Procainamide: Difference between revisions
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{{Short description|An article about the antiarrhythmic medication Procainamide}} | |||
==Procainamide== | |||
Procainamide | [[File:Procainamide.svg|thumb|right|Chemical structure of Procainamide]] | ||
'''Procainamide''' is a medication used to treat a variety of [[cardiac arrhythmias]]. It is classified as a [[Class A antiarrhythmic agent]] and works by blocking [[sodium channels]] in the heart, which helps to stabilize the cardiac membrane and reduce abnormal electrical activity. | |||
==Mechanism of Action== | |||
Procainamide | Procainamide works primarily by inhibiting the influx of sodium ions through the [[sodium channels]] during the depolarization phase of the cardiac action potential. This action prolongs the [[action potential duration]] and the [[effective refractory period]] of cardiac cells, particularly in the [[atria]] and [[ventricles]]. By doing so, it helps to suppress abnormal [[ectopic pacemaker]] activity and reentrant arrhythmias. | ||
==Clinical Uses== | |||
Procainamide is used in the management of several types of arrhythmias, including: | |||
* [[Atrial fibrillation]] | |||
* [[Atrial flutter]] | |||
* [[Ventricular tachycardia]] | |||
* [[Wolff-Parkinson-White syndrome]] | |||
It is often administered intravenously in acute settings, especially in cases of life-threatening ventricular arrhythmias. | |||
==Side Effects== | |||
Common side effects of procainamide include: | |||
* [[Hypotension]] | |||
* [[Nausea]] | |||
* [[Vomiting]] | |||
* [[Rash]] | |||
Serious side effects can include: | |||
* [[Lupus-like syndrome]] | |||
* [[Agranulocytosis]] | |||
* [[QT interval prolongation]] | |||
==Pharmacokinetics== | |||
Procainamide is metabolized in the liver to [[N-acetylprocainamide]] (NAPA), which also has antiarrhythmic properties. The drug and its metabolite are excreted by the kidneys, and dose adjustments may be necessary in patients with [[renal impairment]]. | |||
==History== | |||
Procainamide was first introduced in the 1950s as an alternative to [[quinidine]], another antiarrhythmic agent. It has since become a staple in the treatment of arrhythmias, particularly in emergency settings. | |||
==Related pages== | |||
* [[Antiarrhythmic agent]] | |||
* [[Cardiac arrhythmia]] | |||
* [[Sodium channel blocker]] | |||
[[Category:Antiarrhythmic agents]] | |||
[[Category:Cardiology]] | |||
Latest revision as of 10:52, 15 February 2025
An article about the antiarrhythmic medication Procainamide
Procainamide[edit]

Procainamide is a medication used to treat a variety of cardiac arrhythmias. It is classified as a Class A antiarrhythmic agent and works by blocking sodium channels in the heart, which helps to stabilize the cardiac membrane and reduce abnormal electrical activity.
Mechanism of Action[edit]
Procainamide works primarily by inhibiting the influx of sodium ions through the sodium channels during the depolarization phase of the cardiac action potential. This action prolongs the action potential duration and the effective refractory period of cardiac cells, particularly in the atria and ventricles. By doing so, it helps to suppress abnormal ectopic pacemaker activity and reentrant arrhythmias.
Clinical Uses[edit]
Procainamide is used in the management of several types of arrhythmias, including:
It is often administered intravenously in acute settings, especially in cases of life-threatening ventricular arrhythmias.
Side Effects[edit]
Common side effects of procainamide include:
Serious side effects can include:
Pharmacokinetics[edit]
Procainamide is metabolized in the liver to N-acetylprocainamide (NAPA), which also has antiarrhythmic properties. The drug and its metabolite are excreted by the kidneys, and dose adjustments may be necessary in patients with renal impairment.
History[edit]
Procainamide was first introduced in the 1950s as an alternative to quinidine, another antiarrhythmic agent. It has since become a staple in the treatment of arrhythmias, particularly in emergency settings.