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生脉胶囊治疗慢性充血性心力衰竭的临床研究 被引量:5

Clinical trial of Shengmai capsules in the treatment of patients with chronic congestive heart failure
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摘要 目的观察生脉胶囊治疗慢性充血性心力衰竭的临床疗效和安全性。方法将84例慢性充血性心力衰竭患者随机分为对照组42例和试验组42例。对照组予以安慰剂每次0.3 mg,tid,口服;试验组予以生脉胶囊每次0.3 mg,tid,口服。2组患者均治疗2周。比较2组患者的临床疗效、心率、左心室射血分数(LVEF)、舒张早期最大血流速度(E)、E/舒张晚期最大血流速度(E/A)、肺动脉收缩压(PAS)、慢性心力衰竭超声心动图多参数评分(HF-EMPS),以及药物不良反应的发生率。结果治疗后,试验组和对照组的总有效率分别为90.47%(38例/42例)和73.81%(31例/42例),差异有统计学意义(P<0.05)。治疗后,试验组和对照组的HR分别为(66.54±7.02)和(72.12±8.14)beat·min^(-1),LVEF分别为(46.03±5.56)%和(41.26±5.12)%,E分别为(92.48±14.32)和(75.41±13.62)cm·s^(-1),E/A分别为1.65±0.34和1.35±0.31,PAS分别为(24.85±4.21)和(30.12±4.22)mm Hg,HF-EMPS分别为(7.03±1.12)及(7.68±1.32)分,差异均有统计学意义(均P<0.05)。2组患者治疗期间均未发生药物不良反应。结论生脉胶囊治疗慢性充血性心力衰竭的临床疗效确切,且安全性较高。 Objective To observe the clinical efficacy and safety of Shengmai capsules in the treatment of chronic congestive heart failure. Methods Eighty -four patients with chronic congestive heart failure were randomly divided into control group and treatment group with 42 ca- ses per group. Control group was given placebo 0. 3 mg each time, tid, orally. Treatment group was given Shengmai capsule 0. 3 mg each time, tid, orally. Two groups were treated for 2 weeks. The clinical efficacy, heart rate,left ventricular ejection fraction (LVEF), maximal velocity of bicuspid blood flow in the early (E), E/ maximal velocity of bicuspid blood flow in the advanced ( E/A), pulmonary artery pressure ( PAS), heart function echocardiographic multi - parameter scores ( HF - EMPS) and adverse drug reactions were compared between two groups. Results After treatment, the total effective rates of treatment and control groups were 90.47% (38 cases/42 cases) and 73.81% (31 cases/42 cases) with significant difference ( P 〈 0. 05 ). After treatment, the main inde- xes in treatment and control groups were compared: heart rate were (66.54 ±7.02) and (72.12 ±8.14)beat · min-1, LVEF were(46.03±5.56)% and (41.26 ±5.12)%, E were(92.48 ±14.32)and(75.41 ±13.62)em · s-1,E/A were 1.65 sO, 34 and 1.35 ± 0. 31, PAS were ( 24.85 ± 4. 21 ) and ( 30. 12 ± 4. 22 ) mmHg, I-IF - EMPS were (7.03 ± 1, 12) and (7.68 ± 1.32) points, with significant difference ( all P 〈 0. 05 ). There were no adverse drug reactions occurred during the treatment in two groups Conclusion Shengmai capsules have a definitive clinical efficacy and safety in the treatment of ehronic congestive heart failure.
作者 刘星 吕欢
出处 《中国临床药理学杂志》 CAS CSCD 北大核心 2018年第2期127-130,共4页 The Chinese Journal of Clinical Pharmacology
关键词 生脉胶囊 慢性充血性心力衰竭 安全性 Shengmai capsule chronic congestive heart failure safety
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