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- Publisher Website: 10.1016/j.ophtha.2021.10.002
- Scopus: eid_2-s2.0-85118842746
- PMID: 34627809
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Article: Three-Year Clinical Trial of Low-Concentration Atropine for Myopia Progression (LAMP) Study: Continued Versus Washout: Phase 3 Report
Title | Three-Year Clinical Trial of Low-Concentration Atropine for Myopia Progression (LAMP) Study: Continued Versus Washout: Phase 3 Report |
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Authors | |
Keywords | Atropine Myopia Rebound |
Issue Date | 2022 |
Citation | Ophthalmology, 2022, v. 129, n. 3, p. 308-321 How to Cite? |
Abstract | Purpose: (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 Identifier | http://hdl.handle.net/10722/345153 |
ISSN | 2023 Impact Factor: 13.1 2023 SCImago Journal Rankings: 4.642 |
DC Field | Value | Language |
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dc.contributor.author | Yam, Jason C. | - |
dc.contributor.author | Zhang, Xiu Juan | - |
dc.contributor.author | Zhang, Yuzhou | - |
dc.contributor.author | Wang, Yu Meng | - |
dc.contributor.author | Tang, Shu Min | - |
dc.contributor.author | Li, Fen Fen | - |
dc.contributor.author | Kam, Ka Wai | - |
dc.contributor.author | Ko, Simon T. | - |
dc.contributor.author | Yip, Benjamin H.K. | - |
dc.contributor.author | Young, Alvin L. | - |
dc.contributor.author | Tham, Clement C. | - |
dc.contributor.author | Chen, Li Jia | - |
dc.contributor.author | Pang, Chi Pui | - |
dc.date.accessioned | 2024-08-15T09:25:34Z | - |
dc.date.available | 2024-08-15T09:25:34Z | - |
dc.date.issued | 2022 | - |
dc.identifier.citation | Ophthalmology, 2022, v. 129, n. 3, p. 308-321 | - |
dc.identifier.issn | 0161-6420 | - |
dc.identifier.uri | http://hdl.handle.net/10722/345153 | - |
dc.description.abstract | Purpose: (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.language | eng | - |
dc.relation.ispartof | Ophthalmology | - |
dc.subject | Atropine | - |
dc.subject | Myopia | - |
dc.subject | Rebound | - |
dc.title | Three-Year Clinical Trial of Low-Concentration Atropine for Myopia Progression (LAMP) Study: Continued Versus Washout: Phase 3 Report | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.ophtha.2021.10.002 | - |
dc.identifier.pmid | 34627809 | - |
dc.identifier.scopus | eid_2-s2.0-85118842746 | - |
dc.identifier.volume | 129 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 308 | - |
dc.identifier.epage | 321 | - |
dc.identifier.eissn | 1549-4713 | - |