Anti-Arrhythmia Drugs Flashcards
3 mechanisms for drugs to be anti-arrhythmic
decrease autmaticity
increase refractory period
decrease conduction velocity
what are the five ways to decrease automaticity of a cell?
- increase threshold potential
- decrease phase 4 slope
- increase AP duration
- slow SA/AV node depolarization
- increase maximum diastolic potential
mechanism to increase the depolarization threshold and class of these drugs
block sodium channels
class 1 anti arrhythmics
what are the subsets of class I antiarrhythmics and which of these also blocks potassium channels?
A,B,C
Class IA blocks potassium too
rate class IA-C by increasing strength of Na block
B is weakest
A in the middle
C is strongest
with potassium channel blocking…what is the greatest toxicity?
will lead to lengthened QT…so torsades
name the class IA anti-arrhythmic and its function
Procainamide…Na and K blockers
name the two class IC anti-arrhythmics and its function
Flecainide and Propafenone..Na blockers
what is the warning with class IC drugs?
do not give to patients with structural heart abnormalities
name the class IB anti arrhythmic and its function
lidocaine and Na blocker
how do we decrease the phase 4 slope in the action potential of a nodal cell?
block the HCN channels
what common drugs block the HCN channels?
beta antagonists
class II anti-arrhythmics are what type of drug?
beta blockers
how to increase length of the action potential?
block the K channels that are repolarizing the cells
what class of antiarrhythmics block the K channels to lengthen the action potentials?
Class III and Class IA