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Torsades de pointes (TdP)

Polymorphic VT and Torsades de Pointes (TdP) • LITFL
Torsades de Pointes: Symptoms, Causes, Treatment, and More
  • associated with sudden death
    • pronunciation by Australians commonly associated with sudden death in native French speakers
  • ECG characteristics
    • cyclical multiform ventricular ectopic complexes that vary about an isoelectric axis
      • due to 2 ventricular ectopic foci (a reciprocating tachycardia)
      • usual rate of 150-300/min
  • Other ECG features
    • ectopy
    • bradycardia
    • high grade AV block

Risk factors

  • age: young children normally have a longer QTc without increased risk of TdP
  • gender: males usually have shorter QTc
  • ethnicity: higher risk in black skinned patients
  • causative agent
    • amiodarone increases QTc but does not appear to increase the risk of TdP
  • rapid onset
    • e.g. rapid infusion of a QT-prolonging drug
  • recent conversion from atrial fibrillation
    • especially if a QT-prolonging drug has been used
  • congestive cardiac failure
  • digitalis therapy
  • rapid rate of intravenous infusion with a QT-prolonging drug
  • severe hypomagnesaemia
  • QTc prolongation 
    • caused by inhibition of the rapid component of the delayed rectifier potassium (IKR) channel
    • risk not a linear function of the QT interval
    • risk increases 6% (compound) for every 10% increase in QTc above 500 msec.

Causes of prolonged QT

AntipsychoticsAntiarrhythmicsTricyclicsOther antidepressantsAntihistaminesOthers
ChlorpromazineQuinidineAmitriptylineCitalopramDiphenhydramineErythromycin
HaloperidolProcainamideDoxepinEscitalopramLoratadineClarithromycin
DroperidolDisopyramideImipramineVenlafaxineTerfenadineQuinine
QuetiapineFlecainideDesipramineBupropion Chloroquine
OlanzapineSotalol   Hydroxychloroquine
ThioridazineAmiodarone    

  • Electrolyte abnormalities
    • hypomagnesaemia
    • hypocalcaemia
    • hypokalaemia
      • does not actually cause prolonged QT syndrome
      • U wave of hypokalaemia is commonly misinterpreted as a T wave
  • Heart disease
    • cardiomyopathy
    • severe cardiac failure
    • myocardial ischaemia
    • complete heart block
    • hypertension
  • Poisoning
    • many drugs prolong the QTc to a minor degree, but rarely (if ever) cause TdP on their own
    • type I, III anti-arrhythmics
      • quinine/quinidine
    • antipsychotics
      • clozapine
      • haloperidol/droperidol (much lower risk)
      • quetiapine
      • olanzapine
      • risperidone
    • TCADs
    • carbamazepine
    • methadone
    • lithium
    • organophosphates
    • quinolones
      • erythromycin/clarithromycin/azithromycin
    • ondansetron
    • fluconazole/ketoconazole
  • Congenital
  • Other
    • hypothyroidism
    • SAH

Management

  • cardioversion if pulseless or in extremis
    • 200J
    • may not synchronise, so asynchronous defibrillation may be required
  • MgSO4
    • 1-2 G of MgSO4 over 10 minutes if cardiac arrhythmia, torsades, seizures
    • 1 G of MgSO4 in 100mL Normal Saline over 30 minutes for slow replacement
  • isoprenaline
  • atropine if organophosphates the cause
  • overdrive pacing
  • K+ replacement to 4.5 – 5 mmol/L
  • Calcium gluconate 1 G to replenish Calcium (normally go hand in hand)
  • Admission criteria for ECG monitoring
    • QT interval above the QT Normogram
  • increase in QTc > 60 msec over baseline
  • progressive increase in QTc over hours (e.g. following poisoning)

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