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Ongoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial (ONTARGET): implications for reduced
Philip R Liebson1, Ezra A Amsterdam
1Section of Cardiology, Rush University Medical Center, 1653 West Congress Parkway, Chicago, IL 60612, USA. pliebson@rush.edu
Insights
The Ongoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial (ONTARGET) found that telmisartan (an angiotensin-receptor blocker) was as effective as ramipril (an angiotensin-converting enzyme inhibitor) in preventing cardiovascular events. Combining these drugs increased adverse effects without additional benefit.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Clinical Trials
Background:
- The Ongoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial (ONTARGET) is a significant study comparing angiotensin-receptor blockers (ARBs) and angiotensin-converting enzyme inhibitors (ACEIs).
- Previous research has established the efficacy of both ARBs and ACEIs in managing cardiovascular conditions.
Purpose of the Study:
- To compare the efficacy and safety of telmisartan (an ARB) versus ramipril (an ACEI) in patients with vascular disease or high-risk diabetes.
- To evaluate the benefits and risks of combining telmisartan and ramipril.
Main Methods:
- A large-scale, high-quality noninferiority trial involving patients with vascular disease or high-risk diabetes.
- Participants were randomized to receive telmisartan, ramipril, or the combination therapy.
- Exclusion criteria included patients with heart failure.
Main Results:
- Telmisartan was found to be non-inferior to ramipril in reducing fatal and nonfatal cardiovascular events.
- The combination of telmisartan and ramipril resulted in more adverse effects without a significant increase in cardiovascular benefit.
- The study design differed from others by not always titrating ACEIs to maximum doses and excluding heart failure patients.
Conclusions:
- Telmisartan is a viable alternative to ACEIs like ramipril for reducing cardiovascular events in high-risk populations.
- Combining ARBs and ACEIs is not recommended due to increased adverse effects and lack of added benefit.
- ONTARGET provides robust evidence for ARB and ACEI comparative effectiveness and combination therapy risks.
Abstract:
The recently published Ongoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial (ONTARGET) in patients with vascular disease or high-risk diabetes, as the largest published comparative trial of these agent classes, provides further evidence concerning the comparison between the angiotensin-receptor blockers (ARBs) and the angiotensin-converting enzyme inhibitors (ACEIs). In this trial, telmisartan (an ARB) was non-inferior to ramipril (an ACEI) in reducing fatal and nonfatal cardiovascular events. Moreover, ONTARGET is an example of a high-quality noninferiority trial. However, the combination of the 2 agents was associated with more adverse effects without an increase in benefit. The study differed from several other comparative studies in which the dose and choice of ACEI was left to individual physicians. Further, in ONTARGET, the ACEI was not titrated to the maximum dose and patients with heart failure were excluded.
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