摘要
目的观察坎地沙坦酯片治疗l、2级原发性高血压的临床疗效及其安全性。方法将47例1-2级高血压病人随机分为坎地沙坦酯治疗组(23例)和依那普利对照组(24例),分别给予坎地沙坦4—16mg和依那普利5—20mg,每日1次。每两周测血压一次,如舒张压仍t〉90mmHg,则剂量加倍。进行8周的临床观察。结果两组病人血压均有明显下降(P〈0.01),坎地沙坦酯组的总有效率为82.6%,依那普利组的总有效率为87.5%,两组间未见明显差异(P〉0.05),而坎地沙坦酯治疗组的不良反应较依那普利组要显著减少(P〈0.05)。结论坎地沙坦酯治疗原发性高血压疗效显著,不良反应少,安全有效。
Aim To investigate the clinical efficacy and security of candesartan cilexetil tablets in treatment of 1 - 2 grade essential hypertension. Method 47 patients with 1 - 2 grade essential hypertension were randomly divided into the candesartan cilexetil treatment group (23 cases)and the enalapril control group (24 cases). They were respectively given candesartan cilexetil tablets 4 - 16 mg and enalapril maleate tablets 5 - 20 mg once a day, the blood pressure measured every two weeks. If the patients' diastolic blood pressure 90mmHg,the dose would be doubled. Clinical observation had been carried out for 8 weeks. Result The blood pressures of two groups of patients were both obviously descended( P 〈0.01 ). The total effective rate in candesartan group was 82.6% and that in enalapril group was 87.5%. There was no significant difference between the two groups (P 〉 0.05 ). The adverse effect in candesartan group obviously decreased( P 〈 0.05 ). Conclusion Candesartan has obviously curative effect on essential hypertension with less adverse effect.
出处
《安徽医药》
CAS
2007年第1期19-20,共2页
Anhui Medical and Pharmaceutical Journal
关键词
坎地沙坦酯
原发性高血压
依那普利
随机
双盲
candesartan cilexetil
essential hypertension
enalapril
random
double-blind