Clinical & Hospital Pharmacy
QT Interval & TdP Risk Calculator
Corrects the ECG QT interval for heart rate (QTc) with four formulas, applies sex-specific limits and scores the risk of torsades de pointes.
QTc · Fridericia
453ms
Borderline QTc (450–470 ms)
Moderate risk. Repolarization reserve is slightly impaired.
ECG measurements
Sex (sets the normal limit)
Start of QRS to end of T wave. Uncorrected QT is usually 350–450 ms.
Updates the RR interval. Resting adult 60–100 bpm.
Or enter the RR interval — the heart rate updates to match (60000 ÷ RR).
A pre-treatment QTc, to see the change. A rise of 60 ms or more is critical.
Normal is under 120 ms. Above 120 ms the wide-QRS adjustment is applied automatically.
Formula shown in the result
Working
Every formula, from the same effective QT.
| Formula | Equation | QTc | Notes |
|---|---|---|---|
| Fridericia | QT / ∛RR | 453 ms | Preferred by AHA/FDA across all heart rates |
| Bazett | QT / √RR | 464 ms | Historical; overestimates in tachycardia |
| Framingham | QT + 154(1−RR) | 452 ms | Robust linear population regression |
| Hodges | QT + 1.75(HR−60) | 448 ms | Alternative linear model |
QTc across heart rates (40–130 bpm)
The same QT corrected at other rates. Dashed red: 500 ms danger line; dashed green: the normal limit.
Tisdale QT risk score
For hospitalised patients: predicts QTc prolongation from clinical risk factors.
Score 0 — Low Risk (≤6)
QT-prolonging drug precautions
High-yield drugs with a known or possible risk of TdP (CredibleMeds categories).
Amiodarone (Cordarone / Pacerone)
Known Risk of TdPClass III Antiarrhythmic
Dosing 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.
Sotalol (Betapace)
Known Risk of TdPClass III Antiarrhythmic / Beta-Blocker
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.
Haloperidol (Haldol)
Known Risk of TdPTypical Antipsychotic
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.
Citalopram (Celexa)
Known Risk of TdPSSRI Antidepressant
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.
Azithromycin (Zithromax)
Known Risk of TdPMacrolide Antibiotic
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.
Levofloxacin / Ciprofloxacin (Levaquin / Cipro)
Known Risk of TdPFluoroquinolone Antibacterial
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.
Ondansetron (Zofran)
Possible Risk5-HT3 Receptor Antagonist Antiemetic
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.
Methadone (Dolophine / Methadose)
Known Risk of TdPOpioid Agonist
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.
Fluconazole (Diflucan)
Possible RiskTriazole Antifungal
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.
Rate corrections (RR in seconds = 60 ÷ heart rate)
Fridericia: QTc = QT ÷ ∛RR
Bazett: QTc = QT ÷ √RR
Framingham: QTc = QT + 154 × (1 − RR)
Hodges: QTc = QT + 1.75 × (HR − 60)
Wide QRS (Bogossian)
QT adjusted = QT − 0.5 × (QRS − 100), QRS taken as ≥ 120 ms, result not below 200 ms
Applied when bundle branch block is ticked or QRS is over 120 ms. Every QTc is rounded to the nearest millisecond.
Limits (AHA/ACCF/HRS)
Men: normal < 450 ms, borderline 450–470, prolonged above 470. Women: normal < 460 ms, borderline 460–480, prolonged above 480. Critical at 500 ms or more for both; short below 340 ms. A rise of 60 ms or more from baseline is also critical.
References
1. Drew BJ et al. Prevention of torsade de pointes in hospital settings: a scientific statement from the AHA and ACCF. Circulation. 2010;121(8):1047-1060.
2. Tisdale JE et al. Development and validation of a risk score for QT interval prolongation in hospitalized patients. Circ Cardiovasc Qual Outcomes. 2013;6(4):479-487.
3. Bogossian H et al. QTc evaluation in patients with bundle branch block. Ann Noninvasive Electrocardiol. 2014;19(6):568-575.
Common questions
Bazett divides by the square root of RR, which over-corrects at fast heart rates and under-corrects at slow ones — so a tachycardic patient can look falsely prolonged. Fridericia's cube root stays much closer to the true value across the usual heart-rate range, which is why AHA/ACC and FDA recommend it.
A QTc of 500 ms or more, or a rise of 60 ms or more from baseline, carries a markedly higher risk of torsades de pointes. At that point, non-essential QT-prolonging drugs are usually stopped, potassium and magnesium replaced, and the patient monitored.
A wide QRS lengthens the QT without any change in repolarisation, so the raw QTc overstates risk. Tick the bundle branch block box and enter the QRS duration to subtract half of the excess QRS width before correcting. Any QRS above 120 ms triggers the same adjustment.
It is a validated score for hospitalised patients that adds points for risk factors such as age ≥ 68, female sex, loop diuretics, low potassium, sepsis, heart failure and multiple QT-prolonging drugs. A high score flags patients who need ECG monitoring before and after starting a QT-prolonging drug.
Either. Changing one updates the other (RR in ms = 60000 ÷ heart rate), and the calculation uses the heart rate.
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