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急诊科采用正电子发射断层扫描评估雷诺嗪与微血管性心绞痛:一项初步随机对照试验的结果

Ranolazine and Microvascular Angina by PET in the Emergency Department: Results From a Pilot Randomized Controlled Trial.

作者信息

Safdar Basmah, D'Onofrio Gail, Dziura James, Russell Raymond R, Johnson Caitlin, Sinusas Albert J

机构信息

Department of Emergency Medicine, Yale University School of Medicine, New Haven, Connecticut.

Department of Emergency Medicine, Yale University School of Medicine, New Haven, Connecticut.

出版信息

Clin Ther. 2017 Jan;39(1):55-63. doi: 10.1016/j.clinthera.2016.12.002. Epub 2017 Jan 9.

Abstract

PURPOSE

Coronary microvascular dysfunction (CMD) is a common but underdiagnosed cause of chest pain. Literature is scant regarding effective treatments. We explored the effect of ranolazine on coronary flow reserve (CFR) among symptomatic patients with CMD.

METHODS

This pilot double-blinded randomized controlled trial included emergency department patients with chest pain and CMD admitted to an observation unit between June 2014 and November 2015. Participants were assessed by cardiac Rb-82 positron emission tomography and computed tomography imaging at baseline and 30 days. CMD was defined as CFR <2 corrected for rate pressure product or <2.5 uncorrected, with no evidence of obstructive or nonobstructive coronary artery disease or calcification. Patients with infarction, hypertensive urgency, heart failure, or prescribed QTc-prolonging drugs were excluded. Participants were assigned to ranolazine or placebo in a 2:1 ratio. Primary outcome was change in CFR at 30 days.

FINDINGS

We enrolled 31 patients (71% female, mean [SD] age 50 [6] years) with CMD (mean [SD] corrected CFR 1.6 [0.3]). Ranolazine improved CFR at 30 days by 17% (P = 0.005) compared with 0% with placebo (P = 0.67). However, there was no significant difference in the primary outcome as measured by mean change in CFR (0.27 ranolazine compared with 0.06 placebo; 95% CI, -0.08 to 0.62).

IMPLICATIONS

The emergency department offers a unique venue to diagnose CMD with acute symptoms. In an exploratory randomized controlled trial of symptomatic patients with CMD and no coronary artery disease, promising results were seem with ranolazine and CFR improving at 30 days. Large robust clinical trials are needed to verify improvement of CMD in a sex-specific model. ClinicalTrials.gov identifier NCT02052011.

摘要

目的

冠状动脉微血管功能障碍(CMD)是胸痛常见但诊断不足的病因。关于有效治疗的文献较少。我们探讨了雷诺嗪对有症状的CMD患者冠状动脉血流储备(CFR)的影响。

方法

这项前瞻性双盲随机对照试验纳入了2014年6月至2015年11月间因胸痛和CMD入住观察病房的急诊科患者。在基线和30天时通过心脏Rb-82正电子发射断层扫描和计算机断层扫描成像对参与者进行评估。CMD定义为校正心率血压乘积后的CFR<2或未校正时<2.5,且无阻塞性或非阻塞性冠状动脉疾病或钙化的证据。排除有梗死、高血压急症、心力衰竭或正在服用可延长QTc药物的患者。参与者按2:1的比例分配到雷诺嗪组或安慰剂组。主要结局是30天时CFR的变化。

结果

我们纳入了31例CMD患者(71%为女性,平均[标准差]年龄50[6]岁)(平均[标准差]校正CFR为1.6[0.3])。与安慰剂组改善率为0%(P=0.67)相比,雷诺嗪组在30天时CFR改善了17%(P=0.005)。然而,以CFR的平均变化衡量的主要结局无显著差异(雷诺嗪组为0.27,安慰剂组为0.06;95%CI,-0.08至0.62)。

意义

急诊科为诊断有急性症状的CMD提供了一个独特的场所。在一项针对无冠状动脉疾病的有症状CMD患者的探索性随机对照试验中,雷诺嗪显示出有前景的结果,30天时CFR有所改善。需要大型有力的临床试验来验证在性别特异性模型中CMD的改善情况。ClinicalTrials.gov标识符:NCT02052011。

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