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HITSP/C80: HITSP Clinical Document and Message Terminology Component

1. Introduction

1.1 Overview

The purpose of the Health Information Technology Standards Panel (HITSP) Clinical Document and Message Terminology Component is to define the vocabulary for either document-based or message-based HITSP constructs such as Clinical Document Architecture (CDA) documents, HL7 V2 messages, etc. For more in-depth information about how this Component relates to other HITSP constructs, see HITSP/TN901 Clinical Documents.

1.2 Copyright Permissions

© 2010 ANSI. This material may be copied without permission from ANSI only if and to the extent that the text is not altered in any fashion and ANSI's copyright is clearly noted.
Certain materials contained in this Interoperability Specification are reproduced from HL7 Version 3 Standard: Core Principals with permission of Health Level Seven, Inc. No part of the material may be copied or reproduced in any form outside of the Interoperability Specification documents, including an electronic retrieval system, or made available on the Internet without the prior written permission of Health Level Seven, Inc. Copies of standards included in this Interoperability Specification may be purchased from the Health Level Seven, Inc. Material drawn from these standards is credited where used.

1.3 Reference Documents

A list of key reference documents and background material is provided in the table below. HITSP-maintained reference documents can be retrieved from the HITSP Web Site.

Reference Document Document Description
HITSP Acronyms List Exit Disclaimer [publicaa.ansi.org] Lists and defines the acronyms used in this document
HITSP Glossary Exit Disclaimer [publicaa.ansi.org] Provides definitions for relevant terms used by HITSP documents
TN901 - Clinical Documents TN901 is a reference document that provides the overall context for use of the HITSP Care Management and Health Records constructs
TN903 - Data Architecture TN903 is a reference document that provides the overall context for use of the HITSP Data Architecture constructs

1.4 Conformance

This section describes the conformance criteria, which are objective statements of requirements that can be used to determine if a specific behavior, function, interface, or code set has been implemented correctly.

1.4.1 Conformance Criteria

In order to claim conformance to this construct specification, an implementation must satisfy all the requirements and mandatory statements listed in this specification, the associated HITSP Interoperability Specification or Capability, its associated construct specifications, as well as conformance criteria from the selected base and composite standards. A conformant system must also implement all of the required interfaces within the scope, subset or implementation option that is selected from the associated Interoperability Specification.Claims of conformance may only be made for the overall HITSP Interoperability Specification or Capability with which this construct is associated.

1.4.2 Conformance Scoping, Subsetting and Options

A HITSP Interoperability Specification or Capability must be implemented in its entirety for an implementation to claim conformance to the specification. HITSP may define the permissibility for interface scoping, subsetting or implementation options by which the specification may be implemented in a limited manner. Such scoping, subsetting and options may extend to associated constructs, such as this construct. This construct must implement all requirements within the selected scope, subset or options as defined in the associated Interoperability Specification or Capability to claim conformance.

2.1.1 Value Set Metadata

The Value Sets in this document are defined in a table as shown below.

Element Description
Identifier This is the unique identifier of the value set
Name This is the name of the Value Set
Source This is the source of the Value Set, identifying the originator or publisher of the information
URL A URL referencing the Value Set members or its definition at the time of publication
Purpose Brief description about the general purpose of Value Set
Definition A text definition formally describing how concepts in the Value Set are (intensional) or were (extensional) selected
Version This row contains a string identifying, where necessary, the specific version of the Value Set
Type Extensional (Enumerated) or Intensional (Criteria-based)
Binding Static or Dynamic
Status Active (Current) or Inactive (Retired)
Effective Date The date when the Value Set is expected to be effective
Expiration Date The date when the Value Set is no longer expected to be used
Creation Date The date of creation of the Value Set
Revision Date The date of revision of the Value Set
Code System Source This row identifies the source for the code system
Code System Name This row provides the name of the code system associated with the Value Set

2.2 Rules for Implementing Value Sets

The use of this construct is defined by the Component, Transaction, Transaction Package, Capability or Interoperability Specification that may refer to it

2.2.1 General Information Value Sets

See Value Sets: State, Postal Code, and Country Value Sets for details Demographic Information Value Sets

See Value Sets: Gender, Ethnicity, Marital Status, Personal Relationship, Family Relationship, Contact, Race, Religious Affiliation, Language, Language Ability for details

2.2.2 Administration and Financial Value Sets

See Value Sets: Health Insurance Type, Subscriber Relationship, Financially Responsible Party, Social History for details

2.2.3 Care Management and Health Record Value Sets

See Value Sets: Problem, Problem Type, Diagnosis Type, Diagnosis Priority, Nursing Diagnosis, Problem Severity, Functional Assessment, Problem Status for details Body Site

See Value Sets: Body Site for details Medications

See Value Sets: Medication Fill Status, Medication Product Form, Medication Route FDA, V2 Medication Route, Medication Type, Medication Brand Name, Medication Clinical Drug Name, Medication Drug Class, Medication Packaged Product, Ingredient Name, Medication Vehicle for details Medication Indication

This is the medical condition or problem intended to be addressed by the ordered medication. For example: for chest pain, for pain, for high blood pressure. See Problem for details Medication Route

This indicates the method for the medication received by the individual (e.g., by mouth, intravenously, topically, etc). See Value Sets: Medication Route FDA, V2 Medication Route for details Medication Site

This is the anatomic site where the medication is administered. See Body Site for details Allergies

See Value Sets: Allergy/Adverse Event Type for details Allergy/Adverse Event (Reaction)

