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Published on: April 25, 2014
Impact of collateralisation to a concomitant chronic total occlusion in patients with ST-elevation myocardial
Ivo M van Dongen1, Joëlle Elias1, K Gert van Houwelingen2
1Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Insights
Well-developed coronary collaterals in ST-elevation myocardial infarction (STEMI) patients with chronic total occlusions (CTO) improve left ventricular ejection fraction but not clinical outcomes. Collateral status alone should not dictate CTO revascularization decisions.
Area of Science:
- Cardiology
- Interventional Cardiology
- Myocardial Infarction Research
Background:
- Coronary artery disease management, particularly in ST-elevation myocardial infarction (STEMI) with concomitant chronic total occlusions (CTO), remains complex.
- The role of collateral circulation in influencing cardiac function and clinical outcomes in STEMI patients with CTO is not well-established.
Purpose of the Study:
- To investigate the impact of well-developed versus poorly developed coronary collaterals on cardiac function in STEMI patients with CTO.
- To evaluate whether the presence of good collaterals influences clinical outcomes in this patient population.
Main Methods:
- Analysis of data from the EXPLORE trial, randomizing STEMI patients with CTO to CTO percutaneous coronary intervention (PCI) or no-CTO PCI.
- Angiographic scoring of collateral grades (Rentrop classification) and measurement of left ventricular ejection fraction (LVEF) and end-diastolic volume (LVEDV) via cardiac MRI at 4 months.
Main Results:
- Well-developed collaterals (Rentrop grades 2-3) were present in 54% of patients.
- Patients with well-developed collaterals showed significantly higher LVEF (46.2% vs 42.1%, p=0.004) and a trend for lower LVEDV at 4 months compared to those with poorly developed collaterals.
- No significant difference in scar burden or long-term clinical event rates was observed between groups.
Conclusions:
- In STEMI patients with CTO, well-developed collaterals are associated with improved LVEF at 4 months.
- This improvement in LVEF did not translate to better clinical outcomes.
- Collateral status is an important factor but should not be the sole determinant for revascularization decisions in concomitant CTOs.
Objective:
The impact on cardiac function of collaterals towards a concomitant chronic total coronary occlusion (CTO) in patients with ST-elevation myocardial infarction (STEMI) has not been investigated yet. Therefore, we have evaluated the impact of well-developed collaterals compared with poorly developed collaterals to a concomitant CTO in STEMI.
Methods And Results:
In the EXPLORE trial, patients with STEMI and a concomitant CTO were randomised to either CTO percutaneous coronary intervention (PCI) or no-CTO PCI. Collateral grades were scored angiographically using the Rentrop grade classification. Left ventricular ejection fraction (LVEF) and left ventricular end-diastolic volume (LVEDV) at 4 months were measured using cardiac magnetic resonance imaging. Well-developed collaterals (Rentrop grades 2-3) to the CTO were present in 162 (54%) patients; these patients had a significantly higher LVEF at 4 months (46.2±11.4% vs 42.1±12.7%, p=0.004) as well as a trend for a lower LVEDV (208.2±55.7 mL vs 222.6±68.5 mL, p=0.054) when compared with patients with poorly developed collaterals to the CTO. There was no significant difference in the total amount of scar in the two groups. Event rates were statistically comparable between patients with well-developed collaterals and poorly developed collaterals to the CTO at long-term follow-up.
Conclusions:
In patients with STEMI and a concomitant CTO, the presence of well-developed collaterals to a concomitant CTO is associated with a better LVEF at 4 months. However, this effect on LVEF did not translate into improvement in clinical outcome. Therefore, the presence of well-developed collaterals is important, but should not solely guide in the clinical decision-making process regarding any additional revascularisation of a concomitant CTO in patients with STEMI.
Clinical Trial Registration:
NTR1108.
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