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Verfasst von:Harnek, Jan [VerfasserIn]   i
 Webb, John G. [VerfasserIn]   i
 Kuck, Karl-Heinz [VerfasserIn]   i
 Tschope, Carsten [VerfasserIn]   i
 Vahanian, Alec [VerfasserIn]   i
 Buller, Christopher E. [VerfasserIn]   i
 James, Stefan K. [VerfasserIn]   i
 Tiefenbacher, Christiane [VerfasserIn]   i
 Stone, Gregg W. [VerfasserIn]   i
Titel:Transcatheter implantation of the MONARC coronary sinus device for mitral Regurgitation
Titelzusatz:1-year results from the EVOLUTION phase I study (clinical evaluation of the Edwards Lifesciences Percutaneous Mitral Annuloplasty System for the treatment of Mitral Regurgitation)
Verf.angabe:Jan Harnek, John G. Webb, Karl-Heinz Kuck, Carsten Tschope, Alec Vahanian, Christopher E. Buller, Stefan K. James, Christiane P. Tiefenbacher, Gregg W. Stone
Jahr:2011
Umfang:8 S.
Fussnoten:Gesehen am 03.08.2022
Titel Quelle:Enthalten in: American College of CardiologyJACC Cardiovascular interventions
Ort Quelle:New York, NY : Elsevier, 2008
Jahr Quelle:2011
Band/Heft Quelle:4(2011), 1, Seite 115-122
ISSN Quelle:1876-7605
Abstract:Objectives - This study sought to assess the safety and efficacy of transcatheter valve annuloplasty in patients with mitral regurgitation (MR). - Background - Mitral regurgitation is associated with a worsened prognosis in patients with dilated cardiomyopathy. Surgical mitral annuloplasty reduces the septal-lateral dimension of the mitral annulus resulting in improved leaflet coaptation with a reduction in regurgitation. Percutaneous annuloplasty with the MONARC device (Edwards Lifesciences, Irvine, California) implanted within the coronary sinus is designed to reduce mitral regurgitation through a similar mechanism. - Methods - A total of 72 patients with MR grade ≥2 were enrolled at 8 participating centers in 4 countries. Clinical evaluation and transthoracic echocardiography were performed at baseline and at 3, 6, and 12 months. Multislice cardiac computed tomography and coronary angiography were performed at baseline and 3 months. - Results - The MONARC device was implanted in 59 of 72 patients (82%). The primary safety end point (freedom from death, tamponade, or myocardial infarction at 30 days) was met in 91% of patients at 30 days and in 82% at 1 year. Computed tomography imaging documented passage of the great cardiac vein over an obtuse marginal artery in 55% of patients and was associated with angiographic coronary artery compression in 15 patients and myocardial infarction in 2 patients (3.4%). At 12 months, a reduction in MR by ≥1 grade was observed in 50.0% of 22 implanted patients with matched echocardiograms and in 85.7% of 7 patients with baseline MR grade ≥3. - Conclusions - Implantation of the MONARC device in the coronary sinus is feasible and may reduce MR. However, coronary artery compression may occur in patients in whom the great cardiac vein passes over a coronary artery, necessitating strategies in future studies to avoid this occurrence.
DOI:doi:10.1016/j.jcin.2010.08.027
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1016/j.jcin.2010.08.027
 Volltext: https://www.sciencedirect.com/science/article/pii/S1936879810007971
 DOI: https://doi.org/10.1016/j.jcin.2010.08.027
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:annuloplasty
 coronary sinus
 heart failure
 mitral regurgitation
 mitral valve
K10plus-PPN:1813084491
Verknüpfungen:→ Zeitschrift

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