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    Sex disparity in secondary prevention pharmacotherapy and clinical outcomes following acute coronary syndrome

    Access Status
    Open access via publisher
    Authors
    Dagan, M.
    Dinh, D.T.
    Stehli, J.
    Tan, C.
    Brennan, A.
    Warren, J.
    Ajani, A.E.
    Freeman, M.
    Murphy, A.
    Reid, Christopher
    Hiew, C.
    Oqueli, E.
    Clark, D.J.
    Duffy, S.J.
    Date
    2022
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Dagan, M. and Dinh, D.T. and Stehli, J. and Tan, C. and Brennan, A. and Warren, J. and Ajani, A.E. et al. 2022. Sex disparity in secondary prevention pharmacotherapy and clinical outcomes following acute coronary syndrome. European Heart Journal - Quality of Care and Clinical Outcomes. 8 (4): pp. 420-428.
    Source Title
    European Heart Journal - Quality of Care and Clinical Outcomes
    DOI
    10.1093/ehjqcco/qcab007
    ISSN
    2058-5225
    Faculty
    Faculty of Health Sciences
    School
    Curtin School of Population Health
    Funding and Sponsorship
    http://purl.org/au-research/grants/nhmrc/1111170
    URI
    http://hdl.handle.net/20.500.11937/93092
    Collection
    • Curtin Research Publications
    Abstract

    Aims: We sought to investigate if sex disparity exists for secondary prevention pharmacotherapy following acute coronary syndrome (ACS) and impact on long-term clinical outcomes. Methods and results: We analysed data on medical management 30-day post-percutaneous coronary intervention (PCI) for ACS in 20 976 patients within the multicentre Melbourne Interventional Group registry (2005-2017). Optimal medical therapy (OMT) was defined as five guideline-recommended medications, near-optimal medical therapy (NMT) as four medications, sub-optimal medical therapy (SMT) as ≤3 medications. Overall, 65% of patients received OMT, 27% NMT and 8% SMT. Mean age was 64 ± 12 years; 24% (4931) were female. Women were older (68 ± 12 vs. 62 ± 12 years) and had more comorbidities. Women were less likely to receive OMT (61% vs. 66%) and more likely to receive SMT (10% vs. 8%) compared to men, P < 0.001. On long-term follow-up (median 5 years, interquartile range 2-8 years), women had higher unadjusted mortality (20% vs. 13%, P < 0.001). However, after adjusting for medical therapy and baseline risk, women had lower long-term mortality [hazard ratio (HR) 0.88, 95% confidence interval (CI) 0.79-0.98; P = 0.02]. NMT (HR 1.17, 95% CI 1.05-1.31; P = 0.004) and SMT (HR 1.79, 95% CI 1.55-2.07; P < 0.001) were found to be independent predictors of long-term mortality. Conclusion: Women are less likely to be prescribed optimal secondary prevention medications following PCI for ACS. Lower adjusted long-term mortality amongst women suggests that as well as baseline differences between gender, optimization of secondary prevention medical therapy amongst women can lead to improved outcomes. This highlights the need to focus on minimizing the gap in secondary prevention pharmacotherapy between sexes following ACS.

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