Administration of amiodarone during resuscitation is associated with higher tumor necrosis factor-α levels in the early postarrest period in the swine model of ischemic ventricular fibrillation

J Interferon Cytokine Res. 2013 Jun;33(6):292-6. doi: 10.1089/jir.2012.0123. Epub 2013 May 9.

Abstract

To compare the early postarrest inflammatory cytokine response between animals administered amiodarone (AMIO) and lidocaine (LIDO) intra-arrest during resuscitation from ventricular fibrillation (VF). Domestic swine (n=32) were placed under general anesthesia and instrumented before spontaneous VF was induced by balloon occlusion of the left anterior descending coronary artery. After 7 min of VF, standard ACLS resuscitation was performed and animals were randomized to either bolus AMIO (5 mg/kg, n=13) or LIDO (1 mg/kg, n=14) for recurrent or refractory VF. A non-antiarrhythmic (n=5) was also used for comparison. Following return of spontaneous circulation (ROSC), tumor necrosis factor (TNF)-α levels were drawn at 30 and 60 min. Groups were comparable with respect to prearrest hemodynamics and resuscitation variables. In the postarrest period, the LIDO and non-antiarrhythmic group demonstrated virtually identical TNF-α response trajectories. However, TNF-α levels were significantly higher in AMIO- than LIDO-treated animals at 30 min (geometric mean 539 versus 240 pg/mL, 2.2-fold higher, 95% confidence interval [CI] 1.3-3.8-fold higher, P=0.003) and at 60 min (geometric mean 570 versus 204 pg/mL, 2.8-fold higher, 95% CI 1.1-7.0-fold higher, P=0.03). Significant differences in the postarrest TNF-α levels were observed between animals treated with AMIO as compared to those treated with LIDO. Improved rates of ROSC seen with AMIO may come at the expense of a heightened proinflammatory state in the postcardiac arrest period.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amiodarone / pharmacology*
  • Animals
  • Anti-Arrhythmia Agents / pharmacology*
  • Cardiopulmonary Resuscitation / methods*
  • Coronary Vessels / drug effects
  • Coronary Vessels / metabolism
  • Disease Models, Animal
  • Heart Arrest / drug therapy
  • Heart Arrest / metabolism
  • Heart Arrest / physiopathology
  • Heart Arrest / therapy*
  • Hemodynamics / drug effects
  • Inflammation / drug therapy
  • Inflammation / metabolism
  • Lidocaine / pharmacology
  • Male
  • Myocardial Ischemia / metabolism
  • Myocardial Ischemia / physiopathology
  • Random Amplified Polymorphic DNA Technique
  • Swine
  • Tumor Necrosis Factor-alpha / metabolism*
  • Ventricular Fibrillation / drug therapy*
  • Ventricular Fibrillation / metabolism
  • Ventricular Fibrillation / physiopathology

Substances

  • Anti-Arrhythmia Agents
  • Tumor Necrosis Factor-alpha
  • Lidocaine
  • Amiodarone