Date and time
2019-01-21 20.00 UTC
Zoom Details
Apologies
Objectives
Discussion items
Item | Description | Owner | Notes | Action | |
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1 | Welcome & apologies |
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2 | Conflicts of interest |
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3 | Previous minutes | ||||
4 | Susceptibility test products | Draft 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.xlsx breakpoint 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. Modeling of 703745000 | Sulfamethoxazole and trimethoprim (substance) | seems odd, particularly the | Is modification of | attribute. |
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5 | MRCM rules update | See 2018-10-16 - OBSERVABLE Face-to-face Meeting, Item 6.
What are the requirements for testing MRCM change proposals? Examples of modeling of Observables with | technique | = | Assessment scale | was presented. | |||
6 | Diastolic arterial pressure and how to go forward with existing Observables | See comments on this page. The FSNs are generally under-specified compared to how concepts have been used. We need to decide whether to retire, rename, remodel, add or leave as is. E.g. the blood pressure observables FSNs do not specify time aspect. Can we assume that they are single point in time or not? The guidance given by the EAG was that we should allow more consideration of reasonable clinical interpretation and also to allow updating and clarification of FSNs if deemed necessary. Data concerning clinical use of the concepts should be used to inform decisions. Ambiguous concepts which are not in significant use may be retired. As this might disrupt implementations the updated guidance should be discussed with the MF and CMAG. A briefing note has been sent out. Comments from MF and CMAG should be provided by 2019-01-31. Two comments had been added 2019-01-21. Input from UK is to be expected. | |||
7 | New-project proposals | X | 1) Pragmatic lab/clinical observables ontology for interoperation 2) Neuropathology database for Alzheimers disease registry UNMC has received support for a new project including pathology/autopsy observables. | ||
8 | Target observables | X | Copied from the Vital signs incept./elaborat. document: Target observablesAmong the 46680005 | Vital sign (observable entity) | observables, there are a few "target" observables: 428420003 | Target heart rate (observable entity) |, 315612005 | Target systolic blood pressure (observable entity) |, and 315613000 | Target diastolic blood pressure (observable entity) |. These concepts would not be considered vital signs according to the definition used in this document. While the representation of such targets have not yet been elaborated on, it is clear that a target observable is distinct from a "ordinary" observable, particularly true for e.g. 390734006 | Target weight (observable entity) | and 27113001 | Body weight (observable entity) |. There are related JIRA tickets: IHTSDO-457, PCP-5, IHTSDO-39 and also some potentially related tickets: IHTSDO-356, IHTSDO-308. Here is a presentation from a previous Observables meeting. Here is an updated presentation. This was presented and discussed. Likely, Observables and Settables should be disjoint. Quick comments during the meeting supported the separation of "observation observables" from "observation targets". | ||
10 | Face-to-face meeting |
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11 | Next meeting |
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12 | AOB |
Meeting Files
Recordings
https://snomed.zoom.us/recording/share/4DfdTV5KlKRjIKRp5KFVBYX207uBavq7PkGQbXhy9SewIumekTziMw
Previous Meetings
Title | Creator | Modified | |
---|---|---|---|
E2O meeting 20220825 | Daniel Karlsson | 2022-Aug-25 | |
2022-05-23 - OBSERVABLE Meeting | Daniel Karlsson | 2022-May-24 | |
E2O meeting 20220504 | Daniel Karlsson | 2022-May-05 | |
2022-04-25 - OBSERVABLE Meeting | Daniel Karlsson | 2022-Apr-26 | |
2022-04-06 - OBSERVABLE Face-to-face Meeting | Daniel Karlsson | 2022-Apr-25 | |
2022-03-21 - OBSERVABLE Meeting | Daniel Karlsson | 2022-Mar-31 | |
E2O 23rd meeting 20220223 | Daniel Karlsson | 2022-Feb-23 | |
2022-02-21 - OBSERVABLE Meeting | Daniel Karlsson | 2022-Feb-22 | |
E2O 22st meeting 20220202 | Daniel Karlsson | 2022-Feb-02 | |
2022-01-24 - OBSERVABLE Meeting | Daniel Karlsson | 2022-Jan-24 | |
2021-12-20 - OBSERVABLE Meeting | Daniel Karlsson | 2021-Dec-20 | |
2021-11-15 - OBSERVABLE Meeting | Daniel Karlsson | 2021-Dec-16 |
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