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Winter, Robbert J. de

https://orcid.org/0000-0002-3694-405X

Mayo Clinic

Amsterdam UMC Location University of Amsterdam

Citations 2

Ten-Year All-Cause Death According to Completeness of Revascularization in Patients With Three-Vessel Disease or Left Main Coronary Artery Disease: Insights From the SYNTAX Extended Survival Study
Takahashi, Kuniaki , Serruys, Patrick W. , Gao, Chao , Ono, Masafumi , Wang, Rutao , Thuijs, Daniel J.F.M. , Mack, Michael J. , Curzen, Nick , Mohr, Friedrich‐Wilhelm, Davierwala, Piroze , Milojevic, Milan , Winter, Robbert J. de , Onuma, Yoshinobu , Head, Stuart J., Morice, Marie‐Claude, Holmes, David R. , Investigators, on behalf of the SYNTAX Extended Survival Study, Serruys, Patrick W , Curzen, Nick , Onuma, Yoshinobu , Milojevic, Milan , Wykrzykowska, Joanna J. , Sharif, Faisal , Kappetein, A. Pieter , Investigators, on behalf of the SYNTAX Extended Survival Study

Circulation | May 20, 2021 | Volume: 144 | Issue: 2 | Pages: 96-109

10.1161/circulationaha.120.046289 Get It

Background: Ten-year all-cause death according to incomplete (IR) versus complete revascularization (CR) has not been fully investigated in patients with 3-vessel disease and left main coronary artery disease undergoing percutaneous coronary intervention (PCI) versus coronary artery bypass grafting (CABG). Methods: The SYNTAX Extended Survival study (Synergy Between PCI With TAXUS and Cardiac Surgery: SYNTAX Extended Survival [SYNTAXES]) evaluated vital status up to 10 years in patients who were originally enrolled in the SYNTAX trial. In the present substudy, outcomes of the CABG CR group were compared with the CABG IR, PCI CR, and PCI IR groups. In addition, in the PCI cohort, the residual SYNTAX score (rSS) was used to quantify the extent of IR and to assess its association with fatal late outcome. The rSS of 0 suggests CR, whereas a rSS>0 identifies the degree of IR. Results: IR was more frequently observed in patients with PCI versus CABG (56.6% versus 36.8%) and more common in those with 3-vessel disease than left main coronary artery disease in both the PCI arm (58.5% versus 53.8%) and the CABG arm (42.8% versus 27.5%). Patients undergoing PCI with CR had no significant difference in 10-year all-cause death compared with those undergoing CABG (22.2% for PCI with CR versus 24.3% for CABG with IR versus 23.8% for CABG with CR). In contrast, those with PCI and IR had a significantly higher risk of all-cause death at 10 years compared with CABG and CR (33.5% versus 23.7%; adjusted hazard ratio, 1.48 [95% CI, 1.15–1.91]). When patients with PCI were stratified according to the rSS, those with a rSS≤8 had no significant difference in all-cause death at 10 years as the other terciles (22.2% for rSS=0 versus 23.9% for rSS>0–4 versus 28.9% for rSS>4–8), whereas a rSS>8 had a significantly higher risk of 10-year all-cause death than those undergoing PCI with CR (50.1% versus 22.2%; adjusted hazard ratio, 3.40 [95% CI, 2.13–5.43]). Conclusions: IR is common after PCI, and the degree of incompleteness was associated with 10-year mortality. If it is unlikely that complete (or nearly complete; rSS<8) revascularization can be achieved with PCI in patients with 3-vessel disease, CABG should be considered. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT00114972. URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03417050.
Ten-year all-cause mortality according to smoking status in patients with severe coronary artery disease undergoing surgical or percutaneous revascularization
Takahashi, Kuniaki , Thuijs, Daniel J.F.M. , Gao, Chao , Ono, Masafumi , Holmes, David R. , Mack, Michael J. , Morice, Marie‐Claude, Mohr, Friedrich‐Wilhelm, Curzen, Nick , Davierwala, Piroze , Milojevic, Milan , Dawkins, Keith D., Winter, Robbert J. de , McEvoy, John W. , Onuma, Yoshinobu , Head, Stuart J., Investigators, the SYNTAX Extended Survival Study, de Winter, Robbert J , Serruys, Patrick W , Curzen, Nick , Onuma, Yoshinobu , Milojevic, Milan , Morice, Marie‐Claude, Wykrzykowska, Joanna J. , Kappetein, A. Pieter , Serruys, Patrick W. , Investigators, the SYNTAX Extended Survival Study

European Journal of Preventive Cardiology | January 1, 2021 | Volume: 29 | Issue: 2 | Pages: 312-320

10.1093/eurjpc/zwaa089 Get It

Abstract Aims To evaluate the impact of various smoking status on 10-year all-cause mortality and to examine a relative treatment benefit of coronary artery bypass grafting (CABG) vs. percutaneous coronary intervention (PCI) according to smoking habits. Methods and results The SYNTAX Extended Survival study evaluated vital status up to 10 years in 1800 patients with de novo three-vessel disease and/or left main coronary artery disease randomized to CABG or PCI in the SYNTAX trial. In the present analysis, patients were divided into three groups (current, former, or never smokers), and the primary endpoint of 10-year all-cause mortality was assessed according to smoking status. Smoking status was available in 1793 (99.6%) patients at the time of randomization, of whom 363 were current smokers, 798 were former smokers, and 632 were never smokers. The crude rates of 10-year all-cause mortality were 29.7% in current smokers, 25.3% in former smokers, and 25.9% in never smokers (Log-rank P = 0.343). After adjustment for imbalances in baseline characteristics, current smokers had a significantly higher risk of 10-year all-cause mortality than never smokers [adjusted hazard ratio (aHR): 2.29; 95% confidence interval (CI): 1.60–3.27; P &lt; 0.001], whereas former smokers did not. PCI was associated with a higher risk of all-cause mortality than CABG among current smokers (HR: 1.60; 95% CI: 1.09–2.35; P = 0.017), but it failed to show a significant interaction between revascularization strategies and smoking status (Pinteraction = 0.910). Conclusion Current smokers had a higher adjusted risk of 10-year all-cause mortality, whereas former smokers did not. The treatment effect of CABG vs. PCI did not differ significantly according to smoking status. Clinical trial registration SYNTAX: ClinicalTrials.gov reference: NCT00114972; SYNTAX Extended Survival. ClinicalTrials.gov reference: NCT03417050.