A rationale for the use of β-blockers as standard treatment for heart failure

被引:54
作者
Metra, M [1 ]
Nodari, S [1 ]
D'Aloia, A [1 ]
Bontempi, L [1 ]
Boldi, E [1 ]
Dei Cas, L [1 ]
机构
[1] Univ Brescia, Cattedra Cardiol, I-25100 Brescia, Italy
关键词
D O I
10.1016/S0002-8703(00)90096-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Cardiac sympathetic activation is one of the major and earlier changes observed in patients with heart failure. Its relation to the severity of the disease and its independent prognostic value show that it may directly contribute to the progression of heart failure. beta-Blockers are the most effective tool to counteract the untoward effects of sympathetic activation on the cardiovascular system. Methods and Results We reviewed the results of the placebo-controlled, double-blind studies about the effects of beta-blockers in patients with heart failure. These studies have involved almost 10,000 patients to date and have consistently shown that the long-term administration of beta-blockers is associated with a highly significant improvement in both left ventricular Function and prognosis of the patients with heart failure. The evidence supporting the use of beta-blockers now equals or even surpasses that of angiotensin-converting enzyme inhibitors; therefore pblockers should be considered port of standard therapy. Issues that remain unclarified include the mechanisms through which beta-blockers may improve cardiac function and their tolerability and efficacy in specific groups of patients (such as those with asymptomatic left ventricular dysfunction, severe heart failure, the elderly, or those with left ventricular diastolic dysfunction). It is not currently clear whether the pharmacologic differences between individual beta-blockers are clinically relevant. If they are, the potential for even greater benefit with certain agents exists. It is hoped that these issues will be clarified by the results of ongoing multicenter trials.
引用
收藏
页码:511 / 521
页数:11
相关论文
共 50 条
[1]  
ABRAHAM WT, 1998, CIRCULATION S1, V98
[2]  
ANDERSON JL, 1995, AM J CARDIOL, V75, P1220
[3]   LONG-TERM (2-YEAR) BENEFICIAL-EFFECTS OF BETA-ADRENERGIC-BLOCKADE WITH BUCINDOLOL IN PATIENTS WITH IDIOPATHIC DILATED CARDIOMYOPATHY [J].
ANDERSON, JL ;
GILBERT, EM ;
OCONNELL, JB ;
RENLUND, D ;
YANOWITZ, F ;
MURRAY, M ;
ROSKELLEY, M ;
MEALEY, P ;
VOLKMAN, K ;
DEITCHMAN, D ;
BRISTOW, M .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1991, 17 (06) :1373-1381
[4]  
Basu S, 1997, CIRCULATION, V96, P183
[5]   beta(2)-Adrenergic receptor antagonists protect against ventricular fibrillation - In vivo and in vitro evidence for enhanced sensitivity to beta(2)-adrenergic stimulation in animals susceptible to sudden death [J].
Billman, GE ;
Castillo, LC ;
Hensley, J ;
Hohl, CM ;
Altschuld, RA .
CIRCULATION, 1997, 96 (06) :1914-1922
[6]   Carvedilol produces dose-related improvements in left ventricular function and survival in subjects with chronic heart failure [J].
Bristow, MR ;
Gilbert, EM ;
Abraham, WT ;
Adams, KF ;
Fowler, MB ;
Hershberger, RE ;
Kubo, SH ;
Narahara, KA ;
Ingersoll, H ;
Krueger, S ;
Young, S ;
Shusterman, N .
CIRCULATION, 1996, 94 (11) :2807-2816
[7]   Mechanism of action of beta-blocking agents in heart failure [J].
Bristow, MR .
AMERICAN JOURNAL OF CARDIOLOGY, 1997, 80 (11A) :L26-L40
[8]   DOSE-RESPONSE OF CHRONIC BETA-BLOCKER TREATMENT IN HEART-FAILURE FROM EITHER IDIOPATHIC DILATED OR ISCHEMIC CARDIOMYOPATHY [J].
BRISTOW, MR ;
OCONNELL, JB ;
GILBERT, EM ;
FRENCH, WJ ;
LEATHERMAN, G ;
KANTROWITZ, NE ;
ORIE, J ;
SMUCKER, ML ;
MARSHALL, G ;
KELLY, P ;
DEITCHMAN, D ;
ANDERSON, JL .
CIRCULATION, 1994, 89 (04) :1632-1642
[9]  
Bristow MR, 1997, CIRCULATION, V96, pI
[10]  
BRISTOW MR, 1998, LANCET S1, V352, pS18