Australian Diagnostics and Referral Messaging - Localisation of HL7 Version 2.4, Release 2 is the Australian localisation of the international HL7 V2 Standard covering the Laboratory/Diagnostics/Clinical result reporting, laboratory/radiology ordering specification and patient referral. The term "Diagnostics" covers non laboratory reporting including reporting of diagnostic imaging and non referral related clinical reporting (for example: echocardiography, respiratory function, endoscopy, stress testing, sleep studies). The term pathology in Australia covers all aspects of laboratory medicine including clinical and anatomical pathology domains, while the term “radiology” is understood to include all diagnostic imaging modalities, whether X-ray based or other (e.g. ultrasound). 

The relationship between pathology and radiology practices and their customers in Australia is considered by Government and others as similar to that between other consultant specialists and their customers. For that reason, what HL7 would call an order is generally called a request here and the response by the pathology provider (a formal term meaning the responsible specialist(s)) is called a report.  For some disciplines such as microbiology, anatomical pathology, genetics and genomics the request is more by way of asking a clinical question expecting the pathology provider to understand the best way of answering it - e.g. Is this cancer, if so what type, and what is the prognosis? It is expected this form of requesting will become more common as laboratory medicine evolves. In radiology, it is generally necessary for the request to include clinical information relevant to the purpose of the request, to enable the optimal choice, and interpretation, of the examination.  It is also frequently necessary that the request contain information relevant to safety issues that may arise from performance of the test, such as contrast allergies, renal disease, etc.

The use case here focuses on widely-available, well-standardized methods that will support the secure access to electronic laboratory and radiological requests and results and interpretations for clinical care by authorized parties and is driven by the need for timely electronic access to requested, referred and historical lab results. Requesting clinicians (the Placer) receive test results in the form of a HL7 V2 message, as a response to a request (electronic or paper) or as an unsolicited message by having the report directly sent by the pathology practice (the Filler) to the clinician for importation into their local systems. Images generated in the course of a radiological procedure are not sent in an HL7 message. Depending on the referrer’s requirements, and local technical capabilities, images may be made available on traditional analogue film (rapidly becoming obsolete), portable digital media, or, increasingly, in digital form via an online electronic portal.

Referral messaging covers clinical referral between clinicians and hospitals, as well as hospital discharge and includes a patient history summary suitable for constructing a Virtual Medical Record for use in decision support and can include any pathology/radiology/diagnostics reports relevant to the referral. It also includes a Medication summary. 

This document tries to provide coverage for all laboratory and radiological messaging scenarios in the Australian context including public and private entities, hospital and community and public health entities. The referral messaging covers referral between medical practitioners, allied health and hospitals. It covers referral between practitioners, referral to hospitals and hospital discharge.

The Royal College of Pathologists of Australasia (RCPA) has developed a number of policies around safety in requesting and reporting of pathology including the use of terminology and the transmission of data.  These policies have been incorporated into this document. Similarly, the Royal Australian and New Zealand College of Radiologists has defined minimum requirements for the content of referrals and reports.  Standardised terminology for radiological procedures is being developed, and will be progressively implemented throughout the sector.

This document and the specifications in it supersede those in AS 4700.2-2012 - Implementation of Health Level Seven (HL7) Version 2.4 - Pathology and diagnostic imaging (diagnostics) and HB 262 (Rev)-2012 - Guidelines for messaging between diagnostic providers and health service providers, and AS 4700.6-2006 Implementation of Health Level Seven (HL7) Version 2.4 Part 6: Referral, discharge and health record messaging.

1.1 Purpose

This guide contains the necessary specifications for pathology and radiology requests and reports in Australian healthcare using the HL7 V2.4 protocol. Where appropriate aspects of later versions of HL7 V2 have been incorporated into this localization. Where this is done it is flagged as a variation from v2.4.

1.2 Audience

This guide is designed for use by analysts and developers who require guidance on optional and ambiguous elements of an Australian constrained HL7 Version 2.4.  Users of this guide must be familiar with the details of HL7 message construction and processing.  This guide is not intended to be a tutorial on that subject.

