Drugs For Cardiac Arrhythmias (Konorev) Flashcards
What are the 1B Na channel blocking drugs?
Lidocaine
Mexiletine
Which cell types have a fast AP?
Ventricular contractile cardiomyocytes
Atrial cardiomyocytes
Purkinje fibers
Which cell types have a slow (pacemaker) AP?
SA node cells
AV node cells
What are the 1C Na channel blocking drugs?
Flecainide
Propafenone
What are the class 2 antiarrhythmic drugs?
Beta blockers
Esmolol and propanolol
What are class 3 antiarrhythmic drugs?
K channel blocking drugs Amiodarone Dronedarone Sorta lol Dofetilide Ibutilide
What are class 4 antiarrhythmic drugs?
Cardioactive Ca channel blockers
Verapamil and Diltiazem
Class 1A drugs preferentially bind to __ channels
Open (activated) Na
Class 1A drugs have what effects on the following:
- K channels: ___
- AP duration: ___
- QRS and QT intervals: ___
Block
Prolong
Prolong
This 1a drug is used to tx sustained V tach, directly depresses the activities of SA and AV nodes, and possesses antimuscarinic activity
Procainamide
What are adverse effects of Procainamide?
Cardiac –> QT prolongation, induce Torsade de pointes and syncope
Extracardiac –> lupus syndrome, nausea, diarrhea, and agranulocytosis
This 1a drug is a natural alkaloid from Cinchona bark that is used occasionally for restoring rhythm in A flutter/fib pts with normal (but arrhythmic) hearts
Quinidine
What are adverse effects of quinidine?
Cardiac –> QT prolongation, induce Torsades
Extracardiac –> GI side effects, headache, dizziness, tinnitus, thrombocytopenia, hepatitis, fever
This 1a drug is used for tx of recurrent V Tac
Disopyramide
What are adverse effects of Disopyramide?
Cardiac –> QT prolongation, induce torsades, negative inotropic effect
Extracardiac –> atropine-like symptoms
Class 1B drugs bind to ___ channels
Inactivated Na , preferentially bind to depolarized cells
This 1B drug blocks inactivated Na channels-selectively blocks conduction in depolarized tissue, making damaged tissue completely “electrically silent”. It is used in mono- and polymorphic V Tac
Lidocaine: extensive 1st pass metabolism and only by IV route
This is the least toxic of all Class I drugs