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Antidysrhythmics

ClassEffects on heart/ECGTherapeutic UsesAdverse EffectsDrug InteractionsNotes
Class IB Agents: lidocaine (IV)-> very diff from: phenytoin (dig-induced dys, acute&chronic supp.PK:2C9, 2C19 substrate); memexilitene (symptomatic c dyd. PK:1A2,2D6 substrate) slows conduction in atria, vent, His-Purkinje sys; reduces automaticity in vent and His-Pur sys; accelerates repolarization; minimak ECG changes therapeutic range 1.5-5 mcg/mL (narrow); used for ventricular dysrhythmias CNS effects, drowsiness, confusion, neurologic effects, paresthesias, GI disturbances; dysrhythmias prodysrhythmic drugs and drugs that affect metabolism of Class IB agents
Class II: BB (propranolol-nonselective) Others: acebuterol (cardioselective, for PVCs); esmolol (cardioselective w/ short 1/2life for immediate control of a-flutter and a-fib) decreased automaticity of SA node, decreased velocity of conduction through AV node (prolonged QT interval), decreased myocardial contractility dysrhythmias caused by excessive SNS stim. of heart, in pts w/ supravent. tachydysrhy, propranolol: -supression of excessive discharge, slowing of ventricular rate (by decreasing trans of atrial impulses through AV node) heart block, HF, AV block, sinus arrest, hypotn, bronchospasm (propranolol-nonselective)
Class III: K Channel Blockers (amioderone, bretylium, dofetilide, sotalol, ibutelide)
Class IA Agents: Quinidine, procainamide, disopyramide blocks Na channels, slows impulse conduction, delays repolarization, blocks vagal input to heart (quinidine-increase SA automaticity and AV conduction, so pretreated w/dig. veramipil or BB->suppress AV cond.);widens QRS complex, prolongs QT interval quinidine and procainamide:broad spectrum agents against sv. and v.dysrhythmias (frequently used); disopyramide:only indicated for V.dysrhyth and is reserved for pts. who can't tolerate safer meds (others) GI Effects; hypersensitivity rxns; cardiotoxicity; hypotn;hepatotoxicity (quinidine);+anti-nuclear antibody tier (procainamide-autoimmune); *NB:disopyramide, unlike quinidine, causes a pronounced reduction in contractility, causing severs hypotn 2/2 red. digoxin (quinidine can 2x dig levels); 3A4 inhibitors, drugs that can prolong QT interval (ranolazine, etc)
Class IC Agents: flecainide, propafenone Blocks cardiac Na channels->slowing conduction in atria, ventricles, and His Pur sys, delay ventricular repolarization dysrhythmias, HF, GI effects, bronchospasm (propafenone) drugs that can cause dysrhythmias All class IC agents can exacerbate existing dysrhythmias
Created by: jellyfishh
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