PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY

Detalhes bibliográficos
Autor(a) principal: Ribeiro,Arthur de Góes
Data de Publicação: 2016
Outros Autores: Ricioli Junior,Walter, Silva,Alice Roxo Nobre Sousa e, Polesello,Giancarlo Cavalli, Guimarães,Rodrigo Pereira
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Acta Ortopédica Brasileira (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-78522016000400208
Resumo: ABSTRACT Objective: To compare the efficacy of platelet rich plasma (PRP) against corticosteroid on the treatment of trochanteric pain syndrome . Methods: 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 . Results: 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 . Conclusion: Up to 60 days, PRP infiltration has no influence on pain relief and function improvement in trochanteric syndrome treatment. Level of Evidence II, Prospective Comparative Study.
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spelling PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDYBursitisFemurInjectionsPlatelet-rich plasmaTendinopathyABSTRACT Objective: To compare the efficacy of platelet rich plasma (PRP) against corticosteroid on the treatment of trochanteric pain syndrome . Methods: 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 . Results: 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 . Conclusion: Up to 60 days, PRP infiltration has no influence on pain relief and function improvement in trochanteric syndrome treatment. Level of Evidence II, Prospective Comparative Study.ATHA EDITORA2016-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-78522016000400208Acta Ortopédica Brasileira v.24 n.4 2016reponame:Acta Ortopédica Brasileira (Online)instname:Sociedade Brasileira de Ortopedia e Traumatologia (SBOT)instacron:SBOT10.1590/1413-785220162404159837info:eu-repo/semantics/openAccessRibeiro,Arthur de GóesRicioli Junior,WalterSilva,Alice Roxo Nobre Sousa ePolesello,Giancarlo CavalliGuimarães,Rodrigo Pereiraeng2016-08-26T00:00:00Zoai:scielo:S1413-78522016000400208Revistahttp://www.actaortopedica.com.br/https://old.scielo.br/oai/scielo-oai.php1atha@uol.com.br||actaortopedicabrasileira@uol.com.br1809-44061413-7852opendoar:2016-08-26T00:00Acta Ortopédica Brasileira (Online) - Sociedade Brasileira de Ortopedia e Traumatologia (SBOT)false
dc.title.none.fl_str_mv PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
title PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
spellingShingle PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
Ribeiro,Arthur de Góes
Bursitis
Femur
Injections
Platelet-rich plasma
Tendinopathy
title_short PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
title_full PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
title_fullStr PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
title_full_unstemmed PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
title_sort PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
author Ribeiro,Arthur de Góes
author_facet Ribeiro,Arthur de Góes
Ricioli Junior,Walter
Silva,Alice Roxo Nobre Sousa e
Polesello,Giancarlo Cavalli
Guimarães,Rodrigo Pereira
author_role author
author2 Ricioli Junior,Walter
Silva,Alice Roxo Nobre Sousa e
Polesello,Giancarlo Cavalli
Guimarães,Rodrigo Pereira
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Ribeiro,Arthur de Góes
Ricioli Junior,Walter
Silva,Alice Roxo Nobre Sousa e
Polesello,Giancarlo Cavalli
Guimarães,Rodrigo Pereira
dc.subject.por.fl_str_mv Bursitis
Femur
Injections
Platelet-rich plasma
Tendinopathy
topic Bursitis
Femur
Injections
Platelet-rich plasma
Tendinopathy
description ABSTRACT Objective: To compare the efficacy of platelet rich plasma (PRP) against corticosteroid on the treatment of trochanteric pain syndrome . Methods: 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 . Results: 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 . Conclusion: Up to 60 days, PRP infiltration has no influence on pain relief and function improvement in trochanteric syndrome treatment. Level of Evidence II, Prospective Comparative Study.
publishDate 2016
dc.date.none.fl_str_mv 2016-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-78522016000400208
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-78522016000400208
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1413-785220162404159837
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv ATHA EDITORA
publisher.none.fl_str_mv ATHA EDITORA
dc.source.none.fl_str_mv Acta Ortopédica Brasileira v.24 n.4 2016
reponame:Acta Ortopédica Brasileira (Online)
instname:Sociedade Brasileira de Ortopedia e Traumatologia (SBOT)
instacron:SBOT
instname_str Sociedade Brasileira de Ortopedia e Traumatologia (SBOT)
instacron_str SBOT
institution SBOT
reponame_str Acta Ortopédica Brasileira (Online)
collection Acta Ortopédica Brasileira (Online)
repository.name.fl_str_mv Acta Ortopédica Brasileira (Online) - Sociedade Brasileira de Ortopedia e Traumatologia (SBOT)
repository.mail.fl_str_mv 1atha@uol.com.br||actaortopedicabrasileira@uol.com.br
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