儿童近视控制的局部阿特罗平:阿特罗平治疗长期评估研究
Yong Li1,2, Michelle Yip1, Yilin Ning2
1Singapore Eye Research Institute, Singapore National Eye Centre, Singapore.
JAMA ophthalmology
|November 29, 2023
概括
长期随访儿童近视控制局部氨酸 (0.01%-1.0%) 没有显著差异折射误差或眼部并发症治疗后的几年. 需要进一步研究近视管理的最佳阿特罗宾度和持续时间.
科学领域:
- 眼科医生 眼科 眼科
- 儿科眼科医生 儿科眼科医生
- 临床研究 临床研究
背景情况:
- 局部阿特罗平眼滴用于儿童近视控制,但长期安全性和有效性数据有限.
- 之前的短期研究报告了关于阿特罗宾在近视管理中的有效性不一致的结果.
研究的目的:
- 为了评估儿童近视控制的长期安全性和结果,使用局部氨酸.
- 评估眼部并发症的发生率和长期随访后折射误差的变化.
主要方法:
- 一项前性,双面罩的观察性研究,分析了来自Atropine for the Treatment of Myopia (ATOM) 1和ATOM2试验的数据.
- 成年参与者从ATOM1 (1%的阿特罗宾与安慰剂) 和ATOM2 (0.01%,0.1%,0.5%的阿特罗宾) 被审查了治疗后10-20年.
- 主要结果指标包括循环的球体等价值 (SE) 和轴长 (AL) 的变化,以及眼部并发症的发生率.
主要成果:
- 在被评估的参与者中,在阿特罗平治疗组和安慰剂之间没有观察到最终折射误差 (SE) 或轴长 (AL) 的显著差异.
- 白内障/透镜不透明的发生率,近视性黄斑变性,和 parapapillary 缩在1%的阿托和安慰剂组之间没有差异.
- 长期跟踪 (10-20年) 儿童类药物治疗 (0.01%-1.0%) 没有显示增加的眼部并发症.
结论:
- 短期使用局部阿特罗宾用于儿童近视控制 (0.01%-1.0%) 与折射误差或主要眼部并发症的长期差异无关.
- 研究结果表明,需要进行更长期的研究,以确定近视管理的最佳阿特罗宾度和持续时间.
- 长期来看,阿特罗宾对近视控制的安全性概况似乎有利,但需要对治疗参数进行进一步的研究.
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