Alijanzadeh Dorsa, Moghim Shahrzad, Zarand Paniz, Akbarzadeh Mohammad Ali, Zarinfar Yasaman, Khaheshi Isa
Student Research Committee, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Cardiovasc Drugs Ther. 2024 Dec 10. doi: 10.1007/s10557-024-07652-3.
Ivabradine has been identified as a funny current (If) inhibitor in the sinoatrial node (SAN) and is considered an advocated therapeutic agent in chronic heart failure and stable angina. This therapeutic agent has shown positive benefits in maintaining a reduction in heart rate while sustaining hemodynamic stability. Its clinical application is still evolving and the mechanism of action is becoming clearer daily. The use of this agent to manage atrial fibrillation (AF) has recently been brought under discussion. This study summarizes the mechanism of action of ivabradine and current evidence about the risk of new-onset AF and rate-lowering potential as a therapeutic option in patients suffering from AF.
This review synthesizes findings from preclinical studies, case reports, and clinical trials that assess ivabradine's efficacy in controlling heart rate and its association with new-onset AF.
Studies have shown that this medication may be beneficial in ventricular rate reduction in patients intolerant of first-line AF therapeutic options, including non-dihydropyridine calcium channel blockers and β-blockers. However, it is important to state that ivabradine-treated patients with cardiovascular diseases demonstrated an increased risk for new-onset AF compared with those patients who did not receive it.
While ivabradine demonstrates promise as a therapeutic option for rate control in patients with AF, its use is accompanied by a notable risk of new-onset AF. Further studies should focus on optimal dosing strategies and long-term outcomes of ivabradine treatment in AF management.
伊伐布雷定已被确定为窦房结(SAN)中一种超极化激活的环核苷酸门控阳离子通道电流(If)抑制剂,被认为是慢性心力衰竭和稳定型心绞痛的一种推荐治疗药物。这种治疗药物在维持心率降低的同时保持血流动力学稳定性方面已显示出积极益处。其临床应用仍在不断发展,作用机制也日益清晰。最近,使用这种药物治疗心房颤动(AF)已成为讨论的话题。本研究总结了伊伐布雷定的作用机制以及关于新发房颤风险和作为房颤患者治疗选择的心率降低潜力的现有证据。
本综述综合了临床前研究、病例报告和临床试验的结果,这些研究评估了伊伐布雷定在控制心率方面的疗效及其与新发房颤的关联。
研究表明,这种药物可能对不耐受包括非二氢吡啶类钙通道阻滞剂和β受体阻滞剂在内的一线房颤治疗选择的患者降低心室率有益。然而,必须指出的是,与未接受伊伐布雷定治疗的患者相比,接受伊伐布雷定治疗的心血管疾病患者发生新发房颤的风险增加。
虽然伊伐布雷定作为房颤患者心率控制的治疗选择显示出前景,但其使用伴随着新发房颤的显著风险。进一步的研究应集中在伊伐布雷定治疗房颤的最佳给药策略和长期结果上。