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DICOM PS3.3 2020a - Information Object Definitions​

Page 311​

IE​

Module​

Reference​

Usage​

 

Clinical Trial Series​

C.7.3.2​

U​

Frame of Reference​

Synchronization​

C.7.4.2​

M​

Equipment​

General Equipment​

C.7.5.1​

M​

Document​

SR Document General​

C.17.2​

M​

 

SR Document Content​

C.17.3​

M​

 

SOP Common​

C.12.1​

M​

A.35.7.3.1 Procedure Log IOD Content Constraints​

A.35.7.3.1.1 Template​

The document may be constructed from Baseline TID 3001 “Procedure Log” invoked at the root node.​

Note​

This template defines a container (the root) with subsidiary Content Items, each of which represents a single procedure log​ entry. There is a defined recording observer (the person responsible for recording the log, generally a technician or nurse).​ The log entries follow a canonical model of a coded log entry type (the concept name of the Content Item), the value asso-​ ciated with the concept name as one of the SR Value Types, and optionally a subsidiary free text comment and/or an iden-​ tifier of the author or device source of the log entry (which may be other than the recording observer).​

A.35.7.3.1.2 Observation DateTime​

Each Item in Content Sequence (0040,A730) of the SR Document Content Module that is a target of a "CONTAINS" relationship from​ the root node, i.e., the first level Log Content Items, shall include Observation DateTime (0040,A032) as a Type 1 Attribute. This At-​ tribute shall represent the DateTime at which the event recorded in the Content Item occurred, not the time at which the Item was​ recorded.​

ThefirstlevelProcedureLogContentItemsintheContentSequenceshallbestrictlyorderedbymonotonicallyincreasingObservation​ DateTime (0040,A032) values.​

Observation DateTime (0040,A032) shall be specified to a precision of one second or finer.​

A.35.7.3.1.3 Value Type​

Value Type (0040,A040) in Content Sequence (0040,A730) of the SR Document Content Module is constrained to the following​ Enumerated Values (see Table C.17.3-7 for Value Type definitions):​

Enumerated Values:​

TEXT​

CODE​

NUM​

DATETIME​

DATE​

TIME​

UIDREF​

PNAME​

COMPOSITE​

IMAGE​

WAVEFORM​

CONTAINER​

A.35.7.3.1.4 Relationship Constraints​

Relationships between Content Items in the content of this IOD shall be conveyed in the by-value mode. See Table C.17.3-8 for Re-​ lationship Type definitions.​

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DICOM PS3.3 2020a - Information Object Definitions​

Note​

1.​Relationships by-reference are forbidden. Therefore, Referenced Content Item Identifier (0040,DB73) is not present in​ any of the Content Items within the SR Document Content Module.​

2.​CONTAINERs are not permitted as a target of any relationship.​

Table A.35.7-2 specifies the relationship constraints of this IOD.​

Table A.35.7-2. Relationship Content Constraints for Procedure Log IOD​

Source Value Type​

Relationship Type (Enumerated​

Target Value Type​

 

Values)​

 

CONTAINER​

CONTAINS​

TEXT,CODE,NUM,PNAME,COMPOSITE,IMAGE,​

 

 

WAVEFORM​

any type​

HAS OBS CONTEXT​

TEXT, CODE, NUM, DATETIME, UIDREF, PNAME​

CONTAINER, IMAGE, WAVEFORM,​HAS ACQ CONTEXT​

TEXT, CODE, NUM, DATETIME, DATE, TIME,​

COMPOSITE​

 

UIDREF, PNAME​

any type​

HAS CONCEPT MOD​

TEXT, CODE​

any type (except CONTAINER)​

HAS PROPERTIES​

TEXT, CODE, NUM, DATETIME, UIDREF, PNAME​

TEXT, CODE, NUM​

INFERRED FROM​

IMAGE, WAVEFORM, COMPOSITE​

A.35.8 X-Ray Radiation Dose SR IOD​

A.35.8.1 X-Ray Radiation Dose SR IOD Description​

The X-Ray Radiation Dose SR IOD is used to convey the exposure characteristics and dose from X-Rays generated by imaging​ devices.​

Note​

Therapeutic dose is reported in the RT Dose IOD.​

A.35.8.2 X-Ray Radiation Dose SR IOD Entity-Relationship Model​

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

A.35.8.3 X-Ray Radiation Dose SR IOD Module Table​

Table A.35.8-1 specifies the Modules of the X-Ray Radiation Dose SR IOD.​

Table A.35.8-1. X-Ray Radiation Dose SR 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​

SR Document Series​

C.17.1​

M​

 

Clinical Trial Series​

C.7.3.2​

U​

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DICOM PS3.3 2020a - Information Object Definitions​

Page 313​

IE​

Module​

Reference​

Usage​

Frame of​

Synchronization​

C.7.4.2​

C-shallbepresentifsystemtime​

Reference​

 

 

is synchronized to an external​

 

 

 

reference. May be present​

 

 

 

otherwise.​

Equipment​

General Equipment​

C.7.5.1​

M​

 

Enhanced General Equipment​

C.7.5.2​

M​

Document​

SR Document General​

C.17.2​

M​

 

SR Document Content​

C.17.3​

M​

 

SOP Common​

C.12.1​

M​

A.35.8.3.1 X-Ray Radiation Dose SR IOD Content Constraints​

A.35.8.3.1.1 Template​

The document may be constructed from Baseline TID 10001 “Projection X-Ray Radiation Dose” or Baseline TID 10011 “CT Radiation​ Dose” invoked at the root node.​

Note​

This IOD maybe used with other Templates defined for Dose Reporting. Such other Templates maybe specialized for spe-​ cific modalities or future dose measurement techniques.​

