https://doi.org/10.55788/92a69cb0
HSS may improve diuretic response and outcomes in hospitalised patients with HF, though this has never translated into strong guideline recommendations. Less is known about the efficacy and safety of hypertonic treatment in ambulatory patients with worsening HF. The SALT-HF trial (NCT04533997), presented by Dr Marta Cobo Marcos (Iron Gate Majadahonda University Hospital, Spain), explored whether the addition of HSS to IV furosemide increased 3-hour diuresis or had other positive effects [1].
SALT-HF included participants with:
- worsening HF and 2 signs of volume overload;
- a daily oral loop diuretic dose of ≥80 mg furosemide or equivalent for ≥30 days;
- NT-proBNP >1,000 pg/mL or BNP >250 pg/mL; or
- a need for IV diuretic therapy.
The 168 participants were randomised 1:1 to IV furosemide plus HSS or IV furosemide alone.
The primary outcome of 3-hour diuresis volume did not differ between the groups: 1,099 mL in the HSS group compared with 1,103 mL in the control group (mean difference −4.6 mL; P=0.963). Similarly, no significant differences were observed in 3-hour natriuresis volume or 3-hour weight difference. There were also no differences in any of the other secondary outcomes, assessed 7 days after treatment: NYHA classification and visual analogue scale score, composite congestion score, body-weight difference, inferior vena cava diameter, lung ultrasound B-lines, and biomarker scores.
According to Dr Cobo Marcos, a possible explanation for the negative results is that a single infusion or a 3-hour evaluation period may have been insufficient to show any benefits. Hypertonic saline was safe, with no increased risk of worsening renal function or hypokalaemia.
- Marcos MC, et al. Efficacy of hypertonic saline therapy in ambulatory patients with heart failure. Late breaking clinical trials: drugs and disease management, Heart Failure 2024, 11–14 May, Lisbon, Portugal.
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Table of Contents: HFA 2024
Featured articles
Meet the Trialist: Innovating cardiac monitoring with MONITOR-HF
Trials: Pharmacology
Effects of semaglutide on MACE irrespective of HF status
SEQUOIA-HCM: Aficamten demonstrates clinical efficacy in obstructive HCM
ARIES-HM3 trial: Subgroup analysis in patients with prior need for aspirin
Three diuretic regimens compared in the DEA-HF study
Adding a mineralocorticoid receptor modulator in heart failure with CKD
SGLT2 Inhibitors
Empagliflozin did not reduce mortality for HF after MI regardless of T2D status
SGLT2 inhibitors decrease atrial fibrillation risk in patients with HFrEF
SGLT2 inhibition: Major and early impact on heart failure hospitalisation risk
Trials: Other
Individualised diuretic titration in acute HF without a physician
Intravenous iron deficiency treatment improves exercise capacity in patients with HFpEF
CD34+ stem cells promote reverse cardiac remodelling after acute MI
Registries
Sex-specific outcomes and resource utilisation after HF hospitalisation
Application of guideline-directed medical therapy in patients with HFrEF in the Netherlands
Devices
PAP-guided management system appears safe in patients with HF
Delivery of CRT guided by non-invasive anatomy assessment
RELIEVE-ing HFrEF with interatrial shunting
Miscellaneous
Algorithm-based remote patient monitoring was associated with lower mortality in a retrospective cohort study
High mortality and morbidity in suspected de novo HF in outpatient care
Bio-ADM as a marker for congestion in patients hospitalised for acute HF
Hypertonic saline not effective in ambulatory patients with heart failure?
No effect of low-dose carperitide on mortality or hospitalisation in acute HF
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