Drug-eluting or bare-metal stents for left anterior descending or left main coronary artery revascularization
Permanent lenke
https://hdl.handle.net/10037/23783Dato
2021-10-08Type
Journal articleTidsskriftartikkel
Peer reviewed
Forfatter
Piccolo, Raffaele; Bonaa, Kaare H.; Efthimiou, Orestis; Varenne, Olivier; Urban, Philip; Kaiser, Christoph; Räber, Lorenz; de Belder, Adam; Remkes, Wouter; Van’T Hof, Arnoud W. J.; Stankovic, Goran; Lemos, Pedro A.; Wilsgaard, Tom; Reifart, Jörg; Rodriguez, Alfredo E.; Ribeiro, Expedito E.; Serruys, Patrick W. J. C.; Abizaid, Alex; Sabaté, Manel; Byrne, Robert A.; de la Torre Hernandez, Jose M.; Wijns, William; Esposito, Giovanni; Jüni, Peter; Windecker, Stephan; Valgimigli, MarcoSammendrag
Methods and Results - The Coronary Stent Trialist (CST) Collaboration gathered individual patient data of randomized trials of DES versus BMS for the treatment of coronary artery disease. The primary outcome was the composite of cardiac death or myocardial infarction. Hazard ratios (HRs) with 95% CIs were derived from a 1‐stage individual patient data meta‐analysis. We included 26 024 patients across 19 trials: 13 650 (52.4%) in the LAD/LM and 12 373 (47.6%) in the no‐LAD/LM group. At 6‐year follow‐up, there was strong evidence that the treatment effect of DES versus BMS depended on the target vessel (P‐interaction=0.024). Compared with BMS, DES reduced the risk of cardiac death or myocardial infarction to a greater extent in the LAD/LM (HR, 0.76; 95% CI, 0.68–0.85) than in the no‐LAD/LM territories (HR, 0.93; 95% CI, 0.83–1.05). This benefit was driven by a lower risk of cardiac death (HR, 0.83; 95% CI, 0.70–0.98) and myocardial infarction (HR, 0.74; 95% CI, 0.65–0.85) in patients with LAD/LM disease randomized to DES. An interaction (P=0.004) was also found for all‐cause mortality with patients with LAD/LM disease deriving benefit from DES (HR, 0.86; 95% CI, 0.76–0.97).
Conclusions - As compared with BMS, new‐generation DES were associated with sustained reduction in the composite of cardiac death or myocardial infarction if used for the treatment of LAD or left main coronary stenoses.