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静脉注射双嘧达莫与腺苷后冠状动脉扩张情况的比较

Comparison of coronary vasodilation with intravenous dipyridamole and adenosine.

作者信息

Rossen J D, Quillen J E, Lopez A G, Stenberg R G, Talman C L, Winniford M D

机构信息

Department of Internal Medicine, University of Iowa College of Medicine, Iowa City 52242.

出版信息

J Am Coll Cardiol. 1991 Aug;18(2):485-91. doi: 10.1016/0735-1097(91)90604-8.

DOI:10.1016/0735-1097(91)90604-8
PMID:1856416
Abstract

Although both intravenous dipyridamole and adenosine have been used to produce coronary vasodilation during cardiac imaging, the relative potency of the commonly administered doses of these agents has not been evaluated. Accordingly, the coronary and systemic hemodynamic effects of intravenous adenosine (140 micrograms/kg per min) and intravenous dipyridamole (0.56 mg/kg over 4 min) were compared with a maximally dilating dose of intracoronary papaverine in 15 patients. Coronary blood flow responses were assessed using a Doppler catheter in a nonstenotic coronary artery. The protocol was discontinued in two patients because of transient asymptomatic atrioventricular (AV) block during adenosine infusion. The mean heart rate increased more with adenosine (11 +/- 9 beats/min) and dipyridamole (11 +/- 7 beats/min) than with papaverine (4 +/- 3 beats/min, p less than 0.05 vs. adenosine and papaverine). The mean arterial pressure decreased less with dipyridamole (-10 +/- 3 mm Hg) and papaverine (-9 +/- 4 mm Hg) than with adenosine (-16 +/- 5 mm Hg, p less than 0.01 vs. dipyridamole and papaverine). The peak/rest coronary blood flow velocity ratio was greater with papaverine (3.9 +/- 1.1) than with adenosine (3.4 +/- 1.2, p less than or equal to 0.05 vs. papaverine) or dipyridamole (3.1 +/- 1.2, p less than 0.01 vs. papaverine). A larger decrease in coronary resistance as measured by the coronary vascular resistance index occurred with papaverine (0.25 +/- 0.06) and adenosine (0.26 +/- 0.09) than with dipyridamole (0.31 +/- 0.10, p less than 0.01 vs. papaverine, p less than 0.05 vs. adenosine).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尽管静脉注射双嘧达莫和腺苷都已用于在心脏成像期间产生冠状动脉扩张,但这些药物常用剂量的相对效力尚未得到评估。因此,在15名患者中,将静脉注射腺苷(每分钟140微克/千克)和静脉注射双嘧达莫(4分钟内0.56毫克/千克)的冠状动脉和全身血流动力学效应与冠状动脉内罂粟碱的最大扩张剂量进行了比较。使用多普勒导管在非狭窄冠状动脉中评估冠状动脉血流反应。两名患者因腺苷输注期间出现短暂无症状房室传导阻滞而停止该方案。腺苷(11±9次/分钟)和双嘧达莫(11±7次/分钟)使平均心率增加的幅度大于罂粟碱(4±3次/分钟,与腺苷和罂粟碱相比,p<0.05)。双嘧达莫(-10±3毫米汞柱)和罂粟碱(-9±4毫米汞柱)使平均动脉压降低的幅度小于腺苷(-16±5毫米汞柱,与双嘧达莫和罂粟碱相比,p<0.01)。罂粟碱(3.9±1.1)的峰值/静息冠状动脉血流速度比大于腺苷(3.4±1.2,与罂粟碱相比,p≤0.05)或双嘧达莫(3.1±1.2,与罂粟碱相比,p<0.01)。通过冠状动脉血管阻力指数测量,罂粟碱(0.25±0.06)和腺苷(0.26±0.09)使冠状动脉阻力降低的幅度大于双嘧达莫(0.31±0.10,与罂粟碱相比,p<0.01,与腺苷相比,p<0.05)。(摘要截短于250字)

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