Department of Cardiology, Lady Reading Hospital, Peshawar, Pakistan.
Department of Medicine, Services Hospital, Lahore, Pakistan.
Clin Cardiol. 2024 Nov;47(11):e70033. doi: 10.1002/clc.70033.
This prospective, randomized trial aimed to compare the efficacy and safety of different intravenous diuretic regimens in acute decompensated heart failure (ADHF) patients.
ADHF patients were enrolled and randomized into three groups: continuous intravenous furosemide infusion (cIV), bolus furosemide injection (bI), and furosemide plus hypertonic saline solution (HSS). Clinical outcomes were assessed over 48 h.
In a study involving 1276 patients admitted for ADHF, three therapeutic regimens (T × 1, T × 2, and T × 3) were compared. T × 1 administered an 80 mg furosemide intravenous bolus infusion twice daily to 479 patients, while T × 2 involved a continuous 16-h infusion of 160 mg furosemide daily to 420 patients. T × 3 treated 377 patients with 160 mg furosemide combined with 150 mL of HSS containing 1.95% NaCl over 30 min. Yet, overall changes in renal markers such as BUN, Na, K, and serum creatinine did not differ significantly. Analysis of prespecified study endpoints revealed notable variations in hospitalization length among the treatment arms. T × 1 demonstrated a significantly shorter hospital stay (3.7 days) compared to T × 2 (6.6 days) and T × 3 (7.9 days). Conversely, alterations in serum creatinine at 48 h, overall changes in serum creatinine, body weight loss, and serum potassium levels did not significantly differ among the treatment groups.
While intravenous bolus of furosemide showed potential benefits in reducing hospitalization duration, limitations such as a small sample size and short-term observation emphasize the need for larger studies to validate these outcomes further.
本前瞻性、随机试验旨在比较不同静脉利尿剂方案在急性失代偿性心力衰竭(ADHF)患者中的疗效和安全性。
纳入 ADHF 患者并随机分为三组:持续静脉呋塞米输注(cIV)、呋塞米推注(bI)和呋塞米加高渗盐水(HSS)。在 48 小时内评估临床结局。
在一项纳入 1276 例 ADHF 住院患者的研究中,比较了三种治疗方案(T×1、T×2 和 T×3)。T×1 组给 479 例患者每日两次静脉注射 80mg 呋塞米,T×2 组给 420 例患者每日持续输注 160mg 呋塞米 16 小时,T×3 组给 377 例患者用 160mg 呋塞米加 150ml 含 1.95%NaCl 的 HSS 在 30 分钟内输注。然而,BUN、Na、K 和血清肌酐等肾脏标志物的总体变化无显著差异。对预设研究终点的分析显示,治疗组之间的住院时间存在显著差异。T×1 组的住院时间明显短于 T×2 组(6.6 天)和 T×3 组(7.9 天)。相反,48 小时时血清肌酐的变化、血清肌酐的总体变化、体重减轻和血清钾水平在治疗组之间无显著差异。
虽然静脉推注呋塞米在缩短住院时间方面显示出潜在的益处,但存在样本量小和短期观察的局限性,强调需要更大的研究来进一步验证这些结果。