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DICOM PS3.3 2020a - Information Object Definitions |
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|
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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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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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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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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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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