Evaluation of Reasons for Discontinuation of Atropine 0.01% in Myopia Management: A Single-Center Retrospective Study from Türkiye.

Q3 Medicine
Nilay Akagün, Uğur Emrah Altıparmak
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引用次数: 0

Abstract

Objectives: This study aimed to identify the key factors contributing to non-adherence in patients using 0.01% atropine for progressive myopia control in a specific single-center Turkish population and to propose strategies to enhance adherence.

Materials and methods: This retrospective study included 30 patients (mean age: 10.67±3.47 years; age range: 5-16 years; 14 males and 16 females) diagnosed with progressive myopia and prescribed 0.01% atropine treatment in our clinic between January and June 2021. All participants had discontinued 0.01% atropine treatment before completion. The reasons for discontinuation were analyzed using patient records and categorized into factors such as light sensitivity, difficulties with near vision, ocular or systemic side effects, the need for monthly eye drop renewal, and the long treatment duration. Data on patients' age, sex, treatment adherence, and reasons for discontinuation were collected. Statistical analyses were performed using IBM SPSS Statistics software.

Results: The treatment discontinuation rate in our patient population was 14.92% (95% confidence interval: 10.23-19.61). The most common reasons for discontinuation were the need for monthly drop renewal (80%), long treatment duration (70%), and light sensitivity (60%). Discontinuation rates did not significantly differ by age group (p>0.05). The need for monthly renewal was more frequently reported as a barrier among female patients. Informed consent procedures had highlighted the long treatment duration and the need for monthly renewal, but these still represented barriers to adherence for some families.

Conclusion: To improve adherence to 0.01% atropine treatment for progressive myopia in our patient population, patient education and enhanced support systems are essential. Implementing strategies to address challenges related to monthly renewal and providing better information about the long-term benefits of treatment could help increase adherence rates.

0.01%阿托品在近视治疗中的停药原因评价:一项来自 rkiye的单中心回顾性研究。
目的:本研究旨在确定在特定的单中心土耳其人群中使用0.01%阿托品控制进进性近视的患者不依从性的关键因素,并提出提高依从性的策略。材料与方法:本研究纳入30例患者,平均年龄:10.67±3.47岁;年龄范围:5-16岁;14名男性,16名女性)于2021年1月至6月在我诊所诊断为进行性近视,并使用0.01%阿托品治疗。所有参与者在完成前停止0.01%阿托品治疗。根据患者记录分析停药原因,并将停药原因分类为光敏性、近视力困难、眼部或全身副作用、每月需要更新滴眼液、治疗持续时间长等因素。收集了患者的年龄、性别、治疗依从性和停药原因的数据。采用IBM SPSS统计软件进行统计分析。结果:本组患者停药率为14.92%(95%可信区间:10.23-19.61)。最常见的停药原因是需要每月滴药更新(80%)、治疗时间长(70%)和光敏性(60%)。不同年龄组停药率差异无统计学意义(p < 0.05)。在女性患者中,每月更新的需求更常被报道为障碍。知情同意程序强调了治疗时间长和需要每月更新,但这些仍然是一些家庭坚持治疗的障碍。结论:为了提高0.01%阿托品治疗进行性近视的依从性,患者教育和加强支持系统是必不可少的。实施应对与每月更新有关的挑战的战略,并提供有关治疗长期益处的更好信息,有助于提高依从率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Turkish Journal of Ophthalmology
Turkish Journal of Ophthalmology Medicine-Ophthalmology
CiteScore
2.20
自引率
0.00%
发文量
0
期刊介绍: The Turkish Journal of Ophthalmology (TJO) is the only scientific periodical publication of the Turkish Ophthalmological Association and has been published since January 1929. In its early years, the journal was published in Turkish and French. Although there were temporary interruptions in the publication of the journal due to various challenges, the Turkish Journal of Ophthalmology has been published continually from 1971 to the present. The target audience includes specialists and physicians in training in ophthalmology in all relevant disciplines.
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