Health Conditions

Calcium Channel Blockers: List, Drug Study and Nursing Interventions

GENERAL DESCRIPTION

Calcium Channel Blockers are used to block voltage-dependent Ca2+ channel are called Calcium channel blockers. The main action of this drug is vasodilation. These drugs are used to treat many cardio vascular disease including hypertension, arrhythmia and angina pectoris. Dihyropyridines are more potent vasodilators than Verapamil, which is more potent than diltiazem.

TYPES OF CALCIUM CHANNEL BLOCKERS

There are three types of Calcium channel blockers available so far. Although these drugs are commonly grouped in Calcium channel blockers, but they have different in pharmacological characters, drug interactions and toxicities.

 Class of Calcium channel blockers  Generic Name  Brand Name
Dihydropyridine Nifedipine Adalat CC, Procardia, Nifediac CC
Amlodipine Norvasc, Acord, Amlibon
Nimodipine Nimotop, Nymalize
Nicardipine Cardene
Benzothiazepine Diltiazem Cartia, Dilacor, Tiazac, Cardizem
Phenylalkylamine Verapamil Calan, Isoptin, Verelan

 

MECHANISM OF ACTION

The mechanism of action of calcium channel blockers in hypertension is inhibition of calcium influx into arterial smooth muscles.

The L-type calcium channel is the dominant type in cardiac and smooth muscles. In smooth muscles, calcium influx from these calcium channels is responsible for normal resting tone and contractility. When these channels blocked by calcium channel blockers then inhibit the calcium influx resulted in relaxation of vascular, bronchiolar, gastrointestinal and urinary smooth muscles. Calcium channel blockers also reduce the tonicity of coronary arteries which is befitted for the patient of Variant angina.

Cardiac muscles are highly dependent upon calcium influx for normal function. Impulse generation in Atrioventricular node (AV node) and sinoatrial node (SA node) is highly dependent on calcium dependent, action potential. Firstly, Calcium channel blocker reduce the impulse generation in atrioventricular node and sinoatrial node. Secondly, calcium channel blockers reduce the excitation-contraction coupling in all cardiac cells and reduce cardiac contractility. This reduction in cardiac mechanical function by calcium channel blockers reduce the oxygen requirement in patients with angina.

PHARMACOKINETICS

The calcium channel blockers have complete absorption after oral administration. These drugs have 70-98% bioavailability. Some drugs undergo the first-pass metabolism which reduce their bioavailability. The duration of action of calcium channel blockers is 30-60 min of an oral dose except amlodipine. Most of the calcium channel blockers metabolized by an enzyme CYP3A4.

INDICATIONS

CONTRAINDICATIONS

SIDE EFFECTS & ADVERSE EFFECTS

DRUG INTERACTION

NURSING INTERVENTION

PATIENT EDUCATION

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