Abbo Aharon Ronnie, Gruber Amit, Volis Ina, Aronson Doron, Girerd Nicolas, Lund Kristensen Søren, Zukermann Robert, Alberkant Natalia, Sitnitsky Elena, Kruger Anton, Khasis Polina, Bravo Evgeny, Elad Boaz, Helmer Levin Ludmila, Caspi Oren
Heart Failure Unit, Department of Cardiology and the Rambam Health Care Campus, Haifa, Israel.
Heart Failure Unit, Department of Cardiology and the Rambam Health Care Campus, Haifa, Israel; Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.
JACC Heart Fail. 2024 Aug;12(8):1396-1405. doi: 10.1016/j.jchf.2024.04.014. Epub 2024 May 11.
Limited evidence exists regarding efficacy and safety of diuretic regimens in ambulatory, congestion-refractory, chronic heart failure (CHF) patients.
The authors sought to compare the potency and safety of commonly used diuretic regimens in CHF patients.
A prospective, randomized, open-label, crossover study conducted in NYHA functional class II to IV CHF patients, treated in an ambulatory day-care unit. Each patient received 3 different diuretic regimens: intravenous (IV) furosemide 250 mg; IV furosemide 250 mg plus oral metolazone 5 mg; and IV furosemide 250 mg plus IV acetazolamide 500 mg. Treatments were administered once a week, in 1 of 6 randomized sequences. The primary endpoint was total sodium excretion, and the secondary was total urinary volume excreted, both measured for 6 hours post-treatment initiation.
A total of 42 patients were recruited. Administration of furosemide plus metolazone resulted in the highest weight of sodium excreted, 4,691 mg (95% CI: 4,153-5,229 mg) compared with furosemide alone, 3,835 mg (95% CI: 3,279-4,392 mg; P = 0.015) and to furosemide plus acetazolamide 3,584 mg (95% CI: 3,020-4,148 mg; P = 0.001). Furosemide plus metolazone resulted in 1.84 L of urine (95% CI: 1.63-2.05 L), compared with 1.58 L (95% CI: 1.37-1.8); P = 0.039 collected following administration of furosemide plus acetazolamide and 1.71 L (95% CI: 1.49-1.93 L) following furosemide alone. The incidence of worsening renal function was significantly higher when adding metolazone (39%) to furosemide compared with furosemide alone (16%) and to furosemide plus acetazolamide (2.6%) (P < 0.001).
In ambulatory CHF patients, furosemide plus metolazone resulted in a significantly higher natriuresis compared with IV furosemide alone or furosemide plus acetazolamide.
关于利尿剂方案在非卧床、难治性充血性慢性心力衰竭(CHF)患者中的疗效和安全性,现有证据有限。
作者试图比较CHF患者常用利尿剂方案的效力和安全性。
在一家门诊日间护理单元对纽约心脏协会(NYHA)心功能II至IV级的CHF患者进行了一项前瞻性、随机、开放标签、交叉研究。每位患者接受3种不同的利尿剂方案:静脉注射(IV)250毫克呋塞米;静脉注射250毫克呋塞米加口服5毫克美托拉宗;静脉注射250毫克呋塞米加静脉注射500毫克乙酰唑胺。治疗每周进行一次,采用6种随机序列中的1种。主要终点是总钠排泄量,次要终点是总尿量排泄量,均在治疗开始后6小时测量。
共招募了42名患者。与单独使用呋塞米(3835毫克,95%可信区间:3279 - 4392毫克;P = 0.015)和呋塞米加乙酰唑胺(3584毫克,95%可信区间:3020 - 4148毫克;P = 0.001)相比,呋塞米加美托拉宗导致排泄的钠重量最高,为4691毫克(95%可信区间:4153 - 5229毫克)。呋塞米加美托拉宗导致尿量为1.84升(95%可信区间:1.63 - 2.05升),相比之下,呋塞米加乙酰唑胺给药后收集的尿量为1.58升(95%可信区间:1.37 - 1.8升;P = 0.039),单独使用呋塞米后尿量为1.71升(95%可信区间:1.49 - 1.93升)。与单独使用呋塞米(16%)和呋塞米加乙酰唑胺(2.6%)相比,呋塞米加美托拉宗时肾功能恶化的发生率显著更高(39%)(P < 0.001)。
在非卧床CHF患者中,与单独静脉注射呋塞米或呋塞米加乙酰唑胺相比,呋塞米加美托拉宗导致的利钠作用显著更高。