Difference between revisions of "BiologicallyDerivedProduct FHIR Resource Proposal"
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==Committee Approval Date:== | ==Committee Approval Date:== | ||
<i>Please enter the date that the committee approved this Resource proposal</i> | <i>Please enter the date that the committee approved this Resource proposal</i> | ||
| + | October 5, 2017 | ||
==Contributing or Reviewing Work Groups== | ==Contributing or Reviewing Work Groups== | ||
Revision as of 17:30, 5 October 2017
This page documents a Pending FHIR Resource Proposal
Contents
- 1 BiologicallyDerivedProduct
- 1.1 Owning committee name
- 1.2 Committee Approval Date:
- 1.3 Contributing or Reviewing Work Groups
- 1.4 FHIR Resource Development Project Insight ID
- 1.5 Scope of coverage
- 1.6 RIM scope
- 1.7 Resource appropriateness
- 1.8 Expected implementations
- 1.9 Content sources
- 1.10 Resource Relationships
- 1.11 Timelines
- 1.12 gForge Users
- 1.13 When Resource Proposal Is Complete
- 1.14 FMG Notes
BiologicallyDerivedProduct
Owning committee name
Committee Approval Date:
Please enter the date that the committee approved this Resource proposal October 5, 2017
Contributing or Reviewing Work Groups
FHIR Resource Development Project Insight ID
1128 Patient Care FHIR resource review
Scope of coverage
A material substance originating from a biological entity intended to be transplanted or infused into another (possibly the same) biological entity.
Examples include:
- hematopoietic stem cells (bone marrow, peripheral blood, or cord blood extraction)
- blood (whole, extracted cells, plasma, etc)
- organs
- tissues (porcine valves, skin, bovine cardiac tissue, etc.)
- manipulated cells (e.g. CAR T-cells)
RIM scope
No identified mappings to RIM 2.46 objects.
Resource appropriateness
Organs, tissues, and fluids obtained from one biological entity (person or animal) for the purpose of infusion, transplantation or grafting to another biological entity are neither Specimens ("used for diagnostic and environmental testing") nor Devices ("an instance or a type of a manufactured item") nor Medications (drug, ingredients, and packaging) nor Substances ("homogeneous material with a definite composition"). Furthermore, there is established a relationship between two entities, the donor and the recipient.
Expected implementations
This will be used in reporting clinical outcomes to the Center of Blood and Marrow Transplant Research (CIBMTR) after hematopoietic cell transplant (bone marrow, peripheral blood stem cells, cord blood).
This resource is not used in CCDA.
Content sources
For reporting of clinical outcomes to CIBMTR, source data would come from federated systems at the transplant center, e.g., from the EHR, transplant databases, labs
- Patient undergoes hematopoetic cell transplantation (HCT) using autologous BiologicallyDerivedProduct
- Patient undergoes HCT using HLA-matched BiologicallyDerivedProduct from another person
- Patient receives post-HCT infusion of donor t-cells (BiologicallyDerivedProduct)
- Patient receives blood (BiologicallyDerivedProduct) transfusion
- Patient receives HLA-matched platelets (BiologicallyDerivedProduct)
- Patient receives heart (BiologicallyDerivedProduct) transplant from deceased donor Patient
- Patient donates kidney (BiologicallyDerivedProduct) for transplantation in another Patient
- Patient received pig heart valve (BiologicallyDerivedProduct)
Resource Relationships
ProcedureRequest (for collection)
Patient ("receiver" and "source")
Practitioner (who collected product)
Substance (product processing)
DiagnosticReport (containing HLA-typing)
BiologicallyDerivedProduct ("parent" product for multi-day collections)
Procedure (one for collection and one for transplantation, will need to add BiologicallyDerivedProduct to the "usedReference")
Timelines
ready by Jan 2018 connectathon
??? voting
gForge Users
When Resource Proposal Is Complete
When you have completed your proposal, please send an email to FMGcontact@HL7.org
