Shen Zhidan, Zhou Zhe, Fang Hongge, Zhang Yuehui, Wang Lijun
The Second School of Clinical Medicine, Southern Medical University, Guangzhou 510280, Guangdong, China.
Department of Critical Care Medicine, the Affiliated Bao'an Hospital of Shenzhen, Southern Medical University, Shenzhen 518101, Guangdong, China. Corresponding author: Wang Lijun, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2020 Nov;32(11):1393-1398. doi: 10.3760/cma.j.cn121430-20200817-00629.
Tachycardia is an independent risk factor for mortality of patients with sepsis and multiple organ dysfunction syndrome (MODS), and has attracted extensive attention in recent years. Ivabradine, a specific blocker of hyperpolarization-activated cyclic nucleotide-gated (HCN) channel in sinoatrial node, is capable of inducing heart rate reduction (HRR) via binding specific sites of the channel and promotes ventricular filling because of prolongation of the diastolic period. Ivabradine has no negative effect on inotropic contractility, conductivity, and systemic vascular resistance. While Ivabradine has recently shown its beneficial effects in diverse randomized controlled trials on heart failure, this medicine may be a potential option to treat tachycardia in patients with sepsis and septic cardiomyopathy (SCM). Preliminary findings demonstrate that Ivabradine can remarkably lower heart rate and improve hemodynamic stability in patients with sepsis. In addition, Ivabradine has been reported to ameliorate microcirculation perfusion and suppress the inflammatory response. This review discusses the effects of Ivabradine on heart rate control in patients with sepsis and SCM.
心动过速是脓毒症和多器官功能障碍综合征(MODS)患者死亡的独立危险因素,近年来受到广泛关注。伊伐布雷定是一种特异性窦房结超极化激活环核苷酸门控(HCN)通道阻滞剂,能够通过结合该通道的特定位点来降低心率(HRR),并由于舒张期延长而促进心室充盈。伊伐布雷定对心肌收缩力、传导性和全身血管阻力没有负面影响。虽然伊伐布雷定最近在各种心力衰竭随机对照试验中显示出有益效果,但这种药物可能是治疗脓毒症和脓毒性心肌病(SCM)患者心动过速的一个潜在选择。初步研究结果表明,伊伐布雷定可显著降低脓毒症患者的心率并改善血流动力学稳定性。此外,据报道伊伐布雷定可改善微循环灌注并抑制炎症反应。本综述讨论了伊伐布雷定对脓毒症和SCM患者心率控制的影响。