Low-Dose 0.01% Atropine Eye Drops for Symptomatic Vitreous Floaters: A Noninvasive, Safe, and Effective Therapeutic Option.

IF 0.8 Q4 OPHTHALMOLOGY
Jeanette Du, Osama Sabbagh, Brian K Do, Jason M Huang, Joshua D Levinson, Alexander Melamud, Mohammed K Barazi, Mohsin H Ali
{"title":"Low-Dose 0.01% Atropine Eye Drops for Symptomatic Vitreous Floaters: A Noninvasive, Safe, and Effective Therapeutic Option.","authors":"Jeanette Du, Osama Sabbagh, Brian K Do, Jason M Huang, Joshua D Levinson, Alexander Melamud, Mohammed K Barazi, Mohsin H Ali","doi":"10.1177/24741264251364819","DOIUrl":null,"url":null,"abstract":"<p><p><b>Purpose:</b> To assess whether topical low-dose 0.01% atropine eye drops effectively alleviate floater symptoms, as measured by scores from a modified National Eye Institute Visual Function Questionnaire. <b>Methods:</b> This is a retrospective case series conducted at the Retina Group of Washington. Adults with persistently symptomatic vitreous floaters and either vitreous syneresis without posterior vitreous detachment (PVD) or a history of PVD for at least 3 months were included. Subjects with significant vitreoretinal pathology, significant media opacity, anatomic narrow angles, or a history of pars plana vitrectomy (PPV) were excluded. Patients completed a modified National Eye Institute Visual Function Questionnaire before using topical low-dose 0.01% atropine eye drops once daily for 1 week. The same questionnaire was then completed after the 1-week period to assess treatment response. The primary outcome measure was satisfaction with the drops. <b>Results:</b> A total of 44 patients received 0.01% atropine eye drops prescribed for daily application in either 1 or both eyes. There were 22 patients who completed at least 7 days of consecutive drop use. Of these, 13 patients (59.1%) were \"satisfied\" or \"very satisfied\" with the drops, and 11 patients (50%) reported that they would continue using the medication. <b>Conclusions:</b> Low-dose 0.01% atropine eye drops may be an effective, noninvasive treatment option for select patients with persistently symptomatic vitreous floaters resulting from vitreous syneresis or PVD.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251364819"},"PeriodicalIF":0.8000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12367726/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of VitreoRetinal Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/24741264251364819","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To assess whether topical low-dose 0.01% atropine eye drops effectively alleviate floater symptoms, as measured by scores from a modified National Eye Institute Visual Function Questionnaire. Methods: This is a retrospective case series conducted at the Retina Group of Washington. Adults with persistently symptomatic vitreous floaters and either vitreous syneresis without posterior vitreous detachment (PVD) or a history of PVD for at least 3 months were included. Subjects with significant vitreoretinal pathology, significant media opacity, anatomic narrow angles, or a history of pars plana vitrectomy (PPV) were excluded. Patients completed a modified National Eye Institute Visual Function Questionnaire before using topical low-dose 0.01% atropine eye drops once daily for 1 week. The same questionnaire was then completed after the 1-week period to assess treatment response. The primary outcome measure was satisfaction with the drops. Results: A total of 44 patients received 0.01% atropine eye drops prescribed for daily application in either 1 or both eyes. There were 22 patients who completed at least 7 days of consecutive drop use. Of these, 13 patients (59.1%) were "satisfied" or "very satisfied" with the drops, and 11 patients (50%) reported that they would continue using the medication. Conclusions: Low-dose 0.01% atropine eye drops may be an effective, noninvasive treatment option for select patients with persistently symptomatic vitreous floaters resulting from vitreous syneresis or PVD.

低剂量0.01%阿托品滴眼液治疗症状性玻璃体飞蚊:一种无创、安全、有效的治疗选择。
目的:评估局部低剂量0.01%阿托品滴眼液是否能有效缓解漂浮物症状,通过修改后的美国国家眼科研究所视觉功能问卷得分来衡量。方法:这是在华盛顿视网膜小组进行的回顾性病例系列。研究对象包括有持续症状的玻璃体飞蚊和无玻璃体后脱离(PVD)的玻璃体联合或至少3个月的玻璃体后脱离病史的成年人。有明显玻璃体视网膜病变、明显中膜混浊、解剖角度狭窄或有玻璃体切除史的受试者被排除在外。患者在使用低剂量0.01%阿托品滴眼液前完成修改后的美国国家眼科研究所视力功能问卷,每天1次,持续1周。然后在1周后完成相同的问卷调查以评估治疗反应。主要的结果测量是对下降的满意度。结果:共有44例患者使用0.01%阿托品滴眼液,每日单眼或双眼使用。有22例患者完成了至少7天的连续滴药使用。其中,13名患者(59.1%)对滴药“满意”或“非常满意”,11名患者(50%)表示他们将继续使用药物。结论:低剂量0.01%阿托品滴眼液可能是一种有效的、无创的治疗选择,用于玻璃体联合或PVD引起的持续症状的玻璃体飞蚊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.20
自引率
16.70%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信