Do not launch ANY of the links while your are in create or edit mode. There is a good chance all of your work will be gone.
Template Usage Information:
- Submit template change requests to PMO@HL7.org
- For Reaffirmations, please refer to the FAQ in Hl7 Project Scope Statement Instructions for a list of which sections and fields should be completed
Project Name and ID
Enter the name of the project here: Multiple Chronic Conditions (MCC) Dynamic Electronic Care Planning and Management FHIR IG
Complete this section for all “Direct to Normative” ballot projects and when a project proceeds from “Informative to Normative” or “STU to Normative”.
Forward PSS to the TSC (via tscpm@HL7.org); this triggers American National Standards Institute (ANSI) Project Initiation Notification (PINS) submission.
TSC Notification: Informative/STU to Normative
Date: Submission date
- or - Direct to Normative (no STU) (includes reaffirmations)
Identify ISO, IEC or ISO/IEC standard to be adopted in text box below
Enter info here if an ISO, IEC, or ISO/IEC Standard is to be adopted as an American National Standard; Enter the designation of the standard(s) to be adopted:
Includes text from ISO, IEC or ISO/IEC standard: Check here if this standard includes excerpted text from one or more ISO, IEC or ISO/IEC standards, but is not an identical or modified adoption.
Select the unit of measure used in the standard; if no measurements are in the standard, select N/A
Investigative Project (aka PSS-Lite)
Check this box when the project is investigative or exploratory in nature, which allows limited project scope definition. Sections 1-Project Name, 2-Sponsoring Group(s)/Project Team, 3a-Project Scope, 3b-Project Need, 3e-Project Objectives/Deliverables/Target Dates, 3i-Project Document Repository, 6b-[Realm, if known], and 6d-[applicable Approval Dates] are required for Investigative Project. Investigative Project specific instructions are highlighted in yellow. An investigative project must advance in two WGM cycles, requiring a full scope statement. Otherwise the project will be closed.
2. Sponsoring Group(s) / Project Team
2.a. Primary Sponsor/Work Group
Primary Sponsor/Work Group
Patient Care Work Group
2.b. Co-sponsor Work Group(s)
Co-sponsor Work Group(s):(Enter co-sponsor approval dates in Section 6.d Project Approval Dates)
Clinical decision Support (CDS) - Agreed Feb 26, 2020 Plan Definition and FHIR Clinical Guidelines work
Learning Health System - Agreed March 03, 2020
|Indicate the level of involvement that the co-sponsor will have for this project:|
|Request formal content review prior to ballot|
|Request periodic project updates. Specify period||At WGMs and as requested|
|Other Involvement. Specify details here:|
2.c. Project Team
All names should have confirmed their role in the project prior to submission to the TSC.
Project facilitator (1Mandatory)
Karen Bertodatti, Emma Jones, Gay Dolin
Other interested parties and their roles
PC (Care Plan Team) - Patient-Centered Care Planning
Pharm - Pharmacy Work Group
Vocab - Value set validation etc
Gay Dolin, Emma Jones, Dave Carlson, Jay Lyle
Gay Dolin, Emma Jones
Gay Dolin, Himali Saitwal, Rob Mclure, Rob Hausam
Domain expert rep
Jenna Norton, Arlene Bierman, Stephen Chu, Emma Jones, Laura Heerman
Business requirement analyst
Emma Jones, Gay Dolin
Conformance facilitator (for IG projects)
Gay Dolin, Dave Carlson, Jay Lyle
Other facilitators (SOA, etc)
Bryn Rhodes, Dave Carlson, Sean Muir
Implementers (2Mandatory for STU projects)
FHIR Project Note: The implementer requirement will be handled by the “balloting” project. Therefore work groups do not fill out the above section. However, feel free to list implementers specific to your work group’s resources if you know of any.
1) RTI - leading multiple implementers
3) AHRQ ACTION III Networks https://www.ahrq.gov/research/findings/factsheets/translating/action3/actionIIIpartners.html
3. Project Definition
3.a. Project Scope
Initiated by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) and the Agency for Healthcare Research and Quality (AHRQ), the multiple chronic conditions (MCC) Dynamic electronic care (eCare) Plan Project aims to develop, test, and pilot an interoperable ambulatory eCare plan that will provide a health information technology system agnostic framework for viewing and sharing of critical patient-centered data across home, community, clinic, and research-based settings for persons with MCC, initially focusing on chronic kidney disease (CKD), type 2 diabetes mellitus (T2D), cardiovascular disease (hypertension, ischemic heart disease and heart failure), and pain and expanding as needed to other chronic conditions as needed for an MCC Care Plan. The MCC Dynamic eCare Plan Project will:
- Identify use cases to support the documentation and exchange of MCC eCare plan data within EHRs and other healthcare technology systems.
