TID 10003 Irradiation Event X-Ray Data
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TID 10003 Irradiation Event X-Ray Data

This template conveys the dose and equipment parameters of a single irradiation event.

The template and requirements are structured to consider equipment with various levels of integration between the components (X-Ray Source, Plate or Detector, and Gantry/Table) of the equipment.

An irradiation event is the loading of X-Ray equipment caused by a single continuous actuation of the equipment's irradiation switch, from the start of the loading time of the first pulse until the loading time trailing edge of the final pulse. The irradiation event is the "smallest" information entity to be recorded in the realm of Radiation Dose reporting. Individual Irradiation Events are described by a set of accompanying physical parameters that are sufficient to understand the "quality" of irradiation that is being applied. This set of parameters may be different for the various types of equipment that are able to create irradiation events. Any automatic on-off switching of the irradiation source during the event shall not be treated as separate events, rather the event includes the time between start and stop of irradiation as triggered by the user. E.g., a pulsed fluoro X-Ray acquisition shall be treated as a single irradiation event.

As described in Section 6.2.4, measurement concepts may be post-coordinated, even though not explicitly specified in the Template. In particular, post-coordination using modifier concept (121401, DCM, "Derivation"), with modifier values drawn from CID 10009 “Measured/Calculated” would be appropriate to encode indications of measured or of calculated values.

Type:

Extensible

Order:

Non-Significant

Table TID 10003. Irradiation Event X-Ray Data

NL

Rel with Parent

VT

Concept Name

VM

Req Type

Condition

Value Set Constraint

1

CONTAINER

EV (113706, DCM, "Irradiation Event X-Ray Data")

1

M

2

>

HAS CONCEPT MOD

CODE

EV (113764, DCM, "Acquisition Plane")

1

M

DCID 10003 “Equipment Plane Identification”

3

>

CONTAINS

UIDREF

EV (113769, DCM, "Irradiation Event UID")

1

M

4

>

CONTAINS

TEXT

EV (113605, DCM, "Irradiation Event Label")

1

U

5

>>

HAS CONCEPT MOD

CODE

EV (113606, DCM, "Label Type")

1

MC

IF the value of Row 4 is the value of an Attribute in the images.

DCID 10022 “Label Types”

6

>

CONTAINS

DATETIME

DT (111526, DCM, "DateTime Started")

1

M

7

>

CONTAINS

CODE

EV (113721, DCM, "Irradiation Event Type")

1

M

DCID 10002 “Irradiation Event Types”

8

>

CONTAINS

TEXT

EV (125203, DCM, "Acquisition Protocol")

1

U

9

>

CONTAINS

CODE

EV (T-D0005, SRT, "Anatomical structure")

1

U

DCID 4009 “DX Anatomy Imaged”

10

>>

HAS CONCEPT MOD

CODE

EV (G-C171, SRT, "Laterality")

1

UC

If anatomy is bi-lateral

DCID 244 “Laterality”

11

>

CONTAINS

CODE

EV (111031, DCM, "Image View")

1

U

DCID 4010 “DX View”

DCID 4014 “View for Mammography”

12

>>

HAS CONCEPT MOD

CODE

EV (111032, DCM, "Image View Modifier")

1-n

U

DCID 4011 “DX View Modifier”

DCID 4015 “View Modifier for Mammography”

13

>>

CONTAINS

CODE

EV (113946, DCM, "Projection Eponymous Name")

1

U

DCID 4012 “Projection Eponymous Name”

14

>

CONTAINS

CODE

EV (113745, DCM, "Patient Table Relationship")

1

U

DCID 21 “Patient Equipment Relationship”

15

>

CONTAINS

CODE

EV (113743, DCM, "Patient Orientation")

1

U

DCID 19 “Patient Orientation”

16

>>

HAS CONCEPT MOD

CODE

EV (113744, DCM, "Patient Orientation Modifier")

1

M

DCID 20 “Patient Orientation Modifier”

17

>

CONTAINS

CODE

EV (123014, DCM, "Target Region")

1

M

DCID 4031 “Common Anatomic Regions”

18

>

CONTAINS

NUM

EV (122130, DCM, "Dose Area Product")

1

MC

IFF TID (10001) Row 2 = (113704, DCM, "Projection X-Ray")

UNITS = EV (Gy.m2, UCUM, "Gy.m2")

19

>

CONTAINS

NUM

EV (111634, DCM, "Half Value Layer")

1

U

UNITS = EV (mm, UCUM, "mm")

20

>

CONTAINS

NUM

EV (111638, DCM, "Patient Equivalent Thickness")

1

U

UNITS = EV (mm, UCUM, "mm")

21

>

CONTAINS

NUM

EV (111636, DCM, "Entrance Exposure at RP")

1

MC

IF TID (10001) Row 2 = (P5-40010, SRT, "Mammography") and (TID (10001) Row 9 is absent or value is (R-0038D, SRT, "Yes")) and (TID (10001) Row 10 is absent or value is (R-0038D, SRT, "Yes"))

UNITS = EV (mGy, UCUM, "mGy")

22

>

CONTAINS

TEXT

EV (113780, DCM, "Reference Point Definition")

1

MC

IF Row 21 is present and Row 23 is not present

23

>

CONTAINS

CODE

EV (113780, DCM, "Reference Point Definition")

1

MC

IF Row 21 is present and Row 22 is not present

DCID 10025 “Radiation Dose Reference Points”

24

>

CONTAINS

INCLUDE

DTID 4007 “Mammography CAD Breast Composition”

1

U

25

>

CONTAINS

TEXT

EV (121106, DCM, "Comment")

1

U

26

>

CONTAINS

INCLUDE

DTID 1020 “Person Participant”

1-n

U

$PersonProcedureRole = EV (113851, DCM, "Irradiation Administering")

27

>

CONTAINS

INCLUDE

DTID 10003A “Irradiation Event X-Ray Detector Data”

1

MC

IFF TID (10001) Row 8 is absent or has a value of (R-0038D, SRT, "Yes")

28

>

CONTAINS

INCLUDE

DTID 10003B “Irradiation Event X-Ray Source Data”

1

MC

IFF TID (10001) Row 9 is absent or has a value of (R-0038D, SRT, "Yes")

29

>

CONTAINS

INCLUDE

DTID 10003C “Irradiation Event X-Ray Mechanical Data”

1

MC

IFF TID (10001) Row 10 is absent or has a value of (R-0038D, SRT, "Yes")


Content Item Descriptions

Row 3

If the image generating entity does not assign a DICOM UID to the irradiation event (e.g., for non-digital imaging equipment), the application generating this report shall assign a UID.

In the case of non-integrated cassette-based equipment, a standalone Detector will generate UIDs for the Events it observes. If the X-Ray Source component of the equipment also reports information, it too will generate UIDs for the Events it creates. A downstream system (e.g., a workstation or the Dose Information Reporter itself) may combine the two reports into a composite report, and match up the events based on details such as the time information, and use the UIDs of the X-Ray Source.

Row 6

Provide DateTime the application of X-Ray started. This shall correspond to the start of the first irradiation in the Irradiation Event, which defines the starting point for the calculation of Row 36 "Irradiation Duration".

Row 17

The target region is the anatomy exposed.

Row 21

A text definition of the Reference Point (RP) used for RP-related dose values.

Row 22

A coded definition of the Reference Point (RP) used for RP-related dose values

Row 25

People responsible for the administration of the radiation reported in the irradiation event. May include values that would appear in Performing Physicians' Name (0008,1050), Performing Physician Identification Sequence (0008,1052), Operators' Name (0008,1070) and/or Operator Identification Sequence (0008,1072).
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