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DICOM PS3.3 2020a - Information Object Definitions​ Page 351​

A.43.3 Stereometric Relationship IOD Modules​

Table A.43-1. Stereometric Relationship 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​

 

Stereometric Series​

C.8.18.1​

M​

Equipment​

General Equipment​

C.7.5.1​

M​

Stereometric​

Stereometric Relationship​

C.8.18.2​

M​

Relationship​

Common Instance Reference​

C.12.2​

M​

 

 

SOP Common​

C.12.1​

M​

Note​

The Specimen Identification Module was previously included in this IOD but has been retired. See PS3.3-2008.​

A.44 Hanging Protocol IOD​

A.44.1 Hanging Protocol IOD Description​

AHangingProtocolentityspecifiestheviewingpreferencesofaspecificuserorgroup,foraspecifictypeofStudy(Modality,Anatomy,​ Laterality combination, and optionally Procedure, and/or Reason), that may be exchanged between connecting devices that claim​ conformance to the DICOM Standard. The Hanging Protocol contains information about the Hanging Protocol, the creator, the type​ of Study it addresses, the type of image sets to display, the intended display environment, and the intended layout for the screen(s).​

A.44.2 Hanging Protocol IOD Entity-Relationship Model​

A Hanging Protocol is not related to other Information Entities of the DICOM real-world model, as it is not associated with a specific​ Patient. The E-R model for the Hanging Protocol IOD is shown in Figure A.44.2-1.​

Hanging

Protocol

IOD

Figure A.44.2-1. Hanging Protocol IOD E-R Model​

A.44.3 Hanging Protocol IOD Module Table​

Table A.44.3-1 lists the Modules that make up the Hanging Protocol IOD.​

Table A.44.3-1. Hanging Protocol IOD Modules​

IE​

Module​

Reference​

Usage​

Hanging​

SOP Common​

C.12.1​

M​

Protocol​

Hanging Protocol Definition​

C.23.1​

M​

 

Hanging Protocol Environment​

C.23.2​

M​

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Page 352​

DICOM PS3.3 2020a - Information Object Definitions​

 

IE​

Module​

Reference​

Usage​

 

Hanging Protocol Display​

C.23.3​

M​

A.45 Encapsulated Document IOD​

A.45.1 Encapsulated PDF IOD​

A.45.1.1 Encapsulated PDF IOD Description​

The Encapsulated PDF Information Object Definition (IOD) describes a PDF document that has been encapsulated within a DICOM​ Information Object.​

A.45.1.2 Encapsulated PDF Entity-Relationship Model​

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

A.45.1.3 Encapsulated PDF IOD Module Table​

Table A.45.1-1 specifies the Encapsulated PDF IOD Modules.​

Table A.45.1-1. Encapsulated PDF 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​

Encapsulated Document Series​

C.24.1​

M​

 

Clinical Trial Series​

C.7.3.2​

U​

Equipment​

General Equipment​

C.7.5.1​

M​

 

SC Equipment​

C.8.6.1​

M​

Encapsulated​

Encapsulated Document​

C.24.2​

M​

Document​

SOP Common​

C.12.1​

M​

 

Note​

The Specimen Identification Module was previously included in this IOD but has been retired. See PS3.3-2008.​

A.45.1.4 Encapsulated PDF IOD Content Constraints​

A.45.1.4.1 MIME Type of Encapsulated Document​

Enumerated Values:​

application/pdf​

A.45.2 Encapsulated CDA IOD​

A.45.2.1 Encapsulated CDA IOD Description​

The Encapsulated CDA Information Object Definition (IOD) describes an HL7 Clinical Document Architecture (CDA) document that​ has been encapsulated within a DICOM Information Object.​

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DICOM PS3.3 2020a - Information Object Definitions​

Page 353​

A.45.2.2 Encapsulated CDA Entity-Relationship Model​

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

A.45.2.3 Encapsulated CDA IOD Module Table​

Table A.45.2-1 specifies the Encapsulated CDA IOD Modules.​

Table A.45.2-1. Encapsulated CDA 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​

Encapsulated Document Series​

C.24.1​

M​

 

Clinical Trial Series​

C.7.3.2​

U​

Equipment​

General Equipment​

C.7.5.1​

M​

 

SC Equipment​

C.8.6.1​

M​

Encapsulated​

Encapsulated Document​

C.24.2​

M​

Document​

SOP Common​

C.12.1​

M​

 

A.45.2.4 Encapsulated CDA IOD Content Constraints​

Encapsulated Document (0042,0011) Attribute shall contain an HL7 CDA document of Release 2 or later. Any non-XML multimedia​ content shall be encoded in-line.​

