Pathway definition
Describes the intended model of care. This is the primary business artefact held in the catalogue and should not be tied to named applications, interfaces, provider locations or local procedures.
A proposed approach to representing healthcare pathways as governed, technology-neutral business artefacts that can be catalogued, compared, versioned and related to local implementations.
HPDS is being developed by Agile Health Informatics Ltd for open review and testing against real pathway catalogues. It has not been submitted to, reviewed by or approved by ISO, IEC or a national standards body. The proposal remains subject to change.
Healthcare organisations routinely catalogue applications, interfaces, services, data assets and standards. Pathways are more often distributed across guidance documents, diagrams, spreadsheets, local operating procedures and system configuration. That makes them difficult to discover, compare, govern, reuse and relate consistently to information requirements and technology.
When pathway meaning is dispersed across documents and systems, important distinctions can become implicit: who is responsible, what information is required, which decisions change the route, what outcome is intended, and which parts belong to local implementation rather than to the pathway itself.
HPDS treats the pathway definition as a governed business artefact in its own right. It is intended to remain intelligible to clinicians, managers and architects while also supporting structured processing and controlled lifecycle management.
Keeping these layers separate allows the intended model of care to remain stable and comparable even when organisations use different teams, systems and local operating arrangements.
Describes the intended model of care. This is the primary business artefact held in the catalogue and should not be tied to named applications, interfaces, provider locations or local procedures.
Describes how an organisation or health system realises a pathway definition through particular organisational and technical arrangements, including explicit deviations where they exist.
Represents the actual course of care experienced by an individual. Patient-level instances contain personal health information and sit outside the normative scope of the proposed standard.
The proposed model brings the principal business concerns of a pathway into one governed description while allowing the level of detail to reflect the purpose of the catalogue.
The proposal occupies a catalogue-oriented business layer. Other standards and modelling languages can provide conceptual foundations, semantic bindings, exchange representations, behavioural models and computable implementation artefacts.
ISO 13940 provides a conceptual basis for continuity of care. HL7 FHIR can represent shareable plan definitions and implementation artefacts. BPMN, CMMN and DMN can provide precise behavioural and decision views. WHO SMART Guidelines and Digital Adaptation Kits provide structured, software-neutral guidance artefacts.
HPDS proposes the catalogue-ready pathway business artefact that can reference, map to or be realised through those approaches without requiring one of them to serve every purpose.
The working draft defines four cumulative levels. A higher level is not inherently better. A catalogue used for discovery or commissioning discussion may be fit for purpose without computable expressions.
Governed minimum dataset, persistent identity and a human-readable catalogue record.
Explicit identified elements with complete structural and behavioural relationships.
Important concepts and criteria linked to versioned semantic resources or declared as local terms.
Criteria and temporal constraints expressed under a declared expression profile where appropriate.
Its purpose is to make pathway meaning governable and reusable, while leaving clinical authority and technical implementation with the appropriate people and standards.
Conformance to the representation does not establish that the clinical content is safe, appropriate or approved.
Individual pathway instances and personal health information remain outside the normative pathway definition.
Messages, endpoints, protocols and integration products belong to implementation architecture.
The proposal does not require a particular process notation, terminology, information standard or enterprise architecture tool.
The demonstrator uses a synthetic reference catalogue to show how pathway definitions can remain clinically recognisable while being separated from local delivery arrangements, shared-record capabilities and technical implementation detail.
It includes a guided clinical tour, an interactive pathway catalogue, examples of reference versus local delivery, evidence provenance and a technical view of the draft HPDS mapping.
The working draft is intended to be challenged against real pathway catalogues rather than accepted on the basis of the model alone.
The current material should be read as a proposal for review and practical testing. The name “Healthcare Pathway Description Standard” describes the intended subject and form of the work; it does not imply formal standardisation or accreditation.