Efficacy and Safety of a Stepped-Care Regimen Using Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide in Patients with Moderate-to-Severe Hypertension An Open-Label, Long-Term Study

被引:34
|
作者
Volpe, Massimo [1 ,2 ]
Miele, Cristina [3 ]
Haag, Uwe [4 ]
机构
[1] Univ Roma La Sapienza, Fac Med 2, St Andrea Hosp, Rome, Italy
[2] IRCCS Neuromed, Pozzilli, Italy
[3] Univ Roma La Sapienza, Specialty Sch Cardiol, Rome, Italy
[4] HaaPACS GmbH, Schriesheim, Germany
关键词
ANGIOTENSIN-ALDOSTERONE SYSTEM; BLOOD-PRESSURE CONTROL; DOUBLE-BLIND; PLUS AMLODIPINE; PARALLEL-GROUP; ADULT PATIENTS; HIGH-RISK; COMBINATION; TOLERABILITY; MONOTHERAPY;
D O I
10.2165/00044011-200929060-00002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Treatment guidelines recommend combination therapy to control blood pressure (BP) in the majority of hypertensive patients. This long-term open-label study assessed a treatment algorithm based on olmesartan medoxomil (hereafter olmesartan), amlodipine and hydrochlorothiazide (HCTZ). Methods: Patients with moderate-to-severe hypertension who were inadequately controlled with amlodipine 5 mg/day monotherapy and who subsequently completed 16 weeks of double-blind combination treatment with olmesartan and amlodipine entered a 28-week open-label phase in which all patients initially received olmesartan/amlodipine 40/5 mg/day. After 4, 10 and 19 weeks, patients with inadequately controlled hypertension (seated trough diastolic [DBP] and systolic [SBP] BP >= 90 mmHg and >= 140 mmHg, respectively) had their doses increased in a step-wise manner to: (i) olmesartan/amlodipine 40/10 mg; (ii) olmesartan/amlodipine/HCTZ 40/10/12.5 mg; and (iii) olmesartan/amlodipine/HCTZ 40/10/25 mg. Results: In total, 692 patients entered the open-label phase (691 on olmesartan/amlodipine 40/5 mg). The majority of patients remained on olmesartan/amlodipine 40/5 mg without dose elevation, and, of these, 74.3% achieved goal BP at study completion or early termination. Additional patients achieved goal BP with each successive uptitration of therapy: in patients who finished the study on olmesartan/amlodipine 40/10 mg and olmesartan/amlodipine/HCTZ 40/10/12.5 mg, the respective proportions who reached goal BP were 59.0% and 47.1%. Overall, 66.9% of patients achieved the European guideline recommended goal BP of SBP <140 mmHg and DBP <90 mmHg for patients without diabetes mellitus, and SBP <130 mmHg and DBP <80 mmHg for patients with diabetes. Treatment was generally well tolerated, with no unexpected safety concerns. Conclusions: A treatment algorithm based on olmesartan/amlodipine (+/- HCTZ) provides a high degree of BP control in patients with moderate-to-severe hypertension. The open-label study design suggests similar results are obtainable in clinical practice.
引用
收藏
页码:381 / 391
页数:11
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