TY - JOUR
T1 - Comparison of coronary artery bypass surgery and percutaneous coronary intervention in patients with diabetes
T2 - A meta-analysis of randomised controlled trials
AU - Verma, Subodh
AU - Farkouh, Michael E.
AU - Yanagawa, Bobby
AU - Fitchett, David H.
AU - Ahsan, Muhammad R.
AU - Ruel, Marc
AU - Sud, Sachin
AU - Gupta, Milan
AU - Singh, Shantanu
AU - Gupta, Nandini
AU - Cheema, Asim N.
AU - Leiter, Lawrence A.
AU - Fedak, Paul W.M.
AU - Teoh, Hwee
AU - Latter, David A.
AU - Fuster, Valentin
AU - Friedrich, Jan O.
N1 - Funding Information:
The study was supported by grants from the Heart and Stroke Foundation of Canada and the Canada Research Chairs Program to SV. JOF is supported by a Clinician-Scientist Award from the Canadian Institutes of Health Research. MEF is supported by the Chair of the Heart and Stroke Richard Lewar Centre of Excellence in Cardiovascular Research at the University of Toronto. We thank Neill K J Adhikari for suggesting the addition of the non-diabetic versus diabetic subgroup analysis.
PY - 2013/12
Y1 - 2013/12
N2 - Background: The choice between coronary artery bypass surgery (CABG) and percutaneous coronary intervention (PCI) for revascularisation in patients with diabetes and multivessel coronary artery disease, who account for 25% of revascularisation procedures, is much debated. We aimed to assess whether all-cause mortality differed between patients with diabetes who had CABG or PCI by doing a systematic review and meta-analysis of randomised controlled trials (RCTs) comparing CABG with PCI in the modern stent era. Methods: We searched Medline, Embase, and the Cochrane Central Register of Controlled Trials from Jan 1, 1980, to March 12, 2013, for studies reported in English. Eligible studies were those in which investigators enrolled adult patients with diabetes and multivessel coronary artery disease, randomised them to CABG (with arterial conduits in at least 80% of participants) or PCI (with stents in at least 80% of participants), and reported outcomes separately in patients with diabetes, with a minimum of 12 months of follow-up. We used random-effects models to calculate risk ratios (RR) and 95% CIs for pooled data. We assessed heterogeneity using I2. The primary outcome was all-cause mortality in patients with diabetes who had CABG compared with those who had PCI at 5-year (or longest) follow-up. Findings: The initial search strategy identified 3414 citations, of which eight trials were eligible. These eight trials included 7468 participants, of whom 3612 had diabetes. Four of the RCTs used bare metal stents (BMS; ERACI II, ARTS, SoS, MASS II) and four used drug-eluting stents (DES; FREEDOM, SYNTAX, VA CARDS, CARDia). At mean or median 5-year (or longest) follow-up, individuals with diabetes allocated to CABG had lower all-cause mortality than did those allocated to PCI (RR 0·67, 95% CI 0·52-0·86; p=0·002; I2=25%; 3131 patients, eight trials). Treatment effects in individuals without diabetes showed no mortality benefit (1·03, 0·77-1·37; p=0·78; I2=46%; 3790 patients, five trials; pinteraction=0.03). We identified no differences in outcome whether PCI was done with BMS or DES. When present, we identified no clear causes of heterogeneity. Interpretation: In the modern era of stenting and optimum medical therapy, revascularisation of patients with diabetes and multivessel disease by CABG decreases long-term mortality by about a third compared with PCI using either BMS or DES. CABG should be strongly considered for these patients. Funding: Canadian Institutes of Health Research, Heart and Stroke Foundation of Canada, and Canada Research Chairs programme.
AB - Background: The choice between coronary artery bypass surgery (CABG) and percutaneous coronary intervention (PCI) for revascularisation in patients with diabetes and multivessel coronary artery disease, who account for 25% of revascularisation procedures, is much debated. We aimed to assess whether all-cause mortality differed between patients with diabetes who had CABG or PCI by doing a systematic review and meta-analysis of randomised controlled trials (RCTs) comparing CABG with PCI in the modern stent era. Methods: We searched Medline, Embase, and the Cochrane Central Register of Controlled Trials from Jan 1, 1980, to March 12, 2013, for studies reported in English. Eligible studies were those in which investigators enrolled adult patients with diabetes and multivessel coronary artery disease, randomised them to CABG (with arterial conduits in at least 80% of participants) or PCI (with stents in at least 80% of participants), and reported outcomes separately in patients with diabetes, with a minimum of 12 months of follow-up. We used random-effects models to calculate risk ratios (RR) and 95% CIs for pooled data. We assessed heterogeneity using I2. The primary outcome was all-cause mortality in patients with diabetes who had CABG compared with those who had PCI at 5-year (or longest) follow-up. Findings: The initial search strategy identified 3414 citations, of which eight trials were eligible. These eight trials included 7468 participants, of whom 3612 had diabetes. Four of the RCTs used bare metal stents (BMS; ERACI II, ARTS, SoS, MASS II) and four used drug-eluting stents (DES; FREEDOM, SYNTAX, VA CARDS, CARDia). At mean or median 5-year (or longest) follow-up, individuals with diabetes allocated to CABG had lower all-cause mortality than did those allocated to PCI (RR 0·67, 95% CI 0·52-0·86; p=0·002; I2=25%; 3131 patients, eight trials). Treatment effects in individuals without diabetes showed no mortality benefit (1·03, 0·77-1·37; p=0·78; I2=46%; 3790 patients, five trials; pinteraction=0.03). We identified no differences in outcome whether PCI was done with BMS or DES. When present, we identified no clear causes of heterogeneity. Interpretation: In the modern era of stenting and optimum medical therapy, revascularisation of patients with diabetes and multivessel disease by CABG decreases long-term mortality by about a third compared with PCI using either BMS or DES. CABG should be strongly considered for these patients. Funding: Canadian Institutes of Health Research, Heart and Stroke Foundation of Canada, and Canada Research Chairs programme.
UR - http://www.scopus.com/inward/record.url?scp=84887621557&partnerID=8YFLogxK
U2 - 10.1016/S2213-8587(13)70089-5
DO - 10.1016/S2213-8587(13)70089-5
M3 - Article
C2 - 24622417
AN - SCOPUS:84887621557
SN - 2213-8587
VL - 1
SP - 317
EP - 328
JO - The Lancet Diabetes and Endocrinology
JF - The Lancet Diabetes and Endocrinology
IS - 4
ER -