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特拉唑嗪与其他抗高血压药物联合使用的经验。

Experience with terazosin administered in combination with other antihypertensive agents.

作者信息

Chrysant S G

出版信息

Am J Med. 1986 May 23;80(5B):55-61. doi: 10.1016/0002-9343(86)90853-3.

Abstract

In a randomized, double-blind, placebo-controlled, multicenter trial, the efficacy and safety of terazosin in combination with other antihypertensive agents were assessed using patients with inadequately controlled essential hypertension (supine diastolic blood pressure 95 mm Hg or greater). Of 138 evaluable patients, the terazosin-treated group (n = 84) achieved a significant (p less than 0.05) mean reduction of 7.3 mm Hg in supine diastolic blood pressure when compared with the placebo-treated group (n = 54) who achieved a reduction of 0.6 mm Hg. Analysis of patients by background therapeutic categories (beta blocker, beta blocker plus diuretic, or "other") revealed that terazosin caused a significantly greater decrease in supine diastolic blood pressure than did placebo when added to the combination of beta blocker plus diuretic (decrease of 7.2 mm Hg for the terazosin group versus a decrease of 1.5 mm Hg for the placebo group) and to other antihypertensive drugs (decrease of 7.9 mm Hg for the terazosin group versus a decrease of 1.0 mm Hg for the placebo group). Significant differences between treatment groups were also observed for supine systolic and for standing systolic and diastolic blood pressure variables in select subgroups. The addition of terazosin did not cause significant changes in physical examinations or electrocardiograms. Changes in pulse rates and body weight did not differ significantly between treatment groups for any background therapeutic category. The overall incidence of adverse experiences was only somewhat greater for terazosin-treated than placebo-treated patients. These results suggest that terazosin is safe and effective when administered in combination with other antihypertensive drugs.

摘要

在一项随机、双盲、安慰剂对照、多中心试验中,对患有原发性高血压控制不佳(仰卧位舒张压95毫米汞柱或更高)的患者使用特拉唑嗪联合其他抗高血压药物进行疗效和安全性评估。在138例可评估患者中,与安慰剂治疗组(n = 54,舒张压降低0.6毫米汞柱)相比,特拉唑嗪治疗组(n = 84)仰卧位舒张压平均显著降低(p < 0.05)7.3毫米汞柱。按背景治疗类别(β受体阻滞剂、β受体阻滞剂加利尿剂或“其他”)对患者进行分析显示,当特拉唑嗪添加到β受体阻滞剂加利尿剂组合(特拉唑嗪组降低7.2毫米汞柱,安慰剂组降低1.5毫米汞柱)和其他抗高血压药物中时,其导致仰卧位舒张压降低幅度显著大于安慰剂(特拉唑嗪组降低7.9毫米汞柱,安慰剂组降低1.0毫米汞柱)。在部分亚组中,治疗组在仰卧位收缩压、站立位收缩压和舒张压变量方面也观察到显著差异。添加特拉唑嗪未引起体格检查或心电图的显著变化。在任何背景治疗类别中,治疗组之间的脉搏率和体重变化无显著差异。特拉唑嗪治疗患者的不良事件总发生率仅略高于安慰剂治疗患者。这些结果表明,特拉唑嗪与其他抗高血压药物联合使用时是安全有效的。

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