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基于关联规则挖掘方法推断药物与问题之间关联的验证。

Validation of an association rule mining-based method to infer associations between medications and problems.

出版信息

Appl Clin Inform. 2013 Mar 6;4(1):100-9. doi: 10.4338/ACI-2012-12-RA-0051. Print 2013.

Abstract

BACKGROUND

In a prior study, we developed methods for automatically identifying associations between medications and problems using association rule mining on a large clinical data warehouse and validated these methods at a single site which used a self-developed electronic health record.

OBJECTIVE

To demonstrate the generalizability of these methods by validating them at an external site.

METHODS

We received data on medications and problems for 263,597 patients from the University of Texas Health Science Center at Houston Faculty Practice, an ambulatory practice that uses the Allscripts Enterprise commercial electronic health record product. We then conducted association rule mining to identify associated pairs of medications and problems and characterized these associations with five measures of interestingness: support, confidence, chi-square, interest and conviction and compared the top-ranked pairs to a gold standard.

RESULTS

25,088 medication-problem pairs were identified that exceeded our confidence and support thresholds. An analysis of the top 500 pairs according to each measure of interestingness showed a high degree of accuracy for highly-ranked pairs.

CONCLUSION

The same technique was successfully employed at the University of Texas and accuracy was comparable to our previous results. Top associations included many medications that are highly specific for a particular problem as well as a large number of common, accurate medication-problem pairs that reflect practice patterns.

摘要

背景

在之前的研究中,我们开发了使用关联规则挖掘在大型临床数据仓库中自动识别药物和问题之间关联的方法,并在使用自行开发的电子病历的单个站点进行了验证。

目的

通过在外部站点进行验证来证明这些方法的通用性。

方法

我们从休斯顿大学健康科学中心的德克萨斯大学教职员工诊所收到了 263597 名患者的药物和问题数据,该诊所是一家使用 Allscripts Enterprise 商业电子病历产品的门诊实践。然后,我们进行了关联规则挖掘,以识别药物和问题的关联对,并使用五个有趣性衡量标准(支持度、置信度、卡方、兴趣度和可信度)来描述这些关联,然后将这些关联与黄金标准进行比较。

结果

确定了 25088 对超过我们置信度和支持度阈值的药物-问题对。根据每个有趣性衡量标准对前 500 对进行分析表明,排名较高的对具有高度准确性。

结论

该技术在德克萨斯大学成功应用,准确性与我们之前的结果相当。排名靠前的关联包括许多针对特定问题的高度特异性药物,以及大量反映实践模式的常见、准确的药物-问题对。

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