Nawarskas James J, Bowman Brandi N, Anderson Joe R
From the *University of New Mexico College of Pharmacy, Albuquerque, NM; and †University of New Mexico Hospital, Albuquerque, NM.
Cardiol Rev. 2015 Jul-Aug;23(4):201-11. doi: 10.1097/CRD.0000000000000070.
There has been much research linking elevated resting heart rate to cardiovascular morbidity and mortality. Based on these findings, a lower resting heart rate would be of theoretical benefit in patients with cardiovascular disease. From a pathophysiologic perspective, a lower resting heart rate would be of particular benefit in patients with ischemic heart disease and/or heart failure. Although β-blockers and nondihydropyridine calcium channel blockers are effective at lowering heart rate, they have many other pharmacologic effects that may not be desirable in some patients, such as negative inotropy. Ivabradine is a drug designed to lower heart rate without any other demonstrable pharmacologic effects; in other words, a pure heart rate-lowering drug. It functions by blocking the hyperpolarization-activated cyclic nucleotide gated channels (f-channels) specific for the sinoatrial node and disrupting If ion current flow. This effectively prolongs diastolic depolarization and slows firing in the sinoatrial node, which lowers heart rate. The effects of ivabradine are most pronounced at higher heart rates (use-dependence), which is important in minimizing the development of symptomatic bradycardia. Clinical trials have demonstrated ivabradine to be an effective antianginal drug both alone and in combination with β-blocker therapy, although it has not been shown to produce a demonstrable effect on reducing major adverse cardiovascular events. In patients with heart failure, ivabradine has demonstrated many hemodynamic benefits, but its effect on clinical outcomes have been mixed and dependent on baseline heart rate, ie, the drug may be of benefit with higher baseline heart rates, but detrimental with low baseline heart rates. The adverse effects of ivabradine are not uncommon, but are rarely severe and include visual disturbances, bradycardia, and atrial fibrillation. Although ivabradine is a very interesting new agent, its variable benefits in large-scale clinical trials leave its exact place in therapy still somewhat nebulous. Unanswered questions include which patient populations would benefit most from this drug, and which concomitant medications would produce the best clinical outcomes when used with ivabradine.
已有大量研究将静息心率升高与心血管疾病的发病率和死亡率联系起来。基于这些研究结果,较低的静息心率理论上对心血管疾病患者有益。从病理生理学角度来看,较低的静息心率对缺血性心脏病和/或心力衰竭患者尤其有益。虽然β受体阻滞剂和非二氢吡啶类钙通道阻滞剂在降低心率方面有效,但它们还有许多其他药理作用,在某些患者中可能并不理想,如负性肌力作用。伊伐布雷定是一种旨在降低心率而无任何其他明显药理作用的药物;换句话说,是一种单纯的降低心率药物。它通过阻断窦房结特有的超极化激活环核苷酸门控通道(f通道)并扰乱If离子电流来发挥作用。这有效地延长了舒张期去极化并减慢了窦房结的放电频率,从而降低心率。伊伐布雷定的作用在较高心率时最为明显(使用依赖性),这对于将症状性心动过缓的发生降至最低很重要。临床试验表明,伊伐布雷定单独使用或与β受体阻滞剂联合治疗时都是一种有效的抗心绞痛药物,尽管尚未证明它对减少主要不良心血管事件有明显作用。在心力衰竭患者中,伊伐布雷定已显示出许多血流动力学益处,但其对临床结局的影响不一,且取决于基线心率,即该药物在基线心率较高时可能有益,但在基线心率较低时可能有害。伊伐布雷定的不良反应并不少见,但很少严重,包括视觉障碍、心动过缓和心房颤动。虽然伊伐布雷定是一种非常有趣的新药,但其在大规模临床试验中的益处参差不齐,其在治疗中的确切地位仍有些模糊。未解决的问题包括哪些患者群体将从这种药物中获益最大,以及与伊伐布雷定联合使用时哪些伴随药物将产生最佳临床结局。