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Nebivolol: a third-generation beta-blocker for hypertension
1Massachusetts College of Pharmacy and Health Sciences, Boston, Massachusetts 02115, USA. judy.cheng@mcphs.edu
Insights
Nebivolol effectively lowers blood pressure in hypertension and shows promise for reducing mortality in heart failure patients. This beta-blocker is well-tolerated, offering potential advantages for specific patient groups.
Area of Science:
- Pharmacology and Therapeutics
- Cardiovascular Medicine
Background:
- Nebivolol is a third-generation beta(1)-selective beta-blocker.
- It is approved for hypertension treatment.
Purpose of the Study:
- Review nebivolol's clinical pharmacology.
- Evaluate its efficacy and safety in hypertension and heart failure.
Main Methods:
- Searched MEDLINE and Current Contents (1966-2008).
- Included human clinical trials.
- Reviewed conference abstracts (2006-2008).
Main Results:
- Nebivolol demonstrated comparable blood pressure lowering to other antihypertensives.
- A study indicated a 14% reduction in mortality/hospitalization for heart failure.
- Common side effects included fatigue and headache; it was generally well-tolerated.
Conclusions:
- Nebivolol is effective and well-tolerated for hypertension.
- Preliminary data suggest potential mortality benefits in heart failure.
Background:
Nebivolol is a third-generation beta(1)-selective beta-blocker that is approved for the treatment of hypertension.
Objective:
This article reviews the clinical pharmacology of nebivolol and its efficacy and safety profile in clinical studies of hypertension (the US Food and Drug Administration-approved indication) and heart failure (off-label use).
Methods:
Pertinent articles were identified through searches of MEDLINE and Current Contents from 1966 through December 15, 2008, using the terms nebivolol, drug interaction, pharmacokinetics, and pharmacology. The reference lists of the identified publications were reviewed for additional references. Abstracts presented at meetings of the American Heart Association and the American Society of Hypertension from 2006 through 2008 were also reviewed. All human clinical trials were included, regardless of design.
Results:
Twelve published clinical trials were identified that evaluated the use of nebivolol in the management of hypertension; 1 was placebo controlled, 1 was placebo and active controlled, and 10 involved direct comparisons with other antihypertensive agents. Nebivolol was reported to be as effective in lowering blood pressure (BP) as other beta-blockers (atenolol and bisoprolol), angiotensin-converting enzyme inhibitors (lisinopril and enalapril), the angiotensin-receptor blocker telmisartan, and calcium channel blockers (nifedipine and amlodipine). No published studies were identified that evaluated the effect of nebivolol on long-term cardiovascular outcomes. In data from a study in heart failure, nebivolol was associated with a 14% reduction in all-cause mortality and cardiovascular hospitalization at 12 months (P < 0.05). In comparative clinical studies, nebivolol appeared to be well tolerated relative to the other antihypertensive agents studied. The most commonly reported adverse events with nebivolol were fatigue (4%-79%), headache (2%-24%), paresthesia (7%-13%), bradycardia (6%-11%), rhinitis (1%-7%), and dizziness (2%-5%). Because of differences in its pharmacologic properties, nebivolol may have potential advantages in patients who are unable to tolerate traditional beta-blockers (eg, patients with asthma or chronic obstructive pulmonary disease, or men who experience erectile dysfunction while taking antihypertensive therapy).
Conclusions:
Nebivolol is a cardioselective beta-blocker that has been reported to be efficacious and well tolerated for achieving BP control in patients with hypertension. Preliminary evidence suggests a potential for reduced mortality in patients with heart failure.
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