Identification of extensive coronary artery disease: Incremental value of exercise Tl-201 SPECT to clinical and stress test variables View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2002-03

AUTHORS

Doumit Daou, Nicolas Delahaye, Didier Vilain, Rachida Lebtahi, Marc Faraggi, Dominique Le Guludec

ABSTRACT

BackgroundThe ability of the size of a total myocardial perfusion defect (MPD) to detect extensive coronary artery disease (CAD) is currently suboptimal with exercise thallium 201 single photon emission computed tomography (SPECT). To improve its performance, exercise electrocardiography and indirect scintigraphic markers of extensive CAD were proposed (increased right ventricular Tl-201 uptake, lung-to-heart [L/H] ratio, and left ventricular transient ischemic dilation ratio). We aimed to determine the additive value of these criteria for the detection of extensive CAD.Methods and ResultsThe population included 338 patients who underwent exercise Tl-201 SPECT and coronary angiography. Patients were classified as having extensive CAD (left main, multivessel, or 1-vessel proximal left anterior descending CAD) or limited CAD (1-vessel disease other than proximal left anterior descending CAD or no CAD). First, Tl-201 SPECT provided higher diagnostic value than exercise electrocardiography. Second, age, percent target heart rate achieved, total MPD, and L/H ratio were independent predictors of extensive CAD. Third, visually estimated abnormal right ventricular Tl-201 uptake did not present additional information. Fourth, L/H ratio presented a higher diagnostic accuracy than left ventricular transient ischemic dilation ratio.ConclusionsWith exercise Tl-201 SPECT, age, percent target heart rate achieved, total MPD, and L/H ratio were independent predictors of extensive CAD. (J Nucl Cardiol 2002;9: 161–8.) More... »

PAGES

161-168

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URI

http://scigraph.springernature.com/pub.10.1067/mnc.2002.119974

DOI

http://dx.doi.org/10.1067/mnc.2002.119974

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1000802412

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/11986560


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