- Identify, develop and prioritize the necessary MCC data elements and clinical terminology standards, clinical information models (CIM), and FHIR mappings that will enable the standardized transfer of data across health settings;
- Identify workflow processes required to support basic care coordination requirements such as processes defined in the IHE dynamic care planning technical profile
- Develop, test, and ballot an HL7® Fast Health Interoperability Resource (FHIR®) Implementation Guide based on the defined use cases and MCC data elements.
- The project team recognizes that over the five year project course that FHIR profiles will evolve.
- Given the long project timelines alignment to changing profiles and resources will be maintained as required (e.g., provider specifications).
- This FHIR implementation guide will use the US Core profiles. If this FHIR implementation guide is unable to use a US Core profile, we will request approval from the US Realm Steering Committee, and provide the US Realm Steering Committee an approved rationale for deviation in the implementation guide where applicable.
- In latter part of the project:
- Examine requirements with respect to conflicts in care recommendations and/or care delivery which may exist between chronic conditions within the eCare plan and across systems
- If Plan definitions applied, examine requirements with respect to de-duplication in Plan Definitions applied
- Identify opportunities and challenges of data retrieval.
- Externally to the HL7 Project, the encompassing NIH/AHRQ project will develop and test an open-source clinician facing SMART on FHIR dynamic eCare plan application for managing persons with MCC; leveraging work done in previous FHIR Connectathon Care Planning and management tracks, FHIR Plan Definition and FHIR Clinical Guidelines.
3.b. Project Need
More than 25 percent of Americans have MCC, accounting for more than 65 percent of U.S. health care spending. These individuals have complex health needs handled by diverse providers, across multiple settings of care. As a result, their care is often fragmented, poorly coordinated and inefficient. Therefore, data aggregation is particularly important and challenging for people with MCC. These challenges will increasingly strain the U.S. health system, with the aging of the U.S. population. Projections suggest numbers of adults aged 65 and older will more than double and numbers of those aged 85 and older will triple by 2050.
Care plans are a prominent part of multifaceted, care coordination interventions that reduce mortality and hospitalizations and improve disease management and satisfaction. In addition, proactive care planning promotes person-centeredness, improves outcomes, and reduces the cost of care. By design, care plans take a patient-centered approach, both by making comprehensive health data available across providers and settings and through the incorporation of data elements that have not traditionally been included in health IT systems (e.g., social determinants of health [SDH], patient health and life goals, patient preferences). While Care Plans have been developed, they remain paper-based in many U.S. healthcare settings and are not standardized and interoperable across care settings when electronic. While care plans focused on a single disease or condition are unlikely to be tenable for patients with MCC or their providers, existing care plans infrequently address individuals with MCC. The development of care plans based on structured data has been proposed as a method for enabling electronic systems to pull together and share data elements automatically and dynamically. Such aggregated data would not only provide actionable information to identify and achieve health and wellness goals for individuals with MCC, but also would reduce missingness and improve quality of point-of-care data for use in pragmatic research.
The Fast Healthcare Interoperability Resources (FHIR) specification is an open-source standard for exchanging healthcare information electronically based on emerging industry approaches. The FHIR workflow specification includes a CarePlan request resource that may facilitate the transfer of data for an e-care plan across healthcare settings. SMART (https://smarthealthit.org/) and SMART on FHIR standards include open specifications to integrate applications with health IT systems and may enable the development of an e-care plan application that can integrate with a variety of electronic health record (EHR) systems.
3.c. Security Risks
Will this project produce executable(s), for example, schemas, transforms, style sheets, executable program, etc. If so the project must review and document security risks. Refer to the Cookbook for Security Considerations for additional guidance, including sample spreadsheets that may be used to conduct the security risk assessment.
3.d. External Drivers
National Institutes of Health (NIH) Statement of Work Requirements and Timelines.
