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10 Cards in this Set

  • Front
  • Back
Quinidine
Direct action on AV node to increase Effective Refractory Period [but the anticholinergic effect decreases AV node refractoriness]
Toxicities include depressed myocardial contractility; prolonged Q-T interval can lead to arrhythmias, such as torsades des pointes; slowed conduction
Significant antimuscarinic activity
G.I. Effects (e.g. Nausea or Diarrhea) limit use in up to 30% of Patients
Local anesthetic actions
PROCAINAMIDE
Reversible Lupus-like syndrome without renal or neurological problems
DISOPYRAMIDE
Depresses myocardial contractility (may precipitate heart failure)
Anticholinergic effects even greater than quinidine
LIDOCAINE
Must be given i.v. due to high "first pass" hepatic metabolism
Clearance is directly related to hepatic blood flow (i.e., hepatic intrinsic clearance is exceptionally high)
Adverse effects primarily on the CNS (convulsions, tremors, nystagmus)
Primary uses: Acute management of ventricular arrhythmias [Drug of choice for acute management of ventricular arrhythmias]
FLECAINIDE
PROARRHYTHMIC EFFECTS. Effective suppression of ventricular premature beats, but exacerbates ventricular arrhythmias, increasing mortality
PROPRANOLOL, METOPROLOL
Primary uses: management/prevention of supraventricular and ventricular arrhythmias, particularly in patients with M.I.
AMIODARONE
Prolongs Q-T interval; prolongs period of refractoriness
Actions associated with K+ channel inhibition, but multiple mechanisms and sites for amiodarone and other “Class III” drugs
Complex pharmacokinetics, Very long elimination half-life after chronic use. Accumulates in tissues – many adverse effects
Pulmonary fibrosis (~10%) – can be fatal
ADENOSINE
Mechanism: agonist at adenosine receptors.
Increases ACh-sensitive K+ conductance in SA and AV nodes and atria. Thus, shortened AP, reduced automaticity and slowed conduction.
Decreases cAMP-induced calcium influx.

Denervated hearts are supersensitive
Effects inhibited by adenosine receptor antagonists [caffeine and theophylline], potentiated by adenosine uptake inhibitor [Persantine]
Very short elimination half-life (< 10 sec); only used i.v.

Virtually ALL patients experience chest pain and dyspnea
Primary Use: Rapid management of Paroxysmal Supraventricular Tachycardia
VERAPAMIL
Blocks inward calcium current and prolongs desensitized form of the channel.
Thus, main effects in slow fibers (nodal tissue), and also in damaged fibers [e.g. hypoxic cells] in which sodium channels are refractory and calcium currents are more prominent.
Contraindicated in Wolff-Parkinson-White syndrome
Primary uses: Management of supraventricular arrhythmias and atrial fibrillation
Nifedipine
Is NOT Effective for Treating Arrhythmias