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Genetic Testing Information Standardization in HL7 CDA and ISO13606

机译:HL7 CDA和ISO13606中的遗传测试信息标准化

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Communicating genetic testing reports of a patient in a se-mantically interoperable way remains difficult. Most of the information is stored as non-communicable documents which cannot automatically be processed. The objective of the project was to obtain semantically interoperable genetic testing reports which could be used not only for communication purposes but also for secondary uses, for example clinical trials or clinical decision support. This work describes the first part of the project, the modeling of genetic information reports using EHR standards. We used the Implementation Guide for CDA R2 Genetic Testing Report (GTR) as a basis for modeling the archetypes for both HL7 CDA and CEN/ISO 13606. This approach was validated with the information included in Usher Syndrome reports available at ISS-La Fe. The result of this work were three archetypes following ISOI3606 and three archetypes following HL7 CDA model which contained all the information available in both Usher syndrome genetic testing reports and the implementation guide significant parts.
机译:以SE-SE-SERICLY ITEROMETERATION的方式沟通患者的遗传测试报告仍然困难。大多数信息存储为无法自动处理的非传染文档。该项目的目的是获得语义可互操作的遗传检测报告,该检验报告不仅可以用于沟通目的,还可以用于二次用途,例如临床试验或临床决策支持。这项工作描述了项目的第一部分,使用EHR标准进行遗传信息报告的建模。我们使用CDA R2遗传检测报告(GTR)的实施指南是为HL7 CDA和CEN / ISO 13606建模原型的基础。通过ISS-LA FE的亚瑟综合征报告中包含的信息验证了这种方法。这项工作的结果是ISOI3606之后的三个原型,并且在HL7 CDA模型之后的三个原型包含所有可用的亚瑟综合征遗传检测报告和实施指南的所有信息。

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