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Corticosteroid, Platelet-Rich Plasma, and Ozone Injections for Sinus Tarsi Syndrome

dc.contributor.authorTopal, Murat
dc.contributor.authorToy, Serdar
dc.contributor.authorAydin, Ali
dc.contributor.authorTuncer, Kutsi
dc.date.accessioned2026-01-04T17:46:52Z
dc.date.issued2023-01-01
dc.description.abstractBackground: Sinus tarsi syndrome is characterized by permanent pain on the anterolateral side of the ankle due to chronic inflammation characterized by fibrotic tissue remnants and synovitis accumulation after repeated traumatic injuries. Few studies have documented the outcome of injection treatments for sinus tarsi syndrome. We sought to determine the effects of corticosteroid and local anesthetic (CLA), platelet-rich plasma (PRP), and ozone injections on sinus tarsi syndrome. Methods: Sixty patients with sinus tarsi syndrome were randomly divided into three treatment groups: CLA, PRP, and ozone injections. Outcome measures were visual analog scale, American Orthopedic Foot and Ankle Society Ankle-Hindfoot Scale (AOFAS), Foot Function Index, and Foot and Ankle Outcome Score before injection compared with 1, 3, and 6 months after injection. Results: At the end of months 1, 3, and 6 after injection, significant improvements were observed in all three groups compared with baseline (P < .001 for all). At months 1 and 3, improvements in AOFAS scores were similar in the CLA and ozone groups; those in the PRP group were lower (P = .001 and P = .004, respectively). At month 1, improvements in Foot and Ankle Outcome Score were similar in the PRP and ozone groups and higher in the CLA group (P < .001). At 6-month follow-up, there were no significant differences in visual analog scale and Foot Function Index results among the groups (P > .05). Conclusions: Ozone, CLA, or PRP injections could provide clinically significant functional improvement for at least 6 months in patients with sinus tarsi syndrome.
dc.description.urihttps://doi.org/10.7547/20-221
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/36905621
dc.description.urihttps://avesis.atauni.edu.tr/publication/details/651ca635-8777-4431-8ead-6c931357a7fc/oai
dc.identifier.doi10.7547/20-221
dc.identifier.issn8750-7315
dc.identifier.openairedoi_dedup___::84eeaac204f3761cf415595903e7558d
dc.identifier.orcid0000-0001-8074-4672
dc.identifier.orcid0000-0002-7544-2554
dc.identifier.pubmed36905621
dc.identifier.scopus2-s2.0-85150225897
dc.identifier.urihttps://hdl.handle.net/20.500.12597/40351
dc.identifier.volume113
dc.identifier.wos001112027400018
dc.publisherAmerican Podiatric Medical Association
dc.relation.ispartofJournal of the American Podiatric Medical Association
dc.rightsCLOSED
dc.subjectFoot Diseases
dc.subjectOzone
dc.subjectTreatment Outcome
dc.subjectFasciitis, Plantar
dc.subjectAdrenal Cortex Hormones
dc.subjectPlatelet-Rich Plasma
dc.subjectHumans
dc.subject.sdg3. Good health
dc.titleCorticosteroid, Platelet-Rich Plasma, and Ozone Injections for Sinus Tarsi Syndrome
dc.typeArticle
dspace.entity.typePublication
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Outcome measures were visual analog scale, American Orthopedic Foot and Ankle Society Ankle-Hindfoot Scale (AOFAS), Foot Function Index, and Foot and Ankle Outcome Score before injection compared with 1, 3, and 6 months after injection.</jats:p> <jats:p><jats:bold>Results:</jats:bold> At the end of months 1, 3, and 6 after injection, significant improvements were observed in all three groups compared with baseline (<jats:italic>P</jats:italic> &lt; .001 for all). At months 1 and 3, improvements in AOFAS scores were similar in the CLA and ozone groups; those in the PRP group were lower (<jats:italic>P</jats:italic> = .001 and <jats:italic>P</jats:italic> = .004, respectively). At month 1, improvements in Foot and Ankle Outcome Score were similar in the PRP and ozone groups and higher in the CLA group (<jats:italic>P</jats:italic> &lt; .001). 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