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Bevantolol vs Propranolol: A Double-Blind Controlled Trial in Essential Hypertension
Derek Maclean
Derek Maclean
Clinical Pharmacology Ninewells Hospital & Medical School Dundee DDI 9SY, Scotland
Bevantolol is a novel ß 1-selective beta-adrenoceptor antagonist. The Study Group evaluated its therapeutic utility (100-300 mg bid) compared with pro pranolol (80-240 mg bid) in 266 patients with mild to moderate essential hyper tension (WHO Grades I and II, sitting diastolic blood pressure (DBP) 95 mmHg). There was no difference in their antihypertensive efficacy over six months, 77% being controlled (DBP 90 mmHg) on bevantolol and 81 % on propranolol. Hydrochlorothiazide 25-50 mg bid added later improved BP con trol in those incompletely controlled on bevantolol monotherapy. Both ß- adrenoceptor antagonists also reduced intraocular pressure. Bevantolol caused significantly fewer adverse effects than propranolol with many fewer with drawals during long-term therapy. This unique clinical pharmacologic profile of bevantolol enhances its therapeutic usefulness and may relate to alpha-adreno ceptor antagonist activity, as well as to its ß1-selectivity.
Angiology, Vol. 39, No. 6,
487-496 (1988)
DOI: 10.1177/000331978803900601

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