MusicSarreV3, France, Analysis, bibRecord, 000036

Clinical and angiographic performance of a new‐generation modular stent design for treatment of de novo coronary lesions

Identifieur interne : 000036 ( France/Analysis ); précédent : 000035; suivant : 000037

Clinical and angiographic performance of a new‐generation modular stent design for treatment of de novo coronary lesions

Auteurs : Victor M. Legrand [Belgique] ; Eulogio J. Garcia [Espagne] ; Eberhard Grube [Allemagne] ; Khalife Khalife [France] ; Hans Bonnier [Pays-Bas] ; Philippe Commeau [France] ; Tadeusz Przewlocki [Pologne] ; Carlos Macaya [Espagne] ; Adam Witkowski [Pologne]

Source :

Catheterization and Cardiovascular Interventions [ 1522-1946 ] ; 2001-11.

RBID : ISTEX:4E2113C7A267412B46862F48380B04788ED73C1E

English descriptors

Abstract

The objectives of the Race Car study were to assess the safety and efficacy of the Medtronic AVE S670 stent, a new‐generation stent with a modular design consisting of interconnected sinusoidal rings allowing improved flexibility with good conformability and scaffolding. A total of 285 stents were implanted in 267 patients with (un)stable angina pectoris who underwent angioplasty of a single de novo lesion in a native coronary artery with a diameter between 3.0 and 4.0 mm. Available stent lengths were 9, 12, and 15 mm. The primary endpoint was the 6‐month restenosis rate. Secondary endpoints were device and procedural success and major adverse cardiac event (MACE)‐free survival at 1 and 6 months. All patients received the study stents and no other stents were used (angiographic success: 100%). Eight patients experienced a MACE during hospital admission (Q‐wave MI in 2, non–Q‐wave MI in 4, TLR in 2). A procedural success was obtained in 97% of the patients. There were no additional events at 1 month. The clinical endpoints encountered at 6 months were Q‐wave MI in 1, bypass surgery in 3, and repeat angioplasty in 25 (MACE‐free survival: 86.5%). Quantitative angiographic results were the minimum lumen diameter increased from 1.05 ± 0.32 before to 2.73 ± 0.39 mm after stent implantation. At follow‐up, the loss in diameter was 0.74 ± 0.50 mm. The loss index was 0.45 ± 0.31 and restenosis rate was 13.4%. This study has demonstrated that the S670 stent in patients with (un)stable angina pectoris requiring intervention of a single lesion has a low acute and 6‐month major event rate and a low angiographic restenosis rate. Cathet Cardiovasc Intervent 2001;54:276–282. © 2001 Wiley‐Liss, Inc.

Url:

https://api.istex.fr/document/4E2113C7A267412B46862F48380B04788ED73C1E/fulltext/pdf

DOI: 10.1002/ccd.1284

Affiliations:

Allemagne, Belgique, Espagne, France, Pays-Bas, Pologne
Basse-Normandie, Communauté de Madrid, Grand Est, Lorraine (région), Province de Liège, Région Normandie
Caen, Liège, Madrid, Metz

Links toward previous steps (curation, corpus...)

to stream Istex, to step Corpus: 000826
to stream Istex, to step Curation: 000786
to stream Istex, to step Checkpoint: 000B25
to stream Main, to step Merge: 000D35
to stream Main, to step Curation: 000D34
to stream Main, to step Exploration: 000D34
to stream France, to step Extraction: 000036

Links to Exploration step

ISTEX:4E2113C7A267412B46862F48380B04788ED73C1E

Le document en format XML

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<author><name sortKey="Przewlocki, Tadeusz" sort="Przewlocki, Tadeusz" uniqKey="Przewlocki T" first="Tadeusz" last="Przewlocki">Tadeusz Przewlocki</name>
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<term>coronary disease</term>
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<keywords scheme="Teeft" xml:lang="en"><term>Acute gain</term>
<term>Angina pectoris</term>
<term>Angiographic</term>
<term>Angiographic evaluation</term>
<term>Angiographic result</term>
<term>Angiographic results</term>
<term>Angiographic success</term>
<term>Angiographic success rate</term>
<term>Angiography</term>
<term>Angioplasty</term>
<term>Balloon angioplasty</term>
<term>Benestent</term>
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<term>Cardiac event survival</term>
<term>Cardiovasc intervent</term>
<term>Catharina hospital</term>
<term>Cathet cardiovasc diagn</term>
<term>Cathet cardiovasc intervent</term>
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<term>Coronary artery disease</term>
<term>Coronary stent system</term>
<term>Hospital discharge</term>
<term>Implantation</term>
<term>Infarction</term>
<term>Invas cardiol</term>
<term>John paul</term>
<term>Krankenhaus siegburg gmbh</term>
<term>Legrand</term>
<term>Lesion</term>
<term>Lesion length</term>
<term>Loss index</term>
<term>Lumen</term>
<term>Medtronic</term>
<term>Minimal lumen diameter</term>
<term>Minimum lumen diameter</term>
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<term>Modular stent design</term>
<term>Myocardial infarction</term>
<term>National institute</term>
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<term>Percent diameter stenosis</term>
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<term>Present study</term>
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<term>Procedural success rate</term>
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<term>Reference vessel diameter</term>
<term>Residual diameter stenosis</term>
<term>Restenosis</term>
<term>Restenosis rate</term>
<term>Second stent</term>
<term>Secondary endpoints</term>
<term>Serruys</term>
<term>Single lesion</term>
<term>Statistical analysis</term>
<term>Stenosis</term>
<term>Stent</term>
<term>Stent design</term>
<term>Stent implantation</term>
<term>Stent thrombosis</term>
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<front><div type="abstract" xml:lang="en">The objectives of the Race Car study were to assess the safety and efficacy of the Medtronic AVE S670 stent, a new‐generation stent with a modular design consisting of interconnected sinusoidal rings allowing improved flexibility with good conformability and scaffolding. A total of 285 stents were implanted in 267 patients with (un)stable angina pectoris who underwent angioplasty of a single de novo lesion in a native coronary artery with a diameter between 3.0 and 4.0 mm. Available stent lengths were 9, 12, and 15 mm. The primary endpoint was the 6‐month restenosis rate. Secondary endpoints were device and procedural success and major adverse cardiac event (MACE)‐free survival at 1 and 6 months. All patients received the study stents and no other stents were used (angiographic success: 100%). Eight patients experienced a MACE during hospital admission (Q‐wave MI in 2, non–Q‐wave MI in 4, TLR in 2). A procedural success was obtained in 97% of the patients. There were no additional events at 1 month. The clinical endpoints encountered at 6 months were Q‐wave MI in 1, bypass surgery in 3, and repeat angioplasty in 25 (MACE‐free survival: 86.5%). Quantitative angiographic results were the minimum lumen diameter increased from 1.05 ± 0.32 before to 2.73 ± 0.39 mm after stent implantation. At follow‐up, the loss in diameter was 0.74 ± 0.50 mm. The loss index was 0.45 ± 0.31 and restenosis rate was 13.4%. This study has demonstrated that the S670 stent in patients with (un)stable angina pectoris requiring intervention of a single lesion has a low acute and 6‐month major event rate and a low angiographic restenosis rate. Cathet Cardiovasc Intervent 2001;54:276–282. © 2001 Wiley‐Liss, Inc.</div>
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Clinical and angiographic performance of a new‐generation modular stent design for treatment of de novo coronary lesions

Clinical and angiographic performance of a new‐generation modular stent design for treatment of de novo coronary lesions

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri