FHIR Lab2zorg V3.0.0-beta.3

This FHIR IG is currently under development and can not be considered stable and ready for use.

1 Introduction

This page describes the technical design of Lab2zorg (Lab2healthcare) as a subset of the Information standard lab exchange. This technical specification is implementer centric and complements the functional design. This page uses various terms as defined in the glossary (Dutch: Begrippenlijst). This page implements general principles applicable to FHIR as outlined by a central FHIR IG for R4. Please make sure you familiarize yourself with both the functional design and the FHIR IG for full appreciation of the context of this page.

Many laboratory results have important relationships to other observations and need to be grouped together. The FHIR specification defines several structures to do this:

• Observation and one or more Observation.hasMember elements.
  • Each .hasMember element references another Observation and the Observation with .hasMember elements thus serves as grouper for all Observations it references. Each Observation can be accessed individually. This is useful for panels and/or batteries of tests. This is what NL-CM:13.1.3 LaboratoryTest maps into.
  • Note that while FHIR Observation also allows references to resource types MolecularSequence and QuestionnaireResponse, there is no identified use case for that at time of writing.
  • An Observation without .hasMember elements is expected to be an individual result and has a value when one can be/is determined.
• Observation and one or more Observation.derivedFrom elements.
  • Each .derivedFrom element references another Observation references related measurements the observation is made from. This is what NL-CM:13.1.33 RelatedResult::LaboratoryTestResult maps into.
  • Note that while FHIR Observation also allows references to resource types DocumentReference, ImagingStudy, Media, QuestionnaireResponse and MolecularSequence, there is no identified use case for those at time of writing.
• Observation and one or more Observation.component elements.
  • .components of an Observation are not accessible individually. Whenever you access the Observation, you also access all its components. This is mostly useful when certain context is provided around the result. For lab observations this is expected to be less common. An example outside of the lab realm could be BloodPressure where systolic, diastolic, and cuff size are all in one Observation with 3 components.

This FHIR implementation guide assumes that systems (XIS) are able to make a connection to the right systems. It does not provide information on finding the right XIS nor does it provide information about security including authentication and authorization. Finding the right system, and security aspects of the connection, are dealt with by the infrastructure. Any relevant infrastructure is expected to have a framework in place to deal with this. The only assumption/requirement for an infrastructure is that this allows RESTful FHIR-based exchange as specified here.

2 Boundaries and relationships

2.1 Mappings between profiles and data set

Each transaction starts with links to the functional definition in an ART-DECOR publication and references one or several FHIR profiles. Where the functional definition contains all specific data elements for the transaction (prefixed with ‘lu-concept-v2’), the FHIR profiles only contain a mapping to these data elements that do not have a dependency on a zib counterpart. For example: ‘lu-concept-v2-4266’ (Specimen) has a relation with the zib element with id ‘NL-CM-13.1.2’, therefore no mapping with ‘lu-concept-v2-4266’ can be found in the profiles. On the other hand, ‘lu-concept-v2-4296’ (LaboratoryResultIdentification) has no relation with a zib element, therefore a mapping can be found in the relevant FHIR profile.

Because of open world modeling, the cardinality of elements in the FHIR profiles can be less strict than the cardinalities in the ART-DECOR transactions. However, the latter cardinality is leading when it comes to exchanging building blocks in the context of a specific transaction. For example: in the nl-core-LaboratoryTestResult profile, .performer has a core cardinality of 0..*, while in both the 'Send laboratory results' and ‘Serve laboratory results’ ART-DECOR transactions, the Performer element has a cardinality of 1..1 M. Therefore, .performer is expected to be filled with either a reference to an nl-core-HealthcareProvider-Organization resource.

Each transaction contains a Patient building block with cardinality 1..1 M. This patient is the subject of all other building blocks in the transaction, although no explicit relation exists in the data set. Therefore, a reference to a Patient resource conforming to the nl-core-Patient profile is expected in .subject of each FHIR instance of each building block.

