Volpe Massimo, Miele Cristina, Haag Uwe
Specialty School of Cardiology, University of Rome 'La Sapienza', Rome, Italy.
Clin Drug Investig. 2009;29(6):381-91. doi: 10.2165/00044011-200929060-00002.
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).
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.
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.
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.
治疗指南建议大多数高血压患者采用联合治疗来控制血压(BP)。这项长期开放标签研究评估了一种基于奥美沙坦酯(以下简称奥美沙坦)、氨氯地平和氢氯噻嗪(HCTZ)的治疗方案。
中度至重度高血压患者,接受氨氯地平5mg/天单药治疗血压控制不佳,随后完成16周奥美沙坦与氨氯地平双盲联合治疗后,进入为期28周的开放标签阶段,所有患者最初接受奥美沙坦/氨氯地平40/5mg/天治疗。在4周、10周和19周后,血压控制不佳的高血压患者(坐位谷值舒张压[DBP]和收缩压[SBP]分别≥90mmHg和≥140mmHg)的剂量逐步增加至:(i)奥美沙坦/氨氯地平40/10mg;(ii)奥美沙坦/氨氯地平/氢氯噻嗪40/10/12.5mg;(iii)奥美沙坦/氨氯地平/氢氯噻嗪40/10/25mg。
共有692例患者进入开放标签阶段(691例接受奥美沙坦/氨氯地平40/5mg治疗)。大多数患者维持奥美沙坦/氨氯地平40/5mg治疗且未增加剂量,其中74.3%的患者在研究完成或提前终止时达到目标血压。随着治疗的逐步增加剂量,更多患者达到目标血压:在完成奥美沙坦/氨氯地平40/10mg和奥美沙坦/氨氯地平/氢氯噻嗪40/10/12.5mg治疗的患者中,达到目标血压的比例分别为59.0%和47.1%。总体而言,对于非糖尿病患者,66.9%的患者达到欧洲指南推荐的目标血压,即收缩压<140mmHg和舒张压<90mmHg;对于糖尿病患者,收缩压<130mmHg和舒张压<80mmHg。治疗总体耐受性良好,未出现意外的安全问题。
基于奥美沙坦/氨氯地平(±氢氯噻嗪)的治疗方案能使中度至重度高血压患者的血压得到高度控制。开放标签研究设计表明,在临床实践中可获得类似结果。