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Correlates and Impact of Coronary Artery Calcifications in Women Undergoing Percutaneous Coronary Intervention With Drug-Eluting Stents: From the Women in Innovation and Drug-Eluting Stents (WIN-DES) Collaboration.
Giustino, Gennaro; Mastoris, Ioannis; Baber, Usman; Sartori, Samantha; Stone, Gregg W; Leon, Martin B; Serruys, Patrick W; Kastrati, Adnan; Windecker, Stephan; Valgimigli, Marco; Dangas, George D; Von Birgelen, Clemens; Smits, Pieter C; Kandzari, David; Galatius, Soren; Wijns, William; Steg, P Gabriel; Stefanini, Giulio G; Aquino, Melissa; Morice, Marie-Claude; Camenzind, Edoardo; Weisz, Giora; Jeger, Raban V; Kimura, Takeshi; Mikhail, Ghada W; Itchhaporia, Dipti; Mehta, Laxmi; Ortega, Rebecca; Kim, Hyo-Soo; Chieffo, Alaide; Mehran, Roxana.
Afiliação
  • Giustino G; Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Mastoris I; Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Baber U; Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Sartori S; Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Stone GW; Department of Cardiology, Columbia University Medical Center, New York, New York.
  • Leon MB; Department of Cardiology, Columbia University Medical Center, New York, New York.
  • Serruys PW; Department of Cardiology, Erasmus MC, Rotterdam, the Netherlands.
  • Kastrati A; Department of Cardiology, Herzzentrum, Munich, Germany.
  • Windecker S; Department of Cardiology, Bern University Hospital, Bern, Switzerland.
  • Valgimigli M; Department of Cardiology, Bern University Hospital, Bern, Switzerland.
  • Dangas GD; Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Von Birgelen C; Department of Cardiology, Thoraxcentrum Twente, Enschede, the Netherlands.
  • Smits PC; Department of Cardiology, Maasstad Hospital, Rotterdam, the Netherlands.
  • Kandzari D; Piedmont Heart Institute, Atlanta, Georgia.
  • Galatius S; Department of Cardiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Wijns W; Cardiovascular Center Aalst, Onze-Lieve-Vrouwziekenhuis Ziekenhuis, Aalst, Belgium.
  • Steg PG; Département Hospitalo Universitaire Fibrose, Inflammation et Remodelage, Assistance Publique-Hôpitaux de Paris, Université Paris Diderot, INSERM U114, Paris, France.
  • Stefanini GG; Division of Clinical and Interventional Cardiology, Humanitas Research Hospital, Rozzano, Milan, Italy.
  • Aquino M; Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Morice MC; Department of Cardiology and Cardiovascular Surgery, Institut Cardiovasculaire Paris Sud, Paris, France.
  • Camenzind E; Department of Cardiology, Institut Lorrain du Coeur et des Vaisseaux University Hospital Nancy - Brabois, Vandoeuvre-lès-Nancy, France.
  • Weisz G; Department of Cardiology, Shaare Zedek Medical Center, Jerusalem, Israel; Columbia University Medical Center, New York, New York.
  • Jeger RV; Department of Cardiology, University Hospital Basel, Basel, Switzerland.
  • Kimura T; Department of Cardiology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Mikhail GW; Department of Cardiology, Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Itchhaporia D; Department of Cardiology, Hoag Memorial Hospital Presbyterian, Newport Beach, California.
  • Mehta L; Department of Cardiology, The Ohio State University Medical Center, Columbus, Ohio.
  • Ortega R; Duke Clinical Research Institute, Durham, North Carolina.
  • Kim HS; Department of Cardiology, Seoul National University Main Hospital, Seoul, Korea.
  • Chieffo A; Cardiothoracic Department, San Raffaele Scientific Institute, Milan, Italy.
  • Mehran R; Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York. Electronic address: roxana.mehran@mountsinai.org.
JACC Cardiovasc Interv ; 9(18): 1890-901, 2016 09 26.
Article em En | MEDLINE | ID: mdl-27659564
OBJECTIVES: The aim of this study was to investigate the clinical correlates and prognostic impact of coronary artery calcification (CAC) in women undergoing percutaneous coronary intervention with drug-eluting stents (DES). BACKGROUND: The clinical correlates and the prognostic significance of CAC in women undergoing percutaneous coronary intervention with DES remain unclear. METHODS: Patient-level data from female participants in 26 randomized trials of DES were pooled. Study population was categorized according to the presence of moderate or severe versus mild or no target lesion CAC, assessed through coronary angiography. Co-primary endpoints of interest were the composite of death, myocardial infarction (MI), or target lesion revascularization and death, MI, or stent thrombosis at 3-year follow-up. RESULTS: Among 11,557 women included in the pooled dataset, CAC status was available in 6,371 women. Of these, 1,622 (25.5%) had moderate or severe CAC. In fully adjusted models, independent correlates of CAC were age, hypertension, hypercholesterolemia, smoking, previous coronary artery bypass graft surgery, and worse left ventricular and renal function. At 3 years, women with CAC were at higher risk for death, MI, or target lesion revascularization (18.2% vs. 13.1%; adjusted hazard ratio: 1.56; 95% confidence interval: 1.33 to 1.84; p < 0.0001) and death, MI, or stent thrombosis (12.7% vs. 8.6%; adjusted hazard ratio: 1.48; 95% confidence interval: 1.21 to 1.80; p = 0.0001). The adverse effect of CAC on ischemic outcomes appeared to be consistent across clinical and angiographic subsets of women, including new-generation DES. CONCLUSIONS: Women undergoing PCI of calcified lesions tend to have worse clinical profile and remain at increased ischemic risk, irrespective of new-generation DES.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Stents Farmacológicos / Calcificação Vascular / Intervenção Coronária Percutânea Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: JACC Cardiovasc Interv Assunto da revista: ANGIOLOGIA / CARDIOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Stents Farmacológicos / Calcificação Vascular / Intervenção Coronária Percutânea Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: JACC Cardiovasc Interv Assunto da revista: ANGIOLOGIA / CARDIOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de publicação: Estados Unidos