Carvedilol - A reappraisal of its pharmacological properties and therapeutic use in cardiovascular disorders

被引:87
作者
Dunn, CJ [1 ]
Lea, AP [1 ]
Wagstaff, AJ [1 ]
机构
[1] ADIS INT LTD, AUCKLAND 10, NEW ZEALAND
关键词
D O I
10.2165/00003495-199754010-00015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Carvedilol competitively blocks beta 1, beta 2 and alpha 1 receptors. The drug lacks sympathomimetic activity and has vasodilating properties that are exerted primarily through alpha(1)-blockade. Animal models indicate that carvedilol confers protection against myocardial necrosis, arrhythmia and cell damage caused by oxidising free radicals, and the drug has no adverse effects on plasma lipid profiles. Recent data have confirmed the antihypertensive efficacy of carvedilol in patients with mild to moderate essential hypertension. Carvedilol has similar efficacy to other beta-blocking agents, calcium antagonist, ACE inhibitors and hydrochlorothiazide. Carvedilol also improves exercise tolerance and ischaemic symptoms in patients with stable angina pectoris. Significant reductions in serious cardiac events after acute myocardial infarction and infrequency and severity of ischaemic events in patients with unstable angina have also been demonstrated. Interest in the use of carvedilol in patients with congestive heart failure (CHF) has culminated in the publication of a cumulative analysis of data from 1094 patients with mild to severe CHF who participated in the US Carvedilol Heart Failure Study Program (4 trials). After a median follow-up of 6.5 months, a significant overall reduction in mortality relative to placebo (3.2 vs 7.8%) was revealed in patients who had received carvedilol 6.25 to 50 mg twice daily (plus diuretics and ACE inhibitors). All-cause mortality, risk of hospitalisation for cardiovascular reasons and hospitialisation costs were also reduced significantly (by 65, 28% and 62%, respectively) in these trials. In addition, the Australia and New Zealand Heart Failure Research Collaborative Group showed a 26% reduction in the combined risk of death or hospitalisation with carvedilol 12.5 to 50 mg/day relative to placebo after a mean 19-month follow-up period in 415 patients with CHF (relarive risk 0.74). Adverse events with carvedilol appear to be less frequent than with other beta-blocking agents, are dosage-related and are usually seen early in therapy. Events most commonly reported are related to the vasodilating (postural hypotension, dizziness and headaches) and the beta-blocking (dyspnoea, bronchospasm, bradycardia, malaise and asthenia) properties of the drug. Carvedilol appears to data to have little effect on the incidence of worsening heart failure. Concomitant administration of carvedilol with some medications requires monitoring. Carvedilol is therefore likely to have a beneficial role in the management of controlled CHF, but further clinical studies are required to show the place of beta-adrenoceptor blocking therapy in general in this indication, and the position of carvedilol relative to other similar agents. Carvedilol is also confirmed as effective in the management of mild to moderate hypertension and ischaemic heart disease.
引用
收藏
页码:161 / 185
页数:25
相关论文
共 179 条
[1]  
ABSHAGEN U, 1987, Journal of Cardiovascular Pharmacology, V10, pS23, DOI 10.1097/00005344-198706111-00005
[2]  
Agrawal B, 1996, J HUM HYPERTENS, V10, P551
[3]  
AGRAWAL B, 1995, CAN J CARDIOL SD, V11, pD62
[4]  
Ajima H, 1990, Rinsho Yakuri/Jpn J Clin Pharmacol Ther, V21, DOI [10.3999/jscpt.21.391, DOI 10.3999/JSCPT.21.391]
[5]   COMPARISON OF THE EFFECTS OF CARVEDILOL AND NIFEDIPINE IN PATIENTS WITH ESSENTIAL-HYPERTENSION AND NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
ALBERGATI, F ;
PATERNO, E ;
VENUTI, RP ;
BOERI, D ;
LOMBARDO, I ;
SEMINO, S ;
VIVIANI, GL ;
ADEZATI, L .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1992, 19 :S86-S89
[6]   EFFECTS OF ISCHEMIA AND REPERFUSION ON CARDIAC TOLERANCE TO OXIDATIVE STRESS [J].
AMBROSIO, G ;
SANTORO, G ;
TRITTO, I ;
ELIA, PP ;
DUILIO, C ;
BASSO, A ;
SCOGNAMIGLIO, A ;
CHIARIELLO, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (01) :H23-H30
[7]   PHARMACOLOGICAL CHARACTERISTICS OF THE STEREOISOMERS OF CARVEDILOL [J].
BARTSCH, W ;
SPONER, G ;
STREIN, K ;
MULLERBECKMANN, B ;
KLING, L ;
BOHM, E ;
MARTIN, U ;
BORBE, HO .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 38 :S104-S107
[8]  
BASU S, 1995, CIRCULATION, V92, P91
[9]  
BEERMANN C, 1992, CLIN INVESTIGATOR, V70, pS13
[10]  
*BOEHR MANNH GMBH, 1991, CARV PRESCR INF