针对近视的重复低水平红光治疗的安全性:系统性审查
Yanping Chen1, Ruilin Xiong1, Shaopeng Yang1
1State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou 510060, China.
Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)
|December 13, 2024
概括
针对近视的重复低水平红光 (RLRL) 治疗显示出良好的安全性,没有报告可逆性视力丧失. 建议监测视觉敏度和后视图,以管理暂时的副作用.
科学领域:
- 眼科医生 眼科 眼科
- 生物医学工程 生物医学工程
- 公共卫生 公共卫生
背景情况:
- 近视的患病率在全球范围内不断增加,需要有效和安全的干预措施.
- 重复的低水平红光 (RLRL) 治疗正在成为近视的潜在治疗方法.
- 确定RLRL治疗的安全性对于其临床采用至关重要.
研究的目的:
- 系统地审查和确定RLRL治疗近视的安全性概况.
- 评估与RLRL治疗相关的副作用的发生率和性质.
- 为了比较RLRL治疗与其他近视控制方法的风险对益率.
主要方法:
- 使用近视和RLRL治疗的关键词对七个数据库的系统审查 (开始-2024年2月).
- 对安全结果,风险与益处比率以及副作用发生率的综合分析.
- 将RLRL副作用与已建立的反迷恋干预措施进行比较.
主要成果:
- 分析了20项研究 (2380名参与者,1436人接受RLRL);中位数随访时间为9个月.
- 没有报告永久视力丧失或眼睛结构损伤的病例.
- 暂时的后图像 (在6分钟内解决) 是最常见的副作用;发生率为每100个患者年0.088.
结论:
- 在近视治疗中,RLRL治疗似乎是安全的,没有发现不可逆转的视力或结构损伤.
- 建议监测视力敏度和影像后持续时间,以检测短暂的副作用.
- 需要进一步的长期,充足的研究来充分确定RLRL治疗的安全性.
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