首页> 外文期刊>Ophthalmology and therapy. >Atropine 0.01% Eye Drops for Myopia Control in American Children: A Multiethnic Sample Across Three US Sites
【24h】

Atropine 0.01% Eye Drops for Myopia Control in American Children: A Multiethnic Sample Across Three US Sites

机译:阿托品0.01%滴眼液用于美国儿童近视控制:美国三个地区的多族裔样本

获取原文
获取外文期刊封面目录资料

摘要

Abstract IntroductionTopical atropine eye drops at low concentrations have been shown to slow myopia progression in East Asian studies. This study explored the effect of atropine 0.01% eye drops on controlling myopia progression in a multiethnic cohort of children in the USA.MethodsA multicenter retrospective case–control study ( n =?198) quantified the effect of adding nightly atropine 0.01% eye drops to treatment as usual on the progression of childhood (ages 6–15?years) myopia. Cases included all children treated with atropine for at least 1?year. Controls were matched to cases on both age (±?6?months) and baseline spherical equivalent refraction (SER) (±?0.50?diopters, D) at treatment initiation. The primary endpoint was the average SER myopia progression after 1, 1.5, and 2?years of therapy. A secondary outcome was the percentage of subjects with a clinically significant worsening of myopia, defined as a greater than ??0.75?D SER increase in myopia.ResultsThe average baseline SERs for the atropine ( n =?100) and control ( n =?98) groups were similar (??3.1?±?1.9?D and ??2.8?±?1.6?D, respectively) ( p =?0.23). The average SER increase from baseline was significantly less for the atropine group than the control group at year 1 (??0.2?±?0.8?D compared with ??0.6?±?0.4?D, p ?0.001) and at year 2 (??0.3?±?1.1?D compared with ??1.2?±?0.7?D, p ?0.001). Secondary analysis at year 2 revealed that 80% of the control group vs. 37% of the atropine group experienced clinically significant worsening myopia of at least ??0.75?D ( p ?0.001). There were no major safety issues reported in either group.ConclusionSimilar to results reported in Asia, atropine 0.01% eye drops significantly reduced myopia progression in a cohort of US children over 2?years of treatment.FundingNevakar, Inc.Plain Language SummaryPlain language summary available for this article.
机译:摘要引言在东亚研究中,低浓度的阿托品外用滴眼液可减缓近视进展。这项研究探讨了美国多族裔儿童中阿托品0.01%滴眼液对控制近视进展的作用。方法一项多中心回顾性病例对照研究(n =?198)量化了在夜间向儿童中添加阿托品0.01%滴眼液的效果。对儿童(6至15岁)近视的进展照常进行治疗。病例包括所有接受阿托品治疗至少1年的儿童。在治疗开始时,对照组与年龄(±6?个月)和基线等效球镜屈光度(SER)(±0.50?屈光度,D)的病例相匹配。主要终点是治疗1年,1.5年和2年后SER平均近视进展。次要结果是近视眼临床上显着恶化的受试者百分比,即近视眼SER增加≥0.75?D。结果阿托品(n =?100)和对照(n =?100)的平均基线SERs。 98个)组是相似的(分别为≈3.1≤±1.9≤D和≤2.8≤±1.6μD)(p =≤0.23)。阿托品组在第1年从基线的平均SER增加显着低于对照组(?0.2?±?0.8?D与?0.6?±?0.4?D,p <?0.001)和第1年。 2(±0.3±±1.11.1D与±1.2±±0.70.7D,p <0.001)。在第2年进行的次要分析显示,对照组的80%和阿托品组的37%经历了临床上显着恶化的近视,至少达?? 0.75?D(p <?0.001)。两组均未报告重大安全问题。结论与亚洲报道的结果相似,阿托品0.01%的眼药水可显着降低2岁以上美国儿童队列中的近视进展。FundingNevakar,Inc。对于本文。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号