Related Experiment Video
Updated: Jun 21, 2025

Voltage-Dependent Potassium Current Recording on H9c2 Cardiomyocytes via the Whole-Cell Patch-Clamp Technique
Published on: November 11, 2022
Increased Spironolactone Dosing in Acute Heart Failure Alters Potassium Homeostasis but Does not Enhance Decongestion
Peter S Natov1, Juan B Ivey-Miranda2, Zachary L Cox3
1Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Insights
Spironolactone did not improve congestion in acute heart failure patients. However, this aldosterone antagonist meaningfully limited potassium wasting during treatment, suggesting a role in managing electrolyte balance.
Area of Science:
- Cardiology
- Pharmacology
- Nephrology
Background:
- The ATHENA-HF trial investigated spironolactone's efficacy in acute heart failure.
- No improvements in natriuretic peptide levels or clinical congestion were observed with spironolactone (100 mg/day for 96 hours) in addition to usual care.
Purpose of the Study:
- To conduct a post hoc analysis of the ATHENA-HF trial.
- To determine if spironolactone induced pharmacodynamic effects and if patients with higher aldosterone activity experienced additional decongestion.
Main Methods:
- Excluded patients previously treated with spironolactone.
- Examined renal potassium handling, using baseline serum potassium as a surrogate for spironolactone activity.
- Divided patients into tertiles of baseline serum potassium to explore outcomes.
Main Results:
- Spironolactone significantly increased serum potassium at 72 and 96 hours compared to placebo.
- Spironolactone-treated patients required less potassium supplementation from 48 hours onwards.
- No differences in natriuretic peptide levels, fluid loss, urine output, or dyspnea relief were observed across potassium tertiles.
Conclusions:
- Spironolactone (100 mg/day for 96 hours) offers no significant added decongestive benefit in acute heart failure patients on loop diuretics.
- Spironolactone meaningfully limits potassium wasting in this patient population.
Background:
The ATHENA-HF (Aldosterone Targeted Neurohormonal Combined with Natriuresis Therapy in Heart Failure) clinical trial found no improvements in natriuretic peptide levels or clinical congestion when spironolactone 100 mg/day for 96 hours was used in addition to usual treatment for acute heart failure.
Methods:
We performed a post hoc analysis of ATHENA-HF to determine whether spironolactone treatment induced any detectable pharmacodynamic effects and whether patients with potentially greater aldosterone activity experienced additional decongestion. Trial subjects previously treated with spironolactone were excluded. We first examined for changes in renal potassium handling. Using the baseline serum potassium level as a surrogate marker of spironolactone activity, we then divided each treatment arm into tertiles of baseline serum potassium and explored for differences in laboratory and clinical congestion outcomes.
Results:
Among spironolactone-naïve patients, the change in serum potassium did not differ after 24 hours or 48 hours but was significantly greater with spironolactone treatment compared to placebo at 72 hours (0.23 ± 0.55 vs 0.03 ± 0.60 mEq/L; P = 0.042) and 96 hours (0.32 ± 0.51 vs 0.13 ± 0.72 mEq/L; P = 0.046). Potassium supplementation was similar at treatment start and at 24 hours, but spironolactone-treated patients required substantially less potassium replacement at 48 hours (24% vs 36%; P = 0.048), 72 hours (21% vs 37%; P = 0.013), and 96 hours (11% vs 38%; P < 0.001). When the treatment arms were divided into tertiles of baseline serum potassium, there were no differences in the 96-hour log N-terminal pro-B-type natriuretic peptide levels, net fluid loss, urine output, or dyspnea relief in any of the potassium groups, with no effect modification by treatment exposure.
Conclusions:
Spironolactone 100 mg/day for 96 hours in patients receiving intravenous loop diuresis for acute heart failure has no clear added decongestive ability but does meaningfully limit potassium wasting.
More Related Videos
Related Concept Videos
Antihypertensive Drugs: Potassium-Sparing Diuretics
Heart Failure Drugs: Diuretics
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Heart Failure Drugs: Inotropic Agents
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...

