Title of article
Are there benefits to specific antihypertensive drug therapy?
Author/Authors
William C. Cushman، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2003
Pages
5
From page
31
To page
35
Abstract
Abstract
The antihypertensive drug classes that have reduced cardiovascular events safely either in large placebo-controlled trials or in comparison with other effective antihypertensive drugs in large morbidity trials are diuretics, β-blockers, angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), and calcium channel blockers (CCBs). Although control of blood pressure (BP) is a primary goal of therapy, evidence from several clinical trials suggests that certain antihypertensive agents provide clinical benefits independent of their effect on BP. In the recently reported Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT), an ACE inhibitor, a CCB, and an α-blocker reduced coronary events and mortality to a similar extent as a thiazide-type diuretic, but the diuretic reduced one or more major cardiovascular events, especially heart failure, more than the other agents. In the Losartan Intervention For Endpoint reduction in hypertension (LIFE) trial, the ARB losartan reduced cardiovascular morbidity (primarily stroke) more than the β-blocker atenolol. Although an ARB has not yet been compared with a diuretic in a morbidity trial, as most patients require more than one drug to control BP, and a diuretic plus an ARB is a very effective and well-tolerated combination, this uncertainty applies to a minority of patients. A primary goal in treating hypertension should be to reach a patientʹs goal BP, but initial selection of drugs based on hypertension morbidity study results and other compelling indications should be given priority.
Keywords
diuretics , Renin-angiotensin system. , Blood pressure , antihypertensiveagents , hypertension
Journal title
American Journal of Hypertension
Serial Year
2003
Journal title
American Journal of Hypertension
Record number
648672
Link To Document