医学
射血分数
心力衰竭
临床终点
速尿
置信区间
临床试验
内科学
回廊的
随机对照试验
达帕格列嗪
利尿剂
心脏病学
血管紧张素转换酶抑制剂
利尿剂
重症监护医学
利钠肽
安慰剂
心肌病
物理疗法
扩张型心肌病
心脏病
危险系数
脑利钠肽
肾功能
优势比
心房颤动
作者
Yasuyuki Shiraishi,Nobuhiro Ikemura,Ikuko Ueda,Takashi Kohno,Shintaro Nakano,Toshikazu D. Tanaka,Yuji Nagatomo,Takenori Ikoma,Tomohiko Ono,Yohei Numasawa,Munehisa Sakamoto,Kei Nishikawa,Makoto Takei,Daihiko Hakuno,Ryo Nakamaru,Masaki Ieda,Mitsuyoshi Urashima,Shun Kohsaka
出处
期刊:Heart
[BMJ]
日期:2026-04-20
卷期号:: heartjnl-2025
被引量:1
标识
DOI:10.1136/heartjnl-2025-327642
摘要
BACKGROUND: Introduction of guideline-directed medical therapy (GDMT) has transformed the care of heart failure (HF) with reduced ejection fraction, establishing four foundational drug classes. Yet, in clinical practice, many patients cannot initiate or maintain all four, and clinicians must pragmatically prioritise agents such as angiotensin receptor-neprilysin inhibitor and sodium-glucose cotransporter-2 inhibitor, whose comparative impacts are still explored. Moreover, the optimal loop diuretic to pair with modern GDMT, which enhances natriuresis, remains uncertain. METHODS: Between January 2022 and February 2024, we conducted a multicentre, open-label, randomised, 2×2 factorial design trial for ambulatory patients with symptomatic HF, elevated natriuretic peptide levels and left ventricular ejection fraction (LVEF) <50%, despite conventional therapies (eg, renin-angiotensin-aldosterone system inhibitors and beta-blockers). The patients were assigned to receive either sacubitril/valsartan or dapagliflozin, and torsemide or furosemide. The primary endpoint was the change in the Kansas City Cardiomyopathy Questionnaire Overall Summary Score (KCCQ-OSS) over 6 months; a prespecified secondary endpoint was a hierarchical clinical outcome. RESULTS: Of 231 randomised patients (median age 73 years; median LVEF 36%; 84.0% New York Heart Association class II), changes in KCCQ-OSS did not differ between sacubitril/valsartan and dapagliflozin (adjusted mean difference 2.53 points; 95% confidence interval (CI) -1.81 to 6.88; p=0.25) or between torsemide and furosemide (0.25 points; 95% CI -4.10 to 4.59; p=0.91). Hierarchical composite outcome analyses also showed no significant differences between sacubitril/valsartan and dapagliflozin (win ratio, 1.15; 95% CI 0.71 to 1.88), or between torsemide and furosemide (win ratio, 1.15; 95% CI 0.70 to 1.85). CONCLUSIONS: This trial found no evidence of benefit of one treatment over another for health status over 6 months. Given the sample size and predefined power, modest differences between treatments cannot be excluded. TRIAL REGISTRATION NUMBER: UMIN000045229.
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