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J Hum Hypertens ; 24(2): 93-103, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19458624

ABSTRACT

Most patients inadvertently miss an occasional dose of antihypertensive therapy, and hence drugs that provide sustained blood-pressure (BP) reduction beyond the 24-h dosing interval are desirable. The primary objective of this study was to compare the 24-h mean ambulatory BP reductions from baseline after a simulated missed dose of the direct renin inhibitor aliskiren, irbesartan or ramipril. In this double-blind study, 654 hypertensive patients (24-h mean ambulatory diastolic BP (MADBP) >or=85 mm Hg) were randomized 1:1:1 to once-daily aliskiren 150 mg, irbesartan 150 mg or ramipril 5 mg. Doses were doubled after 2 weeks. At day 42, patients were again randomized equally within each group to receive 1 day of placebo ('missed dose') on either day 42 or day 49. Patients with a successful 24-h ambulatory BP measurement at baseline and on day 42/49 were included in the analyses. The 24-h mean ambulatory systolic BP (MASBP)/MADBP reductions from baseline after a missed dose of aliskiren 300 mg (9.3/7.0 mm Hg) were similar to irbesartan 300 mg (9.5/7.3 mm Hg) and significantly larger than ramipril 10 mg (7.1/5.0 mm Hg, P

Subject(s)
Amides/administration & dosage , Angiotensin II Type 1 Receptor Blockers/administration & dosage , Angiotensin-Converting Enzyme Inhibitors/administration & dosage , Antihypertensive Agents/administration & dosage , Biphenyl Compounds/administration & dosage , Blood Pressure/drug effects , Fumarates/administration & dosage , Hypertension/drug therapy , Medication Adherence , Ramipril/administration & dosage , Tetrazoles/administration & dosage , Adult , Aged , Amides/adverse effects , Angiotensin II Type 1 Receptor Blockers/adverse effects , Angiotensin-Converting Enzyme Inhibitors/adverse effects , Antihypertensive Agents/adverse effects , Biphenyl Compounds/adverse effects , Blood Pressure Monitoring, Ambulatory , Brazil , Canada , Double-Blind Method , Drug Administration Schedule , Europe , Female , Fumarates/adverse effects , Humans , Hypertension/physiopathology , Irbesartan , Male , Middle Aged , Ramipril/adverse effects , Tetrazoles/adverse effects , Time Factors , Treatment Outcome
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