Laboratory results in FHIR R4 overview

The single zib LaboratoryTestResult consists of objects that in FHIR are represented using different (instances of) resources:

• NL-CM:13.1.1 LaboratoryTestResult maps into profile nl-core-LaboratoryTestResult Observation and has .hasMember relationships with individual NL-CM:13.1.3 LaboratoryTests.
  • Note that this level only exists when LaboratoryTestResult contains NL-CM:13.1.4 PanelOrBattery. The concepts NL-CM:13.1.7 ResultType, NL-CM:13.1.5 Comment, and NL-CM:13.1.6 ResultStatus are not mapped in the absence of NL-CM:13.1.4 PanelOrBattery.
• NL-CM:13.1.3 LaboratoryTest also maps into profile nl-core-LaboratoryTestResult Observation and MAY be referenced by a different Observation.hasMember containing NL-CM:13.1.1 LaboratoryTestResult.
• NL-CM:13.1.2 Specimen maps into profile nl-core-LaboratoryTestResult.Specimen Specimen.
  • Note that there could be multiple instances of Specimen: one for the main NL-CM:13.1.16 SpecimenMaterial, and one per isolated NL-CM:13.1.22 Microorganism with a .parent relationship to the main specimen.
• NL-CM:13.1.29 SpecimenSource maps into profile nl-core-LaboratoryTestResult.Specimen.Source Device. This is a special case where the specimen did not come from the Patient directly.

2.2 Patient identification

This implementation guide assumes that the client system is able to make a connection to the right server that contains the patient's information. It does not provide information on finding the right server nor does it provide information about security. Moreover, each transaction is performed in the context of a specific (authenticated) patient, whose context might have been established using the authentication mechanisms described in external specifications such as the MedMij 'Afsprakenstelsel' or through the usage of search parameters for patient identification. Each server is required to perform filtering based on the patient associated with the context for the request or based on the patient identification search parameters, so only the records associated with the authenticated patient are returned.

When patient identification requires the use of search parameters, the following search parameters SHALL be supported:

• Patient: identifier
• Observation: patient

An example of a request that retrieves all Observation resources of a patient with a fake BSN of 11122233:

GET [base]/Observation?patient:identifier=http://fhir.nl/fhir/NamingSystem/bsn|111222333

2.3 Resource identification

All profiles used within the information standard contain .identifier elements with a cardinality of 0..* because of open world modeling. However, all ART-DECOR transactions referenced within this IG assign a 1..1 R cardinality, meaning a stable identifier SHOULD be provided, or the DataAbsentReason extension if a value is missing. Identifiers SHALL contain both a .system and a .value.

Because in HL7v3 (CDA) an identifier can only be composed using OIDs, the .system SHALL be an OID to accommodate compatibility in transformations to and from FHIR. The Dutch HL7v3 datatype variant of II also defines additional restrictions on the maximum length of both @root and @extension (equivalent to respectively .system and .value in FHIR). For the same compatibility reasons, .system SHALL have a maximum of 128 characters and .value SHALL have a maximum of 64 characters.

Systems that encounter or resolve references, either logical or literal, in resources they receive, SHALL NOT rewrite these references to a copy of these resources (with http://nictiz.nl/fhir/StructureDefinition/ext-CopyIndicator present) they may store. This means that relative literal references may need to be rewritten to absolute ones. This also goes for included secondary resources in transactions.

2.4 FHIR Profile Package

All use cases in this specification depend on the same set of FHIR profiles. The table below lists profiles that represent applicable zibs for laboratory result information exchange.

Nictiz uses the FHIR Packaging mechanism. This conveniently bundles all profiles, terminology, example material and other conformance resources you need into a single archive, which can be downloaded or installed using the appropriate FHIR tooling. This version of the information standard uses the following packages: nictiz.fhir.nl.r4.labexchange version 3.0.0-beta.2 or compatible nictiz.fhir.nl.r4.nl-core version 0.8.0-beta.1 or compatible nictiz.fhir.nl.r4.zib2020 version 0.6.0-beta.2 or compatible Note: packages use Semantic Versioning. Other versions can be used at will as long as they have the same major.minor number or a minor number higher than the stated version.

FHIR Profile	FHIR Resource	Based on zib (EN)
nl-core-LaboratoryTestResult	Observation	LaboratoryResult
nl-core-LaboratoryTestResult.Specimen	Specimen
nl-core-LaboratoryTestResult.Specimen.Source	Device
nl-core-Patient	Patient	Patient
nl-core-HealthcareProvider-Organization	Organization	HealthcareProvider

3 Actors involved

Persons		Systems		FHIR Capability Statements
Name	Description	Name	Description	Name	Description
Lab Professional	The user of a LIS	LIS	Laboratory information system	CapabilityStatement: Lab2Healthcare-Results-RetrieveServe	Retrieve [LAB-LRR]/serve [LAB-LRB] lab results requirements. A LIS is only expected to serve results in the context of Lab2zorg.
				CapabilityStatement: Lab2Healthcare-Results-SendReceive	Send [LAB-LRS]/receive [LAB-LRO] lab results requirements. A LIS is only expected to send results in the context of Lab2zorg.
Healthcare professional	The user of a XIS	XIS	(Any) Healthcare information system	CapabilityStatement: Lab2Healthcare-Results-RetrieveServe	Retrieve [LAB-LRR]/serve [LAB-LRB] lab results requirements. A XIS may both retrieve results and serve copies of results in the context of Lab2zorg.
				CapabilityStatement: Lab2Healthcare-Results-SendReceive	Send [LAB-LRS]/receive [LAB-LRO] lab results requirements. A XIS may both send copies of results and receive (copies of) results in the context of Lab2zorg.

4 Use cases

4.1 Health professional orders lab tests and receives results

4.1.1 Introduction

As defined in the functional design, a health professional can order laboratory tests after seeing a patient. Some laboratory tests such as blood gases and EBV serology consist of multiple subtests and are ordered together as one test (a panel). When the order has been received and performed by the laboratory, the results including interpretation are sent to the XIS of the requesting health professional together with the order and patient details. The main FHIR resource to express the laboratory test results is a DiagnosticReport.

4.1.2 Health professional orders lab tests

This transaction is not yet implemented.

4.1.3 Health professional receives lab results resulting from a request

4.1.3.1 Actors

Transaction group	Transaction	Actor	Role
Send laboratory results (PUSH)	Send laboratory results	LaboratoriumresultaatResultaatSturend Systeem [LAB-LRS]	Send lab results to the LAB-LRO
	Receive laboratory results	LaboratoriumresultaatResultaatOntvangend Systeem [LAB-LRO]	Respond to received lab results from the LAB-LRS

4.1.3.2 Invocations

4.1.3.2.1 LAB-LRS: request message

The LIS (LAB-LRS) sends lab results and relevant context information using a HTTP POST method on the endpoint of the XIS of the health professional that requested the laboratory test (LAB-LRO)

4.1.3.2.1.1 Trigger Events

This message is invoked when the LIS needs to send laboratory results to a XIS.

4.1.3.2.1.2 Message Semantics

A FHIR document is used for this use case. This approach is chosen because laboratory results resulting from a request include details about the patient and order, next to the actual laboratory results. In this context, the resources sent by the LIS should be considered a discrete package that is transmitted as-is. It is up to the receiving XIS to extract and persist the resources from the document that it considers relevant.

A FHIR document is sent by performing a HTTP POST command to the Bundle endpoint as shown:

POST [base]/Bundle

The body of the post submission is a Bundle with Bundle.type=document that has a Composition resource as the first resource. The Composition resource should conform to the Composition profile Composition. In this context, a Composition is solely used to send the laboratory results across in a document. Therefore, the Composition only contains one section with a reference to the DiagnosticReport. The DiagnosticReport contains information on the structure of all the resources in the document. All resources referenced by the DiagnosticReport SHALL be present in the Bundle. These resources SHALL conform to the matching profile(s) listed in the profile table. That table contains profiles that represent applicable zibs for laboratory result information exchange.

4.1.3.2.1.3 Identification

Resources SHALL have a stable identifier in the .identifier element for all resources if such an identifier exists in the underlying data. Not all data, like individual results, are currently known to have identifiers in all source systems, but when they exist they are essential and where they do not exist yet they SHOULD be considered. Having stable identification is essential in detection of duplicates and potential clinical decision making issues deriving from duplicates. For more information on dealing with identifiers, see the general FHIR IG.

The .identifier in DiagnosticReport SHALL at least be a Placer Order ID assigned by the placer (ordering application). The Placer Order ID identifies an order uniquely among all orders from a particular ordering application. In this case, a XIS (LAB-LRO). The .identifier MAY additionally be populated with a Filler Order ID, assigned by the filler (fulfilling/receiving application). This identifier is the order number associated with the filling/receiving application and uniquely identifies all orders from the particular filling application. In this case a LIS (LAB-LRS).

The placer/filler order identifiers, specimen identifiers, container identifiers, and observation identifiers are all identifiers issued by an information system, XIS or LIS. Identification always requires specification of the identification system that the identifier is from, and per the central FHIR IG guidance on identifiers this SHALL be an OID. There are a number of ways to get an OID, but most systems are expected to already have (access to) one:

• Your organization may have a UZI Registry Registration Number or URA. See also guidance on OIDs. The URA OID 2.16.528.1.1007.3.3 has a one to one correspondence with uri http://fhir.nl/fhir/NamingSystem/ura, but when you get to the system level this correspondence no longer holds. Hence the use of OIDs. Example:
  • The system ID: system urn:oid:2.16.528.1.1007.3.3.[URA] value [XIS/LIS]
  • Order Numbers: system urn:oid:2.16.528.1.1007.3.3.[URA].1 value 11111111
  • Specimen IDs : system urn:oid:2.16.528.1.1007.3.3.[URA].2 value 22222222
  • Container IDs: system urn:oid:2.16.528.1.1007.3.3.[URA].3 value 33333333
• Your system may have UZI Registry System ID under OID 2.16.528.1.1007.3.2. The system for the UZI System ID has a one to one correspondence with uri http://fhir.nl/fhir/NamingSystem/uzi-nr-sys, but applying to sub systems like order numbers etc. looks the same as the URA:
  • The system ID: system urn:oid:2.16.528.1.1007.3.2 value [UZI System ID]
  • Order Numbers: system urn:oid:2.16.528.1.1007.3.2.[UZI System ID].1 value 11111111
  • Specimen IDs : system urn:oid:2.16.528.1.1007.3.2.[UZI System ID].2 value 22222222
  • Container IDs: system urn:oid:2.16.528.1.1007.3.2.[UZI System ID].3 value 33333333
• Your lab system may have a three digit LABID that you may use as your base for all different kind of identifiers the system may issue. Example:
  • The system ID: system urn:oid:2.16.840.1.113883.2.4.3.11.61.4 value [LABID]
  • Order Numbers: system urn:oid:2.16.840.1.113883.2.4.3.11.61.4.[LABID].1 value [LABID]11111
  • Specimen IDs : system urn:oid:2.16.840.1.113883.2.4.3.11.61.4.[LABID].2 value [LABID]22222
  • Container IDs: system urn:oid:2.16.840.1.113883.2.4.3.11.61.4.[LABID].3 value [LABID]33333

Other common applicable identification systems exist. The main characteristic that the OID strategy SHALL have is persistent globally unique. There SHALL NOT ever be more than one object carrying the same identification, i.e. the same combination of identification system and identification value. If you run out of numbers, and have to restart your numbering because labs typically deal with max 8 characters in their IDs due to barcode constraints, you can still distinguish two identification values 11111111 from one another by changing the identification system value, e.g.:

• system urn:oid:2.16.840.1.113883.2.4.3.11.61.4.[LABID].1 value [LABID]11111
• system urn:oid:2.16.840.1.113883.2.4.3.11.61.4.[LABID].4 value [LABID]11111

While logic is required in creating OIDs, from the point of coming into existence they are plain strings. No semantics may be inferred from individual nodes in an OID. LIS A may have order numbers under a system ending in .1 in DiagnosticRepost.identifier, and LIS B may have specimen IDs under a system ending in .1 in Specimen.identifier. XIS A may even go as far as having a node for production versus test, followed by the node for order numbers, e.g. ending in .1.1 and .2.1.

System administrators SHALL keep record of the OIDs they issue to avoid inadvertent reuse. System administrators MAY delegate record keeping and maintenance, e.g. to a more central part in a larger organization they are part of.

4.1.3.2.1.4 Expected Actions

On receipt of the FHIR Document submission, the XIS (LAB-LRO):

• SHALL process creation of the Bundle;
• SHALL decide which, if any, of the resources in the Bundle are relevant for individual processing;
  • The XIS MAY update pre-existing information with the incoming information;
  • The XIS MAY keep its pre-existing matching resources as-is;
• SHALL be aware that the latest information for a lab result is available in the latest FHIR document that has not been followed up by any other FHIR document;
  • Please note that even a final document MAY be followed up by a document containing corrections.
• SHALL respond using a HTTP code and body that honors the Prefer header and interaction. See FHIR IG Handling Errors for response options in case of errors.

4.1.3.2.1.5 Must Support

The main FHIR resource to express the laboratory test results is a DiagnosticReport. Both the LIS and the XIS shall take into account that the profile contains Must Support flags. The base Must Support guidance requires specifications to define exactly the support expected for profile elements labeled Must Support.

For querying and reading the DiagnosticReport profile, Must Support on any profile data element SHALL be interpreted as follows:

• The LIS (LAB-LRS) SHALL be capable of populating all data elements as part of the query results.
• The XIS (LAB-LRO) SHALL be capable of processing resource instances containing the data elements without generating an error or causing the application to fail.
  • In other words the XIS (LAB-LRO) SHOULD be capable of displaying the data elements for human use or storing it for other purposes.
• In situations where information on a particular data element is not present and the reason for absence is unknown, the LIS (LAB-LRS) SHALL NOT include the data elements in the resource instance returned as part of the query results.
• The XIS (LAB-LRO) SHALL interpret missing data elements within resource instances as data not present in the LIS (LAB-LRS).
• The LIS (LAB-LRS) SHOULD send the reason for the missing information if the reason for the absence of data is known.
  • Refer to the section on Missing Data for guidance on how to handle missing data.
• The XIS (LAB-LRO) SHALL be able to process resource instances containing data elements asserting missing information.

4.1.3.2.2 LAB-LRO: response message

The XIS (LAB-LRO) returns an HTTP Status code appropriate to the processing outcome.

4.1.3.2.2.1 Trigger Events

The XIS (LAB-LRO) completed processing of the send laboratory results message.

4.1.3.2.2.2 Message Semantics

The XIS (LAB-LRO) SHALL return a 201 Created HTTP status code, and SHALL also return a Location header which contains the new Logical Id and Version Id of the created resource version. The XIS (LAB-LRO) SHOULD also return an ETag header with the versionId (if versioning is supported) and a Last-Modified header.

4.1.3.2.2.3 Expected Actions

The XIS/LIS (LAB-LRS) processes the results according to application-defined rules. The most basic of those rules would include marking the transaction as sent/processed successfully or flag a need for action like resending or contacting the LAB-LRO.

4.1.3.2.2.4 Handling Errors

The XIS (LAB-LRO) may be unable to accept a Bundle due to errors or because of technical or business rules. Refer to the Handling Errors section in the FHIR IG for more information.

4.2 Health professional retrieves lab results

4.2.1 Introduction

Healthcare professionals need to be able to retrieve laboratory results directly from a lab (LIS) or a secondary healthcare provider (XIS). Different healthcare professionals may have different needs and/or authorizations. The core FHIR specification offers support for a lot of use cases. This specification only outlines options for the identified scope and associated minimal expectations. As such it is not intended to be limiting to said expectations. Servers SHALL use the CapabilityStatement to advertise their implementation and clients SHOULD use this as means to discover the servers capabilities as per the FHIR specification, as well as publish their own capabilities. [FHIR RESTful] / [CapabilityStatement].

