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Published on: August 28, 2018
CCTA-Guided Invasive Coronary Angiography in Patients With CABG: A Multicenter, Randomized Study.
Grigorios Tsigkas1, Fotios Toulgaridis2, Anastasios Apostolos3
1Department of Cardiology (G.T., G.V., A.M., P.D.), University Hospital of Patras, Greece.
Coronary computed tomography angiography (CCTA)-guided invasive coronary angiography (ICA) in post-coronary artery bypass graft (CABG) patients reduces procedure time and fluoroscopy. However, this strategy increases total contrast volume and radiation exposure without significantly altering complication rates.
Area of Science:
- Cardiovascular Imaging
- Interventional Cardiology
- Radiology
Background:
- Coronary computed tomography angiography (CCTA) accurately visualizes bypass grafts.
- Invasive coronary angiography (ICA) in patients with prior coronary artery bypass graft (CABG) is resource-intensive.
- Previous studies highlight challenges in assessing graft patency post-CABG.
Purpose of the Study:
- To compare CCTA-guided ICA versus classic ICA in patients with prior CABG.
- To evaluate the impact of a CCTA-guided strategy on procedural outcomes.
- To assess the safety and efficacy of CCTA-guided ICA in the CABG population.
Main Methods:
- Multicenter, randomized controlled trial comparing CCTA-ICA versus ICA-only strategies.
- Random assignment of patients with prior CABG to one of two groups (1:1 ratio).
- Primary endpoint: total contrast agent volume administered.
Main Results:
- CCTA-ICA group had higher total contrast volume but lower intra-procedural contrast volume.
- Significant reduction in total fluoroscopy time observed in the CCTA-ICA group.
- No significant differences in contrast-induced nephropathy, complications, or major adverse cardiac events.
Conclusions:
- A CCTA-directed ICA strategy expedites invasive procedures and reduces fluoroscopy time in CABG patients.
- This approach leads to increased total contrast volume and effective radiation dose.
- The CCTA-guided strategy offers procedural efficiencies without compromising patient safety regarding key adverse events.
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