Late thrombotic events after bioresorbable scaffold implantation: a systematic review and meta-analysis of randomized clinical trials
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Collet, Carlos
Department of Cardiology, Academic Medical Center, Universiteit van Amsterdam, Netherlands
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Asano, Taku
Department of Cardiology, Academic Medical Center, Universiteit van Amsterdam, Netherlands
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Miyazaki, Yosuke
Department of Interventional Cardiology, Rotterdam, Netherlands
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Tenekecioglu, Erhan
Department of Interventional Cardiology, Rotterdam, Netherlands
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Katagiri, Yuki
Department of Cardiology, Academic Medical Center, Universiteit van Amsterdam, Netherlands
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Sotomi, Yohei
Department of Cardiology, Academic Medical Center, Universiteit van Amsterdam, Netherlands
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Cavalcante, Rafael
Department of Interventional Cardiology, Rotterdam, Netherlands
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Winter, Robbert J. de
Department of Cardiology, Academic Medical Center, Universiteit van Amsterdam, Netherlands
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Kimura, Takeshi
Department of Cardiovascular Medicine, Kyoto University Hospital, Shogoin Kawaharacho, Sakyo Ward, Kyoto, Japan
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Gao, Runlin
Department of Cardiology, Fu Wai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences, Beijing, China
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Puricel, Serban
Department of Cardiology, University of Fribourg and Hospital, Fribourg, Switzerland
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Cook, Stéphane
Department of Cardiology, University of Fribourg and Hospital, Fribourg, Switzerland
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Capodanno, Davide
Cardio-Thoracic-Vascular Department, Ferrarotto Hospital, University of Catania, Italy
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Onuma, Yoshinobu
Department of Interventional Cardiology, Rotterdam, Netherlands
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Serruys, Patrick W.
Imperial Department of Medicine, Imperial College of London, Kensington, London, UK
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Published in:
- European Heart Journal. - 2017, vol. 38, no. 33, p. 2559-2566
English
To compare the long-term safety and efficacy of bioresorbable vascular scaffold (BVS) with everolimus-eluting stent (EES) after percutaneous coronary interventions.Methods and Results: A systematic review and meta-analysis of randomized clinical trials comparing clinical outcomes of patients treated with BVS and EES with at least 24 months follow-up was performed. Adjusted random-effect model by the Knapp–Hartung method was used to compute odds ratios (OR) and 95% confidence intervals (CI). The primary safety outcome of interest was the risk of definite/probable device thrombosis (DT). The primary efficacy outcome of interest was the risk of target lesion failure (TLF). Five randomized clinical trials (n = 1730) were included. Patients treated with Absorb BVS had a higher risk of definite/probable DT compared with patients treated with EES (OR 2.93, 95%CI 1.37–6.26, P = 0.01). Very late DT (VLDT) occurred in 13 patients [12/996 (1.4%, 95%CI: 0.08–2.5) Absorb BVS vs. 1/701 (0.5%, 95%CI: 0.2–1.6) EES; OR 3.04; 95%CI 1.2–7.68, P = 0.03], 92% of the VLDT in the BVS group occurred in the absence of dual antiplatelet therapy (DAPT). Patients treated with Absorb BVS had a trend towards higher risk of TLF (OR 1.48, 95%CI 0.90–2.42, P = 0.09), driven by a higher risk of target vessel myocardial infarction and ischaemia-driven target lesion revascularization. No difference was found in the risk of cardiac death.Conclusion: Compared with EES, the use of Absorb BVS was associated with a higher rate of DT and a trend towards higher risk of TLF. VLDT occurred in 1.4% of the patients, the majority of these events occurred in the absence of DAPT.
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Faculty
- Faculté des sciences et de médecine
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Department
- Médecine 3ème année
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Language
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Classification
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Pathology, clinical medicine
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License
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License undefined
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Identifiers
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Persistent URL
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https://folia.unifr.ch/unifr/documents/305617
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