HL7 Informative Document: Patient Information Quality Improvement (PIQI) Framework, Edition 1, published by HL7 Cross-Group Projects Work Group. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ballot built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/piqi/ and changes regularly. See the Directory of published versions
The PIQI Framework is structured into four distinct functional but interrelated components: 1) the taxonomy for categorizing dimensions 2) the patient-centric information model for organizing data elements, 3) simple assessment modules (SAMs) to measure quality, and 4) the evaluation criteria to organize and interpret the measures relative to an overarching use case. Together, these components provide a structured and adaptable approach to assess and enhance the quality of patient-oriented healthcare data, ultimately increasing the certainty and usability of this critical information.
This foundational component establishes a well-organized taxonomy that categorizes the various dimensions to be measured in healthcare data quality assessment. A PIQI dimension may be accuracy, completeness, consistency, timeliness or reliability, among others. The taxonomy serves as a structured framework for classifying the aspects of data quality that need to be evaluated. By categorizing these dimensions, it enables a clear understanding of what aspects of data quality are being assessed, providing a standardized and consistent foundation for the assessment process.
This component of the framework focuses on the patient data elements and characteristics assessed for a use case (e.g., USCDI, CACDI, billing). It represents a simplified information model that defines and organizes the patient-centric data elements that are most important to ensuring the accurate representation of a given patient, ensuring alignment with the evolving needs of healthcare information models. This information model serves as the core data structure against which data quality assessments are performed. It may include the data elements related to patient demographics, medical history, treatment records, and any other pertinent healthcare information. The model facilitates the mapping of these elements to the taxonomy of dimensions, ensuring that each data element is assessed against relevant criteria.
A simple assessment module (SAM) is a logical measurement aligned to a qualitative dimension applied to a model element or characteristic according to a pattern. The input parameters of the module are based on the pattern of the assessment, but the returned result is always a ‘pass’ or ‘fail’ (or 0/1). These modules are intended to be organized into one or many hierarchical collections of SAMs to collectively paint a larger qualitative picture as defined by a given use case.
The Evaluation Criteria component represents a use case oriented hierarchical collection of simple assessments aligned to the patient information model. It is the function of the evaluation criteria to describe the relevance of each assessment to the acceptability of each characteristic, element, and essential patient data submission in its entirety, relative to a given use case.
A healthcare specific taxonomy or qualitative dimension applied to a patient-centric information model can establish a common way of expressing and understanding the scope and nature of quality concerns that currently inhibit interoperability partners’ ability to trust patient information, regardless of whether it is local or received from an external entity.
Being aligned to patient information specifically, rather than being a generic quality-oriented framework, provides the benefit of highly relevant, fit-for-purpose, prioritizable results.
The use of a standardized information model coupled with a standard taxonomy as a basis for the deployment of modular assessments should allow for portable evaluation libraries that should function the same regardless of the source of patient information. The evaluation libraries are portable assets that can be shared across institutions and deployed centrally in a transactional manner.
The PIQI Framework is designed to be implemented within a community of practice with encapsulated, portable, content driven components, the ability to share knowledge and evolve, which establishes great potential for rapid evolution and adoption.
The PIQI Framework starts with a simple model intended to support the assessment of core clinical patient data. The simplicity of this model allows for extension through the addition of attributes and data classes. Ideally these extensions would be adopted into the core PIQI model through a standard process.
While many of the foundational, attribute level SAMs are algorithmic, SAMs that apply to codable concepts, elements, data classes, and patient level data often require structured content in the form of value sets, tuples, and other data patterns. These packages of SAMs and related content can be openly shared or licensed in a community portal. More sophisticated algorithmic SAMs, perhaps based on generative AI, could also be hosted as RESTful services through wrapper SAM interfaces.
While the Evaluation Rubrics in PIQI are designed to be configured to support the needs of the implementer, the ability to establish sanctioned standard Evaluation Rubrics is one of the most beneficial features of the PIQI Framework. The ability to publish and share an evaluation Rubrics, along with its dependent SAMs and PIQI components can minimize duplication of effort and provide a powerful way to create a common basis for understanding data quality across the community.