MRI contrast media calculator — gadolinium (GBCA)
AI-enhanced · liveExamination & patient
Select exam · demographics · renal function · adult & pediatric
Select an examination…
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BMI
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BSA m²
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LBW kg (adult)
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eGFR (CKD-EPI)
Protocol reference library
| Study | Adult | Child | Rate |
|---|---|---|---|
| MRI brain / spine | 0.1 mmol/kg | 0.1 mmol/kg | 1.5–2 |
| Breast / liver / prostate | 0.1 mmol/kg | 0.1 mmol/kg | 2–2.5 |
| Hepatobiliary (EOB) | 0.025 mmol/kg | 0.0125 mmol/kg | 1–2 |
| CMR — LGE | 0.1–0.2 mmol/kg | 0.1–0.2 mmol/kg | 2–3 |
| CMR — perfusion | 0.05–0.1 mmol/kg | 0.05–0.1 mmol/kg | 4–5 |
| CE-MRA | 0.1 mmol/kg | 0.1 mmol/kg | 1–2 |
| Ambelvist (any region) | 0.01 mmol/kg | 0.01 mmol/kg | 1–4 |
Pediatric eGFR uses the bedside Schwartz equation (0.413 × height / SCr). GBCA dosing in children is weight-based at the same mmol/kg — fixed dosing is inappropriate. Gadobutrol, gadoterate, gadoteridol and gadoquatrane (Ambelvist) are approved from term neonates; gadopiclenol is adults-only. Check local labeling.
Injection protocol
Delivery · NSF risk · cumulative exposure · cost
Gadolinium load–
Dose administered–
Injection duration–
Gd delivery rate–
NSF risk category–
Cumulative exposure (12 mo)–
Cost analysis
Contrast cost / study–
Saline cost / study–
Total / study–
Cost per mmol Gd–
Annual projection & savings
Annual total cost–
Fixed → weight-dosed savings / yr–
Dose recommendations
Fixed · weight · pediatric · LBW + eGFR · BSA — with NSF guidance
| Method | Factor | mL | mmol Gd |
|---|---|---|---|
| Fixed dose | mL | – | – |
| Weight-based | mmol/kg | – | – |
| Pediatric weight-based | mmol/kg | – | – |
| ★ LBW + eGFR adj. | mmol/kg | – | – |
| BSA-based | mmol/m² | – | – |
★ AI-recommended — adults: LBW + eGFR (eGFR <30: half dose with group II; group I contraindicated). Children: weight-based at the labeled dose (Ambelvist 0.01 mmol/kg = 0.04 mmol Gd/kg). LBW/BSA formulas are adult-derived. Factors editable per site protocol.
AI insight…
eGFR thresholds — NSF risk stratification (ACR / ESUR guidance)
eGFR ≥60 — low risk
Any approved agent acceptable at standard dose. Proceed routinely. In children, use the single lowest adequate dose.
eGFR 30–59 — caution
Prefer group II agents; avoid group I linear agents when possible, especially eGFR <45. Single lowest adequate dose.
eGFR 15–29 — high risk
Group I contraindicated. Group II at ≤0.1 mmol/kg, single administration; avoid repeat within 7 days. Document shared decision.
eGFR <15 / dialysis — very high
Avoid unless essential — group II only, nephrology input, informed consent; consider non-contrast alternatives (TOF, ASL, DWI).
Reference: ACR Manual on Contrast Media (current edition) · ESUR Guidelines v10 · FDA/EMA GBCA safety communications. Ambelvist (gadoquatrane) — FDA initial approval June 2026 (Japan March 2026); not yet authorized in EU/other markets at time of writing. Verify against latest published versions and institutional protocol.
Injection profile monitor
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Injection phase
Distribution / washout
Simplified two-compartment model — educational use
Estimates only — not a medical device. Clinical decisions remain with the treating team.
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