TID 10041 Accumulated Dose Data

TID 10041 Accumulated Dose Data (Current)
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This template documents scope of accumulation summary data for a single radiation source. Some rows are modality-specific and may not apply to all uses.

Type:: Extensible
Order:: Non-Significant
Root:: No

Table TID 10041. Accumulated Dose Data

	NL	Rel with Parent	VT	Concept Name	VM	Req Type	Condition	Value Set Constraint
1			CONTAINER	EV (130500, DCM, "Accumulated Dose Data")	1	M
2	>	CONTAINS	TEXT	EV (113832, DCM, "Identification of the X-Ray Source")	1	M
3	>	CONTAINS	CONTAINER	EV (122505, DCM, "Calibration")	1-n	MC	IFF Calibration Data is available
4	>>	HAS CONCEPT MOD	CODE	EV (113794, DCM, "Dose Measurement Device")	1	M		DCID 10010 “Dose Measurement Devices” DCID 7026 “Radiotherapeutic Dose Measurement Devices”
5	>>	CONTAINS	DATETIME	EV (113723, DCM, "Calibration DateTime")	1	M
6	>>	CONTAINS	NUM	EV (122322, DCM, "Calibration Factor")	1	M		UNITS = EV (1, UCUM, "no units")
7	>>	CONTAINS	NUM	EV (113763, DCM, "Calibration Uncertainty")	1	M		UNITS = EV (%, UCUM, "Percent")
8	>>	CONTAINS	TEXT	EV (113724, DCM, "Calibration Responsible Party")	1	M
9	>>	CONTAINS	TEXT	EV (113720, DCM, "Calibration Protocol")	1	U
10	>	CONTAINS	INCLUDE	DTID 1021 “Device Participant”	1	MC	Required if the irradiating device is not the recording device and the dose was accumulated on a single device.	$DeviceProcedureRole = EV (113859, DCM, "Irradiating Device")
11	>	CONTAINS	NUM	EV (113722, DCM, "Dose Area Product Total")	1	U		UNITS = EV (Gy.m2, UCUM, "Gy.m2")
12	>	CONTAINS	NUM	EV (113726, DCM, "Fluoro Dose Area Product Total")	1	U		UNITS = EV (Gy.m2, UCUM, "Gy.m2")
13	>	CONTAINS	NUM	EV (113727, DCM, "Acquisition Dose Area Product Total")	1	U		UNITS = EV (Gy.m2, UCUM, "Gy.m2")
14	>	CONTAINS	NUM	EV (113730, DCM, "Total Fluoro Time")	1	U		UNITS = EV (s, UCUM, "s")
15	>	CONTAINS	NUM	EV (113855, DCM, "Total Acquisition Time")	1	U		UNITS = EV (s, UCUM, "s")
16	>	CONTAINS	NUM	EV (111637, DCM, "Accumulated Average Glandular Dose")	1-2	U		UNITS = EV (mGy, UCUM, "mGy")
17	>>	HAS CONCEPT MOD	CODE	EV (272741003, SCT, "Laterality")	1	M		DCID 6022 “Side”
18	>	CONTAINS	CODE	EV (113947, DCM, "Detector Type")	1	U		DCID 10030 “Detector Types”
19	>	CONTAINS	NUM	EV (113731, DCM, "Total Number of Radiographic Frames")	1	U		UNITS = EV (1, UCUM, "no units")
20	>	CONTAINS	CONTAINER	EV (130502, DCM, "Reference Point Dosimetry")	1	U
21	>>	CONTAINS	TEXT	EV (113780, DCM, "Reference Point Definition")	1	MC	XOR Row 22
22	>>	CONTAINS	CODE	EV (113780, DCM, "Reference Point Definition")	1	MC	XOR Row 21	DCID 10025 “Radiation Dose Reference Points”
23	>>	CONTAINS	NUM	EV (113725, DCM, "Dose (RP) Total")	1	U		UNITS = EV (Gy, UCUM, "Gy")
24	>>	CONTAINS	NUM	EV (113728, DCM, "FluoroDose (RP) Total")	1	U		UNITS = EV (Gy, UCUM, "Gy")
25	>>	CONTAINS	NUM	EV (113729, DCM, "Acquisition Dose (RP) Total")	1	U		UNITS = EV (Gy, UCUM, "Gy")
26	>>	CONTAINS	NUM	EV (113737, DCM, "Distance Source to Reference Point")	1	U		UNITS = EV (mm, UCUM, "mm")
27	>	CONTAINS	NUM	EV (113812, DCM, "Total Number of Irradiation Events")	1	U		UNITS = EV ({events}, UCUM, "events")
28	>	CONTAINS	TEXT	EV (121106, DCM, "Comment")	1	U

Content Item Descriptions

Row 2	Identification the X-Ray source. This designation shall not change for a given source throughout the entire RDSR. Summary-level values that may traditionally include multiple sources, e.g., Dose Area Product Total from planes A and B of a biplane system, could be described by an instance of this template where the Identification of X-Ray Source indicates multiple sources, e.g., "A and B." Summary-level values that are not traditionally described across multiple sources, e.g., Dose (RP) Total on a biplane system, should not accumulate these values across both sources.
Row 5	Date that the calibration of the equipment's dose indicators was performed.
Row 6	Typically, a value provided by the medical physicist. The recorded dose or dose area product values in this report can be multiplied by this factor to obtain estimated real-world values. Note Note: It is important that this value must not be applied to the measured values before storing them in the report.
Row 7	Value range from 0 to 100 percent. Uncertainty of the 'actual' value expressed as +/- of the mean.
Row 8	Identifies Individual or organization responsible for calibration.
Row 9	Describes calibration protocol according to equipment standards or local guidelines.
Row 10	The device that produced the irradiation accumulated in this template, i.e., the X-Ray source. This is not required to be present if the information is the same as that already recorded in TID 1004 “Device Observer Identifying Attributes” encoded via the inclusion of TID 1002 “Observer Context” in TID 10040 Row 5.
Row 11	The total Dose Area Product for all fluoroscopy and acquisition events for a given X-Ray radiation source.
Row 12	The fluoroscopy component of the total Dose Area Product.
Row 13	The acquisition component of the total Dose Area Product.
Row 14	Total clock time of Fluoroscopy accumulated over the defined scope of accumulation (i.e., the sum of the Irradiation Duration values for accumulated fluoroscopy irradiation events).
Row 15	Total clock time of acquisitions accumulated over the defined scope of accumulation (i.e., the sum of the Irradiation Duration values for accumulated acquisition irradiation events).
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 23	Accumulated dose relative to reference point.
Row 24	The fluoroscopic component of the accumulated dose relative to reference point.
Row 25	The acquisition component of the accumulated dose relative to reference point.
Row 26	A single value for calculating reference point dose based on fixed distance.
Row 27	Total Number of irradiation events.

TID 10041 Accumulated Dose Data

Note