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Autor(en) / Beteiligte
Titel
Mechanically Induced Periprosthetic Osteolysis: A Systematic Review
Ist Teil von
  • HSS Journal, 2019-10, Vol.15 (3), p.286-296
Ort / Verlag
Los Angeles, CA: SAGE Publications
Erscheinungsjahr
2019
Quelle
2022 ECC(Springer)
Beschreibungen/Notizen
  • Background Peri-prosthetic bone loss can result from chemical, biological, and mechanical factors. Mechanical stimulation via fluid pressure and flow at the bone–implant interface may be a significant cause. Evidence supporting mechanically induced osteolysis continues to grow, but there is no synthesis of published clinical and basic science data. Questions/Purposes We sought to review the literature on two questions: (1) What published evidence supports the concept of mechanically induced osteolysis? (2) What is the proposed mechanism of mechanically induced osteolysis, and does it differ from that of particle-induced osteolysis? Methods A systematic review was performed of the PubMed and Web of Science databases. Additional relevant articles were recommended by the senior authors based on their expert opinion. Abstracts were reviewed and the manuscripts pertaining to the study questions were read in full. Studies showing support of mechanically induced osteolysis were quantified and findings summarized. Results We identified 49 articles of experimental design supporting the hypothesis that mechanical stimulation of peri-prosthetic bone from fluid pressure and flow can induce osteolysis. While the molecular mechanisms may overlap with those implicated in particle-induced osteolysis, mechanically induced osteolysis appears to be mediated by distinct and parallel pathways. Conclusions The role of mechanical stimuli is increasingly recognized in the pathogenesis of peri-prosthetic osteolysis. Current research aims to elucidate the molecular mechanisms to better target therapeutic interventions.
Sprache
Englisch
Identifikatoren
ISSN: 1556-3316
eISSN: 1556-3324
DOI: 10.1007/s11420-018-9641-5
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6778158

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