Key result
Early microvascular obstruction, assessed by CMR, was associated with a 66.2% occurrence of the primary composite endpoint compared to 42.4% in patients without MVO, with HR 2.20 indicating a significantly higher risk of adverse outcomes.
Why the study?
Does the presence of early microvascular obstruction assessed by CMR predict adverse clinical outcomes in patients reperfused by pPCI for STEMI?
Population
Patients reperfused by primary percutaneous coronary intervention for first ST-elevation myocardial…
Comparison
Presence of early microvascular obstruction… vs Absence of early microvascular obstruction (eMVO-)
Design
Cohort, Endpoints defined by a consensus of investigators blinded to the CMR…
Follow-up
median 52 months
Authors
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May refine post-STEMI risk stratification; extends observational data but leaves open prospective validation.
Cohort (n=129)
No
Does the presence of early microvascular obstruction assessed by CMR predict adverse clinical outcomes in patients reperfused by pPCI for STEMI?
Effect estimate: HR 2.20 (95% CI 1.11-4.36)
Absolute Event Rate: 66.2% vs 42.4%
p-value: p=0.024
Early microvascular obstruction assessed by first-pass CMR is a strong independent predictor of long-term cardiovascular morbidity at 5 years in patients after STEMI.
Klug et al. (2012) conducted a cohort in acute ST-elevation myocardial infarction (n=129). early microvascular obstruction (MVO) assessment by CMR vs. patients without early MVO was evaluated on composite of death, myocardial re-infarction, stroke, repeat revascularization, recurrence of ischemic symptoms, atrial fibrillation, congestive heart failure and hospitalization (HR 2.20, 95% CI 1.11-4.36, p=0.024). Early microvascular obstruction, assessed by CMR, was associated with a 66.2% occurrence of the primary composite endpoint compared to 42.4% in patients without MVO, with HR 2.20 indicating a significantly higher risk of adverse outcomes.
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