Weeda Erin R, Nguyen Elaine, White C Michael
University of Connecticut/Hartford Hospital, Storrs, CT, USA.
University of Connecticut/Hartford Hospital, Storrs, CT, USA
Ann Pharmacother. 2016 Jun;50(6):475-85. doi: 10.1177/1060028016631571. Epub 2016 Feb 25.
To review the role of heart rate in myocardial ischemia and heart failure with reduced ejection fraction (HFrEF) as well as ivabradine's pharmacology and pharmacokinetics, clinical trials, and place in therapy.
We conducted MEDLINE searches from 1980 to October 2015 using the terms heart failure, HFrEF, angina, f-channel inhibitor, and ivabradine, with forward and backward citation tracking.
English-language trials assessing ivabradine were obtained. Studies and narrative reviews of the topic areas were incorporated if they provided relevant data to inform the practicing clinician.
In the SIGNIFY (Study Assessing the Morbidity-Mortality Benefits of the If Inhibitor Ivabradine in Patients with Coronary Artery Disease) trial, there was no difference in the primary composite end point of cardiovascular (CV) mortality or nonfatal myocardial infarction with ivabradine use in patients with stable coronary artery disease (CAD) versus placebo (P = 0.20). In the subgroup with Canadian Cardiovascular Society angina class ≥II, there was an 18% increase in the primary end point with ivabradine versus placebo (P = 0.02). In HFrEF patients, ivabradine reduced CV mortality or heart failure hospitalizations versus placebo, as seen in the SHIFT (Systolic Heart failure treatment with the If inhibitor ivabradine Trial; P < 0.05).
The SIGNIFY trial negated much of the enthusiasm for using ivabradine in CAD. Ivabradine is a promising therapy in HFrEF based on the results of the SHIFT, but it is an adjunctive therapy, not a substitute for drugs with proven mortality benefits.
综述心率在心肌缺血和射血分数降低的心力衰竭(HFrEF)中的作用,以及伊伐布雷定的药理作用、药代动力学、临床试验和治疗地位。
我们使用“心力衰竭”“HFrEF”“心绞痛”“f通道抑制剂”和“伊伐布雷定”等检索词,对1980年至2015年10月期间的MEDLINE数据库进行了检索,并进行了前后文引用追踪。
获取了评估伊伐布雷定的英文试验。如果研究和叙述性综述提供了相关数据以指导临床医生实践,则纳入这些研究。
在SIGNIFY(评估伊伐布雷定对冠心病患者发病率-死亡率益处的研究)试验中,在稳定型冠心病(CAD)患者中使用伊伐布雷定与使用安慰剂相比,心血管(CV)死亡率或非致命性心肌梗死的主要复合终点没有差异(P = 0.20)。在加拿大心血管学会心绞痛分级≥II级的亚组中,与安慰剂相比,伊伐布雷定组的主要终点增加了18%(P = 0.02)。在HFrEF患者中,与安慰剂相比,伊伐布雷定降低了CV死亡率或心力衰竭住院率,如SHIFT(伊伐布雷定治疗收缩性心力衰竭试验)中所见(P < 0.05)。
SIGNIFY试验削弱了在CAD中使用伊伐布雷定的大部分热情。基于SHIFT试验的结果,伊伐布雷定在HFrEF中是一种有前景的治疗方法,但它是一种辅助治疗,不能替代已证实有死亡率益处的药物。