The identified use cases within the scope of this implementation guide are very broad:

• Get latest X results for one or more specific Observation.codes
• Get latest X results for any Observation.codes
• Get results on/before/after date X
• Get results on/before/after date X for one or more specific Observation.codes
• Get results based on the Observation.identifier

Each server SHALL perform filtering based on the patient, and results associated with the request context and patient identification search parameters, so only the records are returned that the requesting party is authorized for. Example expectations are that any ordering provider will have access to results related to his orders, and any requesting party interested in medication related results only has access to those.

A special word of caution about volume. It has been proven hard to impossible to define an optimum on how much history should be supported. For example some genetic tests are done once at age 15, and are still valid at age 80. Returning all results for someone age 80 could take an enormous toll on both server and client and is seldom relevant. Clients are therefore encouraged to be as specific as possible, by using both code and/or date and/or _count whenever possible. Servers SHOULD implement _count, and SHOULD implement an OperationOutcome that informs the client of a partial result set when the total number exceeds what a server will handle.

4.2.2 Actors

Transaction group	Transaction	Actor	Role
Retrieve laboratory results (PULL)	Retrieve laboratory results request	LaboratoriumresultaatResultaatRaadplegend Systeem [LAB-LRR]	Send a query to the LAB-LRB to retrieve lab results
	Retrieve laboratory results response	LaboratoriumresultaatResultaatBeschikbaarstellend Systeem [LAB-LRB]	Respond to a query from the LAB-LRR to retrieve lab results

4.2.3 Invocations

4.2.3.1 LAB-LRR: request message

The request message represents an HTTP GET parameterized query from the XIS (LAB-LRR) to the XIS/LIS (LAB-LRB).

4.2.3.1.1 Trigger events

When the healthcare professional wants to obtain laboratory results, it issues a retrieve laboratory results request message.

4.2.3.1.2 Message semantics

The XIS (LAB-LRR) executes an HTTP GET conforming to the FHIR RESTful and search specification against the XIS/LIS's Observation endpoint.

• Laboratory results are all under the .category observation, using query parameter category as token.
• Requesting data for a specific .subject is done using query parameter patient as reference, or on some network infrastructures with an authorization token. The FHIR query parameter type reference can take on many forms.
  • If you know what the Patient.id is, e.g. from previous interactions with the same endpoint, you may use:
    • patient=[id]
    • patient=[type]/[id]
    • patient=[url]
  • If you don't know what the Patient.id is, but you know the Patient.identifier, e.g. the Burgerservicenummer (BSN), you may use:
    • patient:identifier=[system]|[value]
• Requesting laboratory results of a specific type is done using query parameter code as token.
• Requesting laboratory results of a specific date (range) is done using query parameter date as token.
• Requesting laboratory results for a specific business identifier is done using query parameter identifier as token.

Basic query syntax

GET [base]/Observation?category=http://terminology.hl7.org/CodeSystem/observation-category|laboratory{&patient=Patient/[id] | &patient:identifier=[system]|[value]}{&[parameter(s)]&_include=[resource(s)]}

Examples

Parameter values have not been uri escaped in these examples for readability. This is likely necessary in practice.

Query parameters overview

Servers SHALL at minimum support all stated parameters and modifiers, and MAY support additional parameters and modifiers. Clients SHALL support required parameters, and MAY support optional parameters.

• category - token - 1..1 required - fixed value http://terminology.hl7.org/CodeSystem/observation-category|laboratory
• patient - token - 0..1 conditional - required if not solved using an alternative method like an authorization token
  • Modifier :identifier - 0..1 optional - required when searching by identifier
• code - token - 0..1 optional
• identifier - token - 0..1 optional - required when searching by unique identifier assigned to the observation
• date - date - 0..1 optional
  • Prefix eq - 0..1 optional - required when searching for results with .effective on exact date
  • Prefix lt - 0..1 optional - required when searching for results with .effective before date
  • Prefix le - 0..1 optional - required when searching for results with .effective on or before date
  • Prefix gt - 0..1 optional - required when searching for results with .effective after date
  • Prefix ge - 0..1 optional - required when searching for results with .effective on or after date
• _count - positiveInt - 0..1 optional
• _include - reference - 0..* optional - useful for request to include secondary related resources, e.g.:
  _include=Observation:patient,Observation:performer,Observation:has-member,Observation:specimen
  • Note that servers MAY, depending on their read capabilities, choose to implement inclusion of resources regardless of a client requesting this to satisfy the generic requirement that references SHALL be resolvable.

