Abstract:AimsTo determine myopia progression in children who continued to wear the defocus incorporated multiple segments (DIMS) lenses or switched from single vision (SV) to DIMS lenses for a 1-year period following a 2-year myopia control trial.Methods128 children participated in this study. The children who had worn DIMS lenses continued to wear DIMS lenses (DIMS group), and children who had worn SV lenses switched to wear DIMS lenses (Control-to-DIMS group). Cycloplegic spherical equivalent refraction (SER) and axi… Show more
“…A further report has shown that this myopia control effect is sustained in the third year. 13,27 While study design differences make direct comparison difficult, the RLRL efficacy results reported here appear at least competitive with these other treatment modalities.…”
Section: Efficacy In Comparison With Other Treatmentsmentioning
confidence: 84%
“…The inclusion and exclusion criteria adopted were the same as for the majority of myopia control trials conducted for low dose atropine eyedrops 12 and defocus incorporated multiple segments (DIMS) spectacle lens 13 , in order to ensure outcomes were comparable across studies. Eligible participants were children aged 8 to 13 years with myopia of cycloplegic spherical equivalent refraction (SER) of -1.00 to -5.00 diopters (D), astigmatism < 2.50 D, anisometropia < 1.50 D, best-corrected visual acuity (BCVA) > 0.0 logMAR (Snellen 1.0 or 20/20) in either eye, and were willing to J o u r n a l P r e -p r o o f participate in the study and accept random allocation in grouping.…”
“…A further report has shown that this myopia control effect is sustained in the third year. 13,27 While study design differences make direct comparison difficult, the RLRL efficacy results reported here appear at least competitive with these other treatment modalities.…”
Section: Efficacy In Comparison With Other Treatmentsmentioning
confidence: 84%
“…The inclusion and exclusion criteria adopted were the same as for the majority of myopia control trials conducted for low dose atropine eyedrops 12 and defocus incorporated multiple segments (DIMS) spectacle lens 13 , in order to ensure outcomes were comparable across studies. Eligible participants were children aged 8 to 13 years with myopia of cycloplegic spherical equivalent refraction (SER) of -1.00 to -5.00 diopters (D), astigmatism < 2.50 D, anisometropia < 1.50 D, best-corrected visual acuity (BCVA) > 0.0 logMAR (Snellen 1.0 or 20/20) in either eye, and were willing to J o u r n a l P r e -p r o o f participate in the study and accept random allocation in grouping.…”
“…In addition to genetic susceptibility, several environmental factors, such as prolonged near work, increased digital screen time, and insufficient time spent outdoors, are recognized as important risk factors for myopic progression [1][2][3][4]. To control the epidemic of myopia, low-concentration atropine eye drops and specially designed contact lenses and spectacle lenses, such as defocus incorporated multiple segments (DIMS) lenses and aspherical lenslets, are recommended to reduce myopic progression and have now reached high levels of evidence [5][6][7].…”
Purpose
The outbreak of coronavirus disease 2019 (COVID-19) has caused many children to stay indoors. Increased near work and insufficient outdoor activities are considered important risk factors for myopic progression. This study aimed to compare the changes in myopic progression before and after COVID-19 in children treated with low-concentration atropine.
Methods
The records of 103 eyes of 103 children who were treated with low-concentration atropine eye drops were retrospectively reviewed. We classified children according to the concentration of atropine eye drops and children’s age. The beginning of the pre-COVID-19 period was set from January 2019 to May 2019, and the endpoint was set in March 2020. The beginning of the post-COVID-19 period was set in March 2020, and the endpoint was set from January 2021 to March 2021. We evaluated the questionnaires administered to children’s parents.
Results
A significant myopic progression was observed in the post-COVID-19 period compared to the pre-COVID-19 period in the 0.05% and 0.025% atropine groups (P < 0.001 and P = 0.020, respectively). For children aged 5 to 7 and 8 to 10 years, the axial elongations were significantly faster in the post-COVID-19 period than in the pre-COVID-19 period (P = 0.022 and P = 0.005, respectively). However, the rates of axial elongation and myopic progression were not significantly different between pre- and post-COVID-19 in children aged 11 to 15 years (P = 0.065 and P = 0.792, respectively). The average time spent using computers and smartphones and reading time were significantly increased, and the times of physical and outdoor activity were significantly decreased in the post-COVID-19 period compared to the pre-COVID-19 period.
Conclusions
The rates of myopic progression have increased substantially after the spread of COVID-19 with an increase in the home confinement of children. Therefore, it is necessary to control the environmental risk factors for myopia, even in children undergoing treatment for the inhibition of myopic progression.
“…Zusätzlich sind in Abb. 3 die aus aktuellen Studiendaten ermittelten mittleren Wachstumsraten der Studien zu den DIMS-Gläsern [ 18 , 20 ], aus der LAMP-Studie (Yam et al. 2020) zur Wirkung von Atropin-Augentropfen auf die Myopieprogression [ 35 ], aus der ROMIO-Studie (Cho et al.…”
Section: Bisherige Studienergebnisseunclassified
“…Gemäß Abb. 3 , nach aktueller Studienlage, erfüllt allein die DIMS-Brille im Beobachtungszeitraum [ 18 , 20 ] das hier vorgestellte praktische Therapiekriterium vollständig, während die Therapie mit 0,05 % Atropin [ 35 ] und danach die Ortho-K-Therapie [ 10 ] und die Therapie mit „High Add“-multifokalen Kontaktlinsen [ 29 ] eine noch tolerierbare Therapieperformance erreichen können. Wie aber kürzlich von Joachimsen et al berichtet [ 14 ], müsse eine Atropin-Konzentration von 0,05 % bei kaukasischen Kindern aufgrund der Nebenwirkungen in der praktischen klinischen Anwendung als kritisch eingestuft werden.…”
Section: Alternative Zu Bekannten Therapieoptionen?unclassified
ZusammenfassungEin übermäßiges Längenwachstum des Auges bei Kindern und Jugendlichen führt zu progredienter Myopie, die im Erwachsenenalter schwerwiegende Augenerkrankungen zur Folge haben kann. Es wurden bereits verschiedene Strategien zur Hemmung der Myopieprogression entwickelt. Das vorgestellte neuartige Einstärkenbrillenglas mit „Defocus Incorporated Multiple Segments (DIMS)“-Technologie erweitert das Portfolio der Myopietherapien um eine leicht anzuwendende nichtinvasive Option. Erste Studien dazu liefern vielversprechende Ergebnisse bei sehr geringem Nebenwirkungsprofil.
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