MeSH
- pojivová tkáň patofyziologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
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.
Department of Dermatology and Allergology Copenhagen University Hospital Gentofte Denmark
Department of Orthopaedic Surgery Stanford University School of Medicine Stanford CA USA
Department of Pathology University Hospital Ostrava Czech Republic
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