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Hyperkalemia in Heart Failure with Reduced Ejection Fraction Patients Treated with Sacubitril/Valsartan: Experience
Sarah M Alyousif1,2, Naif K Alaqil2,3, Mohamad Abdelshafy1,2
1King Abdulaziz Cardiac Center, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh 14611, Saudi Arabia.
Insights
Sacubitril/valsartan use in heart failure with reduced ejection fraction (HFrEF) increases hyperkalemia risk. However, hyperkalemia was manageable, with low discontinuation rates, indicating the therapy is generally safe for HFrEF patients.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Heart failure with reduced ejection fraction (HFrEF) is a significant global health issue.
- Sacubitril/valsartan, an angiotensin receptor neprilysin inhibitor (ARNI), is effective for HFrEF but associated with hyperkalemia risk.
Purpose of the Study:
- To evaluate the incidence of hyperkalemia in HFrEF patients treated with sacubitril/valsartan.
- To assess treatment discontinuation rates due to hyperkalemia.
Main Methods:
- A retrospective cohort study of 238 HFrEF patients initiated on sacubitril/valsartan.
- Potassium levels monitored pre-initiation and at 0-3, 3-6, and 6-12 months post-initiation.
- Hyperkalemia defined as potassium levels >5.0, >5.5, and >6.0 mmol/L.
Main Results:
- Hyperkalemia >5.0 mmol/L increased significantly from 8.2% pre-initiation to 44.4% within three months post-initiation (p < 0.0001).
- Only 17.3% of patients exceeded 5.5 mmol/L.
- Treatment discontinuation occurred in 7.1% of patients, with only 1.3% due to hyperkalemia.
Conclusions:
- Sacubitril/valsartan therapy leads to a higher incidence of hyperkalemia in HFrEF patients.
- Hyperkalemia is generally manageable, with low discontinuation rates, supporting the therapy's safety and efficacy.
- Prospective studies with regular electrolyte monitoring are recommended to further validate findings.
Abstract:
Background/Objectives: Heart failure with reduced ejection fraction (HFrEF) remains a major global health burden. Sacubitril/valsartan, an angiotensin receptor neprilysin inhibitor (ARNI), improves outcomes in HFrEF but may cause hyperkalemia. Methods: A single-center retrospective cohort study was conducted at King Abdulaziz Cardiac Center, Riyadh, including 238 HFrEF patients initiated on sacubitril/valsartan (2016-2021). Potassium levels were assessed pre-initiation and at 0-3, 3-6, and 6-12 months post-initiation. Hyperkalemia was analyzed at thresholds >5.0, >5.5, and >6.0 mmol/L. Results: Median age was 58 years (IQR 48-69); 75.2% were male. Hyperkalemia >5.0 mmol/L occurred in 44.4% (95% CI: 38.1-51.0) within three months post-initiation versus 8.2% (95% CI: 5.3-12.4) pre-initiation. Only 17.3% exceeded 5.5 mmol/L. Treatment discontinuation occurred in 7.1% of patients, with 1.3% stopping due to clinically significant hyperkalemia. McNemar's test confirmed a significant increase in prevalence across time points (p < 0.0001). Conclusions: Despite increased hyperkalemia incidence, discontinuation rates were low, consistent with prior trials (PARADIGM-HF, PARAGON-HF). Sacubitril/valsartan remains an effective and generally safe therapy for HFrEF, with hyperkalemia manageable through monitoring. Limitations include missing potassium data, potential confounding factors, and the lack of a control group; future prospective studies with regular electrolyte monitoring are recommended.
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