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Page 226​

DICOM PS3.3 2020a - Information Object Definitions​

Note​

Digital Luminescence Radiography is an equivalent term for computed Radiography.​

A.2.2 CR Image IOD Entity-Relationship Model​

This IOD uses the E-R Model in Section A.1.2, with only the Image IE below the Series IE. The Frame of Reference IE is not a com-​ ponent of this IOD.​

A.2.3 CR Image IOD Module Table​

Table A.2-1 specifies the Modules of the CR Image IOD.​

Table A.2-1. CR Image IOD Modules​

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​

 

CR Series​

C.8.1.1​

M​

 

Clinical Trial Series​

C.7.3.2​

U​

Equipment​General Equipment​

C.7.5.1​

M​

Image​

General Image​

C.7.6.1​

M​

 

General Reference​

C.12.4​

U​

 

Image Pixel​

C.7.6.3​

M​

 

Contrast/Bolus​

C.7.6.4​

C - Required if contrast​

 

 

 

media was used in this​

 

 

 

image​

 

Display Shutter​

C.7.6.11​

U​

 

Device​

C.7.6.12​

U​

 

Specimen​

C.7.6.22​

U​

 

CR Image​

C.8.1.2​

M​

 

Overlay Plane​

C.9.2​

U​

 

Modality LUT​

C.11.1​

U​

 

VOI LUT​

C.11.2​

U​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

Note​

The Curve Module (Retired) was previously included in the Image IE for this IOD but has been retired. See PS3.3-2004.​

A.3 CT Image IOD​

A.3.1 CT Image IOD Description​

The Computed Tomography (CT) Image Information Object Definition (IOD) specifies an image that has been created by a computed​ tomography imaging device.​

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DICOM PS3.3 2020a - Information Object Definitions​

Page 227​

A.3.2 CT Image IOD Entity-Relationship Model​

This IOD uses the E-R Model in Section A.1.2, with only the Image IE below the Series IE.​

A.3.3 CT Image IOD Module Table​

Table A.3-1 specifies the Modules of the CT Image IOD.​

Table A.3-1. CT Image IOD Modules​

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​

Frame of​

Frame of Reference​

C.7.4.1​

M​

Reference​

 

 

 

Equipment​

General Equipment​

C.7.5.1​

M​

Image​

General Image​

C.7.6.1​

M​

 

General Reference​

C.12.4​

U​

 

Image Plane​

C.7.6.2​

M​

 

Image Pixel​

C.7.6.3​

M​

 

Contrast/Bolus​

C.7.6.4​

C - Required if contrast media​

 

 

 

was used in this image​

 

Device​

C.7.6.12​

U​

 

Specimen​

C.7.6.22​

U​

 

CT Image​

C.8.2.1​

M​

 

Multi-energy CT Image​

C.8.2.2​

C - Required if Multi-energy CT​

 

 

 

Acquisition (0018,9361) is YES.​

 

Overlay Plane​

C.9.2​

U​

 

VOI LUT​

C.11.2​

U​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

A.3.3.1 CT Image IOD Content Constraints​

If Multi-energy CT Acquisition (0018,9361) is YES the following constraints will apply:​

•​The Contrast/Bolus Module shall be present if contrast was administered even if images are processed to remove contrast inform-​ ation from the pixels, e.g. Virtual Non-Contrast images.​

•​The Real World Value Mapping Sequence (0040,9096) shall be present in the General Image Module.​

•​The Defined CID for Measurement Units Code Sequence (0040,08EA) in the Real World Value Mapping Sequence (0040,9096)​ is CID 301 “Multi-energy Material Units”.​

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DICOM PS3.3 2020a - Information Object Definitions​

A.4 MR Image IOD​

A.4.1 MR Image IOD Description​

The Magnetic Resonance (MR) Image Information Object Definition (IOD) specifies an image that has been created by a magnetic​ resonance imaging device.​

A.4.2 MR Image IOD Entity-Relationship Model​

This IOD uses the E-R Model in Section A.1.2, with only the Image IE below the Series IE.​

A.4.3 MR Image IOD Module Table​

Table A.4-1 specifies the Modules of the MR Image IOD.​

Table A.4-1. MR Image IOD Modules​

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​

Frame of​

Frame of Reference​

C.7.4.1​

M​

Reference​

 

 

 

Equipment​

General Equipment​

C.7.5.1​

M​

Image​

General Image​

C.7.6.1​

M​

 

General Reference​

C.12.4​

U​

 

Image Plane​

C.7.6.2​

M​

 

Image Pixel​

C.7.6.3​

M​

 

Contrast/Bolus​

C.7.6.4​

C - Required if contrast​

 

 

 

media was used in this​

 

 

 

image​

 

Device​

C.7.6.12​

U​

 

Specimen​

C.7.6.22​

U​

 

MR Image​

C.8.3.1​

M​

 

Overlay Plane​

C.9.2​

U​

 

