Key result
Deep anesthesia with high-dose ketamine and xylazine significantly reduced the incidence of ventricular tachyarrhythmias to 6.7% compared to 100% with light anesthesia in a rabbit model of acquired long QT syndrome.
Why the study?
Does deep anesthesia with ketamine and xylazine prevent ventricular tachyarrhythmias in a rabbit model of acquired long QT syndrome?
Does deep anesthesia with ketamine and xylazine prevent ventricular tachyarrhythmias in a rabbit model of acquired long QT syndrome?
Deep anesthesia with ketamine suppresses abnormal repolarization-related ventricular tachyarrhythmias in a rabbit model of acquired long QT syndrome, independent of alpha-2-adrenoreceptor agonism.
Answers are grounded in this paper and cite their sources.
Anesthetic protocols warrant standardization in rabbit LQTS models; leaves open translation to clinical arrhythmia risk.
BACKGROUND: Anesthesia sometimes suppresses ventricular tachyarrhythmias (VT) resistant to conventional pharmacological treatment. METHODS AND RESULTS: To know (1) whether deep anesthesia inhibits abnormal repolarization-related VT and (2) if α2-adrenoreceptor (AR) agonistic action is associated with the antiarrhythmic effect of anesthetics, the incidence of VT in a rabbit model of acquired long QT syndrome using different anesthetic regimen was assessed. In Study 1 (n = 30), 15 rabbits were lightly anesthetized with ketamine (123 ± 46 mg/kg) and an α2-AR agonist, xylazine (9.4±3.0mg/kg), while combination of these anesthetics at high doses were used in the other 15 rabbits (343 ± 78 mg/kg and 38.9 ± 3.0 mg/kg). Administration of α1-AR stimulant, methoxamine and nifekalant (Ikr blocker) caused VT in all lightly anesthetized rabbits. In contrast, VT was observed only in 1 of the 15 deeply anesthetized rabbits (P < 0.01). In Study 2 (n = 15), 10 rabbits were anesthetized with high-dose ketamine and low-dose xylazine. In the other 5 rabbits, low-dose ketamine and high-dose xylazine were used. QTc interval in the latter was longer than that of the former (399 ± 56 ms vs. 494 ± 57 ms, P < 0.01). Although no VT appeared in high/low-rabbits, VT occurred in 3 out of 5 low/high-rabbits (P < 0.05). CONCLUSIONS: These results suggest that (1) deep anesthesia suppresses abnormal repolarization-related VT and (2) antiarrhythmic effect of anesthesia on this type of VT is not dependent on α2-AR agonistic action.
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Inaba et al. (2010) studied Acquired long QT syndrome (n=45). Deep anesthesia (high-dose ketamine and xylazine) vs. Light anesthesia (low-dose ketamine and xylazine) was evaluated on Incidence of ventricular tachyarrhythmias (VT) (p=<0.01). Deep anesthesia with high-dose ketamine and xylazine significantly reduced the incidence of ventricular tachyarrhythmias to 6.7% compared to 100% with light anesthesia in a rabbit model of acquired long QT syndrome.
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