Key result
Ivabradine plus nadolol or flecainide suppresses polymorphic nsVT and couplets in CPVT case reports.
Why the study?
Does ivabradine reduce ventricular arrhythmias in patients with CPVT who are intolerant to standard therapy?
Case Report (n=2)
Does ivabradine reduce ventricular arrhythmias in patients with CPVT who are intolerant to standard therapy?
Ivabradine may serve as an effective adjunctive therapy for suppressing ventricular arrhythmias in CPVT patients who cannot tolerate standard treatments, potentially limiting the need for ICDs or sympathetic denervation.
May support ivabradine as adjunct in select CPVT; hypothesis-generating, requiring prospective trials before practice change.
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a potentially lethal hereditary disease characterized by complex ventricular arrhythmias provoked by exercise or emotional stress and by a high mortality rate in young individuals. Nadolol alone or in combination with flecainide is the most effective therapy. However, compliance to treatment is often low due to side effects. We report two patients with CPVT in whom side effects of treatment prompted discontinuation of flecainide or nadolol and in whom ivabradine was successfully added to therapy. In these two patients, ivabradine in combination with nadolol or flecainide was well tolerated and successfully suppressed nonsustained polymorphic ventricular tachycardia and couplets. Thus, ivabradine could limit the use of implantable cardioverter-defibrillators or left cardiac sympathetic denervation in CPVT patients with uncontrollable ventricular arrhythmias.
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Vaksmann et al. (2018) conducted a case report in Catecholaminergic polymorphic ventricular tachycardia (CPVT) (n=2). Ivabradine was evaluated on Suppression of nonsustained polymorphic ventricular tachycardia and couplets. Ivabradine combined with nadolol or flecainide successfully suppressed nonsustained polymorphic ventricular tachycardia and couplets in two patients with CPVT.
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