QT Interval & TdP Risk Calculator
Multi-formula rate correction (Fridericia, Bazett, Framingham, Hodges) with sex-specific thresholds, bundle branch block adjustments, Tisdale risk stratification, and CredibleMeds drug precautions.
1. ECG Parameters
Tisdale QT Risk Score
Validated TdP Risk StratificationQTc Forecast & Arrhythmia Risk
Moderate risk. Repolarization reserve is slightly impaired.
Simultaneous Formula Comparison
| Formula | Equation | Calculated QTc | Clinical Evaluation |
|---|---|---|---|
| Fridericia (Gold Standard) | QT / ∛RR | 453 ms | Preferred by AHA/FDA across all heart rates |
| Bazett | QT / √RR | 464 ms | Historical; overestimates in tachycardia |
| Framingham (Linear) | QT + 154(1−RR) | 452 ms | Robust linear population regression |
| Hodges | QT + 1.75(HR−60) | 448 ms | Alternative linear model |
QTc Trajectory Across Heart Rates (40–130 bpm)
Red Line: 500 ms HazardCredibleMeds QT Drug Precautions
Known & Possible Torsades de Pointes (TdP) RiskDosing Guidance: Reduce dose or discontinue if QTc > 500 ms or increases by > 60 ms over baseline.
Directly blocks IKr channels; lower incidence of TdP than other class III agents due to concurrent calcium/beta blockade, but requires baseline and serial ECGs.
Dosing Guidance: Strict dose reduction in renal impairment. Discontinue if QTc exceeds 500 ms.
Marked reverse use-dependence (highest TdP risk at slower heart rates / bradycardia). 100% renally eliminated.
Dosing Guidance: IV administration carries substantially higher risk than PO. Limit IV doses or switch to atypical agent if QTc > 480 ms.
FDA boxed warning for IV administration. Continuous telemetry recommended during IV therapy.
Dosing Guidance: Max 40 mg/day (Max 20 mg/day in age > 60 yr, hepatic impairment, or CYP2C19 poor metabolizers).
FDA safety communication warns against doses > 40 mg/day due to dose-dependent QTc prolongation.
Dosing Guidance: Avoid in patients with baseline prolonged QTc, hypokalemia, hypomagnesemia, or bradycardia.
FDA warning regarding fatal cardiac arrhythmias; consider Doxycycline or beta-lactams as safer alternatives in high-risk patients.
Dosing Guidance: Dose-adjust for renal clearance. Avoid co-administration with other QT-prolonging agents.
Moxifloxacin carries highest risk among quinolones; Levofloxacin is intermediate; Ciprofloxacin is lowest.
Dosing Guidance: Max single IV dose is 16 mg. Avoid repeat doses in patients with baseline QTc > 480 ms.
ECG monitoring recommended in patients with electrolyte abnormalities or heart failure.
Dosing Guidance: Perform baseline ECG. Obtain follow-up ECG if daily dose exceeds 100 mg/day or if risk factors present.
Potent hERG channel blocker. Clinically significant QTc prolongation commonly observed at doses > 100-120 mg/day.
Dosing Guidance: Renally adjust. Monitor closely when co-administered with CYP3A4/CYP2C9 substrates.
Dual mechanism: direct IKr channel block and CYP inhibition increasing systemic levels of other QT drugs.