群体规模药物流行病学数据集的交互式探索

Tengel Ekrem Skar, Einar J. Holsbø, K. Svendsen, L. A. Bongo
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引用次数: 0

摘要

与药物不良反应(ADR)数据相关的人口规模药物处方数据支持足够大的模型拟合,以检测在较小数据集上使用传统方法无法检测到的药物使用和ADR模式。然而,在大型数据集中检测ADR模式需要可扩展的数据处理工具、用于数据分析的机器学习工具和交互式可视化工具。据我们所知,没有现有的药物流行病学工具支持所有这三个要求。因此,我们创建了一个工具,用于交互式探索处方数据集的模式,其中包含数百万个样本。我们使用Spark对数据进行预处理,以便进行机器学习,并使用SQL查询进行分析。我们已经在Keras和scikit-learn框架中实现了模型。模型结果在Jupyter中使用实时Python编码进行可视化和解释。我们应用我们的工具来探索来自挪威处方数据库的3.84亿处方数据集,以及住院老年人的6200万处方。我们在两分钟内预处理数据,在几秒钟内训练模型,并在几毫秒内绘制结果。我们的研究结果表明,结合计算能力,计算时间短,易于使用的群体规模药物流行病学数据集分析的力量。
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Interactive exploration of population scale pharmacoepidemiology datasets
Population-scale drug prescription data linked with adverse drug reaction (ADR) data supports the fitting of models large enough to detect drug use and ADR patterns that are not detectable using traditional methods on smaller datasets. However, detecting ADR patterns in large datasets requires tools for scalable data processing, machine learning for data analysis, and interactive visualization. To our knowledge no existing pharmacoepidemiology tool supports all three requirements. We have therefore created a tool for interactive exploration of patterns in prescription datasets with millions of samples. We use Spark to preprocess the data for machine learning and for analyses using SQL queries. We have implemented models in Keras and the scikit-learn framework. The model results are visualized and interpreted using live Python coding in Jupyter. We apply our tool to explore a 384 million prescription data set from the Norwegian Prescription Database combined with a 62 million prescriptions for elders that were hospitalized. We preprocess the data in two minutes, train models in seconds, and plot the results in milliseconds. Our results show the power of combining computational power, short computation times, and ease of use for analysis of population scale pharmacoepidemiology datasets.
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