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使用定量血管造影术对氨氯地平和阿替洛尔治疗原发性高血压的血流动力学比较

Haemodynamic comparison of amlodipine and atenolol in essential hypertension using the quantascope.

作者信息

Tham T C, Herity N, Guy S, Silke B

机构信息

Department of Therapeutics and Pharmacology, Queen's University of Belfast, Belfast, Northern Ireland.

出版信息

Br J Clin Pharmacol. 1993 Dec;36(6):555-60. doi: 10.1111/j.1365-2125.1993.tb00414.x.

Abstract

1 We have utilised a non-imaging echo-Doppler cardiac output device, using the principle of attenuated compensation volume flow (ACVF), to assess the cardiovascular effects of amlodipine and atenolol over 3 months in 24 patients with essential hypertension. 2 Both amlodipine and atenolol, at 4 and 12 weeks, similarly reduced mean arterial pressure (12 weeks amlodipine -12.6 mmHg, atenolol -14.9 mmHg; P < 0.01 for each vs baseline). 3 The heart rate fell on atenolol, both at 4 weeks (amlodipine -3 vs atenolol -12 beats min(-1); P < 0.05) and 12 weeks (-1 vs -11 beats min(-1); P < 0.05), without change on amlodipine. 4 Stroke volume initially rose on atenolol without change on amlodipine (4 weeks amlodipine -1.3 ml vs atenolol +10.1 ml; P = 0.05) but between drug effects were not different at 12 weeks. 5 The systemic vascular resistance was reduced on amlodipine (12 weeks: amlodipine -176 dyn s cm(-5): P < 0.05) without change on atenolol (atenolol -48 dyn s cm(-5): NS). 6 The cardiac stroke work was lowered on amlodipine both at 4 weeks (P < 0.01) and 12 weeks (P < 0.05) and statistically different from the unaltered atenolol values at both time points. 7 Skin nutrient flow or fingertip temperature was not altered by either treatment. 8 These results are consistent with contrasting mechanisms of action--vasodilator for amlodipine and decreased cardiac pumping for atenolol. The greater reduction in cardiac stroke work on amlodipine compared with atenolol warrants further investigation during longer-term studies.

摘要
  1. 我们使用了一种非成像的回声多普勒心输出量测定装置,利用衰减补偿体积流量(ACVF)原理,对24例原发性高血压患者进行了为期3个月的氨氯地平和阿替洛尔心血管效应评估。2. 氨氯地平和阿替洛尔在4周和12周时,均同样降低了平均动脉压(12周时氨氯地平降低12.6 mmHg,阿替洛尔降低14.9 mmHg;与基线相比,每种药物P均<0.01)。3. 阿替洛尔使心率下降,在4周时(氨氯地平降低3次/分钟,阿替洛尔降低12次/分钟;P<0.05)和12周时(分别降低1次/分钟和11次/分钟;P<0.05),而氨氯地平对心率无影响。4. 阿替洛尔使每搏输出量最初升高,氨氯地平则无变化(4周时氨氯地平降低1.3 ml,阿替洛尔升高10.1 ml;P = 0.05),但在12周时药物效应无差异。5. 氨氯地平使全身血管阻力降低(12周时:氨氯地平降低176达因秒厘米⁻⁵:P<0.05),阿替洛尔则无变化(阿替洛尔降低48达因秒厘米⁻⁵:无统计学意义)。6. 氨氯地平在4周时(P<0.01)和12周时(P<0.05)均使心脏每搏功降低,且在两个时间点与未改变的阿替洛尔值相比有统计学差异。7. 两种治疗均未改变皮肤营养血流或指尖温度。8. 这些结果与不同的作用机制相符——氨氯地平为血管扩张剂,阿替洛尔为降低心脏泵血功能。与阿替洛尔相比,氨氯地平使心脏每搏功降低幅度更大,这值得在长期研究中进一步探究。

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