Patient

Patient

C.7.1.1

M

Clinical Trial Subject

C.7.1.3

U

Study

General Study

C.7.2.1

M

Patient Study

C.7.2.2

U

Clinical Trial Study

C.7.2.3

U

Series

General Series

C.7.3.1

M

XA/XRF Series

C.8.19.1

M

Clinical Trial Series

C.7.3.2

U

Frame of Reference

Frame of Reference

C.7.4.1

U

Synchronization

C.7.4.2

U

Equipment

General Equipment

C.7.5.1

M

Enhanced General Equipment

C.7.5.2

M

Image

Image Pixel

C.7.6.3

M

Enhanced Contrast/Bolus

C.7.6.4b

C - Required if contrast media was applied and the system is able to register contrast usage.

Mask

C.7.6.10

U

Device

C.7.6.12

U

Intervention

C.7.6.13

U

Acquisition Context

C.7.6.14

M

Multi-frame Functional Groups

C.7.6.16

M

Multi-frame Dimension Module

C.7.6.17

U

Cardiac Synchronization

C.7.6.18.1

C - Required if cardiac synchronization was applied.

Respiratory Synchronization

C.7.6.18.2

C - Required if respiratory synchronization was applied.

Specimen

C.7.6.22

U

X-Ray Tomography Acquisition

C.8.7.7

U

X-Ray Filtration

C.8.7.10

U

X-Ray Grid

C.8.7.11

U

Enhanced XA/XRF Image

C.8.19.2

M

XA/XRF Acquisition

C.8.19.3

C - Required if Image Type (0008,0008) Value 1 equals ORIGINAL. May be present otherwise.

X-Ray Image Intensifier

C.8.19.4

C - Required if X-Ray Receptor Type (0018,9420) is present and equals IMG_INTENSIFIER.

X-Ray Detector

C.8.19.5

C - Required if X-Ray Receptor Type (0018,9420) is present and equals DIGITAL_DETECTOR.

XA/XRF Multi-frame Presentation

C.8.19.7

U

SOP Common

C.12.1

M

Common Instance Reference

C.12.2

U

Frame Extraction

C.12.3

C - Required if the SOP Instance was created in response to a Frame-Level retrieve request