PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY

To compare the efficacy of platelet rich plasma (PRP) against corticosteroid on the treatment of trochanteric pain syndrome From July 2011 to November 2012, eighteen patients (20 hips) with trochanter pain syndrome were randomized in two groups and treated with platelet rich plasma or triamcinolone...

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Published in:Acta ortopedica brasileira Vol. 24; no. 4; pp. 208 - 212
Main Authors: Ribeiro, Arthur de Góes, Ricioli, Junior, Walter, Silva, Alice Roxo Nobre Sousa E, Polesello, Giancarlo Cavalli, Guimarães, Rodrigo Pereira
Format: Journal Article
Language:English
Published: Brazil Departamento de Ortopedia e Traumatologia (DOT/FMUSP) 01-08-2016
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Sociedade Brasileira de Ortopedia e Traumatologia
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Summary:To compare the efficacy of platelet rich plasma (PRP) against corticosteroid on the treatment of trochanteric pain syndrome From July 2011 to November 2012, eighteen patients (20 hips) with trochanter pain syndrome were randomized in two groups and treated with platelet rich plasma or triamcinolone infiltration guided by ultrasound. Pain and function were evaluated prior to the intervention and after 10, 30 and 60 days, through the Facial Expressions Scale for Pain and the Western Ontario McMaster and Harris Hip Score questionnaires. Inter-group analysis was performed by Student t-test and intragroup analysis by ANOVA, followed by Bonferroni post hoc test. Statistical significance was set at p <0.05 There was no difference between the groups. The triamcinolone group showed pain reduction (p=0.004) and improved function (p=0.036) through the Harris Hip Score questionnaire at 10, 30 and 60 days after treatment, when compared with the pre- intervention period. The platelet rich plasma group showed no statistical improvement in any of the variables Up to 60 days, PRP infiltration has no influence on pain relief and function improvement in trochanteric syndrome treatment.
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All the authors declare that there is no potential conflict of interest referring to this article
AUTHORS’ CONTRIBUTION:Each author contributed individually and significantly to the development of the study. AGR (0000-0002-9563-0237)*, WRJ and ARNSS (0000-0003-3252-3511)* performed the literature search and were the main contributors in drafting the manuscript. AGR held all infiltrations. AGR, WRJ, and ARNSS followed up patients and gathered clinical data. GCP (0000-0002-9524-8871)*, RPG (0000-0002-0764-6555)* and WRJ evaluated data from the statistical analysis, reviewed the manuscript and contributed to the intellectual concept of the study. All authors contributed to the intellectual concept of the study. *ORCID (Open Research and Contributor ID).
ISSN:1413-7852
1809-4406
1413-7852
1809-4406
DOI:10.1590/1413-785220162404159837