1.3 Scope

This specification covers the exchange of laboratory results or clinical referral from an appropriate requesting provider or organisation to the testing/consulting source and the transmission of the result from the testing source or clinician to the recipient.  One of the primary features of this implementation guide is its focus on key points of broad interoperability.  These key points include the following:

• Use of strong identifiers for key information objects – These information objects include patients, orders, providers and organizations.  A strong identifier is one that uniquely identifies the object in question in a global fashion.  This means the identifier includes enough information to remain unique when taken out of the context within which the identifier was created.  For patients, providers and organisations this is achieved through the use of the use of the Individual Healthcare Identifier (IHI), Healthcare Provider Identifier–Individual (HPI–I) and Healthcare Provider Identifier–Organisation (HPI–O). In places Medicare Provider numbers are used to provide for location specific provider identifiers. Healthcare Provider Identifier-Organisation (HPI-O) identifiers are not currently available for all organisations at the required level of granularity and alternative organisation identifiers are usually used.
• Use of Vocabulary Standards ­ This guide calls for specific vocabulary standards for the exchange of laboratory information.  Use of standard vocabularies is important for a number of reasons.  Use of standard vocabularies allows broad distribution of healthcare information without the need for individual institutions to exchange master files for data such as test codes, result codes, etc.  Each institution ideally uses the standard codes or maps its own local vocabularies to the standard code, allowing information to be shared broadly, rather than remaining isolated as a single island of information.  Standard vocabularies, particularly coded laboratory results, enable more automated decision support for patient healthcare, as well as more automated public health surveillance of populations.
• Use of consistent specifications across Laboratory/Radiology/Clinical usage. The specification of segment usage and display rules is common to all message types allowing documents to be carried in multiple message types (ORU^R02 or REF^I12) and displayed/processed using common logic in receiving software. This permits the packaging of reports (laboratory/radiology/clinical) for the purpose of  referral messaging with no loss of atomic data, identifiers or terminology, preserving the potential for decision support and allows consistent result filing and display by the receiver.

1.4 Conventions

This guide adheres to the following conventions:

• The guide is constructed assuming the implementer has access to the 2.4 version of the HL7 Standard.  Although some information from the standard is included in this implementation guide, much information from the standard has not been repeated here.
• Data types have been described separately from the fields that use the data types. 
• No conformance information is provided for optional message elements.  This includes length, usage, cardinality, value sets and descriptive information.  Implementers' who want to use optional message elements should refer to the HL7 Standard to determine how these optional message elements will be used. Use of optional message elements should not change the interpretation of data sent using the standard elements.

The following table describes the various attributes used by this guide to document data type attribute tables, message structure attribute tables and segment attribute tables.  Not all attributes apply to all attribute tables.

Table 1-1. Message Element Attributes

Table 1-2. Usage Conformance Testing Recommendations

1.5 Key Words   

In this localisation we have attempted to use 'MUST' to mean that the definition is a mandatory requirement of the specification and 'SHOULD' to mean that there may exist circumstances where it is valid to not adopt the recommendation but the full implications must be understood and carefully weighed before choosing a different course. This is in line with usage with NPAAC and other usage in the Australian Pathology Sector. We have however drawn heavily on HL7 v2 Standards in writing the localisation. These have a wider use of terms meaning the same thing and so it should be the key words:  

“MUST” or the terms "REQUIRED" or "SHALL", mean that the definition is an absolute requirement of the specification.

“MUST NOT” or the phrase "SHALL NOT", mean that the definition is an absolute prohibition of the specification.

“SHOULD” or the adjective "RECOMMENDED", mean that there may exist valid reasons in particular circumstances to ignore a particular item, but the full implications must be understood and carefully weighed before choosing a different course.

“SHOULD NOT” or the phrase "NOT RECOMMENDED" mean that there may exist valid reasons in particular circumstances when the particular behaviour is acceptable or even useful, but the full implications should be understood and the case carefully weighed before implementing any behaviour described with this label.

