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20毫克缓释硝苯地平与25毫克或50毫克阿替洛尔的降压作用比较。轻度至中度重度动脉高血压患者治疗的研究

[Comparative antihypertensive action of 20 mg delayed-action nifedipine with either 25 or 50 mg atenolol. A study on the treatment of patients with mild to moderately severe arterial hypertension].

作者信息

Kraft K, Schiessl S, Vetter H

机构信息

Medizinische Poliklinik, Universität Bonn.

出版信息

Praxis (Bern 1994). 1996 Sep 3;85(36):1081-6.

PMID:8927880
Abstract

In the present double-blind, randomized, placebo-controlled study 36 untreated patients (57.8 +/- 8.4 years) with mild to moderate hypertension were included. After a 14 days' placebo period they were treated with a combination of 20 mg retarded nifedipine and 25 or 50 mg atenolol for six weeks each. Group A started with 25 mg, group B with 50 mg atenolol. Casual sitting blood pressure was measured automatically every second week, routine laboratory parameters and side effects were evaluated at the end of placebo and the verum periods. The blood pressure of the two groups was comparable during placebo and was reduced by 31.6/14.7 mmHg in group A or 29.9/15.8 mmHg in group B (p < 0.001 vs. placebo) after six weeks. In the second treatment period with verum, blood pressure was not further reduced. Both combinations were equally efficient also in the female and the elder subgroups (> 60 years) who were characterized by higher systolic blood pressure. The response rates were 83% and 86% for the combination with 25 and 50 mg atenolol respectively. Heart rate was significantly reduced in all groups during 50 mg atenolol. Laboratory parameters were not altered by treatment. Frequency and severeness of side effects were equal in both groups. It is concluded that in patients with mild to moderate uncomplicated hypertension the combination of 20 mg retarded nifedipine with 25 mg atenolol is equally efficient to the combination with 50 mg atenolol.

摘要

在本双盲、随机、安慰剂对照研究中,纳入了36例未经治疗的轻度至中度高血压患者(57.8±8.4岁)。经过14天的安慰剂期后,他们分别接受20mg缓释硝苯地平与25mg或50mg阿替洛尔的联合治疗,各为期六周。A组起始剂量为25mg阿替洛尔,B组为50mg阿替洛尔。每隔一周自动测量一次随意坐位血压,在安慰剂期和治疗期结束时评估常规实验室参数及副作用。两组在安慰剂期血压相当,六周后A组血压降低31.6/14.7mmHg,B组降低29.9/15.8mmHg(与安慰剂相比,p<0.001)。在第二个治疗期,血压未进一步降低。两种联合治疗方案在女性和年龄较大(>60岁)的亚组中同样有效,这些亚组的收缩压较高。阿替洛尔25mg和50mg联合治疗的有效率分别为83%和86%。在使用50mg阿替洛尔治疗期间,所有组的心率均显著降低。治疗未改变实验室参数。两组副作用的发生频率和严重程度相当。结论是,在轻度至中度单纯性高血压患者中,20mg缓释硝苯地平与25mg阿替洛尔联合治疗与20mg缓释硝苯地平与50mg阿替洛尔联合治疗同样有效。

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