Angiography-Based Blood Flow Quantification After Revascularization in Acute Coronary Syndromes
- PMID: 40576041
- PMCID: PMC12449982
- DOI: 10.1161/JAHA.124.038770
Angiography-Based Blood Flow Quantification After Revascularization in Acute Coronary Syndromes
Abstract
Background: In patients presenting with acute coronary syndromes (ACS), impaired coronary blood flow (CBF) after percutaneous coronary interventions (PCI) is linked to mortality. We developed a novel angiography-based approach for blood flow quantification using automatic contrast bolus tracking. Therefore, this study aimed to investigate the clinical impact of angiography-based blood flow quantification on major adverse cardiovascular events (MACE) after PCI in patients with ACS.
Methods: Prospective, multicenter, nested case-control study of patients presenting ACS. A propensity score was used to match patients with and without MACE at 1 year of follow-up. MACE was defined as cardiovascular death, myocardial infarction, hospitalization for heart failure, or ischemia-driven revascularization. CBF was measured automatically from angiograms after PCI.
Results: One hundred sixty-two patients were included. The mean age was 68.3±13.0 years, 83% were male, and 33% had diabetes. Overall, 66% of patients presented with ST-segment-elevation myocardial infarction. CBF after PCI was lower after ST-segment-elevation myocardial infarction compared with other clinical presentations (74.1±47.0 mL/min ST-segment-elevation myocardial infarction, 89.1±45.8 mL/min, non-ST-segment-elevation myocardial infarction, 95.7±48.8 mL/min, unstable angina, P=0.046). Patients with low post-PCI CBF (<54.3 mL/min) had an increased risk of MACE (hazard ratio, 2.11 [95% CI, 1.35-3.28], P=0.001).
Conclusions: After PCI, automatic quantification of CBF using angiography was associated with MACE in patients with ACS. Risk stratification using post-PCI CBF-derived angiography may enable tailored management strategies for individuals with ACS.
Keywords: acute coronary syndrome; angiography; coronary blood flow; coronary flow velocity; heart failure.
Conflict of interest statement
Takuya Mizukami received consultancy fees from Zeon Medical Inc., research grants from Boston Scientific, and speaker fees from Abbott Vascular, Cathworks, and Boston Scientific. Junichi Yamaguchi was endowed by Abbott Medical Japan LLC, Boston Scientific, Medtronic, and Terumo. Toshiro Shinke received personal fees and research grants from Abbott Medical Japan LLC. Adriaan Wilgenhof has been supported by a research grant provided by the DigiCardiopaTh PhD program. Chris Bouwman and Jean‐Paul Aben are employees of Pie Medical Imaging. Carlos Collet reports receiving research grants from Biosensor, Coroventis Research, Medis Medical Imaging, Pie Medical Imaging, CathWorks, Boston Scientific, Siemens, HeartFlow Inc, Abbott Vascular, and consultancy fees from HeartFlow Inc, OpSens, Abbott Vascular, and Philips Volcano. The remaining authors have no disclosures to report.
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