Sule Sachin S, Frishman William
Department of Medicine, New York Medical College/Westchester Medical Center, Valhalla, New York, USA.
Cardiol Rev. 2006 Sep-Oct;14(5):259-64. doi: 10.1097/01.crd.0000223651.03023.8e.
Nebivolol is a beta-blocker under U.S. Food and Drug Administration review for the treatment of hypertension. The unique pharmacologic properties of nebivolol include high specificity for the beta-1 receptor and a nitric oxide-mediated vasodilatory effect. The agent provides significant blood pressure reduction from baseline values as compared with placebo. Clinical trials have demonstrated that nebivolol reduces blood pressure similarly to atenolol, bisoprolol, amlodipine, nifedipine, lisinopril, and hydrochlorothiazide. The tolerability of nebivolol is similar to or better than that of these agents. In elderly patients (> or = 70 years of age) with clinically stable congestive heart failure, the addition of nebivolol to the treatment regimen improved the time to all-cause mortality and cardiovascular hospital admissions over that of placebo. If approved, nebivolol would likely be a viable alternative therapy for hypertension and heart failure; however, additional studies are needed in patients having coronary artery disease.
奈必洛尔是一种正在接受美国食品药品监督管理局审查用于治疗高血压的β受体阻滞剂。奈必洛尔独特的药理特性包括对β-1受体的高特异性以及一氧化氮介导的血管舒张作用。与安慰剂相比,该药物可使血压从基线值显著降低。临床试验表明,奈必洛尔降低血压的效果与阿替洛尔、比索洛尔、氨氯地平、硝苯地平、赖诺普利和氢氯噻嗪相似。奈必洛尔的耐受性与这些药物相似或更好。在临床病情稳定的老年(≥70岁)充血性心力衰竭患者中,在治疗方案中添加奈必洛尔比安慰剂能延长至全因死亡率和心血管疾病住院的时间。如果获批,奈必洛尔可能成为治疗高血压和心力衰竭的一种可行替代疗法;然而,在患有冠状动脉疾病的患者中还需要进行更多研究。