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替米沙坦治疗轻中度原发性高血压疗效和安全性观察
引用本文:汪艺,姜蕾. 替米沙坦治疗轻中度原发性高血压疗效和安全性观察[J]. 中国医药, 2008, 3(12): 755-756
作者姓名:汪艺  姜蕾
作者单位:中日友好医院高干医疗科,北京,100029
摘    要:目的观察替米沙坦治疗轻中度原发性高血压病的疗效和安全性。方法采用随机双百平行对照试验的方法将符合条件的轻中度原发性高血压患者66例分为替米沙坦组和培哚普利组各33例,2组分别口服替米沙坦80mg和培哚普利4mg,均1次/d,疗程共8周。结果①治疗8周后,替米沙坦组降压总有效率72.7%,培哚普利组总有效率68.8%,2组差异无统计学意义(P〈0.05)。②治疗前后收缩压、舒张压下降幅度分别为:替米沙坦组11.4%和12.3%,培哚普利组8.9%和11.1%,2组比较无统计学意义(P〉0.05)。③不良反应的发生率,替米沙坦组为3.2%,培哚普利组为15.2%,2组差异有统计学意义(P〈0.05)。结论替米沙坦治疗轻中度原发性高血压安全有效,不良反应发生率低于培哚普利。

关 键 词:高血压病  替米沙坦  培哚普利

Efficacy and safety of telmisartan in patients with mild to moderate essential hypertension
WANG Yi,JIANG Lei. Efficacy and safety of telmisartan in patients with mild to moderate essential hypertension[J]. China Medicine, 2008, 3(12): 755-756
Authors:WANG Yi  JIANG Lei
Affiliation:( Department of Senior Ward, China-Japan Friendship Hospital Beijing 100029, China)
Abstract:Objective To observe the efficacy and safety of telmisartan in patients of essential hypertension.Methods This study was a randomized,double-blind and parallel controlled trial.66 eligible mild and moderate hypertension patients were divided randomly into telmisartan group and perindopril group.80mg of telmisartan or 4mg of perindopril was administrated once per day,and the patients were followed up in every two weeks.This trial was continued for 8 weeks.Results After 8 weeks,the effectiveness of telmisartan and perindopril were 72.7% and 68.8%respectively,showing no significant difference between both groups.After 8 weeks,the SBP and DBP of telmisartan group decreased 11.4%and 12.3%.perindopril group decreased 8.9%and 11.1%.Also no significant difference Was observed.The side effect ratio Was significantly lower in telmisartan group(3.2%)than that in perindopril group(15.2%).The most common side effects were COUgh and mild dizziness.Conclusion Telmisartan (80 mg/d)is effective、safe and well tolerated in treatment of mild to moderate essential hypertension.
Keywords:Hypertension  Telmisartan  Perindopril
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