Achieving Safe DICOM Software in Medical Devices

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This paper reports on an investigation on how to produce a reliable software component to extract critical information from DICOM files. The component shall manipulate safety-critical medical information, i.e. patient demographics and data specific to radiotherapy treatments including radiation target volumes and doses intensity. Handling such sensitive data can potentially lead to medical errors, and threaten the health of patients. Hence, guaranteeing reliability and safety is an essential part of the development process. Solutions for developing the component from scratch or reusing all or parts of existing systems and libraries will be evaluated and compared. The resulting component will be tested to verify that it satisfies its reliability requirements. Subsequently, the component is to be integrated within an innovating radiotherapy positioning system developed by a Swedish start-up, Micropos. While remaining objective, I will examine how the outcomes of my practical cases converge with what is discovered in the literature: a massive lack of conformance to DICOM exists among medical systems that produce DICOM files. Endeavors by the manufacturers developing medical devices are still required to universalize the interoperability proclaimed by the creators of the standard. Despite that imperfect context, a reliable software component was achieved and is presented in this report.

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DICOM, Medical Device, Safety-Critical Systems, Software Standards

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