为EU-ROP和打击儿童失明!共同开发一套数据库参数. 在 ROP 登记处注册
Caroline Catt1,2, Johanna M Pfeil3, Daniel Barthelmes2,4
1Department of Ophthalmology, The Children's Hospital at Westmead, Westmead, New South Wales, Australia carolinecatt@hotmail.com.
The British journal of ophthalmology
|September 13, 2023
概括
建议对早产视网膜病变 (ROP) 治疗进行最小的数据集,以跟踪结果. 这种标准化的方法旨在改善患者护理,并使得ROP研究得以一致.
科学领域:
- 眼科医生 眼科 眼科
- 新生儿科学 新生儿科学
- 临床数据管理 临床数据管理
背景情况:
- 早产视网膜病变 (ROP) 的发生率正在上升,治疗选择不断扩大,缺乏全面的安全数据.
- 需要进行标准化数据收集,以有效监测和比较ROP治疗结果.
研究的目的:
- 定义一个最小的,以患者为中心的ROP治疗数据集.
- 建立一个可行的数据集,用于临床实践和协作结果跟踪.
- 通过标准化的ROP治疗研究来改善患者的治疗结果.
主要方法:
- 一个由临床医生和患者代表组成的跨国协会成立.
- 在ROP和注册表开发方面的专业知识指导了数据集的创建.
- 专注于常规临床实践的现实世界,以患者为中心,最小和可行的参数.
主要成果:
- 推的数据点包括患者人口统计,并发症,ROP状态和治疗细节.
- 建议收集眼科和全身并发症,以及短期/长期结果.
- 包括重新治疗事件和后续检查的数据,以全面跟踪.
结论:
- 建议的参数应在ROP注册和研究中采用.
- 标准化将减少报告中的变化,并允许进行有意义的比较.
- 这些参数构成了欧盟-ROP和打击儿童失明的基础! 在 ROP 登记处.
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