Operations

• lastn - shortcut FHIR core operation for getting the latest X results of specified types, or 'any' type
  • Parameter max - positiveInt - optional - default is max=1

4.2.3.1.2.1 Expected actions

The XIS/LIS (LAB-LRB) SHALL process the query to retrieve laboratory results.

4.2.3.2 LAB-LRB: response message

The XIS/LIS (LAB-LRB) returns an HTTP Status code appropriate to the processing as well as a FHIR Bundle including the matching information. Refer to the generic FHIR IG for more information on handling errors and status codes. Not finding a match based on stated parameters does not constitute an error.

4.2.3.2.1 Trigger events

The XIS/LIS (LAB-LRB) completed the processing of the retrieve laboratory results request message.

4.2.3.2.2 Message semantics

The XIS/LIS (LAB-LRB) SHALL process the request and, unless an error is found, respond with a Bundle resource of type searchset. Each Observation matching the request SHALL be marked with .entry.search.mode=match. Each otherwise included resource SHALL be marked with .entry.search.mode=include. If the searchset bundle contains less matching resources than the actual total set, then:

• the Bundle.link that holds the self link, SHOULD include the _count parameter to inform the client of what max was applied
• an OperationOutcome SHOULD be included marked with .entry.search.mode=outcome.

The resources in the response Bundle SHALL be a valid instance of their stated profile. All resources SHALL include their related profile canonical URL in the .meta.profile element in order to show compliance. The exception is the OperationOutcome resource for which there is no profile in this specification.

Example searchset Bundle

Example OperationOutcome

4.2.3.2.3 LAB-LRR: Expected actions

The XIS/LIS (LAB-LRR) SHALL process the response Bundle in accordance with the intentions of the trigger event that caused the retrieve. Actions may include discrete rendering on screen or in context with other information, triggering alerts on trends, ordering of (other) tests and more.

4.3 Health professional sends lab results to other health professional

4.3.1 Introduction

The functional design distinguishes two use cases where lab results may be sent with something else or separate. The process of 'sending' things in FHIR works by means of a RESTful 'create' action. You could create a single Observation on another system using POST Observation and the appropriate Observation in the request body. When you have multiple Observations to create, you could do that for every single Observation, or by means of a Bundle with all resources. This same Bundle approach works for one Observation too.

The added benefit of a Bundle lies in having a solution for all other resources you may want to send, e.g. MedicationRequest, and referenced resources like Patient, PractitionerRole, Practitioner and Organization. Sending the Observation without the resources it references would only work if the receiving server can resolve those. They should then already exist on that server, with references to them or they should be accessible on the source. Without access to the references in the Observation, the target server may not know which patient is involved or what lab this result came from.

4.3.2 Actors

Transaction group	Transaction	Actor	Role
Send laboratory results (PUSH)	Send laboratory results	LaboratoriumresultaatResultaatSturend Systeem [LAB-LRS]	Send lab results to the LAB-LRO
	Receive laboratory results	LaboratoriumresultaatResultaatOntvangend Systeem [LAB-LRO]	Respond to received lab results from the LAB-LRS

4.3.3 Invocations

4.3.3.1 LAB-LRS: request message

The XIS/LIS (LAB-LRS) sends lab results using the HTTP POST method on the target XIS's (LAB-LRO) base. Note that lab results may or may not be sent in tandem with other resources like MedicationRequest. The same principles apply with or without these other resources. The server can only process the incoming request correctly if it understands what is being sent which includes being able to resolve references.

