STEMI patients with multivessel CAD benefit most from complete revascularization during the index procedure

Written By :  Dr. Kamal Kant Kohli
Published On 2022-10-29 04:45 GMT   |   Update On 2022-10-29 07:11 GMT

CHINA: STEMI patients with multivessel coronary artery disease should undergo complete revascularization, and complete revascularization during the index procedure is superior to complete revascularization during a staged procedure in terms of lowering the risk of major adverse cardiac events (MACE) events, states a study published in the Journal, Frontiers in Cardiovascular...

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CHINA: STEMI patients with multivessel coronary artery disease should undergo complete revascularization, and complete revascularization during the index procedure is superior to complete revascularization during a staged procedure in terms of lowering the risk of major adverse cardiac events (MACE) events, states a study published in the Journal, Frontiers in Cardiovascular Medicine.

Multivessel Coronary Artery Disease (CAD), which is linked to increased mortality and a worse prognosis, affects about 50% of individuals with ST-segment elevation myocardial infarction (STEMI). Multiple randomized trials have recently demonstrated that patients with multivessel disease (MVD) frequently seek complete revascularization after percutaneous coronary intervention (PCI) to enhance their prognosis. It has been debatable when the non-culprit artery should be operated on, though.

With regard to ST-segment elevation myocardial infarction (STEMI) patients who had multivessel coronary artery disease, the study sought to identify the best revascularization approach (CAD).

There were 17 randomized controlled trials (RCTs) with 8568 patients that compared three revascularization strategies for STEMI patients with multivessel coronary artery disease: complete revascularization at the index procedure (CR), complete revascularization as a staged procedure (SR), or culprit-only revascularization (COR). Both pairwise and network meta-analyses were carried out by the researchers. Mixed treatment comparison models were used in network meta-analysis. Major adverse cardiac events were the analysis's main result (MACE). Heart failure, stroke, severe hemorrhage, contrast-induced nephropathy, all-cause mortality, cardiac mortality, nonfatal re-MI, unplanned repeat revascularization, re-hospitalization, and stent thrombosis were secondary outcomes.

Key findings of the study:

  • Major adverse cardiac events (MACE) were more likely to occur with phased revascularization at the index procedure compared to full revascularization [odds ratio (OR): 1.93; 95% confidence interval (CI): 1.07-3.49].
  • Complete revascularization decreased the chance of unplanned repeat revascularization (RR: 0.49, 95% CI: 0.33-0.75, p = 0.001), which in turn decreased the incidence of MACE in the pairwise meta-analysis [risk ratio (RR): 0.62, 95% CI: 0.48-0.79, p<0.001].
  • All-cause mortality, cardiac mortality, and nonfatal re-myocardial infarction did not differ significantly from one another.

The authors concluded that revascularization of non-culprit arteries during Primary Percutaneous Coronary Intervention is secure and practical while lowering the risk of re-hospitalization.

According to the authors, the sub-study of the COMPLETE trial suggested that the benefit of complete revascularization over culprit-lesion only PCI was consistent among STEMI patients with multi-vessel disease, regardless of the timing of non-culprit-lesion intervention as determined by the investigator.

More prospective RCTs are required to ascertain the appropriate timing of full revascularization and its effects on all-cause mortality, cardiovascular mortality, and risk of re-MI, they added.

REFERENCE

Feng Y, Li S, Hu S, Wan J, Shao H. The optimal timing for non-culprit percutaneous coronary intervention in patients with multivessel coronary artery disease: A pairwise and network meta-analysis of randomized trials. Frontiers in Cardiovascular Medicine. 2022 ;9:1000664. DOI: 10.3389/fcvm.2022.1000664. PMID: 36225962; PMCID: PMC9548605. 

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Article Source : Frontiers in Cardiovascular Medicine

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