National and Kapodistrian University of Athens School of Medicine, Athens University Hospital Attikon, Athens, Greece.
University of Cyprus Medical School, Nicosia, Cyprus.
Eur J Heart Fail. 2023 Jul;25(7):970-977. doi: 10.1002/ejhf.2861. Epub 2023 May 8.
Atrial fibrillation/flutter (AF) is common in heart failure (HF) with preserved left ventricular ejection fraction (LVEF) and associated with worse outcomes. Empagliflozin reduces cardiovascular death or HF hospitalizations and slows estimated glomerular filtration rate (eGFR) decline in patients with HF and LVEF >40%. We aimed to assess the efficacy and safety of empagliflozin in improving outcomes in patients with HF and LVEF >40% with and without AF.
In this pre-defined secondary analysis of EMPEROR-Preserved, we compared the effects of empagliflozin versus placebo on the primary and secondary endpoints and safety outcomes, stratified by baseline AF, defined as AF reported in any electrocardiogram before empagliflozin initiation or in medical history. Among 5988 patients randomized, 3135 (52%) had baseline AF; these patients were older, with worse functional class, more previous HF hospitalizations and higher natriuretic peptides compared to those without AF (all p < 0.001). After a median of 26 months, empagliflozin reduced cardiovascular death or HF hospitalization compared to placebo to a similar extent in patients with and without AF (hazard ratio [HR] 0.78 [95% confidence interval 0.66-0.93] vs. 0.78 [0.64-0.95], interaction p = 0.96). Empagliflozin also reduced total HF hospitalizations (HR 0.73 [0.57-0.94] vs. 0.72 [0.54-0.95], interaction p = 0.94) and annual eGFR decline (difference = 1.368 vs. 1.372 ml/min/1.73 m /year, interaction p = 0.99) consistently in patients with and without AF. There was no increase in serious adverse events with empagliflozin versus placebo in patients with and without AF.
In patients with HF and ejection fraction >40%, empagliflozin reduced the risk of serious HF events and slowed the eGFR decline regardless of baseline AF.
心房颤动/扑动(AF)在射血分数保留的心力衰竭(HF)中很常见,与预后较差相关。恩格列净可降低射血分数>40%的心力衰竭患者的心血管死亡或心力衰竭住院风险,并减缓估算肾小球滤过率(eGFR)的下降速度。我们旨在评估恩格列净在改善射血分数>40%的心力衰竭伴或不伴 AF 患者结局方面的疗效和安全性。
在 EMPEROR-Preserved 的预先设定的二次分析中,我们比较了恩格列净与安慰剂对主要终点和次要终点以及安全性结局的影响,根据基线 AF 进行分层,定义为恩格列净起始前任何心电图或既往病史中报告的 AF。在 5988 例随机患者中,3135 例(52%)基线时存在 AF;与无 AF 患者相比,这些患者年龄更大,功能状态更差,HF 住院次数更多,利钠肽水平更高(均 P<0.001)。中位随访 26 个月后,与安慰剂相比,恩格列净降低了心血管死亡或 HF 住院的风险,在有和无 AF 的患者中效果相似(风险比 [HR] 0.78 [95%置信区间 0.66-0.93] 与 0.78 [0.64-0.95],交互作用 P=0.96)。恩格列净还降低了总 HF 住院(HR 0.73 [0.57-0.94] 与 0.72 [0.54-0.95],交互作用 P=0.94)和 eGFR 年下降率(差值=1.368 与 1.372 ml/min/1.73 m /year,交互作用 P=0.99),在有和无 AF 的患者中均一致。在有和无 AF 的患者中,与安慰剂相比,恩格列净并未增加严重不良事件。
在射血分数>40%的心力衰竭患者中,无论基线时是否存在 AF,恩格列净均可降低严重 HF 事件的风险并减缓 eGFR 的下降速度。