Suzuki Sho, Motoki Hirohiko, Kanzaki Yusuke, Maruyama Takuya, Hashizume Naoto, Kozuka Ayako, Yahikozawa Kumiko, Kuwahara Koichiro
Department of Cardiovascular Medicine, Minaminagano Medical Center, Shinonoi General Hospital Nagano Japan.
Department of Cardiovascular Medicine, Shinshu University School of Medicine Matsumoto Japan.
Circ Rep. 2019 Feb 27;1(3):137-141. doi: 10.1253/circrep.CR-19-0012.
Clinical evidence of the effects of loop diuretics in patients with heart failure with preserved ejection fraction (HFpEF) is lacking. Thus, we compared the impact of azosemide and furosemide, long- and short-acting loop diuretics, in patients with HFpEF. A prospective multicenter cohort study was conducted between July 2014 and July 2018. We enrolled 301 consecutive patients with HFpEF (median age, 84 years; IQR, 79-88 years; 54.8% female). Azosemide was used in 127 patients (azosemide group), and furosemide in 174 (furosemide group). We constructed Cox models for a composite of cardiac death, non-fatal myocardial infarction, non-fatal stroke, and HF hospitalization (primary endpoints). During a median follow-up of 317 days (IQR, 174-734 days), the primary endpoint occurred in 112 patients (37.2%). On multivariate inverse probability of treatment weighted (IPTW) Cox modeling, the azosemide group had a significantly lower incidence of adverse events than the furosemide group (hazard ratio [HR], 0.46; 95% confidence interval [CI]: 0.27-0.80; P=0.006). Furthermore, on multivariate IPTW Cox modeling for the secondary endpoints, cardiac death (HR, 0.38; 95% CI: 0.17-0.89; P=0.025) and unplanned hospitalization for decompensated HF (HR, 0.50; 95% CI: 0.28-0.89; P=0.018) were also reduced in the azosemide group. Azosemide significantly reduced the risk of adverse events compared with furosemide in HFpEF patients.
关于袢利尿剂对射血分数保留的心力衰竭(HFpEF)患者疗效的临床证据尚缺乏。因此,我们比较了长效袢利尿剂阿佐塞米和短效袢利尿剂呋塞米对HFpEF患者的影响。2014年7月至2018年7月进行了一项前瞻性多中心队列研究。我们纳入了301例连续性HFpEF患者(中位年龄84岁;四分位间距,79 - 88岁;女性占54.8%)。127例患者使用阿佐塞米(阿佐塞米组),174例患者使用呋塞米(呋塞米组)。我们构建了Cox模型,以评估心源性死亡、非致死性心肌梗死、非致死性卒中和心力衰竭住院的复合终点(主要终点)。在中位随访317天(四分位间距,174 - 734天)期间,112例患者(37.2%)发生了主要终点事件。在多变量治疗逆概率加权(IPTW)Cox模型中,阿佐塞米组不良事件发生率显著低于呋塞米组(风险比[HR],0.46;95%置信区间[CI]:0.27 - 0.80;P = 0.006)。此外,在多变量IPTW Cox模型评估次要终点时,阿佐塞米组的心源性死亡(HR,0.38;95% CI:0.17 - 0.89;P = 0.025)和因失代偿性心力衰竭的非计划住院(HR,0.50;95% CI:0.28 - 0.89;P = 0.018)也有所降低。与呋塞米相比,阿佐塞米显著降低了HFpEF患者不良事件的风险。