| Autor: |
Veur, E., Berge, B. S., Donker, A. J. M., May, J. F., Schuurman, F. H., Wesseling, H. |
| Zdroj: |
European Journal of Clinical Pharmacology; September 1985, Vol. 28 Issue: 5 p507-511, 5p |
| Abstrakt: |
After screening two local populations in the northern part of The Netherlands for hypertension, patients with a diastolic pressure (DP) between 95 and 120 mmHg were treated daily either with 50 mg hydrochlorothiazide or 100 mg atenolol. Non-responders were given the combination and if necessary the dose of atenolol was increased to 200 mg. Non-responders to the latter combination were randomized and treated either with 50 mg hydrochlorothiazide and labetalol or with 50 mg hydrochlorothiazide, 200 mg atenolol and prazosin. If after 1 month a DP=90 mmHg had been reached the patient was reassessed after a further 3 months. If a DP>90 mmHg was found the dose of labetalol or prazosin was increased and the patient was re-examined after 1 month. |
| Databáze: |
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| Externí odkaz: |
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