HL7 Standards - Master Grid

The HL7 International Arden Syntax for Medical Logic Modules (MLMs) is an ANSI-approved American National Standard language for encoding medical knowledge and representing and sharing that knowledge among personnel, information systems and institutions. The Arden Syntax for Medica...

This document provides a collection of non-normative recommended best practices, descriptions of common mistakes, and implementation reminders for application developers to consider when creating CCOW-compliant applications. The content of this docume...

Claims Attachments goal is to support the implementation of Health Insurance Portability and Accountability Act (HIPAA) requirements for submitting additional information required for processing a healthcare claim. It is also likely that much of this HL7 product will also support other ...

Claims Attachments questions and answers, gathered through various public presentations circa 2003-2008. Teams within the HL7 ASIG and X12N WG9 formulated the answers. Version 1.2 contains new questions and answers to reflect current information (e.g., what was in the NPRM, curren...

This white paper has been prepared to provide a plain language overview of the recommendation for Healthcare Claims Attachments, expected to be named under the Health Insurance Portability And Accountability Act (HIPAA, 1996) in 2008. While only “claims attach...

GELLO, part of the HL7 Version 3 Normative Edition, is a standard query and expression language that provides a suitable framework for manipulation of clinical data for decision support in healthcare. The GELLO language can be used to build queries to extract and manipulate data from medica...

A Decision Support Service (DSS) facilitates the delivery of clinical decision support by receiving patient data as the input and returning patient-specific conclusions as the output. The HL7 DSS specification provides a standard interface for the provision and consumption of such s...

The HL7 Child Health Functional Profile for EHR Systems (Child Health Profile) is designed to assist children's healthcare providers and associated IT vendors to create functionality that ensures safe and reliable care of children through the effective use of information technology. Specif...

The Pharmacist/Pharmacy Provider Functional Profile will facilitate EHR systems capture of medication and clinical related data at the point of contact or point of care by specifying the functional requirements needed to support messaging among prescribers, pharmacist and pharma...

The HL7 EHR System Long Term Care Functional Profile (LTC EHR-S FP) establishes the functions and conformance criteria for EHR systems in the nursing home setting for the US Realm, and will serve as a key resource to the Certification Commi...

The HL7 International EHR System Functional Model (EHR-S FM) outlines important features and functions that should be contained in an EHR system. Through the creation of functional profiles, this model provides a standard description and common understanding of functions for he...

This HL7 Version 3 CDA implementation guide is a Draft Standard for Trial Use (DSTU) that offers a means for QRDA to use EHR information when creating quality measure definition and reporting.  Health care institutions routinely collect and report performance measure data t...

This Draft Standard for Trial Use (DSTU) is an extension of HL7's Continuity of Care Document (CCD) specification. The purpose of this document is to describe constraints on the CDA Header and Body elements for Personal Healthcare Monitoring Report (PHMR) documents mostly contai...

This implementation guide (IG) (currently a DSTU) describes how HL7 Version 3 Clinical Document Architecture (CDA) Release 2 is used to record information for a Consult Note. The Consult Note may contain both narrative and coded data. For the purpose of this IG a consultation visit is define...

This Draft Standard for Trial Use (DSTU) is based on HL7 Version 3’s Clinical Document Architecture (CDA) and specifies a standard for electronic submission of healthcare associated infection (HAI) Reports to the National Healthcare Safety Network (NHSN) of the Centers for Disease Contro...

This Implementation Guide (IG) facilitates a standard electronic communication for electronic submission to CDA of their Questionnaire Assessments. These allow healthcare facilities and providers a standard way to communicate reports in an industry standard format. Questionnaire Assess...

The purpose of this implementation guide (IG) is to specify a standard for electronic submission of Public Health Case Reports (PHCR) in an HL7 Version 3 Clinical Document Architecture (CDA), Release 2 format. This implementation guide will allow healthcare facilities/providers to commun...

This document describes constraints on the Clinical Document Architecture (CDA) Header and Body elements for Procedure Note documents. The Procedure Note or Report is created immediately following a non-operative procedure and records the indications for the procedure and, when applic...

The Clinical Document Architecture Release 2.0 (CDA R2) addresses universal requirements for exchange and management of structured clinical documents. The approach described in this document, The HL7 Implementation Guide for CDA® Release 2: greenCDA Modules for CCD, Releas...

