Vahdatpour Babak, Kianimehr Lida, Moradi Ahmad, Haghighat Shila
Department of Physical Medicine and Rehabilitation, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Radiology, Isfahan University of Medical Sciences, Isfahan, Iran.
Adv Biomed Res. 2016 Nov 28;5:179. doi: 10.4103/2277-9175.192731. eCollection 2016.
The present study aimed to clinically examine the effects of platelet-rich plasma (PRP) on improvement of plantar fasciitis and its related manifestations.
This single-blind randomized controlled trial was performed on 32 consecutive patients with the final diagnosis of plantar fasciitis that were randomly assigned to the case group (that received PRP, = 16) and the control group (that received corticosteroid as methylprednisolone 1 ml plus lidocaine 1 ml, = 16). The endpoints in the present study were changes in the visual analog scale score and the modified Roles and Maudsley score (RMS) from baseline, 1-month, 3 months, and 6 months follow-up. Plantar fascia was also assessed by B-mode sonography before and also 3 months after primary assessment.
Regarding the pain severity, the PRP group had significantly higher mean pain score at 3 time points of before injection, as well as 1 and 3 months after PRP use when compared to the corticosteroid group ( < 0.05); however, the control group experienced significantly higher pain severity than the PRP group at 6 months after interventions. Also, RMS was lower in PRP group than in corticosteroid group at baseline as well as at 1 and 3 months after injections ( < 0.05). In sonography assessment, no difference was revealed.
Administration of PRP leads to significant improvement in pain severity and physical limitation in patients with plantar fasciitis. This healing effect may be begun at least 3 months after injection.
本研究旨在临床检验富血小板血浆(PRP)对改善足底筋膜炎及其相关症状的效果。
本单盲随机对照试验对32例最终诊断为足底筋膜炎的连续患者进行,这些患者被随机分为病例组(接受PRP治疗,n = 16)和对照组(接受1毫升甲基强的松龙加1毫升利多卡因的皮质类固醇治疗,n = 16)。本研究的终点是从基线、1个月、3个月和6个月随访时视觉模拟量表评分和改良的罗尔斯和莫兹利评分(RMS)的变化。在初次评估前及初次评估后3个月也通过B型超声对足底筋膜进行评估。
关于疼痛严重程度,与皮质类固醇组相比,PRP组在注射前以及使用PRP后1个月和3个月的3个时间点平均疼痛评分显著更高(P < 0.05);然而,在干预后6个月,对照组的疼痛严重程度显著高于PRP组。此外,在基线以及注射后1个月和3个月时,PRP组的RMS低于皮质类固醇组(P < 0.05)。在超声评估中,未发现差异。
PRP给药可使足底筋膜炎患者的疼痛严重程度和身体限制得到显著改善。这种愈合效果可能在注射后至少3个月开始显现。