“MAY” or the adjective "OPTIONAL", mean that an item is truly optional. One software supplier may choose to include the item to enable certain capabilities while another software supplier may omit the same item. In either case, the communication partner cannot be expected to either provide it (sender) or process it (receiver) without clear and voluntary agreement between the partners.

Any further constraining of optional segments/fields/components must be agreed to by both parties and cannot be made pre-requisite to sending/receiving messages to achieve the basic interoperability described in this guide. Therefore, a sender shall not require a receiver to accept any segments/fields/components marked as optional to successfully send a message. Likewise, a receiver shall not require a sender to send any segment/fields/components marked as optional to successfully receive such a message.

1.6 Related Documents

• HL7 V2.4 - Health Level Seven Standard Version 2.4: Health Level Seven Inc.,  Ann Arbor 2000 – www.hl7.org
• LOINC® - Logical Observation Identifier Names and Codes, Users Guide, Indianapolis: Regenstrief Institute - www.regenstrief.org/medinformatics/loinc/
• METeOR - AIHW 2010b. Metadata Online Registry (METeOR), Canberra: AIHW.  Viewed 7 August 2018 – http://meteor.aihw.gov.au/content/index.phtml/itemId/268110
• RFC 1521 - MIME (Multipurpose Internet Mail Extensions) Part One: Mechanisms for Specifying and Describing the Format of Internet Message Bodies – http://www.freesoft.org/CIE/RFC/1521/
• SNOMED CT® - Systematized Nomenclature of Medicine Clinical Terms, International Health Terminology Standards Development Organisation, Copenhagen, Denmark - http://www.snomed.org/
• NPAAC - Requirements for Information Communication (Third Edition, 2013)  National Pathology Accreditation Advisory Council - http://www.health.gov.au/internet/main/publishing.nsf/Content/health-npaac-docs-InfoComm.htm
• APUTS - Australian Pathology Units and Terminology Standards and Guidelines v2.3, 2016. The Royal College of Pathologists Australasia -  https://www.rcpa.edu.au/Library/Practising-Pathology/PTIS/APUTS-Downloads

• AS 4700.2-2012 - Implementation of Health Level Seven (HL7) Version 2.4 - Pathology and diagnostic imaging (diagnostics) - http://infostore.saiglobal.com/store/Details.aspx?ProductID=1602624

• HB 262 (Rev)-2012 - Guidelines for messaging between diagnostic providers and health service providers -  http://infostore.saiglobal.com/store/Details.aspx?ProductID=1507388
• AS 4846:2014 Person and provider identification in healthcare - https://infostore.saiglobal.com/en-au/Standards/AS-4846-2014-1753860/

1.7 Overview of Pathology Messaging

HL7 V2 messaging is widely used in Australia, including the transmission of pathology results from laboratories to providers. This section provides a broad overview of the format and function of pathology messages before detailing specific elements in detail. Electronic ordering is less well developed currently, but is used in some arenas and provides significant potential advantages for the requester and filler of laboratory tests.

HL7 V2 was developed before the introduction of xml or json and the format is text based and unique to HL7 v2. It was originally designed to pass 7 bit channels, optimizes file size and in Australia by default uses the ASCII character set as described in the appendix on parsing HL7 v2. Implementers should read and understand Appendix 1 Parsing HL7v2 (Informative). The file format contains no field names and requires pre-existing knowledge of its structure to process. It is highly storage and bandwidth efficient however.

Most results between laboratories and providers are currently sent in unsolicited mode, where no electronic order was sent, but a paper request was used. An HL7v2 ORU^R01 message is used for this and an example appears below. It should be noted in Australia most paper requests are computer generated and so there is still the opportunity to close the loop between ordering and reporting.

