Common Data Models Harmonization
1.0.0 - STU 1 Publication

Common Data Models Harmonization, published by HL7 International - Biomedical Research and Regulation Work Group. This is not an authorized publication; it is the continuous build for version 1.0.0). This version is based on the current content of https://github.com/HL7/cdmh/ and changes regularly. See the Directory of published versions

CodeSystem: PCORNet Pro Type

Summary

Defining URL:http://hl7.org/fhir/us/cdmh/CodeSystem/pcornet-pro-type
Version:1.0.0
Name:PCORNetProType
Title:PCORNet Pro Type
Status:Active as of 9/6/21
Definition:

The PCORNet Pro Type contains the codes to be used by PCORNet data marts.

Publisher:HL7 International - Biomedical Research and Regulation Work Group
Copyright:

Used by permission of HL7, all rights reserved Creative Commons License

Content:Complete: All the concepts defined by the code system are included in the code system resource
Source Resource:XML / JSON / Turtle

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

This CodeSystem is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)

This code system http://hl7.org/fhir/us/cdmh/CodeSystem/pcornet-pro-type defines the following codes:

CodeDisplayDefinition
PM PROMISSelf-reported and parent-reported measures of global, physical, mental, and social health for adults and children in the general population and those living with a chronic condition.
NQ Neuro-QoLSelf-reported and proxy-reported measures of physical, mental, and social health for adults and children living with a neurological condition.
AM ASQC-MeSelf-reported measures of physical, mental, and social health for adults living with sickle cell disease.
NT NIH ToolboxPerformance tests of cognitive, motor, and sensory function and self-reported measures of emotional function for adults and children in the general population and those living with a chronic condition.
PC PRO_CTCAEA patient-reported outcome measurement system developed by the National Cancer Institute to capture symptomatic adverse events in patients on cancer clinical trials.
LC LOINCTerminology / vocabulary used to describe the PRO item is LOINC.
HC HCAHPSHCAHPS initiative is to provide a standardized survey instrument and data collection methodology for measuring patients perspectives on hospital care.
NI No informationTerminology / vocabulary used to describe the PRO item is No information.
UN UnknownTerminology / vocabulary used to describe the PRO item is Unknown.
OT OtherTerminology / vocabulary used to describe the PRO item is Other.