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Drug-eluting stents appear superior to bare metal stents for vein-graft PCI in vessels up to a stent diameter of 4 mm.
Guttmann, Oliver P; Jones, Daniel A; Safwan, Kassem A; Gallagher, Sean; Rathod, Krishnaraj S; Hamshere, Steve; Smith, Elliot J; Jain, Ajay K; Mathur, Anthony; Wragg, Andrew; Knight, Charles J; Weerackody, Roshan.
Afiliação
  • Guttmann OP; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Jones DA; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Safwan KA; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Gallagher S; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Rathod KS; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Hamshere S; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Smith EJ; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Jain AK; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Mathur A; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Wragg A; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Knight CJ; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
  • Weerackody R; Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London - UK; NIHR Cardiovascular Biomedical Research Unit, Barts Heart Centre, Barts Health NHS Trust, London - UK.
Heart Int ; 11(1): e17-e24, 2016.
Article em En | MEDLINE | ID: mdl-27924213
ABSTRACT

BACKGROUND:

Research trials have shown improved short-term outcome with drug-eluting stents (DES) over bare metal stents (BMS) in saphenous vein graft (SVG) percutaneous coronary intervention (PCI), primarily by reducing target vessel revascularization (TVR) for in-stent restenosis. We compared the outcomes in patients undergoing SVG stent implantation treated with DES or BMS. In exploratory analyses we investigated the influence of stent generation and diameter.

METHODS:

Data were obtained from a prospective database of 657 patients who underwent PCI for SVG lesions between 2003 and 2011. A total of 344 patients had PCI with BMS and 313 with DES. Propensity scores were developed based on 15 observed baseline covariates in a logistic regression model with stent type as the dependent variable. The nearest-neighbour-matching algorithm with Greedy 5-1 Digit Matching was used to produce two patient cohorts of 313 patients each. We assessed major adverse cardiac events (MACE) out to a median of 3.3 years (interquartile range 2.1-4.1). MACE was defined as all-cause mortality, myocardial infarction (MI), TVR and stroke.

RESULTS:

There was a significant difference in MACE between the two groups in favour of DES (17.9% DES vs. 31.2% BMS group; p = 0.0017) over the 5-year follow-up period. MACE was driven by increased TVR in the BMS group. There was no difference in death, MI or stroke. Adjusted Cox analysis confirmed a decreased risk of MACE for DES compared with BMS 0.75 (95% confidence interval (CI) 0.52-0.94), with no difference in the hazard of all-cause mortality (hazard ratio 1.08; 95% CI 0.77-1.68). However, when looking at stent diameters greater than 4 mm, no difference was seen in MACE rates between BMS and DES.

CONCLUSIONS:

Overall in our cohort of patients who had PCI for SVG disease, DES use resulted in lower MACE rates compared with BMS over a 5-year follow-up period; however, for stent diameters over 4 mm no difference in MACE rates was seen.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article