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, PSubject(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