A comparative study on slow down progression of myopia using atropine 0.01% in children

Syeda Sadia Ikram, D. S., S. Puri
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Abstract

The aim of the study was to determine the efficacy of lower concentration of Atropine 0.01% in promoting unaided visual acuity and slowing down the progression of myopia in children over 6 months. It was a hospital-based comparative study in the outpatient department of Ophthalmology, AL, LT, ACD, PPD, SPD, PGP were taken by Lenstar and Lensometer.The Comparative study was performed on 60 children from 9 to 15 years age group with initial myopic spherical equivalence from 0.5 to 6.00 D. The children were screened for visual acuity for distance and near using Snellen’s chart. Cycloplegic Refraction was done to know the presence of Refractive Errors. This study was approved by IRB Ethical Committee. (SCAHS/IRB/2022/JULY/420).The inclusion criteria include Ammetropic children with no binocular vision anomalies and no history of ocular disease. The primary outcome was the rate of myopic progression after 6 months. The participants were instructed to use Atropine 0.01% eye drops during night times for 6 months and the rate of myopic progression and the spherical equivalence, axial length, lens thickness, anterior chamber depth, photopic and scotopic pupil diameter were re-assessed to compare the progression of myopia in the children. Sixty children enrolled for six months study in which the mean progression of myopia was found to be within 0.27D and axial elongation shows 0.23 mm changes respectively, whereas there were no significant changes in the anterior chamber depth, lens thickness, photopic and scotopic pupil diameter before and after assessment in children. Spherical power, Axial Length, Anterior Chamber Depth, Lens Thickness, Photopic Pupil Diameter and Scotopic Pupil Diameter all showed significant progression from pre to post stages, with the average post reading deviating by 0.25 from the normal limits.
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0.01%阿托品延缓儿童近视进展的比较研究
本研究的目的是确定0.01%低浓度阿托品在6个月以上儿童中促进独立视力和减缓近视进展的疗效。本研究是一项以医院为基础的眼科门诊比较研究,Lenstar和Lensometer分别测量AL、LT、ACD、PPD、SPD、PGP。采用Snellen’s视力表对60例初诊近视0.5 ~ 6.00 d的9 ~ 15岁儿童进行了比较研究。通过睫状体麻痹性屈光检查来了解屈光不正的存在。本研究已获IRB伦理委员会批准。(SCAHS / IRB / 2022 / / 420年7月)。纳入标准包括无双眼视力异常和无眼部疾病史的无屈光性儿童。主要观察指标为6个月后近视进展率。要求受试者在夜间使用0.01%阿托品滴眼液,连续6个月,并重新评估近视进展率和球面等效性、眼轴长度、晶状体厚度、前房深度、光瞳和暗瞳直径,比较儿童近视进展。60名儿童参加了为期6个月的研究,其中平均近视进展在0.27D以内,轴向伸长变化0.23 mm,而评估前后儿童前房深度、晶状体厚度、光瞳和暗瞳直径均无显著变化。球体度数、眼轴长度、前房深度、晶状体厚度、光瞳直径和暗瞳直径均表现出明显的变化,平均后读数与正常值相差0.25。
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