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The Templates that comprise the Radiopharmaceutical Radiation Dose SR are interconnected as in Figure A-17.
This Template defines a container (the root) with subsidiary Content Items, each of which corresponds to a single Radiopharmaceutical Administration Dose event entry. There is a defined recording observer (the system and/or person responsible for recording the assay of the radiopharmaceutical, and the person administered the radiopharmaceutical). Multiple Radiopharmaceutical Radiation Dose objects may be created for one study. Radiopharmaceutical Start DateTime in TID 10022 “Radiopharmaceutical Administration Event Data” will convey the order of administrations.
Table TID 10021. Radiopharmaceutical Radiation Dose
DICOM PS3.16 2024e - Content Mapping Resource |
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