HL7’s Version 2.x (V2) messaging standard is the workhorse of electronic data exchange in the clinical domain and arguably the most widely implemented standard for healthcare in the world. This messaging standard allows the exchange of clinical data between systems. It is design...

This document provides assistance to healthcare institutions, hospital information systems vendors, consultants, and other support groups that are considering systems development and implementation activities in a multi-system environment using the Health Level Seven (HL7) protoc...

The Version 2 Implementation Guide: Laboratory Test Compendium Framework, Release 1 is a master file framework Implementation Guide (IG) for the delivery of a laboratory’s Directory of Service to all providers that order lab work including EHRs, HLIS, and others. This provides the me...

This addendum is provided to add clarity to implementations of the HL7 version 2.3.1 messaging standard which choose to follow guidelines for implementing the standard with an XML encoding.  This addendum does not affect implementations of the HL7 version 2.3.1 standard that u...

Technical Corrections to HL7 Version 2.3.1 Messaging Standard

The HL7 Version 2.4 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part of this specification. While HL7 publishes schema...

Technical corrections to HL7 Version 2.4 Messaging Standard.

V2.4 - P03 Post Detail Financial Transaction Implementation Suggestion provides FT1 specific charge update segments vs. the global update segments for the DG1, DRG, GT1 and IN1 segments.

The Version 2.5.1 Implementation Guide: Electronic Laboratory Reporting to Public Health (US Realm), Release 1 describes the transmission of laboratory-reportable findings to appropriate local, state, territorial and federal health agencies using the message. In particular, this guide ...

The Version 2.5.1 Implementation Guide; Orders and Observations; Interoperable Laboratory Result Reporting to EHR (US Realm), Release 1 provides guidance on how to apply the Version 2.5.1 standard to the exchange of laboratory results from the testing source between providers and ot...

The schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part of this specification. While HL7 publishes schema for the HL7 data types, other schemas could be pro...

The HL7 Version 2.6 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part of this specification. While HL7 publishes schema...

The Control chapter of the Health Level Seven (HL7) International® Standard defines the generic rules that apply to all messages, including trigger events and acknowledgements as well as message structure, construction rules, processing rules, segments, fields, delimiters, format...

The Control – Conformance Using Message Profiles chapter of the Health Level Seven® International (HL7) Standard presents the methodology for producing a precise and unambiguous specification called a message profile. Messages that adhere to the constraints of a m...

The organization and delivery of healthcare services is an information-intensive effort. It is generally accepted that the efficacy of healthcare operations is greatly affected by the extent of automation of information management functions. Many believe that healthcare delivery agencies that h...

This chapter defines the rules that apply to queries and to their responses. It also defines the unsolicited display messages because their message syntax is query-like in nature.

A query with its response should be thought of as a message pair. The three generic mode...

This chapter describes the transaction set required for sending structured patient-oriented clinical data from one computer system to another.  A common use of these transaction sets will be to transmit observations and results of diagnostic studies from the producing system (e.g.,...

This chapter currently supports document management and defines the Medical Document Management (MDM) transaction set.  In the future, it is intended also to support the data exchange needs of applications supporting other medical record functions, including chart location and tr...

The Patient Referral chapter defines the message set used in patient referral communications between mutually exclusive healthcare entities.  These referral transactions frequently occur between entities with different methods and systems of capturing and st...

Clinical laboratory automation involves the integration or interfacing of automated or robotic transport systems, analytical instruments, and pre- or post-analytical process equipment such as automated centrifuges and aliquoters, decappers, recappers, sorters, and specimen storage and retrie...

The Personnel Management transaction set provides for the transmission of new or updated administration information about individual healthcare practitioners and supporting staff members.  Since many systems (e.g., security, scheduling, orders, etc.), must be able to closely monito...

This Materials Management chapter defines abstract messages for the purpose of communicating various events related to the transactions derived from supply chain management within a healthcare facility.  There are two basic types of messages defined in this chapter: inventory item master...

The schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part of this specification. While HL7 publishes schema for the HL7 data types, other schemas could be pro...

