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ISO 15189:2012 Management Requirements for Cytopathology Laboratory Information Systems

机译:ISO 15189:2012细胞病理实验室信息系统管理要求

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摘要

During the last decade, there is an increasing need for quality improvement of medical laboratories via the use of quality related standards. Recently regulatory bodies suggest and sometimes enforce the application of ISO 15189, which is designed especially for medical laboratories. Despite the standard does oblige the application of Laboratory Information Systems (LISs), it is evident that without a US it is difficult for laboratories to operate efficiently. Modern cytopathology laboratories form complex systems composed of a multidisciplinaiy human team coupled with medical modalities and capabilities. Hopefully, such laboratories have well standardized and defined workflow. The adoption of the standard, creates numerous management requirements, introduces new functions and associated overhead. In this paper, we present design and implementation issues of an enhanced LIS to support ISO 15189 in a cytopathology laboratoiy. The US designed around ISO 15189 management requirements can improve, enhance andfacilitate the standard application and adoption.
机译:在过去的十年中,越来越需要通过使用质量相关标准来改善医学实验室的质量。最近,监管机构建议并有时强制执行ISO 15189的应用,该ISO 15189专为医学实验室而设计。尽管该标准确实要求实验室信息系统(LIS)的应用,但是很明显,没有美国,实验室就很难有效地运作。现代细胞病理学实验室形成了一个由多学科的人类团队以及医疗模式和能力组成的复杂系统。希望这些实验室具有良好的标准化和定义的工作流程。该标准的采用产生了许多管理要求,引入了新功能和相关的开销。在本文中,我们提出了增强的LIS的设计和实现问题,以在细胞病理学实验室中支持ISO 15189。美国按照ISO 15189管理要求设计,可以改善,增强和促进标准的应用和采用。

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