3.e. Project Objectives / Deliverables / Target Dates
|Clinical Information Model Analysis Mapping and definition (to existing profiles and resources)||March 2020|
|Connectathon 0 (Investigation and informal testing)||May 2020|
|CKD and related Draft Value Set Definitions (not for all chronic conditions)||June 2020|
|Care Planning, Plan Definition, Care Team, Care Coordination and Clinical Guidelines Framework for MCC eCare Plan||June 2020|
|Draft IG (non -balloted, ready for testing)|
|Connectathon 2||January 2021|
|Connectathon 3||January 2022|
|Connectathon 4||May 2022|
|Connectathon 5 (planned)||September 2022|
|Submit for Comment ballot||January 2023|
Submit for STU ballot
Complete STU Reconciliation
|Request STU Publication||May 2024|
|STU Publication Date||September 2024|
Submit for Normative Ballot
Complete Normative Reconciliation
Submit Publication Request
3.f. Common Names / Keywords / Aliases
eCare Plan, Dynamic Care Plan, Multiple Chronic Condition Care Plan, Shared Care Plan, Comprehensive Care Plan, Care Planning and Management
If your project creates a Post-Release 1 version; indicate the name of the prior product and if it is supplanting, replacing or coexisting with a previous release: NA
3.h. Project Dependencies
FHIR Care Plan Resource: http://hl7.org/fhir/R4/careplan.html
Care Team Resource: http://hl7.org/fhir/R4/careteam.html
IHE Dynamic Care Planning Profile: https://wiki.ihe.net/index.php/Dynamic_Care_Planning
FHIR Clinical Guidelines: http://build.fhir.org/ig/HL7/cqf-recommendations/artifacts.html
Plan Definition Resource: https://www.hl7.org/fhir/plandefinition.html
FAST Shared Care Planning Use Case: https://oncprojectracking.healthit.gov/wiki/display/TechLabSC/Ecosystem+Use+Case+Tiger+Team#ecosystem
FHIR Clinical Guidelines:http://build.fhir.org/ig/HL7/cqf-recommendations/artifacts.html
Projects and their Project Insight IDs can be found via http://www.hl7.org/special/Committees/projman/searchableProjectIndex.cfm?ref=common
3.i. HL7-Managed Project Document Repository Location
A template to create a Project Page on the HL7 Wiki is available at: http://wiki.hl7.org/index.php?title=Template:Project_Page.
|Enter the SPECIFIC URL of the HL7-MANAGED SITE where supporting project documents, deliverables, ballot reconciliation work and other project information will be kept.|
|HTTP://Multiple Chronic Conditions (MCC) eCare Plan|
3.j. Backwards Compatibility
Are the items being produced by this project backward compatible?
If you check 'Yes' please indicate the earliest prior release and/or version to which the compatibility applies:
For V3, are you using the current data types?
(Refer to TSC position statement on new projects using R2B for more information on the current V3 data types)
If you check no, please explain the reason:
If desired, enter additional information regarding Backwards Compatibility.
3.k. External Vocabularies
Will this project include/reference external vocabularies?
If Yes, please enter the vocabularies: SNOMED CT, LOINC, ICD10, CPT, RxNorm, CPT
4. Products (check all that apply)
V2 Messages – Administrative
Clinical Information Modeling Initiative (CIMI)
V2 Messages - Clinical
Clinical Context Object Workgroup (CCOW)
V2 Messages - Departmental
Domain Analysis Model (DAM)
V2 Messages – Infrastructure
Electronic Health Record (EHR) Functional Profile
V3 Domain Information Model (DIM / DMIM)
V3 Documents – Administrative (e.g. SPL)
FHIR Implementation Guide (enter FHIR product version below)
V3 Documents – Clinical (e.g. CDA)
FHIR Profiles (enter FHIR product version below)
V3 Documents - Knowledge
V3 Foundation – RIM
Guidance (e.g. Companion Guide, Cookbook, etc)
V3 Foundation – Vocab Domains & Value Sets
V3 Messages - Administrative
V3 Messages - Clinical
New Product Definition (please define below)
V3 Messages - Departmental
New Product Family (please define below)
V3 Messages - Infrastructure
Non Product Project - (Educ. Marketing, Elec. Services, etc.)