The Cardiology (Acute Coronary Syndrome, ACS) Domain Analysis Model will describe the ACS diagnosis, treatment and reporting space to facilitate the exchange and promote reuse of  information between all parties involved in ACS treatment, quality reporting and research and thereb...

The HL7 Version 3 Domain Analysis Model: Vital Records (VR DAM) describes the workflows and stakeholders for transmitting birth and death data to and from U.S. vital records systems. The VR DAM describes how birth, death and fetal death records are p...

This HL7 Version 3 implementation guide offers supplemental material for the January, 2004 annotated ECG (aECG), standard. This implementation guide is not complete in itself and should be used in conjunction with the HL7 aECG standard, R1 as well as the standard’s XML schema...

Describes the basic requirements needed for using the Stability standard and the requirements needed for submitting information to the Food and Drug Administration (FDA) using the standard. This implementation guide is superseded with updates included in HL7 Version 3 Implementation Guide: Drug S...

This document provides technical conformance criteria for Structured Product Labeling (SPL) files based on the drug establishment registration and drug listing process at the United States Food and Drug Administration (FDA). Information on electronic submission may be found in guidance entitl...

This document provides technical conformance criteria for Structured Product Labeling (SPL) files based on the drug establishment registration and drug listing process at the United States Food and Drug Administration (FDA). Information on electronic submission may be found in guidance entitl...

The Context-Aware Knowledge Retrieval (Infobutton), Knowledge Request specification, provides a standard mechanism for clinical information systems to submit knowledge requests to knowledge resources. Context-aware knowledge retrieval into clinical information systems (CIS), such a...

The Health Level Seven Version 3 (V3) Normative Edition—a suite of specifications based on HL7’s Reference Information Model (RIM)—provides a single source that allows implementers of V3 specifications to work with the full set of messages, data types, and termin...

The most fundamental question is always how certain information in HL7 should be transmitted. In most cases, it is information that belongs to the category of "findings" or "observations". The so-called Score or assessment systems are findings. Score systems are so-cal...

HL7 Version 3 Standard: Clinical Trial Registration and Results (CTR&R), Release 1 focuses on the development and maintenance of an HL7 V3 message in support of the global data exchange requirements brought about by the increasing number of national, regional, global and or...

GELLO, part of the HL7 Version 3 Normative Edition, is a standard query and expression language that provides a suitable framework for manipulation of clinical data for decision support in healthcare. Version 1 was approved by ANSI in 2005. See GELLO R2 product for the updated releas...

A Real-Time Location System (RLTS) tracks the location of tags associated with patients, providers, and equipment within a healthcare facility. This document defines storyboards, trigger events, information models and interactions for exchanging information between RTLS a...

This document defines the representation of HL7 V3 messages in XML, including the method to derive XML DTDs plus additional processing rules from HL7 V3 Hierarchical Message Definitions (HMD). 

The Version 2 NCPDP Electronic Prescribing Coordination Mapping Implementation Guide provides mapping requirements for electronic prescribing systems using HL7 Versions 2.4 and later. It specifies functional electronic prescribing communication with systems using NCPDP SCRIPT Standa...

The purpose of this document is to describe constraints on the CDA Document Body elements for a Care Record Summary document. A Care Record Summary document contains patient's relevant health history for some time period. It is intended for communication between healthcare provid...

The purpose of this Quick Start Guide is to aid implementers in developing applications that produce simple CDA documents.

This HL7 Version 3 (V3) standard describes the processes whereby HL7 V3 artifact specifications may be refined, constrained and extended to support implementation designs, conformance profiles, and realm-specific standards.  

The Retrieve, Location, and Updating Service (RLUS) provides a set of interfaces through which information systems can access and manage information. RLUS allows health data to be located, accessed and updated regardless of underlying data structures, security concerns, or delive...

The HL7 Services-Aware Interoperability Framework (SAIF) provides a set of constructs, best practices, processes and more that enable cross-specification discoverable determination of interoperability irrespective of the chosen interoperability paradigm (messages, documents, or servic...

This document is a non-balloted HL7 Recommendation that describes how to send HL7 messages using public Internet mail.

