Achieving blood pressure goals: should angiotensin II receptor blockers become first-line treatment in hypertension?

Michael Weber
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引用次数: 9

Abstract

The benefits of blood pressure control on the risks of major cardiovascular events are well established. In clinical trials conducted in patients with mild-to-moderate hypertension, the angiotensin II receptor blocker (ARB) telmisartan has been shown to provide reduction of blood pressure throughout the 24-h dosing interval. Clinical trials have also demonstrated that ARBs are effective agents in reducing the risk of cardiovascular mortality, stroke, heart failure and new-onset atrial fibrillation. Recently, the ONgoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial (ONTARGET) study established that telmisartan reduces morbidity and mortality in a broad cross-section of patients at high risk for heart and vascular events, to an extent similar to that of the angiotensin-converting enzyme inhibitor ramipril. In addition, ONTARGET demonstrated that telmisartan is somewhat better tolerated than ramipril. Attributes such as effective blood pressure lowering, tolerability and convincing outcomes data mean that ARBs satisfy the requirements for first-line antihypertensive agents.

实现降压目标:血管紧张素受体阻滞剂是否应成为高血压的一线治疗?
控制血压对主要心血管事件风险的益处已得到充分证实。在对轻中度高血压患者进行的临床试验中,血管紧张素II受体阻滞剂(ARB)替米沙坦已被证明可以在24小时给药间隔内降低血压。临床试验也表明,arb是降低心血管死亡、中风、心力衰竭和新发心房颤动风险的有效药物。最近,正在进行的替米沙坦单独和联合雷米普利全球终点试验(ONTARGET)研究证实,替米沙坦在广泛的心脏和血管事件高风险患者中降低了发病率和死亡率,其程度与血管紧张素转换酶抑制剂雷米普利相似。此外,ONTARGET表明替米沙坦的耐受性比雷米普利更好。有效降压、耐受性和令人信服的结局数据等属性意味着arb满足一线降压药的要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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