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STI & AMR · Molecular Assays · Application Insights · Lab Operations
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Rapid molecular AMR markers earn their place by compressing isolation and de-escalation decisions from days to hours. They complement, not replace, culture-based susceptibility testing — and they deliver value only when the assay menu is matched to a specific decision point in the workflow.
Target audienceLab Director, Infectious Disease, Procurement
Compiled from public manufacturer materials and regulatory sources. Not independently verified and not reviewed by a named clinician.
2026-10-06
2026-10-06
professional use
FAQ
No. They complement culture. Markers answer faster for the specific genes they assay, but culture and susceptibility testing remain the reference standard and quantify what markers cannot.
MRSA (mecA/mecC), VRE (vanA/vanB), carbapenemase families (KPC, NDM, VIM, IMP, OXA-48-like), and rifampicin-resistance mutations for tuberculosis are the established, guideline-endorsed set.
Not by itself. A negative result excludes only the mechanisms assayed, and screening specimens can contain organisms below detection or mixed populations. Marker results inform, but clinical decisions still require the full picture.
Start from your institution’s antibiogram and regional surveillance data, then place assays where a faster answer changes a decision — admission screening, positive blood cultures, or outbreak investigations.
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