DICOM PS3.16 2020b - Content Mapping Resource

TID 11021 Imaging Agent Administration Adverse Events

This template provides information on adverse events occurring to a patient as a result of administration of an Imaging Agent.

Type:

Extensible

Order:

Non-Significant

Root:

No

Table TID 11021. Imaging Agent Administration Adverse Events

NL

Rel with Parent

VT

Concept Name

VM

Req Type

Condition

Value Set Constraint

1

CONTAINER

EV (130212, DCM, "Imaging Agent Administration Adverse Events")

1

M

2

>

CONTAINS

CODE

EV (130220, DCM, "Administration discontinued")

1

U

DCID 231 “Yes-No Only”

3

>

CONTAINS

CODE

EV (C41331, NCIt, "Adverse Event")

1-n

M

DCID 60 “Imaging Agent Administration Adverse Events”

4

>>

HAS PROPERTIES

CODE

EV (246112005, SCT, "Severity")

1

U

BCID (3716) Severity

5

>>

HAS PROPERTIES

CODE

EV (118578006, SCT, "Relative Time")

1

U

DCID 61 “Time Relative to Procedure”

6

>>

HAS PROPERTIES

DATETIME

EV (130215, DCM, "Adverse Event Detection DateTime")

1

M

7

>>

HAS PROPERTIES

NUM

EV (130214, DCM, "Estimated Extravasation Volume")

1

UC

IF Row 3 is EV (95384003, SCT, "Injection Site Extravasation")

Units = EV (ml, UCUM, "ml")

8

>>

HAS OBS CONTEXT

UIDREF

EV (130216, DCM, "Referenced Imaging Agent Administration Step UID")

1

U

9

>>

HAS OBS CONTEXT

UIDREF

EV (130262, DCM, "Referenced Imaging Agent Administration Phase UID")

1

U

10

>>

HAS PROPERTIES

TEXT

EV (121106, DCM, "Comment")

1

U


Content Item Descriptions

Row 2

Indicates whether the administration is discontinued due to the adverse event. There is no indication of which adverse event if any contributed to the decision to discontinue the administration.

Row 3

Note that presence of this row means the injector was informed about the adverse event by the operating clinician.

Row 6

Date and time when the adverse event was noted by the observer.

Row 8

UID of the performed step (as recorded in Row 3 of TID 11007) in which the adverse event occurred.

Row 9

UID of the performed phase (as recorded in Row 3 of TID 11008) in which the adverse event occurred.

DICOM PS3.16 2020b - Content Mapping Resource