Medical Alerts

(0010,2000)

Conditions to which medical staff should be alerted (e.g., contagious condition, drug allergies, etc.)

Allergies

(0010,2110)

Description of prior reaction to contrast agents, or other patient allergies or adverse reactions.

Smoking Status

(0010,21A0)

Indicates whether patient smokes.

Additional Patient History

(0010,21B0)

Additional information about the patient's medical history

Pregnancy Status

(0010,21C0)

Describes pregnancy state of patient.

Last Menstrual Date

(0010,21D0)

Date of onset of last menstrual period

Patient's Sex Neutered

(0010,2203)

Whether or not a procedure has been performed in an effort to render the patient sterile.

Patient's Body Mass Index

(0010,1022)

Body Mass Index of the patient in kg/m2.

Measured AP Dimension

(0010,1023)

The thickness in mm of the body part being scanned, in the antero-posterior dimension (per AAPM Report 204).

Measured Lateral Dimension

(0010,1024)

The side-to-side (left to right) dimension in mm of the body part being scanned (per AAPM Report 204).

Special Needs

(0038,0050)

Medical and social needs (e.g., wheelchair, oxygen, translator, etc.)

Patient State

(0038,0500)

Description of patient state (comatose, disoriented, vision impaired, etc.)

Pertinent Documents Sequence

(0038,0100)

List of Documents (e.g., SR, or CDA) that contain information considered pertinent for the patient medical condition.

Zero or more Items shall be included in this Sequence.

>Include Table 10-11 “SOP Instance Reference Macro Attributes”

>Purpose of Reference Code Sequence

(0040,A170)

Describes the purpose for which the document reference is made. Zero or more Items shall be included in this Sequence.

>>Include Table 8.8-1 “Code Sequence Macro Attributes”

No Baseline CID is defined.

>Document Title

(0042,0010)

Title of the referenced document.

Pertinent Resources Sequence

(0038,0101)

List of resources that contain information considered pertinent for the patient medical condition.

Zero or more Items shall be included in this Sequence.

>Retrieve URI

(0040,E010)

Retrieval access path to resource. Includes fully specified scheme, authority, path, and query in accordance with [RFC3986].

>Resource Description

(0038,0102)

Description or title of the resource.

Patient Clinical Trial Participation Sequence

(0038,0502)

Sequence of identifiers for clinical trials or research in which the patient participates.

Zero or more Items shall be included in this Sequence.

>Clinical Trial Sponsor Name

(0012,0010)

The name of the clinical trial or research sponsor, responsible for conducting the clinical trial and for defining the Clinical Trial Protocol.

>Clinical Trial Protocol ID

(0012,0020)

Identifier for the noted protocol, used by the Clinical Trial Sponsor to uniquely identify the investigational protocol.

>Clinical Trial Protocol Name

(0012,0021)

The name or title of the clinical trial or research protocol.

>Clinical Trial Site ID

(0012,0030)

The identifier, issued by the Clinical Trial Sponsor, of the site responsible for submitting clinical trial or research data.

>Clinical Trial Site Name

(0012,0031)

Name of the site responsible for submitting clinical trial or research data.

>Clinical Trial Subject ID

(0012,0040)

The assigned identifier for the patient as a clinical trial or research subject.

>Clinical Trial Subject Reading ID

(0012,0042)

Identifies the patient as a clinical trial or research subject for blinded evaluations.