Progress of <sup>18</sup>F-flurpiridaz in Clinical Trials
Author:
Affiliation:
1. Department of Cardiology, Nihon University Hospital
Publisher
The Japanese Society of Nuclear Cardiology
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/anc/9/1/9_23-00011/_pdf
Reference11 articles.
1. 1. Maddahi J, Lazewatsky J, Udelson JE, et al. Phase-III clinical trial of fluorine-18 flurpiridaz positron emission tomography for evaluation of coronary artery disease. J Am Coll Cardiol 2020; 76: 391–401.
2. 2. Yalamanchili P, Wexler E, Hayes M, et al. Mechanism of uptake and retention of F-18 BMS-747158-02 in cardiomyocytes: A novel PET myocardial imaging agent. J Nucl Cardiol 2007; 14: 782–8.
3. 3. Rozanski A, Gransar H, Hayes SW, et al. Temporal trends in the frequency of inducible myocardial ischemia during cardiac stress testing: 1991 to 2009. J Am Coll Cardiol 2013; 61: 1054–65.
4. 4. Taqueti VR, Hachamovitch R, Murthy VL, et al. Global coronary flow reserve is associated with adverse cardiovascular events independently of luminal angiographic severity and modifies the effect of early revascularization. Circulation 2015; 131: 19–27.
5. 5. van de Hoef TP, van Lavieren MA, Damman P, et al. Physiological basis and long-term clinical outcome of discordance between fractional flow reserve and coronary flow velocity reserve in coronary stenoses of intermediate severity. Circ Cardiovasc Interv 2014; 7: 301–11.
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