'Torsades de pointes' in a patient with history of epilepsy"

(1.) The 12-lead ECG shows bradycard sinus rhythm with left axis deviation, one SVES, borderline PQ interal and QTc prolongation of 508 ms. The T-wave is of low amplitude and double notch appearance. The ECG phenotype and the history of “torsades de pointes” are consistent with the long QT syndrome (LQTS) type 2 phenotype [1]. Subsequent ECG’s confirmed the LQTS type 2 phenotype. (2.) The patient was treated for epilepsy for more than 30 years. She reported that she suffered from witnessed (husband) syncope’s usually in the morning, still lying in the bed, when the telephone rang, which is a typical trigger for ventricular arrhythmias in LQTS type 2 patients [2]. With the background of LQTS “epilepsy” must be considered as haemodynamically relevant ventricular arrhythmia, eg “torsades de pointes” in the context of LQTS. As a consequence phenytoine was stopped, beta-blocker therapy was started and the implantation of an ICD was discussed with the patient. Gene testing was performed and a heterozygous mutation was identified in the KCNH2 gene. Congenital long QT syndrome is an inherited disease characterised by prolonged ventricular repolarisation and a high risk for sudden cardiac death (SCD) due to complex ventricular arrhythmias and “torsades de pointes”. Today eight LQTS phenotypes are known. The most common forms are type 1 and 2, caused by mutations in the potassium channel genes KCNQ1 and KCNH2, respectively, and type 3, caused by mutations in the SCN5A gene encoding the cardiac sodium channel. These types can be distinguished on the surface ECG [1]. LQTS type 1 is characterised by the broadest T-wave, whereas type 2 shows low T-wave amplitude with a double notch appearance as shown in figure 2. Type 3 reveals the most delayed onset of a narrowly peaked Twave which also can be biphasic, depending on