DICOM PS3.16 2018e - Content Mapping Resource

TID 11021 Imaging Agent Administration Adverse Events (Current)
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#### 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 | >> | CONTAINS | CODE | EV (G-C197, SRT, "Severity") | 1 | U |  | BCID (3716) Severity
5 | >> | CONTAINS | CODE | EV (G-D709, SRT, "Relative Time") | 1 | U |  | DCID 61 “Time Relative to Procedure”
6 | >> | HAS PROPERTIES | DATETIME | EV (130215, DCM, "Adverse Event Detection Date Time") | 1 | M |  |
7 | >> | HAS PROPERTIES | NUM | EV (130214, DCM, "Estimated Extravasation Volume") | 1 | UC | IF Row 3 is EV (D0-B0330, SRT, "Injection Site Extravasation") | Units = EV (ml, UCUM, "ml")
8 | >> | CONTAINS | UIDREF | EV (130216, DCM, "Referenced Imaging Agent Administration Step UID") | 1 | U |  |
9 | >> | CONTAINS | UIDREF | EV (130262, DCM, "Referenced Imaging Agent Administration Phase UID") | 1 | U |  |
10 | >> | CONTAINS | 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.

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DICOM PS3.16 2018e - Content Mapping Resource