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Author Spotlight: Enhancing Coronary Artery Revascularization
Published on: September 15, 2023
Infarct-Related Artery as a Donor of Collaterals in ST-Segment-Elevation Myocardial Infarction With Concomitant
Matthias Scholz1,2, Thomas Meyer3,2, Lars S Maier4
1Department of Diagnostic and Interventional Radiology University Medical Center Göttingen Göttingen Germany.
Insights
In ST-elevation myocardial infarction (STEMI) patients with chronic total occlusion (CTO) in a non-infarct-related artery, collaterals from the infarct-related artery distal to the occlusion improve prognosis. This finding challenges the double-jeopardy theory.
Area of Science:
- Cardiology
- Interventional Cardiology
- Myocardial Infarction Research
Background:
- Concomitant chronic total occlusion (CTO) in a non-infarct-related artery (NIRA) is linked to adverse outcomes in ST-segment-elevation myocardial infarction (STEMI).
- The "double-jeopardy effect" describes the acute threat to both the infarct-related artery (IRA) and the CTO area when the IRA provides collaterals to the CTO.
Purpose of the Study:
- To investigate the prognostic significance of intercoronary collateral origins (IRA vs. NIRA) in STEMI patients with coexisting NIRA CTO.
- To evaluate the impact of collateral supply from the IRA proximal versus distal to the STEMI occlusion on patient outcomes.
Main Methods:
- Analysis of data from 93 STEMI patients with single-vessel CTO in a NIRA and well-developed collaterals from a prospective study (FITT-STEMI).
- Comparison of in-hospital mortality rates based on the origin of collaterals supplying the CTO (NIRA, IRA proximal, IRA distal).
- Multivariate regression analysis to identify independent predictors of mortality.
Main Results:
- In-hospital mortality varied significantly based on collateral origin: 15.2% (NIRA), 29.4% (IRA proximal), and 3.3% (IRA distal).
- A proximal collateral origin from the IRA was associated with significantly higher mortality compared to a distal origin (OR=20.8, P=0.027).
Conclusions:
- In STEMI patients with NIRA CTO, collateralization from the IRA distal to the acute occlusion is associated with a better prognosis.
- These findings suggest that the double-jeopardy effect may not be the primary driver of adverse outcomes in this patient population.
Abstract:
BACKGROUND In ST-segment-elevation myocardial infarction (STEMI), a concomitant chronic total occlusion (CTO) in a non-infarct-related artery (NIRA) is associated with adverse outcome. In the case of the infarct-related artery (IRA) as a donor vessel for collaterals to the CTO, the IRA occlusion may lead to an acute threat to both the immediate IRA and the collaterally supplied CTO area, which has been described as a double-jeopardy effect. METHODS AND RESULTS We investigated the role of preformed intercoronary collaterals to the CTO originating from either the IRA or NIRA. Data were obtained from 2 hospitals participating in the prospective FITT-STEMI (Feedback Intervention and Treatment Times in ST-Segment Elevation Myocardial Infarction) study. From a total cohort of 2102 patients with acute STEMI, 93 patients had single-vessel CTO in an NIRA and well-developed intercoronary collaterals to the CTO. In-hospital mortality differed significantly with respect to the origin of the collaterals. Mortality was 15.2% with collaterals originating from the NIRA, 29.4% with a collateral origin from the IRA proximal to the acute STEMI occlusion, and 3.3% with a collateral origin from the IRA distal to the acute occlusion (P=0.044). A multivariate regression model confirmed that a proximal collateral origin had a significant higher mortality compared with a branching in the distal position from the acute STEMI occlusion (P=0.027; odds ratio = 20.8 [95% CI, 1.4-304.1]). CONCLUSIONS In STEMI with CTO in an NIRA, a CTO collateralization from the IRA distal to the acute occlusion is associated with a better prognosis. This finding challenges the double-jeopardy assumption as the main cause of adverse outcome in STEMI with CTO in an NIRA. REGISTRATION URL: https://www.clinicaltrials.gov; Unique identifier: NCT00794001.
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