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首页> 外文期刊>The Journal of Nuclear Medicine >Attenuation of adenosine-induced myocardial perfusion heterogeneity by atenolol and other cardioselective beta-adrenoceptor blockers: a crossover myocardial perfusion imaging study.
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Attenuation of adenosine-induced myocardial perfusion heterogeneity by atenolol and other cardioselective beta-adrenoceptor blockers: a crossover myocardial perfusion imaging study.

机译:阿替洛尔和其他心脏选择性β-肾上腺素受体阻滞剂对腺苷诱导的心肌灌注异质性的减弱:交叉型心肌灌注成像研究。

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Little is known about the effect of chronic beta-blockade on adenosine actions. We sought to investigate the effect of oral beta-blockers on the presence, extent, and severity of myocardial perfusion abnormality induced by adenosine in patients with coronary artery disease. METHODS: In this crossover study, 45 male patients with coronary artery disease on beta-blocker therapy with atenolol, bisoprolol, or metoprolol underwent adenosine myocardial perfusion imaging both on and off beta-blockade in a random order on separate days. Myocardial perfusion was assessed both qualitatively and quantitatively. Hemodynamic response, image analysis, and sensitivity for the detection of coronary stenosis (>or=50% luminal diameter reduction on x-ray coronary angiography) were compared between the on and off beta-blocker studies. RESULTS: Rate pressure product both at baseline and at peak adenosine infusion decreased by 23% +/- 15% and 21% +/- 18%, respectively, after beta-blockade (P < 0.001 for all). The median (interquartile range) summed difference score, a measure of defect reversibility, and quantitative defect size were both significantly lower after beta-blockade (median, 7.0 [interquartile range, 2.0-9.5] vs. median, 5.0 [interquartile range, 0-8.0], P = 0.002; and quantitative defect size, 18% [interquartile range, 9%-34%] vs. quantitative defect size, 6% [interquartile range, 0%-19%], P < 0.001, respectively). The overall sensitivity for the detection of coronary stenosis decreased from 0.76 (95% confidence interval, 0.65-0.88) to 0.58 (95% confidence interval, 0.45-0.71) after beta-blockade (P = 0.03). CONCLUSION: beta-blockade causes a small but significant reduction in the extent and severity of perfusion abnormality by adenosine. This may reduce the diagnostic sensitivity of adenosine myocardial perfusion imaging for the detection of flow-limiting coronary stenosis.
机译:关于慢性β-受体阻滞对腺苷作用的影响知之甚少。我们试图研究口服β-受体阻滞剂对腺苷引起的冠心病患者心肌灌注异常的存在,程度和严重性的影响。方法:在这项交叉研究中,接受阿替洛尔,比索洛尔或美托洛尔接受β受体阻滞剂治疗的45例男性冠状动脉疾病男性患者分别在不同的日子接受了β受体阻滞剂的腺苷心肌灌注成像。定性和定量评估心肌灌注。在开启和关闭β受体阻滞剂研究之间比较了血流动力学响应,图像分析和检测冠状动脉狭窄的敏感性(在X射线冠状动脉造影上≥50%的管腔直径缩小)。结果:β-受体阻滞后,基线和腺苷峰值输注时的速率压力乘积分别降低了23%+/- 15%和21%+/- 18%(所有P均<0.001)。 β受体阻滞后,中位(四分位间距)总和差异得分,缺陷可逆性度量和缺陷数量定量均显着降低(中位数为7.0 [四分位间距2.0-9.5],而中位值为5.0 [四分位间距0 -8.0],P = 0.002;定量缺陷尺寸分别为18%[四分位间距,9%-34%]与定量缺陷尺寸6%[四分位间距,0%-19%],P <0.001) 。 β受体阻滞后,检测冠状动脉狭窄的总体敏感性从0.76(95%置信区间,0.65-0.88)降低到0.58(95%置信区间,0.45-0.71)(P = 0.03)。结论:β-受体阻滞可引起腺苷灌注异常的程度和严重程度的轻微但显着的降低。这可能会降低腺苷心肌灌注成像对限流性冠状动脉狭窄的检测的诊断敏感性。

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