Antiarrhythmic Drugs Flashcards
what are the phases of cardiac action potential ?
Phase 0: Rapid sodium influx through fast acting voltage gated Na+ channel.
Phase 01: inactivation of the voltage-gated Na+ channels along with the activation of transient outward potassium current causes a transient early repolarization.
Phase 02: Influx of L-type calcium channels matches the eflux of K+ through the rectifier K+ channels causing plateau of AP.
Phase 03: L-type calcium channel closes, but the rectfier K+ channels remain opens, this brings the membrane potential to -90 Mv causing repolarization.
What are the main conduction pathways from the SA node to the AV node ?
- Anterior internodal pathway
- Wenckebackh bundle or middle internodal pathway
- Thorel’s bundle or posterior internodal pathway.
what is the pathway of SA nodal impulse propagation to the left atrium ?
Bachmann’s bundle.
What are the intrinsic rates of SA , AV node and Hiss-Purkinje system ?
SAN= 60-100
AVN= 40 -60
HPS= 20-40
What are the spinal levels of cardiac sympathetic nerves
T2 to T4.
What are the preventive and corrective therapies in Tachyarrhythmias?
- Preventive: Medication. Catheter ablation.
- Corrective: Resynchronization therapy (defibrillator)
What are the preventive and corrective therapies in Bradyarrhythmias?
- Preventive: Medication.
- Corrective: Pacemaker.
What are the Pharmacological aims of anti-arrhythmic therapy ?
Rhythm control and rate control
Explain the Vaughan Williams classification of anti-dysrhythmic drugs ?
Ia : Intermediate dissociation Na+ blocker
Ib : Fast dissociation Na+ blocker
Ic: Slow dissociation Na+ blocker
II: Beta adrenoreceptor antagonists.
III: K+ channel blockers
IV: Calcium channel blocker.
What is the action of Vughan Williams class 1a drugs ?
They work by blocking sodium channels in the open or inactivated state, thereby decreasing the rate of rise of the phase 0 depolarization, & slowing conduction velocity.
The examples are Disopyramide, Quinidine, Procainamide.
What is the action of Vughan Williams class II drugs ?
They are beta adreno-receptor antagonists such as propranolol. They inhibit phase 04 of the cardiac AP by negatively modulating pacemaker potentials.
*negative chronotropic: slower SA frequency
*negative dromotropic: slower AV conduction
*negative bathmotropic: lower excitability
leading to reduced cardiac work and metabolic needs.
What is the action of Vughan Williams class III drugs ?
They are drugs such as amiodarone and sotalol. They inhibit the opening of rectifier K+ channels at the phase III of the AP causing cardiac AP prolongation and effective refractory period of the cardiomyocytes.
What is the action of Vughan Williams class IV drugs ?
These are drugs such as delitiazam and verapamil they act on the the plateau phase ( Phase 03) of the cardiac AP. They inhibit the influx of calcium into the cardiomyocytes and reduce the force of contraction and HR.
What are the factors that determine the choice of anti-arrhythmic drugs ?
– Type of arrhythmia
– Cause of arrhythmia
– HF yes/no and type: HF with reduced ejection fraction or HF with preserved ejection fraction.
– Strategy (rhythm or rate control)
– Contra-indications
What are the mechanisms of arrhythmias ?
*enhanced automaticity: Abnormal automaticity (in SA node)
*Reentry: eg Wolf Parkinson White syndrome.
*triggered activity: after depolarization, triggers premature action potentials.