*Department of Orthopedics and Traumatology, Agri Training and Research Hospital, Agri, Turkey. Dr. Toy is now with Basaksehir Pine and Sakura City Hospital, Istanbul, Turkey.
†Department of Orthopedics and Traumatology, Ataturk University Faculty of Medicine, Erzurum, Turkey. Dr. Tuncer is now with the Department of Orthopedics and Traumatology, Altinbas University Medical Park, Bahçelievler Hastanesi, Istanbul, Turkey.
J Am Podiatr Med Assoc. 2023 Jan-Feb;113(1). doi: 10.7547/20-221.
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.
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.
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).
Ozone, CLA, or PRP injections could provide clinically significant functional improvement for at least 6 months in patients with sinus tarsi syndrome.
跗骨窦综合征的特征是由于慢性炎症导致纤维组织残留和滑膜炎积聚,在反复创伤性损伤后,前外侧踝关节出现持续性疼痛。很少有研究记录过注射治疗跗骨窦综合征的结果。我们旨在确定皮质类固醇和局部麻醉剂(CLA)、富含血小板的血浆(PRP)和臭氧注射对跗骨窦综合征的影响。
60 例跗骨窦综合征患者随机分为三组治疗:CLA、PRP 和臭氧注射。在注射前、注射后 1、3 和 6 个月时采用视觉模拟量表、美国矫形足踝协会踝后足量表(AOFAS)、足部功能指数和足部和踝关节结局评分进行评估。
在注射后 1、3 和 6 个月时,所有三组与基线相比,均有显著改善(所有 P<0.001)。在第 1 个月和第 3 个月,CLA 和臭氧组的 AOFAS 评分改善相似;PRP 组较低(分别为 P=0.001 和 P=0.004)。在第 1 个月,PRP 和臭氧组的足部和踝关节结局评分改善相似,CLA 组改善更高(P<0.001)。在 6 个月随访时,各组间视觉模拟量表和足部功能指数结果无显著差异(P>0.05)。
臭氧、CLA 或 PRP 注射至少可在 6 个月内为跗骨窦综合征患者提供有临床意义的功能改善。