Addition of Auricular Acupoint Stimulation to 0.01% Atropine for Myopia: 12-Month Results from a Randomized Trial

被引:2
|
作者
Kong, Xiehe [1 ,2 ]
Yang, Guang [1 ,2 ]
Chen, Zhi [3 ,4 ,5 ,6 ]
Han, Rong [7 ]
Zhao, Yue [1 ,2 ]
Zeng, Li [3 ,4 ,5 ,6 ]
Guo, Xiaocong [1 ]
Shi, Zheng [1 ,2 ]
Zhang, Dan [1 ,2 ]
Yang, Yanting [1 ,2 ]
Liu, Jie [1 ,2 ]
Zhou, Xingtao [3 ,4 ,5 ,6 ,8 ]
Ma, Xiaopeng [1 ,2 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Yueyang Hosp Integrated Tradit Chinese & Western M, Shanghai, Peoples R China
[2] Shanghai Res Inst Acupuncture & Meridian, 650 South Wanping Rd, Shanghai 200030, Peoples R China
[3] Fudan Univ, Dept Ophthalmol & Visual Sci, Eye & ENT Hosp, Shanghai, Peoples R China
[4] Fudan Univ, NHC Key Lab Myopia, Shanghai, Peoples R China
[5] Chinese Acad Med Sci, Lab Myopia, Shanghai, Peoples R China
[6] Shanghai Res Ctr Ophthalmol & Optometry, Shanghai, Peoples R China
[7] Shanghai Qigong Res Inst, Shanghai, Peoples R China
[8] Fudan Univ, Eye & ENT Hosp, 83 Fenyang Rd, Shanghai 200031, Peoples R China
来源
关键词
auricular acupoint; myopia; complementary medicine; atropine; clinical trials; ACCOMMODATION STIMULUS; EYE GROWTH; PREVALENCE; EMMETROPES; LAG;
D O I
10.1089/jicm.2022.0769
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Introduction: A previous 6-month report showed that adjunctive auricular acupoint stimulation (AAS) slowed myopia progression compared with 0.01% atropine (0.01% A) alone. This 12-month report was to determine whether the antimyopic effect of AAS, when added to 0.01% A, continued beyond treatment cessation, and explore the mode of action of AAS from the accommodative response.Design and Interventions: One hundred four children were randomly assigned to either a 0.01% A group or a 0.01% A + AAS group. Participants in the 0.01% A + AAS group received AAS in addition to 0.01% A for 6 months, and then kept using 0.01% A for the following 6 months. Participants in the 0.01% A group only used 0.01% A. The primary outcome was the difference in the mean cycloplegic spherical equivalent refraction (SER) from the baseline to the 12-month visit. Secondary outcomes included axial length (AL) and accommodative lag assessments.Results: The adjusted mean change from baseline to month 12 in the SER was -0.62 D for 0.01% A and -0.46 D for 0.01% A + AAS (difference, 0.16 D; p = 0.01), with a respective mean increase of 0.37 and 0.31 mm in AL (difference, -0.05 mm; p = 0.05). For the 5D near target, there was a reduction in the accommodative lag in children receiving add-on AAS relative to 0.01% A alone at 1 and 6 months (both p = 0.002).Conclusions: AAS treatment produced additional benefits >0.01% A in slowing myopia progression over the 12-month period, where the efficacy was sustained after the cessation of AAS. An effect of add-on AAS on reducing accommodative lag in response to 5D stimulus was found, but its role in mediating therapeutic response remained unclear.Chinese Clinical Trial Registry, ChiCTR1900021316
引用
收藏
页码:574 / 583
页数:10
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