CRE ELR Pain Points
Please post your jurisdiction's CRE-related ELR pain points here!
Comments & Events
Massachusetts CRE ELR Pain Points
- Missing carbapenemase results
- Unclear if carbapenemase test was actually performed (“Demonstrates production of a carbapenemase” but no evidence of that)
- Missing MIC values (we are only getting interpretations of S, I, or R)
- The parent/child linking of organism/susceptibility labs could be a problem, but we don’t actually know without a paper copy of the labs
- Reported as a CRE but there are no carbapenem susceptibilities mapped
Indiana CRE ELR Pain Points
- Comments are sent in multiple result (OBX) segments (OBX|7 “identification and susceptibility” OBX|8 “Testing to follow.”)
- Generic LOINC codes being used, making it difficult for our system to classify results correctly (Our system classifies at the result level)
- No utilization of parent/child linking of susceptibility labs to the organism(s)
- In the example discussed on the conference call, there were 3 organisms identified; and two susceptibility requested tests and results sent. It’s not easy to identify which susceptibility goes with which organism.
- Missing MIC values and only sending the categorical results
- Categorical results sent in the result section and quantitative sent in a note (NTE) segment
From LabCorp: Reporting of MIC values can be rejected by provider's systems. This may require communication with vendors.
Our CT PHL is starting to institute testing for CRE using Phenotype testing, Kirby-Bauer, MIC, and PCR. We just made sending of CRE isolates a requirement in 2017. One of the issues (mentioned in another post) is that what you report to a provider for results and what we want as PH are different levels of detail. Our PHL has a committee working with some hospital ID docs to craft what result message will be sent. Plus I don't know how these results will be reported to us at DPH at this point until they get testing established. So that is a "pain" point as it were. We are moving to getting reportable results from the PHL via an xml file that we will process for our end point surveillance system(s).