Giavarini Alessandra, de Silva Ranil
NIHR Biomedical Research Unit, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
ICMS, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Cardiovasc Drugs Ther. 2016 Aug;30(4):407-417. doi: 10.1007/s10557-016-6678-x.
Stable angina pectoris affects 2-4 % of the population in Western countries and entails an annual risk of death and nonfatal myocardial infarction of 1-2 % and 3 %, respectively. Heart rate (HR) is linearly related to myocardial oxygen consumption and coronary blood flow, both at rest and during stress. HR reduction is a key target for the prevention of ischemia/angina and is an important mechanism of action of drugs which are recommended as first line therapy for the treatment of angina in clinical guidelines. However, many patients are often unable to tolerate the doses of beta blocker or non-dihydropyridine calcium antagonists required to achieve the desired symptom control. The selective pacemaker current inhibitor ivabradine was developed as a drug for the management of patients with angina pectoris, through its ability to reduce HR specifically. The available data suggest that ivabradine is a well-tolerated and effective anti-anginal agent and it is recommended as a second-line agent for relief of angina in guidelines. However, recent clinical trials of ivabradine have failed to show prognostic benefit and have raised potential concerns about safety. This article will review the available evidence base for the current role of ivabradine in the management of patients with symptomatic angina pectoris in the context of stable coronary artery disease.
稳定型心绞痛在西方国家影响2%-4%的人口,每年发生死亡和非致死性心肌梗死的风险分别为1%-2%和3%。心率(HR)无论在静息状态还是应激状态下,均与心肌耗氧量和冠状动脉血流量呈线性相关。降低心率是预防缺血/心绞痛的关键目标,也是临床指南中推荐作为心绞痛一线治疗药物的重要作用机制。然而,许多患者往往无法耐受为实现预期症状控制所需的β受体阻滞剂或非二氢吡啶类钙拮抗剂的剂量。选择性起搏电流抑制剂伊伐布雷定作为一种用于治疗心绞痛患者的药物而被研发,因其具有特异性降低心率的能力。现有数据表明,伊伐布雷定是一种耐受性良好且有效的抗心绞痛药物,在指南中被推荐作为缓解心绞痛的二线药物。然而,伊伐布雷定近期的临床试验未能显示出预后获益,且引发了对安全性的潜在担忧。本文将在稳定型冠状动脉疾病的背景下,综述伊伐布雷定在有症状心绞痛患者管理中当前作用的现有证据基础。