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作 者:刘忠[1] 姚雪艳[1] 陈君柱[1] 朱建华[1] 章黎苹[1] 金争鸣[1] 胡晓晟[1] 王利宏[1] 连苗军[1]
机构地区:[1]浙江大学医学院附属第一医院心内科,杭州310003
出 处:《浙江医学》2005年第7期493-495,共3页Zhejiang Medical Journal
摘 要:目的观察极低剂量培哚普利/吲达帕胺复合制剂(商品名:百普乐)治疗原发性高血压患者的降压疗效及安全性。方法门诊原发性高血压患者经2周的安慰剂选择期后,进入12周随机、双盲平行组治疗期,采用随机、双盲、吲达帕胺缓释剂(商品名:纳催离)作对照。结果治疗后百普乐组患者血压由治疗前的(141.2±9.0)?(97.3±3.0)mmHg下降至(125.9±7.2)?(83.0±5.2)mmHg,有效率91.3%;纳催离组血压由治疗前的(144.1±11.9)?(99.6±4.4)mmHg下降至(125.5±11.3)?(81.9±7.5)mmHg,有效率89.9%。两组经治疗后血压均有效下降(均P<0.001)。百普乐组患者咳嗽发生率20.8%,因不能耐受而退出1例(4.2%);纳催离组低钾血症发生率为25.0%。结论百普乐治疗原发性高血压安全有效。Objective To investigate the efficacy and safety of the combination of Perindopril and Indapamide Biprel in treatment of essential hypertensive patients. Method A randomized double-blind placebo-controlled clinical trial was conducted. Total of 56 outpatients with essential hypertension were recruited in the study after 2-week placebo selection period 48 patients entered in 12-week trial with 2 parallel arms in treatment arm 22 patients received Biprel Perindopril 2mg Indapamide 0.625mg and in control arm 22 patients received Indapamide 1.5mg SRNatrilix. The changes in sitting blood pressure from baseline and the laboratory abnormalities hypokalemia ECG changes and adverse events were compared in two arms. Result Biprel reduced sitting blood pressure from (141.2±9.0) (97.3±3.0)mmHg to (125.9±7.2) (83.0±5.2)mmHg with a response rate of 91.3% Natrilix reduced sitting blood pressure from (144.1±11.9) (99.6±4.4)mmHg to (125.5±11.3) (81.9±7.5)mmHg with a response rate of 89.9% both groups P<0.001. Cough was presented in 20.8% of patients in Biprel group but only one patient withdrew 4.2% the incidence of hypokalemia was 25% in the Natrilix group and none in Biprel group. Conclusions Biprel was effective and well tolerated and offers a promising approach to the treatment of essential hypertension.
关 键 词:培哚普利 吲达帕胺 原发性高血压 降压作用 安全性 血管紧张素
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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