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作 者:谢爽[1,2] 明广华 蒋文 朱兴雷[3] 黎莉[4] 郝玉明[5] 华潞[2] 娄莹[1] 陈国良[1] 刘立伟[1] 李一石[2]
机构地区:[1]北京协和医学院,北京100730 [2]中国医学科学院,北京协和医学院阜外心血管病医院临床药理中心,卫生部心血管药物临床研究重点实验室 [3]山东省立医院,北京100037 [4]山东大学齐鲁医院,济南250021 [5]河北医科大学第二医院,济南250012
出 处:《中国临床药理学杂志》2009年第5期387-390,共4页The Chinese Journal of Clinical Pharmacology
摘 要:目的评价奥美沙坦酯与缬沙坦(均为抗高血压药,血管紧张素Ⅱ受体拮抗剂)治疗轻中度原发性高血压的疗效和安全性比较。方法入选240例轻、中度原发性高血压患者,按照1∶1随机分组,分别接受奥美沙坦酯20~40mg·d-1或缬沙坦80~160mg·d-1治疗,共8周。结果治疗4周后,奥美沙坦酯组与缬沙坦组SeDBP平均下降(10.58±6.82)mmHg及(9.38±7.16)mmHg;奥美沙坦组与缬沙坦组分别有60%及61.74%患者剂量加倍,加量有效率分别为52.22%及51.85%。治疗8周后,2组SeDBP平均下降(15.72±6.03)mmHg及(14.12±6.79)mmHg。治疗4周后,奥美沙坦酯组与缬沙坦组的药物不良反应发生率分别为3.33%及7.5%(P>0.05)。结论每日1次口服奥美沙坦酯胶囊20~40mg·d-1,能24h平稳降压,其8周总有效率79.65%;与缬沙坦80~160mg.d-1的降压疗效相近。2组药物不良反应发生率无显著差异。Objective To evaluate the efficacy and safety of olmesartan medoxomil compared with valsartan in patients with mild to moderate essential hypertension. Methods A total 240 eligible subjects were randomized at 1∶1 ratio to receive olmesartan medoxomil 20-40 mg or valsartan 80-160 mg,once daily for 8 weeks. Results The mean trough reduction in SeDBP from baseline was no difference between olmesartan medoxomil and valsartan groups after 4 weeks [(10.58±6.82) mmHg vs (9.38±7.16) mmHg,P〉0.05] and 8 weeks weeks treatment [( 15.72 ± 6. 03) mmHg vs (14.12 ± 6.79) mmHg,P〉0.05]. After 4 weeks treatment, the patients with double dose in olmesartan and valsartan group were 60% and 61.74%, the double dose efficiency were 52.22% and 51.85% respectively( P 〉 0.05 ). The incidence of study drug-related adverse event (AE) in olmesartan group (3.33%) was similar to that in valsartan group (7.5%, P 〉0. 05). No SAE was occurred. Conclusion Olmesartan medoxomil at oral dase of 20 - 40 mg once daily was effective and safe for hypertension treatment and effect was similar to valsartan 80 - 160 mg once daily.
分 类 号:R544.1[医药卫生—心血管疾病] R972.4[医药卫生—内科学]
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