MSH|^~\&|EQUATORDXTRAY^EQUATORDXTRAY:3.1.2^L|ACME Pathology^7654^AUSNATA|||20160612150255+1000||ORU^R01|BGC06121502965-8968|P|2.4^AUS&&ISO3166_1^HL7AU.ONO.1&&HL7AU|||AL|AL|AUS
PID|||12345678^^^^MR~5432109876^^^AUSHIC^MC||ANTHONY^JENNIFER^KAY||19490709|F|||225 Wises Road^^BUDERIM^QLD^4551||^^^^^^54455055||||||4157269354
PV1|1|O||||||0488077Y^SMITH^RAY^^^DR^^^AUSHICPR^L^^^PRN|0191324T^SPECIALIST^ANDREW^^^DR^^^AUSHICPR^L^^^PRN
ORC|RE||15-57243112-CBC-0^ACME Pathology^7654^AUSNATA||CM|||||||0488077Y^SMITH^RAY^^^DR^^^AUSHICPR^L^^^PRN
OBR|1||15-57243112-CBC-0^ACME Pathology^7654^AUSNATA|CBC^MASTER FULL BLOOD COUNT^7654|||20151221|||||||201512211940||0488077Y^SMITH^RAY^^^DR^^^AUSHICPR^L^^^UPIN||From ACME"ACMEG4399292.oru" 17.03.2016||DR=UMA2P,LN=15-57243112,RC=Y||201603171124||HM|F||^^^201512210000|0488077Y^SMITH^RAY^^^DR^^^AUSHICPR^L^^^UPIN~0191324T^SPECIALIST^ANDREW^^^DR^^^AUSHICPR^L^^^UPIN||||123457Z&Davidson&John&&MBBS&Dr.
OBX|1|ST|15430-2^^LN||FULL BLOOD EXAMINATION||||||F
OBX|2|NM|718-7^Haemoglobin^LN||121|g/L|115-160||||F|||201512212329
OBX|3|NM|789-8^Red Cell Count^LN||3.8|10*12/L|3.6-5.2||||F|||201512212329
OBX|4|NM|4544-3^Haematocrit^LN||0.38||0.33-0.46||||F|||201512212329
OBX|5|NM|787-2^Mean Cell Volume^LN||100|fL|80-98|+|||F|||201512212329
OBX|6|NM|785-6^Mean Cell Haemoglobin^LN||32|pg|27-35||||F|||201512212329
OBX|7|NM|777-3^Platelet Count^LN||393|10*9/L|150-450||||F|||201512212329
OBX|8|NM|6690-2^White Cell Count^LN||8.8|10*9/L|4.0-11.0||||F|||201512212329
OBX|9|NM|770-8^Neutrophils^LN||53|%|||||F|||201512212329
OBX|10|NM|751-8^Neutrophils^LN||4.7|10*9/L|2.0-7.5||||F
OBX|11|NM|736-9^Lymphocytes^LN||30|%|||||F|||201512212329
OBX|12|NM|731-0^Lymphocytes^LN||2.6|10*9/L|1.1-4.0||||F
OBX|13|NM|5905-5^Monocytes^LN||14|%|||||F|||201512212329
OBX|14|NM|742-7^Monocytes^LN||1.2|10*9/L|0.2-1.0|+|||F
OBX|15|NM|713-8^Eosinophils^LN||3|%|||||F|||201512212329
OBX|16|NM|711-2^Eosinophils^LN||0.26|10*9/L|0.04-0.40||||F
OBX|17|NM|706-2^Basophils^LN||0|%|||||F|||201512212329
OBX|18|NM|704-7^Basophils^LN||0.00|10*9/L|< 0.21||||F
OBX|19|FT|5909-7^Interpretation^LN||Comment:\.br\Mild monocytosis and borderline high mean cell volume.  Other significant haematology parameters are within normal limits for age and sex.\.br\||||||F|||201512212329

When this message is received an Acknowledgement message is produced and returned to the laboratory.

