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Serial direct sodium removal in patients with heart failure and diuretic resistance
Veena S Rao1, Juan B Ivey-Miranda1,2, Zachary L Cox3,4
1Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
Insights
Direct sodium removal (DSR) offers a promising approach for heart failure patients with diuretic resistance. This method, involving peritoneal membrane use and diuretic withdrawal, improved diuretic response and cardiorenal parameters, potentially offering a novel therapy.
Area of Science:
- Cardiology
- Nephrology
- Critical Care Medicine
Background:
- Loop diuretics can worsen cardiorenal syndrome (CRS) in heart failure (HF).
- Diuretic resistance is a significant challenge in managing HF patients.
- Direct sodium removal (DSR) presents a potential alternative strategy.
Purpose of the Study:
- To evaluate the feasibility and efficacy of DSR in HF patients with diuretic resistance.
- To assess the impact of DSR on diuretic response and cardiorenal parameters.
- To determine if DSR can reduce reliance on loop diuretics.
Main Methods:
- Two prospective, single-arm studies (RED DESERT and SAHARA) enrolled HF patients requiring high-dose loop diuretics.
- Loop diuretics were withdrawn, and serial DSR was used to achieve and maintain euvolemia.
- Diuretic response was assessed via intravenous furosemide challenge and urine sodium quantification.
Main Results:
- DSR significantly increased diuretic response (81 ± 37 mmol to 223 ± 71 mmol, p < 0.001) after loop diuretic withdrawal.
- Patients maintained euvolemia with DSR, with diuretic re-initiation doses significantly lower than baseline (median 8% of baseline) at 1 year.
- Multiple kidney function parameters and HF biomarkers showed significant improvement (p < 0.05).
Conclusions:
- Serial DSR therapy with loop diuretic withdrawal is feasible in HF patients with diuretic resistance.
- DSR demonstrated substantial and persistent improvements in diuretic resistance and cardiorenal parameters.
- DSR may represent a novel therapeutic option for diuretic resistance and CRS, warranting further investigation in randomized controlled trials.
Aims:
Loop diuretics may exacerbate cardiorenal syndrome (CRS) in heart failure (HF). Direct sodium removal (DSR) using the peritoneal membrane, in conjunction with complete diuretic withdrawal, may improve CRS and diuretic resistance.
Methods And Results:
Patients with HF requiring high-dose loop diuretics were enrolled in two prospective, single-arm studies: RED DESERT (n = 8 euvolaemic patients), and SAHARA (n = 10 hypervolaemic patients). Loop diuretics were withdrawn, and serial DSR was utilized to achieve and maintain euvolaemia. At baseline, participants required a median 240 mg (interquartile range [IQR] 200-400) oral furosemide equivalents/day, which was withdrawn in all participants during DSR (median time of DSR 4 weeks [IQR 4-6]). Diuretic response (queried by formal 40 mg intravenous furosemide challenge and 6 h urine sodium quantification) increased substantially from baseline (81 ± 37 mmol) to end of DSR (223 ± 71 mmol, p < 0.001). Median time to re-initiate diuretics was 87 days, and the median re-initiation dose was 8% (IQR 6-10%) of baseline. At 1 year, diuretic dose remained substantially below baseline (30 [IQR 7.5-40] mg furosemide equivalents/day). Multiple dimensions of kidney function such as filtration, uraemic toxin excretion, kidney injury, and electrolyte handling improved (p < 0.05 for all). HF-related biomarkers including N-terminal pro-B-type natriuretic peptide, carbohydrate antigen-125, soluble ST2, interleukin-6, and growth differentiation factor-15 (p < 0.003 for all) also improved.
Conclusions:
In patients with HF and diuretic resistance, serial DSR therapy with loop diuretic withdrawal was feasible and associated with substantial and persistent improvement in diuretic resistance and several cardiorenal parameters. If replicated in randomized controlled studies, DSR may represent a novel therapy for diuretic resistance and CRS.
Clinical Trial Registration:
RED DESERT (NCT04116034), SAHARA (NCT04882358).
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