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广州中医药大学深圳医院(福田)脑病科,广东深圳 518034
深圳市中西医结合医院
广州中医药大学第二附属医院,广东广州 510120
佛山市中医院
河源市人民医院
✉李哲,副主任医师。E-mail:zhel@gzucm.edu.cn
收稿:2024-11-16,
网络首发:2025-12-02,
纸质出版:2026-02-12
移动端阅览
余泽程, 周志成, 郑春叶, 等. 经皮耳穴迷走神经刺激治疗原发性帕金森病:随机对照单盲试验[J]. 中国针灸, 2026,46(2):168-175.
YU Zecheng, ZHOU Zhicheng, ZHENG Chunye, et al. Transcutaneous auricular vagus nerve stimulation in treatment of primary Parkinson's disease: a randomized, controlled, single-blind trial[J]. Chinese Acupuncture & Moxibustion, 2026, 46(2): 168-175.
余泽程, 周志成, 郑春叶, 等. 经皮耳穴迷走神经刺激治疗原发性帕金森病:随机对照单盲试验[J]. 中国针灸, 2026,46(2):168-175. DOI: 10.13703/j.0255-2930.20241116-0002.
YU Zecheng, ZHOU Zhicheng, ZHENG Chunye, et al. Transcutaneous auricular vagus nerve stimulation in treatment of primary Parkinson's disease: a randomized, controlled, single-blind trial[J]. Chinese Acupuncture & Moxibustion, 2026, 46(2): 168-175. DOI: 10.13703/j.0255-2930.20241116-0002.
目的:
2
观察经皮耳穴迷走神经刺激(taVNS)对原发性帕金森病(PD)自主神经症状和运动症状的治疗效果。
方法:
2
将60例原发性PD患者随机分为观察组30例(剔除1例、脱落1例)和对照组30例(剔除4例、脱落1例)。两组患者予口服复方左旋多巴治疗,若入组时已服用复方左旋多巴类以外的抗PD药物,维持入组前用药方案,连续治疗8周。观察组使用SDZ-ⅡB型电子针疗仪对耳甲区(每次取单侧,两耳交替进行)进行taVNS治疗,选择脉冲频率4 Hz/20 Hz疏密波,电流5~10 mA,每次30 min,每周治疗3次,至少隔天进行,共治疗8周。对照组对耳舟区进行脉冲刺激治疗,操作、疗程均同观察组。于治疗前和治疗后,观察两组原发性帕金森病自主神经症状量表(SCOPA-AUT)评分、世界运动障碍协会修订版帕金森病综合评价量表(MDS-UPDRS)-Ⅲ/Ⅱ评分、中医老年颤证功能障碍评分、改良H-Y分级、帕金森患者生活质量调查量表(PDQ-39)评分,并于治疗后进行安全性评价。
结果:
2
治疗后,观察组患者SCOPA-AUT、MDS-UPDRS-Ⅲ/Ⅱ、中医老年颤证功能障碍评分和PDQ-39评分均较治疗前降低(
P
<
0.001,
P
<
0.05);对照组PDQ-39评分较治疗前升高(
P
<
0.05),其余指标治疗前后比较差异无统计学意义(
P
>
0.05);两组患者H-Y分级治疗后比较差异无统计学意义(
P
>
0.05)。观察组患者SCOPA-AUT、MDS-UPDRS-Ⅱ、
中医老年颤证功能障碍评分
和PDQ-39评分降低幅度均大于对照组(
P
<
0.001)。两组未见明显不良反应。
结论:
2
taVNS辅助复方左旋多巴治疗可以改善原发性PD患者的自主神经症状和运动症状,提高其日常生活质量,且无不良反应。
Objective
2
To explore the therapeutic effect of transcutaneous auricular vagus nerve stimulation (taVNS) on autonomic and motor symptoms in primary Parkinson's disease (PD).
Methods
2
A total of 60 patients with primary PD were randomly divided into an observation group (30 cases
1 case excluded and 1 case dropped out) and a control group (30 cases
4 cases excluded and 1 case dropped out). The patients of the two groups received the oral administration of compound levodopa. If the patients had taken the other anti-PD drugs except compound levodopa preparations before enrolled
the original medication regimen was remained. The treatment lasted 8 weeks. In the observation group
the taVNS was delivered with SDZ-ⅡB type electric acupuncture instrument attached to the concha unilaterally and alternatively
at the frequency of 4 Hz/20 Hz and disperse-dense wave
and at the electric current of 5 mA to 10 mA
for 30 min each time. The taVNS was given 3 times a week
at least once every two days and for 8 weeks. In the control group
the pulse stimulation was given at the scapha
the operation and duration of treatment were the same as the observation group. The scores were observed for the scale for outcomes in Parkinson's disease-autonomic symptoms (SCOPA-AUT)
part Ⅲ/Ⅱof Movement Disorder Society-unified Parkinson's disease rating scale (MDS-UPDRS-Ⅲ
MDS-UPDRS-Ⅱ)
the geriatric tremor syndrome in TCM
the modified Hoehn-Yahr (H-Y) rate
and Parkinson's disease quality of life questionnaire (PDQ-39) before and after treatment; and the safety of treatment was evaluated after treatment in the two groups.
Results
2
After treatment
the scores of SCOPA-AUT
MDS-UPDRS-Ⅲ
MDS-UPDRS-Ⅱ
geriatric tremor syndrome of TCM and PDQ-39 were all lower than those before treatment in the observation group (
P
<
0.001
P
<
0.05); PDQ-39 score was higher in the contro
l group compared with that before treatment (
P
<
0.05)
and the other indexes did not show the statistical differences (
P
>
0.05). There was no difference in H-Y rate after treatment between the two groups (
P
>
0.05). In the observation group
the reduction ranges of SCOPA-AUT
MDS-UPDRS-Ⅱ
geriatric tremor syndrome of TCM and PDQ-39 scores were larger when compared with the control group (
P
<
0.001). The obvious adverse reactions were not presented in the two groups.
Conclusion
2
The taVNS
as an adjunctive therapy to medication with compound levodopa
can attenuate the autonomic and motor symptoms of the patients with primary PD and improve the daily quality of life without adverse reactions.
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