Electronic vs manual approaches to identify patients from the EHR for cancer clinical trials–what’s feasible

N. Bickell, Sylvia Lin, Helena L. Chang, T. Vleck, G. Nadkarni, Hannah Jacobs El, A. Tiersten, M. Shafir, A. Gelijns
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Abstract

Objective: Electronic health records (EHRs) offer a platform to identify patients for clinical trials. We compared an electronic approach combining natural language processing (NLP) with query capabilities of Data Warehouse using structured and unstructured information against manual review to assess feasibility in identifying subjects for a breast cancer trial. Materials and methods: Study included women with new metastatic, ER-positive, HER2-negative breast cancer, treated with letrozole monotherapy between January 2012 and December 2015 who did not receive prior systemic therapy for advanced disease. Concordance between approaches was assessed using Cohen’s kappa statistic. Results: 826 breast cancer cases were identified; 83 were truly metastatic, ER-positive, HER2-negative. Manual review identified 77 (93%) patients compared to 51 (61%) by NLP. Cases missed by electronic approach were due to inaccessibility of data and variability in physician documentation. Cohen’s kappa was 0.36 (95% CI 0.27-0.45), indicating fair agreement. The final eligible study population included 30 women, 28 (93%) identified by manual review and 17 (57%) electronically. The electronic approach markedly reduced time spent: 44 vs. 280 hours. Discussion: While electronic approach offers substantial cost and time savings, variability in physician documentation and inaccessibility of unstructured key data requires manual support to redress misclassification and exclusion of patients by electronic review. Conclusion: Key common data elements need to be developed and incorporated into the clinical care process. Technological innovations are needed to lessen the pain of structured field entry. Whereas the ultimate cost savings can be substantial, there needs to be upfront investment to obtain such efficiencies.
从电子病历中识别癌症临床试验患者的电子vs手动方法-什么是可行的
目的:电子健康档案(EHRs)为临床试验识别患者提供平台。我们比较了一种结合自然语言处理(NLP)和数据仓库查询能力的电子方法,使用结构化和非结构化信息与人工审查相结合,以评估确定乳腺癌试验受试者的可行性。材料和方法:研究纳入了2012年1月至2015年12月期间接受来曲唑单药治疗的新转移性、er阳性、her2阴性乳腺癌患者,且未接受过晚期疾病的全身治疗。采用Cohen’s kappa统计量评估方法间的一致性。结果:共确诊乳腺癌826例;83例确实转移,er阳性,her2阴性。人工检查确定了77例(93%)患者,而NLP检查确定了51例(61%)。电子方法遗漏的病例是由于数据难以获取和医生文件的可变性。Cohen’s kappa为0.36 (95% CI 0.27-0.45),表明基本一致。最终符合条件的研究人群包括30名女性,28名(93%)通过人工评估确定,17名(57%)通过电子评估确定。电子方式显著减少了花费的时间:44小时比280小时。讨论:虽然电子方法节省了大量的成本和时间,但医生文档的可变性和非结构化关键数据的不可访问性需要人工支持,以纠正错误分类和通过电子审查排除患者。结论:需要开发关键的公共数据元素并将其纳入临床护理过程。需要技术创新来减轻结构化油田进入的痛苦。虽然最终节省的成本可能是可观的,但要获得这样的效率,需要进行前期投资。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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