https://doi.org/10.55788/7efb21bb
The single-centre DEA-HF study (NCT05904808) assessed the efficacy and safety of 3 diuretic regimens used commonly in daily practice to treat congestion-refractory, ambulatory chronic HF [1]. Dr Aharon Abbo (Rambam Medical Center, Israel), who presented the study results, said that there is a need for comparative studies to guide contemporary diuretic regimen selection for these patients. Key inclusion criteria of the DEA-HF study were NYHA class II–IV; ≥1 sign of congestion; haemodynamic stability; ≥2 HF drugs plus oral diuretics for 1 month; and rate >20 mL/min/1.73m2.
Three regimens of 3 weeks each were evaluated: 1) 250 mg of IV furosemide; 2) 250 mg of IV furosemide plus 5 mg of oral metolazone; 3) 250 mg of IV furosemide plus 500 mg of IV acetazolamide. The 42 participants were randomised to receive the 3 different regimens in 6 possible sequences. Each participant was followed for 4 consecutive weeks. The median age was 72 years, 60% were men, and most (79%) participants were NYHA class III. The trial was completed by 37 participants.
The primary outcome was sodium excretion 6 hours after treatment. For For regimen 1, this was 3,835 mg (95% CI 3,279–4,392), for regimen 2 it was 4,691 mg (95% CI 4,153–5,229), and for regimen 3 it was 3,584 mg (95% CI 3,020–4,148). “These outcomes demonstrate that IV furosemide plus oral metolazone resulted in a significantly higher natriuresis compared to IV furosemide alone,” Dr Abbo observed.
The secondary endpoint of total urinary volume for the 3 regimens was 1.71L (95% CI 1.49–1.93), 1.84L (95% CI 1.63–2.05), and 1.58L (95% CI 1.37–1.80), respectively. Regimen 2 resulted in a significantly higher rate of worsening renal function, but this did not result in a difference in hospital admissions.
“In these chronic patients receiving high-dose IV furosemide and HF guideline-directed medical therapy, including SGLT2 inhibitors, adding IV acetazolamide did not result in better natriuresis or urine volume excretion,” concluded Dr Abbo.
- Abbo A, et al. DEA-HF: The heart failure diuresis efficacy comparison study. Late breaking clinical trials: medical therapy, 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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