A.27.2 Digital Mammography X-Ray Image IOD Module Table


IE Module Reference Usage
Patient Patient C.7.1.1 M
Clinical Trial Subject C.7.1.3 U
Study General Study C.7.2.1 M
Patient Study C.7.2.2 U
Clinical Trial Study C.7.2.3 U
Series General Series C.7.3.1 M
Clinical Trial Series C.7.3.2 U
DX Series C.8.11.1 M
Mammography Series C.8.11.6 M
Frame of Reference Frame of Reference C.7.4.1 C - Required if multiple images are obtained without releasing breast compression
Equipment General Equipment C.7.5.1 M
Image General Image C.7.6.1 M
Image Pixel C.7.6.3 M
Contrast/Bolus C.7.6.4 U
Display Shutter C.7.6.11 U
Device C.7.6.12 U
Intervention C.7.6.13 U
Specimen C.7.6.22 U
DX Anatomy Imaged C.8.11.2 M
DX Image C.8.11.3 M
DX Detector C.8.11.4 M
X-Ray Collimator C.8.7.3 U
DX Positioning C.8.11.5 U
X-Ray Tomo Acquisition C.8.7.7 U
X-Ray Acquisition Dose C.8.7.8 U
X-Ray Generation C.8.7.9 U
X-Ray Filtration C.8.7.10 U
X-Ray Grid C.8.7.11 U
Mammography Image C.8.11.7 M
Overlay Plane C.9.2 C - Required if graphic annotation is present - See A.27.3
VOI LUT C.11.2 C - Required if Presentation Intent Type (0008,0068) is FOR PRESENTATION. Shall not be present otherwise.
Image Histogram C.11.5 U
Acquisition Context C.7.6.14 M
SOP Common C.12.1 M

Notes: 1. The Curve Module was previously included in this IOD but has been retired. See PS 3.3 2004.

2. The Specimen Identification Module was previously included in this IOD but has been retired, and its functionality replaced by the Specimen Module. See PS 3.3-2008.