TY - JOUR
T1 - White blood cell count and clinical outcomes after left main coronary artery revascularization
T2 - Insights from the EXCEL trial
AU - Claessen, Bimmer E.
AU - Ben-Yehuda, Ori
AU - Mehran, Roxana
AU - Sorrentino, Sabato
AU - Guedeney, Paul
AU - Chen, Shmuel
AU - Dressler, Ovidiu
AU - Kini, Annapoorna S.
AU - Sharma, Samin K.
AU - Mansour, Samer
AU - Noiseux, Nicolas
AU - Li, Ditian
AU - Kappetein, Arie Pieter
AU - Sabik, Joseph F.
AU - Serruys, Patrick W.
AU - Stone, Gregg W.
N1 - Funding Information:
The EXCEL trial was sponsored by Abbott Vascular (Santa Clara, California, USA). R.M.: Institutional Grant Support (funding to the institution) - AstraZeneca, Bayer, Beth Israel Deaconess, BMS, CSL Behring, Eli Lilly/DSI, Medtronic, Novartis Pharamceuticals, OrbusNeich; Consulting Fees - Boston Scientific, Cardiovascular Systems Inc., Medscape, Regeneron Pharmaceuticals (no fee), Roivant Sciences, Siemens Medical Solutions, Sanofi, Abbott Laboratories (personal fees for speaking engagements; consultant (paid to the institution), Abiomed and The Medicines Company (consultant – spouse); Scientific Advisory Board/Advisory Board - PLx Opco Inc./PLx Pharma Inc. (scientific advisory board), Bristol Myers Squibb (advisory board; funding to the institution); Equity <1% - Claret Medical, Elixir Medical; Executive Committee (paid to the institution) - Janssen Pharmaceuticals, Osprey Medical; DSMB Membership (paid to the institution) - Watermark Research Partners. S.M.: Abbott Vascular – grant for CTO program and honoraria as a speaker. A.P.K.: Employee – Medtronic. J.F.S.III: Consultant – Medtronic, Edwards, and Sorin. Advisory board – Medtronic Cardiac Surgery. P.W.S.: Consultant – Abbott, Biosensors, Medtronic, Micell Technologies, SINOMED, Philips/Volcano, Xeltis, HeartFlow. G.W.S.: Speaker or other honoraria from Cook, Terumo, Qool Therapeutics and Orchestra Biomed; Consultant to Valfix, TherOx, Vascular Dynamics, Robocath, HeartFlow, Gore, Ablative Solutions, Miracor, Neovasc, V-Wave, Abiomed, Ancora, MAIA Pharmaceuticals, Vectorious, Reva, Matrizyme; Equity/options from Ancora, Qool Therapeutics, Cagent, Applied Therapeutics, Biostar family of funds, SpectraWave, Orchestra Biomed, Aria, Cardiac Success, MedFocus family of funds, Valfix. For the remaining authors there are no conflicts of interest.
Publisher Copyright:
Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Background: Prior studies have reported an association between elevated white blood cell count (WBCc) and worse clinical outcomes after coronary artery bypass grafting (CABG) and percutaneous coronary intervention (PCI). We assessed the prognostic impact of WBCc in patients undergoing revascularization for left main coronary artery disease (LMCAD). Methods: In Evaluation of XIENCE Versus Coronary Artery Bypass Surgery for Effectiveness of Left Main Revascularization (EXCEL), 1905 patients with LMCAD and low or intermediate SYNTAX scores were randomized to PCI with everolimus-eluting stents versus CABG. The 1895 patients with baseline WBCc available were grouped in tertiles of WBCc (mean 5.6 ± 0.8, 7.5 ± 0.5, and 10.1 ± 1.6 × 109/L). Results: Five-year rates of the primary endpoint (death, myocardial infarction or stroke) were similar across increasing WBCc tertiles (21.2, 18.9, and 21.6%; P = 0.46). Individual components of the primary endpoint, Bleeding Academic Research Consortium (BARC) 3-5 bleeding, stent thrombosis or graft occlusion and ischemia-driven revascularization were all similar across WBCc tertiles. By multivariable analysis, WBCc as a continuous variable was not an independent predictor of adverse events (hazard radio per 1 × 109/L: 1.02; 95% CI, 0.97-1.08; P = 0.43). Results were consistent in the PCI and CABG arms individually. Conclusion: There was no association between baseline WBCc and 30-day or 5-year clinical outcomes after PCI or CABG. The absence of a clear incremental increase in events with increasing WBCc in the current analysis indicates that WBCc should not routinely be used as a prognostic marker or to guide revascularization decisions in patients with LMCAD.
AB - Background: Prior studies have reported an association between elevated white blood cell count (WBCc) and worse clinical outcomes after coronary artery bypass grafting (CABG) and percutaneous coronary intervention (PCI). We assessed the prognostic impact of WBCc in patients undergoing revascularization for left main coronary artery disease (LMCAD). Methods: In Evaluation of XIENCE Versus Coronary Artery Bypass Surgery for Effectiveness of Left Main Revascularization (EXCEL), 1905 patients with LMCAD and low or intermediate SYNTAX scores were randomized to PCI with everolimus-eluting stents versus CABG. The 1895 patients with baseline WBCc available were grouped in tertiles of WBCc (mean 5.6 ± 0.8, 7.5 ± 0.5, and 10.1 ± 1.6 × 109/L). Results: Five-year rates of the primary endpoint (death, myocardial infarction or stroke) were similar across increasing WBCc tertiles (21.2, 18.9, and 21.6%; P = 0.46). Individual components of the primary endpoint, Bleeding Academic Research Consortium (BARC) 3-5 bleeding, stent thrombosis or graft occlusion and ischemia-driven revascularization were all similar across WBCc tertiles. By multivariable analysis, WBCc as a continuous variable was not an independent predictor of adverse events (hazard radio per 1 × 109/L: 1.02; 95% CI, 0.97-1.08; P = 0.43). Results were consistent in the PCI and CABG arms individually. Conclusion: There was no association between baseline WBCc and 30-day or 5-year clinical outcomes after PCI or CABG. The absence of a clear incremental increase in events with increasing WBCc in the current analysis indicates that WBCc should not routinely be used as a prognostic marker or to guide revascularization decisions in patients with LMCAD.
KW - Coronary artery bypass grafting
KW - Left main coronary artery disease
KW - Percutaneous coronary intervention
KW - White blood cell count
UR - http://www.scopus.com/inward/record.url?scp=85121214547&partnerID=8YFLogxK
U2 - 10.1097/MCA.0000000000001052
DO - 10.1097/MCA.0000000000001052
M3 - Article
C2 - 34010180
AN - SCOPUS:85121214547
SN - 0954-6928
VL - 31
SP - 45
EP - 51
JO - Coronary Artery Disease
JF - Coronary Artery Disease
IS - 1
ER -