Pharm - Antiarrhythmic Drugs Flashcards
Most antiarrhythmic agents that target K channels target ___
IKR
Antiarrhythmic drugs can cause ___ but not treat them. These are best treated with ___
Bradyarrhythmias
Implantable devices
Vaughan Williams classification of Antiarrhythmic drugs
I: Na channel blockers (IA, IB, IC)
II: beta receptor blockers
III: K channel blockers
IV: Ca channel blockers
___ has the least effect on Phase 0.
___ has the most effect on Phase 0.
___ also increases the AP duration because ___
- IB
- IC
- IA, side effect: blocks IKR and IKS channels (IB, IC do not)
Avoid class ____ in patients with structural damage (e.g. Post-MI)
IC
Class IA examples:
Quinidine
Procainamide
Disopyramide
Class IB examples:
Lidocaine
Mexiletine
Phenytoin
Class IC examples:
Flecainide
Propafenone
Class ___ has the lowest affinity for Na channels
Class __ has the highest affinity for Na channels
IB
IC
Affinity and kinetics of Class I drugs
Affinity: IC>IA>IB
Kinetics: IB>IA>IC
All class I antiarrhythmic decrease the ___ and reduce the ___
Decrease the upstroke velocity (phase 0) and reduce the amplitude of the cardiac AP
*this may depress conduction velocity and slow impulse propagation
Class IA
Anti-muscarinic
May enhance conduction through the AV node
-also blocks IKR channels (class III effect)
-prolongs QT interval
-increases risk of torsades de pointes
Class IA agents list:
Detailed
- Quinidine (rarely used due to toxicity, blood cos CYP2D6, metabolized by CYP3A4)
- Procainamide (IV only; most used, half life is 3-4 hrs, adverse effect includes lupus like disorder)
- Disopyramide (avoid in heart failure, negative inotropic effect)
Uses of class IA drugs
Atrial and ventricular tachyarrythmias
Uses for class IB agents
Ventricular arrhythmias ONLY