MSH|^~\&|EQUATORDXTRAY^EQUATORDXTRAY:3.1.2^L|Demo Server^1FFA8984-7166-4655-B195-7B4FFFD2F136^GUID|EQUATORDXTRAY^EQUATORDXTRAY:3.1.2 (Build 6387) [win32-i386] {SVV=76;DBV=76}^L|QML^2184^AUSNATA|20160612150923+1000||ACK^R01|HOM06121509607-198|P|2.4^AUS&&ISO3166_1^HL7AU.ONO.1&&HL7AU|||||AUS
MSA|AA|BGC06121502965-8968

These two messages are the backbone of result delivery and acknowledgement of delivery for pathology delivery. The first message is the results of the laboratory evaluation (a document), in this case a Full Blood Count, with a message wrapper to address the message and enable the delivery to be confirmed by the second message which is produced by the recipient and returned to the laboratory. The security and authentication around delivery is out of scope of this standard.

Messages are a stream of text which is divided into segments by the CR (ASCII 13) character. Each segment starts with a three letter code identifying the content of the segment. e.g. "MSH", "PID", "OBX" etc. These segments are further defined by the standard to contain fields which are separated by the "|" character. Each field can optionally repeat and each repeat (if present) is separated by the "~" character. The fields themselves are divided into components by the "^" character and the components are divided into SubComponents by the "&" character. There are no levels of hierarchy possible below this. The text content of Fields/components or subcomponents must escape any delimiters used in HL7 ie |^~\& or Line breaks (ASCII 13/10). Escape sequences are provided for this. e.g. \.br\ replaces a line break in the original text. 

The segments in a message are specified by the standard and are ordered, can be optional and can optionally repeat. Each message type, which is specified in the MSH segment has its own segment structure, but all start with a MSH segment. This creates a hierarchy at the level of the specific message. The full structure of a ORU^R01 message (The main message used to deliver results) is detailed below. This is the full international message structure and in Australia PV1 has been made mandatory and some optional segments have been removed. The Australian message structure is detailed in the section on Observation Reporting.

Legend:

"{}"  Repeat

"[]" Optional 

ORU^R01           Unsolicited Observation Message
MSH Message Header
{
    PID Patient Identification
    [
       [PD1] Additional Demographics
       [{NK1}] Next of Kin/Associated Parties
       PV1 Patient Visit
       [PV2] Patient Visit - Additional Info
    ]
    {
        [ORC] Order common
        OBR Observations Report ID
        [CTD] Contact Data
        {
            [OBX] Observation/Result
        }
    }
}
[DSC] Continuation Pointer

Note that the message structure has been constrained compared with the international standard. This link demonstrates the original message structure: International ORU Structure

In the example message the MSH segment (Line 1) gives this message a Unique ID "BGC06121502965-8968" and Indicated it was sent by ACME Pathology "ACME Pathology^7654^AUSNATA". The response, the ACK^R01 message, indicates that this message has been received using the Message Acknowledgment Segment (MSA, Line 2) with the original message ID "MSA|AA|BGC06121502965-8968" . The "AA" indicates "Application Accept".

In the PV1 segment, in field 9, the provider this message was delivered to is indicated as "0191324T^SPECIALIST^ANDREW^^^DR^^^AUSHICPR^L^^^PRN"

The message contains a report. The report header is in the OBR Segment (Line 5) and the report has a Unique ID which will never change even if the report is updated "15-57243112-CBC-0^ACME Pathology^7654^AUSNATA". It also gives the name of the report and who ordered it and who has been sent copies of the report along with the date the test was done.

The OBX segments, on lines 6-24, contain the atomic data that form the actual result. Each atomic result is identified with a code (e.g. Line 7 "718-7^Haemoglobin^LN") and a data type, in this case mostly Numeric(NM).

The details of the other fields and conventions, localized for Australia,  are specified in this standard, which should be read in concert with the International standard.

In the case of an electronic order a ORM^O01 message is sent to the laboratory and this is responded to with a ORR^O02 message.

