Epicardial electrical heterogeneity after amiodarone treatment increases vulnerability to ventricular arrhythmias under therapeutic hypothermia

PLoS One. 2023 Apr 20;18(4):e0282943. doi: 10.1371/journal.pone.0282943. eCollection 2023.

Abstract

Background: Amiodarone is commonly used during therapeutic hypothermia (TH) following cardiac arrest due to ventricular arrhythmias. However, electrophysiological changes and proarrhythmic risk after amiodarone treatment have not yet been explored in TH.

Methods: Epicardial high-density bi-ventricular mapping was performed in pigs under baseline temperature (BT), TH (32-34°C), and amiodarone treatment during TH. The total activation time (TAT), conduction velocity (CV), local electrogram (LE) duration, and wavefront propagation from pre-specified segments were analyzed during sinus rhythm (SR) or right ventricular (RV) pacing (RVP), along with tissue expression of connexin 43. The vulnerability to ventricular arrhythmias was assessed.

Results: Compared to BT, TH increased the global TAT, decreased the CV, and generated heterogeneous electrical substrate during SR and RVP. During TH, the CV reduction and LE duration prolongation were greater in the anterior mid RV than in the other areas, which changed the wavefront propagation in all animals. Compared to TH alone, amiodarone treatment during TH further increased the TAT and LE duration and decreased the CV. Heterogeneous conduction was partially attenuated after amiodarone treatment. After TH and amiodarone treatment, the connexin 43 expression in the anterior mid RV was lower than that in the other areas, compatible with the heterogeneous CV reduction. The animals under TH and amiodarone treatment had a higher incidence of inducible ventricular arrhythmias than those under BT or TH without amiodarone.

Conclusion: Electrical heterogeneity during amiodarone treatment and TH was associated with vulnerability to ventricular arrhythmias.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amiodarone* / adverse effects
  • Animals
  • Arrhythmias, Cardiac
  • Connexin 43 / metabolism
  • Heart Ventricles
  • Hypothermia, Induced* / adverse effects
  • Swine

Substances

  • Amiodarone
  • Connexin 43

Grants and funding

This work was funded by the Ministry of Science and Technology of Taiwan (109-2314-B-075 -076 -MY3, 111-2314-B-075 -007 -MY3). Chin-Yu Lin is the recipient of the funding award. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.