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DICOM PS3.3 2020a - Information Object Definitions​

Page 361​

A.49.3 RT Ion Plan IOD Modules​

Table A.49-1 identifies and defines the Modules that comprise this IOD. Modules listed are either mandatory or optional as specified​ in PS3.4. Mandatory Modules contain Attributes that are included in all SOP Instances employing this IOD.​

Table A.49-1. RT Ion Plan 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​

Frame of​

Frame of Reference​

C.7.4.1​

M​

Reference​

 

 

 

Equipment​

General Equipment​

C.7.5.1​

M​

Plan​

RT General Plan​

C.8.8.9​

M​

 

RT Prescription​

C.8.8.10​

U​

 

RT Ion Tolerance Tables​

C.8.8.24​

U​

 

RT Patient Setup​

C.8.8.12​

U​

 

RT Fraction Scheme​

C.8.8.13​

U​

 

RT Ion Beams​

C.8.8.25​

C - Required if RT Fraction​

 

 

 

Scheme Module is included and​

 

 

 

Number of Beams (300A,0080) is​

 

 

 

greater than zero for one or more​

 

 

 

fraction groups​

 

Approval​

C.8.8.16​

U​

 

General Reference​

C.12.4​

U​

 

SOP Common​

C.12.1​

M​

 

Common Instance Reference​

C.12.2​

U​

A.50 RT Ion Beams Treatment Record IOD​

A.50.1 RT Ion Beams Treatment Record IOD Description​

The Radiotherapy Ion Beams Treatment Record IOD (RT Ion Beams Treatment Record IOD) addresses the requirements for transfer​ of treatment session reports generated by a treatment verification system during a course of Ion beam treatment, with optional cumu-​ lative summary information. It may also be used for transfer of treatment information during delivery.​

A.50.2 RT Ion 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.50.3 RT Ion Beams Treatment Record IOD Modules​

Table A.50-1 identifies and defines the Modules that comprise this IOD. Modules listed are either mandatory or optional as specified​ in PS3.4. Mandatory Modules contain Attributes that are included in all SOP Instances employing this IOD.​

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Page 362​ DICOM PS3.3 2020a - Information Object Definitions​

Table A.50-1. RT Ion 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​

 

Clinical Trial Study​

C.7.2.3​

U​

 

Patient Study​

C.7.2.2​

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 Ion Beams Session Record​

C.8.8.26​

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​

A.51 Segmentation IOD​

A.51.1 Segmentation IOD Description​

The Segmentation Information Object Definition (IOD) specifies a multi-frame image representing a classification of pixels in one or​ more referenced images. Segmentations are either binary or fractional. If the referenced images have a defined Frame of Reference,​ the segmentation instance shall have the same Frame of Reference and is not required to have the same spatial sampling or extent​ as the referenced images. If the referenced image does not have a defined Frame of Reference, the segmentation instance shall​ have the same spatial sampling and extent as the referenced image.​

The Segmentation IOD does not include the full set of acquisition parameters of the referenced images, e.g., cardiac phase. An ap-​ plication rendering or processing the segmentation may need to access the referenced images for such information.​

A.51.2 Segmentation 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.51.3 Segmentation IOD Module Table​

Table A.51-1 specifies the Modules of the Segmentation IOD.​

Table A.51-1. Segmentation 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​

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DICOM PS3.3 2020a - Information Object Definitions​

Page 363​

IE​

Module​

Reference​

Usage​

 

 

Clinical Trial Study​

C.7.2.3​

U​

 

Series​

General Series​

C.7.3.1​

M​

 

 

Segmentation Series​

C.8.20.1​

M​

 

 

Clinical Trial Series​

C.7.3.2​

U​

 

Frame of​

Frame of Reference​

C.7.4.1​

C - Required if Derivation Image​

Reference​

 

 

Functional Group (C.7.6.16.2.6) is not​

 

 

 

present. May be present otherwise.​

Equipment​ General Equipment​

C.7.5.1​

M​

 

 

Enhanced General Equipment​

C.7.5.2​

M​

 

Image​

General Image​

C.7.6.1​

M​

 

 

General Reference​

C.12.4​

U​

 

 

