Corrected QT Interval (QTc)

Corrects the QT interval for heart rate extremes (includes Bazett, Fridericia, Framingham, Hodges & Rautaharju formulas.

ErstellerDr. Alex Sagie, MD
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Corrected QT Interval (QTc)

The QT interval on an ECG represents the total time for ventricular depolarization and repolarization — essentially, how long it takes the heart's ventricles to contract and then electrically "reset" before the next beat. It's measured from the start of the Q wave to the end of the T wave.

Why "correction" is needed

The raw QT interval isn't constant — it naturally shortens as heart rate increases and lengthens as heart rate slows, since repolarization time is influenced by how much time is available between beats. This means a raw QT value is only meaningful in the context of the heart rate at which it was measured. To make QT values comparable across different heart rates — and therefore clinically useful — the value is mathematically adjusted (corrected) as if the heart were beating at a standard rate of 60 bpm.

Corrected QT interval (QTc)

  • The corrected QT interval (QTc) estimates the QT interval at a standard heart rate of 60 bpm

  • This allows comparison of QT values over time at different heart rates and improves detection of patients at increased risk of arrhythmias

The Life in the Fastlane website provides a concise overview with examples in an article called QT Interval (Burns & Buttner, 2022).

Why QTc Matters Clinically

  1. It's a marker of arrhythmia risk
    A prolonged QTc reflects delayed ventricular repolarization, which creates a vulnerable window where the heart's electrical system can misfire. This raises the risk of Torsades de Pointes, a life-threatening polymorphic ventricular tachycardia that can degenerate into sudden cardiac death.

  2. Drug safety screening
    QTc prolongation is one of the most common reasons drugs get restricted, relabeled, or pulled from the market. Many medications — including certain antibiotics (macrolides, fluoroquinolones), antipsychotics, antiemetics, and antiarrhythmics themselves — can prolong the QT interval as a side effect. Clinicians routinely check baseline and follow-up QTc when starting these medications, especially in combination or in at-risk patients.

  3. Diagnosing Long QT Syndrome
    Congenital Long QT Syndrome is an inherited channelopathy that predisposes people (often young, otherwise healthy individuals) to sudden cardiac events, particularly during exercise, emotional stress, or startling noises (depending on the genetic subtype). QTc is the primary screening measurement used to identify at-risk individuals and family members.

  4. Electrolyte and metabolic monitoring
    Hypokalemia, hypomagnesemia, and hypocalcemia can all prolong QTc, making it a useful marker to track in critically ill patients, those with eating disorders, alcohol use disorder, or anyone on medications affecting electrolyte balance.

 

Formulas

There are multiple formulas used to estimate QTc. It is not clear which formula is the most useful:

  • Bazett formula: QTC = QT / √ RR

  • Fridericia formula: QTC = QT / RR 1/3

  • Framingham formula: QTC = QT + 0.154 (1 – RR)

  • Hodges formula: QTC = QT + 1.75 (heart rate – 60)

 

Note: The RR interval is given in seconds (RR interval = 60 / heart rate).

Prolonged QT (≥440 msec): 

  • QTc is prolonged if ≥ 440ms in men or ≥ 460ms in women

  • QTc > 500 is associated with an increased risk of torsade de pointes

 

Short QT (<350ms)

  • Congenital short QT syndrome has been found to be associated with an increased risk of paroxysmal atrial and ventricular fibrillation and sudden cardiac death

Alle Fragen und möglichen Ergebnisse

Formula Options
Select Formula

Select one option:

  • Bazett
  • Fridericia
  • Framingham
  • Hodges
  • Rautaharju
Enter heart rate (pulse)

A number between 0 and 500, in beats/min.

Select paper speed

Select one option:

  • 25 mm/sec
  • 50 mm/sec
Enter QT interval (paper speed 25 mm/sec)
  • Toggle unit to use msec, small boxes or large boxes
    • 1 small box (1 mm) = 0.04 seconds (40 msec) at 25 mm/sec
    • 1 large box (5 mm) = 0.2 seconds (200 msec) at 25 mm/sec

 

A number between -100 and 1000, in msec or small boxes or large boxes.

