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Risk of developing hyperkalemia in patients with hypertension treated with combination antihypertensive therapy - a
Fatma Luai Mahdi Al-Janabi1, Fatme Moussa2, Sarah Taleb1
1Faculty of Medicine, Aalborg University, Aalborg, Denmark.
Insights
The combination of beta blockers (BB), renin-angiotensin system inhibitors (RASi), and mineralocorticoid receptor antagonists (MRA) significantly increases hyperkalemia risk within 90 days. Careful monitoring for dyskalemia is crucial when initiating this antihypertensive therapy.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Hyperkalemia is a serious adverse effect of antihypertensive therapy.
- The comparative risk of hyperkalemia across different antihypertensive drug combinations is not well understood.
Purpose of the Study:
- To investigate the risk of developing hyperkalemia in relation to various combinations of antihypertensive therapy.
- To identify specific antihypertensive combinations associated with an increased risk of hyperkalemia.
Main Methods:
- Danish register-based study utilizing incidence density matching.
- Matched 793 hyperkalemic patients to 3598 normokalemic patients based on eGFR, age, sex, and time.
- Multivariable conditional logistic regression to estimate hyperkalemia odds within 90 days for eight combination therapy groups.
Main Results:
- The combination of beta blockers (BB) + renin-angiotensin system inhibitors (RASi) + mineralocorticoid receptor antagonists (MRA) showed a significantly increased odds of hyperkalemia (OR 1.95; 95% CI, 1.39-2.72) compared to RASi + thiazides.
- Combinations such as CCB + thiazides and CCB + RASi + thiazides were not significantly associated with hyperkalemia.
- Initiating BB + RASi + MRA therapy was linked to a higher risk of hyperkalemia within 90 days.
Conclusions:
- The combination of BB + RASi + MRA is associated with a significantly increased risk of hyperkalemia.
- Identifying and monitoring patients at high risk for dyskalemia is essential when prescribing combination antihypertensive therapies.
- This finding highlights the need for careful patient selection and monitoring to prevent adverse outcomes associated with hyperkalemia.
Abstract:
The risk of hyperkalemia in relation to different combinations of antihypertensive therapy remains to be elucidated. In this Danish register-based study, we aimed to investigate the risk of developing hyperkalemia in relation to different combinations of antihypertensive therapy. Using incidence density matching, we matched a hyperkalemic patient to five normokalemic patients on eGFR groups, age, sex, and time between study entry and date of potassium measurement. Combination therapies were subdivided into eight groups: beta blockers (BB) + calcium channel blockers (CCB), BB + renin angiotensin system inhibitors (RASi), BB + RASi + mineralocorticoid receptor antagonists (MRA), CCB + RASi, CCB + RASi + thiazides, CCB + thiazides, RASi + thiazides, and other combinations. Multivariable conditional logistic regression was used to estimate the odds of hyperkalemia within 90 days for each of the eight antihypertensive combination therapies. A total of 793 patients with hyperkalemia were matched to 3598 normokalemic patients. In multivariable analysis, odds of developing hyperkalemia when being treated with BB + RASi + MRA was 1.95 (95% CI, 1.39-2.72) compared to RASi + thiazides (reference). CCB + thiazides (OR, 0.76 [95% CI, 0.45-1.28]) and CCB + RASi + Thiazid (OR 0.81 [95% CI, 0.51-1.28]) were among the others not significantly associated with hyperkalemia. Combinations of BB + RASi + MRA were significantly associated with an increased risk of developing hyperkalemia within 90 days of initiating treatment. Patients treated with BB + RASi + MRA within 90 days of treatment initiation, were associated with an increased hyperkalemia risk. When treating hypertensive patients with combination antihypertensive therapy, identifying and monitoring patients with a high risk of dyskalemias is a crucial goal to avoid serious adverse effects and detrimental outcomes related to dyskalemia.
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