Department of Physical Therapy, Monash University, Melbourne, VIC, Australia.
Mobility Impairment Research Center, Department of Physiotherapy, School of Rehabilitation, Babol University of Medical Sciences, Babol, Iran.
Acupunct Med. 2020 Dec;38(6):371-379. doi: 10.1177/0964528420912253. Epub 2020 Apr 27.
To compare the effectiveness of ischaemic compression (IC) applied directly to the knee versus dry needling (DN) with respect to pain, functional status and sensitivity to mechanical stimulation of vastus medialis obliquus (VMO) myofascial trigger points (MTrPs) in patients with patellofemoral pain syndrome (PFPS).
A total of 54 patients with unilateral PFPS aged 20-30 years were selected randomly from patients referred to physical therapy clinics of Babol University of Medical Sciences in Iran. Twenty-seven patients were allocated to either IC or DN groups. Three sessions of treatment were applied over 1 week with follow-up at 1 week, 1 month and 3 months. Primary outcome measures comprised the Kujala questionnaire score for functional status, numerical pain rating scale (NPRS) for pain intensity and pressure pain threshold (PPT) for sensitivity to mechanical stimulation; these were measured and recorded before treatment and 1 week, 1 month and 3 months after the last treatment session.
There were no statistically significant differences in the between-group comparisons of any variables at the various follow-up points. Both groups (n = 27 participants each) had significant improvements (p < 0.05) in pain, functional status and PPT values at follow-up.
There were no differences in markers of pain, function or pressure sensitivity over a 3-month follow-up period between patients with PFPS treated with DN and IC. Temporal improvements in both groups suggested that the two techniques may be similarly effective for the treatment of PFPS.
比较缺血性压迫(IC)直接作用于膝关节与干针(DN)在髌股疼痛综合征(PFPS)患者的股直肌腹内斜肌肌筋膜触发点(MTrPs)的疼痛、功能状态和对机械刺激的敏感性方面的有效性。
从伊朗巴博勒医科大学物理治疗诊所转诊的患者中,共随机选择 54 名年龄在 20-30 岁之间的单侧 PFPS 患者。27 名患者被分配到 IC 或 DN 组。每周进行 3 次治疗,随访 1 周、1 个月和 3 个月。主要结局指标包括功能状态的 Kujala 问卷评分、疼痛强度的数字疼痛评分量表(NPRS)和机械刺激敏感性的压痛阈值(PPT);在治疗前和最后一次治疗后的 1 周、1 个月和 3 个月进行测量和记录。
在各个随访点,两组之间在任何变量的比较中均无统计学差异。两组(每组 27 名参与者)在随访时疼痛、功能状态和 PPT 值均有显著改善(p<0.05)。
在 3 个月的随访期间,接受 DN 和 IC 治疗的 PFPS 患者在疼痛、功能或压痛敏感性标志物方面无差异。两组的时间改善表明,两种技术可能对 PFPS 的治疗同样有效。