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HERO ID
6779131
Reference Type
Journal Article
Subtype
Review
Title
Calcium Channel Blockers
Author(s)
Elliott, WJ; Ram, CVS
Year
2011
Is Peer Reviewed?
Yes
Journal
Journal of Clinical Hypertension
ISSN:
1524-6175
EISSN:
1751-7176
Volume
13
Issue
9
Page Numbers
687-689
Language
English
PMID
21896151
DOI
10.1111/j.1751-7176.2011.00513.x
Web of Science Id
WOS:000294596300010
Abstract
KEY POINTS AND PRACTICAL RECOMMENDATIONS: • Calcium channel blockers, which dilate arteries by reducing calcium flux into cells, effectively lower blood pressure, especially in combination with other drugs, and some formulations of agents of this class are approved for treating angina or cardiac dysrhythmias. • Calcium channel blockers reduce blood pressure across all patient groups, regardless of sex, race/ethnicity, age, and dietary sodium intake. • Nondihydropyridine calcium channel blockers are more negatively chronotropic and inotropic than the dihydropyridine subclass, which is important for patients with cardiac dysrhythmias or who need β-blockers. • Extensive experience in comparative randomized trials indicates that an initial calcium antagonist can prevent all major types of cardiovascular disease, except heart failure (for which a diuretic is superior). Initial dihydropyridine calcium channel blockers have not reduced the rate of progression of renal disease as well as inhibitors of the renin-angiotensin system, although members of the nondihydropyridine subclass can reduce albuminuria. • High doses of dihydropyridine calcium channel blockers often cause edema, headache, flushing and tachycardia; high doses of verapamil can cause constipation. Diltiazem and verapamil have important drug interaction with digoxin and cyclosporine, among others.
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