4.3.3.1.1 Trigger Events

This message is invoked when the XIS needs to send one or more laboratory results to another XIS.

4.3.3.1.2 Message Semantics

Because sending laboratory results will most likely consist of multiple Observations, a transaction interaction is used. This allows for creating a set of resources in a single interaction and makes it possible to include referenced secondary resources if needed.

A transaction interaction is performed by an HTTP POST command as shown:

POST [base]

The body of the post submission is a Bundle with Bundle.type=transaction. Each entry carries request details (Bundle.entry.request) that provides the HTTP details of the action in order to inform the system processing the transaction of what to do for the entry. (Note: .request SHALL be present, even for the resources which aren't Observations. See the overarching principles for more information.)

Identification

Resources SHALL have a stable identifier in the .identifier element for all resources if such an identifier exists in the underlying data. Not all data, like individual results, are currently known to have identifiers in all source systems, but when they exist they are essential and where they do not exist yet they SHOULD be considered. Having stable identification is essential in detection of duplicates and potential clinical decision making issues deriving from duplicates. For more information on dealing with identifiers, see the general FHIR IG.

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• transaction
• create
• HTTP Prefer header

The laboratory result data sent to the XIS SHALL conform to the matching profile(s) listed in the profile table. That table contains profiles that represent applicable zibs for laboratory result information exchange.

4.3.3.1.2.1 Expected Actions

On receipt of the submission, the XIS (LAB-LRO) SHALL:

• process all contained requests successfully or process nothing.
• process creation of or updating all Observation resources.
  • Updating might be in order e.g. when corrections are sent or when previously pending tests have been updated with results.
• match Patient, Practitioner(Role), Organization to pre-existing resources on its server.
  • The server MAY update pre-existing information with the incoming information.
  • The server MAY keep its pre-existing matching resources as-is.
  • The server SHALL create new resources if no matching resource is found (unknown patient, new physician in otherwise known organization, etc.).
• decide if any available Specimen and/or Device resources are relevant.
  • If the server decides to ignore Specimen or Device information, it SHALL not keep the references to them.
• respond using HTTP 200 and a Bundle with detail in case of success. See FHIR IG Handling Errors for response options in case of errors.
  • Note that the response Bundle with type transaction-response SHALL be specific about how the server handled the request Bundle.

4.3.3.2 LAB-LRO: response message

The XIS (LAB-LRO) returns an HTTP Status code appropriate to the processing outcome and returns a Bundle with Bundle.type=batch-response, that contains one entry for each entry in the request, in the same order, with the outcome of processing the entry.

4.3.3.2.1 Trigger Events

The XIS (LAB-LRO) completed processing of the send laboratory results message.

4.3.3.2.2 Message Semantics

The XIS (LAB-LRO) SHALL return a Bundle with Bundle.type=batch-response that contains one entry for each entry in the request, in the same order, with the outcome of processing the entry.

A client may use the returned Bundle to track the outcomes of processing the entry, and the identities assigned to the resources by the server. Each entry element SHALL contain a response element which details the outcome of processing the entry - the HTTP status code, and the location and ETag header values, which are used for identifying and versioning the resources. In addition, a resource may be included in the entry, as specified by the Prefer header sent by the LAB-LRS.

Read more:

• create
• batch
• HTTP Prefer header
• HTTP ETag header

4.3.3.2.3 Expected Actions

The XIS/LIS (LAB-LRS) processes the results according to application-defined rules. The most basic of those rules would include marking the transaction as sent/processed successfully or flag a need for action like resending or contacting the LAB-LRO.

4.3.3.2.4 Handling Errors

The XIS (LAB-LRO) may be unable to accept a Bundle due to errors or because of technical or business rules. Refer to the Handling Errors section in the FHIR IG for more information.

4.4 Health professional reports result leading into a notification "new lab results" for subscribed healthcare professional(s)

This use case will be added in a future release.

5 Release Notes

Please note that we have gained new insights based on the developments in HL7 Europe and the HL7 WGM. The necessary changes based on this feedback will be addressed and released in the next release.