StateChangeReason - HL7 Terminology (THO) v6.0.2

HL7 Terminology (THO)
6.0.2 - UTG Consensus Review Proposal UP-584 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 6.0.2 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

CodeSystem: StateChangeReason

Official URL: http://terminology.hl7.org/CodeSystem/state-change-reason			Version: 2.0.0
Active as of 2020-04-09	Maturity Level: 1	Responsible: Health Level Seven International	Computable Name: StateChangeReason
Other Identifiers: OID:2.16.840.1.113883.4.642.1.0
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

Indicates why the state of the subject changed.

This Code system is referenced in the content logical definition of the following value sets:

StateChangeReason

Last updated: 2020-04-09 21:10:28+0000

This case-sensitive code system http://terminology.hl7.org/CodeSystem/state-change-reason defines the following codes:

Code	Display	Definition	Deprecated
unable-to-participate	Unable to Participate	The subject (ResearchSubject) is not able to take part in the ResearchStudy. Examples: subject has moved away; subject cannot drive and therefore unable to participate, etc.
unwilling-to-participate	Unwilling to Participate	The subject (ResearchSubject) is refusing to take part in the ResearchStudy. Note: Subject refusal is a synonymous term and is used in some studies.
screening-failure	Screening Failure	The failure of the potential subject (ResearchSubject) of meeting one or more criteria required for participation in a trial.
intervention-complete	Intervention Complete	The subject (ResearchSubject) has finished the planned protocol-specified treatment phase.
follow-up-complete	Follow-up Complete	The subject (ResearchSubject) has finished the planned protocol-specified follow-up phase.
adverse-event	Adverse Event	The subject (ResearchSubject) has experienced any unfavorable or unintended disease, sign, or symptom that is temporally associated with the use of a medical treatment or procedure and that may or may not be considered related to the medical treatment or procedure.
consent-withdrawn	Consent Withdrawn	The subject (ResearchSubject) has revoked permission to participate in the study or one or more components of the study.
non-compliance	Non-compliance	The subject (ResearchSubject) has failed to follow medical advice, take medication as directed, or adhere to a prescribed course of treatment.
informedConsentSigned	Informed consent signed	Informed consent signed.	Deprecated
intOrObsComplete	intervention or observation complete	intervention or observation complete.	Deprecated
death	Death	The subject (ResearchSubject) has died.