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Atrial arrhythmias induced during DBT were comparable to that induced during IPN. In patients with IPN-inducible outflow tract premature ventricular contractions, a similar effect was noted with DBT. No major complications occurred during either drug challenge. High-dose DBT is safe and comparable to high-dose IPN in respect of eliciting AF triggers, withtheadvantage to maintain systemic pressure without the need of additional vasopressor support. This studysupports the use of high-dose DBT in electrophysiology laboratories in which IPN

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