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Published on: May 26, 2022
Clinical outcome in hypertensive patients treated with amlodipine plus bisoprolol or plus valsartan
Yi-Heng Li1, Hui-Wen Lin1, Ulrike Gottwald-Hostalek2
1Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Insights
Amlodipine plus bisoprolol (A+B) and amlodipine plus valsartan (A+V) showed similar outcomes for death, atherosclerotic cardiovascular disease events, and heart failure. However, the A+B combination demonstrated a reduced risk of hemorrhagic stroke compared to A+V.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Beta-blockers are not recommended as first-line hypertension treatment due to lower efficacy in stroke prevention.
- Combination therapy is common for blood pressure control.
- Comparing amlodipine plus bisoprolol (A+B) with amlodipine plus valsartan (A+V) provides insights into treatment efficacy.
Purpose of the Study:
- To compare clinical outcomes between amlodipine plus bisoprolol (A+B) and amlodipine plus valsartan (A+V) in hypertensive patients.
- To evaluate the efficacy of A+B versus A+V in preventing all-cause death, atherosclerotic cardiovascular disease (ASCVD) events, hemorrhagic stroke, and heart failure.
Main Methods:
- A population-based cohort study utilized data from the Taiwan National Health Insurance Research Database (2012-2019).
- Adult hypertensive patients initially on amlodipine monotherapy, then switched to A+V or A+B, were included.
- Multivariable Cox proportional hazards models assessed treatment outcomes.
Main Results:
- The study included 4311 patients in the A+B group and 10980 in the A+V group.
- After a mean follow-up of 4.34 years, no significant differences were observed in all-cause death, ASCVD events, or heart failure between the groups.
- The A+B group showed a significantly lower risk of hemorrhagic stroke (aHR 0.70, 95% CI 0.52-0.94).
Conclusions:
- Amlodipine plus bisoprolol (A+B) and amlodipine plus valsartan (A+V) combinations exhibit comparable efficacy regarding mortality, ASCVD events, and heart failure.
- The A+B combination therapy is associated with a reduced risk of hemorrhagic stroke.
- Safety outcomes were similar between the two treatment groups.
Objective:
Several guidelines do not recommend beta-blocker as the first-line treatment for hypertension because of its inferior efficacy in stroke prevention. Combination therapy with beta-blocker is commonly used for blood pressure control. We compared the clinical outcomes in patients treated with amlodipine plus bisoprolol (A + B), a ß1-selective beta-blocker and amlodipine plus valsartan (A + V).
Methods:
A population-based cohort study was performed using data from the Taiwan National Health Insurance Research Database. From 2012 to 2019, newly diagnosed adult hypertensive patients who received initial amlodipine monotherapy and then switched to A + V or A + B were included. The efficacy outcomes included all-cause death, atherosclerotic cardiovascular disease (ASCVD) event (cardiovascular death, myocardial infarction, ischemic stroke, and coronary revascularization), hemorrhagic stroke, and heart failure. Multivariable Cox proportional hazards model was used to evaluate the relationship between outcomes and different treatments.
Results:
Overall, 4311 patients in A + B group and 10980 patients in A + V group were included. After a mean follow-up of 4.34 ± 1.79 years, the efficacy outcomes were similar between the A + V and A + B groups regarding all-cause death (adjusted hazard ratio [aHR] 0.99, 95% confidence interval [CI] 0.83-1.18), ASCVD event (aHR 0.97, 95% CI 0.84-1.12), and heart failure (aHR 1.06, 95% CI 0.87-1.30). The risk of hemorrhagic stroke was lower in A + B group (aHR 0.70, 95% CI 0.52-0.94). The result was similar when taking death into consideration in competing risk analysis. The safety outcomes were similar between the 2 groups.
Conclusions:
There was no difference of all-cause death, ASCVD event, and heart failure in A + B vs. A + V users. But A + B users had a lower risk of hemorrhagic stroke.
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