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Telmisartan to prevent recurrent stroke and cardiovascular events
Salim Yusuf1, Hans-Christoph Diener, Ralph L Sacco
1Population Health Research Institute, McMaster University, Hamilton, ON, Canada.
Insights
Early telmisartan treatment after ischemic stroke did not significantly reduce recurrent stroke or major cardiovascular events. This study found no significant benefit in preventing secondary strokes or related complications with early angiotensin-receptor blocker therapy.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- Lowering blood pressure post-stroke reduces recurrent stroke risk.
- Renin-angiotensin system inhibitors decrease cardiovascular events in high-risk patients.
- The impact of early renin-angiotensin system inhibition post-stroke remains unclear.
Purpose of the Study:
- To evaluate the effects of early telmisartan therapy on recurrent stroke and cardiovascular events.
- To assess the efficacy of an angiotensin-receptor blocker initiated soon after ischemic stroke.
Main Methods:
- A multicenter trial randomized 20,332 ischemic stroke patients.
- Patients received either telmisartan (80 mg daily) or placebo.
- Primary outcome: recurrent stroke; Secondary outcomes: major cardiovascular events, new-onset diabetes.
Main Results:
- Mean blood pressure was 3.8/2.0 mm Hg lower in the telmisartan group.
- No significant difference in recurrent stroke rates (8.7% vs 9.2%).
- No significant differences in major cardiovascular events or new-onset diabetes.
Conclusions:
- Early telmisartan therapy post-ischemic stroke did not significantly reduce recurrent stroke.
- Major cardiovascular events and new-onset diabetes rates were not significantly lowered.
- The study did not establish a significant benefit for early angiotensin-receptor blocker use in this patient population.
Background:
Prolonged lowering of blood pressure after a stroke reduces the risk of recurrent stroke. In addition, inhibition of the renin-angiotensin system in high-risk patients reduces the rate of subsequent cardiovascular events, including stroke. However, the effect of lowering of blood pressure with a renin-angiotensin system inhibitor soon after a stroke has not been clearly established. We evaluated the effects of therapy with an angiotensin-receptor blocker, telmisartan, initiated early after a stroke.
Methods:
In a multicenter trial involving 20,332 patients who recently had an ischemic stroke, we randomly assigned 10,146 to receive telmisartan (80 mg daily) and 10,186 to receive placebo. The primary outcome was recurrent stroke. Secondary outcomes were major cardiovascular events (death from cardiovascular causes, recurrent stroke, myocardial infarction, or new or worsening heart failure) and new-onset diabetes.
Results:
The median interval from stroke to randomization was 15 days. During a mean follow-up of 2.5 years, the mean blood pressure was 3.8/2.0 mm Hg lower in the telmisartan group than in the placebo group. A total of 880 patients (8.7%) in the telmisartan group and 934 patients (9.2%) in the placebo group had a subsequent stroke (hazard ratio in the telmisartan group, 0.95; 95% confidence interval [CI], 0.86 to 1.04; P=0.23). Major cardiovascular events occurred in 1367 patients (13.5%) in the telmisartan group and 1463 patients (14.4%) in the placebo group (hazard ratio, 0.94; 95% CI, 0.87 to 1.01; P=0.11). New-onset diabetes occurred in 1.7% of the telmisartan group and 2.1% of the placebo group (hazard ratio, 0.82; 95% CI, 0.65 to 1.04; P=0.10).
Conclusions:
Therapy with telmisartan initiated soon after an ischemic stroke and continued for 2.5 years did not significantly lower the rate of recurrent stroke, major cardiovascular events, or diabetes. (ClinicalTrials.gov number, NCT00153062.)
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