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Efficacy and safety of hypertonic saline therapy in ambulatory patients with heart failure: The SALT‐HF trial.

Authors :
Cobo Marcos, Marta
de la Espriella, Rafael
Comín‐Colet, Josep
Zegrí‐Reiriz, Isabel
Rubio Gracia, Jorge
Morales‐Rull, Jose Luis
Llàcer, Pau
Díez‐Villanueva, Pablo
Jiménez‐Marrero, Santiago
de Juan Bagudá, Javier
Ortiz Cortés, Carolina
Restrepo‐Córdoba, Maria Alejandra
Goirigolzarri‐Artaza, Josebe
García‐Pinilla, Jose Manuel
Barrios, Elvira
del Prado Díaz, Susana
Montero Hernández, Esther
Sanchez‐Marteles, Marta
Núñez, Julio
Source :
European Journal of Heart Failure; Oct2024, Vol. 26 Issue 10, p2118-2128, 11p
Publication Year :
2024

Abstract

Aims: Combination of hypertonic saline solution (HSS) with intravenous loop diuretics has been suggested to improve diuretic response in patients hospitalized for heart failure (HF). The efficacy and safety of this approach in the ambulatory setting remain unexplored. Methods and results: In this multicentre, double‐blind, randomized study, we allocated ambulatory patients with worsening heart failure (WHF) to a 1‐h infusion of intravenous furosemide (ivFurosemide)‐HSS versus ivFurosemide. The primary endpoint was the volume of diuresis at 3 h. Secondary endpoints included 3‐h natriuresis and weight variation, 7‐day congestion data, kidney function and electrolytes, and 30‐day clinical events. Overall, 167 participants (median age: 81 years, 30.5% female) were randomized across 13 sites between December 2020 and March 2023. There were no differences in 3‐h diuresis between treatments (ivFurosemide‐HSS: 1099 ml vs. ivFurosemide: 1103 ml, p = 0.963), 3‐h natriuresis (∆ +2.642 mEq/L, p = 0.559), or 3‐h weight (∆ +0.012 kg, p = 0.920). Patients in the ivFurosemide‐HSS arm experienced significant weight decrease at 7 days (Δ −0.586 kg, p = 0.048). There were no between‐treatment differences in clinical congestion score, biomarkers, inferior vena cava diameter, or the presence of lung ultrasound B‐lines. At 30 days, 26.5% of the patients in the ivFurosemide‐HSS group versus 33.3% in the ivFurosemide group experienced WHF (hazard ratio 0.76, p = 0.330). The incidence of death from any cause or HF hospitalization was 6% of patients in the ivFurosemide‐HSS group and 8.3% of patients in the ivFurosemide group (hazard ratio 0.69, p = 0.521). The incidence of worsening kidney function or metabolic derangements was not significantly different in the two arms. Conclusions: A single infusion of ivFurosemide‐HSS did not improve 3‐h diuresis or congestion parameters in patients with ambulatory WHF. This therapy showed an appropriate safety profile. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13889842
Volume :
26
Issue :
10
Database :
Complementary Index
Journal :
European Journal of Heart Failure
Publication Type :
Academic Journal
Accession number :
180656273
Full Text :
https://doi.org/10.1002/ejhf.3390