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. 2025 Jul 31:16:1643077.
doi: 10.3389/fphar.2025.1643077. eCollection 2025.

Comparative analysis of furosemide and torsemide efficacy in 24 hours of acute heart failure admission

Affiliations

Comparative analysis of furosemide and torsemide efficacy in 24 hours of acute heart failure admission

Małgorzata Małek-Elikowska et al. Front Pharmacol. .

Abstract

Background: Intravenous (IV) furosemide and torsemide represent a cornerstone of guideline-directed medical therapy for acute heart failure (AHF). However, the evidence regarding the superiority of each agent remains controversial.

Methods: The prospective, open-label, comparative study included 51 adult patients hospitalized due to AHF. Torsemide was administered to 25 patients (49%), and furosemide to 26 patients (51%). The primary endpoint was the change in urinary spot sodium level at 24 h, used to assess diuretic efficacy. Secondary outcomes included lung ultrasound (LUS) B-lines, clinical status evaluation based on the Borg scale, Killip-Kimball classification, and daily urine output.

Results: After 24 h of treatment, urinary sodium levels increased by an estimated marginal mean (EMM) of 21.84 mmol/L in the furosemide group and 0.97 mmol/L in the torsemide group (p = 0.173). The number of B-lines over 24 h decreased, with an EMM of 28.31 in the furosemide group, and 30.12 in the torsemide group (p = 0.779). The severity of dyspnea, measured by the Borg scale, decreased over 24 h with an EMM of 3.58 points in the furosemide group, and 3.62 points in the torsemide group (p = 0.891). Pulmonary congestion, measured by the Killip-Kimball classification, minimized with an EMM of 0.42 points in the furosemide group, and 0.47 points in the torsemide group (p = 0.770). Daily urine output after 24 h of treatment reached an EMM of 3,559.67 mL in the furosemide group, and 2,734.89 mL in the torsemide group (p = 0.068).

Conclusion: Both furosemide and torsemide demonstrated comparable efficacy in the initial treatment of AHF, as assessed by laboratory, ultrasound, and clinical parameters.

Keywords: B-lines; acute heart failure; furosemide; loop diuretics; torsemide; urinary sodium.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
The increase in spot urinary sodium levels, the decrease in the number of B-lines, as well as in the Borg scale and Killip-Kimball classification, along with the volume of daily urine output in the total cohort during the first 24 h of treatment. The values are presented as estimated marginal means ± SE, standard error. The modified Borg Dyspnea Scale assesses ratings of perceived shortness of breath from 0 (nothing at all) to 10 (maximum); the Killip-Kimball classification assesses the severity of heart failure: 1) no clinical signs, 2) mild pulmonary edema, 3) severe pulmonary edema, 4) cardiogenic shock.
FIGURE 2
FIGURE 2
(A) The decrease in the number of B-lines across subgroups during the first 24 h of treatment. (B) The volume of daily urine output across subgroups during the first 24 h of treatment. The values are presented as estimated marginal means. Abbreviations: SE, standard error; AF, atrial fibrillation; COPD, chronic obstructive pulmonary disease; eGFR, estimated glomerular filtration rate (mL/min/1.73 m2); BMI, body mass index (kg/m2), HFpEF, heart failure with preserved ejection fraction; HFmEF, heart failure with mildly reduced ejection fraction.

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