Literature DB >> 2442547

Angiotensin-converting enzyme inhibitors in essential hypertension.

A Zanchetti.   

Abstract

At the Cambridge Conference, the pros and cons of various classes of antihypertensive drugs were extensively discussed, including the place of angiotensin-converting enzyme inhibitors in today's spectrum. A consensus was easily reached that the most important advantage of having the present broad armamentarium of antihypertensive drugs is that a wide choice is now available from which to find the most suitable agent for the individual patient. A revised stepped-care design was proposed, in which the doctor has the choice of starting antihypertensive therapy with a thiazide diuretic, a beta-blocker, an angiotensin-converting enzyme inhibitor, or a calcium antagonist. Small doses of any agent should be used to start with, and doses should not subsequently be increased beyond that at which side effects appear. Should such symptoms occur, the doctor has the choice of either switching to another first-step compound or reducing the dose of the first agent and combining it with one of other available drugs.

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Year:  1987        PMID: 2442547     DOI: 10.1097/00005344-198700003-00002

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol        ISSN: 0160-2446            Impact factor:   3.105


  3 in total

1.  Tolerability of long term therapy with enalapril maleate in patients resistant to other therapies and intolerant to captopril.

Authors:  E J Rucinska; R Small; W S Mulcahy; D L Snyder; P V Rodel; J E Rush; R D Smith; J F Walker; J D Irvin
Journal:  Med Toxicol Adverse Drug Exp       Date:  1989 Mar-Apr

2.  Haemodynamic and hormonal effects of cilazapril in comparison with propranolol in healthy subjects and in hypertensive patients.

Authors:  C H Kleinbloesem; K Erb; J Essig; K Breithaupt; G G Belz
Journal:  Br J Clin Pharmacol       Date:  1989       Impact factor: 4.335

3.  Pharmacokinetic and pharmacodynamic interactions between the ACE inhibitor cilazapril and beta-adrenoceptor antagonist propranolol in healthy subjects and in hypertensive patients.

Authors:  G G Belz; J Essig; K Erb; K Breithaupt; J F Hoogkamer; J Kneer; C H Kleinbloesem
Journal:  Br J Clin Pharmacol       Date:  1989       Impact factor: 4.335

  3 in total

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