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    Outcomes in patients with peripheral vascular disease following percutaneous coronary intervention

    92931.pdf (790.6Kb)
    Access Status
    Open access
    Authors
    Ramzy, J.
    Andrianopoulos, N.
    Roberts, L.
    Duffy, S.J.
    Clark, D.
    Teh, A.W.
    Ajani, A.E.
    Reid, Christopher
    Brennan, A.
    Freeman, M.
    Date
    2019
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Ramzy, J. and Andrianopoulos, N. and Roberts, L. and Duffy, S.J. and Clark, D. and Teh, A.W. and Ajani, A.E. et al. 2019. Outcomes in patients with peripheral vascular disease following percutaneous coronary intervention. Catheterization and Cardiovascular Interventions. 94 (4): pp. 588-597.
    Source Title
    Catheterization and Cardiovascular Interventions
    DOI
    10.1002/ccd.28145
    ISSN
    1522-1946
    Faculty
    Faculty of Health Sciences
    School
    Curtin School of Population Health
    Funding and Sponsorship
    http://purl.org/au-research/grants/nhmrc/1111170
    Remarks

    This is the peer reviewed version of the following article: Ramzy, J, Andrianopoulos, N, Roberts, L, et al. Outcomes in patients with peripheral vascular disease following percutaneous coronary intervention. Catheter Cardiovasc Interv. 2019; 94: 588–597, which has been published in final form at https://doi.org/10.1002/ccd.28145. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.

    URI
    http://hdl.handle.net/20.500.11937/93107
    Collection
    • Curtin Research Publications
    Abstract

    Objectives: To evaluate the clinical characteristics and outcomes of patients with peripheral vascular disease (PVD) undergoing percutaneous coronary intervention (PCI) in a contemporary setting, and to determine whether use of drug-eluting stents (DESs) improves outcomes. Background: PVD was an independent risk factor for adverse outcomes following PCI in the bare-metal stent (BMS) era. It is not known whether outcomes in these patients have improved with advances in interventional techniques and stent technology, as they have for the general population. Methods: Eighteen thousand three hundred and eighty patients undergoing PCI from an Australian registry between 2005 and 2013 were studied. Clinical and procedural data, 30-day and 12-month outcomes were compared in those with and without a reported history of PVD. Outcomes were also compared between patients with PVD who received DES and those who received BMS. Long-term mortality was compared using Australian National Death Index (NDI) linkage. Results: Patients with PVD (n = 1,251, 6.8%) were older and had more prevalent diabetes, hypertension, cerebrovascular disease, heart failure, renal impairment, ostial lesions, left main, and multi-vessel disease (p < 0.001). Patients with PVD had significantly higher rates of major adverse cardiovascular events (MACEs) compared with those without PVD, in-hospital (5.7% vs. 4.1%, p < 0.008), at 30-days (8.6% vs. 5.8%, p < 0.001) and at 12-months (24.6% vs. 13.2%, p < 0.001). At 4.9 ± 2.6 years follow-up, there was significantly greater mortality in the PVD group. PVD patients who received DES experienced significantly less MACE than PVD patients treated with BMS at 30-days (4.8 vs. 10.1%, p < 0.001) and 12-months (19.4 vs. 26.4%, p < 0.005). Conclusions: PVD is an independent predictor of adverse outcomes in patients undergoing PCI. PVD patient who received DES had improved outcomes compared with those receiving BMS.

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