Catherine Hoang Ioana Singureanu Greg Staudenmaier Detailed Clinical Models for Medical Device Domain Analysis Model 1.

Slides:



Advertisements
Similar presentations
Integrating the Healthcare Enterprise IHE Overview Keith W. Boone Interoperability Architect, GE Healthcare Co-chair, IHE Patient Care Coordination PC.
Advertisements

HDF: HL7 Methodology Ioana Singureanu M&M co-chair, HDF Editor Eversolve, LLC.
Medical Device Standards
Device and EMR interoperability (IDCO). Implantable Cardiac Device Information is Collected At Implant … During In Clinic Follow-ups … And in the Home.
QIDAM Issues and proposals for a logical model For discussion during HL7 WG Meeting in Jan 2014 Thursday Q3.
Chapter 22 Object-Oriented Systems Analysis and Design and UML Systems Analysis and Design Kendall and Kendall Fifth Edition.
The HITCH project: Cooperation between EuroRec and IHE Pascal Coorevits EuroRec 2010 Annual Conference June 18 th 2010.
Lecture 5 Standardized Terminology and Language in Health Care (Chapter 15)
L4-1-S1 UML Overview © M.E. Fayad SJSU -- CmpE Software Architectures Dr. M.E. Fayad, Professor Computer Engineering Department, Room #283I.
© 2005 Prentice Hall4-1 Stumpf and Teague Object-Oriented Systems Analysis and Design with UML.
Device and EMR interoperability (IDCO). Implantable Cardiac Device Information is Collected At Implant … During In Clinic Follow-ups … And in the Home.
FHIM Overview How the FHIM can organize other information modeling efforts.
USE Case Model.
September, 2005What IHE Delivers IHE Eye Care Integration Profiles Andrew Casertano Department of Veterans Affairs.
Domain Analysis Models and Detailed Clinical Models A methodological comparison to support a project decision.
Initial slides for Layered Service Architecture
UML - Development Process 1 Software Development Process Using UML (2)
Introduction to RUP Spring Sharif Univ. of Tech.2 Outlines What is RUP? RUP Phases –Inception –Elaboration –Construction –Transition.
® IBM Software Group © 2006 IBM Corporation Rational Software France Object-Oriented Analysis and Design with UML2 and Rational Software Modeler 06. Requirements.
The EHR-S FIM project plans to harmonize the EHR-S FM R2
July 20, 2007 Healthcare Information Technology Standards Panel Principles for Proper Use of HITSP Interoperability Specifications And Proposal for Proper.
HL7 HL7  Health Level Seven (HL7) is a non-profit organization involved in the development of international healthcare.
IHE Profile – SOA Analysis: In Progress Update Brian McIndoe December 6, 2010.
National Institute of Standards and Technology Technology Administration U.S. Department of Commerce 1 Patient Care Devices Domain Test Effort Integrating.
OSEHRA Medical Device Integration Adapter (MDIA) Project Briefing.
Standards Analysis Summary vMR – Pros Designed for computability Compact Wire Format Aligned with HeD Efforts – Cons Limited Vendor Adoption thus far Represents.
Public Health Reporting Initiative: Stage 2 Draft Roadmap.
1 MFI-5: Metamodel for Process models registration HE Keqing, WANG Chong State Key Lab. Of Software Engineering, Wuhan University
Networking and Health Information Exchange Unit 6b EHR Functional Model Standards.
1 HITSP – enabling healthcare interoperability Current Framework and Fundamental Concepts  For those unfamiliar with the HITSP Harmonization Framework.
Sept 13-15, 2004IHE Interoperability Workshop 1 Integrating the Healthcare Enterprise Overview of IHE IT Infrastructure Patient Synchronized Applications.
Sharing Value Sets (SVS Profile) Ana Estelrich GIP-DMP.
Sept 13-15, 2004IHE Interoperability Workshop 1 Integrating the Healthcare Enterprise HIMSS Demonstration XDS Document Content Specifications Keith W.