A.35.8.3.1.2 Value Type​

Value Type (0040,A040) in Content Sequence (0040,A730) of the SR Document Content Module is constrained to the following​ Enumerated Values (see Table C.17.3-7 for Value Type definitions):​

Enumerated Values:​

TEXT​

CODE​

NUM​

DATETIME​

UIDREF​

PNAME​

COMPOSITE​

IMAGE​

CONTAINER​

A.35.8.3.1.3 Relationship Constraints​

Relationships between Content Items in the content of this IOD shall be conveyed by-value. Table A.35.8-2 specifies the relationship​ constraints of this IOD. See Table C.17.3-8 for Relationship Type definitions.​

Table A.35.8-2. Relationship Content Constraints for X-Ray Radiation Dose SR IOD​

Source Value Type​

Relationship Type (Enumerated​

Target Value Type​

 

Values)​

 

CONTAINER​

CONTAINS​

TEXT,CODE,NUM,DATETIME,UIDREF,PNAME,IMAGE,​

 

 

COMPOSITE, CONTAINER​

CONTAINER​

HAS OBS CONTEXT​

DATETIME, CODE, TEXT, UIDREF, PNAME​

TEXT, CODE, NUM​

HAS OBS CONTEXT​

TEXT, CODE, NUM, DATETIME, UIDREF, PNAME,​

 

 

COMPOSITE​

CONTAINER, IMAGE,​

HAS ACQ CONTEXT​

TEXT, CODE, NUM, DATETIME, UIDREF, PNAME,​

COMPOSITE​

 

CONTAINER​

any type​

HAS CONCEPT MOD​

TEXT, CODE​

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DICOM PS3.3 2020a - Information Object Definitions​

Source Value Type​

Relationship Type (Enumerated​

Target Value Type​

 

Values)​

 

TEXT, CODE, NUM​

HAS PROPERTIES​

TEXT,CODE,NUM,DATETIME,UIDREF,PNAME,IMAGE,​

 

 

COMPOSITE, CONTAINER​

PNAME​

HAS PROPERTIES​

TEXT, CODE, DATETIME, UIDREF, PNAME​

TEXT, CODE, NUM​

INFERRED FROM​

TEXT, CODE, NUM, DATETIME, UIDREF, IMAGE,​

 

 

COMPOSITE, CONTAINER​

Note​

TheSOPClassestowhichanIMAGEorCOMPOSITEValueTypemayreferaredocumentedintheConformanceStatement​ for an application (see PS3.2 and PS3.4).​

A.35.8.3.1.4 Completion Flag​

The Completion Flag (0040,A491) of an X-Ray Radiation Dose SR shall have the value "COMPLETE".​

Note​

An RDSR must contain all relevant information from its Scope of Accumulation. The value "PARTIAL" is not be used, as it​ would mean that the RDSR does not contain all the irradiation events within the Scope of Accumulation.​

A.35.9 Spectacle Prescription Report IOD​

A.35.9.1 Spectacle Prescription Report IOD Description​

The Spectacle Prescription Report IOD is used to represent the spectacle prescription for a Patient.​

A.35.9.2 Spectacle Prescription Report IOD Entity-Relationship Model​

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

A.35.9.3 Spectacle Prescription Report IOD Module Table​

Table A.35.9-1 specifies the Modules of the Spectacle Prescription Report IOD.​

Table A.35.9-1. Spectacle Prescription Report 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​

SR Document Series​

C.17.1​

M​

 

Clinical Trial Series​

C.7.3.2​

U​

Equipment​

General Equipment​

C.7.5.1​

M​

 

Enhanced General Equipment​

C.7.5.2​

M​

Document​

SR Document General​

C.17.2​

M​

 

SR Document Content​

C.17.3​

M​

 

SOP Common​

C.12.1​

M​

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DICOM PS3.3 2020a - Information Object Definitions​

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A.35.9.3.1 Spectacle Prescription Report IOD Content Constraints​

A.35.9.3.1.1 Value Type​

Value Type (0040,A040) in Content Sequence (0040,A730) of the SR Document Content Module is constrained to the following​ Enumerated Values (see Table C.17.3-7 for Value Type definitions):​

Enumerated Values:​

TEXT​

CODE​

NUM​

CONTAINER​

A.35.9.3.1.2 Relationship Constraints​

Relationships between Content Items in the content of this IOD shall be conveyed in the by-value mode. See Table C.17.3-8 for Re-​ lationship Type definitions.​

Note​

Relationships by-reference are forbidden. Therefore, Referenced Content Item Identifier (0040,DB73) is not present in any​ of the Content Items within the SR Document Content Module.​

Table A.35.9-2 specifies the relationship constraints of this IOD.​

Table A.35.9-2. Relationship Content Constraints for Spectacle Prescription Report IOD​

Source Value Type​

Relationship Type (Enumerated Values)​

Target Value Type​

CONTAINER​

CONTAINS​

CONTAINER, CODE, NUM, TEXT​

A.35.9.3.1.3 Template Constraints​

The document shall be constructed from TID 2020 “Spectacle Prescription Report” invoked at the root node.​

A.35.10 Colon CAD SR IOD​

A.35.10.1 Colon CAD SR IOD Description​

The Colon CAD SR IOD is used to convey the detection and analysis results of a colon CAD device. The content may include textual​ and a variety of coded information, numeric measurement values, references to the SOP Instances, and spatial regions of interest​ within such SOP Instances. Relationships by-reference are enabled between Content Items.​

A.35.10.2 Colon CAD SR IOD Entity-Relationship Model​

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

A.35.10.3 Colon CAD SR IOD Module Table​

Table A.35.10-1 specifies the Modules of the Colon CAD SR IOD.​

Table A.35.10-1. Colon CAD SR 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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