4.4 Article

Role of chronic continuous intravenous lidocaine in the clinical management of patients with malignant type 3 long QT syndrome

Journal

HEART RHYTHM
Volume 19, Issue 1, Pages 81-87

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.hrthm.2021.09.016

Keywords

Arrhythmias; Genetics; Lidocaine; Long QT syndrome; Sudden cardiac death

Funding

  1. Mayo Clinic Windland Smith Rice Comprehensive Sudden Cardiac Death Program
  2. Dr Scholl Foundation
  3. Mayo Clinic Center for Translational Science Activities from the National Center for Advancing Translational Sciences, a component of the National Institutes of Health [UL1TR002377]

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Chronic continuous intravenous (IV) lidocaine infusion may serve as a potential bridge to transplantation for LQT3 patients who are refractory to standard treatment.
BACKGROUND Type 3 long QT syndrome (LQT3) is caused by pathogenic, gain-of-function variants in SCN5A leading to a prolonged action potential, ventricular ectopy, and torsades de pointes. Treatment options include pharmacotherapy, cardiac denervation, and/or device therapy. Rarely, patients with malignant LQT3 require cardiac transplantation. OBJECTIVE The purpose of this study was to evaluate the role of chronic continuous intravenous (IV) lidocaine as a therapeutic option for select patients with LQT3 refractory to standard therapy. METHODS We performed a retrospective review of patients evaluated and treated at Mayo Clinic and identified 4 of 161 patients with LQT3 (2.5%) who were refractory to standard therapies and therefore treated with IV lidocaine. RESULTS There were 4 patients (2 female [50%]). The median age at first IV lidocaine infusion was 2 months (interquartile range 1.5-4.8 months), and the median cumulative duration on IV lidocaine was 11.5 months (interquartile range 8.7-17.8 months). The main indication for IV lidocaine in all patients was persistent ventricular arrhythmias. Before IV lidocaine, all patients received an implantable cardioverter-defibrillator, and while on intermittent IV lidocaine, all patients underwent bilateral cardiac sympathetic denervation. Additionally, 2 (50%) patients had cardiac ablation for premature ventricular complexes. In all patients, lidocaine infusion resulted in a significant reduction of LQT3-triggered cardiac events. The main side effects of IV lidocaine observed were dizziness (n = 2, 50%) and seizures (n = 2, 50%). During follow-up, 3 of 4 (75%) patients underwent orthotopic cardiac transplantation. The remaining patient continues to receive IV lidocaine bolus for rescue as needed. CONCLUSION For patients with LQT3 who are refractory to standard treatment, chronic IV lidocaine infusion can be used as a potential bridge to transplant.

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