VOI LUT​

C.11.2​

U​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

A.5 Nuclear Medicine Image IOD​

A.5.1 NM Image IOD Description​

TheNuclearMedicine(NM)ImageInformationObjectDefinition(IOD)specifiesanimagethathasbeencreatedbyanuclearmedicine​ imaging device. This includes data created by external detection devices that create images of the distribution of administered radio-​ active materials in the body. Depending on the specific radio pharmaceutical administered and the particular imaging procedure per-​

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DICOM PS3.3 2020a - Information Object Definitions​

Page 229​

formed, problems involving changes in metabolism, function, or physiology can be investigated and various regional pathologies can​ be studied.​

A.5.2 NM Image IOD Entity-Relationship Model​

This IOD uses the E-R Model in Section A.1.2, with only the Image IE below the Series IE.​

A.5.3 NM Image IOD Module Table (Retired)​

This Section was defined in a previous version of the DICOM Standard. The Section is now retired.​

A.5.4 NM Image IOD Module Table​

Table A.5-1 specifies the Modules of the NM Image IOD.​

Table A.5-1. NM Image IOD Modules​

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​

 

NM/PET Patient Orientation​

C.8.4.6​

M​

Frame of​ Frame of Reference​

C.7.4.1​

U​

Reference​Synchronization​

C.7.4.2​

C - Required if time synchronization was​

 

 

 

applied​

Equipment​General Equipment​

C.7.5.1​

M​

Image​

General Image​

C.7.6.1​

M​

 

General Reference​

C.12.4​

U​

 

Image Pixel​

C.7.6.3​

M​

 

Acquisition Context​

C.7.6.14​

U - See Section A.5.4.1​

 

Device​

C.7.6.12​

U​

 

Specimen​

C.7.6.22​

U​

 

NM Image Pixel​

C.8.4.7​

M​

 

Multi-frame​

C.7.6.6​

M​

 

NM Multi-frame​

C.8.4.8​

M​

 

NM Image​

C.8.4.9​

M​

 

NM Isotope​

C.8.4.10​

M​

 

NM Detector​

C.8.4.11​

M​

 

NM TOMO Acquisition​

C.8.4.12​

C - Required if Image Type (0008,0008)​

 

 

 

Value 3 is TOMO, GATED TOMO, RECON​

 

 

 

TOMO or RECON GATED TOMO​

 

NM Multi-gated Acquisition​

C.8.4.13​

C - Required if Image Type (0008,0008)​

 

 

 

Value 3 is GATED, GATED TOMO, or​

 

 

 

RECON GATED TOMO​

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DICOM PS3.3 2020a - Information Object Definitions​

IE​

Module​

Reference​

Usage​

 

NM Phase​

C.8.4.14​

C - Required if Image Type (0008,0008)​

 

 

 

Value 3 is DYNAMIC​

 

NM Reconstruction​

C.8.4.15​

C - Required if Image Type (0008,0008)​

 

 

 

Value 3 is RECON TOMO or RECON​

 

 

 

GATED TOMO​

 

Overlay Plane​

C.9.2​

U​

 

Multi-frame Overlay​

C.9.3​

U​

 

VOI LUT​

C.11.2​

U​

 

ICC Profile​

C.11.15​

U​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

 

Frame Extraction​

C.12.3​

C - Required if the SOP Instance was​

 

 

 

created in response to a Frame-Level​

 

 

 

retrieve request​

Note​

The Curve Module (Retired) was previously included in the Image IE for this IOD but has been retired. See PS3.3-2004.​

A.5.4.1 Acquisition Context Module​

ForAcquisitionContextSequence(0040,0555)theDefinedTIDisTID3470“NM/PETAcquisitionContext”,whichincludesdescription​ of the cardiovascular rest or stress state.​

The Acquisition Context Sequence (0040,0555) shall always apply to all frames in the Image. Patient State shall always apply to all​ frames in the Image, therefore, neither Referenced Frame Numbers (0040,A136) nor Referenced Frame Number (0008,1160) shall​ be present.​

The Acquisition Context information may be entered during acquisition, or obtained from the Modality Worklist using information​ supplied in the Protocol Context, using TID 15101 “NM/PET Protocol Context”.​

A.6 Ultrasound Image IOD​

A.6.1 US Image IOD Description​

The Ultrasound (US) Image Information Object Definition specifies an image that has been created by an ultrasound imaging device.​

A.6.2 US Image IOD Entity-Relationship Model​

This IOD uses the E-R Model in Section A.1.2, with only the Image IE below the Series IE.​

A.6.3 US Image IOD Module Table (Retired)​

This Section was defined in a previous version of the DICOM Standard. The Section is now retired.​

A.6.4 US Image IOD Module Table​

Table A.6-1 specifies the Modules of the US Image IOD.​

Table A.6-1. US Image IOD Modules​

IE​

Module​

Reference​

Usage​

Patient​

Patient​

C.7.1.1​

M​

 

Clinical Trial Subject​

C.7.1.3​

U​

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