Enter QT interval (paper speed 50 mm/sec)
  • Toggle unit to use msec, small boxes or large boxes
    • 1 small box (1 mm) = 0.02 seconds (20 msec) at 50 mm/sec
    • 1 large box (5 mm) = 0.1 seconds (100 msec) at 50 mm/sec

 

A number between -100 and 1000, in msec or small boxes or large boxes.

Mögliche Ergebnisse
Fridericia Corrected QT Interval (QTc) - 25 mm/sec paper speed
Framingham Corrected QT Interval (QTc) - 25 mm/sec paper speed
Bazett Corrected QT Interval (QTc) - 50 mm/sec paper speed
Rautaharju Corrected QT Interval (QTc) - 25 mm/sec paper speed
Rautaharju Corrected QT Interval (QTc) - 50 mm/sec paper speed
Fridericia Corrected QT Interval (QTc) - 50 mm/sec paper speed
Bazett Corrected QT Interval (QTc) - 25 mm/sec paper speed
Hodges Corrected QT Interval (QTc) - 25 mm/sec paper speed
Framingham Corrected QT Interval (QTc) - 50 mm/sec paper speed
Hodges Corrected QT Interval (QTc) - 50 mm/sec paper speed
Prolonged QTc (≥440 msec): Increased risk for torsade de pointes.

#EM3 East Midlands Emergency Medicine Educational Media summarizes actionable resources.

 

The Life in the Fastlane website also provides a concise QTc overview with examples See article called QT Interval (Burns & Buttner, 2022) for more details.

 

 Here are a few key points:

  • QTc is prolonged if ≥ 440ms in men or ≥ 460ms in women
  • QTc > 500 is associated with an increased risk of torsades de pointes (TdP)
  • Viskin (2009) proposes the use of a QT interval scale to aid diagnosis of patients with short and long QT syndromes (once reversible causes have been excluded).
  • Drug-induced QT-prolongation 
    • In the context of acute poisoning with QT-prolonging agents, the risk of TdP is better described by the absolute rather than corrected QT.
    • More precisely, the risk of TdP is determined by considering both the absolute QT interval and the simultaneous heart rate (i.e. on the same ECG tracing).
    • These values are then plotted on the QT nomogram (developed by Chan, 2007) to determine whether the patient is at risk of TdP.
    • The QT nomogram is a clinically relevant risk assessment tool that predicts arrhythmogenic risk for drug-induced QT prolongation can be used for risk stratification
    • A QT interval-heart rate pair that plots above the line indicates the patient is at risk of TdP.

 

Consider potential causes of prolonged QT:

  • Electrolyte abnormalities:
    • Hypokalemia
    • Hypocalcemia
    • Hypomagnesemia
  • Medications:
    • Psychotropic drugs
    • Anti-arrhythmics
    • Other drugs
  • Central causes:
    • Hypothyroid
    • Hypothermia
    • Raised intracranial pressure
    • Autonomic dysfunction
  • Intrinsic cardiac causes:
    • Myocardial ischemia
    • Severe bradycardia, high-grade AV block
    • Congenital long QT syndrome
    • ROSC post-cardiac arrest
    • Coronary artery disease (CAD)
    • Cardiomyopathy
Short QTc (<350ms): Increased risk for paroxysmal atrial and ventricular fibrillation and sudden cardiac death

Viskin (2009) proposes the use of a ‘QT interval scale’ to aid diagnosis of patients with short and long QT syndromes (once reversible causes have been excluded).

 

The Life in the Fastlane website provides a concise overview with examples in an article called QT Interval (Burns & Buttner, 2022). Here are a few key points:

 

Potential causes of a short QTc

  • Hypercalcaemia
  • Congenital short QT syndrome
  • Digoxin effect

 

Short QT syndrome may be suggested by the presence of:

  • Lone atrial fibrillation in young adults
  • Family member with a short QT interval
  • Family history of sudden cardiac death
  • ECG showing QTc < 350 ms with tall, peaked T waves
  • Failure of the QT interval to increase as the heart rate slows

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