Ivabradine approved and other uses in clinical practice: a systematic review

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiovascular Pharmacology Pub Date : 2024-07-08 DOI:10.1097/fjc.0000000000001609
Mohsen Hajiqasemi, Mandana Ebrahimzade, Zahra Ghelichkhan, Xena Huang, Demyana Morkos, Douglas Jennings, Azita H Talasaz
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Abstract

Heart rate (HR) stands as a prognostic indicator of cardiovascular disease and a modifiable risk factor in heart failure (HF). Medication intolerance can curtail the application of conventional HR-lowering β-blockers to the optimum target dose. Ivabradine (IVA), a specific negative-chronotropic agent, selectively inhibits If current in pacemaker cells of the sinoatrial node without depressing myocardial contractility or comprising hemodynamics. This review summarized ivabradine’s clinical labeled and off-label uses, and mechanism of action focusing on the clinical outcomes. PubMed was searched up to January 2024 using the main keywords of IVA, coronary artery disease (CAD), HF, postural orthostatic tachycardia syndrome (POTS) and tachyarrhythmia. To comprehensively review IVA’s clinical indications, mechanisms, and therapeutic effects, all studies investigating treatment with IVA in humans were included, comprising different types of studies such as randomized controlled trials (RCTs) and longitudinal prospective observational studies. After screening, 141 studies were included in our review. A large number of reviewed articles were allocated to HFrEF and CAD, suggesting IVA as an alternative to β-blockers in case of contraindications or intolerance. The beneficial effects of IVA as premedication for coronary computed tomography angiography, HR lowering in POTS, and inappropriate sinus tachycardia constituted most studies among off-label uses. Promising results have been reported on the efficacy of IVA in controlling HR, especially in patients with inappropriate sinus tachycardia or POTS. Due to the unique mechanism of action, IVA has the potential to be used more frequently in future clinical practice.
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伊伐布雷定在临床实践中的批准用途和其他用途:系统综述
心率(HR)是心血管疾病的预后指标,也是心力衰竭(HF)的一个可改变的风险因素。药物不耐受会限制传统的降低心率β受体阻滞剂达到最佳目标剂量。伊伐布雷定(IVA)是一种特异性负性节律调节剂,可选择性地抑制中房结起搏细胞中的If电流,而不会抑制心肌收缩力或影响血液动力学。本综述总结了伊伐布雷定的临床标示和非标示用途以及作用机制,重点关注临床结果。以IVA、冠状动脉疾病(CAD)、高血压、体位性正位性心动过速综合征(POTS)和快速性心律失常为关键词,检索了截至2024年1月的PubMed。为了全面回顾IVA的临床适应症、机制和治疗效果,研究人员纳入了所有研究IVA治疗人类的研究,包括随机对照试验(RCT)和纵向前瞻性观察研究等不同类型的研究。经过筛选,141 项研究被纳入我们的综述。大量的综述文章被分配给高房颤和冠状动脉粥样硬化,这表明在有禁忌症或不耐受的情况下,IVA可作为β受体阻滞剂的替代药物。IVA作为冠状动脉计算机断层扫描血管造影术前用药、降低POTS患者的心率和不适当的窦性心动过速的有益效果,是标示外使用中的大多数研究。关于 IVA 控制心率的疗效,特别是对不适当窦性心动过速或 POTS 患者的疗效,已有令人鼓舞的结果报道。由于其独特的作用机制,IVA 有可能在未来的临床实践中得到更广泛的应用。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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