PRP IN THE TREATMENT OF TROCHANTERIC SYNDROME: A PILOT STUDY
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , |
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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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 |
_version_ |
1752122275538141184 |