TY - JOUR
T1 - Complete revascularisation in ST-elevation myocardial infarction and multivessel disease: Meta-analysis of randomised controlled trials
AU - Kowalewski, Mariusz
AU - Schulze, Volker
AU - Berti, Sergio
AU - Waksman, Ron
AU - Kubica, Jacek
AU - Kołodziejczak, Michalina
AU - Buffon, Antonino Maria Tommaso
AU - Suryapranata, Harry
AU - Gurbel, Paul Alfred
AU - Kelm, Malte
AU - Pawliszak, Wojciech
AU - Anisimowicz, Lech
AU - Navarese, Eliano Pio
PY - 2015
Y1 - 2015
N2 - Background: Current guidelines recommend culpritonly revascularisation (COR) in haemodynamically stable patients with ST-segment elevation myocardial infarction (STEMI) and multivessel (MV) disease. Contrarily, growing body of evidence available from recent randomised controlled trials (RCTs) demonstrates improved outcomes with complete MV-percutaneous coronary intervention (PCI). Methods and results: We performed a meta-analysis of RCTs comparing complete MV-PCI with non-complete MV-PCI in STEMI and MV disease. Complete MV-PCI was defined as revascularisation to non-infarct-related artery lesions during index procedure, non-complete MVPCI-encompassed COR and staged approaches. Multiple databases and congress proceedings from major cardiovascular societies' meetings were screened for relevant studies. Primary endpoint was the composite of major adverse cardiac events (MACE) typically defined as death, recurrent myocardial infarction (MI) and repeat revascularisation. Secondary endpoints were cardiovascular mortality, recurrent MI and repeat revascularisation. Outcomes were analysed at longest available follow-up with differences accounted for with adjusted models by person-years. Seven RCTs (N=1303) were included. The median follow-up was 12 months. Complete MV-PCI reduced the odds of MACE compared with non-complete MV-PCI (OR (95% CIs) 0.59 (0.36 to 0.97), p=0.04) driven by reduction in recurrent MI (0.48 (0.27 to 0.85), p=0.01) and repeat revascularisation (0.51 (0.31 to 0.84), p=0.008). Complete MV-PCI was associated with a non-significant trend towards reduced cardiovascular mortality (0.54 (0.26 to 1.10), p=0.09) as well. In a sensitivity analysis, none of the baseline clinical variables significantly influenced overall estimates. Conclusions: In STEMI and MV disease, complete MVPCI as compared with non-complete strategy reduces MACE by 41%, driven by a 52% reduction in recurrent MI and 49% reduction in repeat revascularisation.
AB - Background: Current guidelines recommend culpritonly revascularisation (COR) in haemodynamically stable patients with ST-segment elevation myocardial infarction (STEMI) and multivessel (MV) disease. Contrarily, growing body of evidence available from recent randomised controlled trials (RCTs) demonstrates improved outcomes with complete MV-percutaneous coronary intervention (PCI). Methods and results: We performed a meta-analysis of RCTs comparing complete MV-PCI with non-complete MV-PCI in STEMI and MV disease. Complete MV-PCI was defined as revascularisation to non-infarct-related artery lesions during index procedure, non-complete MVPCI-encompassed COR and staged approaches. Multiple databases and congress proceedings from major cardiovascular societies' meetings were screened for relevant studies. Primary endpoint was the composite of major adverse cardiac events (MACE) typically defined as death, recurrent myocardial infarction (MI) and repeat revascularisation. Secondary endpoints were cardiovascular mortality, recurrent MI and repeat revascularisation. Outcomes were analysed at longest available follow-up with differences accounted for with adjusted models by person-years. Seven RCTs (N=1303) were included. The median follow-up was 12 months. Complete MV-PCI reduced the odds of MACE compared with non-complete MV-PCI (OR (95% CIs) 0.59 (0.36 to 0.97), p=0.04) driven by reduction in recurrent MI (0.48 (0.27 to 0.85), p=0.01) and repeat revascularisation (0.51 (0.31 to 0.84), p=0.008). Complete MV-PCI was associated with a non-significant trend towards reduced cardiovascular mortality (0.54 (0.26 to 1.10), p=0.09) as well. In a sensitivity analysis, none of the baseline clinical variables significantly influenced overall estimates. Conclusions: In STEMI and MV disease, complete MVPCI as compared with non-complete strategy reduces MACE by 41%, driven by a 52% reduction in recurrent MI and 49% reduction in repeat revascularisation.
KW - Coronary Artery Disease
KW - Electrocardiography
KW - Humans
KW - Myocardial Infarction
KW - Myocardial Revascularization
KW - Outcome Assessment, Health Care
KW - Percutaneous Coronary Intervention
KW - Retreatment
KW - Severity of Illness Index
KW - Survival Analysis
KW - Coronary Artery Disease
KW - Electrocardiography
KW - Humans
KW - Myocardial Infarction
KW - Myocardial Revascularization
KW - Outcome Assessment, Health Care
KW - Percutaneous Coronary Intervention
KW - Retreatment
KW - Severity of Illness Index
KW - Survival Analysis
UR - http://hdl.handle.net/10807/172064
U2 - 10.1136/heartjnl-2014-307293
DO - 10.1136/heartjnl-2014-307293
M3 - Article
SN - 1355-6037
VL - 101
SP - 1309
EP - 1317
JO - Heart
JF - Heart
ER -