慢性肾脏疾病(CKD)的数据建模和可视化:迈向个体化医疗的一步。

Norman Poh, Simon de Lusignan
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引用次数: 10

摘要

背景:个性化医疗包括定制管理以满足患者的需求。慢性肾脏疾病(CKD)在人群水平上,随着年龄的增长,肾功能稳步下降;进行性慢性肾病被定义为明显偏离这一下降速率。目的:建立单个患者肾功能的可视化,显示其肾功能和其他重要协变的平滑趋势线和置信区间。方法:应用生物识别技术开发的先进模式识别技术,收集常规收集的初级保健数据,这些数据是慢性肾脏疾病质量改善(QICKD)试验的一部分。我们绘制了趋势线,使用回归和个体患者的置信区间。我们还创建了一种可视化方法,可以将肾功能与其他六种协变进行比较:糖化血红蛋白(HbA1c)、体重指数(BMI)、血压和治疗。这些产出由一个专家小组审查。结果:成功提取并显示数据。我们证明估计的肾小球滤过(eGFR)是一个嘈杂的变量,并表明许多人将超过“进行性CKD”标准。我们创建了一个可以很容易自动化的数据显示。我们的专家小组对这种显示器很满意,但在临床测试之前需要进行广泛的开发。结论:利用生物识别技术开发的数据可视化方法来查看CKD数据是可行的。“进行性CKD”的定义标准需要重新审视,因为许多患者超过了标准。需要进一步的开发工作和测试来探索这种类型的数据建模和可视化是否可以改善患者护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Data-modelling and visualisation in chronic kidney disease (CKD): a step towards personalised medicine.

Background: Personalised medicine involves customising management to meet patients' needs. In chronic kidney disease (CKD) at the population level there is steady decline in renal function with increasing age; and progressive CKD has been defined as marked variation from this rate of decline.

Objective: To create visualisations of individual patient's renal function and display smoothed trend lines and confidence intervals for their renal function and other important co-variants.

Method: Applying advanced pattern recognition techniques developed in biometrics to routinely collected primary care data collected as part of the Quality Improvement in Chronic Kidney Disease (QICKD) trial. We plotted trend lines, using regression, and confidence intervals for individual patients. We also created a visualisation which allowed renal function to be compared with six other covariants: glycated haemoglobin (HbA1c), body mass index (BMI), BP, and therapy. The outputs were reviewed by an expert panel.

Results: We successfully extracted and displayed data. We demonstrated that estimated glomerular filtration (eGFR) is a noisy variable, and showed that a large number of people would exceed the 'progressive CKD' criteria. We created a data display that could be readily automated. This display was well received by our expert panel but requires extensive development before testing in a clinical setting.

Conclusions: It is feasible to utilise data visualisation methods developed in biometrics to look at CKD data. The criteria for defining 'progressive CKD' need revisiting, as many patients exceed them. Further development work and testing is needed to explore whether this type of data modelling and visualisation might improve patient care.

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