V3 Rules - GELLO
V3 Services – Java Services (ITS Work Group)
Creating/Using a tool not listed in the HL7 Tool Inventory
V3 Services – Web Services (SOA)
If you checked New Product Definition or New Product Family, please define below:
For FHIR IGs and FHIR Profiles, what product version(s) will the profiles apply to?
Versions 4 and 5 and will evolve based on CMS/ONC regulations and ONC Version advancement recommendations over the 3 year time of the project.
5. Project Intent (check all that apply)
Create new standard
Supplement to a current standard
Revise current standard (see text box below)
Implementation Guide (IG) will be created/modified
Reaffirmation of a standard
Project is adopting/endorsing an externally developed IG:
New/Modified HL7 Policy/Procedure/Process
Specify external organization in Sec. 6 below;
Externally developed IG is to be (select one):
White Paper (select one):
Adopted - OR -
Balloted Informative OR
Non-balloted WG White Paper
N/A (Project not directly related to an HL7 Standard)
If revising a current standard, indicate the following:
|- Name of the standard being revised:|
|- Date it was published (or request for publication, or ANSI designation date)|
|- Rationale for revision|
|- The relationship between the new standard and the current standard (is it designed to replace the current standard, a supplement to the current standard, etc.)|
5.a. Ballot Type (check all that apply)
Comment (aka Comment-Only)
Joint Ballot (with other SDOs)
N/A (project won’t go through ballot)
STU to Normative - OR -
Normative (no STU)
If necessary, add any additional ballot information here. If artifacts will be jointly balloted with other SDOs, list the other groups.
5.b. Joint Copyright
Check this box if you will be pursuing a joint copyright. Note that when this box is checked, a Joint Copyright Letter of Agreement must be submitted to the TSC in order for the PSS to receive TSC approval.
Joint Copyrighted Material will be produced?
6. Project Logistics
6.a. External Project Collaboration
Include SDOs or other external entities you are collaborating with, including government agencies as well as any industry outreach. Indicate the nature and status of the Memorandum of Understanding (MOU) if applicable.
For projects that have some of their content already developed:
Joint initiative with the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), the Agency for Healthcare Research and Quality (AHRQ), and the Assistant Secretary for Planning and Evaluation (ASPE).
How much content for this project is already developed?
Requirements and content data elements only
Was the content externally developed ? :
Is this a hosted (externally funded) project? (not asking for amount just if funded)
- OR -
Check here if this standard balloted or was previously approved as realm specific standard
US _ Driven by US NIH and other US Interests - reusing US Core profiles where possible
6.c. Stakeholders / Vendors / Providers
This section must be completed for projects containing items expected to be ANSI approved, as it is an ANSI requirement for all ballots
Clinical and Public Health Laboratories
Clinical and Public Health Laboratories
Quality Reporting Agencies
Local and State Departments of Health
Health Care IT
Medical Imaging Service
Standards Development Organizations (SDOs)
Clinical Decision Support Systems
Healthcare Institutions (hospitals, long term care, home care, mental health)
Other (specify in text box below)
Other (specify in text box below)
Other (specify below)
Other: Indicate other stakeholders, vendors or providers not listed above.
6.d. Project Approval Dates
Click here to go to HL7 Project Scope Statement Instructions#Appendix A for more information regarding this section.
Approvals are by simple majority vote of the approving body
Sponsoring Work Group Approval Date:
Patient Care WG Approval Date
Administrative review – in parallel with Work Group Approval
Co-Sponsor Group Approval Date
CDS WG Approval Date
Learning Health System WG Approval Date
Family Management Group Approval Date(s)
CIMI Projects: CIMI Management Group
CIMI MG Approval Date
CDA Projects: CDA Management Group
CDA MG Approval Date
FHIR Projects: FHIR Management Group
FMG Approval Date
US Realm Projects: US Realm Steering Committee Approval
USRSC Approval Date
Submit PSS to Steering Division after all of the above approvals are received
Steering Division (of Primary Sponsor WG) Approval Date:
SD Approval Date CCYY-MM-DD
ARB and Steering Division approval may be in parallel
Architectural Review Board Approval Date:
(required for externally developed content)
ARB Approval Date
If applicable, TSC has received a Joint Copyright/Distribution Agreement (containing the verbiage outlined within the SOU),
Technical Steering Committee Approval Date:
TSC Approval Date