🔥 Inflammatory Marker Interpretation
UseUse the trend rather than single values; PCT supports antibiotic stewardship and ferritin doubles as an acute…
SourceProcalcitonin-guided antibiotic stewardship and acute-phase reactant interpretation
This-shift next steps
After scoring: open the scene pack, peer scores, and the matching pathway. Local reference — no HIS write.
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Methodology · worked example, guidelines & full notes
All inflammatory markers are non-specific.
When to use
Use the trend rather than single values; PCT supports antibiotic stewardship and ferritin doubles as an acute-phase reactant.
How it works
PCT: < 0.25 argues against bacterial (lower respiratory), > 0.5 possible sepsis, > 2 high-risk. CRP half-life ≈ 19 h.
Key points
- All inflammatory markers are non-specific.
- PCT supports stewardship but is not a standalone decision.
- Ferritin is both an iron-store marker and an acute-phase reactant — interpret with CRP/TSAT.
- Very high ferritin: consider adult Still disease or HLH (HScore).
References
Worked calculation
The values below come from this tool's own example placeholders and are computed server-side with the formula shown on this page, so the arithmetic can be checked quickly. It demonstrates how to substitute values only — it is not clinical advice and not a real case.
| View | Procalcitonin (PCT) |
|---|
→InterpretationProcalcitonin (PCT)
- Behaviour:Rises in bacterial infection/sepsis, lower in viral/localised inflammation
- Common cut-offs:< 0.25 argues against bacterial (lower respiratory); > 0.5 possible sepsis; > 2 high-risk (lab-dependent)
- Use:Antibiotic start/stop support (stewardship), not a standalone decision
| View | CRP/ESR |
|---|
→InterpretationCRP / ESR
- CRP:Acute-phase, responds fast (half-life ≈ 19 h); often higher in bacterial infection; the trend beats a single value
- ESR:Rises slowly, affected by anaemia/globulins; used to follow rheumatic disease/PMR/GCA
- Cue:Both are non-specific — correlate clinically
Verification & sources · governance
FAQ
Frequently asked questions
- What are the limits and cautions when using Inflammatory Marker Interpretation?
- For licensed clinicians and clinical researchers. Interpret results with history, investigations and local protocols; not a diagnosis or prescription, and not a substitute for multidisciplinary decision-making or local guidelines.
- Does Inflammatory Marker Interpretation upload patient data? Where is it calculated?
- Calculation runs locally in the browser; inputs and results are not uploaded. For licensed clinicians only; interpret with history, investigations and local protocols — not a diagnosis or prescription.
- How is Inflammatory Marker Interpretation calculated in practice? Can you show a worked example?
- Inputs: View Procalcitonin (PCT) → Result: Interpretation Procalcitonin (PCT)(Behaviour: Rises in bacterial infection/sepsis, lower in viral/localised inflammation, Common cut-offs: < 0.25 argues against bacterial (lower respiratory); > 0.5 possible sepsis; > 2 high-risk (lab-dependent), Use: Antibiotic start/stop support (stewardship), not a standalone decision) Inputs: View CRP/ESR → Result: Interpretation CRP / ESR(CRP: Acute-phase, responds fast (half-life ≈ 19 h); often higher in bacterial infection; the trend beats a single value, ESR: Rises slowly, affected by anaemia/globulins; used to follow rheumatic disease/PMR/GCA, Cue: Both are non-specific — correlate clinically)