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First head-to-head comparison of effective radiation dose from low-dose 64-slice CT with prospective ECG-triggering versus invasive coronary angiography

B HerzogNuclear Cardiology, University Hospital Zurich, Ramistrasse 100, CH-8091 Zurich, SwitzerlandChristophe WyssNuclear Cardiology, Ramistrasse 100, University Hospital Zurich, 8091 Zurich, SwitzerlandLars HusmannNuclear Cardiology, Ramistrasse 100, University Hospital Zurich, 8091 Zurich, SwitzerlandOliver GaemperliNuclear Cardiology, Ramistrasse 100, University Hospital Zurich, 8091 Zurich, SwitzerlandInes ValentaNuclear Cardiology, Ramistrasse 100, University Hospital Zurich, 8091 Zurich, SwitzerlandV TreyerNuclear Cardiology, Ramistrasse 100, University Hospital Zurich, 8091 Zurich, SwitzerlandUlf LandmesserNuclear Cardiology, Ramistrasse 100, University Hospital Zurich, 8091 Zurich, SwitzerlandPhilipp A. KaufmannNuclear Cardiology, University Hospital Zurich, Ramistrasse 100, CH-8091 Zurich, Switzerland
Heartjournal2009en
ABI

Аннотация

BACKGROUND: Reduction of radiation burden of multidetector computed tomography coronary angiography (CTCA) has remained an important task. OBJECTIVE: To compare effective radiation dose of low-dose 64-slice CTCA using prospective ECG-triggering versus diagnostic invasive coronary angiography (CA). METHODS: 42 patients referred for elective invasive CA owing to suspected coronary artery disease (CAD) were prospectively enrolled to undergo a low-dose CTCA without calcium scoring within the same day before CA. Dose-area product of diagnostic invasive CA and dose-length product of CTCA were measured, converted into effective radiation dose and compared using Mann-Whitney U tests. In addition, accuracy of CTCA to detect CAD (coronary artery narrowing > or =50%) was assessed using invasive CA as standard of reference. On an intention-to-diagnose basis all non-evaluative vessels were included in the analysis and censored as positive. RESULTS: The estimated mean effective radiation dose was 8.5 (4.4) mSv (range 1.4-20.5 mSv) for diagnostic invasive CA, and 2.1 (0.7) mSv (range 1.0-3.3 mSv) for CTCA (p<0.001). 19 patients (42.9%) had no CAD by invasive CA. 40 (95.2%) patients have been correctly classified as having CAD (23/23) or no CAD (17/19). Over 97% (551/567) of segments were evaluable. Vessel-based analysis revealed sensitivity, specificity, positive and negative predictive value of 94.2% (CI 0.8% to 1.0%), 94.8% (CI 09% to 1.0%), 89.0% (CI 0.8% to 1.0%), 97.4% (CI 09% to 1.0%) and an accuracy of 94.6%. CONCLUSIONS: Low dose CTCA allows evaluation of CAD with high accuracy, but delivers a significantly less effective radiation dose to patients compared to diagnostic invasive CA.

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