TY - JOUR
T1 - Anticoagulation for post-operative atrial fibrillation after isolated coronary artery bypass grafting
T2 - a meta-analysis
AU - van de Kar, Mileen R.D.
AU - van Brakel, Thomas J.
AU - van 't Veer, Marcel
AU - van Steenbergen, Gijs J.
AU - Daeter, Edgar J.
AU - Crijns, Harry J.G.M.
AU - van Veghel, Dennis
AU - Dekker, Lukas R.C.
AU - Otterspoor, Luuk C.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/8/1
Y1 - 2024/8/1
N2 - Background and This study aimed to evaluate clinical outcomes in patients developing post-operative atrial fibrillation (POAF) after coronary Aims artery bypass grafting (CABG) and characterize variations in oral anticoagulation (OAC) use, benefits, and complications. Methods A systematic search identified studies on new-onset POAF after CABG and OAC initiation. Outcomes included risks of thromboembolic events, bleeding, and mortality. Furthermore, a meta-analysis was conducted on these outcomes, stratified by the use or non-use of OAC. Results The identified studies were all non-randomized. Among 1 698 307 CABG patients, POAF incidence ranged from 7.9% to 37.6%. Of all POAF patients, 15.5% received OAC. Within 30 days, thromboembolic events occurred at rates of 1.0% (POAF: 0.3%; non-POAF: 0.8%) with 2.0% mortality (POAF: 1.0%; non-POAF: 0.5%). Bleeding rates were 1.1% for POAF patients and 2.7% for non-POAF patients. Over a median of 4.6 years, POAF patients had 1.73 thromboembolic events, 3.39 mortality, and 2.00 bleeding events per 100 person-years; non-POAF patients had 1.14, 2.19, and 1.60, respectively. No significant differences in thromboembolic risks [effect size −0.11 (−0.36 to 0.13)] and mortality [effect size −0.07 (−0.21 to 0.07)] were observed between OAC users and non-users. However, OAC use was associated with higher bleeding risk [effect size 0.32 (0.06-0.58)]. Conclusions In multiple timeframes following CABG, the incidence of complications in patients who develop POAF is low. The use of OAC in patients with POAF after CABG is associated with increased bleeding risk.
AB - Background and This study aimed to evaluate clinical outcomes in patients developing post-operative atrial fibrillation (POAF) after coronary Aims artery bypass grafting (CABG) and characterize variations in oral anticoagulation (OAC) use, benefits, and complications. Methods A systematic search identified studies on new-onset POAF after CABG and OAC initiation. Outcomes included risks of thromboembolic events, bleeding, and mortality. Furthermore, a meta-analysis was conducted on these outcomes, stratified by the use or non-use of OAC. Results The identified studies were all non-randomized. Among 1 698 307 CABG patients, POAF incidence ranged from 7.9% to 37.6%. Of all POAF patients, 15.5% received OAC. Within 30 days, thromboembolic events occurred at rates of 1.0% (POAF: 0.3%; non-POAF: 0.8%) with 2.0% mortality (POAF: 1.0%; non-POAF: 0.5%). Bleeding rates were 1.1% for POAF patients and 2.7% for non-POAF patients. Over a median of 4.6 years, POAF patients had 1.73 thromboembolic events, 3.39 mortality, and 2.00 bleeding events per 100 person-years; non-POAF patients had 1.14, 2.19, and 1.60, respectively. No significant differences in thromboembolic risks [effect size −0.11 (−0.36 to 0.13)] and mortality [effect size −0.07 (−0.21 to 0.07)] were observed between OAC users and non-users. However, OAC use was associated with higher bleeding risk [effect size 0.32 (0.06-0.58)]. Conclusions In multiple timeframes following CABG, the incidence of complications in patients who develop POAF is low. The use of OAC in patients with POAF after CABG is associated with increased bleeding risk.
KW - Anticoagulation
KW - Antiplatelet therapy
KW - Coronary artery bypass grafting
KW - Post-operative atrial fibrillation
KW - Administration, Oral
KW - Humans
KW - Atrial Fibrillation/epidemiology
KW - Male
KW - Anticoagulants/therapeutic use
KW - Hemorrhage/chemically induced
KW - Incidence
KW - Postoperative Complications/epidemiology
KW - Thromboembolism/prevention & control
KW - Female
KW - Coronary Artery Bypass/adverse effects
UR - http://www.scopus.com/inward/record.url?scp=85200574003&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehae267
DO - 10.1093/eurheartj/ehae267
M3 - Article
C2 - 38809189
AN - SCOPUS:85200574003
SN - 0195-668X
VL - 45
SP - 2620
EP - 2630
JO - European Heart Journal
JF - European Heart Journal
IS - 29
ER -