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1.	Mancini, G. B. J., et al. (författare) Pharmacologic Options for the Management of Systolic Heart Failure: Examining Underlying Mechanisms 2015 Ingår i: Canadian Journal of Cardiology. - : Pulsus Group Inc.. - 0828-282X. ; 31:10, s. 1282-1292 Forskningsöversikt (refereegranskat)abstract The optimal management of systolic heart failure includes combination therapy to influence myocardial remodelling favourably by affecting neurohormonal activation and underlying maladaptive pathophysiological pathways. These medications include modulators of the renin-angiotensin-aldosterone system (eg, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, mineralocorticoid receptor antagonists) and β-adrenergic receptor blockers. In addition, an agent with a distinct and complementary mechanism of bradycardic action, the selective pacemaker-current (If) inhibitor ivabradine, provides further reduction of heart rate. Also, a new drug that incorporates neprilysin inhibition combined with angiotensin receptor blockade shows incremental effectiveness. The primary goal of this review is to provide a mechanistic explanation of the complementary role of therapeutic interventions in modulating pathways leading to progressive systolic heart failure. A secondary goal is to summarize the key findings of the pivotal clinical trials that have demonstrated the efficacy of these agents in this population. © 2015 Canadian Cardiovascular Society.

Mancini, G. B. J., et al. (författare)
Pharmacologic Options for the Management of Systolic Heart Failure: Examining Underlying Mechanisms
2015
Ingår i: Canadian Journal of Cardiology. - : Pulsus Group Inc.. - 0828-282X. ; 31:10, s. 1282-1292
Forskningsöversikt (refereegranskat)abstract
- The optimal management of systolic heart failure includes combination therapy to influence myocardial remodelling favourably by affecting neurohormonal activation and underlying maladaptive pathophysiological pathways. These medications include modulators of the renin-angiotensin-aldosterone system (eg, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, mineralocorticoid receptor antagonists) and β-adrenergic receptor blockers. In addition, an agent with a distinct and complementary mechanism of bradycardic action, the selective pacemaker-current (If) inhibitor ivabradine, provides further reduction of heart rate. Also, a new drug that incorporates neprilysin inhibition combined with angiotensin receptor blockade shows incremental effectiveness. The primary goal of this review is to provide a mechanistic explanation of the complementary role of therapeutic interventions in modulating pathways leading to progressive systolic heart failure. A secondary goal is to summarize the key findings of the pivotal clinical trials that have demonstrated the efficacy of these agents in this population. © 2015 Canadian Cardiovascular Society.

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