Enumerated Values for MIME Type of Encapsulated Document (0042,0012):​

text/XML​

A.46 Real World Value Mapping IOD​

A.46.1 Real World Value Mapping IOD Description​

The Real World Value Mapping Information Object Definition specifies a mapping of the stored pixel values of referenced images into​ some Real World value in defined units. This allows the capture of retrospectively determined mappings, e.g., for values that cannot​ be determined at the time of image acquisition and encoding.​

Note​

A particular use case is mapping of PET pixel values to counts, concentration, or standardized uptake values (SUVs) nor-​ malized by one of several factors.​

A.46.2 Real World Value Mapping IOD Entity-Relationship Model​

ThisIODusestheE-RModelinSectionA.1.2,withonlytheRealWorldValueMappingIEbelowtheSeriesIE.TheFrameofReference​ IE is not a component of this IOD.​

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Page 354​ DICOM PS3.3 2020a - Information Object Definitions​

A.46.3 Real World Value Mapping IOD Modules​

Table A.46-1. Real World Value Mapping 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​

 

Real World Value Mapping Series​

C.25.1​

M​

Equipment​

General Equipment​

C.7.5.1​

M​

Real World Value​Real World Value Mapping​

C.25.2​

M​

Mapping​

Common Instance Reference​

C.12.2​

M​

 

 

SOP Common​

C.12.1​

M​

Note​

The Specimen Identification Module was previously included in this IOD but has been retired. See PS3.3-2008.​

A.47 Enhanced XA Image IOD​

A.47.1 Enhanced XA Image IOD Description​

This Section defines the enhanced Information Object for single plane X-Ray Angiographic Imaging that includes those Attributes​ and Information Objects necessary for the interchange of digital X-Ray Angiographic data. This includes images of the heart and all​ blood vessels.​

The enhanced XA IOD is also applicable to clinical areas other than angiography (e.g., Interventional Procedures, Myelography,​ Biopsy/Localization, and Neurology).​

Note​

1.​For the purpose of X-Ray Angiography (XA), this enhanced IOD can be used to encode a single-frame image, or a Cine​ Run, or a single multi-frame image with non-time related dimensions.​

2.​A typical Study might include all the images generated between the time a Patient gets on and gets off the procedure​ table. As several separable diagnostic or therapeutic processes may occur during a single Study (e.g., pre-intervention​ CA, left ventriculography, and post-intervention CA), a Series may be defined as comprising a set of images (single or​ multi-frame) associated with one such process within a Study.​

3.​This enhanced IOD can be used to encode a single plane acquisition, or one plane of a biplane acquisition.​

A.47.2 Enhanced XA 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.47.3 Enhanced XA Image IOD Module Table​

Table A.47-1 specifies the Modules of the Enhanced XA Image IOD.​

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DICOM PS3.3 2020a - Information Object Definitions​

Page 355​

Table A.47-1. Enhanced XA 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​

 

XA/XRF Series​

C.8.19.1​

 

Clinical Trial Series​

C.7.3.2​

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​

 

Mask​

C.7.6.10​

 

Device​

C.7.6.12​

 

Intervention​

C.7.6.13​

 

Acquisition Context​

C.7.6.14​

 

Multi-frame Functional Groups​

C.7.6.16​

 

Multi-frame Dimension​

C.7.6.17​

 

Cardiac Synchronization​

C.7.6.18.1​

 

Respiratory Synchronization​

C.7.6.18.2​

 

Specimen​

C.7.6.22​

 

X-Ray Filtration​

C.8.7.10​

 

X-Ray Grid​

C.8.7.11​

 

Enhanced XA/XRF Image​

C.8.19.2​

 

XA/XRF Acquisition​

C.8.19.3​

 

X-Ray Image Intensifier​

C.8.19.4​

 

X-Ray Detector​

C.8.19.5​

 

XA/XRF Multi-frame Presentation​

C.8.19.7​

 

SOP Common​

C.12.1​

 

Common Instance Reference​

C.12.2​

Usage​

M​

U​

M​

U​

U​

M​

M​

U​

C - Required if C-arm Positioner Tabletop​ Relationship (0018,9474) equals YES. May be​ present otherwise.​

C - Required if C-arm Positioner Tabletop​ Relationship (0018,9474) equals YES. May be​ present otherwise.​

M​

M​

M​

C - Required if contrast media was applied and​ the system is able to register contrast usage.​

U​

U​

U​

M​

M​ U​

C - Required if cardiac synchronization was​ applied.​

C - Required if respiratory synchronization was​ applied.​

U​

U​

U​ M​

C - Required if Image Type (0008,0008) Value​ 1equalsORIGINAL.Maybepresentotherwise.​

C - Required if X-Ray Receptor Type​ (0018,9420) is present and equals​ IMG_INTENSIFIER.​

C - Required if X-Ray Receptor Type​ (0018,9420) is present and equals​ DIGITAL_DETECTOR.​

U​

M​

U​

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