An approach to heart failure and diabetes mellitus

被引:24
|
作者
Fonarow, GC [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Cardiol, Los Angeles, CA USA
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2005年 / 96卷 / 4A期
关键词
D O I
10.1016/j.amjcard.2005.06.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes mellitus is a chronic progressive disease that results in microvascular and macrovascular complications. Diabetes is a significant independent risk factor for heart failure, and there are a substantial number of patients with diabetes and heart failure. Neurohormonal activation plays an important pathophysiologic role in insulin resistance, diabetes, cardiovascular events, and progression of heart failure. Pharmacologic intervention in these neurohormonal systems (ie, angiotensin-converting enzyme [ACE] inhibition, aldosterone antagonism, and P-adrenergic blockade) has been shown to decrease the morbidity and mortality of diabetes and of heart failure. Despite this knowledge, ACE inhibitors, aldosterone antagonists, and P-blockers are grossly underutilized, and deaths and hospitalizations due. to heart failure have steadily increased. Guidelines for the management of heart failure recommend the use of ACE inhibitors and P-blockers in patients with mild, moderate, and severe heart failure with or without diabetes. Aldosterone antagonists are recommended in severe heart failure and recent data also support their use in mild to moderate heart failure. Concerns about increased incidence of hypoglycemia, worsening dyslipidemia, and decreased insulin sensitivity with P-blockers may be preventing physicians from prescribing these agents for their patients with diabetes who have heart failure. P-Blockade, in conjunction with ACE inhibition and aldosterone antagonism, should be standard therapy for all patients with diabetes and heart failure. Furthermore, every effort should be made to ensure that eligible patients are treated with these evidence-based, guideline-recommended, life-prolonging therapies. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:47E / 52E
页数:6
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