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首页> 外文期刊>Journal of International Medical Research >Acebutolol: Efficacy and Acceptability in the Treatment of Essential Hypertension over 22 Months
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Acebutolol: Efficacy and Acceptability in the Treatment of Essential Hypertension over 22 Months

机译:醋丁洛尔:22个月内治疗原发性高血压的疗效和可接受性

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Thirty-three patients were admitted to a 22-month study of acebutolol in the treatment of essential hypertension. Four patients were withdrawn, but only two of them for reasons attributable to the treatment. Twenty-nine patients completed the study, the dose of acebutolol ranging from 400 to 1200 mg/day divided into morning and evening doses. Twenty-four also received diuretics. Although twenty patients had been receiving antihypertensive medication up to the start of the trial, mean systolic and diastolic blood pressures fell significantly by 16% and 15%, respectively, in the first 6 months, and by 20% and 14% at 22 months. Most patients achieved falls to less than 150/90 mm Hg or falls exceeding 20 mm systolic and 10 mm diastolic in at least 2 out of the 3 assessments at 6, 12 and 22 months. The treatment was well tolerated except by the two patients who were withdrawn due to side-effects.
机译:33例患者接受了为期22个月的醋丁洛尔治疗原发性高血压的研究。四名患者退出了治疗,但其中只有两名是由于治疗原因。 29名患者完成了研究,醋丁洛尔的剂量范围为400至1200 mg /天,分为早,晚剂量。二十四也接受了利尿剂。尽管直到试验开始时已有20名患者接受了降压药治疗,但在开始的6个月中平均收缩压和舒张压分别显着下降了16%和15%,在22个月时分别下降了20%和14%。在6、12和22个月的3项评估中,至少有2例的大多数患者跌落至小于150/90 mm Hg或跌落超过20 mm收缩压和10 mm舒张压。除两名因副作用而退出治疗的患者外,治疗耐受性良好。

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