Pharmacotherapy in inherited and acquired ventricular arrhythmia in structurally normal adult hearts

Staniel Ortmans1,2, Charline Daval1,2, Martin Aguilar1,2,3

  • 1Electrophysiology service, Montreal Heart Institute, Montreal, Quebec, Canada.

Insights

This review discusses drug therapies for inherited and acquired ventricular arrhythmias, emphasizing accurate diagnosis and tailored pharmacotherapy to prevent sudden cardiac death (SCD) and manage symptoms.

Area of Science:

  • Cardiology
  • Clinical Pharmacology

Background:

  • Ventricular arrhythmias frequently accompany structural heart disease.
  • A subset of patients with ventricular arrhythmias have structurally normal hearts; these are often inherited, affect younger individuals, and can lead to sudden cardiac death (SCD).
  • Advances in understanding pathophysiology have improved targeted drug therapies over the last two decades.

Purpose of the Study:

  • To review current drug therapies for inherited arrhythmia syndromes.
  • To review current drug therapies for acquired arrhythmias.
  • To provide expert opinion on the optimal use of pharmacotherapy in managing these conditions.

Main Methods:

  • Literature review of drug therapy for specific inherited arrhythmia syndromes (Brugada, early repolarization, long QT, short QT, catecholaminergic polymorphic ventricular tachycardia).
  • Literature review of drug therapy for acquired arrhythmias (idiopathic ventricular fibrillation, short-coupled torsade de pointes, outflow tract ventricular tachycardia, idiopathic left, papillary muscle, and annular ventricular tachycardias).
  • Synthesis of expert opinion on diagnosis, drug selection, and dosing.

Main Results:

  • Pharmacological management is crucial for inherited arrhythmia syndromes, with proper diagnosis and drug selection vital for SCD prevention, often avoiding the need for implantable cardioverter-defibrillators.
  • Pharmacotherapy can offer symptomatic relief and reduce the need for invasive treatments in selected patients with acquired arrhythmias.
  • Current therapies highlight the importance of precise diagnosis and tailored treatment approaches.

Conclusions:

  • Accurate clinical and genetic diagnosis is paramount in inherited arrhythmia syndromes for effective pharmacotherapy and SCD prevention.
  • Pharmacotherapy plays a significant role in managing both inherited and acquired arrhythmias, improving patient outcomes.
  • Further research is necessary to develop novel antiarrhythmic drugs with improved efficacy and reduced side effects.

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