Image Pixel​

C.7.6.3​

M​

 

 

Segmentation Image​

C.8.20.2​

M​

 

 

Multi-frame Functional Groups​

C.7.6.16​

M​

 

 

Multi-frame Dimension​

C.7.6.17​

M​

 

 

Specimen​

C.7.6.22​

U​

 

 

Common Instance Reference​

C.12.2​

C - Required if Derivation Image​

 

 

 

Functional Group (C.7.6.16.2.6) is​

 

 

 

present.​

 

 

SOP Common​

C.12.1​

M​

 

 

Frame Extraction​

C.12.3​

C - Required if the SOP Instance was​

 

 

 

created in response to a Frame-Level​

 

 

 

retrieve request​

 

Note​

The Specimen Identification Module was previously included in this IOD but has been retired, and its functionality replaced​ by the Specimen Module. See PS3.3-2008.​

A.51.4 Segmentation IOD Content Constraints​

The VOI LUT Module shall not be present.​

The Modality LUT Module shall not be present.​

The Overlay Plane Module shall not be present.​

Pixel Padding Value (0028,0120) shall not be present.​

The Defined CID for Purpose of Reference Code Sequence (0040,A170) within Source Instance Sequence (0042,0013) in the Gen-​ eral Reference Module shall be CID 7019 “Segmentation Non-Image Source Purposes of Reference”.​

A.51.5 Segmentation Functional Groups​

TableA.51-2specifiestheuseoftheFunctionalGroupMacrosusedintheMulti-frameFunctionalGroupsModulefortheSegmentation​

IOD.​

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Page 364​ DICOM PS3.3 2020a - Information Object Definitions​

Table A.51-2. Segmentation Functional Group Macros​

Functional Group Macro​

Section​

Usage​

Pixel Measures​

C.7.6.16.2.1​

C - Required if Derivation Image Functional Group (C.7.6.16.2.6) is not present​

 

 

 

andtheFrameofReferenceisdefinedinthepatient-relativeReferenceCoordinate​

 

 

 

System. May be present otherwise if the Frame of Reference is defined in the​

 

 

 

patient-relative Reference Coordinate System. See Section A.51.5.1​

Plane Position (Patient)​

C.7.6.16.2.3​

C - Required if Derivation Image Functional Group (C.7.6.16.2.6) is not present​

 

 

 

andtheFrameofReferenceisdefinedinthepatient-relativeReferenceCoordinate​

 

 

 

System. May be present otherwise if the Frame of Reference is defined in the​

 

 

 

patient-relative Reference Coordinate System. See Section A.51.5.1​

Plane Orientation (Patient)​C.7.6.16.2.4​

C - Required if Derivation Image Functional Group (C.7.6.16.2.6) is not present.​

 

 

 

May be present otherwise. See Section A.51.5.1​

Plane Position (Slide)​

C.8.12.6.1​

C - Required if Derivation Image Functional Group (C.7.6.16.2.6) is not present​

 

 

 

and the Frame of Reference is defined in the Slide Coordinate System. May be​

 

 

 

present otherwise if the Frame of Reference is defined in the Slide Coordinate​

 

 

 

System. See Section A.51.5.1.​

Derivation Image​

C.7.6.16.2.6​

C - Required if Pixel Measures (C.7.6.16.2.1) or either Plane Position (Patient)​

 

 

 

(C.7.6.16.2.3) or Plane Orientation (Patient) (C.7.6.16.2.4) (if the Frame of​

 

 

 

Reference is defined in the patient-relative Reference Coordinate System), or​

 

 

 

Plane Position (Slide) (C.8.12.6.1) (if the Frame of Reference is defined in the​

 

 

 

Slide Coordinate System) Functional Groups are not present. May be present​

 

 

 

otherwise. See Section A.51.5.1​

Frame Content​

C.7.6.16.2.2​

M​

Segmentation​

C.8.20.3.1​

M​

A.51.5.1 Segmentation Functional Groups Description​

When a Frame of Reference UID is present the segment shall be specified within that coordinate system, using the Pixel Measures​ and either the Plane Position (Patient) and Plane Orientation (Patient), or the Plane Position (Slide) Functional Groups. Since this​ defines the spatial relationship of the segment, the size of the segmentation frames need not be the same size, or resolution, as the​ image data used to generate the segment data. The Derivation Image Functional Group may also be present, to specify on which​ images the segmentation was actually performed (since there may be others in the same Frame of Reference that are spatially co-​ located, but were not used to perform the segmentation).​

