atenolol in hypertension: a symposium
TRANSCRIPT
ATENOlOllN HYPERTENSION: A SYMPOSIUM
In a Symposium held by Stuart Pharmaceuticals at the Royal Society of Medicine, 25-26 January 1977, aspects of the treatment of hypertension, with particular reference to atenolol, were discussed. Atenolol is a cardioselective beta-blocking drug which has no membrane stabilising or partial agonist activity. In tests of its relative cardioselectivity in 14 patients with asthma, a single dose of I OOmg of atenolol produc;ed less bronchoconstriction than propranolol I OOmg, pindolol 5 mg or acebutolol 300mg. Both atenolol and acebutolol permitted a bronchodilator response to inhaled isoprenaline (isoproterenol) but propranolol and pindolol blocked such a response. In dose-finding studies in hypertensive patients, I OOmg given once daily appeared to provide good control of blood pressure, similar to that achieved with multiple daily doses, along with a low incidence of adverse effects.
o Compared with Placebo when Added to Existing Regimens In a double-blind crossover study in 51 patients with hypertenSion, atenolol I OOmg once daily or a placebo were added to existing antihypertensive regimens for 4 weeks each, followed by atenolol administered to all patients for 8 weeks. The mean initial blood pressure was 180/ I 07mm Hg. After 4 weeks with a placebo added to the existing treatment this fell to 171/ I OOmm Hg, while the corresponding value with atenolol was 161/91 mm Hg (a significant difference compared with placebo; p < 0.00 I). While a placebo had no effect on heart rate, atenolol produced a mean decrease of 12 beats per minute. Some minor side-effects occurred with atenolol, but the incidence was not statistically greater than with a placebo. 'It is therefore concluded that, where inadequately controlled hypertensives are under consideration, the addition of 100mg of atenolol once a day is a logical next step.'
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