Structured Product Labeling (SPL) in the Clinical Environment: Electronic Health Records (EHR) and Digital Medical References (DMR) Presentation, SPL Usage Discussion Group 9/21/2010

This document provides assistance to healthcare institutions, hospital information systems vendors, consultants and other support groups that are considering systems development and implementation activities in a multi-system environment using the Health Level Seven (HL7) protoc...

This document provides assistance to healthcare institutions, hospital information systems vendors, consultants, and other support groups that are considering systems development and implementation activities in a multi-system environment using the Health Level Seven (HL7) protoc...

The HL7 Version 3 Regulated Product Submissions (RPS) standard provides a common means of exchange of documentation and status between product sponsors and regulatory agencies. The standard facilitates the communication of documents relating to, and the status of, activi...

The HL7 Version 3 Normative Edition’s laboratory domain comprises the models, messages, and other artifacts that are needed to support messaging related to the results or observations association with laboratory tests. It currently supports the results of laboratory testing of any type o...

The purpose of the HL7 Version 3 Annotated Electrocardiogram (aECG) standard is to provide a means to systematically evaluate the ECG waveforms and measurement locations.  The US Food and Drug Association (FDA) continues to be concerned about evaluating noncardiac drugs for negative cardia...

The Healthcare, Community Services and Provider Directory specifies core functionality of a Services and Provider Directory that not only supports semantic interoperability, but also valuable business initiatives such as Wait List Management. This HL7 SFM specifies a means to conduc...

The Personnel Management Domain spans a variety of clinical-administrative information functions associated with organizations, individuals, animals and devices involved in the delivery and support of healthcare services. The domain content includes roles, relationships, creden...

The HL7 Version 3 Accounting and Billing (AB) Messaging Standard supports the communication of acquired patient payor information and specific acquired charges for services to a patient/payer billing system. Examples of services facilitated by this standard include: the creation and manage...

The HL7 Version 3 Claims and Reimbursements Messaging Standard provides non-US realm support for generic, pharmacy, preferred accommodation, physician, oral health, vision care and hospital claims for eligibility, authorization, coverage extension, pre-determination, invoice adjudi...

Common Message Element Types (CMETs) are standardized model fragments intended to be building blocks that individual content domains can "include" in their designs. These blocks reduce the effort to produce a domain-specific design and assure that similar conten...

The HL7 Version 3 Implantable Device Cardiac (IDC) Follow-up Summary is a message model for describing an observation of an interrogator at a physical location who is performing an interrogation of a therapeutic medical device (bound to a patient) using identifiable interr...

The Implementation Technology Specification (ITS) is a section in the Version 3 Normative Edition that shows how to map the HL7 data types to the Object Management Group’s (OMG) Unified Modeling Language (UML) and their Object Constraint Language (OCL) kernel data types when needed...

The Infrastructure Management section of the HL7 Version 3 Normative Edition focuses on the development and management of specifications that support the routing of messages to their specified destination(s). Infrastructure Management’s current domains are: Master File/Registry; Message Contro...

The HL7 Version 3 Data Access Consent standard allows two or more health IT systems to communicate a patient’s consent or to withdraw an existing expression of consent for the collection, access, use or disclosure of their personal health information. The Data Access Consen...

The HL7 Version 3 Tuberculosis Domain Analysis Model (DAM) represents the clinical processes associated with managing pulmonary tuberculosis (TB) from the point at which patients present themselves at treatment sites, through diagnosis and treatment. The process model has been s...

HL7 Version 3 Shared Messages are a work product produced for expressing common, useful and reusable message types. A Shared Message can be envisioned as a message type that is reusable in interactions in any of the domains within the HL7 standard. This document provides data on common messag...

The purpose of the MLLP Protocol (Minimum Lower Layer Protocol) is to provide both a minimalistic Open Systems Interconnection (OSI)-session layer framing protocol as well as a minimalistic reliable transport protocol. If security is an issue, additional protocols or techno...

The Version 3 Regulated Product Submission (RPS) Implementation Guide provides technical details (conformance criteria) on using the Regulated Product Submission (RPS) standard. The RPS standard provides a common means of exchange of documentation and status between product sponso...

The HL7 standards define several different types of objects that implement various characteristics of vocabulary. (In HL7, encoded information is referred to as vocabulary.) Whereas other elements of the HL7 standards are primarily concerned with structure, vocabulary deals with conten...