DICOM PS3.3 2019d - Information Object Definitions

A.41.3 Ophthalmic Photography 8 Bit Image IOD Modules

Table A.41-1. Ophthalmic Photography 8 Bit Image IOD Modules

IE

Module

Reference

Usage

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

Ophthalmic Photography Series

C.8.17.1

M

Clinical Trial Series

C.7.3.2

U

Frame of Reference

Synchronization

C.7.4.2

M

Equipment

General Equipment

C.7.5.1

M

Image

General Image

C.7.6.1

M

General Reference

C.12.4

U

Image Pixel

C.7.6.3

M

Enhanced Contrast/Bolus

C.7.6.4b

C - Required if contrast was administered, see Section A.41.4.2

Cine

C.7.6.5

C - Required if there is a sequential temporal relationship between all frames

Multi-frame

C.7.6.6

M

Device

C.7.6.12

U

Acquisition Context

C.7.6.14

U

Ophthalmic Photography Image

C.8.17.2

M

Ocular Region Imaged

C.8.17.5

M

Ophthalmic Photography Acquisition Parameters

C.8.17.4

M

Ophthalmic Photographic Parameters

C.8.17.3

M

ICC Profile

C.11.15

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


Note

The Specimen Identification Module was previously included in this IOD but has been retired. See PS3.3-2008.

DICOM PS3.3 2019d - Information Object Definitions