坎地沙坦西莱地酯实现高质量的24小时血压控制。

Blood pressure. Supplement Pub Date : 2000-01-01
P Meredith
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引用次数: 0

摘要

流行病学证据表明,最佳的血压控制需要在24小时内持续和完全降低血压的策略。为了最大限度地提高依从性,抗高血压药物也需要具有良好的耐受性,并且在方便的每日一次剂量下有效。新型血管紧张素II型1 (AT1)受体阻滞剂坎地沙坦与AT1受体紧密结合并缓慢解离,从而对肾素-血管紧张素系统提供持久的抑制作用。这很可能解释了其明显的降压效果,在24小时内保持平稳。谷峰比是测量给药间隔结束时降压效果持久性的有用指标。该比率接近于坎地沙坦西列地酯8和16毫克的理想比率1.0,而原型at1受体阻滞剂氯沙坦50毫克的理想比率为0.7。通过给药后0-36小时的动态血压测量和48小时的临床测量,16毫克坎地沙坦西列地尔的降压作用也明显大于100毫克氯沙坦。坎地沙坦西列地尔通过控制血压远远超过正常给药间隔,即使对那些偶尔可能错过给药间隔的患者也能提供心血管保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Achieving quality 24-h blood pressure control with candesartan cilexetil.

Epidemiological evidence suggests that optimal blood pressure control requires strategies that lower blood pressure consistently and fully throughout 24 h. In order to maximize compliance, antihypertensive agents also need to be well tolerated and effective when administered at a convenient once-daily dose. The new angiotensin II type 1 (AT1) receptor blocker candesartan binds tightly to, and dissociates slowly from, the AT1-receptor and thereby provides long-lasting suppression of the renin-angiotensin system. This is likely to explain its pronounced antihypertensive efficacy, which is maintained smoothly over 24 h. The trough-to-peak ratio is a useful measure of the persistence of antihypertensive efficacy at the end of the dosing interval. This ratio was found to be close to the ideal of 1.0 for candesartan cilexetil, 8 and 16 mg, whereas it was 0.7 for the prototype AT1-receptor blocker losartan, 50 mg. The antihypertensive effect of candesartan cilexetil, 16 mg, was also significantly greater than that of losartan, 100 mg, as demonstrated by ambulatory blood pressure measurements 0-36 h after dosing and by clinic measurements 48 h after dosing. By controlling blood pressure well beyond the normal dosing interval, candesartan cilexetil provides cardiovascular protection even in those patients who may occasionally miss doses.

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