HL7 FHIR Implementation Guide: Common Terminology Criteria (CTC) Adverse Events Release 1 - DRAFT
0.0.1 - DRAFT
HL7 FHIR Implementation Guide: Common Terminology Criteria (CTC) Adverse Events Release 1 - DRAFT
0.0.1 - DRAFT
HL7 FHIR Implementation Guide: Common Terminology Criteria (CTC) Adverse Events Release 1 - DRAFT, published by HL7 International Clinical Interoperability Council. This guide is not an authorized publication; it is the continuous build for version 0.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/standardhealth/fsh-ae/ and changes regularly. See the Directory of published versions
| Official URL: http://hl7.org/fhir/us/ctcae/ValueSet/ctcae-grade-value-set | Version: 0.0.1 | |||
| Draft as of 2024-02-28 | Computable Name: CTCAEGradeVS | |||
CTCAE Grades 0 through 5. The grade of the adverse event, determined by CTCAE criteria, where 0 represents confirmation that the given adverse event did NOT occur, and 5 represents death. Note that grade 0 events are generally not reportable, but may be created to give positive confirmation that the clinician assessed or considered a particular AE.
References
http://hl7.org/fhir/us/ctcae/CodeSystem/ctcae-grade-code-system
Expansion based on codesystem CTCAE Grade Code System v0.0.1 (CodeSystem)
This value set contains 6 concepts.
| Code | System | Display | Definition |
| 0 | http://hl7.org/fhir/us/ctcae/CodeSystem/ctcae-grade-code-system | Absent Adverse Event | The absence of adverse events or within normal limits or values. |
| 1 | http://hl7.org/fhir/us/ctcae/CodeSystem/ctcae-grade-code-system | Mild Adverse Event | An experience that is usually transient, and requires no special treatment or intervention. The event does not generally interfere with usual daily activities. Includes transient laboratory test alterations. |
| 2 | http://hl7.org/fhir/us/ctcae/CodeSystem/ctcae-grade-code-system | Moderate Adverse Event | An experience that is alleviated with simple therapeutic treatments. The event impacts usual daily activities. Includes laboratory test alterations indicating injury, but without long-term risk. |
| 3 | http://hl7.org/fhir/us/ctcae/CodeSystem/ctcae-grade-code-system | Severe Adverse Event | An adverse event experience that requires intensive therapeutic intervention and interrupts usual daily activities. |
| 4 | http://hl7.org/fhir/us/ctcae/CodeSystem/ctcae-grade-code-system | Life Threatening or Disabling Adverse Event | Any adverse event that places the patient, in the view of the initial reporter, at immediate risk of death from the adverse event as it occurred, i.e., it does not include an adverse experience that, had it occurred in a more severe form, might have caused death. |
| 5 | http://hl7.org/fhir/us/ctcae/CodeSystem/ctcae-grade-code-system | Death Related to Adverse Event | The termination of life associated with an adverse event. |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |