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引用次数: 16

摘要

阻断肾素-血管紧张素系统(RAS)已成为治疗心血管风险增加患者不可或缺的组成部分。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)研究了23400名高危心血管患者,并比较了替米沙坦和雷米普利的有效性,结果表明两种药物“治疗等效”。替米沙坦是目前唯一一种具有与雷米普利相当的心血管保护临床试验证据的血管紧张素II受体阻滞剂,雷米普利被广泛认为是心血管风险增加患者RAS阻断的“参考”药物。尽管先前排除了对血管紧张素转换酶抑制剂药物不耐受的患者,但替米沙坦组中停药的患者较少,因此替米沙坦具有优越的总体疗效/耐受性比。
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Focus on the ONTARGET results.

Blockade of the renin-angiotensin system (RAS) has become an integral component of the treatment of patients at increased cardiovascular risk. The ONgoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial (ONTARGET) studied 23 400 high-risk cardiovascular patients and compared the effectiveness of telmisartan with that of ramipril and showed that the two drugs were 'therapeutically equivalent'. Telmisartan is now the only angiotensin II blocker with clinical trial evidence of cardiovascular protection equivalent to that of ramipril, which is widely regarded as the 'reference' drug for RAS blockade in patients at increased cardiovascular risk. Despite the prior exclusion of patients intolerant of angiotensin-converting enzyme inhibitors drugs, there were fewer discontinuations in the telmisartan group, and so telmisartan had a superior overall efficacy/tolerability ratio.

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