Briefing: HL7 Working Group Meeting Update for the VCDE Community Dianne M. Reeves Associate Director, Biomedical Data Standards NCI CBIIT VCDE Meeting.
1 Introduction to Software Engineering Lecture 1.
Software Engineering Prof. Ing. Ivo Vondrak, CSc. Dept. of Computer Science Technical University of Ostrava
Unified Modeling Language* Keng Siau University of Nebraska-Lincoln *Adapted from “Software Architecture and the UML” by Grady Booch.
L6-S1 UML Overview 2003 SJSU -- CmpE Advanced Object-Oriented Analysis & Design Dr. M.E. Fayad, Professor Computer Engineering Department, Room #283I College.
Networking and Health Information Exchange Unit 5b Health Data Interchange Standards.
IHE Profile – SOA Analysis: In Progress Update Brian McIndoe January 18, 2011.
S&I Integration with NIEM (DRAFT) Standards Development Support June 8, 2011.
1 Capturing Requirements As Use Cases To be discussed –Artifacts created in the requirements workflow –Workers participating in the requirements workflow.
FDT Foil no 1 On Methodology from Domain to System Descriptions by Rolv Bræk NTNU Workshop on Philosophy and Applicablitiy of Formal Languages Geneve 15.
1 Healthcare Information Technology Standards Panel Care Delivery - IS01 Electronic Health Record (EHR) Laboratory Results Reporting July 6, 2007.
Data Segmentation for Privacy November 16 th, 2011.
This material was developed by Duke University, funded by the Department of Health and Human Services, Office of the National Coordinator for Health Information.
PCD User Handbook 2010 Purpose The Handbook is designed to help healthcare professionals implement IHE on a new clinical system purchase or upgrade an.
Networking and Health Information Exchange Unit 6a EHR Functional Model Standards.
Ontology-Based Interoperability Service for HL7 Interfaces Implementation Carolina González, Bernd Blobel and Diego López eHealth Competence Center, Regensurg.
Device and EMR interoperability (IDCO). Implantable Cardiac Device Information is Collected At Implant … During In Clinic Follow-ups … And in the Home.
OOD OO Design. OOD-2 OO Development Requirements Use case analysis OO Analysis –Models from the domain and application OO Design –Mapping of model.
Helping the Cause of Medical Device Interoperability Through Standards- based Test Tools DoC/NIST John J. Garguilo January 25,
Integrating the Healthcare Enterprise The IHE Process: Developing Standards-based Solutions Kevin O’Donnell Co-chair, IHE Radiology Planning Committee.
Chapter 7 Part II Structuring System Process Requirements MIS 215 System Analysis and Design.
How To Edit an IHE Profile Webinar Presentation for QRPH Editors Vassil Peytchev, Epic October 19, 2009.
Integrating the Healthcare Enterprise Retrieve Information for Display (RID) Integration Profile Ellie Avraham Kodak Health Imaging IHE IT Infrastructure.
ITI Infrastructure - Wednesday November 7th, IHE IT infrastructure “Terminology Sharing” Christel Daniel (AP-HP, INSERM, Paris), Ana Esterlich (GIP-DMP),
Informatics for Scientific Data Bio-informatics and Medical Informatics Week 9 Lecture notes INF 380E: Perspectives on Information.
Copyright © 2009 by The McGraw-Hill Companies, Inc. All Rights Reserved. McGraw-Hill/Irwin Chapter 2 Clinical Information Standards – Unit 3 seminar Electronic.
eHealth Standards and Profiles in Action for Europe and Beyond
Healthcare Information Technology Standards Panel
Current Framework and Fundamental Concepts
an alliance among HL7, CEN and OpenEHR ?
Retrieve Protocol for Execution (RPE)
Object Oriented Analysis and Design
, editor October 8, 2011 DRAFT-D
Software Development Process Using UML Recap
Presentation transcript:

Catherine Hoang Ioana Singureanu Greg Staudenmaier Detailed Clinical Models for Medical Device Domain Analysis Model 1

Overview Detailed Clinical Model (DCM) – Atomic clinical information – Promote semantic clarity and reuse Standard Terminology is built-in rather than an afterthought (e.g. primary and secondary standard-based coding system) Structured information to support – Process improvement – Interoperability and automation Reusable in many contexts – New standards – Profiling existing standards – Application development – Interoperability Domain Analysis Model (DAM) – Describe the stakeholders requirements to a integrators, developers, vendors, etc. – Assist communication among stakeholder groups – Uses a Std. modeling language (UML) improves communication, identifies main concepts, and leads to consensus – Models can be used to generate code or other models (e.g. ontology) – Methodology that supports the development of DCMs Context for DCMs 2

Glossary DAM: Domain Analysis Model UML: Unified Modeling Language – a standard developed by the Object Management Group DCM: Detailed Clinical Model – reusable information models, standardized LOINC: Logical Observation Identifiers Names and Codes – standard codes for laboratory SNOMED-CT: Systematized Nomenclature of Medicine-- Clinical Terms – Terminology System ISO: International Organization for Standardization – standards development organization HL7: Health Level Seven- healthcare interoperability standards development organization IHE: Integrating the Healthcare Enterprise – standards-related consortium Continua Health Alliance – standards-related consortium specialized in personal healthcare devices 3

May 2011: Ballot Details This ballot is informative and will expanded as new requirements and use cases are identified The ballot artifacts are intended to be used: – by providers To express semantic interoperability requirements (e.g. RFP) – by consortia (e.g. IHE, Continua Health Alliance) To develop Integration and Content Profile – by standard development organizations (e.g. HL7, ISO) To develop new standards for interoperability Ballot: V3 Ballot  Domain Analysis Models: – Project Site: – Releases: – Latest project artifacts 4

Specification history September Draft for Comment Initial version documenting the Domain Analysis for the following use cases: Intubate Patient - Unplanned Manage Patient on Ventilator Liberate Patient from Ventilator, Planned May Informative In addition to addressing the ballot comments, this ballot includes additional use cases that are a high priority for the project stakeholders.: Post-Operative Patient Transport Patient-to-device Association Time Synchronization for Networked Devices and for Legacy Devices 5

Approach 1.Gathered requirements illustrated by scenarios, standard operating procedures, and stakeholder requirements 2.Use cases that were derived from clinical scenario illustrate the requirements in a precise way. Use cases identify the capabilities and user or system roles involved. 3.Next we elaborated the use cases as workflows, step by step, identify the type of information produced or required by each step 4.Refine the information structures (correspond to device data) required to support workflow – Includes standard terminology bindings – Interoperability requirements with the information systems between devices Consistent, repeatable approach/methodology Ballot Document Structure and Process

Actors to specify roles for business users relative to the use cases in scope Identify the users roles and/or system roles for users and systems involved in the clinical scenario(s) 7 Is a Care Team Member… Clinician roles Is a Clinician… Care Team Member roles

Business Use Case Analysis to specify… Use Cases – Active verb – Based on requirements and clinical scenarios – Narrative description Preconditions Steps  Workflow Postconditions Actors – Participants in use cases – A role relative to the use case Users, systems Actor participation …based on Workflow Use Case Business Use Case Reference to workflow Technical Use Case

Device State Transition Condition Device to Patient Association – State Transitions Patient associated to one more devices Device undergoes state changes – connected/disconnected to patient – settings configured 9 Patient Ready Patient Not Available Device Assigned to a Patient

Clinical Workflow 10 Role Process Step Information as input into a step Information produced by a step Trigger Device Data produced by a step Decision

Post-0perative Transport 11 EHR Data

Post-0perative Transport 12 Device Data

Post-0perative Transport 13 Information Received

Technical Use Case Actors: System Roles The process steps are described as system interactions Synchronize Time is a high-priority requirements 14 System role Technica l Use Case System role Technical Use Case

Time Synchronization for Legacy Devices Legacy Devices are unable to synchronize time automatically – Missing network connection – Missing support for protocol (SNTP) Device Manager required to – report device observation and parameters – Synchronized – It supplies time correction information (synchronized time) 15 Device Manager Medical Device Network Time Server

Time Synchronization +Time Correction 16 Time correction Synchronization Use case is realized differently for legacy devices vs. networked/interoperable devices

Patient to Device Association – Interoperable Medical Device 17 Choice 1: Using Hospital Info System (ADT) Choice 2: Enter at point-of-care

Patient to Device Association – Legacy Medical Device 18 Choice 1: Location based Choice 3: Patient association using Device Manager Device Manager Choice 2: Patient assigned at point-of-care

Information Derived from Workflow Analysis High-level, identifies the information used or produced, precursors to DCMs 19 Device Observation Device Configuration Common/ Shared Information EHR Data Required

Focus of the analysis: Medical Device Interoperability Emphasis on device-to-device and device-to-system interoperability and automation We specify the structure of relevant types of data 20 Device Observation Device Configuration Common/ Shared Information

Information Analysis to specify context for DCMs 21 attribute class association repetitions data type for date/time

DCMs provide the final level of detail : Standard Terminology 22 DCM Candidate Parameter properties Terminology Constraints Inherited Constraints Is a “Ventilator Setting” Reusable data that may be used in information exchanges