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R5 Planning


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Resource/Implementation GuideCurrent FMMOpen gForgeDependencyPriorityTarget FMMPlan/TimelineConference CallPrime Facilitator
Owned  
 
  

BiologicallyDerivedProduct01
?? 1-2?

 Discuss with Bob M who will review and summarize and present to OO whether vote on moving from draft to FMM1

goal = 1?

Monday, 1-2pm ETBob Milius

Device06

What Needs It:

  • Dozens of resources (TNTC)

What Does it Depend On:


 HN
  • Update Resource Proposal and re-approve with FMG by May 2019.
  • FHIR Prod Mgmt would like to aim for Normative.


Monday, 1-2pm ET

Hans Buitendijk

Jose Costa-Teixeira


DeviceDefinition00

H for 1

M for >1

1-2
  • Update Resource Proposal and approve with FMG by May.
  • Work with LIVD and Catalog to make sure
Monday, 1-2pm ET

Hans Buitendijk

Jose Costa-Teixeira


DeviceRequest01
 L1

Discuss with Jose, HB, Device WG who will review, summarize and present to WG.

goal = 1?

Monday, 1-2pm ET

Hans Buitendijk

Jose Costa-Teixeira


DeviceUseStatement00
 H to determine punt or not?
  • Need to determine whether needed?
    • Use case never fleshed out and never garnered strong interest from community.
    • Needs a Champion to commit to resubmitting a fully fleshed out resource proposal to FMG and shepherding through draft.
    • Barring that consider removing from Specification.

goal = ?

Monday, 1-2pm ET

Hans Buitendijk

Jose Costa-Teixeira


Substance22


Plan was to move ownership to BRR - need a status update on why that has not happened?

Determine ownership.

Monday, 1-2pm ETHans Buitendijk

SupplyDelivery11


Discuss with Jose, who will review, summarize and present to WG.

goal = ?

Monday, 1-2pm ET

SupplyRequest11


Discuss with Jose who will review, summarize and present to WG.

goal = ?

Monday, 1-2pm ET

DiagnosticReport34

What Needs It:

  • ClinicalNotes

What Does It Depend On:

  • Imaging Profile
 HN
  •  EH to review QA criteria and trackers.
  • Recently Major concerns due to Overlap with DocRef brought up because of us core Clinical Notes work. (although this is really because DocRef overlaps with everything that uses attachment) The use case and boundaries for Diagnostic report are well defined. DocRef boundaries are underspecified.
  • How do Procedures and DR overlaps still needs clarification. Work with PC on that.
  • Boundaries between DR and Composition. And whether more DR like structures are coming to FHIR.
  • There may be substantive changes if Media changes
  • More imaging and anatomic path examples needed.
  • FHIR Prod Mgmt would like to aim for Normative.
Tuesday, 2-3pm ETEric Haas

Media12
 H2-3
  •  Nail down the boundary issues.
    • Reworked as an 'ObservationMedia' in R4 and valueAttachment removed from Observation to remove duplicate functionality from specification
    • Post Ballot comments suggests the desire for valueAttachment and a "non Observation", "Non docref" Media Object. JT II, SD, OO
    • Discussion this week on how to move ahead to clarify boundaries and use cases.
Tuesday, 2-3pm ET

Eric Haas,, Hans Buitendijk,

Elliot Silver


ObservationN15

What Needs It:

  • "Everything"

What Does It Depend On:

 HN for planned
  • Trackers:
  • Value Attachment see above
  • Consider other profile (e.g., Physical Activity ) in light of substantial effort to gain and maintain consensus. What lessons learned from this experience
  • Normative:
    • vitals profile
    • operation
    • searchparameters
    • elements
Tuesday, 2-3pm ETEric Haas

ObservationDefinition01

What Needs it:

  • CatalogEntry
  • LIVD
  • Various Pharmacy

What Does it Depend On:

 H3-4
  • Finalize Resource Proposal with FMG.
  • Needs examples
  • Test implementations to show ObsDef magically turns into Observation instances.
  • Additional Search Parameters.
  • Possibly define a new operation.
Wednesday, 1-2pm ETFrançois Macary, Rob Hausam

Specimen20

What Needs It:

  • "Everything"

What Does It Depend On:

  • Observation
  • BodyStructure
 H4
  • Review QA criteria and trackers.
  • Collection into Procedure??
  • Look for vendor implementation.
Tuesday, 3-4pm ET

Eric Haas

Riki Merrick


SpecimenDefinition04
 M1-2
  • Finalize Resource Proposal with FMG
Wednesday, 1-2pm ETFrancois Macary

ServiceRequest22

What Needs It:

  • CarePlan
  • Task

What Does It Depend On:

  • ActivityDefinition
 H4-5
  •  Continue to work closely with PC on trackers and documentation.
  • Review QA criteria and trackers. Look for vendor implementation.
Tuesday, 1-2pm ETEric Haas

Task25

What Needs It:

  • DME IG?
  • BSeR
  • eCR


 H3-4

  • Review QA criteria and trackers.
  • Look for vendor implementation.


 TBD (Monday or Wednesday old Workflow slots)Vassil Peytchev

BodyStructure10

What Needs It:

  • Specimen
  • (SpecimenDefinition)

What Does It Depend On:

  • Patient
M2-3
  • EH to review Connectathons and Poll implementers
  • check QA criteria
  • summarize and present findings to OO with recommendations whether to move from 1 to 2.
  • Address that BodyStructure has Patient mandatory. Or do we need a BodyStructureDefinition. Consider gForge.
 Tuesday, 2-3pm ETEric Haas

CatalogEntry00

What Needs It:

  • LIVD
  • Order Service
  • Compendium

What Does It Depend On:

  • Composition
 H1-2

 Discuss with Jose, Francois who will review, summarize and present to WG.

 Wednesday, 1-2pm ETFrancois Macary, Rob Hausam

NutritionOrder23

What Needs It

  • CarePlan
  • PlanDefinition

What Does it Depend On:

  • Request Pattern

3
  • Review QA criteria and trackers.
  • Clarifications on recommendations for outpatient setting.
  • Establish a profile/IG.
  • Look for vendor implementation.


 Reinstate.Margaret Dittloff, Eric Haas
Strong Interest








ClinicalNotes




 SD sponsor of US Core


DeviceMetric




 see comments re device resources


DocumentReference




 SD sponsor


Procedure

















Implementation Guides
Owned








LIVD





Friday, 1-2pm ET

DME?








Catalog








Nutrition Order/Recommendation







Strong Interest

















Healthcare Product

Link to Healthcare Product project page, including: Device, DeviceDefinition, Substance, BiologicallyDerivedProduct, and Supply.  The goal is to define this constructs better, combine or split as necessary, and clarify when to use which one(s) with a particular focus on medication space, nutrition, and specimen.  This will also address any UDI related topics to ensure the resources that require it have the appropriate UDI information (which to date has focused on implantable devices).


  • No labels

3 Comments

  1. Where are the Clinical Genomics aspects represented?  Their IG has a different data model & needs.  Is it considered part of the LRI IG as in v 2.51?  There has been quite a bit of work in FHIR by CG WG.

    1. CG uses OO owned resources and would contribute to those like any other contributor.  Not sure what else we need to represent here, short of having to then list all other workgroups specifically that use OO capabilities.

  2. Wouldn't we want to list dependencies and IGs?