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Published on: February 26, 2013
Triple Combination Therapy for Global Cardiovascular Risk: Atorvastatin, Perindopril, and Amlodipine
Michel E Bertrand1, Charalambos Vlachopoulos2, Jean-Jacques Mourad3
1Lille Heart Institute, 139 C-76 rue de Lille Lambersart, 59037, Lille, France. mbertrand2007@gmail.com.
Insights
Combining statins, ACE inhibitors, and CCBs significantly reduces cardiovascular events in high-risk patients. Triple therapy offers an effective approach to managing global cardiovascular risk, improving outcomes for coronary artery disease patients.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Coronary artery disease (CAD) management is complex, involving multiple risk factors like hypertension and hypercholesterolemia.
- Statins, ACE inhibitors, and calcium channel blockers (CCBs) are cornerstone therapies for cardiovascular risk reduction.
- Current guidelines advocate a comprehensive approach to managing cardiovascular risk factors.
Purpose of the Study:
- To review the evidence supporting the combination of statins, ACE inhibitors, and CCBs in hypertensive patients with hypercholesterolemia or CAD.
- To evaluate the efficacy of triple therapy in reducing major adverse cardiovascular events.
- To explore the benefits of single-pill formulations for treatment adherence.
Main Methods:
- Literature search for studies combining statins with antihypertensive drugs in patients with hypertension and hypercholesterolemia or stable CAD.
- Analysis of existing trial data, including a post hoc analysis from the EUROPA trial.
- Review of evidence on the impact of combination therapy on cardiovascular event reduction and patient adherence.
Main Results:
- Triple therapy with statins, ACE inhibitors, and CCBs is associated with a significant reduction in major cardiovascular events.
- A post hoc analysis of the EUROPA trial showed a 46% reduction in cardiovascular death, myocardial infarction, or resuscitated cardiac arrest with triple therapy.
- Single-pill formulations combining these drug classes enhance treatment adherence.
Conclusions:
- Triple therapy with statins, ACE inhibitors, and CCBs is an effective strategy for managing global cardiovascular risk in high-risk patients.
- This combination therapy offers significant benefits in reducing cardiovascular events for patients with CAD.
- Single-pill formulations represent a promising approach to improve patient adherence and therapeutic outcomes.
Abstract:
Statins, angiotensin-converting enzyme (ACE) inhibitors, and calcium channel blockers (CCBs) have markedly changed the clinical progression of patients with coronary artery disease (CAD). The goal of this paper is to review the rationale and evidence for combining these three drug classes in hypertensive patients with hypercholesterolemia or CAD. Data sources include a literature search for publications on the use of a statin combined with various antihypertensive drugs in patients with hypertension and hypercholesterolemia or stable CAD. Hypercholesterolemia and hypertension constitute major physiological risk factors of ischemic heart disease. Current guidelines recommend a global approach to risk management, using agents that address as many risk factors as possible. Dual combination therapies are an important component of guideline-recommended therapy in hypertension. Our review of the literature indicates that triple therapy with a statin, ACE inhibitor, and CCB is associated with a significant reduction in major cardiovascular events. For example, a post hoc analysis in 1056 patients with stable CAD participating in the EUROPA trial indicated that the addition of perindopril to a CCB and a lipid-lowering agent was associated with a 46 % reduction in the composite of cardiovascular death, myocardial infarction, and resuscitated cardiac arrest (p = 0.023). In addition, single pill formulations are known to result in better adherence to the treatment. Single-pill formulations that combine a statin, an ACE inhibitor, and a CCB appear to offer an effective approach to the management of global cardiovascular risk.
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