Böhm Michael, Reil Jan-Christian
Klinik für Innere Medizin III (Kardiologie/Angiologie/Internistische Intensivmedizin), Universitätsklinikum des Saarlandes, Homburg/Saar, Germany.
Drugs. 2007;67 Suppl 2:43-9. doi: 10.2165/00003495-200767002-00006.
High heart rates predict cardiovascular morbidity and mortality in the healthy population, in hypertensive patients, and in those with coronary heart disease (CHD) or heart failure. I(f) channel inhibition with ivabradine is an effective approach to reduce heart rate pharmacologically, with the prospect of preventing complications. The antianginal effects of heart rate-lowering with ivabradine have been shown to be similar to those with beta-adrenoceptor antagonists (beta-blockers) in patients with CHD. The BEAUTIfUL and SHIfT trials will provide evidence on whether I(f) channel inhibition with ivabradine is able to reduce mortality and morbidity in patients with CHD with impaired left ventricular function and heart failure. Future perspectives for additional study are potential roles of ivabradine in the treatment of hypertension and atherosclerosis, and their complications. Further clinical and mechanistic studies to clarify the pathophysiological background are needed to fully define the role of heart rate reduction in the broad spectrum of cardiovascular interventions.
在健康人群、高血压患者以及冠心病(CHD)或心力衰竭患者中,心率升高预示着心血管疾病的发病率和死亡率。使用伊伐布雷定抑制I(f)通道是一种通过药物降低心率的有效方法,有望预防并发症。在冠心病患者中,伊伐布雷定降低心率的抗心绞痛作用已被证明与β肾上腺素能受体拮抗剂(β阻滞剂)相似。BEAUTIfUL试验和SHIfT试验将为使用伊伐布雷定抑制I(f)通道是否能够降低左心室功能受损的冠心病和心力衰竭患者的死亡率和发病率提供证据。伊伐布雷定在高血压和动脉粥样硬化及其并发症治疗中的潜在作用是未来进一步研究的方向。需要进一步的临床和机制研究来阐明病理生理背景,以便全面确定降低心率在广泛的心血管干预措施中的作用。