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Article: Three-Year Clinical Trial of Low-Concentration Atropine for Myopia Progression (LAMP) Study: Continued Versus Washout: Phase 3 Report

TitleThree-Year Clinical Trial of Low-Concentration Atropine for Myopia Progression (LAMP) Study: Continued Versus Washout: Phase 3 Report
Authors
KeywordsAtropine
Myopia
Rebound
Issue Date2022
Citation
Ophthalmology, 2022, v. 129, n. 3, p. 308-321 How to Cite?
AbstractPurpose: (1) To compare the efficacy of continued and stopping treatment for 0.05%, 0.025%, and 0.01% atropine during the third year. (2) To evaluate the efficacy of continued treatment over 3 years. (3) To investigate the rebound phenomenon and its determinants after cessation of treatment. Design: A randomized, double-masked extended trial. Participants: A total of 350 of 438 children aged 4 to 12 years originally recruited into the Low-Concentration Atropine for Myopia Progression (LAMP) study. Methods: At the beginning of the third year, children in each group were randomized at a 1:1 ratio to continued treatment and washout subgroups. Cycloplegic spherical equivalent (SE) refraction and axial length (AL) were measured at 4-month intervals. Main Outcome Measures: Changes in SE and AL between groups. Results: A total of 326 children completed 3 years of follow-up. During the third year, SE progression and AL elongation were faster in the washout subgroups than in the continued treatment groups across all concentrations: –0.68 ± 0.49 diopters (D) versus –0.28 ± 0.42 D (P < 0.001) and 0.33 ± 0.17 mm versus 0.17 ± 0.14 mm (P < 0.001) for the 0.05%; –0.57 ± 0.38 D versus –0.35 ± 0.37 D (P = 0.004) and 0.29 ± 0.14 mm versus 0.20 ± 0.15 mm (P = 0.001) for the 0.025%; –0.56 ± 0.40 D versus –0.38 ± 0.49 D (P = 0.04) and 0.29 ± 0.15 mm versus 0.24 ± 0.18 mm (P = 0.13) for the 0.01%. Over the 3-year period, SE progressions were –0.73 ± 1.04 D, –1.31 ± 0.92 D, and –1.60 ± 1.32 D (P = 0.001) for the 0.05%, 0.025%, and 0.01% groups in the continued treatment subgroups, respectively, and −1.15 ± 1.13 D, –1.47 ± 0.77 D, and –1.81 ± 1.10 D (P = 0.03), respectively, in the washout subgroup. The respective AL elongations were 0.50 ± 0.40 mm, 0.74 ± 0.41 mm, and 0.89 ± 0.53 mm (P < 0.001) for the continued treatment subgroups and 0.70 ± 0.47 mm, 0.82 ± 0.37 mm, and 0.98 ± 0.48 mm (P = 0.04) for the washout subgroup. The rebound SE progressions during washout were concentration dependent, but their differences were clinically small (P = 0.15). Older age and lower concentration were associated with smaller rebound effects in both SE progression (P < 0.001) and AL elongation (P < 0.001). Conclusions: During the third year, continued atropine treatment achieved a better effect across all concentrations compared with the washout regimen. 0.05% atropine remained the optimal concentration over 3 years in Chinese children. The differences in rebound effects were clinically small across all 3 studied atropine concentrations. Stopping treatment at an older age and lower concentration are associated with a smaller rebound.
Persistent Identifierhttp://hdl.handle.net/10722/345153
ISSN
2023 Impact Factor: 13.1
2023 SCImago Journal Rankings: 4.642

 

