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Extending the Bridg Model with Hematopoietic Cell Transplant Concepts
Extending the Bridg Model with Hematopoietic Cell Transplant Concepts
Track: Poster Abstracts
Wednesday, February 26, 2014, 6:45 PM-7:45 PM
Longhorn Hall E (Exhibit Level 1) (Gaylord Texan)
Organizing data into coherent groups, i.e. data domains, is key to understanding relations between
complex subject areas such as information collected around one simple hematopoietic cell transplant
(HCT) event. Multiplying this by the number of transplants that are part of the CIBMTR Outcomes
Research Database underlines the need for structures that document this 'data about data'
(Metadata). The difficulty is showing how the complete set of data around a transplant event is
connected in a way that transcends the collection method, i.e. form. Our aim was to demonstrate
that a domain-driven architecture aligns with the forms-based model, and eases the introduction of
collecting more data about HCT transplant events.
The Biomedical Research Integrated Domain Group (BRIDG) model is publically available. The goal of
BRIDG group is to have a common view of the data exchanged for semantic interoperability. The BRIDG
model is intended to balance the concerns of the larger health care community, while being specific
enough to apply to a particular subject area such as HCT. We extracted all Common Data Elements
(CDEs) for all CIBMTR-mandated forms and associated each element to one of three contexts,
Recipient, Donor and stem-cell product; most elements were in the Recipient context. Because no
element could be described in isolation, instance diagrams were created to describe how one simple
concept needed multiple BRIDG entities to be fully described. Some CDEs were described as
relationships between entities rather than an attribute of an entity.
We extended the generic BRIDG model to contain all identified elements. To this end, we requested
the expansion of the BRIDG model to include a 'PerformedSubstanceExtraction' entity at the same
level of inheritance as 'PerformedSubstanceAdministration'. While the collection of a stem-cell
product could have been described in the context of a 'Product' and a 'SpecimenCollection', the
richness of the relationship between a Donor and a Recipient would not have been as obvious. This as
well as other enhancements to the BRIDG model were included in BRIDG version 3.2.
With this effort, we have documented each data point (CDE) collected on all the CIBMTR-mandated
forms and the relationships between them. We intend to use the UML BRIDG model with the added HCT
content as the specification for a physical database model. This physical model will help remove
barriers that transplant centers experience in electronic transfer of HCT data to the Stem Cell
Transplant Outcomes Database by providing a foundation upon which to develop their own in-house data
systems, and eventual development of Electronic Medical Record (EMR) integration engines to submit
data to the Outcomes Database.
Disclosures:
Nothing To Disclose
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