射血分数
达帕格列嗪
心力衰竭
医学
肾功能
内科学
心脏病学
糖尿病
血管紧张素转换酶抑制剂
人口
血管紧张素受体
血管紧张素转换酶
血管紧张素II
2型糖尿病
内分泌学
血压
环境卫生
作者
Felipe Augusto,Patrícia Paiva,Camilo Félix,Inês Jordão,M. Costa,Patrícia Dias,Francisco Parente,Lino Gonçalves,Francisco Pereira Machado,Natália António
摘要
Abstract Dapagliflozin has demonstrated multiple benefits in clinical trials for heart failure with reduced ejection fraction (HFrEF), but older patients with multiple comorbidities were often excluded. This study aimed to evaluate the effectiveness and safety of dapagliflozin in a real‐world population of HFrEF patients. This retrospective study included HFrEF patients from a tertiary hospital, who initiated dapagliflozin between January 202 and December 2022. The mean follow‐up was 15.3 ± 8.3 months. Each patient served as their own control to compare left ventricular ejection fraction (LVEF), laboratory parameters, and time‐dependent events, such as heart failure (HF) readmissions. A total of 155 HFrEF patients (mean age 68.5 ± 14.5 years; 75.5% male) were included. Of these, 47.1% had non‐ischemic heart disease, 49.0% had type 2 diabetes mellitus, and most were on beta‐blockers, loop diuretics and angiotensin‐converting enzyme inhibitor, angiotensin II receptor blocker, or angiotensin receptor neprilysin inhibitor. LVEF improved from 29.2% to 34.3% ( P < .001), with significant reductions in body weight and heart rate ( P < .001). HF‐related emergency room visits decreased (0.68 ± 1.06 to 0.58 ± 0.96; P = .329). Renal function declined, with glomerular filtration rate decreasing from 67.6 ± 25.2 to 55.2 ± 30.8 mL/min/1.73 m 2 ( P < .001), particularly in older patients (HR 1.033; 95% CI: 1.004–1.063) and those with higher baseline heart rate (HR 1.028; 95% CI: 1.011–1.045). Severe adverse drug reactions occurred in 3.9% of patients, with hypotension (12.9%) being the most common. In conclusion, dapagliflozin demonstrated a favorable safety profile and significant hemodynamic benefits, improving LVEF and stabilizing HF progression in a real‐world HFrEF population.
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