Key result
Multivessel intervention showed no credible mortality advantage over culprit-vessel intervention in patients with STEMI and multivessel coronary disease (global summary OR 1.10; 95% BCI 0.74-1.51).
Why the study?
Does multivessel intervention reduce mortality compared to culprit-vessel intervention in patients with STEMI and multivessel coronary disease?
Meta-Analysis (n=48,398)
Does multivessel intervention reduce mortality compared to culprit-vessel intervention in patients with STEMI and multivessel coronary disease?
A Bayesian cross-design meta-analysis found no credible mortality advantage for multivessel intervention over culprit-vessel intervention in STEMI patients with multivessel disease.
No mortality benefit supports culprit-only PCI as default in STEMI; confirms prior RCTs and tempers routine multivessel intervention.
INTRODUCTION: During primary percutaneous coronary intervention (PCI), patients with ST-elevation myocardial infarction (STEMI) and multivessel coronary disease can undergo either multivessel intervention (MVI) or culprit-vessel intervention (CVI) only. BACKGROUND: Randomized controlled trials (RCTs) support the use of MVI, but cohort studies support the use of CVI. METHODS: We developed Bayesian models that incorporated parameters for study type and study outcome after MVI or CVI. RESULTS: A total of 18 studies (4 RCTs, 3 matched cohort studies, and 11 unmatched observational studies) enrolled 48,398 patients with STEMI and multivessel CAD and reported outcomes after MVI or CVI-only at the time of primary PCI. Using a Bayesian hierarchical model, we found that the point estimates replicated previously reported trends, but the wide Bayesian credible intervals (BCI) excluded any plausible mortality difference between MVI versus CVI in all three study types: RCTs (odds ratio [OR] 0.60, 95% BCI 0.31-1.20), matched cohort studies (OR 1.37, 95% BCI 0.86-2.24), or unmatched cohort studies (OR 1.16, 95% BCI 0.70-1.89). Both the global summary (OR 1.10, 95% BCI 0.74-1.51) and a sensitivity analysis that weighted the RCTs 1-5 times as much as observational studies revealed no credible advantage of one PCI strategy over the other (OR 1.05, 95% BCI 0.64-1.48). CONCLUSIONS: Bayesian approaches contextualize the comparison of different strategies by study type and suggest that neither MVI nor CVI emerges as a preferred strategy in an analysis that accounts mortality differences.
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Bittl et al. (2015) conducted a meta-analysis in ST-elevation myocardial infarction (STEMI) and multivessel coronary disease (n=48,398). Multivessel intervention (MVI) vs. Culprit-vessel intervention (CVI) only was evaluated on Mortality (OR 1.10, 95% CI 0.74-1.51). Multivessel intervention showed no credible mortality advantage over culprit-vessel intervention in patients with STEMI and multivessel coronary disease (global summary OR 1.10; 95% BCI 0.74-1.51).
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