Date and time
2019-04-08 13.30 UTC
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Item | Description | Owner | Notes | Action | |
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1 | Welcome & apologies |
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2 | Conflicts of interest | ||||
3 | Previous minutes | ||||
4 | Susceptibility observables | Daniel Karlsson Farzaneh Ashrafi Suzanne Santamaria | BackgroundDraft editorial guidelines: Editorial Guidelines for Diagnostic Products Used for Susceptibility Testing It was decided to recommend representation the physical form of the susceptibility test product, and also to use the | has presentation strenght... | attributes (as opposed to other strength attributes). Two issues were discovered while re-reading the Inception/Elaboration document for susceptibility testing: 1. "oral form antibiotic susceptibility" exists as components in LOINC tests. 2. when other methods than culture are used, e.g. PCR or sequencing, to determine susceptibility, we might need to use another way of modeling, e.g. beta-lactamase producing ~ resistance towards beta-lactam antibiotics. While the Susceptibility test products are needed for the mycobacteria tests (with strength-specified antibiotics), we might reconsider the approach for other cases, and use substances where products are not needed, together with a role chain | towards | o | ingredient | → | towards |. Rob: Aren't all susceptibility tests strength-specified, even though the strength is not part of the definition? Xavier: EUCAST breakpoint for diffusion disks : http://www.eucast.org/clinical_breakpoints/ the xls is at http://www.eucast.org/fileadmin/src/media/PDFs/EUCAST_files/Breakpoint_tables/Preliminary_v_9.0_Breakpoint_Tables_for_consultation.xlsxbreakpoint requires a definite antibio amount in the disk. Most tests (mycobacteria tests being an exception) are based on there being a concentration gradient (e.g. disk diffusion, etest, MIC procedures) and thus not a single concentration. 2019-02-11: An OWL ontology with Diagnostic test products and susceptibility observables is attached. The combination substances are to be inactivated, so modeling cannot rely on use of such concepts. 2019-03-25: An alternative version not using combination substances was presented and discussed. Current objectiveGive recommendations on representation given two alternatives: (1) use | Susceptibility test product | as values of the | towards | attribute OR (2) use Substance together with | direct substance | = | Susceptibility test product | only when needed. | ||
James R. Campbell | (Cognitive) Function observables | See this page. | |||
James R. Campbell | AP/MP/Genomics observables | An inception/elaboration document is published here. | |||
James R Campbell Daniel Karlsson | Lab observables interoperability | See this page. | |||
Daniel Karlsson | Existing observables (primarily vital signs) | The modeling of the (few) existing defined Observables have some issues as highlighted by the NHS, including a mix of actual and target observables and near same/similar observables. See this page, particularly the comments. | |||
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