MSH|^~\&|MERIDIAN^MERIDIAN:3.1.4 (Build 6934) [win32-i386]^L|Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID||ACME Pathology^7654^AUSNATA|20160814205041+1000||ORM^O01^ORM_O01|XX08142050015-2604|P|2.4^AUS&&ISO3166_1^HL7AU.ONO.1&&HL7AU|||AL|AL|AUS
PID|1|....
PV1||O||||||||||||||V1||||BULKBILL
ORC|NW|BGC-00013065-1^Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID||BGC-00013065^Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID|||||201608142050+1000|||0191324T^SPECIALIST^ANDREW^K^^DR^^^AUSHICPR^L^^^UPIN|||201608142049+1000||||||Buderim GE Centre
OBR|1|BGC-00013065-1^Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID||26604007^Full Blood Count^SCT|||||||L|||||0191324T^SPECIALIST^ANDREW^K^^DR^^^AUSHICPR^L^^^UPIN|||||||||||^^^^^R|254327KW^BLOGGS^DAMIEN^^^DR^^^AUSHICPR^L^^^UPIN|||||||||||^Pregnant:False~^Fasting:True~^Radiotherapy:False~^Hormonal Therapy:False
OBX|1|FT|11492-6^History and Physical Notes^LN||This is a test message\.br\||||||F|||201608142050+1000

This message is requesting a Full Blood Count encoded as "26604007^Full Blood Count^SCT" from ACME Pathology Laboratories encoded as "ACME Pathology^7654^AUSNATA" with an order number of "BGC-00013065-1^Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID". "ORC|NW|" indicates this is a new order. In the order we specify the ordering provider in the ORC segment which is "0191324T^SPECIALIST^ANDREW^K^^DR^^^AUSHICPR^L^^^UPIN" and request a copy be sent to "254327KW^BLOGGS^DAMIEN^^^DR^^^AUSHICPR^L^^^UPIN" in the OBR Segment.

The response to this message is as below

MSH|^~\&|EQUATORDXTRAY^EQUATORDXTRAY:3.1.4 (Build 6896) [win32-i386] {SVV=78;DBV=76}^L|Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID|MERIDIAN^MERIDIAN:3.1.4 (Build 6934) [win32-i386]^L|Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID|20160814205104+1000||ORR^O02|BGC08142051838-6830|P|2.4^AUS&&ISO3166_1^HL7AU.ONO.1&&HL7AU|||AL|AL|AUS
MSA|AA|XX08142050015-2604
PID|1|....
ORC|OK|BGC-00013065-1^Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID||BGC-00013065^Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID|||||201608142050+1000|||0191324T^SPECIALIST^ANDREW^K^^DR^^^AUSHICPR^L^^^UPIN|||201608142049+1000||||||Buderim GE Centre
OBR|1|BGC-00013065-1^Buderim GE Centre^7C3E3681-91F6-11D2-8F2C-444553540000^GUID||26604007^Full Blood Count^SCT|||||||L|||||0191324T^SPECIALIST^ANDREW^K^^DR^^^AUSHICPR^L^^^UPIN|||||||||||^^^^^R|254327KW^BLOGGS^DAMIEN^^^DR^^^AUSHICPR^L^^^UPIN|||||||||||^Pregnant:False~^Fasting:True~^Radiotherapy:False~^Hormonal Therapy:False

The ORR message confirms the tests ordered back to the placer and may contain the laboratory number(s).

The MSA segment "MSA|AA|XX08142050015-2604" indicates this message has been accepted and the ORC value of "ORC|OK|" indicates the order has been accepted.

The combination of the ORU^R01 report message and its response and the ORM^O01 order message and its acknowledgement are the backbone of pathology messaging. The details of the order and report messages are covered in subsequent sections. Segments common to all message processing are covered in this section. In some settings the messages and segments used in the examples will be all that is encountered in normal usage but the international standard covers similar messages used in queries for orders and results and these will be seen in some settings but are not covered in this guide.

Messages can be batched into files using a single batch inside a File Header structure as illustrated below. In Australia only one Batch is supported but a batch can contain any number of messages. The main purpose of this wrapper is to ensure the collection of messages has not been truncated in transport as the file should end with a BTS and FTS and this should be checked for when processing files.  The specification of the segments used in many HL7v2 message types is provided in section 2.1, where usage notes and some example values are provided.