This indicates the reaction that may be caused by the product or agent. See Problem for details Allergy/Adverse Event Severity

This is a description of the level of the severity of the allergy or intolerance. See Problem Severity for details Allergy/Adverse Event Product

This identifies the product or agent that causes the intolerance. See Value Sets Ingredient Name, Medication Drug Class, Medication Clinical Drug Name for details Immunizations

See Value Sets: Vaccine Administered, Vaccine Manufacturer, No Immunization Reason, Immunization Information Source, Immunization Service Funding Eligibility for details Measurements and Laboratory Results

See Value Sets: Laboratory Observation Identifier, Laboratory Finding Identifier, Laboratory Order, Result Normalcy Status, V2 Result Status Code System, V3 Result Status, Vital Sign Result, Unit of Measure Code System, Order Control Code System, Order Status Code System, Order Setting Type Code System, Order Priority Code System, Specimen Action Code, Specimen Risk Code System, Specimen Type, Specimen Collection Method, Newborn Screening Order, Newborn Screening Results - Observation and Findings for details Laboratory Observation

This identifies laboratory results. See Laboratory observation identifier, Laboratory Finding Identifier, Laboratory Order for details Result Status

This identifies the status for the results (observation). See V2 Result Status Code System, V3 Result Status for details Procedures

See Value Sets: Procedure for details Providers

See Value Sets: Provider Role, Provider Type for details Admissions and Encounters

See Value Sets: Admission Source, Admission Type, Encounter Type, Discharge Disposition, Patient Class for details Advance Directives

See Value Sets: Advance Directive Type for details Genetic Testing

The following sections describe the value sets selected for reporting the results of genetic tests. See Value Sets: Genetic Test Result Identifier, Genetic Test Result for details Genetic Disease

This identifies genetic diseases. See Value Set Problems for details Medication Assessed in Genetic Test

This identifies the medication assessed for the genetic test. See Value Set Medication Clinical Drug Name for details Document Metadata

The following sections describe the value sets selected for recording document metadata in transactions used to register and exchange clinical documents. Descriptions of the value sets in this section are drawn from the IHE IT Infrastructure Technical Framework, Volume II, Release 4.0. Only those metadata elements that require coded values are listed in this section; other fields should be provided as described in the relevant base standard. See Value Sets: Document Class, Document Type, Healthcare Facility Type, Clinical Specialty, Format Code, Author Role for details

Download an Excel spreadsheet containing all C80 Value Set Information with values.
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SortValue Sets:
OID Sort
Purpose Sort
Newborn Screening Order Value Set This identifies the newborn screening order
Newborn Screening Results - Observation and Findings Value Set This identifies the newborn screening results - observation and findings
Laboratory Order Value Set This identifies the laboratory order
Confidentiality Value Set 2.16.840.1.113883.1.11.10228 This is the code specifying the level of confidentiality of the document, which may be used by IT systems to make an authorization decision about access to the document. More than one value may be applied to any document
Financially Responsible Party Type Value Set 2.16.840.1.113883.1.11.10416 This identifies the party that has responsibility for all or a portion of the patient's healthcare; includes health insurance, the patient directly, a guardian or other guarantor, or other third party that is not a health insurance plan
Language Value Set 2.16.840.1.113883.1.11.11526 This identifies the name of a human language.
Marital Status Value Set 2.16.840.1.113883.1.11.12212 Demographic Information
Language Ability Mode Value Set 2.16.840.1.113883.1.11.12249
Race Value Set 2.16.840.1.113883.1.11.14914 Classifying data based upon race
Ethnicity Value Set 2.16.840.1.113883.1.11.15836 Demographic Information
Coverage Role Type Value Set 2.16.840.1.113883.1.11.18877 Describes the role recognized through the issuance of insurance coverage to an identified covered party who has this relationship with the policy holder such as the policy holder themselves (self), spouse, child, etc.
Religious Affiliation Value Set 2.16.840.1.113883.1.11.19185 Demographic Information
Personal Relationship Role Type Value Set 2.16.840.1.113883.1.11.19563 Demographic Information
Family Member Value Set 2.16.840.1.113883.1.11.19579 Demographic Information
No Immunization Reason Value Set 2.16.840.1.113883.1.11.19717 This identifies the reason why the immunization did not occur
Administrative Gender Value Set 2.16.840.1.113883.1.11.1 Demographic Information
Advance Directive Type Value Set 2.16.840.1.113883. This identifies the type of the Advance Directive
Result Normalcy Status Value Set 2.16.840.1.113883.1.11.78 A rough qualitative interpretation of the observation, such as "normal", "abnormal", "below normal", "change up", "resistant", "susceptible", etc.
Order Setting Type Code System Table Value Set 2.16.840.1.113883.12.482 This value set describes the care setting type associated with an order.
Specimen Collection Method Value Set 2.16.840.1.113883.12.488 This value set describes the procedure or process by which the specimen was collected
Specimen Risk Code System Table Value Set 2.16.840.1.113883.12.489 This value set encodes any known or suspected specimen hazards, e.g., exceptionally infectious agent or blood from a hepatitis patient
Specimen Action Code Value Set 2.16.840.1.113883.12.65 This value set identifies the action to be taken with respect to the specimens that accompany or precede an order
Author Role Value Set 2.16.840.1.113883. This is the code specifying the role of the document author when the document was created.
Contact Type Value Set 2.16.840.1.113883. Demographic Information
Provider Role Value Set 2.16.840.1.113883. This classifies providers according to the role they play in the healthcare of the individual
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