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CRISP-TDM0 for standardized knowledge discovery from physiological data streams: Retinopathy of prematurity and blood oxygen saturation case study

机译:CRISP-TDM 0 用于从生理数据流中发现标准化知识:早产儿视网膜病变和血氧饱和度案例研究

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The CRoss Industry Standard Process for Temporal Data Mining (CRISP-TDM) that supports physiological stream temporal data mining and CRISP-DM0 that supports null hypothesis driven confirmatory data mining in combination was proposed by prior research. This combined CRISP-TDM0 is utilised as the standardised approach to managing, reporting and performing retrospective clinical research and is designed to solve the limitation in knowledge discovery amongst physiological data streams [1]. The temporal abstractions (TA) of high fidelity blood oxygenation saturation (SpO2) levels of nine premature neonates are analysed using data collected by the Artemis Platform that complies with the Big Data concept [2] and correlated with Retinopathy of Prematurity (ROP) data. The hourly SpO2, TA pattern visualisation manifested three clusters and this is further supported by mathematical review of time percentage spent in target, below and over oxygenation. Clustering based on ROP stage and gestational age identified probable association within these three clusters. However known risk factors showed no association with ROP.
机译:结合先前的研究,提出了支持生理流时间数据挖掘的CRoss时间数据挖掘行业标准过程(CRISP-TDM)和支持空假设驱动的确认数据挖掘的CRISP-DM0。这种组合的CRISP-TDM0被用作管理,报告和进行回顾性临床研究的标准化方法,旨在解决生理数据流中知识发现的局限性[1]。使用符合大数据概念[2]且与早产儿视网膜病变(ROP)数据相关的Artemis平台收集的数据,分析了九名早产儿的高保真血液氧饱和度(SpO2)水平的时间抽象(TA)。每小时的SpO 2 ,TA模式可视化显示了三个簇,数学上检查了目标,低于和高于氧化的时间百分比进一步支持了这一点。基于ROP阶段和胎龄的聚类确定了这三个聚类中的可能关联。但是,已知的危险因素与ROP无关。

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