DC FieldValueLanguage
dc.contributor.authorYam, Jason C.-
dc.contributor.authorZhang, Xiu Juan-
dc.contributor.authorZhang, Yuzhou-
dc.contributor.authorWang, Yu Meng-
dc.contributor.authorTang, Shu Min-
dc.contributor.authorLi, Fen Fen-
dc.contributor.authorKam, Ka Wai-
dc.contributor.authorKo, Simon T.-
dc.contributor.authorYip, Benjamin H.K.-
dc.contributor.authorYoung, Alvin L.-
dc.contributor.authorTham, Clement C.-
dc.contributor.authorChen, Li Jia-
dc.contributor.authorPang, Chi Pui-
dc.date.accessioned2024-08-15T09:25:34Z-
dc.date.available2024-08-15T09:25:34Z-
dc.date.issued2022-
dc.identifier.citationOphthalmology, 2022, v. 129, n. 3, p. 308-321-
dc.identifier.issn0161-6420-
dc.identifier.urihttp://hdl.handle.net/10722/345153-
dc.description.abstractPurpose: (1) To compare the efficacy of continued and stopping treatment for 0.05%, 0.025%, and 0.01% atropine during the third year. (2) To evaluate the efficacy of continued treatment over 3 years. (3) To investigate the rebound phenomenon and its determinants after cessation of treatment. Design: A randomized, double-masked extended trial. Participants: A total of 350 of 438 children aged 4 to 12 years originally recruited into the Low-Concentration Atropine for Myopia Progression (LAMP) study. Methods: At the beginning of the third year, children in each group were randomized at a 1:1 ratio to continued treatment and washout subgroups. Cycloplegic spherical equivalent (SE) refraction and axial length (AL) were measured at 4-month intervals. Main Outcome Measures: Changes in SE and AL between groups. Results: A total of 326 children completed 3 years of follow-up. During the third year, SE progression and AL elongation were faster in the washout subgroups than in the continued treatment groups across all concentrations: –0.68 ± 0.49 diopters (D) versus –0.28 ± 0.42 D (P < 0.001) and 0.33 ± 0.17 mm versus 0.17 ± 0.14 mm (P < 0.001) for the 0.05%; –0.57 ± 0.38 D versus –0.35 ± 0.37 D (P = 0.004) and 0.29 ± 0.14 mm versus 0.20 ± 0.15 mm (P = 0.001) for the 0.025%; –0.56 ± 0.40 D versus –0.38 ± 0.49 D (P = 0.04) and 0.29 ± 0.15 mm versus 0.24 ± 0.18 mm (P = 0.13) for the 0.01%. Over the 3-year period, SE progressions were –0.73 ± 1.04 D, –1.31 ± 0.92 D, and –1.60 ± 1.32 D (P = 0.001) for the 0.05%, 0.025%, and 0.01% groups in the continued treatment subgroups, respectively, and −1.15 ± 1.13 D, –1.47 ± 0.77 D, and –1.81 ± 1.10 D (P = 0.03), respectively, in the washout subgroup. The respective AL elongations were 0.50 ± 0.40 mm, 0.74 ± 0.41 mm, and 0.89 ± 0.53 mm (P < 0.001) for the continued treatment subgroups and 0.70 ± 0.47 mm, 0.82 ± 0.37 mm, and 0.98 ± 0.48 mm (P = 0.04) for the washout subgroup. The rebound SE progressions during washout were concentration dependent, but their differences were clinically small (P = 0.15). Older age and lower concentration were associated with smaller rebound effects in both SE progression (P < 0.001) and AL elongation (P < 0.001). Conclusions: During the third year, continued atropine treatment achieved a better effect across all concentrations compared with the washout regimen. 0.05% atropine remained the optimal concentration over 3 years in Chinese children. The differences in rebound effects were clinically small across all 3 studied atropine concentrations. Stopping treatment at an older age and lower concentration are associated with a smaller rebound.-
dc.languageeng-
dc.relation.ispartofOphthalmology-
dc.subjectAtropine-
dc.subjectMyopia-
dc.subjectRebound-
dc.titleThree-Year Clinical Trial of Low-Concentration Atropine for Myopia Progression (LAMP) Study: Continued Versus Washout: Phase 3 Report-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.ophtha.2021.10.002-
dc.identifier.pmid34627809-
dc.identifier.scopuseid_2-s2.0-85118842746-
dc.identifier.volume129-
dc.identifier.issue3-
dc.identifier.spage308-
dc.identifier.epage321-
dc.identifier.eissn1549-4713-

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