Evaluation of the short- and long-term safety and therapy outcomes of the everolimus-eluting bioresorbable vascular scaffold system in patients with coronary artery stenosis: Rationale and design of the German-Austrian ABSORB RegIstRy (GABI-R)

被引:25
|
作者
Nef, Holger [1 ]
Wiebe, Jens [1 ]
Achenbach, Stefan [2 ]
Muenzel, Thomas [3 ]
Naber, Christoph [4 ]
Richardt, Gert [5 ]
Mehilli, Julinda [6 ]
Woehrle, Jochen [7 ]
Neumann, Till [8 ]
Biermann, Janine [8 ]
Zahn, Ralf [9 ]
Kastner, Johannes [10 ]
Schmermund, Axel [11 ]
Pfannebecker, Thomas [12 ]
Schneider, Steffen [13 ]
Limbourg, Tobias [13 ]
Hamm, Christian W. [1 ,14 ]
机构
[1] Univ Giessen, Med Klin 1, Dept Cardiol, Klin Str 33, D-35392 Giessen, Germany
[2] Univ Erlangen Nurnberg, Dept Cardiol, Med Klin 2, Erlangen, Germany
[3] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Med 2, Mainz, Germany
[4] Elisabeth Hosp, Klin Kardiol & Angiol, Essen, Germany
[5] Segeberger Kliniken GmbH, Herzzentrum, Bad Segeberg, Germany
[6] Ludwig Maximilians Univ Munchen, Dept Cardiol, Klinikum Grosshadern, Munich, Germany
[7] Univ Ulm, Dept Internal Med 2, Ulm, Germany
[8] Univ Essen Gesamthsch, Dept Cardiol, Essen, Germany
[9] Herzzentrum Ludwigshafen, Abt Kardiol, Ludwigshafen, Germany
[10] Univ Vienna, Sch Med, Dept Cardiol, Vienna, Austria
[11] CCB, Frankfurt, Germany
[12] Abbott Vasc Deutschland GmbH, Wetzlar, Germany
[13] Inst Herzinfarktforsch, Ludwigshafen, Germany
[14] Kerckhoff Heart & Thorax Ctr, Dept Cardiol, Bad Nauheim, Germany
关键词
Coronary artery disease; Bioresorbable scaffolds; BVS; Stenosis;
D O I
10.1016/j.carrev.2015.09.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Third-generation drug-eluting metal stents are the gold standard for treatment of coronary artery disease. The permanent metallic caging of the vessel, however, can result in limited vasomotion, chronic inflammation, and late expansive remodeling, conditions that can lead to late and very late stent thrombosis. The development of bioresorbable scaffolds (BRSs) promises advantages over metal stents due to complete biodegradation within 2-4 years. Theoretically, since vessel scaffolding is temporary and no permanent implant remains in the vessel, BRSs, as opposed to metal stents, once degraded would no longer be potential triggers for stent-related adverse events or side effects. Methods/design: The short-and long-term outcome after implantation of an everolimus-eluting, poly-L-lactic acid-based bioresorbable scaffold system (ABSORB, Abbott Vascular, Santa Clara, CA, USA) in the world-wide greatest all-comers cohort will be evaluated in the prospective, non-interventional, multicenter German-Austrian ABSORB RegIstRy (GABI-R). GABI-R will include over 5000 patients from about 100 study sites in Austria and Germany. Safety endpoints such as cardiac death, myocardial infarction, and clinically driven percutaneous or surgical target lesion and vessel revascularization will be evaluated during hospitalization and in the follow-up period (minimum of 5 years). Conclusion: Although two randomized controlled trials and several registries have documented safety and efficacy as well as non-inferiority of this everolimus-eluting ABSORB device compared with drug-eluting metal stents, the current knowledge regarding clinical application, treatment success, and long-term safety of using this BRS in daily routine is limited. Thus, the goal of GABI-R is to address this lack of information. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:34 / 37
页数:4
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