The relationship of polyethylene wear to particle size, distribution, and number: A possible factor explaining the risk of osteolysis after hip arthroplasty
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20524192
DOI
10.1002/jbm.b.31638
Knihovny.cz E-resources
- MeSH
- Algorithms MeSH
- Humans MeSH
- Arthroplasty, Replacement, Hip adverse effects MeSH
- Osteolysis etiology MeSH
- Polyethylenes chemistry MeSH
- Prosthesis Failure * MeSH
- Particle Size MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Polyethylenes MeSH
The most critical factor in the development of periprosthetic osteolysis (OL) in total hip arthroplasty (THA) is the biological reaction to wear debris. This reaction is dependent, in part, on the size and concentration of particles, which are determined predominantly by the polyethylene (PE) wear rate. This implies that the risk for developing OL and prosthesis failure can be estimated from wear measurements. We developed a computational algorithm for calculating the total number of PE particles for volumetric wear when particle size and distribution are known. We found that: (i) total number of PE wear particles decreases up to 5 orders of magnitude if the average size of particles increases and the total volumetric wear remains constant; (ii) total amount of PE wear particles decreases up to 4 orders of magnitude if the width of the distribution increases and total volumetric wear remains constant; (iii) for the same volumetric wear, the number of particles significantly decreases/increases with the increase/decrease in their average size and range. These findings suggest that the risk for the development of OL in THA cannot be simply estimated from the volumetric wear alone.
References provided by Crossref.org
Surface protolytic property characterization of hydroxyapatite and titanium dioxide nanoparticles
Innate immunity sensors participating in pathophysiology of joint diseases: a brief overview
Particle disease: biologic mechanisms of periprosthetic osteolysis in total hip arthroplasty