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Published on: February 8, 2022
Impact of Large Thrombus Burden on Very Long-Term Clinical Outcomes in Patients Presenting With ST-Segment Elevation
Paola Scarparo, Menno van Gameren, Jeroen Wilschut
1Interventional Cardiology, Thoraxcenter, Erasmus MC, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands. r.diletti@erasmusmc.nl.
Insights
Large thrombus burden (LTB) in ST-segment elevation myocardial infarction (STEMI) patients increases early risks like no-reflow and distal embolization. However, LTB does not impact very long-term clinical outcomes or mortality after percutaneous coronary intervention.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Thrombosis Research
Background:
- Large thrombus burden (LTB) is a recognized complication in ST-segment elevation myocardial infarction (STEMI).
- The very long-term clinical impact of LTB in STEMI patients remains incompletely understood.
- Previous studies have not extensively evaluated outcomes beyond 10 years post-intervention.
Purpose of the Study:
- To compare very long-term clinical outcomes between STEMI patients with LTB and small thrombus burden (STB).
- To assess the impact of LTB on major adverse cardiac events (MACE) and mortality up to 15 years post-percutaneous coronary intervention (PCI).
- To identify potential early risks associated with LTB in STEMI patients.
Main Methods:
- A cohort of 812 STEMI patients undergoing PCI between 2002-2004 was analyzed.
- Thrombus burden (TB) was assessed, with LTB defined as thrombus ≥2 vessel diameters.
- Outcomes including 10-year MACE and up to 15-year survival data were collected and analyzed.
Main Results:
- Patients with LTB (28.0%) had higher rates of no-reflow and distal embolization compared to STB patients (72.0%).
- No significant differences in 10-year MACE rates (42.5% vs 42.4%) or 10/15-year mortality were observed between LTB and STB groups.
- LTB was an independent predictor of MACE within 30 days post-PCI, but not beyond.
Conclusions:
- LTB in STEMI patients is associated with increased early procedural complications like no-reflow and distal embolization.
- Despite early risks, LTB does not appear to influence very long-term MACE or mortality rates.
- LTB may help identify a high-risk subpopulation for early ischemic events, warranting closer monitoring.
Objectives:
The impact of large thrombus burden (LTB) on very long-term clinical outcomes in patients with ST-segment elevation myocardial infarction (STEMI) is unknown. We compared very long-term clinical outcomes in STEMI patients with either LTB or small thrombus burden (STB).
Methods:
Between 2002 and 2004, thrombus burden (TB) was evaluated in consecutive patients with STEMI undergoing percutaneous coronary intervention (PCI). In occluded infarct-related arteries, TB was reclassified after flow restoration. LTB was defined as thrombus ≥2 vessel diameters. Major adverse cardiac event (MACE) rate was evaluated at 10-year follow-up and survival data were collected up to 15 years post PCI.
Results:
A total of 812 patients were enrolled, and TB assessment was available for 806 patients (99.3%); 580 patients (72.0%) had STB and 226 patients (28.0%) had LTB. Patients with LTB experienced more no reflow (4.0% vs 0.5%; P<.01) and distal embolization (17.3% vs 3.4%; P<.001) than STB patients. Ten-year MACE rate (42.5% vs 42.4%; P=.59), 10-year mortality rate (27.0% vs 26.4%; P=.75), and 15-year mortality rate (31.9% vs 35.9%; P=.29) were similar between STB and LTB groups, respectively. By landmark analysis, MACE rate was higher in the LTB group (15.9% vs 8.8%; P<.01) at 30 days, but not beyond (31.6% vs 36.9%; P=.28). There was no difference in mortality at any time point (at 30 days, 9.7% vs 6.2%; P=.08; beyond 30 days, 17.3% vs 20.5%; P=.48). LTB was an independent predictor of MACE at 30 days post PCI (hazard ratio, 1.60; 95% confidence interval, 1.01-2.51; P=.04).
Conclusions:
In STEMI patients, LTB might identify a subpopulation at high risk of no-reflow, distal embolization, and early ischemic events, but is not associated with worse clinical outcomes at long-term follow-up.
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