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Proceedings Paper

Design requirements for DICOM patient, study, and results management
Author(s): Steven L. Fritz; Steven R. Roys; Sunita Munjal
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Paper Abstract

The DICOM services for patient, study and results management are recent additions to the ACR-NEMA standard. Commercially available RIS systems and the HL7 standard do not match the DICOM state transition models for these management tasks well. The purpose of this effect is to model the interaction between a DICOM-compliant PACS and an RIS, based on the DICOM management models, to provide a basis for standards-based PACS-RIS integration. We report on a state transition model for a RIS that correlates both to the HL7 trigger events usually supported and to the major features of the various state transition models incorporated in DICOM.

Paper Details

Date Published: 1 May 1996
PDF: 11 pages
Proc. SPIE 2711, Medical Imaging 1996: PACS Design and Evaluation: Engineering and Clinical Issues, (1 May 1996); doi: 10.1117/12.239237
Show Author Affiliations
Steven L. Fritz, Univ. of Maryland/Baltimore (United States)
Steven R. Roys, Univ. of Maryland/Baltimore (United States)
Sunita Munjal, Univ. of Maryland/Baltimore (United States)


Published in SPIE Proceedings Vol. 2711:
Medical Imaging 1996: PACS Design and Evaluation: Engineering and Clinical Issues
R. Gilbert Jost; Samuel J. Dwyer, Editor(s)

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