Effect of Thick-Needle Therapy in Patients with Bell's Palsy at Recovery Stage: A Multi-center Randomized Controlled Trial

被引:5
作者
Yu, Bin-yan [1 ]
Wang, Yan-ping [2 ]
Shang, Hong-cai [3 ]
Wang, Li-ying [2 ]
Wan, Yi-jia [1 ]
Zhao, Chen [4 ]
Xuan, Li-hua [1 ]
机构
[1] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Dept Acupuncture & Moxibust, Hangzhou 310000, Peoples R China
[2] China Acad Chinese Med Sci, Inst Basic Res Clin Med, Beijing 100700, Peoples R China
[3] Beijing Univ Chinese Med, Affiliated Dongzhimen Hosp, Minist Educ & Beijing, Key Lab Chinese Internal Med, Beijing 100700, Peoples R China
[4] Tianjin Univ Tradit Chinese Med, Grad Sch, Tianjin 300193, Peoples R China
关键词
Bell's palsy; acupuncture; thick-needle therapy; randomized controlled trial; Chinese medicine; PERIPHERAL FACIAL PALSY; ACUPUNCTURE;
D O I
10.1007/s11655-020-3081-z
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objective: To compare the clinical effects of thick-needle therapy (TNT) and acupuncture therapy (AT) on patients with Bell's palsy (BP) at the recovery stage. Methods: A total of 146 eligible participants from 3 hospitals in China were randomized into the TNT group (73 cases) and the AT group (73 cases) using a central randomization. Both groups received Western medicine thrice a day for 4 weeks. Moreover, patients in the TNT group received subcutaneous insertion of a thick needle into Shendao (GV 11) acupoint, while patients in the AT group received AT at acupoints of Cuanzhu (BL 2), Yangbai (GB 14), Dicang (ST 4), Xiaguan (ST 7), Jiache (ST 6), Yingxiang (LI 20) and Hegu (LI 4), 4 times a week, for 4 weeks. Both groups received 2 follow-up visits, which were arranged at 1 month and 3 months after treatment, respectively. The primary outcome measure was House-Brackmann Facial Nerve Grading System (HBFNGS) grade. And the clinical recovery rates of both groups were evaluated according to the HBFNGS grades after treatment. The secondary outcome measures included the facial disability index (FDI) and electroneurogram (EnoG). The adverse events were observed and recorded in both groups. Results: Three cases withdrew from the trial, 2 in the TNT group and 1 in the AT group. There was no signifificant difference in the clinical recovery rates between the TNT and AT groups after 4-week treatment [40.85% (29/71) vs. 34.72% (25/72), P>0.05]. At the 2nd follow-up visit, more patients in the TNT group showed reduced HBFNGS grades than those in the AT group (P<0.01). No significant difference was observed between the two groups in FDI score, EnoG latency and maximum amplitude ratio at all time points (all P>0.05). Conclusion: The clinical effect of TNT was equivalent to that of AT in patients with BP at recovery stage, while the post-treatment effect of TNT was superior to that of AT. (Registration No. ChiCTR-INR-16008409)
引用
收藏
页码:455 / 461
页数:7
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