ActConsentType - HL7 Terminology (THO) v7.1.0

HL7 Terminology (THO)
7.1.0 - Continuous Process Integration (ci build) International flag

HL7 Terminology (THO), published by HL7 International - Vocabulary Work Group. This guide is not an authorized publication; it is the continuous build for version 7.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/UTG/ and changes regularly. See the Directory of published versions

ValueSet: ActConsentType

Official URL: http://terminology.hl7.org/ValueSet/v3-ActConsentType	Version: 3.0.0	Highlight text changes?
	Responsible: Health Level Seven International	Computable Name: ActConsentType
Other Identifiers: OID:2.16.840.1.113883.1.11.19897
Copyright/Legal: This material derives from the HL7 Terminology THO. THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license.html

Definition: The type of consent directive, e.g., to consent or dissent to collect, access, or use in specific ways within an EHRS or for health information exchange; or to disclose health information for purposes such as research.

References

Included into ActConsentDirectiveType
Included into SecurityCategoryObservationValue

Logical Definition (CLD)

Language: en

Include codes fromhttp://terminology.hl7.org/CodeSystem/v3-ActCode version 📦10.0.0 where concept is-a _ActConsentType

Expansion

Expansion performed internally based on codesystem ActCode v10.0.0 (CodeSystem)

This value set contains 10 concepts

Level	System	Code	Display (en)	Definition	JSON	XML
1	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	_ActConsentType	ActConsentType	Definition: The type of consent directive, e.g., to consent or dissent to collect, access, or use in specific ways within an EHRS or for health information exchange; or to disclose health information for purposes such as research.
2	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	ICOL	information collection	Definition: Consent to have healthcare information collected in an electronic health record. This entails that the information may be used in analysis, modified, updated.
2	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	IDSCL	information disclosure	Definition: Consent to have collected healthcare information disclosed.
2	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	INFA	information access	Definition: Consent to access healthcare information.
3	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	INFAO	access only	Definition: Consent to access or "read" only, which entails that the information is not to be copied, screen printed, saved, emailed, stored, re-disclosed or altered in any way. This level ensures that data which is masked or to which access is restricted will not be. Example: Opened and then emailed or screen printed for use outside of the consent directive purpose.
3	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	INFASO	access and save only	Definition: Consent to access and save only, which entails that access to the saved copy will remain locked.
2	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	IRDSCL	information redisclosure	Definition: Information re-disclosed without the patient's consent.
2	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	RESEARCH	research information access	Definition: Consent to have healthcare information in an electronic health record accessed for research purposes.
3	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	RSDID	de-identified information access	Definition: Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes, but without consent to re-identify the information under any circumstance.
3	`http://terminology.hl7.org/CodeSystem/v3-ActCode`	RSREID	re-identifiable information access	Definition: Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes re-identified under specific circumstances outlined in the consent. Example:: Where there is a need to inform the subject of potential health issues.