Akagün Nilay, Altıparmak Uğur Emrah
Acıbadem Ankara Hospital, Clinic of Ophthalmology, Ankara, Türkiye.
Turk J Ophthalmol. 2025 Apr 24;55(2):61-66. doi: 10.4274/tjo.galenos.2025.86584.
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.
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.
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.
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.
本研究旨在确定在特定的单中心土耳其人群中,使用0.01%阿托品控制近视进展的患者不依从的关键因素,并提出提高依从性的策略。
这项回顾性研究纳入了2021年1月至6月期间在我们诊所被诊断为近视进展并开具0.01%阿托品治疗处方的30例患者(平均年龄:10.67±3.47岁;年龄范围:5 - 16岁;男性14例,女性16例)。所有参与者在完成治疗前均已停用0.01%阿托品治疗。使用患者记录分析停药原因,并将其分类为畏光、近视力困难、眼部或全身副作用、每月需要更换眼药水以及治疗持续时间长等因素。收集患者的年龄、性别、治疗依从性和停药原因的数据。使用IBM SPSS Statistics软件进行统计分析。
我们患者群体中的治疗停药率为14.92%(95%置信区间:10.23 - 19.61)。最常见的停药原因是每月需要更换眼药水(80%)、治疗持续时间长(70%)和畏光(60%)。停药率在不同年龄组之间无显著差异(p>0.05)。女性患者更频繁地将每月更换眼药水作为停药障碍。知情同意程序已经强调了治疗持续时间长和每月需要更换眼药水,但这些仍然是一些家庭依从性的障碍。
为了提高我们患者群体对0.01%阿托品治疗近视进展的依从性,患者教育和强化支持系统至关重要。实施应对每月更换眼药水相关挑战的策略,并提供有关治疗长期益处的更好信息,可能有助于提高依从率。