摘要
A direct switch of candesartan to the fixed-dose combination olmesartan/amlodipine in uncontrolled hypertension is a frequent clinical requirement but is not covered by current labeling. An open-label, prospective, single-arm phase IIIb study was performed in patients with 32mg candesartan followed by olmesartan/amlodipine 40/10mg. The primary endpoint was change in mean daytime systolic blood pressure (BP). Mean daytime systolic BP was reduced by 9.2 +/- 12.6mmHg (P<.0001) after substituting candesartan for olmesartan/amlodipine (baseline BP 140.2 +/- 9.7mmHg). The reduction in office BP was 9.4 +/- 18.4/4.0 +/- 9.6mmHg; P<.002). Overall, 61.3% of patients achieved a target BP <140/90mmHg using office BP and <135/85mmHg using ambulatory BP measurement. There were 8 adverse events with a possible relation to study drug and 1 unrelated serious adverse events. In conclusion, patients with uncontrolled moderate arterial hypertension being treated using candesartan monotherapy achieve a further reduction of BP when switched directly to a fixed-dose combination of olmesartan 40mg/amlodipine 10mg.
- 出版日期2013-11
- 单位河北医科大学