TID 10003 Irradiation Event X-Ray Data

TID 10003 Irradiation Event X-Ray Data
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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
Root:: No

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
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”
17b	>>	HAS CONCEPT MOD	CODE	EV (G-C171, SRT, "Laterality")	1	UC	If anatomy is bi-lateral	DCID 244 “Laterality”
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	The DateTime that the application of X-Rays started for this irradiation event. 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 17b	Previously, a CODE content item (T-D0005, SRT, "Anatomical structure") along with CODE concept modifier (G-C171, SRT, "Laterality") were used to identify bilateral anatomy. This duplicated the function of Row 17 and was retired. See PS3.16 2017c.
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 26	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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