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🩸 PLASMIC Score (TTP Probability)

UsePredict severe ADAMTS13 deficiency.

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SourceBendapudi PK, et al. Derivation and external validation of the PLASMIC score for rapid assessment o…

Runs locally in your browser (no PHI uploaded). For licensed clinicians — not a substitute for clinical judgement.
Stored on this device for revisit reminders

This-shift next steps

After scoring: open the scene pack, peer scores, and the matching pathway. Local reference — no HIS write.

Score + version; reference only — not a substitute for care · no HIS write

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Methodology · worked example, guidelines & full notes
Clinical takeaway

High scores predict severe ADAMTS13 deficiency (< 10%).

When to use

Predict severe ADAMTS13 deficiency.

How it works

Seven points (platelets, haemolysis, no cancer, no transplant, MCV, INR, creatinine). 0–4 low, 5 intermediate, 6–7 high probability.

Key points

  • High scores predict severe ADAMTS13 deficiency (< 10%).
  • Validated in adults with thrombotic microangiopathy.

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.

Platelet count < 30 ×10⁹/LNo
Haemolysis (retic > 2.5%, haptoglobin undetectable, or indirect bili > 2)No
No active cancerNo
No solid-organ/stem-cell transplantNo
MCV < 90 fLNo
INR < 1.5No
Creatinine < 2.0 mg/dLNo

→PLASMIC0/7

  • Interpretation:Low (0–4%) probability of severe ADAMTS13 deficiency
  • Action:Lower likelihood — pursue alternative TMA causes.
Platelet count < 30 ×10⁹/LYes (+1)
Haemolysis (retic > 2.5%, haptoglobin undetectable, or indirect bili > 2)Yes (+1)
No active cancerYes (+1)
No solid-organ/stem-cell transplantYes (+1)
MCV < 90 fLYes (+1)
INR < 1.5Yes (+1)
Creatinine < 2.0 mg/dLYes (+1)

→PLASMIC7/7

  • Interpretation:High (62–82%) — strongly consider TTP
  • Action:PLASMIC predicts severe ADAMTS13 deficiency (C statistic 0.96 in the original study); diagnosis relies on ADAMTS13 activity.
Verification & sources · governance
FAQ

Frequently asked questions

What are the limits and cautions when using PLASMIC Score (TTP Probability)?
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 PLASMIC Score (TTP Probability) 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 PLASMIC Score (TTP Probability) calculated in practice? Can you show a worked example?
Inputs: Platelet count < 30 ×10⁹/L No, Haemolysis (retic > 2.5%, haptoglobin undetectable, or indirect bili > 2) No, No active cancer No, No solid-organ/stem-cell transplant No, MCV < 90 fL No, INR < 1.5 No, Creatinine < 2.0 mg/dL No → Result: PLASMIC 0 /7(Interpretation: Low (0–4%) probability of severe ADAMTS13 deficiency, Action: Lower likelihood — pursue alternative TMA causes.) Inputs: Platelet count < 30 ×10⁹/L Yes (+1), Haemolysis (retic > 2.5%, haptoglobin undetectable, or indirect bili > 2) Yes (+1), No active cancer Yes (+1), No solid-organ/stem-cell transplant Yes (+1), MCV < 90 fL Yes (+1), INR < 1.5 Yes (+1), Creatinine < 2.0 mg/dL Yes (+1) → Result: PLASMIC 7 /7(Interpretation: High (62–82%) — strongly consider TTP, Action: PLASMIC predicts severe ADAMTS13 deficiency (C statistic 0.96 in the original study); diagnosis relies on ADAMTS13 activity.)
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