Which of the following is the treatment of choice for torsades de pointes?

Occasional patients will have recurrent episodes of torsade [“Torsade storm”].  Each individual episode may be treated with magnesium or defibrillation, if needed [Treatment step #1 above].  However, additional therapies are required to stop recurrence and end the storm.

re-load magnesium if needed
  • Recurrent torsade may reflects inadequate magnesium dosing [e.g., patient is bolused with 2-4 grams, without an infusion].  The first step when managing recurrent torsade is therefore to ensure that the patient has truly received an adequate dose of magnesium.
  • If the patient was bolused with magnesium a few hours ago without an infusion, re-load with 2-4 grams IV immediately [8-16 mM].
  • If the patient is a candidate for magnesium infusion [GFR >30 ml/hr], this should be started.
  • If the patient has renal failure and has already received 4-6 grams of magnesium [16-24 mM], then check magnesium levels and ensure that a high level is achieved.   Note that a therapeutic level for torsade is roughly 3.5-5 mg/dL [1.5-2 mM] – not a “normal” level.
  • More on magnesium above.📖
treat any other precipitating factors
  • Hypokalemia, should be treated aggressively, targeting a high-normal potassium level [>4.5 mEq/L].[29084733]
  • Hypocalcemia may promote torsade and should be treated if present.📖
  • Hypothermia should be aggressively reversed.📖
speed up the heart
  • Speeding up the heart rate will generally decrease the QT interval and reduce the risk of acquired torsade.  However, this probably doesn't work in Type-I congenital long-QT syndrome, which is not a pause-dependent arrhythmia. 📄 [34039680]  
  • The usefulness of chronotropy depends on the patient's baseline heart rate.
    • Chronotropy is most beneficial for patients starting out with bradycardia.
    • If the patient is already significantly tachycardic, chronotropy is unlikely to provide benefit.  The usual target heart rate is 100-110 b/m, but occasionally heart rates up to 140 b/m may be needed.[26183037]  There's no high-quality data on this.
  • Medical chronotropy is generally the easiest & fastest way to stabilize the patient.  The ideal chronotrope depends on the patient's hemodynamics and baseline blood pressure.
    • Baseline severe hypotension:  epinephrine infusion.
    • Baseline normotension or mild hypotension:  dobutamine or isoproterenol infusion.
    • ⚠️ Caution:  If chronotropic therapy causes lots of premature ventricular complexes, this may be counterproductive [since premature ventricular complexes can trigger torsade].[31114687]  In this situation, consider transvenous pacing and/or lidocaine.
    • ⚠️ Caution:  Beta-adrenergic agonists are contraindicated in patients with congenital long-QT syndrome.
  • Electrical chronotropy may be used if medical chronotropy fails or is contraindicated:
    • Transcutaneous pacing may work, but this is painful for conscious patients.
    • Transvenous pacing is more comfortable, but this is more invasive and takes a bit longer to achieve.
    • Patients with a pacemaker may have the device rate increased.
lidocaine 💊
  • Lidocaine is the preferred antiarrhythmic drug for torsade, although there isn't a ton of evidence supporting its use.
    • Do not use amiodarone, procainamide, beta-blockers, or most other antiarrhythmics.  Most of these will stretch out the QT interval even further!  Beta-blockers will slow down the heart rate, increasing the risk of torsade [although beta-blockers may be beneficial in some patients with congenital long-QT syndrome].📄 [34039680] 
  • Start with a loading dose of 1-1.5 mg/kg lidocaine followed by a 1 mg/min infusion.  For recurrent arrhythmias, re-load with another 1 mg/kg bolus and increase the maintenance infusion to 2-3 mg/min.
consider an alternative diagnosis
  • Acquired torsade is generally fairly easy to control with a combination of high-dose magnesium, heart rate augmentation, and occasionally some lidocaine.  Failure to respond to these interventions suggests an alternative diagnosis [e.g. polymorphic VT due to ischemia, catecholaminergic ventricular tachycardia, or congenital long-QT syndrome].

podcast

[back to contents]

Follow us on iTunes

The Podcast Episode

//traffic.libsyn.com/ibccpodcast/Torsades_Final.mp3

Want to Download the Episode?
Right Click Here and Choose Save-As

questions & discussion

[back to contents]

To keep this page small and fast, questions & discussion about this post can be found on another page here.

What is the best treatment for torsades de pointes?

Intravenous magnesium is the first-line pharmacologic therapy in Torsades de Pointes. Magnesium has been shown to stabilize the cardiac membrane, though the exact mechanism is unknown. The recommended initial dose of magnesium is a slow 2 g IV push.

How is torsades treated?

The torsades rhythm is treated with magnesium sulfate 2 g IV over 1 to 2 minutes, correction of hypokalemia, pacing or isoproterenol to increase heart rate, and correction of the cause.

Which of the following is not a treatment for torsades de pointes?

Do not use amiodarone, procainamide, beta-blockers, or most other antiarrhythmics. Most of these will stretch out the QT interval even further! Beta-blockers will slow down the heart rate, increasing the risk of torsade [although beta-blockers may be beneficial in some patients with congenital long-QT syndrome].

Does amiodarone treat torsades de pointes?

Background Amiodarone is an effective antiarrhythmic drug rarely associated with torsade de pointes arrhythmias [TdP]. The noniodinated compound dronedarone could resemble amiodarone and be devoid of the adverse effects.

Chủ Đề