Isaac A Bernstein, Karen S Fernandez, Joshua D Stein, Suzann Pershing, Sophia Y Wang
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引用次数: 0
Abstract
The digitization of health records through electronic health records (EHRs) has transformed the landscape of ophthalmic research, particularly in the study of glaucoma. EHRs offer a wealth of structured and unstructured data, allowing for comprehensive analyses of patient characteristics, treatment histories, and outcomes. This review comprehensively discusses different EHR data sources, their strengths, limitations, and applicability towards glaucoma research. Institutional EHR repositories provide detailed multimodal clinical data, enabling in-depth investigations into conditions such as glaucoma and facilitating the development of artificial intelligence applications. Multicenter initiatives such as the Sight Outcomes Research Collaborative and the Intelligent Research In Sight registry offer larger, more diverse datasets, enhancing the generalizability of findings and supporting large-scale studies on glaucoma epidemiology, treatment outcomes, and practice patterns. The All of Us Research Program, with a special emphasis on diversity and inclusivity, presents a unique opportunity for glaucoma research by including underrepresented populations and offering comprehensive health data even beyond the EHR. Challenges persist, such as data access restrictions and standardization issues, but may be addressed through continued collaborative efforts between researchers, institutions, and regulatory bodies. Standardized data formats and improved data linkage methods, especially for ophthalmic imaging and testing, would further enhance the utility of EHR datasets for ophthalmic research, ultimately advancing our understanding and treatment of glaucoma and other ocular diseases on a global scale.
通过电子病历(EHR)实现的健康记录数字化改变了眼科研究的面貌,尤其是在青光眼研究方面。电子病历提供了大量结构化和非结构化数据,可对患者特征、治疗史和治疗结果进行全面分析。本综述全面讨论了不同的电子病历数据来源、其优势、局限性以及对青光眼研究的适用性。机构电子病历库提供详细的多模态临床数据,有助于对青光眼等疾病进行深入研究,并促进人工智能应用的开发。视力结果研究合作组织(Sight Outcomes Research Collaborative)和视力智能研究登记处(Intelligent Research In Sight registry)等多中心计划提供了更大、更多样化的数据集,提高了研究结果的可推广性,并为有关青光眼流行病学、治疗结果和实践模式的大规模研究提供了支持。我们所有人研究计划特别强调多样性和包容性,通过纳入代表性不足的人群和提供电子病历以外的全面健康数据,为青光眼研究提供了一个独特的机会。挑战依然存在,如数据访问限制和标准化问题,但可以通过研究人员、机构和监管机构之间的持续合作来解决。标准化的数据格式和改进的数据链接方法,尤其是眼科成像和检测方面的数据链接方法,将进一步提高电子病历数据集在眼科研究中的实用性,最终在全球范围内促进我们对青光眼和其他眼科疾病的了解和治疗。