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癫痫发作:雷加曲班在心肌灌注成像中的不良反应。

Seizure: An Adverse Effect of Regadenoson in Myocardial Perfusion Imaging.

作者信息

Radwan Sohab S, Schwartz Owen G

机构信息

Department of Internal Medicine, MedStar Washington Hospital Center, USA.

出版信息

Case Rep Cardiol. 2019 Apr 8;2019:6240605. doi: 10.1155/2019/6240605. eCollection 2019.

DOI:10.1155/2019/6240605
PMID:31089430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6476027/
Abstract

Regadenoson is a selective adenosine 2a (A2a) receptor agonist that is used in cardiac stress testing to evaluate for ischemic heart disease and has largely replaced adenosine in the modern era. Since adenosine receptors are involved in synaptic transmission between neurons throughout the central nervous system (CNS) including the cerebral cortex, hippocampus, and other structures as well, regadenoson can lower the seizure threshold in susceptible individuals. Epileptogenic activity is an uncommon yet potentially severe adverse effect of regadenoson use, and therefore, more awareness is required in screening patients at risk and evaluating alternate ways to investigate coronary artery disease (CAD) in susceptible individuals.

摘要

雷加曲班是一种选择性腺苷2A(A2a)受体激动剂,用于心脏负荷试验以评估缺血性心脏病,在现代已基本取代了腺苷。由于腺苷受体参与包括大脑皮层、海马体等在内的整个中枢神经系统(CNS)中神经元之间的突触传递,雷加曲班可降低易感个体的癫痫发作阈值。致痫活性是使用雷加曲班时一种罕见但可能严重的不良反应,因此,在筛查高危患者以及评估易感个体中研究冠状动脉疾病(CAD)的替代方法时,需要提高认识。

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Severe Shivering as an Adverse Effect of Regadenoson Myocardial Perfusion Imaging.严重寒战作为雷加曲班心肌灌注成像的不良反应
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本文引用的文献

1
ASNC imaging guidelines for SPECT nuclear cardiology procedures: Stress, protocols, and tracers.美国核医学与分子影像学会(ASNC)单光子发射计算机断层扫描(SPECT)核心脏病学检查的成像指南:负荷试验、方案及示踪剂
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Adenosine receptors: expression, function and regulation.腺苷受体:表达、功能与调控
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Regadenoson.雷加曲班
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Advances in pharmacologic stress agents: focus on regadenoson.药理学应激剂的进展:聚焦于雷加曲班。
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Regadenoson.雷卡弹。
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Regadenoson: a new myocardial stress agent.瑞加德松:一种新型心肌应激剂。
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J Nucl Cardiol. 2007 Sep-Oct;14(5):645-58. doi: 10.1016/j.nuclcard.2007.06.114.
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Modulation of glutamate release and excitotoxicity by adenosine A2A receptors.腺苷A2A受体对谷氨酸释放和兴奋性毒性的调节作用。
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