TY - JOUR
T1 - All-cause mortality and major cardiovascular outcomes comparing percutaneous coronary angioplasty versus coronary artery bypass grafting in the treatment of unprotected left main stenosis
T2 - A meta-analysis of short- and long-term randomised trials
AU - Kunutsor, Setor
AU - Laukkanen, Jari A
AU - Niemelä,, Matti
AU - Thuesen,, Leif
AU - Mäkikallio, Timo H.
PY - 2017
Y1 - 2017
N2 - Objective We compared percutaneous coronary intervention (PCI) with coronary artery bypass grafting (CABG) for the treatment of left main coronary artery (LMCA) disease by conducting a systematic review and meta-analysis of randomised controlled trials (RCTs). Methods Randomised controlled trials of PCI versus CABG in patients with LMCA stenosis were identified from MEDLINE, the Cochrane Library, and search of bibliographies to November 2016. Study specific hazard ratios with 95% CIs were aggregated for all-cause mortality, major adverse cardiac and cerebrovascular events (MACCE), and other cardiovascular events at time-points of 30 days, 1 year, and 3 years and beyond. Results Six RCTs comprising 4,700 patients were included. There were no significant differences in risk of all-cause mortality in pooled analysis of relevant trials at 30 days (0.61, 95% CI: 0.27-1.36), 1 year (0.66, 95% CI: 0.42-1.04), and 3 years and beyond (1.04, 95% CI: 0.81-1.33), comparing PCI with CABG. There was no significant difference in the risk of MACCE at 30 days (0.72, 95% CI: 0.51-1.03) and 1 year (1.16, 95% CI: 0.94-1.44); however, PCI was associated with a higher risk of MACCE compared with CABG during longer term follow-up (1.27, 95% CI: 1.12-1.44). Composite outcome of death, stroke, or myocardial infarction was lower with PCI at 30 days (0.67, 95% CI: 0.49-0.92). Repeat revascularization was increased at 1 year and at 3 years and beyond for PCI. Conclusions All-cause mortality rates are not significantly different between PCI and CABG at shortand long-term follow-up. However, PCI is associated with a reduction in the risk of major cardiovascular outcomes at short-term follow-up in LMCA stenosis patients; but at long term, MACCE rate is increased for PCI.
AB - Objective We compared percutaneous coronary intervention (PCI) with coronary artery bypass grafting (CABG) for the treatment of left main coronary artery (LMCA) disease by conducting a systematic review and meta-analysis of randomised controlled trials (RCTs). Methods Randomised controlled trials of PCI versus CABG in patients with LMCA stenosis were identified from MEDLINE, the Cochrane Library, and search of bibliographies to November 2016. Study specific hazard ratios with 95% CIs were aggregated for all-cause mortality, major adverse cardiac and cerebrovascular events (MACCE), and other cardiovascular events at time-points of 30 days, 1 year, and 3 years and beyond. Results Six RCTs comprising 4,700 patients were included. There were no significant differences in risk of all-cause mortality in pooled analysis of relevant trials at 30 days (0.61, 95% CI: 0.27-1.36), 1 year (0.66, 95% CI: 0.42-1.04), and 3 years and beyond (1.04, 95% CI: 0.81-1.33), comparing PCI with CABG. There was no significant difference in the risk of MACCE at 30 days (0.72, 95% CI: 0.51-1.03) and 1 year (1.16, 95% CI: 0.94-1.44); however, PCI was associated with a higher risk of MACCE compared with CABG during longer term follow-up (1.27, 95% CI: 1.12-1.44). Composite outcome of death, stroke, or myocardial infarction was lower with PCI at 30 days (0.67, 95% CI: 0.49-0.92). Repeat revascularization was increased at 1 year and at 3 years and beyond for PCI. Conclusions All-cause mortality rates are not significantly different between PCI and CABG at shortand long-term follow-up. However, PCI is associated with a reduction in the risk of major cardiovascular outcomes at short-term follow-up in LMCA stenosis patients; but at long term, MACCE rate is increased for PCI.
KW - Percutaneous coronary intervention
KW - coronary artery bypass grafting,
KW - left main coronary artery stenosis
KW - meta-analysis
U2 - 10.1136/openhrt-2017-000638
DO - 10.1136/openhrt-2017-000638
M3 - Article (Academic Journal)
C2 - 29259788
SN - 2053-3624
VL - 4
JO - Open Heart
JF - Open Heart
IS - 2
M1 - e000638
ER -