If the Frame of Reference UID is not present, each pixel of the segmentation shall correspond to a pixel in a referenced image, using​ the Derivation Image Functional Group. Hence, the rows and columns of each referenced image will match the segmentation image.​ If both the Frame of Reference UID and the Derivation Image Functional Group are present, the segmentation and referenced image​ pixels need not correspond.​

The value of Purpose of Reference Sequence (0040,A170) in the Derivation Image Functional Group Macro shall be (121322, DCM,​ "Source Image for Image Processing Operation"). The value of Derivation Code Sequence (0008,9215) shall be (113076, DCM,​ "Segmentation").​

Note​

Non-image source instances used during segmentation, such as real world value maps, can be described in the top level​ Data Set in the Source Instance Sequence (0042,0013) of the General Reference Module and are implied to have been​ used for the derivation of all frames. I.e., there is no mechanism for selectively specifying on a per-frame basis which non-​ image instances were used. Real World Value Map instances already contain a means of selectively applying different scale​ factors to different frames.​

A.52 Ophthalmic Tomography Image IOD​

ThisSectiondefinesanInformationObjecttobeusedwithopticalophthalmictomographicimagingdevices,includingopticalcoherence​ scanners and confocal scanning laser ophthalmoscopes, but excluding ophthalmic ultrasound devices.​

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DICOM PS3.3 2020a - Information Object Definitions​

Page 365​

A.52.1 Ophthalmic Tomography Image IOD Description​

The Ophthalmic Tomography Image IOD specifies a single-frame or a multi-frame image acquired on an Ophthalmic Tomography​ modality. This IOD can be used to encode both single and multi-frame ophthalmic images.​

A.52.2 Ophthalmic Tomography 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.52.3 Ophthalmic Tomography Image IOD Modules​

Table A.52.3-1. Ophthalmic Tomography Image IOD Modules​

IE​

Module​

Reference​

Patient​

Patient​

C.7.1.1​

 

Clinical Trial Subject​

C.7.1.3​

Study​

General Study​

C.7.2.1​

 

Patient Study​

C.7.2.2​

 

Clinical Trial Study​

C.7.2.3​

Series​

General Series​

C.7.3.1​

 

Clinical Trial Series​

C.7.3.2​

 

Ophthalmic Tomography Series​

C.8.17.6​

Frame of​ Frame of Reference​

C.7.4.1​

Reference​

 

Synchronization​

C.7.4.2​

Equipment​General Equipment​

C.7.5.1​

Enhanced General Equipment​

C.7.5.2​

Image​ Image Pixel​

C.7.6.3​

Enhanced Contrast/Bolus​

C.7.6.4b​

Multi-frame Functional Groups​

C.7.6.16​

Multi-frame Dimension​

C.7.6.17​

Acquisition Context​

C.7.6.14​

Cardiac Synchronization​

C.7.6.18.1​

Ophthalmic Tomography Image​

C.8.17.7​

Ophthalmic Tomography Acquisition​

C.8.17.8​

Parameters​

 

Ophthalmic Tomography Parameters​

C.8.17.9​

Ocular Region Imaged​

C.8.17.5​

SOP Common​

C.12.1​

Common Instance Reference​

C.12.2​

Frame Extraction​

C.12.3​

Usage​

M​

U​

M​

U​

U​

M​

U​

M​

C - Required if Ophthalmic Photography​ Reference Image available or if​ Ophthalmic Volumetric Properties Flag​ (0022,1622) is YES. May be present​ otherwise.​

C - Required if Ophthalmic Photography​ Reference Image available​

M​

M​

M​

C-Requiredifcontrastwasadministered​

M​

M​

M​

C - Required if cardiac synchronization​ was used​

M​ M​

M​

M​

M​

U​

C - Required if the SOP Instance was​ created in response to a Frame-Level​ retrieve request​

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