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

**Authors:** Małgorzata Małek-Elikowska, Andrzej Szyszka, Julita Fedorowicz, Rafał Dankowski, Cyntia Szymańska, Artur Baszko

PMC · DOI: 10.3389/fphar.2025.1643077 · 2025-07-31

## TL;DR

This study compared furosemide and torsemide in treating acute heart failure and found both drugs to be similarly effective within 24 hours.

## Contribution

The study provides direct comparative evidence of furosemide and torsemide efficacy in acute heart failure treatment.

## Key findings

- Furosemide and torsemide showed similar changes in urinary sodium levels after 24 hours.
- Both drugs reduced lung congestion and dyspnea similarly based on clinical and ultrasound assessments.
- Furosemide had a slightly higher urine output, but the difference was not statistically significant.

## Abstract

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.

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.

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).

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

## Linked entities

- **Chemicals:** furosemide (PubChem CID 3440), torsemide (PubChem CID 41781)

## Full-text entities

- **Diseases:** Pulmonary congestion (MESH:D001261), dyspnea (MESH:D004417), AHF (MESH:D006333)
- **Chemicals:** furosemide (MESH:D005665), Torsemide (MESH:D000077786), sodium (MESH:D012964)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12350330/full.md

---
Source: https://tomesphere.com/paper/PMC12350330