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Congestive heart failure: what should be the initial therapy and why?
1Chatterjee Center for Cardiac Research, Moffitt/Long Hospital, University of California, San Francisco, California 94143-0124, USA. chatterj@medicine.ucsf.edu
Insights
Neurohormonal activation worsens heart failure by promoting ventricular remodeling. Effective treatments for systolic heart failure include ACE inhibitors, ARBs, and beta-blockers to improve function and survival.
Area of Science:
- Cardiology
- Pharmacology
- Heart Failure Research
Background:
- Left ventricular systolic dysfunction triggers neurohormonal activation, leading to progressive ventricular remodeling and heart failure.
- Both symptomatic and asymptomatic patients with left ventricular systolic dysfunction exhibit activation of the renin-angiotensin-aldosterone and sympathetic nervous systems.
- Angiotensin and adrenergic system activation negatively impacts hemodynamics, promotes myocyte hypertrophy and fibroblast growth, and can cause myocyte necrosis and apoptosis.
Purpose of the Study:
- To outline pharmacologic strategies for managing left ventricular systolic dysfunction.
- To emphasize the importance of therapies that prevent ventricular remodeling and improve prognosis.
- To review current treatment options for heart failure.
Main Methods:
- Review of existing studies on pharmacologic interventions for systolic heart failure.
- Analysis of the efficacy of ACE inhibitors, ARBs, digitalis, diuretics, beta-blockers, and spironolactone.
- Consideration of risk factor modification for patients with heart failure secondary to ischemic heart disease.
Main Results:
- ACE inhibitors improve exercise tolerance and decrease treatment failure in symptomatic patients, and reduce mortality.
- Angiotensin II receptor blockers (ARBs) offer similar survival benefits to ACE inhibitors but may be better tolerated.
- Long-term adrenergic inhibition with beta-blockers, combined with ACE inhibitors, attenuates remodeling, improves function, and enhances survival in symptomatic systolic heart failure.
Conclusions:
- Initial pharmacotherapy for systolic heart failure should prioritize maximal tolerated doses of ACE inhibitors or ARBs if ACE inhibitors are not tolerated.
- Diuretics should be used judiciously for symptom relief, not long-term therapy.
- Combination therapy including ACE inhibitors/ARBs, potentially with digoxin, hydralazine/isosorbide dinitrate, diuretics, and spironolactone, alongside risk factor modification, is crucial for managing systolic heart failure and improving patient outcomes.
Abstract:
Left ventricular systolic dysfunction is associated with neurohormonal activation which contributes to progressive ventricular remodeling and worsening clinical heart failure. Renin-angiotensin-aldosterone and sympathetic nervous systems are activated, not only in patients with clinically overt heart failure, but also in patients with asymptomatic or minimally symptomatic left ventricular systolic dysfunction. Activation of the angiotensin and adrenergic systems produces deleterious effects on systemic and coronary hemodynamics, promotes myocyte hypertrophy and fibroblast growth, and myocyte necrosis and apoptosis. Thus, therapy of heart failure should consist of pharmacologic agents not only to relieve symptoms but also to prevent and attenuate ventricular remodeling and progressive heart failure, thereby improving prognosis. In patients who are symptomatic, ACE inhibitors along with digitalis and diuretics as initial therapy (triple therapy) have the greater potential to improve exercise tolerance and decrease the incidence of treatment failure compared with diuretics alone or a combination of diuretics and digitalis. Diuretics alone should not be considered for long-term therapy as plasma renin activity, angiotensin II, aldosterone, norepinephrine and vasopressin levels may increase. ACE inhibitors decrease mortality in patients with heart failure resulting from left ventricular systolic dysfunction. The results of presently available studies indicate that angiotensin II receptor blockers (ARBs) do not provide any advantage over ACE inhibitors regarding survival benefit but may be better tolerated. Long-term adrenergic inhibition with the use of ss-adrenoceptor antagonists added to ACE inhibitors is associated with attenuation of ventricular remodeling, improvement in ventricular function and clinical class and survival of patients with symptomatic systolic left ventricular failure. Thus, initial pharmacotherapy for systolic heart failure should consist of: maximal tolerated dosages of ACE inhibitors;ARBs if ACE inhibitors are not tolerated because of intractable cough or angioedema;adequate dosages of hydralazine and isosorbide dinitrate if ACE inhibitors or ARBs are not tolerated; relatively low dosages of digoxin (serum concentrations of < or = 1.0 ng/dl) if not contraindicated; and diuretics to relieve congestive symptoms. Addition of spironolactone to ACE inhibitors can result in a significant reduction in the risk of sudden death in patients with symptomatic severe heart failure. Myocardial infarction resulting from ischemic heart disease is the most common cause of systolic left ventricular failure and the therapeutic modalities with potential to reduce the risks of myocardial infraction, such as risk factor modification, adequate control of diabetes and hypertension, antiplatelet agents and lipid-lowering agents, should also be included in the initial therapy.
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