Platelet-Rich Plasma and Cartilage Repair View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-12

AUTHORS

Mitchell I. Kennedy, Kaitlyn Whitney, Thos Evans, Robert F. LaPrade

ABSTRACT

PURPOSE OF REVIEW: To assess the utilization and efficacy of platelet-rich plasma (PRP), for the treatment of articular cartilage injury, most commonly characterized by progressive pain and loss of joint function in the setting of osteoarthritis (OA). RECENT FINDINGS: PRP modulates the inflammatory and catabolic environment through a locally applied concentrate of platelets, leukocytes, and growth factors. Clinically, PRP has been shown to be possibly a viable treatment adjuvant for a variety of inflammatory and degenerative conditions. Recent efforts have focused on optimizing delivery methods that enable platelets to slowly degranulate their biological constituents, which may promote healing and improve OA symptoms for a longer duration. There are various factors that affect the progression of OA within joints, including inhibition of inflammatory cytokines and altering the level of enzymatic expression. PRP therapy aims to mediate inflammatory and catabolic factors in a degenerative environment through the secretion of anti-inflammatory factors and chemotaxic effects. There are a growing number of studies that have demonstrated the clinical benefit of PRP for non-operative management of OA. Additional randomized controlled trials with long-term follow-up are needed in order to validate PRP's therapeutic efficacy in this setting. Additionally, continued basic research along with well-designed pre-clinical studies and reporting standards are necessary in order to clarify the effectiveness of PRP for cartilage repair and regeneration for future clinical applications. More... »

PAGES

573-582

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s12178-018-9516-x

    DOI

    http://dx.doi.org/10.1007/s12178-018-9516-x

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1106903178

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/30203333


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