FHS
BHS
  {
    MSH
    {Any segments required by message}
  }
BTS
FTS

FHS|^~\&|EQUATORDXTRAY:0.12.8 (Build 310)|1FFA8984-7166-4655-B195-7B4FFFD2F136|||20050417220634+1000
BHS|^~\&|EQUATORDXTRAY:0.12.8 (Build 310)|1FFA8984-7166-4655-B195-7B4FFFD2F136|||20050417220634+1000
MSH|^~\&|EQUATORDXTRAY^EQUATORDXTRAY:0.12.8 (Build 310)^L|Demo Practice^1FFA8984-7166-4655-B195-7B4FFFD2F136^GUID|||20050417220634+1000||ORU^R01|20050417.736428|P|2.4^AUS&&ISO3166_1^HL7AU.ONO.1&&HL7AU|||AL|AL|AUS
PID|1||100333^^^Medical-Objects&7C3E3682-91F6-11D2-8F2C-444553540000&GUID^SR^Demo Practice&1FFA8984-7166-4655-B195-7B4FFFD2F136&GUID||TESTER^Testy^^^Mr^^L||19900101|M|||3 Drury Lane^^NAMBOUR^QLD^4560^AUS^H||61(07)54455055^PRN^PH^^61^07^54455055|||||||||||||||||N
PV1|1|O||||||0191322W^ANDERSON^THOMAS^^^DR^^^AUSHICPR^L^^^UPIN|0191322W^ANDERSON^THOMAS^^^DR^^^AUSHICPR^L^^^UPIN|||||||N
ORC|RE||E062CF28-A67B-45D6-A5F8-B1423EDFB093^Demo Server^1FFA8984-7166-4655-B195-7B4FFFD2F136^GUID||CM|||||||0191322W^ANDERSON^THOMAS^^^DR^^^AUSHICPR^L^^^UPIN
OBR|1||E062CF28-A67B-45D6-A5F8-B1423EDFB093^Demo Practice^1FFA8984-7166-4655-B195-7B4FFFD2F136^GUID|11486-8^Chemotherapy Record^LN|||20050417+1000|||||||||0191322W^ANDERSON^THOMAS^^^DR^^^AUSHICPR^L^^^UPIN||From Demo Practice in File 20050417.736425 dated 17.04.2005||LN=E062CF28-A67B-45D6-A5F8-B1423EDFB093||200504172206+1000||PHY|C||^^^20050417+1000|0191322W^ANDERSON^THOMAS^^^DR^^^AUSHICPR^L^^^UPIN||||0191322W&ANDERSON&THOMAS&&&Dr&&AUSHICPR&AUSHICPR
OBX|1|NM|3141-9^Weight^LN||70|kg^^ISO+|||||F
OBX|2|NM|28325-9^Performance Status^LN||2||||||F
OBX|3|ST|21946-9^Chemotherapy Rx^LN||CHOP||||||F
OBX|4|FT|11486-8^^LN||This is a record of chemo being given.\.br\||||||F
BTS|1||1
FTS|1

1.8 ACKNOWLEDGEMENT PROCESSING

The International HL7 standard specifies two levels of acknowledgement processing: Original and Enhanced Modes.

(a) Original Mode, specifies that the message be acknowledged at the application level. The reasoning is that it is not sufficient to know that the underlying communications system guaranteed delivery of the message. It is also necessary to know that the receiving application processed the data successfully at a logical application level.

(b) Enhanced mode, The HL7 acknowledgment paradigm has been extended to distinguish both accept and application acknowledgments. With a positive accept acknowledgment, the receiving system commits the message to safe storage in a manner that releases the sending system from the need to resend the message. After the message has been processed by the receiving system, an application acknowledgment may be used to return the resultant status to the sending system.

This Australian HL7 standard requires the use of Enhanced Mode Acknowledgment and this is described in 8 Acknowledgement.