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金叶千里光纳米凝胶经皮给药改善膝骨关节炎患者的功能能力:一项随机对照试验。

Phonophoresis of Phyllanthus amarus nanoparticle gel improves functional capacity in individuals with knee osteoarthritis: A randomized controlled trial.

机构信息

Department of Physical Therapy, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.

Department of Pharmaceutical Sciences. Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.

出版信息

J Bodyw Mov Ther. 2020 Jan;24(1):15-18. doi: 10.1016/j.jbmt.2019.04.013. Epub 2019 May 4.

DOI:10.1016/j.jbmt.2019.04.013
PMID:31987536
Abstract

OBJECTIVE

This study examined the effects of treatment with Phyllanthus amarus nanoparticle gel applied by phonophoresis (PP) and ultrasound therapy (UT) in patients with symptomatic knee osteoarthritis (OA) using a randomized, double-blind, controlled trial.

METHODS

Patients with knee OA (n = 40; mean age ± SD, 64.30 ± 9.71 years), who had visual analogue scale (VAS) scores for knee pain intensity of 68.00 ± 9.58 (UT group) and 71.00 ± 8.74 (PP group, respectively) before treatment, were randomly allocated into two groups. Both groups were treated with an ultrasound program in continuous mode, 1.0 W/cm, 10 min per session, for 10 sessions. Nanoparticles of P. amarus were used in the PP group, whereas a nondrug coupling gel was used in the UT group. The 6-min walk test (6-MWT) was performed to evaluate functional capacity. The VAS and the 6-MWT were evaluated before and after 10 treatment sessions in both groups using a double-blind procedure.

RESULTS

VAS and 6-MWT showed significant improvement after treatment in both groups (p < 0.05). The PP group showed more significant effects than the UT group, in terms of both reducing the VAS pain score (p < 0.05) and improving 6-MWT (p < 0.05).

CONCLUSIONS

PP is suggested as an effective method for the treatment of symptomatic knee OA for reducing pain and improving functional capacity.

摘要

目的

本研究采用随机、双盲、对照试验,考察了叶下珠纳米凝胶经声透(PP)和超声疗法(UT)治疗对有症状膝骨关节炎(OA)患者的影响。

方法

40 例膝 OA 患者(平均年龄±标准差,64.30±9.71 岁),治疗前视觉模拟评分(VAS)膝关节疼痛强度分别为 68.00±9.58(UT 组)和 71.00±8.74(PP 组),随机分为两组。两组均采用连续模式的超声程序,1.0 W/cm,每次 10 分钟,共 10 次。PP 组使用叶下珠纳米粒子,UT 组使用无药物耦合凝胶。采用 6 分钟步行试验(6-MWT)评估功能能力。两组均采用双盲程序,在治疗前和治疗后 10 次治疗后评估 VAS 和 6-MWT。

结果

两组 VAS 和 6-MWT 治疗后均显著改善(p<0.05)。与 UT 组相比,PP 组在降低 VAS 疼痛评分(p<0.05)和改善 6-MWT 方面效果更为显著(p<0.05)。

结论

PP 被认为是治疗有症状膝骨关节炎的有效方法,可减轻疼痛,提高功能能力。

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