Andrew J. Sheean, M.D., Adam W. Anz, M.D., and James P. Bradley, M.D.
The authors report the following potential conflicts of interest or sources of funding: A.J.S. reports personal fees from Arthroscopy and grants from Embody, Inc., outside the submitted work. A.W.A. reports grants and personal fees from Arthrex, personal fees from Ossur, and grants from KLSMC Stem Cell, outside the submitted work. J.P.B. reports royalties from Arthrex, outside the submitted work. Full ICMJE author disclosure forms are available for this article online, as supplementary material.
Received February 16, 2021; accepted July 6, 2021.
Address correspondence to Andrew J. Sheean, M.D., San Antonio Military Medical Center, San Antonio, Texas 78234 U.S.A. E-mail: ajsheean@gmail. com
Published by Elsevier on behalf of the Arthroscopy Association of North America
0749-8063/21978/$36.00
https://doi.org/10.1016/j.arthro.2021.07.003

Abstract:
Platelet-rich plasma (PRP) is perhaps the most widely studied of the biologic therapies, with an
ever-growing body of evidence supporting its safety and efficacy in decreasing inflammation and pain and
promoting healing in the setting of both nonoperative and operative treatments. PRP is produced by the
centrifugation of whole blood, isolating its constituent parts based on their unique densities. These density
gradients can be selectively harvested so as to obtain different concentrations of various blood product
components, such as platelets and leukocytes. A precise and consistent method for describing the essential
characteristics of different PRP formulations is critical for both practical and research purposes. The concentration
of platelets, method of activation, and the total number of red blood cells (RBCs), white blood
cells (WBCs), and neutrophils relative to baseline values are all of particular importance in accurately
describing a PRP formulation. The biologic activity of PRP is manifold: platelet α granules promote the
release of various growth factors, including vascular endothelial growth factor and tissue growth factor b,
while inflammation is modulated through inhibition of the nuclear factor-κB pathway. PRP has been
convincingly shown to be efficacious in the setting of patellar tendinopathies, knee osteoarthritis, and
lateral epicondylitis. In fact, several recent randomized controlled trials have demonstrated the superiority
of PRP over both corticosteroids and hyaluronic acid in treating knee OA-related symptoms. There is also
substantial promise for the utility of PRP in treating partial hamstring tears and as an adjunct to rotator cuff
(RC) repair, especially in the setting of small- to medium-sized tears, where it appears to exert substantial
analgesic effects and promote enhanced rates of RC repair healing.
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