Department of Computer Science, Stanford, CA.
Stanford Center for Biomedical Informatics Research, Stanford, CA.
AMIA Annu Symp Proc. 2022 Feb 21;2021:641-650. eCollection 2021.
Advancing diagnostic testing capabilities such as clinical next generation sequencing methods offer the potential to diagnose, risk stratify, and guide specialized treatment, but must be balanced against the escalating costs of healthcare to identify patient cases most likely to benefit from them. Heme-STAMP (Stanford Actionable Mutation Panel for Hematopoietic and Lymphoid Malignancies) is one such next generation sequencing test. Our objective is to assess how well Heme-STAMP pathological variants can be predicted given electronic health records data available at the time of test ordering. The model demonstrated AUROC 0.74 (95% CI: [0.72, 0.76]) with 99% negative predictive value at 6% specificity. A benchmark for comparison is the prevalence of positive results in the dataset at 58.7%. Identifying patients with very low or very high predicted probabilities of finding actionable mutations (positive result) could guide more precise high-value selection of patient cases to test.
推进诊断检测能力,如临床下一代测序方法,具有诊断、风险分层和指导专门治疗的潜力,但必须与医疗保健成本的不断上升相平衡,以确定最有可能从中受益的患者病例。Heme-STAMP(斯坦福血液淋巴恶性肿瘤可操作突变面板)就是这样的下一代测序测试之一。我们的目标是评估在测试订购时可获得的电子健康记录数据的情况下,Heme-STAMP 病理变异的预测效果。该模型的 AUROC 为 0.74(95%置信区间:[0.72, 0.76]),特异性为 6%时,阴性预测值为 99%。一个比较基准是数据集阳性结果的患病率为 58.7%。识别预测发现可操作突变(阳性结果)可能性极低或极高的患者,可以指导更精确地选择具有高价值的患者进行测试。