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The effectiveness of dry needling in patients with chronic low back pain: a prospective, randomized, single-blinded study

干刺 医学 Oswestry残疾指数 可视模拟标度 物理疗法 腰痛 安慰剂 止痛药 随机对照试验 麻醉 外科 针灸科 病理 替代医学
作者
Joanna Rajfur,Katarzyna Rajfur,Łukasz Kosowski,Karolina Walewicz,Robert Dymarek,Kuba Ptaszkowski,Jakub Taradaj
出处
期刊:Scientific Reports [Springer Nature]
卷期号:12 (1) 被引量:5
标识
DOI:10.1038/s41598-022-19980-1
摘要

Abstract Dry needling (DN) is a standard procedure for treating musculoskeletal disorders. However, there are no clear recommendations for using DN in low back pain (LBP). Therefore, this study aimed to assess the effectiveness of the novel DN program for reducing pain intensity and improving functional efficiency in patients with chronic LBP. A group of 40 patients with chronic LBP due to the L5-S1 discopathy were eligible and randomized into experimental (n = 20) and control (n = 20) groups. The DN program was performed for the experimental group according to the Five Regulatory Systems (FRS) concept. The control group received sham therapy using placebo needles. DN sessions were performed twice a week for 4 weeks. A single needling application lasted 60 min. Both groups received standard treatment and physical exercise of LBP for 1 month. Subjective pain was measured by a visual analog scale (VAS), functional efficiency was assessed with the Oswestry Disability Index (ODI), and the lower spine range of motion was measured with the Schober test. There were significant differences in pain reduction (VAS) in both groups ( p < 0.001). The strongest analgesic effect in the DN group yielded 6.45 points immediately after the therapy, 6.2 points after 1 month, and 6 points after 3 months. The DN group scored higher VAS reduction than the control group ( p < 0.001). There were significant differences in the functional state (ODI) in the experimental group ( p < 0.001). There was a significant ODI decrease by 18.1 points, after 1 month by 18.9 points, and after 3 months by 17.6 points. No significant differences were found in the control group ( p > 0.05). Intergroup differences were observed in the functional efficiency in ODI in all measurement time-points ( p < 0.001). There were significant differences in the range of motion (Schober test) in the DN group (main effect: p < 0.001). For all measurements, differences ( p < 0.001) were observed in favor of DN compared to the control. In conclusion, DN program according to the FRS concept stands for the novel treatment method supplemented by an exercise program, effectively reducing pain and improving functional efficiency in LBP patients.
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