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将阿托品添加到次极量运动负荷试验联合Tl-201单光子发射计算机断层扫描用于诊断心肌缺血的安全性和可行性。

Safety and feasibility of atropine added to submaximal exercise stress testing with Tl-201 SPECT for the diagnosis of myocardial ischemia.

作者信息

Cosín-Sales Juan, Maceira Alicia M, García-Velloso María J, Macías Alfonso, Gimenez Marta, García-Bolao Ignacio, Coma-Canella Isabel

机构信息

Department of Cardiology, Clínica Universitaria de Navarra, Universidad de Navarra, Pamplona, Navarra, Spain.

出版信息

J Nucl Cardiol. 2002 Nov-Dec;9(6):581-6. doi: 10.1067/mnc.2002.125469.

Abstract

BACKGROUND

We aimed to assess whether atropine administration is safe and feasible in patients unable to reach the minimal heart rate (HR) required (80% of age-predicted HR) in myocardial scintigraphic studies after exercise stress testing (EST).

METHODS AND RESULTS

We studied 108 patients who underwent myocardial perfusion scintigraphy after EST; 0.5 mg of atropine was administered to those showing signs of fatigue before reaching minimal HR (group A, n = 44). The scintigraphic results for group A were compared with those of patients who spontaneously achieved minimal HR (group B, n = 64). Coronary angiographic results, if available, and clinical follow-up were also compared. In group A, atropine increased HR by 13.7 +/- 7.4 beats/min. The percentage of maximal age-related HR achieved was 83.3% +/- 7.5%; 74% achieved minimal HR. No major adverse effects occurred. When groups A and B were compared, baseline and peak HR, rate pressure product, and maximal metabolic equivalents achieved were higher in group B. There were no differences in number of perfusion studies positive for ischemia (group A, 26/44, and group B, 30/64; P =.2), coronary lesions, or clinical follow-up.

CONCLUSIONS

Atropine added to EST in patients who cannot achieve their 80% age-related HR is a safe and potentially useful method for myocardial perfusion studies.

摘要

背景

我们旨在评估在运动负荷试验(EST)后心肌闪烁显像研究中,对于无法达到所需最低心率(HR)(年龄预测心率的80%)的患者,给予阿托品是否安全可行。

方法与结果

我们研究了108例在EST后接受心肌灌注闪烁显像的患者;对于在达到最低HR之前出现疲劳迹象的患者给予0.5mg阿托品(A组,n = 44)。将A组的闪烁显像结果与自发达到最低HR的患者(B组,n = 64)的结果进行比较。还比较了冠状动脉造影结果(若有)及临床随访情况。在A组中,阿托品使HR增加了13.7±7.4次/分钟。达到的最大年龄相关HR百分比为83.3%±7.5%;74%的患者达到了最低HR。未发生重大不良反应。比较A组和B组时,B组的基线和峰值HR、心率血压乘积及达到的最大代谢当量更高。缺血阳性灌注研究的数量(A组,26/44;B组,30/64;P = 0.2)、冠状动脉病变或临床随访方面无差异。

结论

对于无法达到其年龄相关HR的80%的患者,在EST中加用阿托品是一种安全且可能有用的心肌灌注研究方法。

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