A.3.1 Header

Enhanced SR Information Object Definition (IOD) header relevant for TID 2000 as specified in DICOM PS 3.3. The contents of any module not covered by this transformation guideline will not be included in the generated CDA document.

Table A.3.1-1

DICOM Enhanced SR IOD Modules

IE Module Reference Usage Covered by this Transformation Guideline
Patient Patient C.7.1.1 M Yes
Clinical Trial Subject C.7.1.3 U No
Study General Study C.7.2.1 M Yes
Patient Study C.7.2.2 U No
Clinical Trial Study C.7.2.3 U No
Series SR Document Series C.17.1 M Yes
Clinical Trial Series C.7.3.2 U No
Equipment General Equipment C.7.5.1 M Yes
Document SR Document General C.17.2 M Yes
SR Document Content C.17.3 M Yes
SOP Common C.12.1 M Yes

DICOM SR Header Modules:

Refer to section 6.1 for details.

Patient Module

The patient module specifies the Attributes of the Patient that describe and identify the Patient who is the subject of a diagnostic Study. This Module contains Attributes of the patient that are needed for diagnostic interpretation of the Image and are common for all studies performed on the patient.

Clinical Trial Subject Module

The Clinical Trial Subject Module contains attributes that identify a Patient as a clinical trial Subject. This Annex does not provide mappings for this module since they are outside the scope of this transformation.

General Study Module

The General Study Module specifies the Attributes that describe and identify the Study performed upon the Patient.

Patient Study Module

The Patient Study Module defines the attributes that provide information about the Patient at the time the Study was performed. This Annex does not provide mappings for the module since they would need to be inserted in the content tree.

Clinical Trial Study Module

The Clinical Trial Study Module contains attributes that identify a Study in the context of a clinical trial. This Annex does not provide mappings for this module.

SR Document Series Module

The SR Document Series Module defines the Attributes of the SR Document Series. A Series of SR Documents may contain any number of SR Documents.

Clinical Trial Series Module

The Clinical Trial Series Module contains attributes that identify a Series in the context of a clinical trial. This Annex does not provide mappings for this module.

General Equipment Module

The General Equipment Module specifies the Attributes that identify and describe the piece of equipment that produced a Series of Composite Instances.

SR Document General Module

The SR Document General Module defines the general Attributes of an SR Document Instance. These Attributes identify the SR Document and provide context for the entire document.

SOP Common Module

The SOP Common Module defines the Attributes which are required for proper functioning and identification of the associated SOP Instances.

SR Document Content Module

The Attributes in this Module convey the content of an SR Document. It specifies the root content item and the content tree (refer to Figure 2 SR Document Structure).