Материал: part03

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Page 256​

DICOM PS3.3 2020a - Information Object Definitions​

A.27.3 Digital Mammography X-Ray Image IOD Module Table​

Table A.27-1 specifies the Modules of the Digital Mammography X-Ray Image IOD.​

Table A.27-1. Digital Mammography X-Ray 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​

 

DX Series​

C.8.11.1​

M​

 

Mammography Series​

C.8.11.6​

M​

Frame of​

Frame of Reference​

C.7.4.1​

C - Required if multiple images are​

Reference​

 

obtained without releasing breast​

 

 

 

compression​

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​

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 Tomography 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 Section 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​

- Standard -​

 

DICOM PS3.3 2020a - Information Object Definitions​

Page 257​

IE​

Module​

Reference​

Usage​

 

Acquisition Context​

C.7.6.14​

M​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

Note​

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

2.​TheSpecimenIdentificationModulewaspreviouslyincludedinthisIODbuthasbeenretired,anditsfunctionalityreplaced​ by the Specimen Module. See PS3.3-2008.​

A.27.4 Overlay Plane Module​

If the Overlay Plane Module is present, any Overlays defined in that Module shall store the overlay data in Overlay Data (60xx,3000),​ and not any unused high bits in Pixel Data (7FE0,0010).​

A.28 Digital Intra-Oral X-Ray Image IOD​

A.28.1 Digital Intra-Oral X-Ray Image IOD Description​

The Digital Intra-Oral X-Ray Image Information Object Definition specifies an image that has been created by an intra-oral projection​ radiography imaging device.​

Note​

It meets all of the requirements of the DX IOD in Section A.26 in addition to those specified in this section.​

The Digital Intra-Oral X-Ray Image IOD is used in two SOP Classes as defined in PS3.4 Storage Service Class, a SOP Class for​ storageofimagesintendedforpresentation,andaSOPClassforstorageofimagesintendedforfurtherprocessingbeforepresentation.​ These are distinguished by their SOP Class UID and by the Enumerated Value of the mandatory Attribute in the DX Series Module,​ Presentation Intent Type (0008,0068).​

A.28.2 Digital Intra-Oral X-Ray 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.28.3 Digital Intra-Oral X-Ray Image IOD Module Table​

Table A.28-1 specifies the Modules of the Digital Intra-Oral X-Ray Image IOD.​

Table A.28-1. Digital Intra-Oral X-Ray 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​

 

DX Series​

C.8.11.1​

M​

 

Intra-Oral Series​

C.8.11.8​

M​

- Standard -​

Page 258​

DICOM PS3.3 2020a - Information Object Definitions​

 

IE​

Module​

Reference​

Usage​

Frame of​

Frame of Reference​

C.7.4.1​

U​

Reference​

 

 

 

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​

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 Tomography 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​

 

Intra-Oral Image​

C.8.11.9​

M​

 

Overlay Plane​

C.9.2​

C - Required if graphic​

 

 

 

annotation is present - See​

 

 

 

Section A.28.3​

 

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​

 

Common Instance Reference​

C.12.2​

U​

Note​

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

2.​TheSpecimenIdentificationModulewaspreviouslyincludedinthisIODbuthasbeenretired,anditsfunctionalityreplaced​ by the Specimen Module. See PS3.3-2008.​

A.28.4 Overlay Plane Module​

If the Overlay Plane Module is present, any Overlays defined in that Module shall store the overlay data in Overlay Data (60xx,3000),​ and not any unused high bits in Pixel Data (7FE0,0010).​

- Standard -​

DICOM PS3.3 2020a - Information Object Definitions​

Page 259​

A.29 RT Beams Treatment Record IOD​

A.29.1 RT Beams Treatment Record IOD Description​

The focus for this Radiotherapy Beams Treatment Record IOD (RT Beams Treatment Record IOD) is to address the requirements​ for transfer of treatment session reports generated by a treatment verification system during a course of external beam treatment,​ with optional cumulative summary information. It may also be used for transfer of treatment information during delivery.​

A.29.2 RT Beams Treatment Record IOD Entity-Relationship Model​

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

A.29.3 RT Beams Treatment Record IOD Module Table​

Table A.29.3-1 specifies the Modules of the RT Beams Treatment Record IOD.​

Table A.29.3-1. RT Beams Treatment Record 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​

RT Series​

C.8.8.1​

M​

 

Clinical Trial Series​

C.7.3.2​

U​

Equipment​

General Equipment​

C.7.5.1​

M​

Treatment​

RT General Treatment Record​

C.8.8.17​

M​

Record​

RT Patient Setup​

C.8.8.12​

U​

 

 

RT Treatment Machine Record​

C.8.8.18​

M​

 

Measured Dose Reference Record​

C.8.8.19​

U​

 

Calculated Dose Reference Record​

C.8.8.20​

U​

 

RT Beams Session Record​

C.8.8.21​

M​

 

RT Treatment Summary Record​

C.8.8.23​

U​

 

General Reference​

C.12.4​

U​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

Note​

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

A.30 RT Brachy Treatment Record IOD​

A.30.1 RT Brachy Treatment Record IOD Description​

The focus for this Radiotherapy Brachy Treatment Record IOD (RT Brachy Treatment Record IOD) is to address the requirements​ for transfer of treatment session reports generated by a treatment verification system during a course of Brachytherapy treatment,​ with optional cumulative summary information. It may also be used for transfer of treatment information during delivery.​

- Standard -​

Page 260​

DICOM PS3.3 2020a - Information Object Definitions​

A.30.2 RT Brachy Treatment Record IOD Entity-Relationship Model​

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

A.30.3 RT Brachy Treatment Record IOD Module Table​

Table A.30.3-1 specifies the Modules of the RT Brachy Treatment Record IOD.​

Table A.30.3-1. RT Brachy Treatment Record 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​

RT Series​

C.8.8.1​

M​

 

Clinical Trial Series​

C.7.3.2​

U​

Equipment​

General Equipment​

C.7.5.1​

M​

Treatment​

RT General Treatment Record​

C.8.8.17​

M​

Record​

RT Patient Setup​

C.8.8.12​

U​

 

 

RT Treatment Machine Record​

C.8.8.18​

M​

 

Measured Dose Reference Record​

C.8.8.19​

U​

 

Calculated Dose Reference Record​

C.8.8.20​

U​

 

RT Brachy Session Record​

C.8.8.22​

M​

 

RT Treatment Summary Record​

C.8.8.23​

U​

 

General Reference​

C.12.4​

U​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

Note​

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

A.31 RT Treatment Summary Record IOD​

A.31.1 RT Treatment Summary Record IOD Description​

ThefocusforthisRadiotherapyTreatmentSummaryRecordIOD(RTTreatmentSummaryRecordIOD)istoaddresstherequirements​ for transfer of cumulative summary information, normally generated at the completion of a course of treatment.​

A.31.2 RT Treatment Summary Record IOD Entity-Relationship Model​

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

A.31.3 RT Treatment Summary Record IOD Module Table​

Table A.31.3-1 specifies the Modules of the RT Treatment Summary Record IOD.​

- Standard -​

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