Randomized controlled trial of patching vs acupuncture for anisometropic amblyopia in children aged 7 to 12 years
Item
Title
Randomized controlled trial of patching vs acupuncture for anisometropic amblyopia in children aged 7 to 12 years
Author(s)
Journal Publication
Date
2010
volume
128(12)
pages
1510-1517
Research Type
RCT
Keywords
Abstract
OBJECTIVE: To compare the effectiveness of 2-hour daily patching with the effectiveness of acupuncture in treating anisometropic amblyopia in children aged 7 to 12 years who have worn optimal spectacles for at least 16 weeks. METHODS: In a single-center randomized controlled trial, 88 eligible children with an amblyopic eye who had a best spectacle-corrected visual acuity (BSCVA) of 0.3 to 0.8 logMAR at baseline were randomly assigned to receive 2 hours of patching of the sound eye daily or 5 sessions of acupuncture weekly. All participants in our study received constant optical correction, plus 1 hour of near-vision activities daily, and were followed up at weeks 5, 10, 15, and 25. The main outcome measure was BSCVA in the amblyopic eye at 15 weeks. RESULTS: The mean BSCVA of the amblyopic eye at 15 weeks improved from baseline by 1.83 and 2.27 lines in the patching and acupuncture groups, respectively. After baseline adjustment, the mean difference of BSCVA between the 2 groups was 0.049 logMAR (95% confidence interval, 0.005-0.092; P = .03), meeting the definition of equivalence (difference within 1 line). The BSCVA had improved by 2 lines or more in 28 (66.7%) and 31 (75.6%) eyes in the patching and acupuncture groups, respectively. Amblyopia was resolved in 7 (16.7%) and 17 (41.5%) eyes in the patching and acupuncture groups, respectively. CONCLUSION: Acupuncture produced equivalent treatment effect for anisometropic amblyopia, compared with patching, and was statistically superior. Further studies are warranted to investigate its value in the treatment of amblyopia. CLINICAL RELEVANCE: Acupuncture could potentially become an alternative treatment to occlusion therapy for amblyopia. TRIAL REGISTRATION: Centers for Clinical Trials Registry Identifier: CUHK_CCT00248.
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has health condition studied
Eye Diseases
plan
>1/WK
has study population number
88
has duration
25 Weeks