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      Platelet-rich plasma in osteoarthritis treatment: review of current evidence

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          Abstract

          Platelet-rich plasma (PRP) is defined as a volume of plasma with a platelet concentration higher than the average in peripheral blood. Many basic, preclinical and even clinical case studies and trials report PRP’s ability to improve musculoskeletal conditions including osteoarthritis, but paradoxically, just as many conclude it has no effect. The purpose of this narrative review is to discuss the available relevant evidence that supports the clinical use of PRP in osteoarthritis, highlighting those variables we perceive as critical. Here, recent systematic reviews and meta-analyses were used to identify the latest randomized controlled trials (RCTs) testing a PRP product as an intra-articular treatment for knee osteoarthritis, compared with an intra-articular control (mostly hyaluronic acid). Conclusions in the identified RCTs are examined and compared. In total, five recent meta-analyses and systematic reviews were found meeting the above criteria. A total of 19 individual trials were identified in the five reviews but only 9 were level of evidence I RCTs, and many had moderate or high risks of bias. At present, results from these RCTs seem to favor PRP use over other intra-articular treatments to improve pain scales in the short and medium term (6–12 months), but the overall level of evidence is low. As a result, clinical effectiveness of PRP for knee osteoarthritis treatment is still under debate. This is, prominently, the result of a lack of standardization of PRP products, scarceness of high quality RCTs not showing high risks of bias, and poor patient stratification for inclusion in the RCTs.

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          Platelet-rich plasma: Growth factor enhancement for bone grafts.

          Platelet-rich plasma is an autologous source of platelet-derived growth factor and transforming growth factor beta that is obtained by sequestering and concentrating platelets by gradient density centrifugation. This technique produced a concentration of human platelets of 338% and identified platelet-derived growth factor and transforming growth factor beta within them. Monoclonal antibody assessment of cancellous cellular marrow grafts demonstrated cells that were capable of responding to the growth factors by bearing cell membrane receptors. The additional amounts of these growth factors obtained by adding platelet-rich plasma to grafts evidenced a radiographic maturation rate 1.62 to 2.16 times that of grafts without platelet-rich plasma. As assessed by histomorphometry, there was also a greater bone density in grafts in which platelet-rich plasma was added (74.0% +/- 11%) than in grafts in which platelet-rich plasma was not added (55.1% +/- 8%; p = 0.005).
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            Principles and Methods of Preparation of Platelet-Rich Plasma: A Review and Author's Perspective

            The utility of platelet-rich plasma (PRP) has spanned various fields of dermatology from chronic ulcer management to trichology and aesthetics, due to its role in wound healing. Though PRP is being used over a long time, there is still confusion over proper terminology to define, classify and describe the different variations of platelet concentrates. There is also a wide variation in the reported protocols for standardization and preparation of PRP, in addition to lack of accurate characterization of the tested products in most articles on the topic. Additionally, the high cost of commercially available PRP kits, precludes its use over a larger population. In this article, we review the principles and preparation methods of PRP based on available literature and place our perspective in standardizing a safe, simple protocol that can be followed to obtain an optimal consistent platelet yield.
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              Platelet-rich plasma: the PAW classification system.

              Platelet-rich plasma (PRP) has been the subject of hundreds of publications in recent years. Reports of its effects in tissue, both positive and negative, have generated great interest in the orthopaedic community. Protocols for PRP preparation vary widely between authors and are often not well documented in the literature, making results difficult to compare or replicate. A classification system is needed to more accurately compare protocols and results and effectively group studies together for meta-analysis. Although some classification systems have been proposed, no single system takes into account the multitude of variables that determine the efficacy of PRP. In this article we propose a simple method for organizing and comparing results in the literature. The PAW classification system is based on 3 components: (1) the absolute number of Platelets, (2) the manner in which platelet Activation occurs, and (3) the presence or absence of White cells. By analyzing these 3 variables, we are able to accurately compare publications. Copyright © 2012 Arthroscopy Association of North America. Published by Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Ther Adv Chronic Dis
                Ther Adv Chronic Dis
                TAJ
                sptaj
                Therapeutic Advances in Chronic Disease
                SAGE Publications (Sage UK: London, England )
                2040-6223
                2040-6231
                19 February 2019
                2019
                : 10
                : 2040622319825567
                Affiliations
                [1-2040622319825567]Grupo de Investigación en Reumatología (GIR), Agrupación Estratégica CICA-Instituto de Investigación Biomédica (INIBIC), Complexo Hospitalario Universitario A Coruña (CHUAC), Sergas, Universidad de A Coruña (UDC), A Coruña, Spain
                [2-2040622319825567]Grupo de Investigación en Reumatología (GIR), Agrupación Estratégica CICA-Instituto de Investigación Biomédica (INIBIC), Complexo Hospitalario Universitario A Coruña (CHUAC), Sergas, Universidad de A Coruña (UDC), A Coruña, Spain
                [3-2040622319825567]CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Spain
                [4-2040622319825567]Grupo de Investigación en Reumatología (GIR), Agrupación Estratégica CICA-Instituto de Investigación Biomédica (INIBIC), Complexo Hospitalario Universitario A Coruña (CHUAC), Sergas, Universidad de A Coruña (UDC), A Coruña, Spain
                [5-2040622319825567]CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Spain
                [6-2040622319825567]Grupo de Investigación en Reumatología (GIR), Agrupación Estratégica CICA-Instituto de Investigación Biomédica (INIBIC), Complexo Hospitalario Universitario A Coruña (CHUAC), Sergas, Universidad de A Coruña (UDC), A Coruña, Spain
                [7-2040622319825567]Red de Investigación en Inflamación y Enfermedades Reumáticas, INIBIC-CHUAC, A Coruña, Spain
                [8-2040622319825567]ProteoRed/ISCIII, INIBIC-CHUAC, A Coruña, Spain
                [9-2040622319825567]Grupo de Investigación en Reumatología, Agrupación Estratégica CICA-INIBIC, Hospital Universitario A Coruña, Xubias de Arriba 84, 15006 A Coruña, Spain
                Author notes
                Author information
                https://orcid.org/0000-0001-9327-7639
                Article
                10.1177_2040622319825567
                10.1177/2040622319825567
                6383098
                30815245
                0c5525f9-b1f8-466a-9a30-2818e3a46426
                © The Author(s), 2019

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 6 July 2018
                : 28 December 2018
                Funding
                Funded by: Interreg (POCTEP)-EU Program, ;
                Award ID: 0245_IBEROS_1_E
                Funded by: axencia galega de innovación, FundRef https://doi.org/10.13039/501100010769;
                Award ID: IN607A 2017/11
                Funded by: instituto de salud carlos iii, FundRef https://doi.org/10.13039/501100004587;
                Award ID: CPII15/00013
                Funded by: Instituto de Salud Carlos III, FundRef https://doi.org/10.13039/501100004587;
                Award ID: PI12/00329
                Funded by: Instituto de Salud Carlos III, FundRef https://doi.org/10.13039/501100004587;
                Award ID: PI16/02124
                Funded by: Instituto de Salud Carlos III, FundRef https://doi.org/10.13039/501100004587;
                Award ID: PMP15/00032
                Funded by: Ministerio de Educación y Cultura, FundRef https://doi.org/10.13039/501100008743;
                Award ID: FPU13/06041
                Categories
                Review
                Custom metadata
                January-December 2019

                allogenic products,anti-inflammatory intra-articular therapies,clinical evidence,clinical trials,knee osteoarthritis,patient stratification,platelet-rich plasma

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