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      Efficacy of combined orthokeratology and 0.01% atropine solution for slowing axial elongation in children with myopia: a 2-year randomised trial

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          Abstract

          Eighty Japanese children, aged 8–12 years, with a spherical equivalent refraction (SER) of − 1.00 to − 6.00 dioptres (D) were randomly allocated into two groups to receive either a combination of orthokeratology (OK) and 0.01% atropine solution (combination group) or monotherapy with OK (monotherapy group). Seventy-three subjects completed the 2-year study. Over the 2 years, axial length increased by 0.29 ± 0.20 mm ( n = 38) and 0.40 ± 0.23 mm ( n = 35) in the combination and monotherapy groups, respectively ( P = 0.03). Interactions between combination treatment and age or SER did not reach significance level (age, P = 0.18; SER, P = 0.06). In the subgroup of subjects with an initial SER of − 1.00 to − 3.00 D, axial length increased by 0.30 ± 0.22 mm ( n = 27) and 0.48 ± 0.22 mm ( n = 23) in the combination and monotherapy groups, respectively ( P = 0.005). In the − 3.01 to − 6.00 D subgroup, axial length increased by 0.27 ± 0.15 mm ( n = 11) and 0.25 ± 0.17 mm ( n = 12) in the combination and monotherapy groups, respectively ( P = 0.74). The combination therapy may be effective for slowing axial elongation, especially in children with low initial myopia.

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          Most cited references32

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          Retardation of myopia in Orthokeratology (ROMIO) study: a 2-year randomized clinical trial.

          This single-masked randomized clinical trial aimed to evaluate the effectiveness of orthokeratology (ortho-k) for myopic control. A total of 102 eligible subjects, ranging in age from 6 to 10 years, with myopia between 0.50 and 4.00 diopters (D) and astigmatism not more than 1.25D, were randomly assigned to wear ortho-k lenses or single-vision glasses for a period of 2 years. Axial length was measured by intraocular lens calculation by a masked examiner and was performed at the baseline and every 6 months. This study was registered at ClinicalTrials.gov, number NCT00962208. In all, 78 subjects (37 in ortho-k group and 41 in control group) completed the study. The average axial elongation, at the end of 2 years, were 0.36 ± 0.24 and 0.63 ± 0.26 mm in the ortho-k and control groups, respectively, and were significantly slower in the ortho-k group (P 0.54) but was correlated with the initial age of the subjects (P 1.00D per year) were 65% and 13% in younger (age range: 7-8 years) and older (age range: 9-10 years) children, respectively, in the control group and were 20% and 9%, respectively, in the ortho-k group. Five subjects discontinued ortho-k treatment due to adverse events. On average, subjects wearing ortho-k lenses had a slower increase in axial elongation by 43% compared with that of subjects wearing single-vision glasses. Younger children tended to have faster axial elongation and may benefit from early ortho-k treatment. (ClinicalTrials.gov number, NCT00962208.).
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            Increased prevalence of myopia in the United States between 1971-1972 and 1999-2004.

            To compare US population prevalence estimates for myopia in 1971-1972 and 1999-2004. The 1971-1972 National Health and Nutrition Examination Survey provided the earliest nationally representative estimates for US myopia prevalence; myopia was diagnosed by an algorithm using either lensometry, pinhole visual acuity, and presenting visual acuity (for presenting visual acuity > or =20/40) or retinoscopy (for presenting visual acuity -2.0 diopters [D]: 17.5% vs 13.4%, respectively [P -7.9 D: 22.4% vs 11.4%, respectively [P < .001]; < or =-7.9 D: 1.6% vs 0.2%, respectively [P < .001]). When using similar methods for each period, the prevalence of myopia in the United States appears to be substantially higher in 1999-2004 than 30 years earlier. Identifying modifiable risk factors for myopia could lead to the development of cost-effective interventional strategies.
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              Five-Year Clinical Trial on Atropine for the Treatment of Myopia 2: Myopia Control with Atropine 0.01% Eyedrops.

              To compare the safety and efficacy of different concentrations of atropine eyedrops in controlling myopia progression over 5 years.
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                Author and article information

                Contributors
                nozomik@omiya.jichi.ac.jp
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                29 July 2020
                29 July 2020
                2020
                : 10
                : 12750
                Affiliations
                [1 ]ISNI 0000000123090000, GRID grid.410804.9, Department of Ophthalmology, Saitama Medical Centre, , Jichi Medical University, ; 1-847 Amanuma-cho, Omiya-ku, Saitama-shi, Saitama, 330-8503 Japan
                [2 ]Konno Eye Clinic, Saitama, Japan
                [3 ]Omiya Hamada Eye Clinic, Saitama, Japan
                [4 ]ISNI 0000000123090000, GRID grid.410804.9, Department of Hematology, Saitama Medical Centre, , Jichi Medical University, ; Saitama, Japan
                Article
                69710
                10.1038/s41598-020-69710-8
                7391648
                32728111
                d41aa676-8e66-41bf-99b5-ebd50d4aea46
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 December 2019
                : 17 July 2020
                Funding
                Funded by: JSPS KAKENHI
                Award ID: JP26462646
                Award Recipient :
                Categories
                Article
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                © The Author(s) 2020

                Uncategorized
                diseases,medical research
                Uncategorized
                diseases, medical research

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