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Clinical factors associated with hyperkalemia in patients with congestive heart failure
F H Ramadan1, N Masoodi, A A El-Solh
1Division of Geriatrics, Department of Medicine, State University of New York, Millard Fillmore Hospital, Buffalo, NY 14209, USA. Framadan@kaleidahealth.org
Insights
Congestive heart failure patients are at risk for hyperkalemia. Key factors include diabetes, poor kidney function, and use of certain medications like ACE inhibitors and spironolactone.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Patients with congestive heart failure (CHF) face increased risk of hyperkalemia due to comorbidities and medications affecting potassium excretion.
- Angiotensin-converting enzyme (ACE) inhibitors are commonly used in CHF and can impair potassium excretion.
Purpose of the Study:
- To identify clinical factors associated with hyperkalemia in patients hospitalized for CHF.
- Investigate predictors of hyperkalemia upon initial presentation in CHF patients.
Main Methods:
- A case-control study design was employed.
- Data from 938 non-dialysis-dependent CHF patients were analyzed.
- Hyperkalemia defined as serum potassium (K) ≥ 5.6 mmol/L; normokalemia as serum K 3.5–5.5 mmol/L.
Main Results:
- Diabetes mellitus, creatinine clearance <40 mL/min, and use of spironolactone were significantly associated with hyperkalemia.
- Use of ACE inhibitors also showed an independent association with hyperkalemia.
- Mean potassium levels were significantly higher in hyperkalemic cases compared to controls.
Conclusions:
- Hyperkalemia in CHF patients is independently linked to diabetes, reduced creatinine clearance, and use of spironolactone and ACE inhibitors.
- Clinical practice guidelines for spironolactone and ACE inhibitor use in CHF require clarification.
- Enhanced monitoring of serum potassium is recommended for CHF patients at higher risk.
Background:
Patients with congestive heart failure (CHF) are at risk for hyperkalemia because of coexisting comorbidities and use of multiple medications that impair potassium (K) excretion such as angiotensin converting enzyme (ACE) inhibitors.
Objective:
To identify clinical factors associated with hyperkalemia on initial presentation in patients hospitalized for CHF.
Design:
A case-control study.
Setting:
Two university-affiliated tertiary-care hospitals.
Subjects:
Using ICD-9 code for CHF, CHF admissions with hyperkalemia on presentation (cases) were identified from a population of 938 non-dialysis-dependent CHF patients. CHF admissions with normokalemia on presentation were used as controls. Hyperkalemia was defined as serum K > or = 5.6 mmol/L, and normokalemia as serum K > or = 3.5 and < or =5.5.
Methods:
Data were collected on demographic characteristics, clinical variables, comorbidity and medication use. Factors associated with hyperkalemia on initial presentation were examined.
Results:
Mean age did not differ between cases [76 years, standard deviation (SD) = 12] and controls (75 years, SD = 12) (P = 0.824). Mean potassium levels for cases and controls were 6.2 mmol/L (range 5.6 to 8.2) and 4.3 mmol/L respectively (P < 0.001). On multivariate analysis, diabetes mellitus [odds ratio (OR) = 2.42, 95% confidence interval (CI) = 1.04-5.59], creatinine clearance <40 mL/min (OR = 8.36, CI = 2.73-25.56), use of spironolactone (OR = 4.18, CI = 1.27-13.79), and use of ACE inhibitors (OR = 2.55, CI = 1.06-6.13) were independently associated with hyperkalemia.
Conclusions:
In CHF patients, hyperkalemia on presentation is independently associated with diabetes, creatinine clearance <40 mL/min, use of spironolactone, and use of ACE inhibitors. Recommendations for use of spironolactone and ACE inhibitors in CHF, and the intensity of serum K monitoring need to be clarified to account for patients at higher risk for hyperkalemia.
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